| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs74703437 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11027046 | AGGCGATTGAGGAAG[A/C]TTCTGTTTTCTTTGA | 9678 |
| rs74719549 | snp | C/T | 0.158632 | 0.232706 | intron-variant | PHF14 | GRCh38.p7 | 7:11153400 | CTTTTTTAGTGGGGG[C/T]AGGGGAAGTTTAGGG | 9678 |
| rs74722607 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11046367 | GTGTTGCCTTTTCCA[A/G]TTGTTTGAAGAATAT | 9678 |
| rs74789084 | snp | A/T | 0.0659589 | 0.169201 | intron-variant | PHF14 | GRCh38.p7 | 7:11081359 | ATTAGCTCAATTTTT[A/T]TATAAGAATATTCTT | 9678 |
| rs74789711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045711 | AAAAGATGGATACAG[A/T]TACAGAAGTAATTAT | 9678 |
| rs74790522 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | PHF14 | GRCh38.p7 | 7:11059327 | ACTACATGATACATT[G/T]GCTAGTTCATTACCT | 9678 |
| rs74795853 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11058713 | AGTTTAAGTATTTAC[A/G]TGCAATAAGAGATTT | 9678 |
| rs74846870 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | PHF14 | GRCh38.p7 | 7:11047994 | AAACCTCTTGGTATT[C/T]CAACATGAAAGTTAT | 9678 |
| rs74871510 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11025105 | CTTTGAAGGGGTTGA[A/G]GAATTCAGTGGAGGA | 9678 |
| rs74874929 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11015821 | TTAGCTCATGCATAG[A/T]TTTTTTTTTTTTTTT | 9678 |
| rs74914205 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967020 | GAGTCCATTCATTAC[A/G]GTGTCTTCAACAAGG | 9678 |
| rs74920226 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10980782 | CCATGGACTTCACTG[G/T]GGGTATTAGTGTAAT | 9678 |
| rs74926055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151130 | TTTTCTGAGTAATTG[C/T]TGAACATGTATATTA | 9678 |
| rs74937198 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11008147 | TGCCCTCAGGTTTAG[G/T]TGCTATTCATTAAAT | 9678 |
| rs74969214 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11149020 | TAGGGTTTTTTTTTT[G/T]TTTTGTTTTGTTTTC | 9678 |
| rs74969979 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PHF14 | GRCh38.p7 | 7:11095662 | GGATTTTAAATTGTA[C/T]TCATTATCTACTAAA | 9678 |
| rs74985104 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:10989297 | CTGTTGAAATGATGG[C/T]TCCAAATGTTACTTT | 9678 |
| rs75003737 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119909 | GGAATCTTTCCTAGG[C/T]GTGATAAGTTGTAAA | 9678 |
| rs75014528 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11081869 | TCAAAAAAAAAAAAA[A/G]AGATTTATGATCTTA | 9678 |
| rs75016615 | snp | A/C | 0.109108 | 0.206518 | intron-variant | PHF14 | GRCh38.p7 | 7:11117721 | AGGAGTATCTTGCCA[A/C]AATACATTAAACAAG | 9678 |
| rs75060983 | snp | A/T | 0.109108 | 0.206518 | intron-variant | PHF14 | GRCh38.p7 | 7:11059817 | CATTATGCAAATTAG[A/T]TAATAGAGTACCAAA | 9678 |
| rs75088490 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | PHF14 | GRCh38.p7 | 7:11158925 | CCTAACTGAAAATCT[A/G]TTATCTAGATATTTT | 9678 |
| rs75142165 | snp | A/G/T | 0.0001237 | 0.00786349 | nc-transcript-variant, synonymous-codon, missense | PHF14 | GRCh38.p7 | 7:11111389 | CCATTTTGGCTGTTT[A/G/T]GATCCTCCTTTGAAA | 9678 |
| rs75173620 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11083099 | AATGTTCAGAGAATC[A/G]GGTCTAGCTTAGATT | 9678 |
| rs75198836 | snp | A/T | 0.0126979 | 0.078662 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108075 | ATTTTGGCCATCCAC[A/T]TTGTTCTTTGATTTC | 9678 |
| rs75204543 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11016764 | TTACCCTCTTTAAGT[A/T]ATTTTTAAGTGTACA | 9678 |
| rs75235655 | in-del | -/ATT/TTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145296 | TCTCTTTTTCTCTCT[-/ATT/TTA]TWTTTAAAATTCCAT | 9678 |
| rs75236554 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072699 | CTGTTTACATTGCTA[G/T]AAATACCTGAGGCTA | 9678 |
| rs75271767 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151073 | AATAGAATCTTAGAC[-/A]AAAAAAACCTGTCAT | 9678 |
| rs75273318 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074094 | TTCAATGCCTTTCCC[C/T]CATGTCTTGGCTATT | 9678 |
| rs75284265 | snp | A/C | 0.0437281 | 0.141251 | intron-variant | PHF14 | GRCh38.p7 | 7:11001301 | TGATTACTGCAGCTT[A/C]ATAGTAAGTCTTGAA | 9678 |
| rs75290373 | snp | A/C | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11029213 | CTGTGTCTTTAGTAT[A/C]TCTGTTACTATCTCT | 9678 |
| rs75327686 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11082414 | CATGAAACAAAGTCA[A/G]TTCTCTTTTTGTTTG | 9678 |
| rs75328279 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11119029 | CCACTTTCTAAATTA[C/T]GCTTACTACAAACTT | 9678 |
| rs75331171 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | PHF14 | GRCh38.p7 | 7:11001562 | TTAGTTCTTTGATTT[C/T]TTTCATCAGAGTTTT | 9678 |
| rs75345872 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11109810 | AGTACTGTTGGTCCT[A/G]TTGGTCCTATTTGAT | 9678 |
| rs75376130 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | PHF14 | GRCh38.p7 | 7:11119202 | TTTAAAAGTCGCAAA[C/T]CTCATACTGTCCTGT | 9678 |
| rs75430591 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11164942 | ACATTCTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 9678 |
| rs75431535 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | PHF14 | GRCh38.p7 | 7:11067037 | GGTAAAAAGGTTAAC[C/T]CATAGGATAGGGGGG | 9678 |
| rs75443787 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11048868 | TCTGCATTGGCAGTT[A/T]CATTTGTTTTGATTT | 9678 |
| rs75450917 | snp | A/G | 0.0789645 | 0.182653 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066385 | TCACCTCAGCCTCCC[A/G]AGTAGCTGAGACTTG | 9678 |
| rs75459403 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137129 | TTCTTAAGATTTAAT[A/C]TCTCAGGTTTTCTTG | 9678 |
| rs75496100 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11134870 | ATTCAGTAGAGCAAC[A/T]TATAGACCACCAAGT | 9678 |
| rs75519634 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11154979 | AGCTAGAAAAAAAAA[G/T]CACTGTTTTTGAAGA | 9678 |
| rs75522083 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | PHF14 | GRCh38.p7 | 7:11127960 | TTCCTGAACTCCTCT[C/G]AAGACCTCCAGGCCA | 9678 |
| rs75537646 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11110295 | CAGATTTCTTGACAT[C/T]TGAAGTTTTAAATCA | 9678 |
| rs75556694 | snp | C/T | 0.104504 | 0.2033 | intron-variant | PHF14 | GRCh38.p7 | 7:11114807 | CAAAACATACCTTCT[C/T]GCATAGGCTATGCTT | 9678 |
| rs75572557 | snp | C/T | 0.0271762 | 0.113356 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968885 | TATTTGAAGTTTTAT[C/T]CAGGAGAGAAATGCT | 9678 |
| rs75601401 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955894 | AAAATACACGTAAAC[A/G]TAGTTGGCCCATGGT | 9678 |
| rs75612541 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107386 | ATTTTGTTAATGGGT[A/G]AAAGACCATATATTA | 9678 |
| rs75636689 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PHF14 | GRCh38.p7 | 7:10994527 | ACTGGGTGAGCAAGC[C/T]GGTTAGTGGTGGGAG | 9678 |
| rs75648961 | snp | A/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11094048 | CATTCCTTAAAGGAG[A/T]AGGGTCTGGGTGAGA | 9678 |
| rs75658225 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11052662 | TCCAGTGTGGTACAG[A/G]GAAAATAGTATCTTG | 9678 |
| rs75669786 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PHF14 | GRCh38.p7 | 7:11151721 | GTCATGCATGGCCCT[A/G]GCTCTGTAGAGGCTT | 9678 |
| rs75707029 | snp | C/T | 0.110519 | 0.207473 | intron-variant | PHF14 | GRCh38.p7 | 7:11100361 | CCCAGACTATGTTTT[C/T]TGGTCTTTGACTCTA | 9678 |
| rs75764265 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11003426 | TAAGCCAGTGTTTAC[C/T]GTTTGTCTTCCTGTT | 9678 |
| rs75766306 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061713 | ACATTTAACAGAGGA[A/C]ATTTATATTTATTAT | 9678 |
| rs75768974 | snp | A/G | 0.0752113 | 0.178743 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973113 | CCTTTGCATAGAGGT[A/G]TACCACTTTGTAACT | 9678 |
| rs75774863 | in-del | -/TTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004364 | GGCTTTTTTTTTTTT[-/TTT]GGTTGCTTGCTCATA | 9678 |
| rs75789907 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11007195 | CGAAACTCCGTCTCA[A/C]AAAAAAAAAAGAAAG | 9678 |
| rs75791995 | snp | A/G | 0.040671 | 0.13668 | intron-variant | PHF14 | GRCh38.p7 | 7:11121187 | CTTTTTATTATATAC[A/G]TGTGGGATCTTTTAA | 9678 |
| rs75890304 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11003427 | AAGCCAGTGTTTACC[A/G]TTTGTCTTCCTGTTA | 9678 |
| rs75893503 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11035121 | GTTTGAAAAAAAAAA[A/G]GCGTAATAAAAAAGA | 9678 |
| rs75906406 | snp | A/C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11144610 | ATATATTTATATAAT[A/C/T]ATATATAATTATATT | 9678 |
| rs75924081 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11009387 | TTTATTTTCTTAAAT[A/G]TGAGTTGTGTACATT | 9678 |
| rs75970759 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11166836 | TCCTCAGCACAAAGA[A/C]AGGTGTGAAACAGTT | 9678 |
| rs75979260 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:10981635 | ATTCATCAATTTCTT[C/T]CATTCTAGAGCATAT | 9678 |
| rs75990525 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11014890 | TGCCATCTTCCATGT[G/T]TTTTTTTTTTTTACA | 9678 |
| rs76006772 | snp | G/T | 0.030665 | 0.119967 | intron-variant | PHF14 | GRCh38.p7 | 7:11067626 | TCTCTTAGTCCATTT[G/T]ATGTTGCTAAGAAGA | 9678 |
| rs76029462 | snp | A/G/T | 0.070099 | 0.173832 | intron-variant | PHF14 | GRCh38.p7 | 7:11028307 | TGGATTCTGCTGAGC[A/G/T]TGTATTGTTTTTGCA | 9678 |
| rs76037354 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11000304 | CTTTCTGTTGTATGA[C/T]GTGGAGTATCTTTTC | 9678 |
| rs76054340 | snp | C/T | 0.081446 | 0.184634 | intron-variant | PHF14 | GRCh38.p7 | 7:11111111 | TCTACTGTCAGTGTT[C/T]TAAATATTTGTTTTG | 9678 |
| rs76121455 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11051224 | TTTCTTTTTTTTTTT[G/T]TGAAGACAGTCTCTC | 9678 |
| rs76152108 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:10990465 | AGAGGAGAGAGAATA[C/T]GAAGCTTGCAGAGAA | 9678 |
| rs76176059 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10980081 | ATTAATTGGCATTGG[C/T]AACTACCAAAACAAA | 9678 |
| rs76178093 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11067754 | AGGACCTCAAGGTGC[C/T]TTCACTCATGGTGAA | 9678 |
| rs76206106 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089106 | GATATAAAAAAAAAA[-/AA]CCGTAGCCCTGATCA | 9678 |
| rs76221436 | snp | A/T | 0.0807149 | 0.183963 | intron-variant | PHF14 | GRCh38.p7 | 7:11122765 | CCACATTGTCCTTCC[A/T]CTGCCCTATAGTTCC | 9678 |
| rs76241129 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | PHF14 | GRCh38.p7 | 7:11021920 | TGTAGCATGCATAGC[C/T]TCTGAAGTTGTGATA | 9678 |
| rs76258662 | snp | A/G | 0.5 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963657 | GCACTGTCAACATTA[A/G]ACAGATCAATGAGAC | 9678 |
| rs76259824 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11054833 | TCTGTCTTGTAATAC[A/G]TTATTATAGTATTTT | 9678 |
| rs76261133 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10984425 | GTTGTCATTTGGGAA[A/G]TAGTGTAATATTTTT | 9678 |
| rs76262122 | snp | A/G | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10969812 | TGTTGCCTTTTTTTA[A/G]GGTAACACAAATTCA | 9678 |
| rs76322253 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105521 | CAGAATATTTACATC[A/G]TTAAATTTTTAAAAA | 9678 |
| rs76352451 | snp | G/T | 0.0659589 | 0.169201 | intron-variant | PHF14 | GRCh38.p7 | 7:11067632 | AGTCCATTTTATGTT[G/T]CTAAGAAGAAATACC | 9678 |
| rs76391370 | snp | C/T | 0.0450141 | 0.143111 | intron-variant | PHF14 | GRCh38.p7 | 7:11038901 | AGTTCTTGCTCCCTA[C/T]ATGATTTTCAAAGAA | 9678 |
| rs76404209 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PHF14 | GRCh38.p7 | 7:11052223 | TAGGTTTTGAATTTC[A/G]TATGAATGGAATCAA | 9678 |
| rs76427517 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966384 | TGTAGAAAGTGCATG[C/T]TGATTGGTCTATGGG | 9678 |
| rs76455189 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106074 | CTAATTCTTCTCTCA[G/T]GCTGTGAAGAGTTGC | 9678 |
| rs76476085 | snp | A/G | 0.112631 | 0.208878 | intron-variant | PHF14 | GRCh38.p7 | 7:11161900 | GCATACACTTCATGC[A/G]TATTTCCCAGATATT | 9678 |
| rs76481989 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:10989385 | ATGAAAAATATATAT[C/T]GTGTATTGTATGAAA | 9678 |
| rs76487214 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11156493 | TCACTTGGTAGTAAA[A/G]TTTTAGAAATTCACT | 9678 |
| rs76510195 | snp | A/T | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10969296 | GTGAGGTAATTCACA[A/T]GTTCAATTAGTTTAA | 9678 |
| rs76520082 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11127611 | ACAAACTCTGAGTAA[A/T]TTTTAGAAAATTCCT | 9678 |
| rs76528857 | snp | A/C | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11054024 | GCATGTTGAAGCTCC[A/C]AAAAAAAAAAATCCT | 9678 |
| rs76549024 | snp | A/C | 0.0166325 | 0.0896639 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170178 | TTTCTTTGGCTTAGA[A/C]ATTTTTCAAAATTCA | 9678 |
| rs76569318 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:11013519 | CCTTTAATGCTTTTA[C/T]AGTAGGACTAAAACT | 9678 |
| rs76595498 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | PHF14 | GRCh38.p7 | 7:11089730 | AGTGTGACTTTATGA[C/T]GTGACTTTAGTGTAG | 9678 |
| rs76602008 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11004271 | AAAAAAAAAAAAAAG[A/G]AAAGAAAAAGAAAAC | 9678 |
| rs76635182 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11069547 | TTTATGTATTTTTTT[A/T]AATTTTATTTGCTAA | 9678 |
| rs76639500 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959940 | CTGGAGGGTGAGCAA[A/G]GCAGAGAAGAGCTTT | 9678 |
| rs76737879 | snp | G/T | | | splice-donor-variant, intron-variant | PHF14 | GRCh38.p7 | 7:10983161 | GCAAGAGTAATGAGG[G/T]AGATCAACCCAATTT | 9678 |
| rs76777262 | snp | C/T | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:10980077 | ATTAATTAATTGGCA[C/T]TGGCAACTACCAAAA | 9678 |
| rs76777324 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144578 | AATTTATAATATATA[A/G]AATATAAATTAATGT | 9678 |
| rs76780745 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11012865 | ATCATAGAGTTAGAG[A/G]TTGGCTCAGTTGTGC | 9678 |
| rs76804313 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11056162 | GAAGAGATCTACTCT[G/T]TGGGTGTCCTTAGCT | 9678 |
| rs76812969 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170261 | CGGTTCTAATTTCCA[A/G]GCTGCCATTTGCCAA | 9678 |
| rs76830840 | snp | C/G | 0.109108 | 0.206518 | intron-variant | PHF14 | GRCh38.p7 | 7:11163576 | ACTTTACTTAATGAT[C/G]CAAGTGTTTATTACT | 9678 |
| rs76848887 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11076586 | TTTTTTTTTTTTTTT[G/T]AGGCAGAGTCTCACT | 9678 |
| rs76849442 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHF14 | GRCh38.p7 | 7:11057102 | ATTGATATGTCAACA[A/G]AAACACAAGTGTTAA | 9678 |
| rs76853356 | snp | C/T | 0.040671 | 0.13668 | intron-variant | PHF14 | GRCh38.p7 | 7:11162470 | ATAAATTTATAGAAT[C/T]GGGATTGTGCCCATT | 9678 |
| rs76905773 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11031686 | ATATACCCGGGAGTT[C/T]GAGGCTGCATTGAAC | 9678 |
| rs76925263 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10986357 | GTTGATATTTACCAC[C/T]TCAAATTAAAACTGA | 9678 |
| rs76930539 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11019164 | AGGATCTTTGCGTCA[A/G]TGTTCATCAGAGATA | 9678 |
| rs76932908 | snp | C/T | 0.0858192 | 0.188533 | intron-variant | PHF14 | GRCh38.p7 | 7:11133003 | ATGAATCTAACAAAA[C/T]ATACACAAAACCTGT | 9678 |
| rs76958051 | snp | A/T | 0.0655868 | 0.168795 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066339 | TTCTTGACGCAGTAC[A/T]GCCTCTGCCTCCCGG | 9678 |
| rs77005239 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:10980637 | GTGTTTTGTAAGGTT[C/G]ACACAAACTTACTTG | 9678 |
| rs77027227 | snp | C/T | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11010271 | TGGAAATAAAACTGA[C/T]CCCAAGAATAAAATT | 9678 |
| rs77028971 | snp | A/G | 0.46875 | 0.121031 | intron-variant | PHF14 | GRCh38.p7 | 7:11019052 | TGTTGATTGATTTGC[A/G]TATGTTGAATCATCC | 9678 |
| rs77043289 | snp | A/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:10999114 | TCCTGGGCTCAAACA[A/G]TCTTCTTGTTTCAGC | 9678 |
| rs77056449 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11078949 | ATAAGTATTTTTAGC[A/G]TTTCTCATATTTATT | 9678 |
| rs77061787 | snp | C/T | 0.0295035 | 0.117819 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968862 | AGACTTCCCCCTTAG[C/T]AGAGCTGTATTTGAA | 9678 |
| rs77115565 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11004366 | CTTTTTTTTTTTTTT[G/T]GGTTGCTTGCTCATA | 9678 |
| rs77117259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11049078 | GTTTTTAAAACAAAA[C/G]AAAACAATGATTTAT | 9678 |
| rs77118159 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF14 | GRCh38.p7 | 7:11085256 | ATTTTTTAATTACAC[A/G]TTGCGACATTAGCTT | 9678 |
| rs77129811 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11091257 | AATGAAAAATGGAAA[A/G]GCAAGGAAGAAAGGG | 9678 |
| rs77140421 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11037281 | CACTTTGTGTGCCAG[G/T]CATAATTTTGATCTC | 9678 |
| rs77155628 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11007888 | CTTATTGAATTTATA[A/G]TTGTTTACTGTAATT | 9678 |
| rs77162211 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11158794 | GTCATAGTTGCTTAC[A/G]GATTAGCCTGAAGTC | 9678 |
| rs77165189 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:11028268 | AAAGTGGAAAACAGA[A/G]TGGTCGTATGGGTAC | 9678 |
| rs77190524 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11025636 | GTCTCTCCTAAAAAA[A/T]TACAAAAAATTAGCC | 9678 |
| rs77200814 | snp | A/C | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11007196 | GAAACTCCGTCTCAC[A/C]AAAAAAAAAGAAAGA | 9678 |
| rs77205870 | snp | A/G | 0.0655868 | 0.168795 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063698 | TATATTGGAAATTAG[A/G]AACCTGAGAAATACA | 9678 |
| rs77211613 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11074855 | ATTGTCCCTTGTCTT[C/T]CTGTCTTCTTCTCAG | 9678 |
| rs77235263 | snp | C/G | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:11002005 | TAGTTTCTTTATGCT[C/G]TAGTTGAGGAAATTA | 9678 |
| rs77237782 | snp | C/G/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11019863 | TGATGTAGGTACCTA[C/G/T]AGCTATAAACCTCCC | 9678 |
| rs77243649 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11031786 | AAGTAAAAAAATACC[A/G]AGCTATTGTGCAGGC | 9678 |
| rs77246225 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11166417 | TTGGTAAAAAGCTTC[C/G]TTTGCAATTTTATTT | 9678 |
| rs77247123 | snp | C/T | 0.113685 | 0.209567 | intron-variant | PHF14 | GRCh38.p7 | 7:11083862 | AAACCAGTGGGGCTG[C/T]ACAAAAATTGGCTAG | 9678 |
| rs77256367 | snp | A/G | 0.0592355 | 0.161582 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064365 | CTATCTTTACATGCT[A/G]TTTTTTTAACTTTCA | 9678 |
| rs77258229 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | PHF14 | GRCh38.p7 | 7:11075715 | TATCCAAACTATATC[A/G]ATATGTATCAGGTAT | 9678 |
| rs77277979 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062346 | CAAGAGAAATTGACA[G/T]TGCTCTCTATTTAGA | 9678 |
| rs77287875 | snp | G/T | 0.0726307 | 0.176182 | intron-variant | PHF14 | GRCh38.p7 | 7:10975773 | TAAATAAAATGAGAA[G/T]TAAAAGCCTTTCCAG | 9678 |
| rs77297315 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020120 | ATCAGACGGGGCCTG[A/G]CTCTGTTCCCCAGGC | 9678 |
| rs77310025 | snp | A/G | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10969932 | TGTCCACAACAAGCT[A/G]TTTATTTTACTATCT | 9678 |
| rs77341141 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11124258 | TTGGTGGTATGTCCT[A/G]CTACAACCTACTTTA | 9678 |
| rs77372952 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11093114 | CTTTCTCTTTAACTC[A/C]TGGGTTATTTAGAAG | 9678 |
| rs77401436 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11113798 | TTTGCTAGTATTACA[A/G]CCTAAGAAGAAAGCA | 9678 |
| rs77429552 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10981572 | AATGTCTTCAGCCTA[A/C]CTTTTTAGTAACCTC | 9678 |
| rs77444093 | snp | C/T | 0.112631 | 0.208878 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107060 | GCATAGGAGGTGCAC[C/T]TAATTGTTTCAGTTA | 9678 |
| rs77444407 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | PHF14 | GRCh38.p7 | 7:11089415 | GTGAAATTCAGCTGG[G/T]CATGGTGGCTCATAC | 9678 |
| rs77445361 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11077310 | CAAAGAAAAAAAAAA[A/G]GCCAGATTCAGCCGG | 9678 |
| rs77482632 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11156932 | TTAAAGATTCACAAT[A/G]CTCACCTTTGGGCAT | 9678 |
| rs77488043 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11123918 | GCGAGACTCCATCTC[A/C]AAAAAAAAAAAACTA | 9678 |
| rs77491257 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11168019 | CGAAAGAGTCCGTCT[A/C]AAAAAAAAAAAAAAA | 9678 |
| rs77492939 | snp | A/C | 0.104504 | 0.2033 | intron-variant | PHF14 | GRCh38.p7 | 7:11009162 | CCTGTTTTATATATA[A/C]CGAAATATAATTAGG | 9678 |
| rs77519926 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | PHF14 | GRCh38.p7 | 7:11164293 | GTTTGTTCATATGGC[A/C]AAATTATAAAGGGAC | 9678 |
| rs77535763 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11128383 | AAAAGTCTTTGTTAT[G/T]TTCCCTACTTCATTC | 9678 |
| rs77593040 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11076903 | TTTTTGGCAAAATTA[C/T]ACCTTTTTCAGATAA | 9678 |
| rs77596686 | snp | G/T | | | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111386 | CTACCATTTTGGCTG[G/T]TTGGATCCTCCTTTG | 9678 |
| rs77604712 | snp | A/G | 0.0861826 | 0.188849 | intron-variant | PHF14 | GRCh38.p7 | 7:11133161 | TTCAGTGCAATCCCA[A/G]TCGAACTCTCAGCAA | 9678 |
| rs77610123 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11151046 | CAATGATTTTAAAAA[C/T]AAGAAAAGCAAAATA | 9678 |
| rs77610315 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | PHF14 | GRCh38.p7 | 7:11059705 | CTTGAACCTGGGAGG[C/T]GGAAACTACAGTGAG | 9678 |
| rs77629149 | snp | G/T | 0.0225045 | 0.103662 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104820 | TAACAAGTTCCCAGC[G/T]GATGCTGATGCTACT | 9678 |
| rs77715497 | snp | A/G | 0.00329669 | 0.0404658 | intron-variant | PHF14 | GRCh38.p7 | 7:11071251 | TGATATTCAAAGACT[A/G]TATATTCCATGTTCC | 9678 |
| rs77749069 | snp | C/T | 0.114738 | 0.210248 | intron-variant | PHF14 | GRCh38.p7 | 7:11161481 | AGTAATTTTTAGTCA[C/T]TTACGTCTCTGAAAA | 9678 |
| rs77772495 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PHF14 | GRCh38.p7 | 7:11080574 | AAATAAACATTAACT[C/T]TGCTGGTTTTTCTCC | 9678 |
| rs77776547 | snp | A/G | 0.1652 | 0.235179 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956644 | TGGGGTGGGCCCTGA[A/G]TCAAATGACTTGGTA | 9678 |
| rs77778775 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | PHF14 | GRCh38.p7 | 7:11075371 | GCCCACGGATCTGCC[A/G]GCTGTACAAGCAGCA | 9678 |
| rs77789469 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120050 | AAGTGATAATAGTTA[A/T]TTTTTCCCAAAAAAT | 9678 |
| rs77801652 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | PHF14 | GRCh38.p7 | 7:11003923 | GTAGATATATGTCCT[C/T]TGTGGAAAACATCAG | 9678 |
| rs77831168 | snp | A/C | | | stop-gained, intron-variant | PHF14 | GRCh38.p7 | 7:10982534 | AAGAAGTACTATCAT[A/C]AGAAAAACAATTAAT | 9678 |
| rs77846653 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11029104 | GCATTTCAGCCCCAT[C/G]AATTATAGTTAAAAA | 9678 |
| rs77899184 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038929 | GAACAGATTTTTGAT[A/T]CAACTGTCATTTGAC | 9678 |
| rs77919539 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11129550 | TGTGTGTATGTTTCT[C/T]TTTTTTTTTTTTTTT | 9678 |
| rs77971470 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11027833 | TAAGAATTAGTATAG[A/C]TTGATGGTGGGCTTT | 9678 |
| rs77978955 | snp | A/G | 0.084364 | 0.187256 | intron-variant | PHF14 | GRCh38.p7 | 7:11130000 | TATGCTAAGTTATGC[A/G]GCAAAAAAAAGAATC | 9678 |
| rs78032961 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11011748 | TTACATTAGGGCAGT[G/T]CCTTCCTTTTTAGAG | 9678 |
| rs78035475 | snp | A/T | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:11000093 | TGTATAATTAATTTA[A/T]TGGTAGTAATTTGAA | 9678 |
| rs78039124 | snp | C/T | 0.0360663 | 0.129354 | intron-variant | PHF14 | GRCh38.p7 | 7:11021336 | TTAATTACAAAGTTA[C/T]AAATAATGTGCATCT | 9678 |
| rs78044349 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:10987246 | ACCTTTTCTAAAAAT[A/G]TAGAGGAAGTATGAT | 9678 |
| rs78057022 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091346 | TAGAAACAGAAAAAA[G/T]ATGAGTTGGCTATAT | 9678 |
| rs78064851 | snp | C/T | 0.167158 | 0.235875 | intron-variant | PHF14 | GRCh38.p7 | 7:11010792 | AGCACCTGAGACTAC[C/T]GTGTGTGCCACCATG | 9678 |
| rs78122770 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:10993206 | AAAGTTATTTTTTCT[C/T]ACCAATTAATTATTA | 9678 |
| rs78126347 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047570 | GGAGGCTGAGGCGGG[C/T]GGATCACTTGAGGTC | 9678 |
| rs78127547 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:10997004 | GGCCTCAGGAATATT[C/G]AGTTCTAAGTGTCGC | 9678 |
| rs78208494 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987280 | TCAAGCTTTTTGTTA[C/T]AATAATTTTTTCTTA | 9678 |
| rs78209733 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11168020 | GAAAGAGTCCGTCTC[A/C]AAAAAAAAAAAAAAG | 9678 |
| rs78214261 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11080369 | AAACACTACTTGGTG[G/T]TTTTTTCCCCCCTCA | 9678 |
| rs78217421 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967274 | TTTCATTGGAGGGCT[C/G]AGTGATGGTGGTGCC | 9678 |
| rs78231701 | snp | A/C | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11092559 | CACTCTTGAAGATTC[A/C]AATCAGTAGGTGAAC | 9678 |
| rs78255902 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11011324 | GGTTGTGAGAGGTCA[C/T]GCTCCAATTTAGGCT | 9678 |
| rs78257122 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | PHF14 | GRCh38.p7 | 7:11006144 | GATTGACTACCAAAA[A/G]GACTGTACTAATTAC | 9678 |
| rs78294348 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11058573 | AATCAAGTTAGTATG[C/T]AGTATGGAGCTACCA | 9678 |
| rs78354762 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11045880 | ACTGTGGAAAAATCA[A/G]ACTGACTTGCTGAGG | 9678 |
| rs78382724 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | PHF14 | GRCh38.p7 | 7:11123348 | TTCCTCTTATAGTCT[C/T]CTTTTACTAAGTAGT | 9678 |
| rs78385112 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | PHF14 | GRCh38.p7 | 7:10998731 | ACATGTTACTGCTGC[G/T]TATATCCATGAATGT | 9678 |
| rs78388261 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11008056 | TGATATCCTGATTGT[A/C]GTGTGTCTGAATTCA | 9678 |
| rs78389128 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11024573 | CAGTGCTCCTATACT[A/G]TTGTGAAAATCCTAG | 9678 |
| rs78418712 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | PHF14 | GRCh38.p7 | 7:11002866 | GAAGGTTGAGGGTCA[A/G]TGCAGATGGAAGCTT | 9678 |
| rs78420469 | snp | A/T | 0 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966095 | TTGTCCTCTGTGTGC[A/T]GCACCCACTGTCCAA | 9678 |
| rs78437354 | snp | C/G | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10970106 | TTGAGGCAGTTTGTG[C/G]TCGCTGTTTTTTGGA | 9678 |
| rs78472808 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | PHF14 | GRCh38.p7 | 7:11073679 | ATTCTGTGTGAGGGT[A/T]CCAACTCCACATTTC | 9678 |
| rs78525906 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043329 | GAATCACTACATTTG[A/G]TAAAGGTTATAGTAT | 9678 |
| rs78565859 | snp | A/G | 0.175897 | 0.238765 | intron-variant | PHF14 | GRCh38.p7 | 7:10980066 | TTGAAAAAATAATTA[A/G]TTAATTGGCATTGGC | 9678 |
| rs78584567 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | PHF14 | GRCh38.p7 | 7:11126385 | CTTTTATAAGCAGGC[C/T]AAGTGCTGTAAAGGA | 9678 |
| rs78606321 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11098710 | CATTATTCCAAGGCT[A/G]TCTTGGACATTTACT | 9678 |
| rs78625014 | snp | A/G | 0.113685 | 0.209567 | intron-variant | PHF14 | GRCh38.p7 | 7:11157822 | GCTGAAATCATAGAA[A/G]TACTGAAACCCCATT | 9678 |
| rs78704490 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11164943 | CATTCTTTTTTTTTT[G/T]AGACGGAGTCTCGCT | 9678 |
| rs78705181 | snp | C/T | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 7:10969017 | TGTCTCTTACCTAAG[C/T]GTTATGCAGAGAATG | 9678 |
| rs78705952 | snp | A/C/T | 0.00756178 | 0.0610554 | intron-variant | PHF14 | GRCh38.p7 | 7:11011582 | GATGGTTGCTATTTT[A/C/T]TCTTTAGAAATGACC | 9678 |
| rs78714121 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11055767 | TTTTACGCATATACA[A/G]AGTACCTATTTAATA | 9678 |
| rs78748629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999812 | TGAGTGGTAATGCCA[A/G]TTAAGTCAACAGGAT | 9678 |
| rs78787885 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11158050 | AGGTTAACATCTTAT[A/G]TAAGCATAGAACAAT | 9678 |
| rs78794797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129850 | ATGCCATTAAGAAGT[A/G]TAGGTAAGGTACAGT | 9678 |
| rs78811024 | snp | A/G | 0.146985 | 0.227789 | intron-variant | PHF14 | GRCh38.p7 | 7:11010092 | TTGCCTACTTGTGTG[A/G]ATGCACATTTTATCT | 9678 |
| rs78813880 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11022580 | TTTAAGAATAGATAA[A/G]TGCAAAGTGCAGTGA | 9678 |
| rs78821040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099805 | ATTTCAAAACAAATA[C/T]ACAGTTTCAAAAAAG | 9678 |
| rs78833426 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:11043087 | CTTGTTTTATTGTTC[A/G]GAATTTCTCAAATGC | 9678 |
| rs78846664 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:10974662 | GCCCGTGGAGCTGTC[A/C]AGCCCTCCCCACCCT | 9678 |
| rs78862271 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956000 | GGTTTCATAAGCAAA[A/G]TGCTGTATCTTCAAG | 9678 |
| rs78869247 | in-del | -/CAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060913 | ACAGTGTACTTGAYA[-/CAT]TSAAGAATTGAAATT | 9678 |
| rs78874237 | snp | A/G | 0.179425 | 0.239831 | intron-variant | PHF14 | GRCh38.p7 | 7:11030235 | TCAGGATGGTGGGCA[A/G]AAGTACGAGAGGGCA | 9678 |
| rs78921195 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | PHF14 | GRCh38.p7 | 7:11049050 | AAAAGAGAAGCGAAG[A/G]GGAAATATTTCAGTT | 9678 |
| rs78923238 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122107 | ATGAGTGAGAACATG[C/T]GGTGTTTGATTTTCT | 9678 |
| rs78959742 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122677 | TTTCTGGGAATATCA[C/G]ATATGCTGTTGTTAA | 9678 |
| rs78967610 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10999757 | TTTTCAGAAACATTT[A/G]AAAAGTCTGAATCAA | 9678 |
| rs78974846 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10998813 | CTCTTATGATGCTGA[A/G]GGCACTATCTCTATT | 9678 |
| rs78997187 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11121818 | GCTCTTCAGAATGGT[A/G]TGCAATTTAAAACTT | 9678 |
| rs79000237 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11003748 | TCATTAAAATATTCT[C/T]AATTATAAGTGACAT | 9678 |
| rs79008379 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10985560 | TAATTACTGCTCTTA[A/C]TGGCCTTAACATATG | 9678 |
| rs79009556 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PHF14 | GRCh38.p7 | 7:10996341 | AGAAATTTAAATTTG[A/G]GACTTATCAGCCTGA | 9678 |
| rs79017307 | snp | C/T | 0.111224 | 0.207945 | intron-variant | PHF14 | GRCh38.p7 | 7:11121127 | ACAAAAGTTTCATCA[C/T]CCCTAAAGAATGACT | 9678 |
| rs79024414 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:11142848 | TTATTCTAAGTATAC[A/C]TTGATAAAACTCCGT | 9678 |
| rs79058980 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11085688 | TCACTGTGTTACCCA[A/G]GCTGGAGTGCGGGAA | 9678 |
| rs79075713 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11151476 | AGGCCAGAGGATCAT[C/T]TGAGCCCAGGAGGTT | 9678 |
| rs79090939 | snp | A/G | 0.103794 | 0.20279 | intron-variant | PHF14 | GRCh38.p7 | 7:11113994 | TACATTTGCTTAGGT[A/G]GAATATTATTTGCTA | 9678 |
| rs79094851 | snp | C/T | 0.0140754 | 0.0827018 | intron-variant | PHF14 | GRCh38.p7 | 7:10990895 | ATGGCTGACTGTGGC[C/T]CTTTTACATTTGTAC | 9678 |
| rs79102418 | snp | A/G | 0.5 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963689 | GTGTTAAAGTCTCCC[A/G]TGATTATTGTGTGGG | 9678 |
| rs79116224 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11167620 | TTCAGTGCTACATAT[A/C]AAAAATTTCTTGCCA | 9678 |
| rs79142703 | snp | G/T | 0.0168055 | 0.0901129 | intron-variant | PHF14 | GRCh38.p7 | 7:11163111 | GGGAGATCTCTTTGA[G/T]TATCTTTTGTTTGCA | 9678 |
| rs79146837 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | PHF14 | GRCh38.p7 | 7:11078483 | CCTCTCTGCGAGCCA[A/G]TTTTCTCATTCATAG | 9678 |
| rs79150310 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959861 | CAGGAAAGTGGTGTT[C/T]CAGCCATTCAGTGAG | 9678 |
| rs79170164 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11118154 | AAAAAGTTGTTTCTA[C/T]TGTGTCCTATATTAG | 9678 |
| rs79173355 | snp | A/G | 0.0217504 | 0.102186 | intron-variant | PHF14 | GRCh38.p7 | 7:11006094 | ATTTCTTAGTCAAAA[A/G]ATAAGTGTATTTAAA | 9678 |
| rs79195215 | snp | C/G | 0.0376037 | 0.131863 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960253 | CCAGCACCCCACCCC[C/G]CTACAGGCCTCAGTG | 9678 |
| rs79199561 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11141118 | TCCTCATCAGGGAAT[A/G]AATTGGTTCTCCAAG | 9678 |
| rs79218934 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11007995 | AATATCTTTGTGGGA[A/G]GATCTTCTAATATTA | 9678 |
| rs79352237 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | PHF14 | GRCh38.p7 | 7:11067874 | TATCAAAGGAACTAA[C/T]AGAGTTAGAACACAC | 9678 |
| rs79377697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967557 | GAGTCAAGCAGTTAA[C/T]GTCAGCTGGATGTAG | 9678 |
| rs79392245 | snp | A/G | 0.029116 | 0.117091 | intron-variant | PHF14 | GRCh38.p7 | 7:10990156 | ATTTCTGAATTTCCC[A/G]GTACTTAAGGAGTAT | 9678 |
| rs79397621 | snp | C/T | 0.029116 | 0.117091 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065270 | ATGCAATCTAAATGC[C/T]AAAGGTCAAGTTGAA | 9678 |
| rs79398746 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | PHF14 | GRCh38.p7 | 7:11001249 | TTGTTCATCAACTGA[C/T]CTATATATCTATTCT | 9678 |
| rs79410317 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11126558 | TAAACTTTCTCTCTT[C/T]GTTATTTAGCTGTTT | 9678 |
| rs79432044 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11067219 | AGATGCTCAACATCA[C/T]GAATCATTCAGGAAG | 9678 |
| rs79433407 | snp | G/T | 0.0528381 | 0.153711 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149723 | GAATAATCTGTAGTT[G/T]TATTTTTTGTTATCT | 9678 |
| rs79466587 | snp | A/G | 0.111576 | 0.20818 | intron-variant | PHF14 | GRCh38.p7 | 7:11094435 | GCTATAGTCACATCT[A/G]TTTATCTCTCTGATT | 9678 |
| rs79484118 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | PHF14 | GRCh38.p7 | 7:10978053 | GCAAAGTAAAATGGG[G/T]TTAACTTTAGATCTT | 9678 |
| rs79490106 | snp | A/G | 0.0759472 | 0.179459 | intron-variant | PHF14 | GRCh38.p7 | 7:11083376 | AGGTGTGTGCACACC[A/G]TCTCTCTTTCTCCCC | 9678 |
| rs79499497 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11092213 | TTGCTTCTATTCCTT[C/T]TTCTTTGTGGTTACC | 9678 |
| rs79509947 | snp | C/T | 0.105214 | 0.203807 | intron-variant | PHF14 | GRCh38.p7 | 7:11012930 | ACTTTTCAAACTGTT[C/T]TATAGCTTTAGGTGC | 9678 |
| rs79530451 | snp | A/C | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11005450 | TGAGAGTCCTTTAAG[A/C]AGGCCCTTGTGTATA | 9678 |
| rs79533387 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:10996099 | CTATCATTATGATGG[A/G]TGTGGGAAGCCATAA | 9678 |
| rs79565747 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10982346 | TATACATATGTGTGG[G/T]TTTTTTTTTCTCATA | 9678 |
| rs79572418 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | PHF14 | GRCh38.p7 | 7:11074660 | TTCAAACTTCCATAG[A/T]TCCCAAGAACATGCA | 9678 |
| rs79577254 | snp | A/G/T | 0.5 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963727 | ACAGCAAGTCCTTAG[A/G/T]GACCTACAAAGAGAC | 9678 |
| rs79674108 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | PHF14 | GRCh38.p7 | 7:10978757 | TCACCTCCACCTCCA[C/T]TTCCACTGTTGTGGC | 9678 |
| rs79697056 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11011612 | CTATTTTGAGATGTA[A/G]TAAATGTGTCTCAGG | 9678 |
| rs79710593 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11027406 | CACTTTGAATACTTA[C/T]ATTAAACAATTCTTT | 9678 |
| rs79729158 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017407 | CGCCAGCATTTGTTA[C/T]TGCCTATCTTTGGCT | 9678 |
| rs79738171 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:11027153 | AACATATTACATGAA[A/G]TTATCCAGATAATCT | 9678 |
| rs79752602 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11051241 | GAAGACAGTCTCTCA[C/G]TATGTTGTGAGCAGT | 9678 |
| rs79788440 | snp | A/G | 0.0821764 | 0.185298 | intron-variant | PHF14 | GRCh38.p7 | 7:11132057 | ATAGTTCAAGTTAGC[A/G]TATCCATCATGTCAC | 9678 |
| rs79823425 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11077622 | AAAAAAAAAAAAAAA[A/G]ACAGATTCAAGCACA | 9678 |
| rs79832957 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958320 | CCAAAGTCAATCCAT[G/T]CTACCTAAATATTGA | 9678 |
| rs79862111 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11120055 | ATAATAGTTATTTTT[C/T]CCCAAAAAATTGCCA | 9678 |
| rs79868680 | snp | C/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11024553 | TGGTGACTTTAAGTT[C/G]AAGCCAGTGCTCCTA | 9678 |
| rs79879397 | snp | A/C | 0.0948562 | 0.196037 | intron-variant | PHF14 | GRCh38.p7 | 7:11166941 | TCAACAACAAAAAGA[A/C]AAACATTATATTAAG | 9678 |
| rs79887248 | snp | A/G | 0.0232847 | 0.105357 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065378 | ACTTAGTGATACCTT[A/G]TTTATTTTTGTTTCG | 9678 |
| rs79908927 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11069917 | GGCCTTCTGAATGGA[A/G]TTGGAAAAAGTGTTC | 9678 |
| rs79953724 | snp | A/G | 0.0591753 | 0.161511 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169514 | CTGTAGTGTTTTTGA[A/G]AAGTTTGCAGCTTAT | 9678 |
| rs79965218 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11082387 | CAATTTAATAAAACC[A/G]TTATGGAAAGGCATG | 9678 |
| rs79997265 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11166352 | AAAACCCTCCTGTAT[A/G]TCAGAAGAAATTTTT | 9678 |
| rs80014362 | snp | C/G | 0.0452528 | 0.143452 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066430 | ATTAACTTTTCTGTT[C/G]TAACTAGTATGGAGG | 9678 |
| rs80048234 | snp | A/G | 0.0659589 | 0.169201 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066237 | ATGTATTACATTTTA[A/G]TTTCAAATATTAGTC | 9678 |
| rs80048603 | snp | C/T | 0.170084 | 0.236883 | | | GRCh38.p7 | 7:10970880 | AATATAGTAATATAC[C/T]ATATTGAAAAAATAA | 9678 |
| rs80061577 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:11024971 | AGTAAATTGAAAACC[C/T]TCTAGAAAGGGGTCA | 9678 |
| rs80081872 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | PHF14 | GRCh38.p7 | 7:11093724 | CAGCCTTCAGCCTCC[A/G]AAGAATCACAAGCTT | 9678 |
| rs80095790 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10991779 | TTTTTTTTTTTTTTG[G/T]TAGAGACAGGGTTTT | 9678 |
| rs80110297 | in-del | -/TTA | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11145295 | CTCTCTTTTTCTCTC[-/TTA]TTTTTTAAAATTCCA | 9678 |
| rs80112715 | snp | A/G | 0.0119091 | 0.0762411 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108116 | AATGGTATCTCTTAT[A/G]TTTGTCCACAGTTTA | 9678 |
| rs80124589 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11110674 | GAAAGTGACAGGTAA[A/T]TTGTGAGAATAAAAC | 9678 |
| rs80146615 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968088 | AGCAAATAGAAAACA[C/G]TACATATATTTCATG | 9678 |
| rs80149003 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | PHF14 | GRCh38.p7 | 7:10987142 | ATCAGTTGTCTTTTT[A/G]CACATTGCAAAATGA | 9678 |
| rs80193059 | snp | C/G | 0.0410537 | 0.137264 | intron-variant | PHF14 | GRCh38.p7 | 7:11053869 | CATTCCTTTCATCTT[C/G]TTCTTTGTCTCTAGT | 9678 |
| rs80237190 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157239 | TGAGGGAGGAAGAAA[G/T]GAAGGATTCTAGGAA | 9678 |
| rs80255804 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:11061642 | ACAAAGTGCAGTAGT[A/C]CAATATAGTATTAAT | 9678 |
| rs80264667 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11155782 | TTTTTTGTTTTTTTT[A/T]AGCAACTAGCACAGT | 9678 |
| rs80279712 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11034127 | AATTGCCTCATATGC[C/T]TTTTTTTTAATATTA | 9678 |
| rs80287057 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | PHF14 | GRCh38.p7 | 7:11079976 | GCATATTGCTAGAGC[C/T]GATTATACAAGGAAA | 9678 |
| rs80327338 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11059501 | GCCCTGTAGGCCAGG[C/T]GCAGTGGTTCACACC | 9678 |
| rs80343009 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11042434 | ATGTAATTCTTTAGA[A/G]GGTTTGACTCTAGTA | 9678 |
| rs111237629 | snp | A/T | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11010357 | GTGATGAAGATGATG[A/T]TTGCCAACCACAATT | 9678 |
| rs111243695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989499 | AATGTTAAGCACAAT[A/C]TATTAAATATGCAAG | 9678 |
| rs111247443 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10970692 | CAGTTTACAACCAAT[A/G]AAGACAAATTCTTTA | 9678 |
| rs111262339 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11088417 | AAACACACACACACA[C/T]GCACACACACACACA | 9678 |
| rs111274371 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11121486 | AATTGCAGGGGTTAT[A/G]TTCCAAGACCCCTAG | 9678 |
| rs111284731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035507 | TTATGTACAAAAATT[A/T]TTTTTGTAATTTATT | 9678 |
| rs111286363 | in-del | -/T | 0.5 | 0 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973998 | TTTTTCTTTCTTTAA[-/T]TTTTTTTTCTTCTAG | 9678 |
| rs111309016 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11087282 | CTGCAACCTCTGCCT[C/T]CTGGGTTCAAGCGAT | 9678 |
| rs111330414 | in-del | -/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11076878 | AGCTTTCAAATATGG[-/T]TTTTTTTTTTTTTTG | 9678 |
| rs111376221 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11145652 | TTAATATACTTCATC[A/G]AACTATTTAAAGAAC | 9678 |
| rs111403587 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959208 | ATGTTTTTGTGGCTG[C/T]CCAAACCATAACCAC | 9678 |
| rs111431399 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11140634 | AAATAATATAATCCA[-/T]AACTGCAAGAATATA | 9678 |
| rs111449959 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11152878 | AGTCAGAGGAAACAC[C/T]TACTGCATTTTGTTC | 9678 |
| rs111452639 | in-del | -/T | 0.197082 | 0.244335 | intron-variant | PHF14 | GRCh38.p7 | 7:11020687 | TCTTTCTTTTTTTTT[-/T]CTTTAAAATTCTAGA | 9678 |
| rs111469776 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11001437 | TCTACAAAATTACAT[C/G]CTGGAATTTTGATTG | 9678 |
| rs111484274 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981899 | GTAAAATAAATGAAG[C/G]AGTTTTATGGGTTAG | 9678 |
| rs111521152 | snp | C/T | 0.0225045 | 0.103662 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106373 | GGTTCAAGCCCTCCA[C/T]GTTAGTCTTATATTT | 9678 |
| rs111523895 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11002735 | AGACGTGAGCCACCG[C/T]GCCCGGCCAAAAATT | 9678 |
| rs111540292 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11072220 | GGCATCTTATGTGGC[A/C]GGGGCCAGGGGCAAA | 9678 |
| rs111550873 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11042376 | GTTTTAAGTAATAAC[C/T]AAAATTAAAATGAAT | 9678 |
| rs111566893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983695 | CACCAAATCTTTGCT[C/T]TATGTGTATGGGACA | 9678 |
| rs111573299 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030552 | GCATCTCCGTCTAAA[G/T]GCATGCAAATTAAAT | 9678 |
| rs111574057 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11086492 | CTTCTCAATCACTTA[C/T]ACTTAGTCCATATGT | 9678 |
| rs111576751 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:11010055 | ATTGGATAGCTCCTT[A/G]AGGGCTTTATTCTCT | 9678 |
| rs111584225 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11010380 | CCACAATTTAATGAC[A/G]TTAAAGAAATTAATG | 9678 |
| rs111586769 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PHF14 | GRCh38.p7 | 7:11159273 | TTGGTTTTTGACATG[A/G]TGTGATCTATAACTA | 9678 |
| rs111592387 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11151703 | TTCCCAAGACCCCCA[A/G]GAGTCATGCATGGCC | 9678 |
| rs111598244 | snp | G/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:10993988 | CACTTTGGCCTGGGT[G/T]ACAGAGGGTGACTCT | 9678 |
| rs111598592 | in-del | -/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10986149 | TGCTTTTATTTTTGA[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs111599018 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11096129 | TCCCAGTCATGCAAA[G/T]TTCATTTTGGTTCTT | 9678 |
| rs111608826 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11153476 | TTATTAAAAAGTTTA[G/T]TGGAGACAAGTAGCA | 9678 |
| rs111613427 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11147861 | TTCATATATTCAAAT[A/G]TTTGCCTGACATTCC | 9678 |
| rs111617841 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11146500 | ACCAGAGTTGGAAAT[A/G]TTTTAAGAAATAAGT | 9678 |
| rs111632425 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11073924 | ACCTGGGGCTCTGTG[C/T]ATCAGCTGGAGCTGG | 9678 |
| rs111642574 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972143 | GTTTCATCATGTTGG[A/G]CAGGCTGGTCTCGAA | 9678 |
| rs111658295 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11145840 | TGCTCTTTTACTTCT[A/G]TCGTATACGTTATAC | 9678 |
| rs111659857 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11151552 | CGACAGCAAGACCCT[A/G]TCTCAAAATAAATAA | 9678 |
| rs111661839 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11145137 | ATTATAAAAATGATT[A/T]AAAAAAAACCCTCGG | 9678 |
| rs111697974 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PHF14 | GRCh38.p7 | 7:11164024 | GAGATAATTCTGACT[A/G]TTAATTTGGATCCAG | 9678 |
| rs111698959 | snp | C/T | 0.112631 | 0.208878 | intron-variant | PHF14 | GRCh38.p7 | 7:11124359 | CAGTTTACCATGTTG[C/T]TAAATACTCTTACAT | 9678 |
| rs111743740 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959188 | TCAGAAAGCTGATGC[C/T]GTTAATGTTTTTGTG | 9678 |
| rs111744978 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10986290 | CACATAGCCCCTTTA[C/T]AGTTTTAAAAATTAT | 9678 |
| rs111748045 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10992303 | AAGTGATCCACCCGA[C/G/T]TCAGCTTCCCAAAGT | 9678 |
| rs111756524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148163 | ATCTCTGTATTTGTG[C/T]TCTTTCCTAATTTCT | 9678 |
| rs111758172 | in-del | -/T | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11096162 | TTCTTTTTCGGTGTC[-/T]TGAGTATATGCATGC | 9678 |
| rs111784427 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11006985 | TTTGATACCAGCCTG[A/G]TTAATGTGGTGAAAC | 9678 |
| rs111786067 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | PHF14 | GRCh38.p7 | 7:11055227 | CATAAATTAGCTTAC[C/G]CATATCCCTTTTGAA | 9678 |
| rs111792238 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11152142 | CTTAGGACCTTTTAA[A/G]ATAACTGAATAATAA | 9678 |
| rs111805460 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11003088 | TGGGATTACAGGCGT[A/G]TGCCACCACACCCAG | 9678 |
| rs111807867 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:10995482 | ACTCGGGAGCCTAGC[A/T]GGCTTCACCCAGTGG | 9678 |
| rs111818961 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11028518 | AATTACGTTTTTTCA[C/T]ATAAACTCTTGGCTC | 9678 |
| rs111861141 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11003627 | GTTTACCAAGTCCAT[C/T]CTTCTGCAGAAATTA | 9678 |
| rs111864377 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11086209 | TTTGTTACTATTGTA[C/G]TCAAATTTGTCCAGA | 9678 |
| rs111890152 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:10992644 | CTCCAGCCTGGGCGA[C/T]AGAGGAAGACTGTCT | 9678 |
| rs111910121 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11017356 | AATATACATTTCATG[A/C]AACAGTGTACAAGGG | 9678 |
| rs111914745 | snp | A/C | 0.0225045 | 0.103662 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11107929 | TTGCAGCTTTTAGGT[A/C]GCAGATGATTATAGT | 9678 |
| rs111915546 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11145298 | CTCTTTTTCTCTCTT[A/T]TTTAAAATTCCATTG | 9678 |
| rs111939165 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | PHF14 | GRCh38.p7 | 7:11030404 | GCTTTCTTTTTTACT[A/G]TGGTAGTTTGGATTC | 9678 |
| rs111958339 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | PHF14 | GRCh38.p7 | 7:11111733 | ATTAAATAGTGCTCC[A/G]AAAGCCCAAACAGAT | 9678 |
| rs111960690 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11004983 | GATTCTGTCACTGCA[A/C]TCCAGCCTGGGCAAT | 9678 |
| rs111961817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135878 | CAAAGCTTGTTTAAA[A/G]CTAATTTATAGCTTA | 9678 |
| rs111978077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159991 | TGTGATGCTGAGTTT[G/T]GGGGTGTGATTCATC | 9678 |
| rs111985280 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11150966 | CAGTTTATTTTCTAC[C/T]TTAAAAGAAAAGTAA | 9678 |
| rs111988747 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11145891 | TTGGATTAGCATCAG[A/C]AAGTAAACTGAGGAA | 9678 |
| rs111992605 | snp | A/T | 0.00279162 | 0.0372561 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169844 | CTCTGTGTTCTTCTT[A/T]AAGGGCCTTAACATA | 9678 |
| rs111998388 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11093647 | GACTGTCACATATTA[C/T]TCAGTGCTTGCTGGT | 9678 |
| rs112002770 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11100063 | AACTTCTAGTTGAAA[A/G]GCCAACTATATTGTT | 9678 |
| rs112014523 | in-del | -/TTT | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11076428 | ATTTAATATTATTTT[-/TTT]AAAATGTACTGTCTG | 9678 |
| rs112046224 | snp | G/T | 0.5 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958774 | CATTGCATCTCACTG[G/T]GTCCTCAAACACCTG | 9678 |
| rs112049318 | in-del | -/CC | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11128731 | CTTTCCTCCCGTTCT[-/CC]TTCCGTCTCTCCCAT | 9678 |
| rs112053588 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10996592 | CTATCCCAGAGGTTA[C/T]TGAAAAAAAAAACTA | 9678 |
| rs112055977 | snp | C/T | 0 | 0 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973433 | CTTTCTTTGCTTTGC[C/T]GGGCGTTTTGTCCAA | 9678 |
| rs112063142 | snp | C/T | 0.5 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965011 | TGCGATGGGTTAGAA[C/T]ATGCTCCTTTAGCTC | 9678 |
| rs112069568 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11156527 | TGGCCGGGCGTGGTG[G/T]CTCATGCCTGTAATC | 9678 |
| rs112086958 | snp | C/T | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:10969851 | GCCTAGACCAAAATT[C/T]GGATCTCCAGACTCT | 9678 |
| rs112095596 | snp | C/T | 0.0803491 | 0.183626 | intron-variant | PHF14 | GRCh38.p7 | 7:11112567 | ATGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 9678 |
| rs112120827 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10980053 | ATTTACCTCTCATTT[A/G]AAAAAATAATTAATT | 9678 |
| rs112136682 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11009788 | GAAGCTGAAGAAAAA[A/G]TACATACAGACTTGC | 9678 |
| rs112147980 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11155532 | CTTCCCTCCATTGTT[C/T]GCTTGACCAACTCTT | 9678 |
| rs112156713 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11100236 | ACTGAATTTGAAAAT[A/G]GGACTGGACACAAAT | 9678 |
| rs112162816 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11059656 | GTGCACACCTGTAAA[A/C]CCAGCTACTTGCAAG | 9678 |
| rs112169715 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11087223 | TTAAGATGGAGTCTC[G/T]CTCTGTCATCCAGGC | 9678 |
| rs112180411 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147011 | GCCACGACACCTGGC[A/T]AATTTTGTATTTTTT | 9678 |
| rs112207822 | in-del | -/TTTTAG | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10975932 | TATTACTGTTGCTAC[-/TTTTAG]TAGCATCAACAGCAG | 9678 |
| rs112225716 | in-del | -/TG | 0.29278 | 0.246313 | | | GRCh38.p7 | 7:10969611 | ACAATTAATTCTAAC[-/TG]TTATTTTCTTTTTCT | 9678 |
| rs112230004 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11158065 | ATAAGCATAGAACAA[G/T]TCTCAAACCTAAGAA | 9678 |
| rs112252658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150054 | ATATATACATGTAAT[A/G]TTGAAAATACATTGC | 9678 |
| rs112253699 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11096512 | ACTTACAGGAGAAAG[A/G]GAACTGGATGCCATT | 9678 |
| rs112261492 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967466 | CTTTTGCCACAGGGC[C/G]AAAGAATTATCTGGC | 9678 |
| rs112266828 | snp | C/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11122641 | TTTCCCTTCATGTTA[C/G]TTTAAAAATTGAATT | 9678 |
| rs112279901 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11006925 | CACACCTTTAATCCC[A/G]GCATGTTGGGAGGCT | 9678 |
| rs112290359 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963208 | TTTCTGCTTTCTCTT[G/T]TGGGCATTTAGGGTT | 9678 |
| rs112309490 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165175 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 9678 |
| rs112323642 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11145294 | TGCTCTCTTTTTCTC[C/T]CTTTTTTAAAATTCC | 9678 |
| rs112325754 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149387 | AATTGGCTATGGGAC[C/T]CTGGGGAAGTTCATT | 9678 |
| rs112331061 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11089782 | TTTTTTTTTTTTTTT[C/T]TTTTTGAGACGGAGT | 9678 |
| rs112337047 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11074959 | TTTTTTTTTTTTTAG[A/G]TGGAGTCTTGCTCTG | 9678 |
| rs112347661 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11027888 | GCCTTACATTTACTT[C/T]CTTTGTTATTTTTGG | 9678 |
| rs112349754 | snp | G/T | 0.0178098 | 0.0926698 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105969 | GCTTGAGCTCAGCAG[G/T]TTGTACTGCTGAAAA | 9678 |
| rs112369088 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11004478 | TATGGTTTCTCCACA[C/T]CCCACAGGATCCATT | 9678 |
| rs112408206 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11145758 | ATTATAGATACATGG[A/C]ATATTATTATCTTAT | 9678 |
| rs112412294 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:11109292 | CAAAAATTGAATACA[A/G]GAATTCAAATAGAAC | 9678 |
| rs112413130 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PHF14 | GRCh38.p7 | 7:11160113 | TATTATTGCCATCTT[C/T]ATGTCCCTGTGTACC | 9678 |
| rs112415373 | in-del | -/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064311 | ATTGTTTGAAAATCA[-/C]CCCCCAAAAGTCTAC | 9678 |
| rs112421929 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11087494 | TGCGCCTGGCCAGCA[C/T]TGTTCTTCTTTCTTG | 9678 |
| rs112425470 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | PHF14 | GRCh38.p7 | 7:11162275 | TTGTATTTTTAGTGG[A/T]GACGGGGTTTCTCCT | 9678 |
| rs112430361 | snp | A/C | 0.0267878 | 0.112589 | intron-variant | PHF14 | GRCh38.p7 | 7:11056598 | ACAGAAACAGATGAC[A/C]CCTTGTTCATAATTT | 9678 |
| rs112432610 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11074856 | TTGTCCCTTGTCTTC[C/G]TGTCTTCTTCTCAGC | 9678 |
| rs112441952 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11037919 | TTTTTCATTGGGAAA[A/G]TAGTGGAAATACATC | 9678 |
| rs112464442 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11074411 | GAGGCAGGGTTTCGC[C/T]GTGTTAGCCAGGATG | 9678 |
| rs112478967 | in-del | -/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11165668 | CCATTGTTAGGAGTT[-/G]GTTACGTCCTAAGAG | 9678 |
| rs112481265 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | PHF14 | GRCh38.p7 | 7:11112939 | GAGAGAACATATTTA[A/G]TTTTAAAGATTTTAT | 9678 |
| rs112484055 | snp | A/G | 0.48 | 0.0979796 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149334 | AAACAATTCCTGACT[A/G]CAACTTAGGAGACAT | 9678 |
| rs112498886 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11088416 | CAAACACACACACAC[A/G]CGCACACACACACAC | 9678 |
| rs112506745 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11121113 | TGCAGTTTCTGATAA[C/G]AAAAGTTTCATCATC | 9678 |
| rs112509416 | snp | C/G | 0.0225045 | 0.103662 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106329 | CATTATTGGCTGATA[C/G]AGAAGTCTGTAGTGG | 9678 |
| rs112526356 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10982169 | CTTCATTAGCACTAT[A/C]CTGAACTAAAACCAT | 9678 |
| rs112552865 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11136282 | AGAATTTTAATTATA[A/C]TTTTTTTTCAAGATG | 9678 |
| rs112570324 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11154948 | CTTCTATTTAATAAC[A/G]TAATGATGGTTATTT | 9678 |
| rs112587148 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139771 | AACTTTTGGTACTCT[C/G]TAAGGTACAAAAAGT | 9678 |
| rs112593541 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11133176 | ATCGAACTCTCAGCA[A/G]GTTATTTTGTGGATT | 9678 |
| rs112671182 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064311 | TTGAAAATCACCCCC[A/C]AAAAGTCTACACTTT | 9678 |
| rs112675549 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11038260 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 9678 |
| rs112684019 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11047663 | ATGGTGATGGGGATT[C/T]GTAATCCCTGCTACT | 9678 |
| rs112693107 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11017254 | GATTTCCTTTCTTTC[A/G]GATGTATACCCAACA | 9678 |
| rs112703224 | snp | A/T | 0.444444 | 0.157135 | intron-variant | PHF14 | GRCh38.p7 | 7:11037387 | AACTGAATCCTGAAG[A/T]AGTTAAATAATTTGC | 9678 |
| rs112726768 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11138727 | GAGAGATAAGTGCTC[A/T]AAGTCTTAACATGAG | 9678 |
| rs112736370 | snp | A/G/T | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964354 | TAGTTTGGCTGGATA[A/G/T]GAAATTCTGGGTTGA | 9678 |
| rs112807225 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158647 | GAAACTGATTTCATA[C/T]TTTTGTCAATCTAGT | 9678 |
| rs112822978 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11158704 | AATAAGATATCTTAG[G/T]ACTCTTTCACCTTTA | 9678 |
| rs112844620 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11123832 | CCAGCCTGGGTGAAT[C/T]GCTTGAACCCAGGAG | 9678 |
| rs112847887 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973944 | CCCTCGCGCTGTGCA[A/G]TTTCTGGTCTTTCGT | 9678 |
| rs112854713 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10991997 | GACTATTTTAGTCTG[A/G]TAGAAAACATTCTTA | 9678 |
| rs112895610 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10975770 | TTTAAATAAAATGAG[-/A]AAGTAAAAGCCTTTC | 9678 |
| rs112899699 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11160087 | TCCCCATTCTAGTAG[C/T]CTCCAGTGTCTATTA | 9678 |
| rs112901486 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11044326 | ATAAAAGTTGAAATT[-/T]AAAAAAAAAAGAAAA | 9678 |
| rs112904471 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11165458 | AAGGTACTTACATCA[A/G]CATCTATAAAGATAT | 9678 |
| rs112907197 | snp | C/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11060915 | CAGTGTACTTGATAT[C/G]AAGAATTGAAATTAA | 9678 |
| rs112957856 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106374 | GTTCAAGCCCTCCAC[A/G]TTAGTCTTATATTTG | 9678 |
| rs112959261 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11095907 | CTTTTTCTAGTTGTT[C/T]TCTAGTCAGGGGATA | 9678 |
| rs112967392 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10988557 | TTTTTTTTTTTTTAA[C/G]CTAGATGTGGTATTC | 9678 |
| rs112983478 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11147163 | TATTTTTTATTCAAA[C/G]TGAAAGCTGAGAAAC | 9678 |
| rs112993406 | in-del | -/A | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11077300 | ACCAGTAGTGCAAAG[-/A]AAAAAAAAAAGCCAG | 9678 |
| rs113009193 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11026434 | CTTTATTGAAGTGGT[C/T]TGGAGCTGAACTTGG | 9678 |
| rs113009618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073388 | AAAACCCAGCCAGGC[A/G]TACATTAAACCTTAA | 9678 |
| rs113021470 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11148724 | TTTGTAGGTTAATAG[A/T]CAAACATTTATATAA | 9678 |
| rs113023343 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:10994605 | TTTTAGATTTTATTA[C/T]TGTGTCCGGAATTGG | 9678 |
| rs113039741 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11122695 | ATGCTGTTGTTAACA[C/T]GTTTCTCCTTGGCAA | 9678 |
| rs113041968 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11041017 | GGAACTGGAAAATTA[C/T]TTTAGATAACATTAT | 9678 |
| rs113044401 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11072141 | GTAAGGGAAGCATAG[C/T]GGTTTCTGCTTCTGG | 9678 |
| rs113046342 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11155678 | TGTGTCATAATTGCA[A/G]TGATACAGTTACTTG | 9678 |
| rs113060616 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11099972 | AATTGACTATTGACA[A/G]TTTCTCTAAATGAGC | 9678 |
| rs113080694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132883 | CCTTTTCATATACCT[A/G]TTGATGATGTTTACC | 9678 |
| rs113087789 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11085260 | TTTAATTACACATTG[C/T]GACATTAGCTTAATA | 9678 |
| rs113096175 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11082002 | AAAGCTAATAGTGTA[C/T]GTAGAATTCTAACAG | 9678 |
| rs113102015 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:10977016 | AATTGAATCATATTT[C/T]TGACTCTTGTTTTAG | 9678 |
| rs113116656 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11148117 | CCAAGTTACCATCAT[G/T]CCTGATCTGTTTGCA | 9678 |
| rs113135296 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11155835 | TGATGTTCAATCAGG[A/G]AGGAATGAATAGATG | 9678 |
| rs113137879 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11062429 | ATGTCAGAAAACAAT[A/T]AAGTTACTAAGCTCT | 9678 |
| rs113140412 | snp | C/G | 0.0729998 | 0.176553 | intron-variant | PHF14 | GRCh38.p7 | 7:11030981 | CTGTCTTGTCTATTT[C/G]TAGATGGTTGTACTT | 9678 |
| rs113149071 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135719 | TTTCCACAGCCTGCT[C/G]TAAGAGATAAACCTA | 9678 |
| rs113153617 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11097620 | GTTGTTATGCAGCTA[C/T]TGTTTGAATACTTTC | 9678 |
| rs113153837 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11116320 | TCCTTTTAGTGGAAA[A/G]CGATATTTAGAAACC | 9678 |
| rs113158788 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11000903 | TTCTCTTGTTTATTA[C/T]GCTTTTGGTCTTGTA | 9678 |
| rs113170104 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10986870 | ATTGGCATTTTTGTT[C/T]TGTAAAAGAAAGAAG | 9678 |
| rs113178318 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146860 | TTTACTTATGTATTT[A/G/T]TTTAGAGACAGAGTC | 9678 |
| rs113197853 | in-del | -/ACC | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10988815 | TTGTTAATTCTTATA[-/ACC]TCCTGAAGTAGATAT | 9678 |
| rs113198861 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10988738 | AGAGATACAGCGGAA[A/T]GGAAAAGGCATTGAC | 9678 |
| rs113232668 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11070332 | ATCCTCTATCCTCAG[C/T]CTCCCAAAGTGGTGG | 9678 |
| rs113238518 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11134698 | TGCCATCATTTATTG[A/G]TTCAGTCTATCATTA | 9678 |
| rs113243701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11038140 | ATATGGAGGCCGAGC[A/G]CAGTGGCTCATGCCT | 9678 |
| rs113252395 | snp | A/T | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11001063 | TTTGGGTCTGAATTT[A/T]TTTTTGTTACGAGTA | 9678 |
| rs113286944 | snp | A/G | 0.233235 | 0.249437 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965146 | TGGAGGAGAAGAGGT[A/G]TTCTGGCTTTTGGAA | 9678 |
| rs113287745 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10991073 | TCGGTTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 9678 |
| rs113328700 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11098331 | CTTCCTTGAGACCTT[C/T]CGCAGTGTCTAGCCT | 9678 |
| rs113334343 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047571 | GAGGCTGAGGCGGGC[A/G]GATCACTTGAGGTCA | 9678 |
| rs113393816 | in-del | -/GAA | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11154335 | TAAACATCATTTCAA[-/GAA]GGTGAATTAAATTAC | 9678 |
| rs113412473 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11152105 | ATTTGAAAATTGCTT[G/T]TGATCAGTACTGCAA | 9678 |
| rs113418162 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11024914 | ACATTTCATAAGGCT[A/G]TAGCTGCCATACATA | 9678 |
| rs113419194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989549 | TTAAAGTTTAAATCT[A/G]TAATGCAGAAGGTTT | 9678 |
| rs113431712 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11098462 | CTCTCTGTCTGCCTT[G/T]CCTCTCCTCATTTTT | 9678 |
| rs113449540 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11160098 | GTAGTCTCCAGTGTC[C/T]ATTATTGCCATCTTC | 9678 |
| rs113450078 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11147561 | GCTGTCTGAATCTTA[C/T]TTGACCTCTCAATGT | 9678 |
| rs113481455 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11157041 | TCATGGTTCAGTTAT[C/T]TTTATCACCTCCATG | 9678 |
| rs113497369 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106258 | ATTTTTCTAATTTTT[A/T]AAAATTAATTTTTAT | 9678 |
| rs113505111 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959868 | GTGGTGTTTCAGCCA[C/T]TCAGTGAGTCCTGAG | 9678 |
| rs113510496 | snp | A/G/T | 0.0260255 | 0.111165 | intron-variant | PHF14 | GRCh38.p7 | 7:11124475 | ATAAGAAAGTATCAT[A/G/T]CTAATAATAATAATA | 9678 |
| rs113516970 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11032587 | TAGATGGATTTTGTT[A/T]GTTAGGAGTAGAGTT | 9678 |
| rs113522759 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11071613 | TTCAACGATCATTAC[A/G]GTCCAGTTTTTAGAG | 9678 |
| rs113525859 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11039247 | TGTATTTTTTTTTCT[A/C]TTCTTTGGATGTATA | 9678 |
| rs113530198 | in-del | -/ATGAA | 0.180383 | 0.240111 | intron-variant | PHF14 | GRCh38.p7 | 7:11009488 | ACACACTGAGCACAT[-/ATGAA]ATGAGTTTTATGTGT | 9678 |
| rs113531835 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149622 | CTTCCTAGAACTACA[C/G]TTGGTGGGCAATATT | 9678 |
| rs113534213 | in-del | -/CA | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11067914 | GGTCAATAATCTCTT[-/CA]TGAAGGATTCATCTT | 9678 |
| rs113545824 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | PHF14 | GRCh38.p7 | 7:11074683 | AACATGCACAAAATA[C/T]AGCCAAGTTCTTTGC | 9678 |
| rs113546754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040009 | TAAAATACTATCTAC[C/T]ATAAAAGACATTTTC | 9678 |
| rs113549812 | snp | C/G | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:11087226 | AGATGGAGTCTCGCT[C/G]TGTCATCCAGGCTGG | 9678 |
| rs113572603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11003946 | AACATCAGTAGAAAT[A/G]AGCTAAGAAAACATC | 9678 |
| rs113581229 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973320 | TTTGGACTCAAGATT[C/G]TGTATCCGGGCCCTT | 9678 |
| rs113582813 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11081834 | ACACTCCAGCCTGGG[C/T]GACAGAATGAGACTC | 9678 |
| rs113584285 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068289 | CCGGAGGCAGGGCTT[A/G]CAGTGAGCCAAGATC | 9678 |
| rs113586134 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11025972 | CAAAAATTAGCTGGG[C/T]GTGGTGGCACGTGCC | 9678 |
| rs113588281 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10995718 | GGCAGCTGAGGCCCG[A/G]CGAGAATTTGAGAGC | 9678 |
| rs113614622 | snp | A/C | 0.000265622 | 0.0115213 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982661 | GGAAAGAGAGAAGGA[A/C]AAAGAAAAAGCAACA | 9678 |
| rs113615231 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:10994846 | CGTACCCGAAGAGTG[A/C]GCAGCAGCAAGATTT | 9678 |
| rs113622468 | in-del | -/A | 0.380138 | 0.213458 | intron-variant | PHF14 | GRCh38.p7 | 7:11032498 | CAGGGAGCTTTGTTT[-/A]AAAAAAAAAAAAAGA | 9678 |
| rs113643901 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11152197 | AATTGGATTGTTTTG[G/T]AAAAGTATGTGAAGC | 9678 |
| rs113651964 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11146673 | AAAGCATTTAGAGAA[C/T]TCTACTATGTTTGAG | 9678 |
| rs113663006 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958998 | GGAGTCTTTTTAAAA[C/T]GCGTATCAGTCAAAG | 9678 |
| rs113675814 | in-del | -/C | 0.130008 | 0.219321 | intron-variant | PHF14 | GRCh38.p7 | 7:10996483 | CAGAGAAAACTGTTT[-/C]AAAAAGAGAGTCAGT | 9678 |
| rs113692954 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | PHF14 | GRCh38.p7 | 7:11093930 | TGTAGGAGTAGAGGA[-/T]TTTTTTTTTCCTCTT | 9678 |
| rs113693202 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11049856 | TCTTTGTTAATGATG[A/G]TAATCTGACAACCTA | 9678 |
| rs113696390 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10986759 | GTTTTTTGGGGACGG[C/T]AGTGTACTATTTTCA | 9678 |
| rs113720351 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11076572 | TTTTCTTTTTCTTTT[C/T]TTTTTTTTTTTTTGA | 9678 |
| rs113731675 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | PHF14 | GRCh38.p7 | 7:11152886 | GAAACACCTACTGCA[C/T]TTTGTTCAGGAATCA | 9678 |
| rs113735022 | snp | A/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11128171 | AAATTCATGCCTTCT[A/T]ATTTAAACCAGACCT | 9678 |
| rs113747217 | in-del | -/A | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11031399 | AGCATGTTATGACAC[-/A]ACATGCTTTATTAGA | 9678 |
| rs113761815 | snp | A/G | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11117285 | ACTACAAGGTGAGCT[A/G]TCTTAGCTTGGAGAC | 9678 |
| rs113767403 | snp | C/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11013515 | CCCACCTTTAATGCT[C/T]TTACAGTAGGACTAA | 9678 |
| rs113773958 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959990 | TATTTTTTAATATAC[A/G]TAGAAAGTTTATCTG | 9678 |
| rs113797139 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11016902 | CACCCTTTCCCTGCA[C/G]TATCCTTCCCAACGT | 9678 |
| rs113807892 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | PHF14 | GRCh38.p7 | 7:10991938 | TTTAAATTTTTAAAA[A/G]TTATTTCTAGTTTTT | 9678 |
| rs113813206 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHF14 | GRCh38.p7 | 7:11155976 | AAACTTTATACTTAT[A/G]TAGTAGCTAATAGGT | 9678 |
| rs113814966 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11146090 | TCTAGTGCTGTAAAC[A/T]GTGAAAATGTCAGAA | 9678 |
| rs113828326 | snp | C/G | 0.48 | 0.0979796 | intron-variant | PHF14 | GRCh38.p7 | 7:11068427 | GCTAAGTAAAATAAA[C/G]CAGTTACAGAAGGGT | 9678 |
| rs113830762 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11037482 | TCATGTGACTCTGTT[C/T]TCTATTTCTAATCAA | 9678 |
| rs113840207 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11149972 | TTTAACTTGAATGTT[G/T]CTAGTGTGTGAGGCT | 9678 |
| rs113840923 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | PHF14 | GRCh38.p7 | 7:11162357 | GGCCTTCCACAGTGC[C/T]GGGATTACAGGTGTG | 9678 |
| rs113841394 | snp | A/C | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11148722 | CATTTGTAGGTTAAT[A/C]GACAAACATTTATAT | 9678 |
| rs113848229 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11098461 | CCTCTCTGTCTGCCT[C/T]GCCTCTCCTCATTTT | 9678 |
| rs113870009 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | PHF14 | GRCh38.p7 | 7:11060157 | GTTGAGATTATGGCC[C/G]TGAGCCATGGTGCCT | 9678 |
| rs113875208 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11051926 | TTTTTTTTCTATATT[A/G]TGAAATATACCACAT | 9678 |
| rs113886805 | snp | G/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11030083 | TTCATTTATATAGCT[G/T]TTCCAGTCTCTTGAT | 9678 |
| rs113894837 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:10994320 | GGCATGTGCCTGTAG[G/T]CCTAGTTACTCAGGA | 9678 |
| rs113922926 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11150587 | TTGCATCATTAAATT[C/T]TTAAGTAAAGCTTAC | 9678 |
| rs113960309 | in-del | -/TTAA | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165249 | TTTGAAGACTACTGT[-/TTAA]TTATATTGTAGAGGG | 9678 |
| rs113964954 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11002813 | AAGAGGCAAAAATGA[A/G]ATGCTGATGACAAAA | 9678 |
| rs113970843 | snp | C/T | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 7:10970044 | TTTAGTTTGCTTAAT[C/T]AGACAGAATTGTGGA | 9678 |
| rs113974070 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10992524 | AAAAATTAGCCGGGC[A/G]TGGTGGCTTATACCT | 9678 |
| rs113987669 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11058114 | ATCCTACAGTTTTAT[G/T]GTTGCTAAAGTAGTT | 9678 |
| rs113995080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11000438 | TCTGTCTCCCAGGTT[C/T]CTGCGATTCTCGTGC | 9678 |
| rs114006010 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11024102 | GTGAAGCTGCCTTAT[A/T]GCTGATAATGGAGAA | 9678 |
| rs114040035 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11083713 | TGACCCACCCCCTTG[A/G]CCTCCCAAAGTGCTA | 9678 |
| rs114047609 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11048519 | GAGGTTACAGTGAGC[A/C]TTAGATCATGCCACT | 9678 |
| rs114053230 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150265 | GGTTATTGTTACTGG[C/T]TATAGTTATGGTTAT | 9678 |
| rs114128892 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11132256 | CTCTACTTGCCCATT[C/T]TCTTCCCACTGATAA | 9678 |
| rs114144536 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11098510 | GGGTTCTACAGCTCT[A/G]CTATGTCTCACTTCC | 9678 |
| rs114147574 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11132423 | GTTGTGGCAGATGGC[A/G]AGATCTCATTCTTTT | 9678 |
| rs114153973 | snp | G/T | 0.175254 | 0.238565 | intron-variant | PHF14 | GRCh38.p7 | 7:10979974 | TAAAACATTAAAAAT[G/T]TTTTAAAAAATTGCT | 9678 |
| rs114186887 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11047476 | GTTGTAGTTGTATGG[C/T]GCTAGAAACATATAG | 9678 |
| rs114191284 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11128920 | TCAATTTCTTTTGCA[C/T]TTTTTTTGCTAGGCT | 9678 |
| rs114206218 | snp | A/G | 0.0271762 | 0.113356 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106620 | TTAAGATGTTTAATC[A/G]AAATAATTGGCCACT | 9678 |
| rs114209178 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11086099 | GTAGTGCTTATTCTC[C/T]TTCATCAACTCTCTC | 9678 |
| rs114264484 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10987018 | CGTTAAGTACATTAG[A/G]TGTCATGTTGAGAAA | 9678 |
| rs114266097 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11069817 | CGTGGCTTGGTATTA[C/G]CACCACACCACCATG | 9678 |
| rs114279617 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965917 | GCACGGGAGGGAATC[C/T]CCTGGTCTGCCTGCT | 9678 |
| rs114289730 | snp | A/G/T | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11122782 | TGCCCTATAGTTCCA[A/G/T]CTTAGTCCAGTCCTG | 9678 |
| rs114290478 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11147560 | CGCTGTCTGAATCTT[A/G]CTTGACCTCTCAATG | 9678 |
| rs114296653 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964657 | AGATCTCCTGAATAA[A/G]ATTCTGAAGAGTGTT | 9678 |
| rs114322767 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10987251 | TTCTAAAAATGTAGA[A/G]GAAGTATGATTGGTC | 9678 |
| rs114343275 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11019281 | ATTCCCTCTTCCTCT[A/G]TTTTTTGGAATAGTT | 9678 |
| rs114466463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047365 | AGCTACTGTGCCTGG[C/T]TTAAATTAGTACACT | 9678 |
| rs114468575 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11027889 | CCTTACATTTACTTT[C/T]TTTGTTATTTTTGGC | 9678 |
| rs114470394 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11015446 | TGTATTGACATGAAT[C/T]TGTGGTCTGTATCAT | 9678 |
| rs114479165 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10983861 | TCTACTTGAAGTTCT[A/G]CTACTGAAAGTTAGG | 9678 |
| rs114497478 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11134613 | CAGAGTAGCCACAGG[A/G]TCACACAACTTTTTG | 9678 |
| rs114500298 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | PHF14 | GRCh38.p7 | 7:11098572 | AAAATGGCCAGAACT[A/T]GAACTCCAGTTCTTG | 9678 |
| rs114510215 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11067118 | TTGGACAACTCAGCA[A/G]TAAGAAACAACCCCA | 9678 |
| rs114524377 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11120875 | AGATCTAACTCATAC[A/G]GAAACTTGTTTTTTA | 9678 |
| rs114528204 | snp | A/G/T | 0.0326105 | 0.123535 | intron-variant | PHF14 | GRCh38.p7 | 7:11039742 | TATACCAGCTTTGAA[A/G/T]ATGCTTTATGTGAAA | 9678 |
| rs114530549 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11138369 | TAAAGAGACTCCTTA[C/G]AAGGTGATAATGAAA | 9678 |
| rs114560031 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11139588 | CAAATTTAAAGGATT[C/T]TACCAAGTTGTACTA | 9678 |
| rs114572389 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:10980239 | TGATTGATAAAAAGC[C/T]TTCTAGAAGGTTGAT | 9678 |
| rs114584374 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965428 | TATTGCTGACTGATC[C/T]TTCCTCTAGAAGCTT | 9678 |
| rs114584815 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11033788 | CTAGATCTGGGTATT[A/T]GGGCTGAGGTTCGGT | 9678 |
| rs114589610 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001610 | GATCTTGGCAATATT[A/T]TTTTATTTTTTGGGG | 9678 |
| rs114592013 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | PHF14 | GRCh38.p7 | 7:11076541 | TCTTCTTTAGAGATG[A/C]TTATCTTGGATATTT | 9678 |
| rs114597711 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11039294 | GGCAAACTAGAGATA[C/T]TCATTTTTATGTTAA | 9678 |
| rs114600074 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11142498 | TTCTGATATCATGTA[A/G]AAAACTATCTAAATC | 9678 |
| rs114607343 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11102414 | GTTTGTTAGTATGTT[G/T]CATAAGACATAGTGC | 9678 |
| rs114614781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075957 | TAATACGATGAAACC[C/T]CGTCTCTACCAAAAA | 9678 |
| rs114619394 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11029536 | GTAAAATGTAAAACA[G/T]TGCCACTCTCCTCAC | 9678 |
| rs114646865 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11145470 | CAAATCTCCAAATTC[A/C]TTAGGCAGTTACTTC | 9678 |
| rs114675992 | snp | A/G | 0.0256215 | 0.110247 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972320 | AATCTCCTTCTAGAA[A/G]TTAGTTTTACATAAA | 9678 |
| rs114680266 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11132267 | CATTTTCTTCCCACT[A/G]ATAACCAGGGTTTTG | 9678 |
| rs114716702 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11059274 | AGAATTGAAAACATG[A/G]ACTTGCAGCATTAAA | 9678 |
| rs114719422 | snp | A/G | 0.0119302 | 0.0763069 | intron-variant | PHF14 | GRCh38.p7 | 7:11040808 | TAATGATAGAATAAT[A/G]TTGTGTATTTTTTTA | 9678 |
| rs114722624 | snp | A/G | 0.108402 | 0.206034 | intron-variant | PHF14 | GRCh38.p7 | 7:10995585 | GTGGTCGATGGGACC[A/G]CGCCACAGAGCGGGG | 9678 |
| rs114730662 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11007881 | AATTTCGCTTATTGA[A/G]TTTATAATTGTTTAC | 9678 |
| rs114731177 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11077937 | TGCTTCTCTCTTCAG[C/T]GTGCATGAAACTGAG | 9678 |
| rs114750830 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11041687 | GAACATTAGCACATT[C/G]TCAGGCCAGCTTTTT | 9678 |
| rs114833008 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11086084 | AATGAATAAAAATAT[G/T]TAGTGCTTATTCTCC | 9678 |
| rs114834781 | snp | A/G | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11005833 | GAGTCTCGTTCTTTC[A/G]CCAGGCTACAGTGCA | 9678 |
| rs114839777 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11035258 | ATGTAAACTAGATGC[A/G]AATACCACACCATTT | 9678 |
| rs114841950 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11023130 | ATTGATAGTAGTTTT[C/T]CTAGAAAGCCAATAA | 9678 |
| rs114842222 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11158644 | GAAGAAACTGATTTC[A/T]TATTTTTGTCAATCT | 9678 |
| rs114845338 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11138463 | ATAGTAAACATTAAA[A/T]ATTATTTTTAAGCAA | 9678 |
| rs114860498 | snp | C/T | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11017784 | TGATATGATATCTTT[C/T]GTCTGTTTTTGCTTC | 9678 |
| rs114863698 | snp | A/C | 0.030665 | 0.119967 | intron-variant | PHF14 | GRCh38.p7 | 7:11055795 | ATAATGTTTAAGCTT[A/C]AGTCTTGAGAATCTG | 9678 |
| rs114865147 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11035466 | TGACATACAAGATCA[A/T]GTTTCTAAAGAAGTA | 9678 |
| rs114867919 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11109238 | TATCAGGAAGCAGTG[C/G]CTGATAGTTTTCAGG | 9678 |
| rs114870424 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | PHF14 | GRCh38.p7 | 7:11003862 | ATGTATCTACCCCAT[A/C]TGTTGTACCTTGTGT | 9678 |
| rs114876983 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | PHF14 | GRCh38.p7 | 7:11074511 | CACCGTGCCTGGCCC[C/T]GTTAGTTCCAACTTT | 9678 |
| rs114878529 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11054011 | TAGAAATTCCAATGC[A/G]TGTTGAAGCTCCAAA | 9678 |
| rs114881351 | snp | C/G | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11033809 | GAGGTTCGGTATAAT[C/G]TTTATTTCCATTTAA | 9678 |
| rs114909455 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11072756 | TTTGGCTCATAGTTC[C/T]GCAGGCTGTTCAAGC | 9678 |
| rs114911240 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11054509 | GAGTGATCAGTCATT[C/T]TGGTCTTGATCTTAC | 9678 |
| rs114935200 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:10975463 | GGGCCTTTCAGATGT[C/T]TCTGAAGTATAAGTC | 9678 |
| rs114952329 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11142303 | CCTTTTCTGTTCTTA[C/T]AGTGATACACATAGC | 9678 |
| rs114952973 | snp | C/T | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064326 | CAAAAGTCTACACTT[C/T]TTTATTACATTGCAT | 9678 |
| rs115013884 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159276 | GTTTTTGACATGGTG[C/T]GATCTATAACTATTT | 9678 |
| rs115043533 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11008563 | GTGATGCCTGATGAT[C/G]TGAGGTGGAACAGTT | 9678 |
| rs115045790 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | PHF14 | GRCh38.p7 | 7:11070224 | CTGTGACTACAAGTG[C/T]GCGCCACCATGCCCA | 9678 |
| rs115047073 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11118835 | TATATACTTCAGTAA[A/G]TTATTCCTTAAGCAT | 9678 |
| rs115052574 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | PHF14 | GRCh38.p7 | 7:11089933 | TGTGCCGTCACGACC[A/G]GCTAATTTTGTATTT | 9678 |
| rs115057333 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11049496 | AAAAAAAAAAAAAGT[A/G]TAAATTAGAACTGTT | 9678 |
| rs115069171 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165367 | ATACATCGTATCAGG[A/G/T]TGTTAATATATATTA | 9678 |
| rs115070702 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11129250 | GGCTGTTTATTGAAA[C/T]AACAAATGATGTTTG | 9678 |
| rs115073334 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11155485 | GCTTTGGCTGACTTA[A/C]CCTTCCCACTGTTCC | 9678 |
| rs115076747 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11052587 | ACCAGTTCACACTCA[C/T]ACCAGCAATGGATAA | 9678 |
| rs115082919 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11033141 | GATCTTGAAAGCTCC[A/G]TTTCTCCAAGCAGGT | 9678 |
| rs115090373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995586 | TGGTCGATGGGACCG[C/T]GCCACAGAGCGGGGG | 9678 |
| rs115102687 | snp | C/G | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:10998869 | GTACCATCTCTACTT[C/G]TTAAGTCATTCTTAG | 9678 |
| rs115111170 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | PHF14 | GRCh38.p7 | 7:11010570 | TATATAGTTTAATTT[A/G]TAACTATTAATATTA | 9678 |
| rs115115039 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11027357 | TATTGAAGTTTTTAA[A/G]TTTTCCTTGTATTTG | 9678 |
| rs115118856 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11042298 | TATAGTTTTAGAAAA[C/T]TGGAAAATTACTTTG | 9678 |
| rs115121612 | snp | A/G | 0.0858192 | 0.188533 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964914 | GTGGTTTTCAGCTCC[A/G]TTAGGTCATTTAAGC | 9678 |
| rs115166444 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11044420 | AGAGCCTTTTCATTG[G/T]TGTTAGTGGTTTTTA | 9678 |
| rs115174550 | snp | G/T | 0.084728 | 0.187577 | intron-variant | PHF14 | GRCh38.p7 | 7:11122456 | ACGTATATATATATA[G/T]TGTGTGTGTGTGTGT | 9678 |
| rs115175483 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | PHF14 | GRCh38.p7 | 7:11141233 | TTTAAATTTAGAGCA[A/C]CTGGCCAAATTCTTT | 9678 |
| rs115177723 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11139600 | ATTTTACCAAGTTGT[A/G]CTATATTTAAATGAA | 9678 |
| rs115180109 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11060498 | TTTCTACACTGGTGT[A/C]CTTAAACTTATGTGT | 9678 |
| rs115203542 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11072416 | ATTCAACATGAGATT[A/T]GAGTGGGACACGTAT | 9678 |
| rs115203698 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11094691 | GCTCCCAAGGCTTCT[A/G]TACTCTGATATTAGC | 9678 |
| rs115210491 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10987136 | TTATTAATCAGTTGT[C/G]TTTTTACACATTGCA | 9678 |
| rs115220364 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11014646 | GCTGAAAAGCCCCTC[C/T]GTTCTACGAGACCTC | 9678 |
| rs115253699 | snp | C/T | 0.0437281 | 0.141251 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066312 | TCACTCAGGCTAGAG[C/T]GCAGTGGCACTTTCT | 9678 |
| rs115257228 | snp | G/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11037997 | AAACTGTAAAAGAAG[G/T]TATAAACGTAGTTAC | 9678 |
| rs115264905 | snp | C/T | 0.0839998 | 0.186933 | intron-variant | PHF14 | GRCh38.p7 | 7:11091744 | GCCTGGGTGACGGAG[C/T]GAGACCCTTTCTCAA | 9678 |
| rs115266699 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11075448 | ATGGCAGAAGGCAAA[C/G]GGGGAGCTGGCATAT | 9678 |
| rs115302965 | snp | C/G | 0.0267878 | 0.112589 | intron-variant | PHF14 | GRCh38.p7 | 7:11096203 | GCATGTAAACTTCAA[C/G]TGGGATTAAAACCAT | 9678 |
| rs115319303 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11083525 | CCAGGCTGCAGTGCA[A/G]TCTCGGCTCACTGGA | 9678 |
| rs115320271 | snp | C/G | 0.195704 | 0.244033 | intron-variant | PHF14 | GRCh38.p7 | 7:11022860 | AAAATCATATCTTCT[C/G]TTCTTAGATGGGTTC | 9678 |
| rs115321100 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:11168919 | TGAAACTGTAGAAGA[C/T]TGTAAGCATTCTAAG | 9678 |
| rs115322277 | snp | A/C/G | 0.0422008 | 0.138995 | intron-variant | PHF14 | GRCh38.p7 | 7:10995873 | CGCTGGCCCGCAAGC[A/C/G]CCTTGCACAGCCCCG | 9678 |
| rs115326219 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF14 | GRCh38.p7 | 7:11096936 | GTACCTGTTTACTTC[A/G]TTGATAGTATTTTGC | 9678 |
| rs115328326 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11116277 | ATCTCCATTCCTGGA[A/G]TCAGCTGTTTCTCCA | 9678 |
| rs115339842 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | PHF14 | GRCh38.p7 | 7:11034780 | TCTCGAACTCCCAAC[C/T]TCAAGTGATCTGCTT | 9678 |
| rs115344153 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11133626 | GCTAATCTCCAGAGT[A/G]CTTCCCCTAGCAAGA | 9678 |
| rs115349983 | snp | A/G | 0.0252325 | 0.109451 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104433 | GTATAAAATTATTCC[A/G]TGTCCATAATCGGTC | 9678 |
| rs115355132 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11137567 | TTAAACATTAATCAC[C/T]TTTACATTTTAACTT | 9678 |
| rs115362391 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11108568 | GTAATTCTGAAAGGT[A/G]TCACTAATGAAGGAA | 9678 |
| rs115411901 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11009557 | AAATATGTTTCCCAT[A/G]CTCATGTTTTATATG | 9678 |
| rs115418148 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11122022 | CCCCTTGCCCTACCC[C/G/T]CCGACAGGCCTCTGG | 9678 |
| rs115421877 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:10977892 | CATAGGGTTGGGTGT[A/G]TGATAGGAGACTTAT | 9678 |
| rs115421974 | snp | C/T | 0.0252325 | 0.109451 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105347 | CACTCCATTCTATTT[C/T]CCTGTATTCACATCC | 9678 |
| rs115426877 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11058725 | TACGTGCAATAAGAG[A/G]TTTGCATTCTGAATG | 9678 |
| rs115429899 | snp | A/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11039876 | GATTTTTGGAAGATT[A/T]TGTTTTATACTTAAT | 9678 |
| rs115437535 | snp | G/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11017484 | GATTTGCATTTCTCT[G/T]ATGATCAAGGATTTT | 9678 |
| rs115444290 | snp | A/G/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11137013 | TAAGACATATGCTAC[A/G/T]CATTTTCAGTGGGGA | 9678 |
| rs115448614 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:10998403 | AAACTGAATAAGGAA[A/G]CATATACCTAAAATA | 9678 |
| rs115452004 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11016316 | TCGAGAAGCCTTTTA[G/T]TATATGAGCTTCAAA | 9678 |
| rs115467248 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959219 | GCTGCCCAAACCATA[A/G]CCACCTAACAGCCAC | 9678 |
| rs115472402 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11084570 | TAAGCCAGTTTTTAA[A/G]TAGCTACAAAATATA | 9678 |
| rs115480512 | snp | A/G | 0.00332784 | 0.0406552 | intron-variant | PHF14 | GRCh38.p7 | 7:11013945 | TCATATGTTTGCTTT[A/G]TAATGTGTCTGCCTT | 9678 |
| rs115571531 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11148114 | ACTCCAAGTTACCAT[C/T]ATTCCTGATCTGTTT | 9678 |
| rs115605324 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11140705 | GAAGTTGAAATAATA[A/G]GATTTTAAACATGGT | 9678 |
| rs115635300 | snp | A/G | 0.110167 | 0.207236 | intron-variant | PHF14 | GRCh38.p7 | 7:11022339 | TCTGGAAAGGAAGTT[A/G]AAACTGTATACAAAA | 9678 |
| rs115641659 | snp | A/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11134504 | CTAAATTGATTTTAC[A/T]GCCACTTGTATGGTT | 9678 |
| rs115652333 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | PHF14 | GRCh38.p7 | 7:11159367 | TTTGCCTAGAACATC[A/G]AGACTCAGCAAAGGA | 9678 |
| rs115655384 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11141429 | TCTGGTGCTCATTTT[C/G]TGATTAAATCTCTTA | 9678 |
| rs115655533 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11023542 | TGAAATTGAAATTTG[A/G]CCAATTAGGGCTGGG | 9678 |
| rs115665709 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10988985 | GGCAGATTTTTGTTT[C/G]CTTACTCTGGTACTG | 9678 |
| rs115665987 | snp | A/G/T | 0.0158469 | 0.0875917 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968545 | CATAGTATATAATAC[A/G/T]TAGTGTTGATGGCCA | 9678 |
| rs115673943 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11020462 | GGCTCATTGTAAACC[C/T]CCGCCTCCTAGGCTC | 9678 |
| rs115780993 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11136644 | TTAAGAAATGCATTT[A/G]TAATTCTTAATCATG | 9678 |
| rs115805856 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11148042 | CATTCCTAATTACTT[C/T]CTTTTGTTTAATTCC | 9678 |
| rs115813944 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066739 | GGCTTTTTCAATGTG[A/G]GCTTATTTCTAGACT | 9678 |
| rs115827670 | snp | G/T | 0.0252325 | 0.109451 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106763 | TTCTTGTGATGGAAT[G/T]TTTACACAGAAATGA | 9678 |
| rs115829276 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11033177 | GGATATTCCATGTCA[A/C]CCAATGCATTAATTA | 9678 |
| rs115831727 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11044902 | CTACTGGTCGAGTAT[C/T]CCAAATCTGAAAATC | 9678 |
| rs115839373 | snp | A/C | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103687 | AATGGAAAATAGTTT[A/C]AACTTTAGGAATAGA | 9678 |
| rs115877553 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985038 | ATTCTATTATTCAAG[C/G]TCTACAGTAGTTTTT | 9678 |
| rs115878383 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | PHF14 | GRCh38.p7 | 7:11029174 | GGGTAACCTTGCTCT[A/G]TTTTTCTTTAAATAA | 9678 |
| rs115880285 | snp | C/G | 0.0256215 | 0.110247 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968831 | CCTGTTTTCCATTCT[C/G]GTAATCTCTGAAGTT | 9678 |
| rs115882298 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:10991955 | TATTTCTAGTTTTTA[A/T]ATAAAATTCAGAAGT | 9678 |
| rs115886186 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11137326 | CCATGTGGATACTTC[C/T]TATGCTTGATCTTAA | 9678 |
| rs115890165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11166716 | CTTCATAATGCTTTT[C/T]TGCACCTAGGTTACA | 9678 |
| rs115925375 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11053656 | TGACTAGTATTATCA[C/T]CCTTAACTTTGGAGT | 9678 |
| rs115934334 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11048936 | ACATTTCTATTTTCT[A/G]GGAATTAGCCAAATT | 9678 |
| rs115943943 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | PHF14 | GRCh38.p7 | 7:11152073 | CTTCAGGTAGCAGAA[C/T]TGTCAAGCTGTTTTG | 9678 |
| rs115950803 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11045875 | AACTTACTGTGGAAA[A/T]ATCAAACTGACTTGC | 9678 |
| rs115952186 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | PHF14 | GRCh38.p7 | 7:11039528 | TAAATTACAGTTTTC[A/G]CAAATATTTTTTATT | 9678 |
| rs115971163 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11133632 | CTCCAGAGTGCTTCC[C/T]CTAGCAAGACACTCT | 9678 |
| rs115991049 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11013062 | AGTTTGATCTTTTAT[A/G]TATATATTTTAGTAC | 9678 |
| rs116012220 | snp | A/G | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11005070 | GTGATAGTTTAGGTG[A/G]TGTCAACCACAGACC | 9678 |
| rs116016983 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11039967 | TTTGGCTTGATTTGC[A/C]AGTTTTTCTCATAAG | 9678 |
| rs116064302 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11134360 | TATCATTTAGAGAGA[C/T]TTGCAAACTTTTTAA | 9678 |
| rs116070482 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11093215 | ATCTTTAATATCTCC[A/G]TCATCCCAGAGTTTG | 9678 |
| rs116073268 | snp | G/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11139967 | CAGCCTAACAGGCTG[G/T]TTTGTTGGAGCAGTA | 9678 |
| rs116115904 | snp | A/G | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062988 | AAAAAGAATAAACAT[A/G]TTGATAAAACAAATA | 9678 |
| rs116116644 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | PHF14 | GRCh38.p7 | 7:11085201 | AGTTTTGCTTGACAT[G/T]TTTTAAAGATTTACT | 9678 |
| rs116118160 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | PHF14 | GRCh38.p7 | 7:11045648 | TCTTCAGTCCATCCC[A/G]GAGTTCTGTGGACTG | 9678 |
| rs116119580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11023390 | GTAATTGTTTTGGGG[C/T]GTGCCGTTAACATGC | 9678 |
| rs116126278 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11093492 | TTGGATTTCTTTACT[A/C]TTTCCTGTGTTTCTG | 9678 |
| rs116126941 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11113473 | TGTGGTTGAATACCA[A/G]TATAAACAACTAACA | 9678 |
| rs116136011 | snp | G/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11033280 | TATACAATTCCAGGC[G/T]GATTGGATACTGAGG | 9678 |
| rs116136130 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11059856 | AAATAATTTAAACTT[C/T]TTGTCAAATTTTTAT | 9678 |
| rs116160071 | snp | A/G | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11017586 | TCAAATCTTTTGTCT[A/G]TTTTTAATCAGATTA | 9678 |
| rs116162054 | snp | G/T | 0.104504 | 0.2033 | intron-variant | PHF14 | GRCh38.p7 | 7:11026840 | CCTCTTGCTTATTTT[G/T]CTTTAAGAAAACATC | 9678 |
| rs116176470 | snp | C/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11032169 | GCTCAGGAGGCTGAG[C/G]TGGGAGGATTGCTGA | 9678 |
| rs116190630 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11119691 | AATTAGTTCATAATT[C/T]TATAAAATATTTGTT | 9678 |
| rs116194975 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11155475 | TTCTCACTGGGCTTT[G/T]GCTGACTTACCCTTC | 9678 |
| rs116198309 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11145843 | TCTTTTACTTCTATC[A/G]TATACGTTATACATT | 9678 |
| rs116254078 | snp | A/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11137370 | TGACAGCTCTACACA[A/T]TTCCCTAGTTAAGAG | 9678 |
| rs116274739 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:10998182 | ATTGAGTAGATAAGA[A/G]TAACCATAGTAATTA | 9678 |
| rs116276734 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11053666 | TATCATCCTTAACTT[A/T]GGAGTTATCATATAG | 9678 |
| rs116283398 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11092951 | AGATTGGCATGGCAA[C/T]GTTCTAGATTGCTCT | 9678 |
| rs116287464 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11076961 | TATATTAATATAATA[C/G]TAATATATATGTTGT | 9678 |
| rs116290698 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11142866 | GATAAAACTCCGTTA[A/T]TGACTTAATGGTTAA | 9678 |
| rs116302231 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | PHF14 | GRCh38.p7 | 7:11011340 | GCTCCAATTTAGGCT[C/T]CTGGTTGTCTGGTTA | 9678 |
| rs116316736 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | PHF14 | GRCh38.p7 | 7:11122273 | CACAGTTTACCATGG[A/G]TAACTGAAACCTGGG | 9678 |
| rs116344227 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11069225 | CCCCAACCAGCACCC[C/T]ACACCACACATACCC | 9678 |
| rs116346286 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PHF14 | GRCh38.p7 | 7:11134408 | TATTGTTTGCTATAT[A/G]ATTTAAAGATTTCAT | 9678 |
| rs116349861 | snp | C/G/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11140040 | TGTTACCCTGTAACA[C/G/T]CTTACACGTTCCTAC | 9678 |
| rs116353275 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065410 | CAGTTCATGGCACAT[G/T]TAATGATCAGAAAAT | 9678 |
| rs116353334 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11121729 | GGTAGCACATACAGT[A/G]TGGACATATTCTGGG | 9678 |
| rs116354168 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11163559 | TATCACACACATTTC[A/G]CACTTTACTTAATGA | 9678 |
| rs116429694 | snp | C/G/T | 0.039522 | 0.134904 | intron-variant | PHF14 | GRCh38.p7 | 7:11010886 | TCTGAAACTCCTGGG[C/G/T]TCAAGCGATCATCCT | 9678 |
| rs116447173 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11095741 | AAATGAGAAGCTCCT[A/G]TAATCACCTACAAAA | 9678 |
| rs116458170 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | PHF14 | GRCh38.p7 | 7:11002333 | GACAGCCACAGGTGT[A/G]GGTCAAGGGGGGAGC | 9678 |
| rs116499849 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11055105 | TTGTAAAGGCAGCCT[A/G]AGATAGTTCTGTTTA | 9678 |
| rs116509038 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11111597 | ACCAGTACACCTTAA[C/G]AATATATTGCTATGG | 9678 |
| rs116533401 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11029810 | GTAATTTTTATTGCA[C/T]ATTCATGATGGCTTT | 9678 |
| rs116562607 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11133935 | AAGGACTAACCTGGA[C/T]CAGGTGACCCAAGTG | 9678 |
| rs116563960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130919 | GTCATATAGTATGTA[G/T]CCTGTTCAATTTGGC | 9678 |
| rs116589995 | snp | G/T | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11023320 | TTTACTTTTGAAGTG[G/T]AATTTGTCAAAATTA | 9678 |
| rs116597291 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PHF14 | GRCh38.p7 | 7:11014851 | TTTGTTAACACATTT[A/G]AGCACTTGTCATCAT | 9678 |
| rs116620545 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:10975607 | TTCAGTGTACCTTAT[A/G]TATATATACAGTTTC | 9678 |
| rs116623870 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11031785 | TAAGTAAAAAAATAC[C/T]GAGCTATTGTGCAGG | 9678 |
| rs116628363 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11006640 | TGGTCAGCAGAAACT[G/T]GATGATGGTATAGTA | 9678 |
| rs116654363 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11132179 | ACCTGTAGCCCTCAT[A/G]TTGTATATTTTATCT | 9678 |
| rs116667641 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF14 | GRCh38.p7 | 7:11125720 | TTTTATGTTTAATAT[A/G]TTGTTCTCTTTTTTT | 9678 |
| rs116669972 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11160708 | TGTTTGTTGGCTGTT[A/T]GTATGTCTTCTGAGA | 9678 |
| rs116674872 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965001 | CTACCTTCTTTGCGA[C/T]GGGTTAGAACATGCT | 9678 |
| rs116684950 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PHF14 | GRCh38.p7 | 7:11018214 | CTTTTTTGCTTAGGA[C/T]AGCTTTGGCTCTTCT | 9678 |
| rs116691397 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11050419 | AAATATGAGTAAAAA[C/T]TTACTTTTAACAACT | 9678 |
| rs116694880 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11084819 | GTATTTTGTAACAAT[C/T]AGTTTCAATGTTTAT | 9678 |
| rs116740401 | snp | A/T | 0.00297375 | 0.0384452 | intron-variant | PHF14 | GRCh38.p7 | 7:11038867 | GCAGGTTAGTTTCTT[A/T]CCAATTGCTGTCTCC | 9678 |
| rs116741869 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11033734 | ATCTCTAATGACTCA[A/G]TTTCAACCTCATTTA | 9678 |
| rs116747132 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11135198 | CAAGTGGCATAATGG[C/T]TCTGTGCCTCAGTTT | 9678 |
| rs116751817 | snp | A/G | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11031617 | AAAAAAATTAGCTGG[A/G]TGTGATGTTGCCTGT | 9678 |
| rs116769513 | snp | A/G | 0.00676609 | 0.0577691 | | | GRCh38.p7 | 7:10969915 | CTTTTTCTTACAGTA[A/G]GTGTCCACAACAAGC | 9678 |
| rs116796841 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | PHF14 | GRCh38.p7 | 7:11047654 | TAGCTAGGAATGGTG[A/G]TGGGGATTCGTAATC | 9678 |
| rs116807609 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11083110 | AATCGGGTCTAGCTT[A/G]GATTGTGCAGTCCAA | 9678 |
| rs116824642 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11160757 | TTGCCCACTTTTTAA[A/T]TGAGTCATTTGTTTT | 9678 |
| rs116836332 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | PHF14 | GRCh38.p7 | 7:11073512 | CTGTGGCTTTCCAGG[A/G]TTCAGCCCCCTTGGC | 9678 |
| rs116837601 | snp | A/C | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11035120 | TGTTTGAAAAAAAAA[A/C]AGCGTAATAAAAAAG | 9678 |
| rs116865317 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11085670 | TTTTTTTGAGACAGT[C/G]TCTCACTGTGTTACC | 9678 |
| rs116867228 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | PHF14 | GRCh38.p7 | 7:11036246 | GATATAGTTTATTGT[A/C]ACTCAAAAATTATAC | 9678 |
| rs116892920 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063835 | ATTACTCTATGTTAT[G/T]TATTTCTTTAGTTTC | 9678 |
| rs116894722 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11071694 | CCCCATTTCCAGCGT[C/T]AGGCAACCACTGCAA | 9678 |
| rs116903067 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11052995 | AACCTTTAAGTGCTG[C/G]CTTACAGTTATGAAT | 9678 |
| rs116935509 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11141414 | CTGTATAGTATAGAA[C/T]CTGGTGCTCATTTTC | 9678 |
| rs116940701 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11085928 | TGCTTGAATTCTGGA[A/G]CCTAGTTATTTGGGT | 9678 |
| rs116947933 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | PHF14 | GRCh38.p7 | 7:11079828 | TTTTTCTTCATTGTC[A/G]TCATCCTGTTTTTTC | 9678 |
| rs116974833 | snp | A/G | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:10971601 | AATAACCTAAATGCA[A/G]TATTGTCTTCTGGAT | 9678 |
| rs117013062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150135 | TATAACAATATGCCA[C/G]GGAGTGATTAATATT | 9678 |
| rs117020725 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11165986 | CACTACAATTCTGTC[C/T]GTGTAAAAAGAGCAA | 9678 |
| rs117036540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027402 | AGTTCACTTTGAATA[C/T]TTATATTAAACAATT | 9678 |
| rs117038122 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | PHF14 | GRCh38.p7 | 7:11075002 | GAGTGCAGTGGCATG[A/G]TTTTCGTTTACTGCA | 9678 |
| rs117040107 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11117420 | GGAGATTTTCTAGAA[C/T]TACAAATGCGTGACA | 9678 |
| rs117044467 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11037624 | AATTTGAATTTTCAT[A/G]TACCTCTTCATCGTA | 9678 |
| rs117054218 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PHF14 | GRCh38.p7 | 7:11057282 | CTAAAGAATTAATTA[A/G]AATACATTACATGTT | 9678 |
| rs117079853 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11012163 | TGATTTACCAAGATA[C/T]TGTCAATGAAGTCCT | 9678 |
| rs117089337 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11092448 | TAAAGCCCTTATGCT[A/G]AAGTCCTAAGATAGT | 9678 |
| rs117151440 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11098485 | TCATTTTTATTGCTA[C/G]TGTATAATTGGGTTC | 9678 |
| rs117154562 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11039487 | ATTTCTTTGAATGCC[C/T]TTTTTAGTACTGTGT | 9678 |
| rs117176042 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11138377 | CTCCTTACAAGGTGA[C/T]AATGAAAAAAAAACA | 9678 |
| rs117180674 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11030036 | TTTTGATACATGTAG[C/G]TGTTTTTGATACATA | 9678 |
| rs117182717 | snp | A/G | 0.0449849 | 0.143069 | intron-variant | PHF14 | GRCh38.p7 | 7:11111510 | TATTGGTGTCCTTCC[A/G]TTTGATAGCTTTCCC | 9678 |
| rs117204127 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11005958 | CCACCTCACCCGGCT[A/G]TATTTTTGTATTTTG | 9678 |
| rs117205775 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:11129321 | AAGACCAAGAAGATA[C/T]CTGTTCAGCAAGTTT | 9678 |
| rs117224471 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | PHF14 | GRCh38.p7 | 7:11114457 | CTTTTATAGAAATTC[C/T]GTAAGTCTAATAAGA | 9678 |
| rs117234467 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11077768 | TTGAGAGGCAGGTTC[A/G]GTTAAATGAGTGGAG | 9678 |
| rs117240702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062822 | AGAGAGCTAATTTAA[A/G]AGAGGCATCAGACTT | 9678 |
| rs117256719 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | PHF14 | GRCh38.p7 | 7:11072089 | ACTGGTAATTTACTA[A/G]GAAAAGATATTTAAT | 9678 |
| rs117276422 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11033939 | TATATGAAGTAATTG[G/T]AAGTAAACCCTGTTT | 9678 |
| rs117282371 | snp | A/G | 0.0189856 | 0.0955633 | | | GRCh38.p7 | 7:10969852 | CCTAGACCAAAATTC[A/G]GATCTCCAGACTCTT | 9678 |
| rs117291087 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:10996803 | TTTGCTAATGCTGCG[G/T]TTGTGAGAACCAGAG | 9678 |
| rs117308428 | snp | A/G | 0.0496679 | 0.149556 | intron-variant | PHF14 | GRCh38.p7 | 7:11038871 | GTTAGTTTCTTTCCA[A/G]TTGCTGTCTCCTTCA | 9678 |
| rs117327377 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11000963 | ATCTAGATTTTCTCC[C/T]GTGTTATTTTCTAGT | 9678 |
| rs117331072 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11008757 | AAAATCTTTTTTGGC[C/T]GGGCGCGGTGGCTCA | 9678 |
| rs117331265 | snp | C/T | 0.162253 | 0.234095 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962208 | CTATTCAGTATGATA[C/T]TGGGTGTGAGTTTGT | 9678 |
| rs117337306 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:10989492 | TATATGTAATGTTAA[A/G]CACAATCTATTAAAT | 9678 |
| rs117351779 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11145118 | ATGTCTATTTTATAC[C/T]ACAATTATAAAAATG | 9678 |
| rs117359527 | snp | A/G | 0.0189856 | 0.0955633 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973480 | CCAAGAACCTGGACA[A/G]CTTGCAGTCACGATC | 9678 |
| rs117385809 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966599 | ATCAAAACCTTGAAA[A/G]CCCATCTAATTGGTG | 9678 |
| rs117402889 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PHF14 | GRCh38.p7 | 7:11013052 | GTTTTGCATGAGTTT[C/G]ATCTTTTATATATAT | 9678 |
| rs117442726 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11021465 | ACTCAAGTTGGTATC[A/C]TCACATGAGTGGTTG | 9678 |
| rs117444431 | snp | C/T | 0.00744079 | 0.0605395 | nc-transcript-variant, synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:11169460 | TATATCTCAGGAGCT[C/T]AACATGGAACAGAAA | 9678 |
| rs117462988 | snp | A/G | 0.030278 | 0.119257 | intron-variant | PHF14 | GRCh38.p7 | 7:11167522 | GATTGGACTACAACT[A/G]TATACTAAGTATGTC | 9678 |
| rs117474868 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11016177 | AAAATTCTTTTATAT[A/G]CTATTTGAACACTTG | 9678 |
| rs117485183 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11166325 | TGTCTTATCTCAGCA[G/T]AGAGAAAAAAAAAAA | 9678 |
| rs117491489 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | PHF14 | GRCh38.p7 | 7:11003703 | AACATGAATCCCATA[C/G]ACAGTACAAGTTTAT | 9678 |
| rs117510366 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11080727 | GTGCGGATATATATC[C/G]TAATGGTTTCAACCA | 9678 |
| rs117535227 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | PHF14 | GRCh38.p7 | 7:11075710 | ACATATATCCAAACT[A/G]TATCAATATGTATCA | 9678 |
| rs117539992 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10977196 | TGTTGAAGTTGTGGA[C/T]TCCCAGCCCTACTTA | 9678 |
| rs117558820 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:10995352 | ATTTACAAGCCTTGC[A/G]CTAGACACAGAGTGC | 9678 |
| rs117588474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040969 | TGTTGCTGTTTTAAC[C/G]TAAACTCTATGGAAA | 9678 |
| rs117611768 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11020541 | ATGCCACGACACCTG[C/G]CTAAATTTTGTATTT | 9678 |
| rs117631582 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11038386 | CAGTGACACAAGATC[A/G]TGCTACTGCACTCTA | 9678 |
| rs117660600 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | PHF14 | GRCh38.p7 | 7:11002070 | TTTGTTTTGAGACAG[A/G]GTCTCACTCTGCTGC | 9678 |
| rs117665999 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11004082 | GTGAAACCCTGTCTC[C/T]ACAAAATACAGAAAA | 9678 |
| rs117668771 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11028508 | CCATATAGGTAATTA[C/T]GTTTTTTCATATAAA | 9678 |
| rs117683238 | snp | A/G | 0.0356815 | 0.128715 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065351 | TTCTTTGTTGGAAGT[A/G]GTTATGGAACTACTT | 9678 |
| rs117687097 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11067206 | CAAGCATATGAAAAG[A/T]TGCTCAACATCACGA | 9678 |
| rs117695550 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11037586 | CTTGAATTATATTAT[A/G]ATGTTTGGAATAAAA | 9678 |
| rs117716847 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11000855 | CACAGAGCAGAAGTT[C/T]TACATTTTAATGGAG | 9678 |
| rs117724228 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | PHF14 | GRCh38.p7 | 7:11018819 | CTGCTTGTCGTGTTC[C/T]AGATCTTAGAGGAAA | 9678 |
| rs117761700 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11092825 | GCCAAAATGGTATTA[C/T]AAAATGTTGAAGCCA | 9678 |
| rs117768737 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965972 | TATTTGGGCAGGAGT[G/T]TACAGTTCCTCCAGG | 9678 |
| rs117808190 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11040039 | CATTTATTAAAAGAC[G/T]TTTAACAGAGGTTTG | 9678 |
| rs117810067 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11167309 | GGCTGTTTTGGCTCA[C/T]GTTGCTTCAAACATT | 9678 |
| rs117841431 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11129865 | ATAGGTAAGGTACAG[C/T]GGGAATTTTGAGAGT | 9678 |
| rs117862850 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11072916 | ACAACCATCTTTCAT[A/G]TGAACTAACAGCAAG | 9678 |
| rs117876767 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:10998922 | ATTGACTATGGATGT[A/C]TTTTTTTAGGCCAGC | 9678 |
| rs117917608 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11163876 | AGATGGAAGCCAAGT[A/G]GTGTATCTGTTTTTC | 9678 |
| rs117920041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975625 | TATATACAGTTTCAA[C/T]TGAAGGAATCTGAGA | 9678 |
| rs117932204 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11077417 | ACCATCCTGGCCAAC[A/G]TGGTAAAACCCCGTC | 9678 |
| rs117951766 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11076403 | CTATTCTTATAAGTA[C/T]GCTGTTTAGTTGTAT | 9678 |
| rs117951923 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11013318 | GGGCGCCTGCCACCA[C/T]GCCTGGATAATTTTT | 9678 |
| rs117983516 | snp | C/T | 0.046775 | 0.145601 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063867 | GTTATGAAATTTTTA[C/T]TTCTAATTGCATTAT | 9678 |
| rs117990660 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11006815 | GCCTTGAAAGCCTTC[C/G]GTTTGGCTTCAGCTT | 9678 |
| rs117992414 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11079958 | TTGATTGTCACTTTT[C/G]TTGCATATTGCTAGA | 9678 |
| rs117992770 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11017956 | ATGGCAAGAGATGGC[A/G]TCTAGTTTCCTTCTT | 9678 |
| rs117993536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094870 | CAGGCCACTTGGTTG[C/T]CCTCTGACATCAGCT | 9678 |
| rs118014074 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102844 | CTTGTCAGAATTGTC[A/G]TATTAAGTAATGTCT | 9678 |
| rs118023399 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066268 | TCTCGTTATTCTGAT[G/T]ATAATTTTTTTGTTG | 9678 |
| rs118030845 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11121152 | ATGACTTTTTAACAG[A/G]TAAATATCAGCAACA | 9678 |
| rs118030880 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134959 | ATAAACATGCTGATA[C/T]CTTTGTCCTCTGGCA | 9678 |
| rs118038020 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11019856 | TCTCTTTTGATGTAG[A/G]TACCTATAGCTATAA | 9678 |
| rs118046676 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11088673 | AAGGAAATAGTCAAA[C/G]AAAGAAATGCTAATA | 9678 |
| rs118075160 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:10995632 | AGGCTCAGGCCACGC[A/G]GGAGCCCATGGCGGG | 9678 |
| rs118090490 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11007213 | AAAAAAAAGAAAGAA[A/G]AGAAAAGCTTAGTTA | 9678 |
| rs118099360 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:10976776 | TGTTAGGTTGATATA[G/T]CTATATATCCCTTAA | 9678 |
| rs118150047 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11128707 | CTCTCTCTCCCCCCG[C/T]CCCCACTGCTTTCCT | 9678 |
| rs118170990 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11077659 | TTGCATTTTGTGAGT[A/G]TGATTTGGAGAACAG | 9678 |
| rs137876205 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11153117 | AAGATTACTGTCTCC[C/T]GTATAAAGAATAGGT | 9678 |
| rs137906843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033775 | TTAGAATAATTATCT[A/G]GATCTGGGTATTTGG | 9678 |
| rs137945936 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11140008 | GTCTTTGACTAGAAC[G/T]CACAGTAAGAAATAC | 9678 |
| rs137946796 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11002227 | CAGGAGATGGGAAGG[A/T]TCATCCTTTGAGAGA | 9678 |
| rs137956166 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104595 | GGAAGAAACATGAAA[A/G]TATCAGGAAGGAGAT | 9678 |
| rs137962069 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11090706 | CAGATTTACTTTTGA[A/G]TTTATTTCATATTAA | 9678 |
| rs137962293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11066979 | AGTTGGACTAAATTC[A/G]AAGTTAAAAACTTTT | 9678 |
| rs137973257 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10997815 | AAAGAGAGAAAGAGA[C/T]GGAAGCAGTTGTATC | 9678 |
| rs137982428 | snp | G/T | 0.0130921 | 0.0798413 | | | GRCh38.p7 | 7:10969435 | AGACAATTCATTTTT[G/T]TCTTCATTTATCTTA | 9678 |
| rs137993534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960673 | CCACACTGTCTTCCA[C/T]AATGGTTGAACTAGT | 9678 |
| rs137998015 | in-del | -/GTTA | 0.494187 | 0.0535994 | intron-variant | PHF14 | GRCh38.p7 | 7:11055849 | AAATATTTTTTAGAT[-/GTTA]GTTTAGGAAAAATGT | 9678 |
| rs138015266 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | PHF14 | GRCh38.p7 | 7:11025669 | GCATGGTAGCAGGTG[C/T]CTGTAGTCTCAGCTA | 9678 |
| rs138023949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130062 | TTCTCATTCATGTAA[C/T]GTATCAGTACAGGTT | 9678 |
| rs138025500 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11094198 | GTGTCTGTTAGTTTT[C/T]TCTGGCTGTTAGAAC | 9678 |
| rs138035868 | in-del | -/AAG | 0.02016 | 0.0983543 | intron-variant | PHF14 | GRCh38.p7 | 7:11154333 | TGTAAACATCATTTC[-/AAG]AAGGTGAATTAAATT | 9678 |
| rs138063340 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11138843 | ATTTGCTTCACTGTC[A/G]TTTGCTTCATTGTGT | 9678 |
| rs138081122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11061487 | TCATAATTATGGACA[A/G]TTATGAAGTGTGGAG | 9678 |
| rs138085493 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11085534 | GAACAATGAATTGCT[A/G]AATTTAATCGTTTTT | 9678 |
| rs138097628 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11166902 | GCATGCATTTATAAA[C/G]TGTACTTTATTTCTA | 9678 |
| rs138100847 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11021550 | GTACTTGTGTACTAC[A/T]TTTTAAGAAGGTCAG | 9678 |
| rs138135496 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11046736 | ACCCATAATGCAGAA[G/T]TAGGAGGGACTGAGG | 9678 |
| rs138136375 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11123302 | TAAGACAATATAGCA[A/G]TAAATTTACATATAT | 9678 |
| rs138148504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981410 | AGATTGTTATTTACT[G/T]AATTGGGTACAAAAA | 9678 |
| rs138149666 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990980 | CAAAGTATGGATGCT[A/G]TTTTTCAGGTTATCT | 9678 |
| rs138177842 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11078062 | TATTTTAGTTCACAC[C/T]GTGGTATTTGAATAG | 9678 |
| rs138179694 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10985237 | TTGGGTCTTAATCTT[C/G]CTGGTTATTTTAGCT | 9678 |
| rs138231189 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017118 | ACTCCATTGTGTATT[C/G]TGTACCACAATTTCT | 9678 |
| rs138244960 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11051124 | TAGCTCACTGCAGCC[G/T]CCACCTCCTGGGCTC | 9678 |
| rs138293321 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11153511 | GAATATGAGTTTAAA[A/G]CATGGTATAGATGTG | 9678 |
| rs138307196 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11158245 | GTGGCAATTCTTTAC[C/T]TTTTCCTTGCCTTTC | 9678 |
| rs138370058 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11112078 | ACATTGTAGTAATAC[A/G]TAGTTTATTTTGTGG | 9678 |
| rs138398492 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11041180 | TGCCTTTGTAGGCAG[C/T]GGATAATGAAGATAA | 9678 |
| rs138412237 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11148099 | TGACTACATTACAGT[A/G]CTCCAAGTTACCATC | 9678 |
| rs138419229 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11099465 | GGTATTTCTGGGGTA[C/T]ACAATTTTAGAGTAA | 9678 |
| rs138453515 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104744 | TGGATCTGCCCTCTG[C/G]CCACTTTACTCCCTC | 9678 |
| rs138480517 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10998516 | GAATATAAAGAGCTC[A/G]TTAATATAAATATAT | 9678 |
| rs138487340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067580 | ACTGATGGATTAAAG[G/T]ATAAACAAAATGTAG | 9678 |
| rs138487472 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11111006 | ATTTAATGGGCAAAT[A/G]ATTAATTCTTTAAGT | 9678 |
| rs138507063 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11045791 | ATTTCAGTGATATAG[G/T]AGTCTGTTGAGAGGG | 9678 |
| rs138547644 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11002717 | CCAAAGTGCTGGGAT[A/T]ACAGACGTGAGCCAC | 9678 |
| rs138571276 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963170 | TCTTTTAATTGTGAT[C/G]TTAGGGTGTCGATAT | 9678 |
| rs138601262 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965237 | GATGTTGGTGACCTA[C/T]GGATGTGGTTTTGGT | 9678 |
| rs138623218 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092946 | GAATCAGATTGGCAT[A/G]GCAACGTTCTAGATT | 9678 |
| rs138651754 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168132 | TCTATTCACTGGAGA[C/T]AAAATAAGGAAAAAA | 9678 |
| rs138656401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990363 | TTACTTGTGGATTCA[C/T]TTTTCGTTTTTCCTA | 9678 |
| rs138703875 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11162979 | AGAAAAGAAATAGTT[A/T]TTTATGTATTCCCAT | 9678 |
| rs138703912 | in-del | -/A | 0.0930568 | 0.194599 | intron-variant | PHF14 | GRCh38.p7 | 7:11145136 | ATGATTAAAAAAAAA[-/A]CCCTCGGGAGGGGTT | 9678 |
| rs138708394 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11135652 | AGCAACAATTTCCTG[C/T]ACTGGCAATGTTAAA | 9678 |
| rs138725750 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | PHF14 | GRCh38.p7 | 7:11128399 | TTCCCTACTTCATTC[G/T]ATTTCCTGTCTCAGA | 9678 |
| rs138754483 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042521 | ACTAACAGTTACTGA[C/T]ATTGTAAAAAGATGT | 9678 |
| rs138761507 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11014747 | AGAAATTCTGTCCAT[C/T]ATTGCAGAGTAGGTA | 9678 |
| rs138766006 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080687 | CTCTTTTCTAGATCA[A/G]AAGTACTATTCAGGA | 9678 |
| rs138805215 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11134552 | TTGATCTCATCCAAG[C/T]GCTTTATTTTACAGA | 9678 |
| rs138810776 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11139634 | TGTATCTATTTCACA[C/G]TAACCCTAAAGTACT | 9678 |
| rs138835523 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11017785 | GATATGATATCTTTC[A/G]TCTGTTTTTGCTTCG | 9678 |
| rs138839546 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085035 | TAATGGTATGTTTTG[C/T]TGAATTGAAATTTAC | 9678 |
| rs138843089 | in-del | -/CT | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11034226 | TTGGGTTGTAAAACT[-/CT]ACTTAGAGACACTTT | 9678 |
| rs138855477 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:10980225 | CTATCGTGAAGTTTT[C/G]ATTGATAAAAAGCCT | 9678 |
| rs138859077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065333 | TTTGTCTGTGATAGG[C/T]CATTCTTTGTTGGAA | 9678 |
| rs138872263 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11023238 | CTGGCAGTGTTCACA[A/G]TGCCTAATACATAGA | 9678 |
| rs138880923 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984752 | TTTATTAAACCTGTA[C/T]TTCATAAATACTGCC | 9678 |
| rs138883877 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11157689 | GTTCTTAAACTGCAA[A/G]CGTTTAAAAACATGA | 9678 |
| rs138886737 | in-del | -/TTAT | 0.125182 | 0.216612 | intron-variant | PHF14 | GRCh38.p7 | 7:11148584 | TATCAAAATATGAAA[-/TTAT]TTTATCTGTTAACAG | 9678 |
| rs138910779 | snp | C/G | 0.0707826 | 0.174302 | intron-variant | PHF14 | GRCh38.p7 | 7:11025522 | TTGCCAGCCGGGCAC[C/G]GTGGCTCACACCTGT | 9678 |
| rs138912277 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | PHF14 | GRCh38.p7 | 7:11013226 | GAGTGCAGTGGCGCA[A/G]TCTTGGCTCACTGCA | 9678 |
| rs138915419 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11111747 | CGAAAGCCCAAACAG[A/G]TCACTCTCTGCTAAC | 9678 |
| rs138992960 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071916 | TAAAAAAGTAAGCCT[C/G]CTAAATTTATATTAA | 9678 |
| rs139002471 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11148997 | AAACCCAAAGTCATT[C/G]CTTGAAATAGGGTTT | 9678 |
| rs139018909 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11030189 | TTATAATTATACGGT[A/G]AAGGTAGTCTGGATT | 9678 |
| rs139022268 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11059318 | AAATTCAAAACTACA[A/T]GATACATTTGCTAGT | 9678 |
| rs139032478 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | PHF14 | GRCh38.p7 | 7:11165481 | AAAGATATAAAGAAT[A/T]GGGAGAGTTGCCTCT | 9678 |
| rs139043840 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11119947 | TTAGAAACATAAAGT[A/G]CATTATGCCATGTTA | 9678 |
| rs139080134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116962 | GTATTGTAATTTAAA[A/G]AGTAGGACATAGCTC | 9678 |
| rs139093645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074819 | GCCACAACCACTTAA[C/T]AATACTCTAAGAAGT | 9678 |
| rs139158319 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11077226 | TTATAAATTGAAGAA[A/C]CCTCTGAATATATAG | 9678 |
| rs139173040 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11015167 | AGGGTATATTATGTC[C/T]TAAAATAAAGGATAG | 9678 |
| rs139184129 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11004891 | AAATACAAAAATTAG[C/G]CTGTAATCCCAGCTG | 9678 |
| rs139185297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072898 | GGTGTCAGGCTCCTT[C/T]AAACAACCATCTTTC | 9678 |
| rs139220191 | in-del | -/GATAA | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11165848 | CAAGTTTTATTTAGT[-/GATAA]GATAAACATGGCAGT | 9678 |
| rs139272326 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11079797 | ATGATTTTGTTTGTT[C/G]TTTACAGTTAATTTT | 9678 |
| rs139279947 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068073 | ATGAAATTCTGGGCC[G/T]GGTGCGGTGGCTCAC | 9678 |
| rs139289572 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11145870 | CATTACCATATGTTA[G/T]ACTTGTTGGATTAGC | 9678 |
| rs139291211 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11038004 | AAAAGAAGGTATAAA[C/T]GTAGTTACCATTATT | 9678 |
| rs139303463 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11160672 | TCGCTGACAATTAGC[G/T]ATGTTGAGCATTTTT | 9678 |
| rs139309135 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961770 | GGTTTGTAGTTCTCC[A/G]TGAAGAGGTCCTTCA | 9678 |
| rs139311747 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11163885 | CCAAGTAGTGTATCT[A/G]TTTTTCTTTCTACAC | 9678 |
| rs139322859 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10973840 | CCCTCAATTCCTGCT[C/G]CTCTCAGGGCTGCGC | 9678 |
| rs139333043 | snp | A/G | 0.000736648 | 0.0191776 | intron-variant | PHF14 | GRCh38.p7 | 7:11040649 | CTTAAAACAATATAT[A/G]CTACATTTGTTCAAA | 9678 |
| rs139338170 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11038919 | GATTTTCAAAGAACA[G/T]ATTTTTGATACAACT | 9678 |
| rs139350135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081483 | ATTTTCATCCTCTTA[C/T]TTGACCCCTTATTCA | 9678 |
| rs139352043 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11027139 | CCTTGCTCAATTTCA[A/G/T]CATATTACATGAAAT | 9678 |
| rs139379781 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11043244 | AGTCATTTAAATTCA[A/G]CCATTCTTTGACATC | 9678 |
| rs139395027 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11140627 | TACAAAGAAATAATA[A/T]AATCCATAACTGCAA | 9678 |
| rs139398222 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10976203 | TGGTTACTAATTGAA[G/T]TCATCCGCAGCAATC | 9678 |
| rs139429435 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11136541 | GTTTAAGTCTTTTGC[A/G/T]TAGTTATTACTTTTT | 9678 |
| rs139453670 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090946 | AGACACAAATAAAGA[A/C]AAAGTGGGACCATAT | 9678 |
| rs139483579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019410 | TTTATTATGGCTTCA[A/G]TCTCGTTACTTGTTA | 9678 |
| rs139488452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986758 | AGTTTTTTGGGGACG[A/G]CAGTGTACTATTTTC | 9678 |
| rs139497183 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11087377 | TTATATTTTTAGTAG[A/G]GACGGGGTATCACCA | 9678 |
| rs139522263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023565 | GGGCTGGGTGCTCAC[A/G]CCTGTTATCCCAGCA | 9678 |
| rs139523079 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11142462 | TCAGCTATAATTCAT[C/T]GCTTGAAAAGAAATG | 9678 |
| rs139561388 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10986470 | GAGAAATAATGTCTT[A/G]GTATCATTATGAAAA | 9678 |
| rs139561863 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11086802 | GAATATAATTTGTAT[A/G]GTAATTTAATTCATT | 9678 |
| rs139571102 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11155102 | GGAAAGAATAGACTT[C/G]ATTGTGCTTTCTGTG | 9678 |
| rs139589422 | in-del | -/TGT | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11140341 | CAGCTTTAAAACAAA[-/TGT]TGTTCACAGCTCAGT | 9678 |
| rs139593481 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10981857 | TTGACTATCATAAAT[A/G]TCTATGCTTATTTTA | 9678 |
| rs139609215 | snp | C/T | 0.00121786 | 0.0246464 | intron-variant | PHF14 | GRCh38.p7 | 7:11035595 | GTCTTTTATGACTCT[C/T]GGGAGTACAAATGTT | 9678 |
| rs139672619 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096543 | TTCCAGTTCATTTAC[A/G]GGTATTTCATATCGT | 9678 |
| rs139719421 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10993628 | GTTGGTGGCCCAGAT[A/G/T]CTGAAGAAAAATGAA | 9678 |
| rs139726592 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11100457 | ACTGGGGTACATAGA[C/G]ACTAAGCAGTGTGAA | 9678 |
| rs139727541 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059888 | TTATTTTATTTTTTT[A/G]AGACAAAGTCTCGTC | 9678 |
| rs139729863 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11151681 | TCTTGAGTTTGAGCT[A/G]TCAATGTTCCCAAGA | 9678 |
| rs139733669 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063405 | CATAATGGAGTAAAT[A/G]AAACAATAAAAATAA | 9678 |
| rs139745531 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11031443 | CCATGTTATGACACA[A/G]CATCTTATTTTTAAA | 9678 |
| rs139747238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11101384 | GCATTATACTTTTCC[A/G]GTAGTAAACTACAGA | 9678 |
| rs139784812 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PHF14 | GRCh38.p7 | 7:10995604 | CACAGAGCGGGGGCA[A/G]CACTCATAAGGGAGG | 9678 |
| rs139813269 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11160991 | AAATTCTTTCCACAG[A/G]CAGATGTCCAGAATG | 9678 |
| rs139833926 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960834 | TTCATTTCTCTGATG[A/G]CCAGTGATGATGAGC | 9678 |
| rs139848437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154881 | ATTATATTGTAATAC[C/T]AACAGTTGAAATTGC | 9678 |
| rs139900658 | in-del | -/ATTAT | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11027305 | ACTGTTATTAGAGAA[-/ATTAT]ATTAACTAGGCAGTA | 9678 |
| rs139903057 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11035278 | CCACACCATTTAACA[C/T]AAGACGCTTGAGCAT | 9678 |
| rs139912759 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106802 | GAAAATCCAACCCAT[C/T]AGTTCTCTGGATATT | 9678 |
| rs139913603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11043786 | CAGAAACTGCTATAG[C/T]ATATTCAAATCCCAA | 9678 |
| rs139933910 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11007158 | AGATCGCGCCATTGC[A/G]CTCCAGCCCGGGTAA | 9678 |
| rs139939164 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11123665 | TGAACCTTTAGTCCC[A/C]CCTACTCGGGAGGCT | 9678 |
| rs139941640 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11038209 | ACGAGGTCAAGAGAT[A/C]GAGACCATCCTAGGA | 9678 |
| rs139941697 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10999521 | ATGACCCTCGCTCTC[C/T]ATTTTGTTGTTTTTG | 9678 |
| rs139953306 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11010427 | CTTATCTTGTGTGTT[A/G]TAGTCTAACTCCTTT | 9678 |
| rs139960909 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11095672 | TTGTATTCATTATCT[A/G]CTAAATTGGGAGAAG | 9678 |
| rs139961530 | in-del | -/C | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11012314 | TCACCCCTCAGTATA[-/C]CTAGGGAATTGGTTC | 9678 |
| rs139983233 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11003972 | ACATCTCCCAGTTGG[A/G]CTTGGTGGCTCACGC | 9678 |
| rs139992786 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992125 | GCGACACAATCTCAG[C/G]TCACTGCAACCTCTG | 9678 |
| rs140017740 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002114 | CAGTGGCGCAATTTC[A/G]GCTCACTGCAACCTC | 9678 |
| rs140045435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10975056 | AAGTGAAAGCACGTA[A/G]ACTTCATTTATTTTG | 9678 |
| rs140120902 | snp | A/C | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063795 | AAAGTGCCATCTTCT[A/C]ATTTTGATAAGATTT | 9678 |
| rs140124538 | in-del | -/TG/TGTGTG | 0.0919065 | 0.197371 | intron-variant | PHF14 | GRCh38.p7 | 7:11041424 | AGATGCTGGTGTTTT[-/TG/TGTGTG]TGTGTGTGTGTGTGT | 9678 |
| rs140127823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044989 | AAACATTTGGATTTT[A/G]GAGCACTTCAGATTT | 9678 |
| rs140128286 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11141016 | ATATGTTCTGAGGAA[C/G]ATAAGACAGACCTGG | 9678 |
| rs140134461 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145503 | TATAAGCAGAATAGA[A/C]TTGAGCATTTTCTTA | 9678 |
| rs140144616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11024465 | CATCTAGGACTTACC[A/G]TAGCTAGAGAGGAGA | 9678 |
| rs140152752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958017 | TGTAAACCATGAAAG[G/T]GTAAATTTTATGGTA | 9678 |
| rs140153453 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11067837 | GAGAGGGGGAGATGC[C/T]AGGCTCTTTTTACTA | 9678 |
| rs140157371 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11087477 | TTACAGGCATGAGCC[A/T]CTGCGCCTGGCCAGC | 9678 |
| rs140165209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11026539 | TTAGAACTAGAAAAG[A/G]CTCAGAGATGCCCAC | 9678 |
| rs140166910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11007396 | TTACAATTTTCTGTA[C/T]AGTTAACACCTGTAG | 9678 |
| rs140230936 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103920 | AAACTAGTAGACTTT[C/T]GTTTAAAAGAATAAG | 9678 |
| rs140238557 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11074111 | ATGTCTTGGCTATTA[A/T]CATTTGTCTCTTTTT | 9678 |
| rs140247703 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11152648 | ACTTATAAGGATATC[A/G]TAATAAGAAAAACAG | 9678 |
| rs140272429 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965358 | GAGTTTGCTGGAGGT[C/T]CTCTCCAGACCTTGT | 9678 |
| rs140278896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11049238 | AGCACTTTGGAAGGC[C/T]GAGGCGGGAGGATCA | 9678 |
| rs140288938 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997193 | CTCATTTTGTTTCTC[C/T]ATAGTAGAGTTTAAT | 9678 |
| rs140334747 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985443 | CAGGCAGACATTTTT[C/T]TTAGCTGCTAAGTTC | 9678 |
| rs140337936 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:11036040 | TGAGGAAATTACTCT[A/G]TCAGTGCAATATATT | 9678 |
| rs140355036 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058533 | ATAAATGCTAAATAA[G/T]AGTGCTGTAATTACT | 9678 |
| rs140366924 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11015353 | CCATGTGTTGATGTT[C/T]AGGACAAATGACTAA | 9678 |
| rs140382416 | snp | C/T | 0.107694 | 0.205546 | intron-variant | PHF14 | GRCh38.p7 | 7:11089990 | TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 9678 |
| rs140384101 | in-del | -/A | 0.0228947 | 0.104514 | intron-variant | PHF14 | GRCh38.p7 | 7:10978812 | GTTGTCCTCTGGGGG[-/A]AAAAAATGTTCCCGT | 9678 |
| rs140397560 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964826 | CATTTGATCTACAAT[C/T]GCTGATATCCTTCCT | 9678 |
| rs140433841 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11060973 | TATAATGTAATTCTG[C/T]TTAGAATTATTTGGT | 9678 |
| rs140436142 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PHF14 | GRCh38.p7 | 7:11134809 | TAAAATAATTTTGCA[A/G]AAAAACATGAGTAAA | 9678 |
| rs140500781 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | PHF14 | GRCh38.p7 | 7:11138654 | AATATTTTAATTTCT[A/G]ATATTTATCTCACTT | 9678 |
| rs140516495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11089731 | GTGTGACTTTATGAT[A/G]TGACTTTAGTGTAGA | 9678 |
| rs140540266 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055483 | TGACTTACAAATTCT[C/G]GTTGTGTTTTATATA | 9678 |
| rs140548896 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11133750 | TTGGATTATCCTCAA[C/T]CACAAACACATCTTT | 9678 |
| rs140549149 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020805 | ATATGTAAATGAACA[A/T]CCTCCTACTCAACAG | 9678 |
| rs140578053 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107574 | TACTTCTTTAAGCAT[A/C]CAGTTTTTATTTTAT | 9678 |
| rs140579548 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11091612 | ATACAAGAATTAGCC[A/G]AGTGTGGTGGTGGTG | 9678 |
| rs140588858 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10984934 | ATTCCAAAGTGCTTC[G/T]TCGAAAAGTGCCCAT | 9678 |
| rs140616736 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988424 | GGGTAAACCTTTTTT[C/G]CAGGGCTGAATAATT | 9678 |
| rs140691324 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11112646 | CATGGTGGCGAGTGC[C/T]TCTAATCCCAGCTAC | 9678 |
| rs140693189 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11069303 | CAAAGGTTCCTGCTG[C/T]TTTATGGACCCAGGG | 9678 |
| rs140719785 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11079258 | CCAGAATTAGGTTGT[C/T]TTTGTGAGATGGCTC | 9678 |
| rs140733578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153423 | GTTTAGGGTTGGGAA[G/T]CAAGAATTTGGCTTT | 9678 |
| rs140738446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011988 | GGTGGTAGTAATAAC[A/T]AACTTTTAGGCATCT | 9678 |
| rs140754179 | in-del | -/A | 0.115788 | 0.21092 | intron-variant | PHF14 | GRCh38.p7 | 7:10990085 | TATCTCTGTGTATTC[-/A]ATATACCTACGCAGG | 9678 |
| rs140754784 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11072350 | TGAGAAATCTACCCC[C/T]GTGATCCAGTCACCT | 9678 |
| rs140759164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071051 | GGTTTTTGATTAACT[A/G]ATAATCTTTATTTTT | 9678 |
| rs140760343 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972216 | GTTGGGATTACAGGC[A/G]TGAGCCACCGCACCC | 9678 |
| rs140762730 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004485 | TCTCCACACCCCACA[C/G]GATCCATTCAGGTAC | 9678 |
| rs140788376 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11156178 | AGTAGTAGCTAAGAC[A/C]TAACCAGTAAATCCA | 9678 |
| rs140794150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147584 | CTCAATGTTATTTAA[C/G]AATGTCAACCATTCT | 9678 |
| rs140801809 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11006603 | ATGTTGTTGTCTTCT[A/G]TCTTCTTCATGGCAG | 9678 |
| rs140802799 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11110346 | AAAATCTGACAGATT[A/G]GTTGAGAAAGTATTA | 9678 |
| rs140814915 | snp | G/T | 0.00177888 | 0.0297704 | intron-variant | PHF14 | GRCh38.p7 | 7:11037123 | ATATGCAACATAATG[G/T]GATAGATCTTACTGA | 9678 |
| rs140828362 | snp | A/G | 0.00149016 | 0.0272555 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028782 | TGTGACCTGTGCTCA[A/G]AAGGAAGGTCTGCTT | 9678 |
| rs140840977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966210 | GACCGGAGCTGTTTC[C/T]ATTGGGCCATCTTGG | 9678 |
| rs140852193 | snp | A/C/T | 0.00319074 | 0.0398324 | intron-variant | PHF14 | GRCh38.p7 | 7:11002246 | TCCTTTGAGAGACAT[A/C/T]GGTTTAGAAGAAAGT | 9678 |
| rs140854152 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11039978 | TTGCAAGTTTTTCTC[A/G]TAAGAATCTCCTGTT | 9678 |
| rs140868327 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PHF14 | GRCh38.p7 | 7:11113638 | GAAAAATGAAATTTA[A/G]TATAATATTTAAGCT | 9678 |
| rs140902383 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143248 | AAAATATATAAACTT[C/T]ATTTAGCATAAATGT | 9678 |
| rs140932506 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11025270 | TGGTTTCTCGAGTTG[G/T]AATCTACTCCTGGTG | 9678 |
| rs140933552 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11091898 | ATGACTGCGTCTTTC[A/G]GTGGATATTGAAGGT | 9678 |
| rs140953952 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10988829 | AACCTCCTGAAGTAG[A/G]TATTATTTTTATCGC | 9678 |
| rs140997792 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11005043 | GTATAATGTCAATTT[A/G]TTGCATTATTGGTGA | 9678 |
| rs141036672 | in-del | -/GAT | 0.0879971 | 0.190408 | intron-variant | PHF14 | GRCh38.p7 | 7:11145957 | TTTAAAGCAATGGCA[-/GAT]AACTCTTGAATATGT | 9678 |
| rs141050506 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11049916 | AAGTGTAGCAATAGA[C/T]ACATAAAAGTTTTCT | 9678 |
| rs141059503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984131 | CTGAAGTAAGTTAAA[C/T]GGGTAGAAAGATTTT | 9678 |
| rs141097360 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001870 | GTTTCCCTTTCTTGT[C/T]TTATTACCTGATGTT | 9678 |
| rs141113681 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973371 | TCCGTACAGAGCGTG[C/T]TTTAATTTTCAATAA | 9678 |
| rs141113723 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11016151 | ACCTCCTGTGATGGT[C/G]CAATCTGGCAAAAAT | 9678 |
| rs141152384 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978620 | CAACCTTGGCGCTAT[G/T]GGCATTTTGTGTTGG | 9678 |
| rs141218789 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11134185 | CTTTACAGTAGGCTT[G/T]TAGAATCTAACTTGC | 9678 |
| rs141228053 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11056366 | TTACTTGTCATGTAG[A/C]ATACATATTTTATTA | 9678 |
| rs141253149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11090266 | GGAGAAGTTCTGCTT[C/T]GAATGAAACTGGTAG | 9678 |
| rs141259698 | snp | A/T | 0.002788 | 0.0372321 | intron-variant | PHF14 | GRCh38.p7 | 7:11051585 | ATAATAATAAATGCA[A/T]GACTTAAATTTTTCC | 9678 |
| rs141272388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017319 | TAGGAACCTCCAAAG[C/T]TTTCTTCATCATGGT | 9678 |
| rs141283054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060566 | CTAATTCAGTGTGTC[A/G]GAGTCAGCCTGAGAT | 9678 |
| rs141321670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143873 | CCAAAAATTGACAAA[C/T]GGAACTATATCAAAC | 9678 |
| rs141332027 | snp | C/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065618 | GATAGTTTTTCCTCT[C/G]CTGTATTTTAAGTAA | 9678 |
| rs141335312 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11159169 | TTCCTTAAGAAAATT[G/T]GTTACCTTTCATTTT | 9678 |
| rs141336287 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11147134 | ATTACGGGCATAAGC[C/T]GCCACACCCAGCCTA | 9678 |
| rs141345369 | snp | C/T | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11020603 | AGGCTGGTCTCAAAC[C/T]CCTGAGCTTAAGTGA | 9678 |
| rs141373300 | in-del | -/ATATGTATAAATACAAATATGTATTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117595 | ATAAATATGTATTTA[-/ATATGTATAAATACAAATATGTATTT]TATGTATAAATACAA | 9678 |
| rs141389263 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11028294 | GGTACTGAAAGTGTG[G/T]ATTCTGCTGAGCGTG | 9678 |
| rs141425399 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PHF14 | GRCh38.p7 | 7:11046026 | CCAGGGATGTGAAAA[A/G]CTAGTAAAGAATATT | 9678 |
| rs141425591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123010 | CCTCCTTTTAAAAAT[A/G]CTTCTTTCTCGCCTT | 9678 |
| rs141445436 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11009594 | AGAAAGATTTTAGAA[C/T]GTATTTAGTCACTAA | 9678 |
| rs141459451 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11111070 | CATGATTATACATAT[A/T]CGTTCATTCATATGC | 9678 |
| rs141482591 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106204 | ACTGAATTGATCCCA[A/C]TCTTTAAGTGACTAT | 9678 |
| rs141533922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11031703 | AGGCTGCATTGAACT[A/G]TGTTCTCACCACTGC | 9678 |
| rs141551051 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | PHF14 | GRCh38.p7 | 7:11005918 | CCGCCTCAGCCTCCT[C/G]AGTAGCTGGGACTAC | 9678 |
| rs141576061 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10996052 | GTGCCAAGAGTGAGC[A/G]AGGGCTGTGAGGGCT | 9678 |
| rs141596015 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11074465 | TCCGCCTGCTTCAGC[C/T]TCCCAAAGTGCTGGG | 9678 |
| rs141607553 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11140232 | GTTATACGACCCTAC[C/T]GTATATACACATGCA | 9678 |
| rs141624726 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11062301 | AGTGATAATCTGCCT[C/G]TTTAACACAGGGAAT | 9678 |
| rs141625776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965844 | CGTCCCAGGTTGATC[C/T]CAGACTGCTGCACTA | 9678 |
| rs141648660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956874 | TCTGACTTCCAAAAC[C/T]GTGAGAAAATAAATT | 9678 |
| rs141699603 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | PHF14 | GRCh38.p7 | 7:11123750 | ACACCACTACACTCC[A/G]GCCTGGGTGAATCGC | 9678 |
| rs141703492 | in-del | -/TA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038671 | AAAAAAAAAAAAAAT[-/TA]TATATATATATATGT | 9678 |
| rs141709984 | snp | C/T | 0.0807149 | 0.183963 | intron-variant | PHF14 | GRCh38.p7 | 7:11162278 | TATTTTTAGTGGAGA[C/T]GGGGTTTCTCCTTGC | 9678 |
| rs141715714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135051 | AATATCCCTCATTGC[A/G]TCTGTTACAAAATGT | 9678 |
| rs141744813 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11019088 | ACCCAGGGATAAATC[C/G]TACTTGGTCATAATG | 9678 |
| rs141745397 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11080079 | AATGAATGTCATAAA[C/G]TTATTCCACGTAAAA | 9678 |
| rs141746332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11085590 | TGGCCTCGTTTCAAC[A/G]TTTAACATTGGTGAC | 9678 |
| rs141750548 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11025481 | ATGAATCTATGCAGC[-/A]AACTTCATTGTTTTA | 9678 |
| rs141760123 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11083443 | CAGGAAGTTGCCACA[C/T]AGAAATATTCTGCTT | 9678 |
| rs141765293 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11129613 | CTTTATTTACCAAAA[C/T]ATTTTCTTTCTGTTG | 9678 |
| rs141768445 | snp | A/C | 0.00244998 | 0.034914 | intron-variant | PHF14 | GRCh38.p7 | 7:11040652 | AAAACAATATATACT[A/C]CATTTGTTCAAATCA | 9678 |
| rs141774562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11166162 | ACATTAAGAGGTAAG[C/T]CTGTCTACTTTCCAG | 9678 |
| rs141808618 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11014978 | TTTCGTGGAGATCAC[A/G/T]CTCTGCCTCTTCCTC | 9678 |
| rs141809783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045629 | GTTCTAGATTTGGAT[A/G]CTTTCTTCAGTCCAT | 9678 |
| rs141828018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979889 | TATTTGGAGAATGAG[A/G]GGTTGGGTAAGCTAT | 9678 |
| rs141867331 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983375 | GGAGCTCACAATCTC[C/T]GTCCTCAAGGAGAAA | 9678 |
| rs141872178 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11041944 | TGTACTTTCCAAATA[C/T]AAATATACTTTAGAT | 9678 |
| rs141884674 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080951 | AGTGTTGCTGGTGAT[G/T]TGGCCTAAGGTGATA | 9678 |
| rs141915610 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11150359 | GTGTTTGCTGGTTAT[A/G]AAGACGAACAGAGGC | 9678 |
| rs141955797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017870 | GGATTCCCCAATGTT[G/T]TCTTGTAGTATTTTC | 9678 |
| rs141977186 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11037794 | ACGTTTCCAATAATC[A/T]GCTACACTGTGTAGT | 9678 |
| rs141986247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980725 | CTGTAAATAGGATTT[A/G]TACTTTTCTCCGCAG | 9678 |
| rs142033631 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11144613 | TATTTATATAATAAT[A/G]TATAATTATATTTAC | 9678 |
| rs142048919 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | PHF14 | GRCh38.p7 | 7:11165073 | GGGACTATAGGCGCC[C/T]GCCACCACACCCAGC | 9678 |
| rs142069544 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11082062 | TGCCTTAGAAAATCA[A/G]TTTGAGTGCAGTGGC | 9678 |
| rs142082737 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001385 | TCTTCTGGGTTTTTT[-/T]GCCTCTCCATGTAAA | 9678 |
| rs142088107 | in-del | -/A | 0.084364 | 0.187256 | intron-variant | PHF14 | GRCh38.p7 | 7:11130098 | GCAGCTCTGCTCATT[-/A]TATAGTCACTTGGGG | 9678 |
| rs142099284 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11145721 | CAAGGAAATATACTA[A/G]TGAGCATAAAAAGTA | 9678 |
| rs142119360 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11152436 | AGGATTATAAATAAC[A/G]AACGTAAATACAAGC | 9678 |
| rs142138013 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044781 | GCATCTGGATGGTAG[A/G]AAAAAAATGATAAAC | 9678 |
| rs142162729 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150076 | ATACATTGCAAGTCA[C/T]GGAAGATTTACATAG | 9678 |
| rs142164135 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11098514 | TCTACAGCTCTACTA[C/T]GTCTCACTTCCCCCA | 9678 |
| rs142173904 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103084 | TTGTAAAACAACTAT[A/G]GACTCATATTAAATG | 9678 |
| rs142174329 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11061605 | AATTTGTTACTTTTT[A/G]TTTCCTATGGCATAA | 9678 |
| rs142239672 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065113 | TCATTACATGTTTTC[G/T]AAAATGATTAGATTG | 9678 |
| rs142243178 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11038550 | GTAGTCCCACCTACT[C/T]GGGAAACTGCAGCAG | 9678 |
| rs142245229 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11112743 | GCCATTGCATGCCAA[A/C]CTGGGCGACAGGGCG | 9678 |
| rs142245449 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10996801 | TCTTTGCTAATGCTG[C/T]GGTTGTGAGAACCAG | 9678 |
| rs142248232 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11097465 | GGGATCACCATTAGG[C/T]GTAGTAGTAGGCCTT | 9678 |
| rs142262526 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | PHF14 | GRCh38.p7 | 7:11004815 | CCGAGGTGGGTGGAT[C/T]ACTTGAAGTCAGGAG | 9678 |
| rs142274427 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11100346 | AGATGCTTACTGTAT[C/T]CCAGACTATGTTTTC | 9678 |
| rs142286434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000449 | GGTTCCTGCGATTCT[C/T]GTGCCTCAGCTTCCT | 9678 |
| rs142286584 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959400 | TTGCCTCACCAGCTG[A/G]AAACCTCTATGGGCA | 9678 |
| rs142325625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11033850 | ACCAAGATTTAGAGC[A/G]TGTCATGAGAAAGCA | 9678 |
| rs142343631 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104618 | AAGGAGATGAAATGT[C/T]TCTGAAATACAGGAA | 9678 |
| rs142350181 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10995152 | GTGTGTTACAAACCT[G/T]GAGCTAGACACAGAG | 9678 |
| rs142366416 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997841 | GTATCAGAGTGCTAG[A/T]ATATTTTATAATCTA | 9678 |
| rs142377541 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962134 | TGTTGAATAGGAGAG[G/T]TGAGAGAGGGCATCC | 9678 |
| rs142380251 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11091583 | CAAAATGGTGAAACC[A/C]GTCTCTACTAAAAAT | 9678 |
| rs142392098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999269 | CTCCAGTTCACTCCA[C/G]TCCTCTCTCAAACCA | 9678 |
| rs142413570 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053231 | TATAATCACTTAAAA[G/T]ATCTTATTCAGGAGA | 9678 |
| rs142521527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049058 | AGCGAAGAGGAAATA[C/T]TTCAGTTTTTAAAAC | 9678 |
| rs142529190 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11122037 | CCCGACAGGCCTCTG[A/G]TGTGTGTTGCTTCTC | 9678 |
| rs142542849 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11126562 | CTTTCTCTCTTCGTT[A/T]TTTAGCTGTTTCAAA | 9678 |
| rs142542998 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11076970 | ATAATACTAATATAT[A/G]TGTTGTACTTATGTT | 9678 |
| rs142556172 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11124752 | TATATATTAAAATAG[A/G/T]TATTTTCTATTTCTT | 9678 |
| rs142566001 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026127 | AAAAAAAAAAAAAAA[-/A]GAGAGAGAAATTGCC | 9678 |
| rs142574463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167288 | AAAGGGTATGAGCTT[C/G]ATAATGGCTGTTTTG | 9678 |
| rs142585533 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11108348 | ATTGGATTCTTTTCT[C/T]TTTTTCCCCTTCTGT | 9678 |
| rs142585582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011931 | ATACTCTCTCAGAAC[A/T]TTTCAATTTCCATTT | 9678 |
| rs142588185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11012696 | GATTTTTATTACATT[A/G]GCTGCCTAAATAATA | 9678 |
| rs142594554 | snp | G/T | 0.101301 | 0.200969 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960931 | CCCACTTTTTGATGG[G/T]TTTTTTTTTTCTTGT | 9678 |
| rs142604478 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11079685 | TGACTCTCTGTTTTC[A/C]AAATAAATTAATTAA | 9678 |
| rs142703380 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11047041 | TTTTAACTTACACGA[A/G]TAAAATTCTCTAAAT | 9678 |
| rs142707689 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11136177 | GGTCAATGTAAGGCT[A/G]TAAGGTCAATGTGGT | 9678 |
| rs142711618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058537 | ATGCTAAATAAGAGT[A/G]CTGTAATTACTTTGG | 9678 |
| rs142718465 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11075139 | AGACAGAGTTTCACC[A/G]TGTTGCCCAGGCTGG | 9678 |
| rs142751323 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064721 | TCATTGAACAATTGC[A/G]TGCAATTTGTCAGTA | 9678 |
| rs142752347 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11128323 | CTCTTATTTTCACTG[A/T]GGAAAGGGGGGTGAT | 9678 |
| rs142761008 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11051185 | AGCTGGGATTATAGG[C/T]GTGTGCCACCAAGCC | 9678 |
| rs142765552 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11139653 | CCCTAAAGTACTGGA[A/G]GTTTAAAAGGGAAGT | 9678 |
| rs142770871 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11142522 | CTAAATCATTTCAGC[C/T]GCAAGCTTATAACCA | 9678 |
| rs142771067 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966983 | AGAATCAGCATCCCT[C/T]TGCAAAGTAATGAAC | 9678 |
| rs142771271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061771 | TTTTGTTTTTTGTTT[G/T]TTTTTTTGTTTTTTT | 9678 |
| rs142771678 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11019383 | GTCCCAGGCTTTTCT[G/T]TACCGGGAGACTTTA | 9678 |
| rs142779631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014052 | ATGACCAGTGGGATA[C/T]AGATGGAGAAGGGTG | 9678 |
| rs142792536 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11023307 | CCTAATTTCTGACTT[G/T]ACTTTTGAAGTGGAA | 9678 |
| rs142813056 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PHF14 | GRCh38.p7 | 7:11025621 | ACACGGTGAAACCCC[A/G]TCTCTCCTAAAAAAA | 9678 |
| rs142876136 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082519 | CAGATAAGCTTAATT[A/T]TCCCTTGTTATTCAA | 9678 |
| rs142896200 | in-del | -/GGAGCAGCCAGGATTCTG | 0.0648419 | 0.167978 | intron-variant | PHF14 | GRCh38.p7 | 7:11073938 | GCATCAGCTGGAGCT[-/GGAGCAGCCAGGATTCTG]GGAGCAGTGTCCTGA | 9678 |
| rs142912264 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11101081 | TGCACAGTTTTTTGT[C/T]CTGGGAAGATAGGAG | 9678 |
| rs142914337 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11031089 | GTGAGCATATCTTGC[C/T]TTCTATTTCCATTTT | 9678 |
| rs142930754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087610 | AGGAATCTTTACTCA[C/T]GCAATTATTCCTTTT | 9678 |
| rs142979315 | snp | C/T | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105617 | CAGAATCATTTTTTC[C/T]ACCTGTCTGAATCAG | 9678 |
| rs142997630 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10983864 | ACTTGAAGTTCTACT[A/G]CTGAAAGTTAGGTTT | 9678 |
| rs143008625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144596 | TATAAATTAATGTAA[C/T]ATATTTATATAATAA | 9678 |
| rs143011129 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11037292 | CCAGGCATAATTTTG[A/T]TCTCTTTACATGTAT | 9678 |
| rs143016762 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11153787 | GGGTGGTTATAGGAT[C/T]AATTAAAGAAGACTT | 9678 |
| rs143018028 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10998989 | TTAGACATTGGGAAA[G/T]CGTACACATTTAGGA | 9678 |
| rs143019651 | snp | G/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10969805 | GGCTCAATGTTGCCT[G/T]TTTTTAGGGTAACAC | 9678 |
| rs143024338 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | PHF14 | GRCh38.p7 | 7:11074964 | TTTTTTTTAGATGGA[A/G]TCTTGCTCTGTCACC | 9678 |
| rs143046231 | in-del | -/GAGG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015004 | TCCTCTCCAATATAA[-/GAGG]GGGGGTGGGTACTTA | 9678 |
| rs143096826 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11067661 | CCTGAGGGTGGATAA[C/T]TGATAAAGAAGGAAA | 9678 |
| rs143114074 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | PHF14 | GRCh38.p7 | 7:11032071 | GGATTTTGAGATGAG[C/T]CTGGGCAACATAGCA | 9678 |
| rs143114714 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | PHF14 | GRCh38.p7 | 7:11139327 | CACTGTATTTATTTT[G/T]ATTGTATTCTCACCT | 9678 |
| rs143118216 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103202 | GCATTAATATTATTA[A/G]CATGAAATTTTTACT | 9678 |
| rs143121136 | in-del | -/T | 0.0260105 | 0.111035 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063661 | GAGGTTTTTATTAGG[-/T]TTTTTTGTTTTGCTT | 9678 |
| rs143139070 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11157850 | ATTTTCCATAACTCT[A/G]ATTGCCTCTGCACAT | 9678 |
| rs143174779 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11090096 | TTCTTTATGTGTGTA[C/G/T]GTGTGTCATTTTTTT | 9678 |
| rs143179576 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11023044 | TTAGTTTACCTGGCT[C/T]TTTATTTGTATTATG | 9678 |
| rs143188006 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11038077 | TACTGCTGAATAATT[G/T]GATAGCCTTGTCTCT | 9678 |
| rs143245221 | snp | C/T | 0.00517822 | 0.0506191 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973937 | GCAGCCGCCCTCGCG[C/T]TGTGCAATTTCTGGT | 9678 |
| rs143252463 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11113942 | AAAAGAAACCCAGAA[A/T]GAAAGTTCATATGCT | 9678 |
| rs143275095 | in-del | -/TTTT | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11053408 | AACTGTTTATAACTC[-/TTTT]TTTAGGCTTCAAAAA | 9678 |
| rs143280357 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11084527 | ACTTCACAATGCATA[A/T]TGGACTTTTTCTCAG | 9678 |
| rs143288831 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166596 | AGCTTTATTAGATCA[A/T]ATTTTAATGTTATTT | 9678 |
| rs143306054 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11045960 | TTCTTGAATTATGCT[C/G]TGCTGCCCAGGAGAA | 9678 |
| rs143314388 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10980212 | CTTACTTTTGCGTCT[A/G]TCGTGAAGTTTTGAT | 9678 |
| rs143315896 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11118704 | CATTTTCAGTAAAAC[A/G]TAGATTGTTTATTAG | 9678 |
| rs143331205 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11075859 | TAGCTAGGCTGGGCG[C/T]GGTGACTCATGCCTG | 9678 |
| rs143357356 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11007339 | TGTTTTTTATGTTTT[C/G]CATCCTGTTCTGTAT | 9678 |
| rs143382134 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11161855 | TGAAGGAAAGTTACC[A/T]ATGTAGGAGCCTCTT | 9678 |
| rs143407686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11040394 | TTTTAAACCTCCTAC[A/G]TATGTGTCTTTGTCT | 9678 |
| rs143413395 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11115059 | CTTCCATCCGTTCAC[C/G]CAAGTCACATATCTG | 9678 |
| rs143427862 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11005753 | TATATATATGTAATA[A/G]TTTCTGTGGGATAGA | 9678 |
| rs143429438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11099848 | GTAATCTCACCATTC[A/G]TCTGACACTTGATTT | 9678 |
| rs143438358 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090912 | GGTCAGGAGGTAGCA[C/G]TCATTCAAGGGAATA | 9678 |
| rs143463060 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125183 | AAGGTGATTTTTTTT[-/T]ATTAGACACTAAGCA | 9678 |
| rs143526250 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11070254 | AGCTGATTTTTTAAT[C/T]GTTTGTAGAAATGGG | 9678 |
| rs143531289 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11001979 | ATGATGTTAGCTATA[C/G]GTTTTTTTTGTAGTT | 9678 |
| rs143552987 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082523 | TAAGCTTAATTTTCC[A/C]TTGTTATTCAATCAT | 9678 |
| rs143558104 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11052315 | TGATCCATGTAGTTG[C/T]AGTTTATTTATTGTC | 9678 |
| rs143594580 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11057616 | TTACCTCAGGTGATC[A/T]ACCCGCCTCGGCCTC | 9678 |
| rs143659366 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11024975 | AATTGAAAACCTTCT[A/G]GAAAGGGGTCACTTT | 9678 |
| rs143673074 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11138325 | GGATTACAGGCGTGA[A/G]CCACTGCGCCTGGCC | 9678 |
| rs143698030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11127722 | CTTCTCCTTTAATGA[A/G]TTACCATACCAAATT | 9678 |
| rs143731334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080108 | AATGAGTTCAAAGTT[C/T]ATTTGCACCTGTGAG | 9678 |
| rs143740680 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11142014 | AATCAGAAAAATAAG[A/C]AAATAGCTTCAATGC | 9678 |
| rs143784663 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11024493 | AGAAGTCACTATCTG[C/G]CTTCTAAGGGCAGGC | 9678 |
| rs143786083 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11158423 | TGTGCATCAGAGCAG[A/G]GGAACATGATGTCAG | 9678 |
| rs143814865 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11095830 | TGAGATAAAACCTCA[A/G]CTGGATTCTGTAGAT | 9678 |
| rs143822693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156517 | ATTCACTTTCTGGCC[A/G]GGCGTGGTGGCTCAT | 9678 |
| rs143823231 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026609 | GGAACCAAAGTAAGG[A/C]AATTACTTAATTGAC | 9678 |
| rs143841480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098484 | CTCATTTTTATTGCT[A/G]GTGTATAATTGGGTT | 9678 |
| rs143841881 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11076732 | ACCACCACACCCGAC[C/T]AATTTTTGTATTTTT | 9678 |
| rs143857676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067165 | GACTTGAAAATATTT[C/T]TCCAAAGAAGATATA | 9678 |
| rs143858319 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11038233 | CCTAGGAGTTTGAGA[C/T]CAGCCTGGCCAACAT | 9678 |
| rs143929948 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11116841 | AAAAATTAACTTTTT[A/G]GAATTTTAAATTTTA | 9678 |
| rs143946541 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11131086 | TTTGTTTGTTTTGTA[C/T]ACAACAGTCTTGTTT | 9678 |
| rs143947204 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11026051 | CAGTAGGTGTAGGTT[A/G]CAGTGAGCCGAGATT | 9678 |
| rs143972394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11015302 | ATACAAGATTGCTGG[A/G]ATAGCGTAGAATCTA | 9678 |
| rs143992271 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11006113 | AGTGTATTTAAACTT[C/G]TAAAAACCATTTCCA | 9678 |
| rs144031519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155553 | ACCAACTCTTTCTTA[C/T]CCTTCATGTCTCATT | 9678 |
| rs144035521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076123 | CAGCCTGGGCAACAG[C/T]GAGAAAGTTGCGTAA | 9678 |
| rs144060559 | in-del | -/AA | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11117846 | CCTTTAAAGTTCTTT[-/AA]AATTTGAAGCATATA | 9678 |
| rs144070547 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11079025 | AATTCTTAAGTGCCT[A/G]AATTCCTTCTGTGAA | 9678 |
| rs144077775 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11039286 | TTAAAAAAGGCAAAC[A/T]AGAGATATTCATTTT | 9678 |
| rs144087067 | snp | A/G | 0.0752113 | 0.178743 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971995 | GGCTGGAATGCAGTG[A/G]CGTGATCTCTGCTCA | 9678 |
| rs144098007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11043654 | TGAAATTTTTTCACT[A/G]TTTTCACATGATTGC | 9678 |
| rs144150325 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11078410 | AAAATTAAGAGGTTG[A/C]AATTTTGGTTAAGTC | 9678 |
| rs144153293 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11132720 | TTACATTCCTACTAA[C/T]AGTGTACATGAGTTC | 9678 |
| rs144157235 | in-del | -/T | 0.0803491 | 0.183626 | intron-variant | PHF14 | GRCh38.p7 | 7:11088072 | TCCGTGGGGCATTGA[-/T]TCCAGGACCGCTCTC | 9678 |
| rs144160122 | in-del | -/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957251 | TCTGTTATATTTTCC[-/C]AATAAATTTTTAAAA | 9678 |
| rs144167142 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11158669 | CAATCTAGTATTTTC[A/T]TACAAACAATGGGGA | 9678 |
| rs144171043 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10986123 | ACAGGTGTACGACAA[C/T]GACTGGCTAATGCTT | 9678 |
| rs144188552 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11012087 | AGATACCGGCAGCCT[C/G]ATCAATGCTGACTGA | 9678 |
| rs144188653 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11052810 | TGTTGGGGTGTTTAC[A/C]TTTTTCTCATTGCAA | 9678 |
| rs144201728 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | PHF14 | GRCh38.p7 | 7:11038417 | GCCTGGGCGACAGAG[C/T]GAGACTCCATCTCAA | 9678 |
| rs144202875 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11015392 | ACCTCTTCTTCCTTA[C/T]TGTCTATCCAAAAAT | 9678 |
| rs144217955 | snp | C/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:10970584 | TCCCCCTACAGCTCC[C/G]CCAAAAAATTCTGAG | 9678 |
| rs144226360 | in-del | -/A | 0.173643 | 0.238054 | intron-variant | PHF14 | GRCh38.p7 | 7:11154096 | AAACACATTTGAAAG[-/A]AAACTAATGGATTTA | 9678 |
| rs144267396 | in-del | -/ACACTATA | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11029360 | AAAACTATTTTCATT[-/ACACTATA]AAAATGTTACTTACT | 9678 |
| rs144286295 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11153564 | AAGTCATCATAAAGT[A/G]GTTGGCATTTGTGGC | 9678 |
| rs144345552 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11097142 | GCACCACCATGCCCG[A/G]CTAATTTTATATTTG | 9678 |
| rs144357890 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | PHF14 | GRCh38.p7 | 7:11059985 | AAGTTATCTTCCCAC[C/G]ACAGCCTCCTGAGTA | 9678 |
| rs144383257 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10993730 | AATTGATAAGGGGCT[A/G]GGTACGGTGGCTCAT | 9678 |
| rs144384831 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10999014 | TTAGGATTTCAAGCT[G/T]CTTTTGCAAAGTTCT | 9678 |
| rs144420751 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | PHF14 | GRCh38.p7 | 7:10995529 | ACATGTGGAGCTGCC[C/T]GCCAGTCCCATGCCG | 9678 |
| rs144424471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063446 | TAACAATCTTATATA[A/G]TGAACAAAAATTTAA | 9678 |
| rs144464750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957171 | GATGTGGATGGTGTT[C/T]ATAAGGGTGTTTACT | 9678 |
| rs144484603 | snp | C/T | 9.04609e-05 | 0.00672475 | intron-variant | PHF14 | GRCh38.p7 | 7:11061784 | TTTTTTTTTTGTTTT[C/T]TTCCAGAGAACCAGA | 9678 |
| rs144490409 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11168870 | CCATGTTCCACAGGA[A/G]CCTGCTATGAATTAT | 9678 |
| rs144500575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048118 | GTCCATGGGAATTAT[A/G]AATTTTAGGACTCTA | 9678 |
| rs144519700 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955905 | AAACATAGTTGGCCC[A/G]TGGTGAGGTTAAATA | 9678 |
| rs144556358 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11146908 | CTGGAGTCCAGTGGT[A/G]CGATCACAGCTCACT | 9678 |
| rs144566721 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11069792 | CCTCCTGAGTAGCTG[G/T]AATTACCACCGTGGC | 9678 |
| rs144568835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11151029 | TACAATAAAAGATAT[A/G]TCAATGATTTTAAAA | 9678 |
| rs144580284 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:11072361 | CCCCCGTGATCCAGT[C/T]ACCTCCCATCAGGTC | 9678 |
| rs144585019 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110747 | GTTCTGTTTTTTAAC[A/G]TGTAAAGGTTATTTT | 9678 |
| rs144602219 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11163609 | GAGGTAAATGCACCA[C/T]TTAAAGAATTATGGT | 9678 |
| rs144608134 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | PHF14 | GRCh38.p7 | 7:11002631 | TATTTTTATTAGAGA[C/T]GGGATTTCTCCATGT | 9678 |
| rs144614492 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11117036 | AACTTGTATCTGCTG[A/C]AACACTTAAAATGAT | 9678 |
| rs144620700 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11031444 | CATGTTATGACACAA[C/T]ATCTTATTTTTAAAA | 9678 |
| rs144623427 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11043189 | TTTTATTTTTGGATT[A/G]GAGTCAAAGGCTTTA | 9678 |
| rs144634773 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964634 | GGCCTGTCTTGCCAG[C/G]TTGGGGAAGATCTCC | 9678 |
| rs144641599 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11018560 | TATTCACTGTTGTCA[C/G]GTAGACATGCTCCTG | 9678 |
| rs144676720 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966507 | CCCACAGGCTTCAGG[C/T]CATCCCTGGCTTGAA | 9678 |
| rs144720572 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11005084 | GATGTCAACCACAGA[C/T]CTCTTAATTTTAAAG | 9678 |
| rs144723441 | in-del | -/TCTC | 0.0475351 | 0.146656 | | | GRCh38.p7 | 7:10969407 | GATCTGCAGTTTCTC[-/TCTC]AACAAAATAAGACAA | 9678 |
| rs144735475 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112044 | AATTACATCTTTTTA[A/G]TATTAACATTCTAAA | 9678 |
| rs144759046 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965159 | GTGTTCTGGCTTTTG[G/T]AATTTTCAGCCTTTT | 9678 |
| rs144769222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072095 | AATTTACTAAGAAAA[G/T]ATATTTAATTGACTT | 9678 |
| rs144792556 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963699 | CTTGCATTATTATTG[G/T]GTAGGACTCTAAGTC | 9678 |
| rs144834596 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11136910 | TAGCACATGCTTATT[A/G]TAGAAAACTTGGAGA | 9678 |
| rs144872054 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | PHF14 | GRCh38.p7 | 7:11008024 | TAGGGTACCTCTGAC[C/T]GTGATGTCACTTATC | 9678 |
| rs144890952 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11128336 | TGAGGAAAGGGGGGT[C/G]ATATTTTTATCTTTC | 9678 |
| rs144909210 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11076493 | TTTATATTTTATTTT[G/T]AATGAAGACCATCGC | 9678 |
| rs144910454 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11133152 | AACTATAGATTCAGT[A/G]CAATCCCAATCGAAC | 9678 |
| rs144923878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11051430 | TTAAATATTATATTC[A/G]TAGTAGTCACTCTTA | 9678 |
| rs144936245 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11056984 | TGATTTTGGAATTTT[A/G]CCCATGAATAAGCAT | 9678 |
| rs144970405 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11016542 | GGAGAGTAAGACTTA[C/T]AAACCTGACTGTGGG | 9678 |
| rs144972419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083165 | AGGGGCAGGATTTGC[A/G]TCAGGGATAAAAACT | 9678 |
| rs144984782 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | PHF14 | GRCh38.p7 | 7:11087398 | GGTATCACCATGTTG[G/T]CCATACTGGTCTCGA | 9678 |
| rs144987183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976463 | CAAACATAGTTGGGT[C/T]GTGGAAGTTACGAAT | 9678 |
| rs144997834 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11017528 | TATGCCTGTTTTAGC[A/G]TATGAGCTTCTTTTT | 9678 |
| rs145022487 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11073338 | AAATGAGAAATTAAC[C/G]AAAAGAAACAGGCAG | 9678 |
| rs145036922 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152058 | ATTTTCATAAATAAT[C/G]TTCAGGTAGCAGAAC | 9678 |
| rs145070489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031921 | TATAATTTGGTGCTA[C/T]TGAACATTGCTGTAC | 9678 |
| rs145088736 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:10986588 | TGCATTTTCCGCAAA[C/T]GGACACCTGTTTTTG | 9678 |
| rs145099742 | in-del | -/C | 0.0349115 | 0.127424 | intron-variant | PHF14 | GRCh38.p7 | 7:11112551 | TCGAGGGAGGTGGAT[-/C]ATGAGGTCAGGAGTT | 9678 |
| rs145164192 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11148668 | GTTCACCACTATTAC[C/T]CCATCTCCTAGAACA | 9678 |
| rs145183451 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11071868 | TACACCATTTTATTC[A/T]TTCTTCAACTCAGTA | 9678 |
| rs145207039 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11152915 | CAGAGGGAAGAGCAG[C/T]ATGTTTGGAGCCAGG | 9678 |
| rs145208701 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11146680 | TTAGAGAACTCTACT[A/G]TGTTTGAGATTTTCC | 9678 |
| rs145224513 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11134091 | TTGTCAGGAGTCAGA[A/G]TTTGAAATAGGCCTT | 9678 |
| rs145234703 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11027438 | ATTGTCCATTGTCAG[A/T]CTTTCATAATTTAAC | 9678 |
| rs145247482 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965625 | AGGCAGGATGTTTAA[A/G]TCTGTAGAAGTTGTC | 9678 |
| rs145254835 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10993784 | GAGGCCAAGGCAAGC[A/G]GATCACCTGAGGTCA | 9678 |
| rs145256609 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033468 | CCTTTCAAGGGCATG[A/G/T]TCTGGGCATTTCATA | 9678 |
| rs145285105 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990648 | ATTTTAGTGATTAAG[-/T]TTTTTTTTTACTTTA | 9678 |
| rs145320424 | snp | A/C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102913 | TTTGGACTTACTGAA[A/C/G]AGTTACTGAAGCCTG | 9678 |
| rs145321569 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11031825 | GCTGACTACAACTTA[C/T]GTTACTATGTTTTAC | 9678 |
| rs145326388 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107103 | TAGTTGTAGTTTACT[C/G]CTCTAATGAAATTAG | 9678 |
| rs145329768 | in-del | -/TCTT | 0.0352857 | 0.128054 | intron-variant | PHF14 | GRCh38.p7 | 7:10990869 | TTGCTTTCTTTTCTC[-/TCTT]TTTAGAAATGGCTGA | 9678 |
| rs145342679 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10996133 | GGCTTTTCAGCAGAG[A/G]ATTAATATGGTTTGA | 9678 |
| rs145373600 | snp | A/C/T | 3.31539e-05 | 0.00407137 | synonymous-codon, missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036556 | ATTCGTAAACTTATG[A/C/T]GGAAAGCAGAACTCA | 9678 |
| rs145391078 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968865 | CTTCCCCCTTAGTAG[A/G]GCTGTATTTGAAGTT | 9678 |
| rs145410191 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11004053 | AGGAGTTTGAGACCA[C/G]CCTGGGCAATGTGGT | 9678 |
| rs145415796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161214 | AAGTTTGGTAAAACT[G/T]AATTTTAGGGCCTGA | 9678 |
| rs145419154 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11079488 | GTGAAAAGATGTTCT[A/G]GAATAATAGTAACAT | 9678 |
| rs145426273 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:10987641 | AGTTATTTTCTAGGT[A/G]GTACTTTTTTGCCAT | 9678 |
| rs145518228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166184 | ACTTTCCAGTAGCCT[C/G]AAAGGATACATTTTC | 9678 |
| rs145522506 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155458 | TTCCACTACTTTGCT[C/G]TTTCTCACTGGGCTT | 9678 |
| rs145545357 | snp | A/G/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11035918 | AGGAAATGGATTGTG[A/G/T]TTAAGGTAAATAGTG | 9678 |
| rs145563540 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166875 | GTCCTGAACAGCAGG[C/G]AGTGTTAGAAGGCAT | 9678 |
| rs145572918 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11085329 | TCTGTTGATTTAAAA[C/T]AATTTATTAGTTTTC | 9678 |
| rs145579688 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107680 | AATAATGTGCTATTC[A/G]TATAATAATCTGTTT | 9678 |
| rs145594515 | in-del | -/CAGAGTGAGACTCT | 0.0154538 | 0.0865337 | intron-variant | PHF14 | GRCh38.p7 | 7:11047767 | CTCCAATCTGGGTGA[-/CAGAGTGAGACTCT]GTCTCACAAAAAGAC | 9678 |
| rs145623656 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11001260 | CTGACCTATATATCT[A/G]TTCTTTGATTAATAC | 9678 |
| rs145624236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089792 | TTTTTTTTTTTGAGA[C/T]GGAGTTTCACTCTTG | 9678 |
| rs145640943 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10985062 | AGTTTTTTGATGATT[A/T]TAGTTTATTTAAATT | 9678 |
| rs145683950 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11050859 | CTTTTTTTTCCCCCA[A/G]CACTTCTTGGAGTCT | 9678 |
| rs145689587 | snp | A/T | 0.0402882 | 0.136092 | intron-variant | PHF14 | GRCh38.p7 | 7:11049457 | TCCAGCCTGGGCGAC[A/T]TAGCAAGACTGTCTC | 9678 |
| rs145703033 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11043644 | ATTAGGAAGCTGAAA[-/T]TTTTTCACTATTTTC | 9678 |
| rs145705978 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11125985 | CTTTGAAAAGTTCAA[A/G]CTGTATCAAAGCACT | 9678 |
| rs145725292 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11102233 | GAAAGATAGGTTTAT[G/T]TTGACAACCAAAAGT | 9678 |
| rs145736005 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10988642 | TCATTGGAGCTTGCA[A/G]CTTTTCTTTTGGGGG | 9678 |
| rs145741882 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11055824 | TGAAAATATGAAATA[C/T]GTTTCATATAAATAT | 9678 |
| rs145752229 | in-del | -/TTTG | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11011242 | CTTTCTCGTGGGTGA[-/TTTG]TTTAACTCAGTATTC | 9678 |
| rs145758720 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064430 | ACAGATATATTTCAG[C/T]GCTTACTCAGACATA | 9678 |
| rs145758930 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10995858 | CCCACCCGGAACTCG[C/T]GCTGGCCCGCAAGCG | 9678 |
| rs145768969 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11127218 | GTTTGGAAGTGGGGC[A/G]TTCTAGATTTTGATT | 9678 |
| rs145778344 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10958466 | AGAATTCTGATTCCT[A/G]TTCCTTTGTAAATAT | 9678 |
| rs145873576 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11019852 | TTTTTCTCTTTTGAT[G/T]TAGGTACCTATAGCT | 9678 |
| rs145875018 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11120092 | TGGCGGAGTTCTTAT[A/T]ATTGGATGCGTCGTA | 9678 |
| rs145884387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098551 | TGGCTCGTTTCCTCA[C/T]CTGATAAAATGGCCA | 9678 |
| rs145893746 | in-del | -/TTTGTTAGATTTATATCTAAG | 0.496842 | 0.0396107 | intron-variant | PHF14 | GRCh38.p7 | 7:11001608 | AGATCTTGGCAATAT[-/TTTGTTAGATTTATATCTAAG]TATTTTATTTTTTGG | 9678 |
| rs145900020 | snp | C/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104722 | GGTGACTACCCTATT[C/G]CTCTCCTGGATCTGC | 9678 |
| rs145912806 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11034117 | CACACTACAGAATTG[C/G]CTCATATGCTTTTTT | 9678 |
| rs145923741 | in-del | -/T | 0.116488 | 0.211364 | intron-variant | PHF14 | GRCh38.p7 | 7:11002040 | TTATTTCTGTTTGTG[-/T]TTTTTTTTTACTTGT | 9678 |
| rs145957871 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069549 | TATGTATTTTTTTTA[A/T]TTTTATTTGCTAATA | 9678 |
| rs145975250 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11164504 | GTATATTTCAGTGTA[A/G]AGGCTACAGGTGCCT | 9678 |
| rs145987150 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11043718 | GAGATATTCATACTG[A/G]CCTGTTCTTTTGAAA | 9678 |
| rs145989196 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:10994819 | TGAGTGTTACAGCTC[A/G]TAAAGGCAGCGCGTA | 9678 |
| rs146010102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167387 | CTAGAAGTGTGAGTA[C/T]TAGCAATCTTAATTT | 9678 |
| rs146010248 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:11118191 | ATAGAACAAATCTGC[A/G]GTGTTTTGTAGACTT | 9678 |
| rs146029004 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | PHF14 | GRCh38.p7 | 7:11123578 | CAAGGTCAGGAGTTC[C/G]AGACCAGCCTAGTCA | 9678 |
| rs146029549 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11047386 | TTAGTACACTTTCTT[G/T]TCTAAGCACTATTAA | 9678 |
| rs146040210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11010329 | CATTTAAAGTAATGT[A/G]TATCTACCCAAGGTG | 9678 |
| rs146051334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014283 | GTATAACTTTATATC[A/G]GGAGATAGAACTTAA | 9678 |
| rs146111536 | snp | A/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063504 | GTGGAGTTGAGGACT[A/G]TGATTTTGAAACAGT | 9678 |
| rs146120331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065306 | TTCATGGAATTGGGA[A/G]GTCTTAAAGGCTTTG | 9678 |
| rs146139737 | in-del | -/AGAT | 0.0248432 | 0.108648 | intron-variant | PHF14 | GRCh38.p7 | 7:11084254 | TGTTTCAGCATACAC[-/AGAT]AGCCATTTATTTTGA | 9678 |
| rs146146365 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11067804 | TGATCAGGGATCACA[C/T]GATAAGAGAGGAATC | 9678 |
| rs146150689 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11144801 | GAGATGTACTACAAC[A/G]TATATGAACCTTAAG | 9678 |
| rs146160913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961100 | ATATCCCATTTGTCA[A/G]TTTTGGCTTTTGTTG | 9678 |
| rs146163619 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | PHF14 | GRCh38.p7 | 7:11026512 | TTAACAGATGTATTT[A/T]TTGGGCAGCACTTAG | 9678 |
| rs146166545 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093445 | TTCTTGTTGCTCTGC[-/T]TTACCTCAGTGTACC | 9678 |
| rs146172210 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963541 | TGGTGCTGAGAAGAA[G/T]GTATATTCTGTTGAT | 9678 |
| rs146175353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11030127 | ACTTTGATGAAGGCT[A/G]CTAGATGAACAGTGA | 9678 |
| rs146213497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124058 | TTTTTCCTTTTCTTT[C/T]TTCTAACTCCACTTT | 9678 |
| rs146229944 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11011457 | TGTTAAATGTTTCTC[A/G]CTGTGGCTTATTTAA | 9678 |
| rs146232186 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11078922 | TAGATTAATATGAAT[A/T]ATATTATCTACATAA | 9678 |
| rs146248122 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959717 | TATGCTGTGGGTACC[A/G]GCATCTGGATGAGGG | 9678 |
| rs146281379 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10976153 | CTTGGATCCCAAGAG[C/T]TGATGGACGGAATCT | 9678 |
| rs146292956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980748 | CTCCGCAGAAATAAT[A/G]TTTGATTATAGGATA | 9678 |
| rs146325153 | snp | C/G | 0.030278 | 0.119257 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962140 | ATAGGAGAGGTGAGA[C/G]AGGGCATCCTTGTGT | 9678 |
| rs146343418 | in-del | -/TTTTC | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11131947 | TGGACTACTGGAATT[-/TTTTC]TTGTTGGGTTTTTTT | 9678 |
| rs146349615 | snp | C/G/T | 0.00159649 | 0.0282165 | intron-variant | PHF14 | GRCh38.p7 | 7:11027116 | TTCCTTATATTCACT[C/G/T]TGAAATCCCTTGCTC | 9678 |
| rs146374751 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11096157 | CTTTTATTCTTTTTC[A/G]GTGTCTGAGTATATG | 9678 |
| rs146375311 | snp | G/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150081 | TTGCAAGTCACGGAA[G/T]ATTTACATAGCATCA | 9678 |
| rs146392282 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11030494 | TGTGAAGCAGCCATG[A/T]TTGGGACAGTGGGGT | 9678 |
| rs146393373 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | PHF14 | GRCh38.p7 | 7:11100451 | GAGGTAACTGGGGTA[C/T]ATAGACACTAAGCAG | 9678 |
| rs146403019 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10995440 | AATCCCTTAGCTAGA[C/T]ATAAAGGTTCTCCAA | 9678 |
| rs146438877 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11155916 | TTATTTTATAAAATA[A/G]TTTTGTCCTTATGTT | 9678 |
| rs146442445 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11110317 | TTTAAATCAGTGAAA[G/T]ATAAACAATAAAGAA | 9678 |
| rs146448538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11036872 | TATTTGTAAATATAC[C/T]TAAAAGTTTTAAACT | 9678 |
| rs146459612 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11039521 | TAATTGATAAATTAC[A/G]GTTTTCGCAAATATT | 9678 |
| rs146459819 | snp | A/T | 0.0356815 | 0.128715 | intron-variant | PHF14 | GRCh38.p7 | 7:11113336 | GCCAGTAGCCATTGG[A/T]TAAGGTTTTAGTTTT | 9678 |
| rs146463909 | in-del | -/TATATATATA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122332 | ACTGTTTGTACTTTT[-/TATATATATA]TATATATATATACAC | 9678 |
| rs146515942 | snp | A/G | 0.067446 | 0.170804 | intron-variant | PHF14 | GRCh38.p7 | 7:11007148 | CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCCA | 9678 |
| rs146555824 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11091845 | TTCTTTACCCCTTAA[A/G]TATTCAATTCTAATT | 9678 |
| rs146570144 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10988821 | ATTCTTATAACCTCC[G/T]GAAGTAGATATTATT | 9678 |
| rs146574418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056064 | TACGAGTCAGATTAT[A/G]AAACCTCTATCTGTC | 9678 |
| rs146578081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060508 | GGTGTCCTTAAACTT[A/G]TGTGTATTTGACCTA | 9678 |
| rs146602868 | in-del | -/GTTAAAAAAAAAAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031190 | GTTTTATATAGGCTG[-/GTTAAAAAAAAAAAA]TTAAAAAAAAAAGGT | 9678 |
| rs146632474 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957859 | AGACAGAACATAGAT[C/T]AGTGATTATCAAGGT | 9678 |
| rs146672956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11114137 | GGTAAAATGTCTCCA[A/G]CTTCTTTCTCTGCGG | 9678 |
| rs146688120 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | PHF14 | GRCh38.p7 | 7:11005412 | TGTTTCTGTTACTTA[A/C/T]TACATTGTCCAAGTT | 9678 |
| rs146691723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11074053 | CCTGTGATGGGCTGC[A/G]CTGCCTGGAAGATCT | 9678 |
| rs146691780 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11118995 | CTATATTGATAATTT[A/G]CAAAATTGAAAAACT | 9678 |
| rs146695433 | snp | A/C/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11075860 | AGCTAGGCTGGGCGC[A/C/G]GTGACTCATGCCTGT | 9678 |
| rs146699735 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11007357 | TCCTGTTCTGTATCC[G/T]TTAACTTTGTGATTT | 9678 |
| rs146703433 | in-del | -/A | 0.0322114 | 0.122752 | intron-variant | PHF14 | GRCh38.p7 | 7:11002316 | GTCATGCTGGAGCTT[-/A]AGACAGCCACAGGTG | 9678 |
| rs146707123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009421 | TATATTAGTCAAAGA[C/T]TGATGCTAATTAAAT | 9678 |
| rs146709375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11077036 | TAATTCATATATACT[A/G]CATTTAATACTATCT | 9678 |
| rs146710676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126938 | ACCACTCTTACGTTT[C/T]TATTGTGATTTAAGT | 9678 |
| rs146712277 | snp | A/G | | | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968536 | ATTTGTGTTCATAGT[A/G]TATAATACGTAGTGT | 9678 |
| rs146754382 | snp | C/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10971560 | CCTTCTCTTACTTTC[C/T]TTCAATACATGAATT | 9678 |
| rs146777286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013185 | ATTTTTTATGAGATG[G/T]AATTTTGCTCTTGGC | 9678 |
| rs146777709 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10970097 | AATCCTACATTGAGG[C/G]AGTTTGTGCTCGCTG | 9678 |
| rs146804674 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11142341 | CACTGCGCCATAATG[A/G]ATCATTTTTATCTGC | 9678 |
| rs146805476 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11089241 | AAAACAACATTAAAG[A/T]TATCAGCTGTTTGCG | 9678 |
| rs146810208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11020792 | AAACCAATTCTTCAT[A/G]TGTAAATGAACAACC | 9678 |
| rs146823973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091611 | AATACAAGAATTAGC[C/T]GAGTGTGGTGGTGGT | 9678 |
| rs146833992 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10988333 | AGCAAAATGGAAAAA[C/T]AGGAAAATAGAGGAA | 9678 |
| rs146876185 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10993074 | TTATTTGTGCAGTTA[C/T]TGGTGATATTACTAT | 9678 |
| rs146899717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11079718 | ATGTTAGGAACATGG[C/T]TTTTCTCCTTTTACA | 9678 |
| rs146916413 | snp | C/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973649 | GGTGAATTAGGCGCG[C/G]AGAGGGCGGAGCCTT | 9678 |
| rs146926128 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10979215 | TTATTTGATATTGTA[A/G]AGGGATTCTTGAAGG | 9678 |
| rs146955857 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11139837 | AGTAAAATTTTCCAT[A/G]GGGTATGACTTAGTG | 9678 |
| rs146959015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144086 | AAATTTCTCAAAAGT[C/T]ATACAAGCAGTCAAT | 9678 |
| rs146975567 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11094057 | AAGGAGAAGGGTCTG[G/T]GTGAGACTTTGGGTC | 9678 |
| rs146976101 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11147212 | GTGTTGTTTGGTTGT[A/G]CAGGATATATTTTTA | 9678 |
| rs146985942 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11028481 | AATTAGTTGAATTTT[G/T]ATTTATTTGAACCAT | 9678 |
| rs146985983 | snp | C/G | 5.57647e-05 | 0.00528008 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990778 | ATTTGCTGTGTTTGT[C/G]TGGGAGATAATAGTG | 9678 |
| rs147022088 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10994517 | TATGGCTAGAACTGG[C/G]TGAGCAAGCTGGTTA | 9678 |
| rs147060131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11158012 | TGGAGTGTTCTGATA[C/T]ACCCTTTACCCAGCT | 9678 |
| rs147063420 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | PHF14 | GRCh38.p7 | 7:11162296 | GGTTTCTCCTTGCTG[A/G]CCAGGCTGGTCTCAA | 9678 |
| rs147079907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11116346 | AAACCAAGATCTGGT[A/G]TGGTCATTGTTACTG | 9678 |
| rs147081262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041146 | GTATCATATATGTAT[A/G]TATATAGAATGAATC | 9678 |
| rs147091128 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11045663 | AGAGTTCTGTGGACT[A/G]TGCTGGGCAGGTTAA | 9678 |
| rs147127007 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11008513 | TTGTGAACTGCACAT[A/G]TGAGGGATCTAGGTT | 9678 |
| rs147130332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090915 | CAGGAGGTAGCAGTC[A/G]TTCAAGGGAATAAAC | 9678 |
| rs147160155 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11094287 | ACATAAGTCCAAAAC[C/T]AGTTTCATTTGGTCA | 9678 |
| rs147166474 | in-del | -/T | 0.47743 | 0.103805 | intron-variant | PHF14 | GRCh38.p7 | 7:11132303 | TCTGTATAATTGAGA[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs147174105 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10991454 | GTGTTGGATTACAGG[C/T]GTGAACTACCGCGCC | 9678 |
| rs147176398 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058446 | TTCTTGGTTGGAGGA[C/G]TTGGTATTTTGTATA | 9678 |
| rs147186150 | in-del | -/A | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11017760 | GTGATCCTGCTTTTT[-/A]AAAAAACCTGATATG | 9678 |
| rs147221830 | in-del | -/TGAT | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11005390 | TTATAATCTATTAAC[-/TGAT]TGCTGTTTCTGTTAC | 9678 |
| rs147271772 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11116863 | TAAATTTTAAAACAA[C/T]GTGTATAACCCAAGT | 9678 |
| rs147272280 | snp | A/T | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11072301 | GAACTCACCATCATG[A/T]GAACAGCACCAAGAG | 9678 |
| rs147275382 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11074686 | ATGCACAAAATATAG[C/T]CAAGTTCTTTGCTAG | 9678 |
| rs147280189 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964624 | TTTGAATGTTGGCCT[A/G]TCTTGCCAGGTTGGG | 9678 |
| rs147280507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11006516 | ACCTTGGCCACATCA[A/G]TGTCACAGAGCTCCT | 9678 |
| rs147290186 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966187 | CATCGATCTTGCAGG[C/G]AGCTGTAGACCGGAG | 9678 |
| rs147332130 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11132973 | GGCACCAGAAAACCC[A/G]TGAAATTCTTAGGTA | 9678 |
| rs147377281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11019387 | CAGGCTTTTCTTTAC[C/T]GGGAGACTTTATTAT | 9678 |
| rs147377462 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11087316 | TCTGCCCCAGCCTCC[C/T]GAGTAGCTGGGACTA | 9678 |
| rs147380982 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11090300 | CTCCCTGTAATTGCC[C/T]AGTGAATCAGGTTGA | 9678 |
| rs147387249 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11023487 | TTCCCCTATCTTTCT[C/T]CCTGACTTGGTTGGG | 9678 |
| rs147397319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10986415 | TTCATGTAGTGTCTG[A/G]AAAACTTCATGGTAC | 9678 |
| rs147436952 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11151463 | ACTTGGGGAGCTGAG[G/T]CCAGAGGATCATTTG | 9678 |
| rs147466021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154139 | TATGGAATTTACATT[A/G]CAGTGAAACTTCATT | 9678 |
| rs147480776 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966639 | TCATATCTATAATCC[C/T]AGTTTTAAGTGAGTC | 9678 |
| rs147482711 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | PHF14 | GRCh38.p7 | 7:11034840 | AGGCATGTGCCACCA[C/T]GCCTGGCCCTTAATT | 9678 |
| rs147540384 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170189 | TAGAAATTTTTCAAA[A/G]TTCACCTGTCCCCTG | 9678 |
| rs147549767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983356 | TATTTGTCACCGTTC[C/T]CAAGGAGCTCACAAT | 9678 |
| rs147622016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098402 | GCTGTTTTCTCTTGC[C/T]GCCTTTCTCTGTTCC | 9678 |
| rs147645544 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996625 | TGATAAAATGTTTAT[A/G]TCACATGATTCATTA | 9678 |
| rs147647595 | snp | C/T | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107447 | TATTAATCTGATAGC[C/T]AGGAAGTTGTATTTA | 9678 |
| rs147647871 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064932 | TAAAATGTTAGAACA[A/G]TAGTATTATTTAGTA | 9678 |
| rs147655412 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11000203 | TACGCTACTACTTTC[A/T]TCCTCTAGTTTAAAT | 9678 |
| rs147656003 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959239 | CTAACAGCCACAACA[C/G]TCATATCTAGACACT | 9678 |
| rs147691850 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962076 | TGAATACCTTTTATT[G/T]CTTTCTCTTGCCTGA | 9678 |
| rs147731600 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121560 | AGTGAAAGGAAATAT[A/C]TTATGGCTTCCCTTT | 9678 |
| rs147734962 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126068 | TTTTTAAAGACCAAT[A/G]GTATTCTTTATATTC | 9678 |
| rs147743778 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11049500 | AAAAAAAAAGTGTAA[A/G]TTAGAACTGTTTGAG | 9678 |
| rs147746864 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11053026 | TCTTAGGGCATACTT[C/T]CCTTGCTTGAGCTGA | 9678 |
| rs147750036 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11012653 | CAAGTTATCTTGTCT[G/T]TTGGGTGTGTTCATG | 9678 |
| rs147760151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016121 | TTGGATACTGTGGAC[C/G]TTACATAAGTAGACA | 9678 |
| rs147762358 | in-del | -/AAATATGTATTTATATGTATAAATAC | 0.493293 | 0.0575177 | intron-variant | PHF14 | GRCh38.p7 | 7:11117582 | CCAAACGATATATAT[-/AAATATGTATTTATATGTATAAATAC]AAATATGTATTTATA | 9678 |
| rs147835798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11143498 | TTCAAGAAATAATAC[A/G]TTTTTGACTGTATTA | 9678 |
| rs147848036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070173 | AGCCTGAACTCTTAG[A/G]CTCAGGTGATCTTCC | 9678 |
| rs147851171 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11072658 | ACTCTGATATAACAT[A/G]TATAGTGCTTATTGT | 9678 |
| rs147855667 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11028111 | AATACACCTAACTTA[C/G]TGAGCACAGCTTAGT | 9678 |
| rs147859641 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962218 | TGATATTGGGTGTGA[A/G]TTTGTCATAAATGGC | 9678 |
| rs147863846 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964659 | ATCTCCTGAATAAAA[C/T]TCTGAAGAGTGTTTT | 9678 |
| rs147865774 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11031654 | AGCTACTAGAGAGGC[C/T]GAGGTGAGAGGATCA | 9678 |
| rs147944706 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11165545 | GTTTAAGAAATCTTT[G/T]AAACTTGGCAGTCTA | 9678 |
| rs147961098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979465 | TTTTTTTCAAACGTA[A/C]GAAAGGTTTATTGTA | 9678 |
| rs147963073 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11045560 | ATAACTATTTTAAGC[A/C]CTTGCTATCCAGCCT | 9678 |
| rs147970909 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965673 | CAGATATGCCCTGCC[C/T]TAAGAGGTGGAATCT | 9678 |
| rs147977531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11099905 | CAGGGAATGAGCTTT[A/G]TCAAGGATAGAGCTG | 9678 |
| rs147993844 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11062273 | TTATACTCTGGATTT[A/C]AATGTAAATAAGAGT | 9678 |
| rs148041066 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11057938 | AGTTTTAAACTTTCA[C/T]TTACTTTTAATAGGT | 9678 |
| rs148044788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134894 | ACCAAGTAAATTTTT[A/T]TCAAAAGACTGAATG | 9678 |
| rs148056718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019032 | CCTGTTGATGTGATA[C/T]ATCATGTTGATTGAC | 9678 |
| rs148098621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127819 | AGCTTAGACCATTTA[C/T]GAGAGATTGAGAAAA | 9678 |
| rs148102164 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11080191 | TAAGAATTTTGTAGC[A/G]TTAGATTTTCAGTTT | 9678 |
| rs148109020 | snp | A/G | 1.74689e-05 | 0.00295536 | intron-variant | PHF14 | GRCh38.p7 | 7:11013948 | TATGTTTGCTTTATA[A/G]TGTGTCTGCCTTTGA | 9678 |
| rs148119167 | snp | C/T | 0.00167581 | 0.0288981 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974299 | TCCCTAAGTCTTCTC[C/T]AAACGACCACCTCAC | 9678 |
| rs148134928 | snp | A/G | 0.00795532 | 0.062565 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150234 | AGAGAGCTACAATAC[A/G]CATTAGAATGCTTAT | 9678 |
| rs148156349 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076932 | AATTCTAAGATATGT[C/T]AGTATCTCAATGGTA | 9678 |
| rs148167378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037733 | TAAAACGGGTATTGA[C/G]TTATTGTTAGAAAAC | 9678 |
| rs148206271 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11026060 | TAGGTTACAGTGAGC[C/T]GAGATTGCACCACTG | 9678 |
| rs148226472 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032146 | GGTGTGTGCCTATAG[G/T]CCTAACTGCTCAGGA | 9678 |
| rs148236683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997017 | TTGAGTTCTAAGTGT[C/T]GCATATATGTTTAAT | 9678 |
| rs148258750 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11090135 | GATTATGCATGAAGC[A/C]TCAAGTGTGATTTAA | 9678 |
| rs148262233 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11051483 | TTCATTATGTACCCT[A/G]TAATCACATTACCTG | 9678 |
| rs148268108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986329 | ACCATTAATATTTGT[A/G]TAGATTATATCTGTT | 9678 |
| rs148310110 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11166659 | GTTATAGCAATTTTA[A/T]TATTATACTCTAGCA | 9678 |
| rs148313137 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122769 | ATTGTCCTTCCACTG[C/G]CCTATAGTTCCAGCT | 9678 |
| rs148315373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045993 | AGAGGGGAAAACCTA[C/G]GGGCTTCTTAGGTTG | 9678 |
| rs148317653 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11153716 | AAGGATTCTTTAACA[G/T]AAAACCCACCTACTT | 9678 |
| rs148325276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11009456 | ATAGAAACATGTCTT[C/T]TGTGTTACCCATTGG | 9678 |
| rs148365744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115387 | TATATAACATCTTTT[C/T]AAATTTTCATGTTTG | 9678 |
| rs148381698 | snp | A/C | 0.0652144 | 0.168387 | intron-variant | PHF14 | GRCh38.p7 | 7:11074429 | GTTAGCCAGGATGGT[A/C]TCGATCTCCTGACCT | 9678 |
| rs148382766 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11005847 | CACCAGGCTACAGTG[C/T]AAAGGTGAGATCTCG | 9678 |
| rs148404002 | snp | A/C | 0.00927196 | 0.0674538 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169525 | TTGAAAAGTTTGCAG[A/C]TTATGTAATAGCAGA | 9678 |
| rs148414064 | snp | C/G | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:10995082 | TTCTCCAAGTCCGCA[C/G]AGAGCACTGATTGGT | 9678 |
| rs148423661 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956424 | CTTGATTTTAAAACT[C/G]TGCACGGACTTTCAC | 9678 |
| rs148432018 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11011671 | TGATACTTCAGGACA[A/G]GAATTAAGTTGCAAT | 9678 |
| rs148474055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117105 | ATATTTCTTTTAAAA[A/G]TGCTTCCTCCAGGTC | 9678 |
| rs148483513 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11007038 | AAAAATTTGCCAGGT[A/G]TGGTAGTGGGCACCT | 9678 |
| rs148503923 | snp | A/G | 0.118235 | 0.212457 | intron-variant | PHF14 | GRCh38.p7 | 7:11075073 | CTCCTGAGTAGCTGG[A/G]ACTACAGACACATGC | 9678 |
| rs148520140 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966775 | CTACTCAGCAACCAG[A/G]TACACCCTTCTATCC | 9678 |
| rs148556728 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11072185 | AACTTCTAATCATGG[C/T]AGAAAGCAAAGGGGG | 9678 |
| rs148562329 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11137086 | GGTTTGTGACTCCAC[A/G]GCTTAAACCCTTCCC | 9678 |
| rs148566605 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11030616 | CATTCTGTGGTCTGT[A/G]TATCTTACCTATAAG | 9678 |
| rs148571338 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963971 | GAGCCTATGTGTGTC[C/T]TTGCAAATGAGATGG | 9678 |
| rs148614324 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11131116 | TGTTTCCAAGTTTTG[G/T]CAGTTATGAATAACG | 9678 |
| rs148639360 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:10977006 | AGTCAACAGAAATTG[A/G]ATCATATTTTTGACT | 9678 |
| rs148677906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11078429 | TTTGGTTAAGTCTCT[A/G]CCAGGGAGAGGCTGT | 9678 |
| rs148691041 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10970585 | CCCCCTACAGCTCCC[C/T]CAAAAAATTCTGAGT | 9678 |
| rs148693707 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | PHF14 | GRCh38.p7 | 7:11038533 | TGTGGTGGTGCACAC[A/C]TGTAGTCCCACCTAC | 9678 |
| rs148715796 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11146822 | TTTTGTGCAAATCAA[C/T]GATGCAGCTTTTTTG | 9678 |
| rs148765636 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106020 | ATGGAAATCAGTTTA[C/T]TAAAGAACAAAGCAG | 9678 |
| rs148773435 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11091371 | CTATATTTATTTTTT[A/G]GAGAAAAATATAATA | 9678 |
| rs148782654 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10999033 | TTGCAAAGTTCTGGC[C/G]GCACTAGGGTTTTTT | 9678 |
| rs148790311 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11053091 | GGGAGATACAAAGAT[A/G]TTTTTAGGGTTAGTT | 9678 |
| rs148822363 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | PHF14 | GRCh38.p7 | 7:11115026 | CTCAACTTTTCTCTT[A/C/T]TTTTTCCCTTATTTC | 9678 |
| rs148823010 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11040375 | GTGTACTGTGTTTTG[G/T]TTTTTTTAAACCTCC | 9678 |
| rs148832903 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11005503 | TCTCACTGTTTCTCT[G/T]TTTTGTCCACCACTT | 9678 |
| rs148875938 | snp | A/G | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11107971 | TTTTTTAAATGGTCT[A/G]AATTTGCAACATAGC | 9678 |
| rs148877384 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11093252 | TGATTGCTTTGTTTC[C/T]TGACAGTGGATTTTC | 9678 |
| rs148879290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070236 | GTGCGCGCCACCATG[C/G]CCAGCTGATTTTTTA | 9678 |
| rs148938949 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064431 | CAGATATATTTCAGC[A/G]CTTACTCAGACATAC | 9678 |
| rs148946590 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958635 | TCTCCATAACAAAGG[A/C]TTTATGATCTCTTTA | 9678 |
| rs148963832 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11127429 | CCTTTCTAGAGTCTT[G/T]CTCTTTAACGGGCCC | 9678 |
| rs148979664 | snp | G/T | 0.0941369 | 0.195465 | intron-variant | PHF14 | GRCh38.p7 | 7:11013344 | TTTTTGTGTTTTTAG[G/T]AGAGATGAGGTTTCA | 9678 |
| rs149016582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120896 | TTGTTTTTTACTGAC[A/G]ACATATTTTAGTAAC | 9678 |
| rs149031364 | snp | C/G | 0.0755793 | 0.179102 | intron-variant | PHF14 | GRCh38.p7 | 7:11008190 | ACTAAGAGATGTTTC[C/G]CCCTATTTATTTTTC | 9678 |
| rs149032857 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PHF14 | GRCh38.p7 | 7:11076718 | GATTACAGGTGCACA[C/G]CACCACACCCGACTA | 9678 |
| rs149079579 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11073624 | TCTGGAAGGCAACAG[C/T]GCCCTTCCCACAGCT | 9678 |
| rs149083534 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11152293 | TTTATAGTCAGAGCT[C/G]AGTTTGGAATCCTAG | 9678 |
| rs149092027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139291 | AAATTAGGCATTCAT[C/T]TATCTTTCACCATCC | 9678 |
| rs149092373 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965155 | AGAGGTGTTCTGGCT[C/T]TTGGAATTTTCAGCC | 9678 |
| rs149094936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031976 | GAAACAATATAAAAC[C/T]GGGTGTGGTGGCACA | 9678 |
| rs149140593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11097327 | TTGCCACAATGGAGA[A/G]TTATTATGACACCTA | 9678 |
| rs149146862 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11027631 | TTTCTCTTTTTATAC[A/G]GAAAGAATGTACATA | 9678 |
| rs149154968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084284 | TTGAAGATAATAGCA[A/G]TTAGAACATAAGTAT | 9678 |
| rs149156634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10993866 | GTACAAAAATTAATC[C/T]GGCATGGTGGCACGT | 9678 |
| rs149191471 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11045956 | ATTTTTCTTGAATTA[C/T]GCTCTGCTGCCCAGG | 9678 |
| rs149209243 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10987750 | TACTTTCTCTGAAAC[C/T]TTGAAAGATGATATA | 9678 |
| rs149227608 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161372 | ATTGTTTCCACAATG[A/G/T]CCAATCCTAAACAAT | 9678 |
| rs149232288 | in-del | -/ATC | 0.447291 | 0.153545 | intron-variant | PHF14 | GRCh38.p7 | 7:11060912 | AACAGTGTACTTGAT[-/ATC]ATGAAGAATTGAAAT | 9678 |
| rs149249620 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | PHF14 | GRCh38.p7 | 7:11029413 | CTTTCATGAGTATTA[C/G]TGGAGACTTCCAGAG | 9678 |
| rs149251532 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11099719 | GTTACCTCTAAGATC[A/G]TTGTCTTATCTTTAA | 9678 |
| rs149259618 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:10995059 | AATCCCTGAGATAGA[C/G]ACAAAAGTTCTCCAA | 9678 |
| rs149283313 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11168499 | TCAATGATTTAATTT[A/G]GTTTCATCAGATACA | 9678 |
| rs149311664 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10990432 | GTAGTTAGTTGCATG[C/T]GTGCTTTTTCATATC | 9678 |
| rs149336883 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11163297 | ACAAAAAAATTCTTA[C/T]GCTTTTTACAGTAAA | 9678 |
| rs149340001 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11117015 | ATTCTTGATAAAGAT[C/T]TCAACAACTTGTATC | 9678 |
| rs149345622 | snp | A/G | 0.000555764 | 0.0166605 | intron-variant | PHF14 | GRCh38.p7 | 7:11042669 | AAATCTTTACTTGCT[A/G]CCTTTATTAAAAGTT | 9678 |
| rs149355842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11006658 | TGATGGTATAGTAGT[C/T]AAGCTTGTTTCTCCT | 9678 |
| rs149404067 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11072009 | ATGATTAAGTATGAG[G/T]ATTTATAACCATTCT | 9678 |
| rs149408560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003181 | CCTGACCTCGTGGTC[C/T]GCCCGCCTTGGCCTC | 9678 |
| rs149418886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963672 | TTAATATTGACAGTG[C/T]GGTGTTAAAGTCTTG | 9678 |
| rs149458513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067030 | ACCAGATGGTAAAAA[C/G]GTTAACCCATAGGAT | 9678 |
| rs149463172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144567 | TGTAGCACTATAATT[C/T]ATAATATATAAAATA | 9678 |
| rs149471474 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960739 | TTCTCCACATCCTCT[C/G]CAGCATCTGTTGTTT | 9678 |
| rs149473240 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | PHF14 | GRCh38.p7 | 7:11025693 | TCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT | 9678 |
| rs149497036 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | PHF14 | GRCh38.p7 | 7:11130823 | TCCTGTGCTCTGCCT[A/G]TTCACCACTCCCTCT | 9678 |
| rs149525155 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022505 | TAATGAACGTGACTA[C/T]CTTTCCTTGCATATG | 9678 |
| rs149543893 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11123388 | ATTTACTTAAGTAGG[C/T]GAATGTATATTAATT | 9678 |
| rs149559930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078231 | ATTGTTGACATACAT[C/G]GAGAGGTTTGTTAAC | 9678 |
| rs149561305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10986117 | GAGACTACAGGTGTA[C/T]GACAACGACTGGCTA | 9678 |
| rs149603390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11153540 | TGAGGGCTGAAGATA[C/T]AAATGGGAAAGTCAT | 9678 |
| rs149618372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140640 | TATAATCCATAACTG[C/T]AAGAATATACTATAC | 9678 |
| rs149654636 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11079404 | TCTTTCAAATGCCAC[A/G]TTAAACCTAGAGGAA | 9678 |
| rs149658568 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11161102 | TGCATATGGTGAAAT[A/G]TAGGGCTCCAGTTTC | 9678 |
| rs149661118 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987186 | GAGTCCTAAAAAAAG[A/G]TTAGTTCTGTAACAT | 9678 |
| rs149666604 | in-del | -/AAT | 0.109461 | 0.206758 | intron-variant | PHF14 | GRCh38.p7 | 7:11152150 | CTTTTAAGATAACTG[-/AAT]AATAATCTGGTCAGT | 9678 |
| rs149668807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040008 | TTAAAATACTATCTA[C/T]CATAAAAGACATTTT | 9678 |
| rs149711949 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11155148 | TAGGCTCCTCATATT[C/T]TATTTTATTTAATAA | 9678 |
| rs149716753 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11047669 | ATGGGGATTCGTAAT[C/T]CCTGCTACTCAGGAG | 9678 |
| rs149720638 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11035877 | AGTGACATGTGACGT[A/G]TAATAGGAAGTTTGG | 9678 |
| rs149742019 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107598 | ATTTTATTAAAAAAT[C/G]TTAGTGTTTCTTTAC | 9678 |
| rs149756904 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000983 | TATTTTCTAGTTCTA[G/T]AATTTTTTAATTATA | 9678 |
| rs149775353 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11101519 | AGCAAATTGACCTCT[A/C]TTATTTCTTATATGT | 9678 |
| rs149805425 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064008 | TAAGAAGATAATATC[A/G]TAAATTGTCTGCAAA | 9678 |
| rs149809191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995606 | CAGAGCGGGGGCAGC[A/G]CTCATAAGGGAGGCT | 9678 |
| rs149831388 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11086418 | CATCTTGCTTTTATT[-/A]ATACTTTATGTTATA | 9678 |
| rs149854560 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11165505 | TGCCTCTTTGTGTAA[C/T]CCTTTTATATAAAGG | 9678 |
| rs149859616 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11059555 | CCAAGGCAGGTGGAT[C/T]GCTTTAGGTCAGGAG | 9678 |
| rs149863580 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11136869 | ATGGTCATAATTATT[G/T]TAATTACTTAAAAAA | 9678 |
| rs149873825 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11019664 | AAAGGTTTGTCAGTG[G/T]TGTTTACCTTTTCAA | 9678 |
| rs149877086 | in-del | -/A | 0.0543909 | 0.155886 | intron-variant | PHF14 | GRCh38.p7 | 7:11029114 | CCATGAATTATAGTT[-/A]AAAAAAAAATAGCAT | 9678 |
| rs149918365 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113154 | ACCTTTTTTAAATAT[A/G]CCTTTTTGCATATAT | 9678 |
| rs149925817 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11015270 | AATTGGTGGACTGAT[C/T]CTTGAGAAATGTTGC | 9678 |
| rs149931020 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11004898 | AAAATTAGCCTGTAA[A/T]CCCAGCTGGTTGGGA | 9678 |
| rs149935839 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976260 | ACTGTTTTTTTATCC[A/T]TTGCTTCTCAGCTCT | 9678 |
| rs149967768 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965027 | ATGCTCCTTTAGCTC[A/G]GAGAAGTTTGTTATT | 9678 |
| rs149988305 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | PHF14 | GRCh38.p7 | 7:11068307 | GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC | 9678 |
| rs149999630 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961902 | TATAGGAATGCTTGT[A/C]ATTTTTGCACCTTGA | 9678 |
| rs150006016 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11145978 | TCTTGAATATGTTGA[A/G]CCTAAATTTATCACA | 9678 |
| rs150019590 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11133789 | TTGCACATATTACAT[C/G]ATAAAACGATTCCTC | 9678 |
| rs150021190 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11027343 | TGTCAGGATTTGACT[A/G]TTGAAGTTTTTAAGT | 9678 |
| rs150072211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11024230 | TGAGAGAGGTGAGGA[A/G]GCTGCAGAAGAAAGG | 9678 |
| rs150094166 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972552 | AGGATTTTAACTGGA[A/C]GAATAAATATCTGAA | 9678 |
| rs150113841 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11147789 | GCAGTTGTACCTGTA[G/T]TTGGGGGACTTTTAA | 9678 |
| rs150121849 | snp | C/T | 0.000198804 | 0.00996807 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028792 | GCTCAAAAGGAAGGT[C/T]TGCTTTCAGAGGCAG | 9678 |
| rs150160744 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PHF14 | GRCh38.p7 | 7:11143367 | GTCAAGTGATTCTTC[C/T]GCCTCTGCCTCCGAA | 9678 |
| rs150173923 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11025511 | ATTTTAAGAACTTGC[C/T]AGCCGGGCACGGTGG | 9678 |
| rs150177066 | in-del | -/T | 0.0471551 | 0.14613 | intron-variant | PHF14 | GRCh38.p7 | 7:11054292 | ATCAATTAGAATTTA[-/T]GGGGTTTGACTAAGC | 9678 |
| rs150177317 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11092085 | GTTTTGCTGACTGAA[A/G]TACCTCTGTGTATAA | 9678 |
| rs150183536 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:10990192 | CCTTAAGTGTGCCAT[C/T]ACATACATACTTGCT | 9678 |
| rs150185086 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11080377 | CTTGGTGTTTTTTTC[C/T]CCCCTCAGAATTATA | 9678 |
| rs150230348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089067 | AGCCTCATTTTGAGC[A/T]CAGACAGACACAAAG | 9678 |
| rs150233821 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050543 | TAGCCACATATGGCT[A/G]TTTAAATTTAAATCA | 9678 |
| rs150236216 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156825 | GAAAAGAAATTAACT[C/T]TCTACACTTAAGTTT | 9678 |
| rs150264775 | snp | C/T | 0.0155214 | 0.0867166 | intron-variant | PHF14 | GRCh38.p7 | 7:11111513 | TGGTGTCCTTCCGTT[C/T]GATAGCTTTCCCATG | 9678 |
| rs150268476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037908 | GATCCTTAGTTTTTT[C/T]CATTGGGAAAATAGT | 9678 |
| rs150298015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007531 | AGTAGCTAGTATTGC[A/T]AGAGTCTTTTGTTTT | 9678 |
| rs150317823 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104234 | CTTGCATTTTCAGTG[A/G]TGGTGGATATTCTAT | 9678 |
| rs150334643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066373 | CAAGCAATCCTCTCA[C/T]CTCAGCCTCCCGAGT | 9678 |
| rs150336615 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10997663 | GATTTGCTTCTAAGC[A/T]AAGTCAAATAGTTGT | 9678 |
| rs150345817 | in-del | -/A | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11044970 | GTAATGTCAGTGCTC[-/A]AAAAAACATTTGGAT | 9678 |
| rs150346267 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960511 | ACATTTGGGTTGGCT[C/G]CAAGTCTTTGCTATT | 9678 |
| rs150354024 | in-del | -/CA/CACGCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088418 | ACACACACACACACG[-/CA/CACGCA]CACACACACACACAG | 9678 |
| rs150379592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138813 | TTCTGTTATTTTATA[C/T]TCAATTTCAGTGTCA | 9678 |
| rs150393329 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11123093 | GGTTTTTTTGATAGG[C/G]TTCTCTAGGTTGGTT | 9678 |
| rs150394381 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11021127 | ACTCTACTTAGTCTG[C/G]TTTATTAAAATATAT | 9678 |
| rs150446815 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11016915 | CACTATCCTTCCCAA[C/T]GTCTAGTAACCATCC | 9678 |
| rs150456570 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:10979992 | TTAAAAAATTGCTTT[C/T]TATTCAGGCATGGTT | 9678 |
| rs150477866 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | PHF14 | GRCh38.p7 | 7:11074499 | ACAGGCATGAGCCAC[A/C]GTGCCTGGCCCCGTT | 9678 |
| rs150497036 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | PHF14 | GRCh38.p7 | 7:11023718 | CTGTAATCCCAGCCA[C/T]TCAGGAGGCTGAGGC | 9678 |
| rs150501696 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956957 | AACAAATGTAGATTT[C/T]GGTATCAGAAGTGAT | 9678 |
| rs150537618 | snp | A/C | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11135481 | TTCTTTATTTGAAGA[A/C]CATTTAAAATTATTT | 9678 |
| rs150555547 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019244 | CAGAGTAACACTGGC[C/G]TCATAGAATGAGTTT | 9678 |
| rs150578562 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11155012 | ATCCTTACTATCTAT[C/G]TGTAGGTACCTATCT | 9678 |
| rs150587931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075233 | TGTGGGCCACTGCAC[C/G]TGGCCTTTCAGACAT | 9678 |
| rs150617896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974763 | GGTCATCTTTATGTT[C/G]TCTTAGCACCACAAC | 9678 |
| rs150641736 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11101180 | AGCTTTTTAGTTTTT[A/G]TCAAACTTATCAACT | 9678 |
| rs150694514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095546 | ATCCCTAGAAGTAAA[G/T]GGAAATAAGATCAGG | 9678 |
| rs150710413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059294 | GCAGCATTAAAATAC[A/G]TACTTGAAAAATTCA | 9678 |
| rs150723557 | in-del | -/G | 0.00953873 | 0.0683987 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169745 | GAACAGAGACAGAAT[-/G]TTATTTTTTTTGTAA | 9678 |
| rs150742871 | in-del | -/A | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11015728 | TGTCTCCTTACTCTT[-/A]ACTACTGCCGTTACT | 9678 |
| rs150763937 | snp | A/C/G | 0.00149991 | 0.0273452 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051768 | ACCCAAGAAGATTCC[A/C/G]ATAAGAAACACGGTA | 9678 |
| rs150779538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160159 | TATGAGTAAGAACAT[A/G]TGGCATTTGATTTTC | 9678 |
| rs150781170 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11129970 | AGTAGGATTTGACAG[A/G]AGTATTAATTAGGAT | 9678 |
| rs150795864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015131 | TATCACCATCATTTC[C/T]CATATTTTAACATAA | 9678 |
| rs150847987 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11009762 | AGTATGGATCATTTT[C/T]CAGGGACAGTGAAGC | 9678 |
| rs150853108 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11068020 | GTATCCAAACCATAG[C/G]ATACATACAGTAGAA | 9678 |
| rs150858669 | snp | A/C/G | 0.0287743 | 0.116735 | | | GRCh38.p7 | 7:10970386 | GCCAGCCTGGCCAAC[A/C/G]TGGTGAAACCCTGTC | 9678 |
| rs150892929 | in-del | -/CTGT | 0.0279526 | 0.114869 | intron-variant | PHF14 | GRCh38.p7 | 7:11114432 | TTTCTATCTTTACCC[-/CTGT]CTATTACTTTTATAG | 9678 |
| rs150905431 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11140260 | GCATACACCCCCACA[C/T]GGAAATAAAACTTTT | 9678 |
| rs150907355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063300 | GTAAAGTAGTAAGTA[G/T]TTCCAAGTTCAGGAG | 9678 |
| rs150918172 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965922 | GGAGGGAATCCCCTG[G/T]TCTGCCTGCTGTGAA | 9678 |
| rs150939385 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11125248 | TGTTTGTCATGAGTT[A/G]TGAAGTTTGAAAACC | 9678 |
| rs150955516 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11079120 | AGCTCTAACTATTAC[A/C]ATGAACTTAAAAGGA | 9678 |
| rs150957222 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11011969 | TCCATGTTTATTATA[C/T]TTTGGTGGTAGTAAT | 9678 |
| rs150963232 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11070837 | TGCTTGTTAATTTAC[C/T]GATACACTGCCATAT | 9678 |
| rs150966747 | snp | A/C | 0.0752113 | 0.178743 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972181 | CCTCAAGTGATCCAC[A/C]CGCCTCAGCCTCCCA | 9678 |
| rs151014570 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11035384 | CCCAAATAATACATT[A/G]TATTTGATTTCAATA | 9678 |
| rs151014735 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11142625 | AAAATGCTTGTGACA[A/G]CTTTAACCTATCATC | 9678 |
| rs151017873 | in-del | -/T | 0.108402 | 0.206034 | intron-variant | PHF14 | GRCh38.p7 | 7:11110165 | TTTCTTTGTGTGTTG[-/T]TTTATGTAAGAAGAG | 9678 |
| rs151018430 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967003 | AAGTAATGAACTCAG[C/T]TGAGTCCATTCATTA | 9678 |
| rs151026783 | in-del | -/ATTC | 0.102726 | 0.202016 | intron-variant | PHF14 | GRCh38.p7 | 7:11008067 | TTGTAGTGTGTCTGA[-/ATTC]AGGAGAATGTCAGGT | 9678 |
| rs151046691 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11025195 | TGACTGAACTGCTGC[A/G]ATCTCATGATAAAAA | 9678 |
| rs151068657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137883 | TGAGCCACTGCGCCC[A/G]GCCCTGTTGAGTCAT | 9678 |
| rs151076623 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10995561 | GTGCCCGCATTCCTC[A/T]GCCCTTGGGTGGTCG | 9678 |
| rs151098499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11088091 | AGGACCGCTCTCGGA[C/T]ATCAAAATCTGAAGA | 9678 |
| rs151103124 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11156569 | GGAGGCCGAGGCGGC[A/G]GATCACCTAAGGTCG | 9678 |
| rs151115921 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983890 | GGTTTATTCATTGAT[A/C]TCAGAGATGCATCAT | 9678 |
| rs151150557 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | PHF14 | GRCh38.p7 | 7:11165134 | TTCACCATGTTGGCC[A/G]GGATAGTCTCGGTCT | 9678 |
| rs151152435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082223 | TAGTGACACGTGCCT[A/G]TAGTCCCAGCTACTT | 9678 |
| rs151163672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044984 | TCAAAAAACATTTGG[A/G]TTTTGGAGCACTTCA | 9678 |
| rs151166914 | in-del | -/ATA | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11143217 | TGAAGATAATATGCT[-/ATA]ATAATTTGTAAATAA | 9678 |
| rs151168017 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10977504 | ATAAACATAATTTAA[C/G]TCTATCATAAAATAG | 9678 |
| rs151215500 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11038590 | TTGAACCCCAGAGGC[A/G]GAGGTTGTAGTGAGC | 9678 |
| rs151225571 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | PHF14 | GRCh38.p7 | 7:11004851 | GACCAGCTTGGTCAA[C/G]ATGGTGAAATCCCGT | 9678 |
| rs151227623 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11098212 | ACATTTAAAAAACTT[C/T]AGCCATGTATATAAT | 9678 |
| rs151256715 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11060826 | ATTTACTTTTTTTGA[A/G]TGACTAATTTAGTTG | 9678 |
| rs151257933 | in-del | -/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11153395 | TAAGTCTTTTTTAGT[-/G]GGGGTAGGGGAAGTT | 9678 |
| rs151320198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016663 | TGAGATGTTTTGATA[C/T]AGGCATGCAATGTGA | 9678 |
| rs180752566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083758 | AGTCACCACACCTGG[C/T]CTGCTTTCCCTAATT | 9678 |
| rs180760202 | snp | A/G | 0.00233133 | 0.0340621 | intron-variant | PHF14 | GRCh38.p7 | 7:11040645 | CTTTCTTAAAACAAT[A/G]TATACTACATTTGTT | 9678 |
| rs180765363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020235 | TGCAGGTTATAGGTG[G/T]GCGCCACCACACCAG | 9678 |
| rs180766912 | snp | A/C | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065637 | TATTTTAAGTAAGGA[A/C]ATAGATTTGAGAATA | 9678 |
| rs180773013 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11000755 | CCTTGTATATTTTGG[A/G]TATCAGTTCTTTATC | 9678 |
| rs180784176 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103567 | GATTTAGAAGAGACT[C/G]TTTGCTGAAATTGAA | 9678 |
| rs180787321 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11075082 | AGCTGGGACTACAGA[C/T]ACATGCCATCACACC | 9678 |
| rs180788644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11056388 | ATTTTATTATATATC[A/G]TTAGACCCATAGTTA | 9678 |
| rs180796259 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093633 | CTTACTTAGCAGTAG[A/G]CTGTCACATATTACT | 9678 |
| rs180820887 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047858 | AAGGGAGGGAGGGAG[G/T]GCGGGAAAAAGAGAG | 9678 |
| rs180833658 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133592 | AGAGGAAGTTAGGGA[A/T]CAGAAGAGGACAGGA | 9678 |
| rs180848744 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11167455 | TGTATTAATTCAGGC[A/G]TACCTTTTATTCGTT | 9678 |
| rs180849783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11150881 | CTGCTTTAATCAGTC[C/T]TTTGAAATTCAGTAT | 9678 |
| rs180858280 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11112728 | GTGAACCGAGATCAC[A/G]CCATTGCATGCCAAC | 9678 |
| rs180904194 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10969417 | TTCTCTCTCAACAAA[A/G]TAAGACAATTCATTT | 9678 |
| rs180904653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10994299 | AAAAAATTAGCTGGG[C/T]ATGGTGGCATGTGCC | 9678 |
| rs180910971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987327 | ATTCTTTTAATTCTA[A/G]TTTTACAGGAAATGT | 9678 |
| rs180946781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11154102 | ATTTGAAAGAAACTA[A/G]TGGATTTAACCAGGT | 9678 |
| rs180947667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029307 | GTTGTTTTCAGTGTT[G/T]GGGGACTGGTTAAGA | 9678 |
| rs180952837 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961336 | TTATTAAATAGGGAA[A/T]CCTTTTCCCATTGCT | 9678 |
| rs180967232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010615 | AACTATTAACATAGT[A/G]TATATGAAATCCATA | 9678 |
| rs180971512 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11146913 | GTCCAGTGGTGCGAT[C/G]ACAGCTCACTGCAGC | 9678 |
| rs180990930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976768 | ATGAGTTTTGTTAGG[C/T]TGATATATCTATATA | 9678 |
| rs181032513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164489 | CTGTTAATTATAGCT[A/G]TATATTTCAGTGTAG | 9678 |
| rs181046452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968151 | TAAAAGACTGAAGGA[A/G]TGAAAGTCAGAGATT | 9678 |
| rs181082787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977178 | ATCACTGGTTTCCAA[A/T]CATGTTGAAGTTGTG | 9678 |
| rs181085641 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10994761 | TCTTTCTGGTGGGTT[C/T]GTGGTCTCGCTGGCT | 9678 |
| rs181098310 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012375 | ATATTCAAGTCCCAC[A/C]GTCGGACCTGGGGAA | 9678 |
| rs181116758 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056205 | TTCAGAACCCTGAGA[C/T]TCCTGTTTTGCTTTT | 9678 |
| rs181119246 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10986586 | ACTGCATTTTCCGCA[A/C]ACGGACACCTGTTTT | 9678 |
| rs181125563 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11040180 | ACTGAGAAATGACTT[C/T]GATAGATGGTTGCTG | 9678 |
| rs181127546 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066364 | TCCCGGGCTCAAGCA[A/G]TCCTCTCACCTCAGC | 9678 |
| rs181130923 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11019712 | TCATTGATCTTTTGT[A/G]TATGTTTTTTATTTC | 9678 |
| rs181134526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000131 | AACTTTATATATGTT[C/G]CAAGTAAAGATGCAA | 9678 |
| rs181137813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11049190 | TTTAAAAGTAAATTA[C/G]AGCCTGGCGCGGTGG | 9678 |
| rs181145158 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11111594 | TTAACCAGTACACCT[A/T]AAGAATATATTGCTA | 9678 |
| rs181145471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093117 | TCTCTTTAACTCATG[A/G]GTTATTTAGAAGTGT | 9678 |
| rs181148677 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11030477 | GCTAATTAACAAAAA[C/T]GTGTGAAGCAGCCAT | 9678 |
| rs181157164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149124 | AAGCAGGATTCAAAA[G/T]AAGATTTGTCTGACA | 9678 |
| rs181157208 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104404 | ATAATCTCTTAAATG[A/C/T]TCTCATATCCACAGT | 9678 |
| rs181158752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121997 | AGGTATTTGTCCTAA[C/T]GCACTTCCTCCCCTT | 9678 |
| rs181162032 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11074561 | GTATCGATTCATAGG[C/G]TGTTATAAGCAGCCA | 9678 |
| rs181162308 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11166897 | AGAAGGCATGCATTT[A/G]TAAACTGTACTTTAT | 9678 |
| rs181171312 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11133163 | CAGTGCAATCCCAAT[C/T]GAACTCTCAGCAAGT | 9678 |
| rs181172712 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11085422 | ATCATTGATGTAACC[C/T]TTTGTGTAATGTATT | 9678 |
| rs181280091 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973549 | CTTAAGGTAGCAAAC[A/G]TCCCTTTGTGGAACG | 9678 |
| rs181285626 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11108732 | GAAATCAGCAACAGA[G/T]TGGAACTGTGTTAGT | 9678 |
| rs181287826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153539 | GTGAGGGCTGAAGAT[A/G]TAAATGGGAAAGTCA | 9678 |
| rs181289136 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11116226 | CAGGTACTTTCTTGC[C/T]GAAGGTCTTCCAGGC | 9678 |
| rs181292863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089383 | CGTATTTGAACACAC[C/T]GTGGTTTCTCTAAAA | 9678 |
| rs181298599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145667 | GAACTATTTAAAGAA[C/G]TACTTTTCTGATCAA | 9678 |
| rs181305929 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163568 | CATTTCGCACTTTAC[G/T]TAATGATCCAAGTGT | 9678 |
| rs181308980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127536 | TGCATCTTTGCTTTG[C/T]TACTACAGACAGACA | 9678 |
| rs181320769 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11044763 | AGGTTATTTAAGTCT[A/G]TTGCATCTGGATGGT | 9678 |
| rs181325476 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024265 | AAGGTAGCAGAGGTT[A/G]GTTCATGAGGTTTAA | 9678 |
| rs181345181 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964943 | GCTCTTCTCTACACT[A/G]GTTATTCTAGTTAGC | 9678 |
| rs181345296 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11004537 | ATCTCTTTAGTCTCC[A/G]TTAATCTAGAACAAT | 9678 |
| rs181348721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11077889 | AATAAATGTCAGTTT[A/G]TTCCTCAGTTGAGAA | 9678 |
| rs181362073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11060521 | TTATGTGTATTTGAC[C/T]TACTTAGGATTCTTG | 9678 |
| rs181363486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958999 | GAGTCTTTTTAAAAC[A/G]CGTATCAGTCAAAGT | 9678 |
| rs181374358 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11136738 | CAGATGTATATAAAC[A/G]TAAGATTAGATATAT | 9678 |
| rs181393414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070615 | CTTATGTGGCCCCAT[A/G]TTGATCGTCTTACAT | 9678 |
| rs181450510 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11052211 | GGTTTATTTTTGTAG[A/G]TTTTGAATTTCATAT | 9678 |
| rs181456035 | snp | C/T | 8.35708e-05 | 0.00646362 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982772 | TCCCACTACGACAAC[C/T]GCTACAGAGGAACAA | 9678 |
| rs181465817 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017619 | AGATTTTTTCCTGTG[C/G]AGTTATTTGAACTCC | 9678 |
| rs181523274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068983 | TGTTTTTGATGCTAT[C/T]GTATAGGTTATCTTT | 9678 |
| rs181529813 | snp | A/G | 0.000797342 | 0.0199508 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051758 | TGCCACCAGAACCCA[A/G]GAAGATTCCGATAAG | 9678 |
| rs181534217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033959 | AAACCCTGTTTTACT[A/G]ATGTGGTAACTGAGG | 9678 |
| rs181540121 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108102 | TTTCTTGGGTTCTTA[A/G]TGGTATCTCTTATAT | 9678 |
| rs181544885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127179 | CTCAGCAGCTCAGAC[C/T]TCCTTTAAACTGGGA | 9678 |
| rs181547664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088882 | GGAATGAGGAAACCT[A/G]TTTTATGTCATAAGT | 9678 |
| rs181551192 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11154500 | ATTTAATAAACTATA[G/T]TTGTCTAATTTCTGT | 9678 |
| rs181590353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098665 | AATCCCCACTGCACC[C/T]GGCTGTTCTTTACTT | 9678 |
| rs181593731 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11035215 | TTATAAGTAATGTAG[A/G]GACTGCTTAAAATAT | 9678 |
| rs181596987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996273 | AGGAATTGGTTTTGA[A/G]GTAGATAGTAAAAGT | 9678 |
| rs181661765 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11016239 | CTGGAAATTATAGGC[C/T]TTCACAATATTTCCA | 9678 |
| rs181672838 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11062632 | TGTTTTGTCTTTGTT[G/T]CTTTGTTTCGTTTTG | 9678 |
| rs181689886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162934 | CAATCTGCTCCAGAA[C/T]CATGAATTGGAGAGA | 9678 |
| rs181691565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137839 | GATCTGCCCACCTCG[A/G]CCTCCCTAAAGTGTT | 9678 |
| rs181703792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099651 | AATCATTTGGAAAGA[C/T]TGAGACTCTTACCAC | 9678 |
| rs181759853 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11080063 | ATACATTTTTACTAC[A/G]AATGAATGTCATAAA | 9678 |
| rs181771773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078535 | ATTTAAAAATCCCTT[C/T]TAATTTTCAAATTTC | 9678 |
| rs181773693 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11062189 | GATAAGACCTTTCTT[A/G]AAATATTATATAGTG | 9678 |
| rs181780589 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11046868 | GGCTTAGACATAAGA[A/G]AAAAAAAAACTCTGG | 9678 |
| rs181785311 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981188 | ATTACAGAGGTTAAG[C/G]CTAGTTGAGTTAATA | 9678 |
| rs181787684 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117296 | AGCTGTCTTAGCTTG[A/G]AGACTTCTATTTGGT | 9678 |
| rs181788362 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10995814 | AAGCCCCTCACTGCC[C/T]GGGGCTGGCAGTGCC | 9678 |
| rs181790312 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11137127 | TATTCTTAAGATTTA[A/G]TCTCTCAGGTTTTCT | 9678 |
| rs181795118 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11099252 | TATTTATTGTATCAC[A/G]TTCTTTGACTTAAAA | 9678 |
| rs181796722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11116658 | GCTTGTCATTTGATA[A/G]CTTTTAAACTGAATT | 9678 |
| rs181796873 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10995544 | CGCCAGTCCCATGCC[A/G]TGTGCCCGCATTCCT | 9678 |
| rs181803298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11015475 | ATAGGCATAGGCATT[A/G]CTCTAAGTTGGGCCT | 9678 |
| rs181809146 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11033565 | TCTAGCAGGGTAGCC[A/G]TATGCCCAGTAAAAA | 9678 |
| rs181815300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145120 | GTCTATTTTATACCA[A/C]AATTATAAAAATGAT | 9678 |
| rs181816586 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964863 | TGATCGAATTGGTTA[C/T]TGAAGCTTGTGTATG | 9678 |
| rs181848861 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141227 | GTATAATTTAAATTT[A/G]GAGCAACTGGCCAAA | 9678 |
| rs181883509 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094442 | TCACATCTATTTATC[G/T]CTCTGATTCTGACTC | 9678 |
| rs181899913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964401 | GAATGTTGACTATTG[A/G]CCCCCACTATCTTCT | 9678 |
| rs181908547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113168 | TACCTTTTTGCATAT[A/G]TTCTTTTGAGAAGGC | 9678 |
| rs181922514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151425 | TTAGCTGGTTGTGGT[A/G]GTGCACACCTATAGT | 9678 |
| rs181923913 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11004768 | TGGCTGGGTGCGGTG[A/G]CTCATGCCTGTAATC | 9678 |
| rs181941042 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168047 | AAAGAAATGTCATCT[C/G]TAGGAACTTTTTTCT | 9678 |
| rs181951461 | snp | A/G | 0.0193772 | 0.0965046 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974073 | CGCTGCCTGGGCCGG[A/G]GGTCTTCTCCGGCCA | 9678 |
| rs181975144 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046013 | TTCTTAGGTTGGGCC[A/G/T]GGGATGTGAAAAGCT | 9678 |
| rs182013895 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961406 | TGTATGGTGTTATTT[C/T]TGAGGCTTCTGTTCT | 9678 |
| rs182015709 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10976918 | TCTCAGGTCACAAAT[G/T]TGTATGTATAGTTCT | 9678 |
| rs182034657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981650 | CCATTCTAGAGCATA[C/T]AGTAGTTACTGCGTA | 9678 |
| rs182077351 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:10994612 | TTTTATTATTGTGTC[C/T]GGAATTGGTGGGTTC | 9678 |
| rs182078616 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11158968 | CTGAGTTGTTTCTTA[G/T]TCTCAAAATTGTCAG | 9678 |
| rs182083816 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011805 | GTATGTCCACTACCA[A/T]TTGGGAAAAAGAAAT | 9678 |
| rs182126155 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11121519 | GATGCCTTAAACCAG[A/T]TATTTTTTCCTAGAC | 9678 |
| rs182146315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085113 | TGGTATGTTATGAAA[C/T]AGACAACAGATATAT | 9678 |
| rs182170520 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11158597 | GGGGAGTTGTTTTAT[G/T]TTTAAGTCACTAAGC | 9678 |
| rs182186843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989201 | ACAAATCTGCCGCAA[A/T]TTTAGATGTTATACA | 9678 |
| rs182192566 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11002339 | CACAGGTGTAGGTCA[A/T]GGGGGGAGCCAGAGC | 9678 |
| rs182204156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022020 | AAAGTGCTAAGATCT[A/G]CTGTTTAAATTTCAA | 9678 |
| rs182223438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024739 | AAAAGATTCCTTTCA[A/G]AAGATTACTGCTTAT | 9678 |
| rs182225325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986122 | TACAGGTGTACGACA[A/G]CGACTGGCTAATGCT | 9678 |
| rs182226254 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959451 | GAGTTTTGTTCATGC[C/T]TGCTGGGCTCATTCT | 9678 |
| rs182227812 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11051286 | CTCCTGAAGTGCTGG[G/T]ATTATGGGAGTGAGC | 9678 |
| rs182234243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10991324 | CTGGGATTACAGGCA[C/T]GAGCCACCATGCCTG | 9678 |
| rs182247138 | snp | C/T | | | | | GRCh38.p7 | 7:10971549 | TCTCCTTCTTTCCTT[C/T]TCTTACTTTCTTTCA | 9678 |
| rs182251032 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104693 | GAATCACAGGAAGGA[C/T]TTGTAAAAACACAGG | 9678 |
| rs182262424 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058097 | TTCCACATATTATTT[C/T]CATCCTACAGTTTTA | 9678 |
| rs182269712 | snp | A/T | 3.65103e-05 | 0.00427245 | intron-variant | PHF14 | GRCh38.p7 | 7:11042642 | ACTGTTTCACTATGA[A/T]AATTATTATTGAAAT | 9678 |
| rs182281192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11159701 | TAAAAGGTACAAGGG[A/G]TCTCTGTATTATTTC | 9678 |
| rs182287353 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11097147 | ACCATGCCCGGCTAA[A/T]TTTATATTTGTAGTA | 9678 |
| rs182289966 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11122518 | CTTCAGAACCCTATC[C/T]TTATGCCCTACAATT | 9678 |
| rs182292131 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11076507 | TGAATGAAGACCATC[A/G]CACAGATTGGGAACT | 9678 |
| rs182294967 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11141781 | CTAGTCTGAACGTGT[A/G]TCTAACAGCTGTAAG | 9678 |
| rs182329152 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11048919 | GTGGTGTTCAGGGTG[A/T]AACATTTCTATTTTC | 9678 |
| rs182365067 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11135519 | ATGCTGGCTGAACTA[G/T]AATTTTTGGAAATGC | 9678 |
| rs182384706 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11100342 | TGTTAGATGCTTACT[A/G]TATCCCAGACTATGT | 9678 |
| rs182398572 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081792 | GCCCCGGAGGCAGAG[A/G]TTGCAGTGAGCTGAG | 9678 |
| rs182412032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155540 | CATTGTTTGCTTGAC[C/G]AACTCTTTCTTATCC | 9678 |
| rs182417779 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103886 | AACATTGGAGGAAAA[A/G]TATTCATAATCTTTA | 9678 |
| rs182423074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11119197 | TGTCTTTTAAAAGTC[A/G]CAAACCTCATACTGT | 9678 |
| rs182425208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138357 | GAAAAATATTTCTAA[A/G]GAGACTCCTTACAAG | 9678 |
| rs182431153 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11140146 | AACCTTCTCATACCC[C/T]TGCACACACCTGTAC | 9678 |
| rs182502454 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956933 | ATGATTTTTACAGCA[A/G]TCCTAGAAAACAAAT | 9678 |
| rs182510370 | snp | A/G | 0.00755907 | 0.0610114 | | | GRCh38.p7 | 7:10970718 | CTTTATATGACATCA[A/G]AATGTAATTTCCTTT | 9678 |
| rs182517534 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11030951 | TAATGAAGTTTGCAT[G/T]TGACAGTAATCATTC | 9678 |
| rs182517824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994931 | GTTGCCATTGCTGGC[C/T]GGGGCAGCTTGCTCT | 9678 |
| rs182542893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966910 | TGTCCTTGCCCCTTC[A/G]AACATACTGGGATCT | 9678 |
| rs182544743 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066541 | TGTTTTCTTCTAGAA[C/G]CTTTGTAGTTTTGGC | 9678 |
| rs182547925 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11030092 | ATAGCTGTTCCAGTC[A/T]CTTGATTTTAAGGAA | 9678 |
| rs182563088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988280 | ATGTGGAGAGAAATT[A/G]GCGTAGAGATATGAT | 9678 |
| rs182590764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066124 | TTGTTGTTCGCACTT[C/T]TATTTATTTTACATT | 9678 |
| rs182608306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11147849 | CCAAGATCTAAATTC[A/G]TATATTCAAATGTTT | 9678 |
| rs182616473 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11165013 | CACTGCAGCCTCCAC[C/T]TCCTGGGTTCAAGCG | 9678 |
| rs182640544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962537 | GGATATTGGCCTGCA[A/G]TTCTTTTTGTTGTAT | 9678 |
| rs182680534 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063011 | AACAAATATATTAGT[A/G]TTGTTGTATGTTTTT | 9678 |
| rs182688891 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11109401 | GATGACCTGAGATGA[C/G]AAATATAAATTATAT | 9678 |
| rs182689708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047114 | CGCTCTGTCACCCAG[C/G]CTGGGGTGCAGTGGC | 9678 |
| rs182698199 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11025943 | GTGGCAAAACCCTGT[A/G]TCTACTAAAAATACA | 9678 |
| rs182716484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099970 | ACAATTGACTATTGA[C/T]AATTTCTCTAAATGA | 9678 |
| rs182717730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080822 | AGGGCCATCAAGCAC[A/G]AAGTCTTGAATTTTG | 9678 |
| rs182766233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977520 | TCTATCATAAAATAG[A/G]AACAAATCAACATTG | 9678 |
| rs182766344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11049335 | CCAAAATTAACTGTG[C/T]GTGGTGGCACACACC | 9678 |
| rs182782669 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012730 | TGAACTCCTCTCAGA[A/C]TGTTGAGTTTTGTGA | 9678 |
| rs182812370 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085751 | TTTTTAAGAGACAGG[A/G]TCTCACTATATTGTC | 9678 |
| rs182813770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992344 | CAGGCATGAGCCACC[A/G]TGCCTGGCTGACAGT | 9678 |
| rs182820910 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005821 | TTTTTTGAGACGGAG[C/T]CTCGTTCTTTCACCA | 9678 |
| rs182827276 | snp | C/G | 1.83155e-05 | 0.00302612 | intron-variant | PHF14 | GRCh38.p7 | 7:11036712 | AGACACTGGTACATG[C/G]ACATTTTCACTGAGA | 9678 |
| rs182828402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11114151 | AACTTCTTTCTCTGC[A/G]GTAGTCATGTTGTTA | 9678 |
| rs182845177 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11075932 | GTCAGGAGATCGAGA[C/G]CATCCTGGCTAATAC | 9678 |
| rs182847156 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090627 | AAAGCTTGTAACTGT[A/G]AAGAAATTGTGGAAT | 9678 |
| rs182851972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001476 | TTGAATCTATAGATC[A/C]AGTTGGGAAGAAATG | 9678 |
| rs182853341 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11072362 | CCCCGTGATCCAGTC[A/G]CCTCCCATCAGGTCC | 9678 |
| rs182863428 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11053636 | ATTGTTTCAAGAAAG[C/T]CTTTTGACTAGTATT | 9678 |
| rs182869347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128755 | TCTCCCATTCTCCCT[C/T]CTCTCTCCCTCTCTT | 9678 |
| rs182870261 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11041469 | GTGTATATTTATCTA[C/T]GTATATGCATACATA | 9678 |
| rs182875553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147543 | AGACCCAATAGTTAT[A/G]CCGCTGTCTGAATCT | 9678 |
| rs182878206 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11109778 | TTTTAGATGTGTGAT[A/G]TTGTCATAGTAAATA | 9678 |
| rs182968567 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11127821 | CTTAGACCATTTACG[A/G]GAGATTGAGAAAATT | 9678 |
| rs182972042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087117 | CATTCTATTCTGAAA[G/T]AAATTTGTTAACAAA | 9678 |
| rs182974023 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10991585 | AAAGTGCTGGGATTA[C/T]AGGCGTAAGCCACCG | 9678 |
| rs182979738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004907 | CTGTAATCCCAGCTG[A/G]TTGGGAGGCTGAGGC | 9678 |
| rs182986867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067359 | TGGAGTTCTTGTACA[A/G]TTGCCCTTGGGAATA | 9678 |
| rs182994723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168770 | CTCTCATTGCTTATA[C/T]TTTGAAGGTTACCAT | 9678 |
| rs182999127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11143066 | AAGCATTTTAGTTTT[A/G]TCAGAAATATTTGCC | 9678 |
| rs183006103 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106353 | GTAGTGGTATTAATG[A/G]AATAGGTTCAAGCCC | 9678 |
| rs183008648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018884 | CTGTGGGTCTGTCAT[A/G]TATCGCTTTTATTAT | 9678 |
| rs183011021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125115 | GATGATTTATGTAGA[C/T]ACAGCAGAAACTAAT | 9678 |
| rs183041743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118394 | TTGCTTCTAGCATGT[G/T]CCTTGGCAAGTGAAA | 9678 |
| rs183048120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11054680 | AGACCAGGCATACAA[C/T]AGCTTACTAACTTGT | 9678 |
| rs183055688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11154970 | TGGTTATTTAGCTAG[A/G]AAAAAAAAGCACTGT | 9678 |
| rs183063430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965272 | ATGTCCTTTTTGTTG[A/T]TGTTGATGCTATTCC | 9678 |
| rs183074533 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10983368 | TTCTCAAGGAGCTCA[C/G]AATCTCTGTCCTCAA | 9678 |
| rs183075117 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11090960 | ACAAAGTGGGACCAT[A/G]TGAGTCATGTGTGAT | 9678 |
| rs183082345 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960091 | GTTACAAGTGGATTT[A/T]AAAAAAATTATTATT | 9678 |
| rs183084370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10997232 | GCAGAGCAAAAAGAC[A/G]TTATTACTGAGAATA | 9678 |
| rs183096538 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10975201 | GATTTCTCTGTTTTA[C/T]ACCTTAAAATATATT | 9678 |
| rs183105549 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11053028 | TTAGGGCATACTTTC[C/T]TTGCTTGAGCTGAGG | 9678 |
| rs183109449 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035337 | CTGGAACCAGTCCCC[C/G]ATGGATATTGAAGGG | 9678 |
| rs183120988 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962141 | TAGGAGAGGTGAGAG[A/C]GGGCATCCTTGTGTT | 9678 |
| rs183126650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018168 | GGCTACTGTAGGTTT[A/G]TGGTATAATTTGAAG | 9678 |
| rs183162730 | snp | C/G/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11057625 | GTGATCTACCCGCCT[C/G/T]GGCCTCCCAAAGTAC | 9678 |
| rs183217513 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960450 | CTGCATAGTATTCCA[C/T]GGTGTATATGTGCCA | 9678 |
| rs183229517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139523 | TTTGATGAATTTTAT[A/G]TTGTGAGAAATTAAA | 9678 |
| rs183236388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11049703 | TTTCTGGGGTTTTCA[A/C]AGTTCTGCTAATAAA | 9678 |
| rs183244172 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075687 | TTTCAACCTGAGATT[G/T]GGAGGAGACATATAT | 9678 |
| rs183244409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031920 | GTATAATTTGGTGCT[A/G]TTGAACATTGCTGTA | 9678 |
| rs183244945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164939 | TTGACATTCTTTTTT[C/T]TTTGAGACGGAGTCT | 9678 |
| rs183247715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057339 | GAGAAATGTTTAATT[A/G]TTTGTTTTAGATGAA | 9678 |
| rs183269306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013637 | TTCTTATAAACCATT[C/G]GTGTTTCATATCTTT | 9678 |
| rs183304574 | snp | A/T | 0.0872718 | 0.189788 | intron-variant | PHF14 | GRCh38.p7 | 7:11073239 | CAAGTTCCTTCCATC[A/T]ATGAGCCTGTAAAAT | 9678 |
| rs183313759 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11038071 | AACAAATACTGCTGA[A/T]TAATTGGATAGCCTT | 9678 |
| rs183330363 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025675 | TAGCAGGTGCCTGTA[A/G]TCTCAGCTACTTGGG | 9678 |
| rs183330468 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10997629 | CTGTAGTCATTTTAA[G/T]ATTTGGCTGGACCTG | 9678 |
| rs183333435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137993 | ATAAACAGACCAGCA[A/G]TATATCTGTGGCATT | 9678 |
| rs183339438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110077 | TTGGACTTTTGTATC[A/G]TAATATGAAATTTCT | 9678 |
| rs183358778 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965629 | AGGATGTTTAAGTCT[C/G]TAGAAGTTGTCTGCT | 9678 |
| rs183416641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962998 | TCTTGCTAGCAGTCT[A/G]TCTATTTTGTTGATC | 9678 |
| rs183422466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10975541 | AGGTCGTATATTCAC[A/G]TTGTACTAAACTGGA | 9678 |
| rs183423343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10978931 | TCTTCAAGACATATA[C/T]GGTTTTGGTCAAACA | 9678 |
| rs183430931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995079 | AAGTTCTCCAAGTCC[A/G]CACAGAGCACTGATT | 9678 |
| rs183435387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041291 | TTACTTTCTTTGCTC[A/C]ATATTTTCGGTGTTC | 9678 |
| rs183453916 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125742 | TCTTTTTTTCCTCTG[G/T]ACTATATTCATATGA | 9678 |
| rs183462347 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099016 | TTCATTTCAAAAATG[C/G]TTTTCTATTAGTAAA | 9678 |
| rs183462615 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11077938 | GCTTCTCTCTTCAGC[A/G]TGCATGAAACTGAGG | 9678 |
| rs183473156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060856 | GACTCTTGGTTATCT[A/G]GGAACAGATTAAATG | 9678 |
| rs183473713 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156198 | CAGTAAATCCAAGAT[A/G]TGGAAATAATGAAAA | 9678 |
| rs183489307 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143921 | GCAAAGGAAACAATC[A/T]ACAGAGTAAAGAGAC | 9678 |
| rs183494259 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11161587 | TGCCTATCTTGAACA[A/T]TTTTAGATATTATTT | 9678 |
| rs183495644 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116240 | CCGAAGGTCTTCCAG[A/G]CTCAGCTTATCTACT | 9678 |
| rs183535676 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140877 | TGGGAAGCGTCTTTG[A/G]TATATGGTCAGTTTC | 9678 |
| rs183541002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113661 | TTTAAGCTGAAACTT[C/G]CGGAGACTTAATTGA | 9678 |
| rs183600932 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11018769 | GGAAGCTAGGGCTTC[C/T]AGTACTATGTTGAAT | 9678 |
| rs183607917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10983944 | TTTGTGTCTCTTTGT[C/G]TGTGTGTTTTTGTAT | 9678 |
| rs183707953 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964389 | TCTTTTCTTTAAGAA[A/T]GTTGACTATTGGCCC | 9678 |
| rs183719784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975718 | AAATTATGTGTAATT[C/T]CACCTCTTTTGAAAA | 9678 |
| rs183734302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047442 | CTGAAATTCCATTGG[A/G]TCATCATTCTGATTA | 9678 |
| rs183738327 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071585 | TTAATGATTTTTAGT[A/G]CATTTGTCATTGTTC | 9678 |
| rs183752359 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006429 | TTTGTTGGCAAGATT[C/G]AAAGCATTGTAATCA | 9678 |
| rs183757758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121367 | ATGCAAAAGAAAACC[G/T]TACACTTAAGTAAGG | 9678 |
| rs183762660 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11139914 | CATATAATAATGATA[C/T]TGACTTTGAGATTCT | 9678 |
| rs183763040 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103622 | AACATGTAATTTGGA[A/G]TTTTCTGATTAATAA | 9678 |
| rs183779350 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11134381 | AACTTTTTAAACAAA[A/G]GATTCATTTTATATT | 9678 |
| rs183787089 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11096341 | TTTTGAATGCTCATA[C/G]AGACCTGACAATTTC | 9678 |
| rs183799573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157674 | AATAATTTTCTAATG[A/G]TTCTTAAACTGCAAG | 9678 |
| rs183823835 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11160549 | TTTCTCTGCAGCCTT[C/G]CCAGCATCGTTGTTT | 9678 |
| rs183854955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014510 | TGGATGGAGAGAAGG[A/C]CCTCTGTGTTGAGAG | 9678 |
| rs183855107 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972957 | TCCCTTTGCAAACCC[C/T]CACTTTTTCTGCAGG | 9678 |
| rs183861405 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990547 | AGTATATATTTCTCA[A/G]ATATAATGTACTTTG | 9678 |
| rs183875453 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032265 | TGATAATGCATAATT[A/C/G]AGAAGATAAGTTTGA | 9678 |
| rs183881757 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960796 | TAACTGGCATGAGGT[G/T]GTATCTCCTTGTGGT | 9678 |
| rs183884363 | snp | C/T | 0.00159617 | 0.0282053 | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10958947 | GATTGCCAGGTTAAC[C/T]CTGCAAGGTAAGAAG | 9678 |
| rs183889947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074054 | CTGTGATGGGCTGCA[C/T]TGCCTGGAAGATCTC | 9678 |
| rs183892751 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055371 | CTTTTCATCTTTTGT[A/G]GAAGTGCCAAAGGAC | 9678 |
| rs183900301 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11038385 | GCAGTGACACAAGAT[A/C/T]GTGCTACTGCACTCT | 9678 |
| rs183919806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086935 | TCACTGAAATCTCTG[C/T]GTTATCTTTAATCTA | 9678 |
| rs183933951 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063581 | CCTGTATGAGTATCT[A/G]CTGTGTCTTACTAAT | 9678 |
| rs183939111 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11090018 | TCAGGTGATTCGCCC[G/T]CCTTAGCCTCCCAAA | 9678 |
| rs183942385 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10993233 | ATTATTATTATTATT[A/T]TTTTTTAATCAGGGC | 9678 |
| rs183944469 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11027312 | TTAGAGAAATTATAT[A/T]AACTAGGCAGTAGGA | 9678 |
| rs183946209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11160331 | TAGGTTGATTACATG[C/T]CTTCGCTATTATGAA | 9678 |
| rs183956553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123131 | CTTTTTTTCTCGCTG[C/T]AGTTGATAGCATCTA | 9678 |
| rs183992671 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11010579 | TAATTTGTAACTATT[A/C]ATATTAACTATATTT | 9678 |
| rs184015449 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11047743 | ATGAGCTGAGATTGC[A/G]CCAGTGCTCTCCAAT | 9678 |
| rs184019470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028631 | TGAGAATGCAGTCTT[C/T]AGTCTGGAAATAAGT | 9678 |
| rs184045938 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11082851 | TTCAAATAGCCTATT[A/C]ATCCTTTATTCTTTA | 9678 |
| rs184050999 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065304 | ATTTCATGGAATTGG[A/G]AAGTCTTAAAGGCTT | 9678 |
| rs184072342 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103000 | CAAACAAGAAAGACA[A/G]TGCATTCCATTAGTC | 9678 |
| rs184075444 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149403 | CTGGGGAAGTTCATT[A/T]TGTATTCTGGGAATG | 9678 |
| rs184076075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120616 | AAACCATGGCATTCA[C/T]GGCTCCCTAAATTTT | 9678 |
| rs184077164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956628 | TGAGTTCATACTGGA[C/T]TGGGGTGGGCCCTGA | 9678 |
| rs184083665 | snp | A/T | 0.0189856 | 0.0955633 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105532 | CATCATTAAATTTTT[A/T]AAAAAATTTAAAAAT | 9678 |
| rs184084188 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11021221 | TTTATGTGATGCTTA[C/T]TTCCTGTTCCTTTCC | 9678 |
| rs184097339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987885 | GCTGGGCGTGGTGGT[A/G]CATACCTGTAATCCC | 9678 |
| rs184097755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066735 | AGTTGGCTTTTTCAA[C/T]GTGGGCTTATTTCTA | 9678 |
| rs184104911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11142463 | CAGCTATAATTCATC[A/G]CTTGAAAAGAAATGC | 9678 |
| rs184130265 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106998 | AGTCTATGTTATGGA[A/T]TTTGCTTCTTTCTAA | 9678 |
| rs184131912 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136969 | TCAAGAAATAACCAC[A/T]ACTAACATTTCGTTA | 9678 |
| rs184202363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001171 | GTGCTCCCTTATATT[A/G]CCTTTGCTCCTTTGT | 9678 |
| rs184239290 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969892 | GTCTTTTGTATACAT[A/G]TTTGTTTCTTTTTCT | 9678 |
| rs184255051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976014 | CTTAATTTTCACAGT[A/G]ACTTAGTGAAGGAGA | 9678 |
| rs184265193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993485 | TTTAGTAATGTTTGT[C/T]GAGTACCTTCTATGT | 9678 |
| rs184282531 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11153649 | CAGCATTAAACAGAG[A/G]GAAAAACTCATAGAA | 9678 |
| rs184299612 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11032618 | AAAAAAGAAAACCTT[A/G]AATTTAAATGACTTT | 9678 |
| rs184300661 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11028233 | TAACTATCTCATGTA[A/G]TTTATTGAATACCCT | 9678 |
| rs184311430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007323 | TTTCCATCCTTGCAA[A/G]TGTTTTTTATGTTTT | 9678 |
| rs184318354 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966235 | TCTTGGAAGTGCCCC[C/T]CAAGGAGCTTTATTG | 9678 |
| rs184324077 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10984541 | ATGCATGCAGTTTAC[A/G]TTATAGCAGTTAATA | 9678 |
| rs184331541 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10995494 | AGCTGGCTTCACCCA[G/T]TGGATCCCGCACCAG | 9678 |
| rs184338175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068257 | TTGGGAGGCTGAGGC[A/T]GGAGAATGGCATGAA | 9678 |
| rs184357515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111256 | ACAGTGTTGAAGTTG[A/G]AATATACAATAGTTT | 9678 |
| rs184362034 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11092764 | TTACTCGCTGAACCT[G/T]ATCATTGACTCTTAG | 9678 |
| rs184364579 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11074378 | ACCACGCCCAGCTAA[C/T]TTTTTGTATTTTTAG | 9678 |
| rs184370370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148872 | AATTTTTGGAAATAT[A/G]TTTTAAACTTTATAA | 9678 |
| rs184375459 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11166700 | AATGCCTTTTTCACC[C/G]CTTCATAATGCTTTT | 9678 |
| rs184379854 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11132491 | TCTTTACCCATTTGT[A/C]TGTTAATGGGCGGTT | 9678 |
| rs184393960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980796 | GGGGGTATTAGTGTA[A/G]TATATGGTGCATGTT | 9678 |
| rs184413851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957927 | TATGGGGTTTCTTTT[C/G]AGGTTGATGTAAGTG | 9678 |
| rs184438981 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11023625 | TGAGATTAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9678 |
| rs184445000 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11050292 | AAGATACTGATATAA[A/G]CATATAAACTAAATA | 9678 |
| rs184447084 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11004079 | GTGGTGAAACCCTGT[C/G]TCTACAAAATACAGA | 9678 |
| rs184464052 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11015308 | GATTGCTGGGATAGC[A/G]TAGAATCTACCATTG | 9678 |
| rs184467525 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11050896 | ATAGTTTCTTTAAGT[A/G]GTATATTCAGCACAA | 9678 |
| rs184480636 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11084053 | GGATATGAGAAGATA[C/T]GTTAAAGACACTATT | 9678 |
| rs184480652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110755 | TTTTAACATGTAAAG[A/G]TTATTTTTATTTGTT | 9678 |
| rs184487171 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011313 | ATTTCTTTGATGGTT[G/T]TGAGAGGTCACGCTC | 9678 |
| rs184495739 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11048529 | TGAGCCTTAGATCAT[A/G]CCACTGCACTCCAGC | 9678 |
| rs184512802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11056140 | TAGAACTCACTTTGG[C/T]TACTTGGAAGAGATC | 9678 |
| rs184519788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148236 | CAAAAGCAAATCATA[C/T]TATTTAAATTCTTAA | 9678 |
| rs184582478 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029326 | GACTGGTTAAGATTC[A/G]TTCAAGTATTCTGAG | 9678 |
| rs184611044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994581 | GGGTCTTGCAGATTC[C/T]GGTACTGATTTTAGA | 9678 |
| rs184612855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065716 | CCTATATGAAAAGGA[A/G]GTGGGCCTGTCTTTC | 9678 |
| rs184612886 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11131225 | GGGATCATATGGTAA[A/G]AGTGTGTTTGGCTGC | 9678 |
| rs184618278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092111 | TATAAATAATACTTA[A/T]CTCTGCTTAGTTGTA | 9678 |
| rs184635422 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165770 | TATAAATAAAGAAAA[A/G]CCGAGGGTCTCCTCT | 9678 |
| rs184640032 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10979978 | ACATTAAAAATTTTT[A/T]AAAAAATTGCTTTCT | 9678 |
| rs184659416 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PHF14 | GRCh38.p7 | 7:11156679 | AGGCGCCTGTAATCC[C/T]AGCTACTCGGGAAGC | 9678 |
| rs184673585 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133267 | TATTAAAGGAGAACA[A/G]AGTCAGAGGACTGAC | 9678 |
| rs184708934 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162987 | AATAGTTATTTATGT[A/G]TTCCCATACATGAAA | 9678 |
| rs184716689 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170247 | CTCTTTACTCTCCCC[A/G]GTTCTAATTTCCAAG | 9678 |
| rs184730446 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PHF14 | GRCh38.p7 | 7:10995221 | AAGGTTCTCCAAGTC[C/T]CCACCAGATTAGCTA | 9678 |
| rs184766740 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:10985539 | TATTTTAGCAGGGCC[C/T]TTTTATAATTACTGC | 9678 |
| rs184774065 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10999092 | GTGCCCCAGGCTTGC[C/T]TCAAACTCCTGGGCT | 9678 |
| rs184779265 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963765 | TGGGTGCTCCTGTAT[G/T]GTGTGCATATATATT | 9678 |
| rs184787850 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018998 | CAGTTGAAATGATCA[C/T]ATGGTTTTTATCCTT | 9678 |
| rs184795343 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961052 | ACTCTGATGATAGTT[A/T]CTTTTTCTGTGCAGA | 9678 |
| rs184809180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111732 | TATTAAATAGTGCTC[C/T]GAAAGCCCAAACAGA | 9678 |
| rs184811938 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966663 | GTGAGTCTGAGAAAC[A/G]TAGTTTTTATTCTAA | 9678 |
| rs184822356 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10993965 | AGTGAGCCAAGATTG[C/T]GCCAGTGCACTTTGG | 9678 |
| rs184915334 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10981484 | TAAGTAGTGTTGGGT[G/T]GAGAGGGACTGGGCT | 9678 |
| rs184918777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998877 | TCTACTTCTTAAGTC[A/C]TTCTTAGGTCTACTT | 9678 |
| rs184923470 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995710 | CGCAGGGAGGCAGCT[C/G]AGGCCCGGCGAGAAT | 9678 |
| rs184927015 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:10976502 | TATGGGAACAATTCT[A/G]AAACTTACATTAAGT | 9678 |
| rs184933498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016015 | GTGGTTACTTCATGC[C/T]ATCATAATAGACAAA | 9678 |
| rs184951734 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964605 | GTTCTCTGTATTTCC[C/T]GAATTTGAATGTTGG | 9678 |
| rs184961912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139841 | AAATTTTCCATAGGG[C/T]ATGACTTAGTGTACT | 9678 |
| rs184963232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068862 | GATCATGGTATATCT[C/G]TCCATTTATTCAGAT | 9678 |
| rs184967329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098244 | TGAAAGCTGAAAATA[C/T]CAGAATATTTTGGGA | 9678 |
| rs184970755 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11115518 | CTATTGATTTGCATC[A/G]TCAAAAATAGCTTTC | 9678 |
| rs184976505 | snp | A/G | 0.000662981 | 0.0181948 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051633 | CTCGGAATGTGACCA[A/G]GCAGGGAGCAGTGAC | 9678 |
| rs184985120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033862 | AGCATGTCATGAGAA[A/G]GCAGCTGTTTGTATG | 9678 |
| rs184985440 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11077190 | TCTTGTCTTAAAGAT[C/G]AACACATATTATTGC | 9678 |
| rs184987444 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11152339 | TGGATATGTGACCAA[C/G]GGCAGTTCCTGAGTG | 9678 |
| rs184997987 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170055 | TTTGACGGTCTCTGG[C/T]AGAAGTAATGCCATG | 9678 |
| rs185007416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135741 | ATAAACCTATTGCAA[A/G]TGAAGACAGCCTTCA | 9678 |
| rs185036818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964998 | TTTCTACCTTCTTTG[C/T]GATGGGTTAGAACAT | 9678 |
| rs185036819 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11004580 | TTGTGGTGTTCATGA[G/T]GTTGACATATTGAAG | 9678 |
| rs185041136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983296 | ATGAGCACCCTAACT[A/G]TAACATTTTTTCATT | 9678 |
| rs185050908 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996740 | ACCACACTACCTAAA[A/T]AAATCCTGGGGTACA | 9678 |
| rs185055797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045338 | CTGTTACTGGACTCT[A/T]ATTTCATGACTGTGC | 9678 |
| rs185065322 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11024286 | TGAGGTTTAAGGAAA[A/G]AAGCCATCTCCGTAA | 9678 |
| rs185073642 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10991211 | TTTGAGATGATGTCT[C/T]GCACTGTTGCCCAGG | 9678 |
| rs185096672 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11119558 | CAATTGTGAAAATAT[C/T]GCCTAAATAATAGAA | 9678 |
| rs185149070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967521 | AATCACAGAAGCTCT[C/T]TGTGTGTTGGAACAA | 9678 |
| rs185153481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100924 | CAGGCAATTCTAACT[A/G]TATAAGATACAGAAT | 9678 |
| rs185158415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039244 | TGCTGTATTTTTTTT[C/T]CTATTCTTTGGATGT | 9678 |
| rs185163284 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10999900 | TTGATGGCAGTCCAA[A/G]TTATAAATATTTTTG | 9678 |
| rs185163562 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11145669 | ACTATTTAAAGAACT[A/G]CTTTTCTGATCAAAT | 9678 |
| rs185169387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064882 | ATTAGGTACCTTATG[A/G]ATAATTGCTGAGTGA | 9678 |
| rs185175677 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11000761 | ATATTTTGGATATCA[A/G]TTCTTTATCAGATAG | 9678 |
| rs185176290 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PHF14 | GRCh38.p7 | 7:11163810 | GCTGTTGAGAGTTAC[A/T]TATCTAGCATATGTT | 9678 |
| rs185197447 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11041147 | TATCATATATGTATA[G/T]ATATAGAATGAATCT | 9678 |
| rs185208113 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11020323 | TTGAGCTCCTGGGCT[A/C]AAGCAGTCCTCCCAC | 9678 |
| rs185211922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987745 | TTAACTACTTTCTCT[A/G]AAACCTTGAAAGATG | 9678 |
| rs185220775 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093702 | CTTAATTTTCCTCAT[G/T]CAAACTCAGCCTTCA | 9678 |
| rs185236140 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075363 | TTTATTTGGCCCACG[A/G]ATCTGCCGGCTGTAC | 9678 |
| rs185237811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047614 | CAACATGATGAAACC[A/C]TGTCTCTACTAAAAA | 9678 |
| rs185244152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056489 | CTGTTAACATAAGCT[A/G]AATTAGATAAAAAGA | 9678 |
| rs185266676 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986147 | AATGCTTTTATTTTT[G/T]ATTTTTTTTTTTTTT | 9678 |
| rs185277034 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044555 | AGCAGTTAACTGGGT[A/G]TATTAATTTTGGAGT | 9678 |
| rs185278017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11082530 | AATTTTCCCTTGTTA[C/T]TCAATCATTTATGCT | 9678 |
| rs185284147 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019448 | GTACAGGCTTTGGAT[G/T]TCTTCATGGTTCAAT | 9678 |
| rs185309667 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077586 | GGCCTGGCAACAGAG[C/G]GAGACTCTGTCTTAA | 9678 |
| rs185319659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159706 | GGTACAAGGGATCTC[C/T]GTATTATTTCTTTCA | 9678 |
| rs185325421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122656 | CTTTAAAAATTGAAT[G/T]ATCTTTTTCTGGGAA | 9678 |
| rs185326278 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11153425 | TTAGGGTTGGGAATC[A/T]AGAATTTGGCTTTGT | 9678 |
| rs185334126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11116134 | TTTATTGTTATTTTC[A/G]AATTACTACAAATTC | 9678 |
| rs185434293 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11060178 | CATGGTGCCTGGCCT[A/G]TCAGTCAGATCTTTT | 9678 |
| rs185457801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136575 | TTAAAAAAGTGGAGG[A/T]TGAGCATGTCTTTTG | 9678 |
| rs185460717 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162305 | TTGCTGGCCAGGCTG[A/G]TCTCAAACTCCTGGC | 9678 |
| rs185473026 | snp | C/G | 0.000399281 | 0.0141238 | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10968369 | CTACACGAACATGGC[C/G]TCTGCCTCCCTTACA | 9678 |
| rs185485414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986831 | CATGAGAATTAATCC[A/G]TGACCGTAAATTATA | 9678 |
| rs185491552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11000465 | GTGCCTCAGCTTCCT[A/G]TGTAGCTGGGATTAC | 9678 |
| rs185581005 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058818 | ACTGAAGTGACAGTT[G/T]AGATAACTGAGTTTC | 9678 |
| rs185587782 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989908 | TGTATTTGGGATTAC[C/T]GGTGTGAGCCACTGT | 9678 |
| rs185598103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023333 | TGGAATTTGTCAAAA[C/T]TATGAAAAAGAATAT | 9678 |
| rs185602971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11144468 | TATGTACCTATACCC[C/T]ATGTTTATTGCAGAG | 9678 |
| rs185608690 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104572 | TTGTTTATCACACAG[C/T]AGGGAAAGGAAGAAA | 9678 |
| rs185615595 | snp | C/T | 0.0810805 | 0.184299 | intron-variant | PHF14 | GRCh38.p7 | 7:11122400 | ATACATACACACACA[C/T]ATATATATACACGTA | 9678 |
| rs185619785 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085509 | TGTTTCTATTGTAGA[C/T]GTCAGTGGTGAACAA | 9678 |
| rs185634252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11159051 | TTAAGTATTGAAATA[C/T]TTAAATCAGGCTATT | 9678 |
| rs185639972 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11126741 | GTAAAATACAGTTAG[C/T]TGTATTTTTTTAACC | 9678 |
| rs185650615 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141420 | AGTATAGAATCTGGT[A/G]CTCATTTTCTGATTA | 9678 |
| rs185651458 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11088744 | TTCCCACCGTAAATA[C/T]ATAACTCCCCAAATT | 9678 |
| rs185706678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11075765 | TCATTTAGATACCCT[A/G]TGAAATAAGTATTAA | 9678 |
| rs185718797 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972232 | TGAGCCACCGCACCC[A/G]GCAGTACAGTTTTTC | 9678 |
| rs185720106 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11133971 | TTTAAGGATATTAAT[C/T]ACTTAAGTAGAAAGC | 9678 |
| rs185722917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043980 | CCAGCATGTGAGAGT[G/T]TCTGCAGCTAAAAAA | 9678 |
| rs185731254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11003536 | GTTATGGGATACATA[C/T]AGATAGTAAAAAGGT | 9678 |
| rs185738263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11095124 | AACAAATTGTAGTGA[C/T]AGTAAGAGTGGTTGA | 9678 |
| rs185738420 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113263 | AACATTGAAAAGGCA[A/G/T]GGGGGCATATTTTAG | 9678 |
| rs185757124 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11151537 | GCCCTCCAGCCTGGG[C/T]GACAGCAAGACCCTA | 9678 |
| rs185766591 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107261 | TATGGATCATAGCAC[A/G]TATGAAGGTAAATCA | 9678 |
| rs185766803 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11035253 | AATGCATGTAAACTA[C/G]ATGCAAATACCACAC | 9678 |
| rs185767553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11168581 | AATACTTAAATTGAT[A/G]TTTATGCTTTAATTA | 9678 |
| rs185779766 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066522 | TGACAAAAACTTTCT[G/T]CTTTGTTTTCTTCTA | 9678 |
| rs185785703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049197 | GTAAATTAGAGCCTG[C/G]CGCGGTGGCTCACAC | 9678 |
| rs185788814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109105 | CTCAGTAGCAATTAT[C/T]ATTTTCATGTATTTT | 9678 |
| rs185793949 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11030919 | TTCAAAACCCAGAAT[A/G]TTGCATGAATCAATA | 9678 |
| rs185801257 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070707 | TTGTGTCATTATTGT[C/G]TGTCAATTAATTTAC | 9678 |
| rs185891665 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11052392 | TTCTTTTGCTTTGTT[C/G]ATGGGCAGTTAGGTT | 9678 |
| rs185905738 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11017768 | GCTTTTTAAAAAAAC[C/G]TGATATGATATCTTT | 9678 |
| rs185908837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049119 | ACCTGCTTCTATACC[C/T]AGGGGATTTAGATAA | 9678 |
| rs185918224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089525 | GTGAGACTCCATTCT[C/G]CACAAAAAGGAAAAA | 9678 |
| rs185919849 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11030118 | AGGAATTGTACTTTG[A/C]TGAAGGCTACTAGAT | 9678 |
| rs185938696 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973591 | AATCCTTAAAAAACA[A/G]ATCAGAAACAAAAAC | 9678 |
| rs185957354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127537 | GCATCTTTGCTTTGC[C/T]ACTACAGACAGACAG | 9678 |
| rs185961035 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11155136 | CAGGATTTGTGCTAG[A/G]CTCCTCATATTTTAT | 9678 |
| rs186051303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10994678 | CCTCGCGGTGAGTGT[G/T]AACAGTTTTTAAAGG | 9678 |
| rs186061557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011895 | AAGTAGTTCAGCATG[A/G]TTTTTTATAGTCTGA | 9678 |
| rs186083814 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956420 | ATTACTTGATTTTAA[A/T]ACTGTGCACGGACTT | 9678 |
| rs186084203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961570 | GCTGTTTTTGGTGCC[A/G]TATGAAATTTAAAGT | 9678 |
| rs186090645 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10976959 | TGTAAAAGGGAATTT[A/C]GAAGAAAATGATTGT | 9678 |
| rs186102996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167680 | CAGTGTCTCTCCTGA[A/G]GAAGACAGGGGAAAG | 9678 |
| rs186139946 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11151024 | CTGTTTACAATAAAA[G/T]ATATATCAATGATTT | 9678 |
| rs186140279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112826 | AGATATAATATTTGC[A/C]TATATTTTATTTAAT | 9678 |
| rs186146308 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086119 | TCAACTCTCTCCTGG[A/G/T]CCGTTGCAATAACCA | 9678 |
| rs186158910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090213 | AGTACATGAAAGTAA[G/T]TCTTTAAGTATATTC | 9678 |
| rs186169239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137672 | ACAATCTCGGCTCCC[A/T]GTACCCAGGTTCAAG | 9678 |
| rs186173263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099509 | AAGCACCTACAGCAG[G/T]GAAATAGTTCTCATT | 9678 |
| rs186175418 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11071927 | GCCTGCTAAATTTAT[A/G]TTAAGAGCCTAGATT | 9678 |
| rs186180226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116991 | TCATGCTTCAGTCTT[C/T]TCCAGGATATTCTTG | 9678 |
| rs186182351 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11053230 | TTATAATCACTTAAA[A/T]GATCTTATTCAGGAG | 9678 |
| rs186195039 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10991907 | CAGGCCTTATTTCCA[G/T]TTTTTTTTTTTTAAT | 9678 |
| rs186202806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154165 | TCATTGCTATGACTT[A/G]GACTATTATTTACTA | 9678 |
| rs186204091 | snp | A/C | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11004924 | TGGGAGGCTGAGGCA[A/C]AAGAATAGCTTGAAC | 9678 |
| rs186215752 | snp | A/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10969448 | TTTTCTTCATTTATC[A/T]TATTTTACTTTCCCT | 9678 |
| rs186218526 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11025719 | AGAATGGCGTGAACC[C/T]GGGAGGCAGAGCTTG | 9678 |
| rs186222732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051816 | CATAAGCATCATACA[A/G]TTCTGAGGCCAAAAT | 9678 |
| rs186233627 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960344 | GAACAGGTGGTGTTT[G/T]GTTTTCTGTCCTTGT | 9678 |
| rs186235400 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10975224 | AATATATTTATGCTT[A/G]TATTATAGAGGAAAA | 9678 |
| rs186241546 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108115 | TAATGGTATCTCTTA[C/T]ATTTGTCCACAGTTT | 9678 |
| rs186255898 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089010 | TAAAATCTTCAACAC[C/T]ATTTTAAGGACATTA | 9678 |
| rs186257455 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11046912 | GTTCTTGATGACTGA[A/G]AAAGATAAATTGTGG | 9678 |
| rs186261011 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11069328 | CCAGGGGCTTCTGGA[A/G]GGGAGATGGGGAAGG | 9678 |
| rs186264467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133796 | TATTACATCATAAAA[C/T]GATTCCTCCTGGATG | 9678 |
| rs186273300 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104708 | TTTGTAAAAACACAG[A/G]TGACTACCCTATTCC | 9678 |
| rs186281791 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127420 | GGCTAGATTCCTTTC[C/T]AGAGTCTTGCTCTTT | 9678 |
| rs186319385 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961375 | TCAGGTTTGTCAAAG[A/T]TCAGATGGTTGTAGA | 9678 |
| rs186349742 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11036263 | CTCAAAAATTATACA[A/G]TATACCTTAAGGATC | 9678 |
| rs186371891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962162 | TCCTTGTGTTGTGCA[A/G]CTTTTCAAAGGGAAT | 9678 |
| rs186373782 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964869 | AATTGGTTATTGAAG[A/C]TTGTGTATGCTTCAC | 9678 |
| rs186398112 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11056257 | TTTTATTTATTCCCA[A/G]GAGTATGAAATAAAG | 9678 |
| rs186409280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019868 | TAGGTACCTATAGCT[A/G]TAAACCTCCCTCTTA | 9678 |
| rs186458791 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093241 | GTTTGTTCTGCTGAT[G/T]GCTTTGTTTCTTGAC | 9678 |
| rs186463000 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:10994769 | GTGGGTTCGTGGTCT[C/T]GCTGGCTCAGGAGTG | 9678 |
| rs186468137 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002726 | TGGGATTACAGACGT[A/G]AGCCACCGCGCCCGG | 9678 |
| rs186537753 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041363 | AAATAAATAGGTTAC[A/G]ATCTCACTTTTTCCC | 9678 |
| rs186545146 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066190 | AAATTTGTTTGTGTC[A/G]TAAATTATTAGGAAA | 9678 |
| rs186574248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11001240 | GGGCTCAGTTTGTTC[A/G]TCAACTGACCTATAT | 9678 |
| rs186585391 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103986 | TGTTGGTAATTATTA[C/T]TGTTGCTGAACTCTG | 9678 |
| rs186599750 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:10985150 | TAGTTATATTTCTAG[A/T]TTTCTTATTTGTATG | 9678 |
| rs186600339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140340 | TTCAGCTTTAAAACA[A/G]ATGTTCACAGCTCAG | 9678 |
| rs186609756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999032 | TTTGCAAAGTTCTGG[C/T]GGCACTAGGGTTTTT | 9678 |
| rs186619014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040420 | TGTCTTTGAAAGCTG[A/G]AATAGAAGTTTAATT | 9678 |
| rs186625741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063090 | TCTTAATTTCTCAAA[A/G]AAAGGCATGAAGTCT | 9678 |
| rs186629622 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018937 | CGTTTTTGGGGAGTT[A/G/T]TTATGATGAAGGGAT | 9678 |
| rs186635588 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11047215 | CTGGGACTACAGGCG[C/T]GTGCCACCACGCCCA | 9678 |
| rs186635777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966342 | TGTCTGAGTCTGGCT[A/G]AGTCTGAGGTTTTTA | 9678 |
| rs186641798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11026052 | AGTAGGTGTAGGTTA[C/T]AGTGAGCCGAGATTG | 9678 |
| rs186646107 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10977240 | AAATTGGAAGTAGAG[A/C]AATGGTAGCTAAACA | 9678 |
| rs186654269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074736 | TTACTCCAGTTCCCA[A/G]TAAGTTCTTCATTTC | 9678 |
| rs186654975 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11100071 | GTTGAAAAGCCAACT[A/T]TATTGTTTTTGATTT | 9678 |
| rs186658374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118730 | ATTAGTCATTCTTAA[C/T]AGTATTAATAGAATT | 9678 |
| rs186658855 | snp | G/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11012406 | CTTGGGTTATGAAAA[G/T]TTGATGCTTTGTTTA | 9678 |
| rs186667341 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11081065 | TATATATGTATATAT[A/G]TGTGTGTGTATTTAT | 9678 |
| rs186680250 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11138107 | GTGCAGTGGCACGAT[C/G]TTGGCTCACTGCAGG | 9678 |
| rs186744714 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962624 | ATTCCCTCTTTTTCT[A/G]TTGATTGGAATAGTT | 9678 |
| rs186746208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978388 | ATGAGATTAGATTGA[C/T]GTAGAACAATTTCAT | 9678 |
| rs186776129 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021695 | AGCTGCTTGTTGAAG[A/T]TGTGTATCTTTATAT | 9678 |
| rs186778984 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11154730 | AGTTAAAAATGCTAA[A/T]CAGATGCCCGTGGGG | 9678 |
| rs186804318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11114320 | TGGACCAGGGGAAAC[C/T]CTAAAATATTGCTAT | 9678 |
| rs186807689 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11097820 | CAAATCTTGTTTGTC[C/G/T]CTTCCTCTATTCTAT | 9678 |
| rs186812134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121673 | CTGCAGTACTGTGAT[A/G]GTCGATCTAGTCACT | 9678 |
| rs186812955 | snp | C/T | 0.030665 | 0.119967 | intron-variant | PHF14 | GRCh38.p7 | 7:11076571 | TTTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTG | 9678 |
| rs186815431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057478 | CTCCCAGGATCGAGC[A/G]ATTCTCATGCCTCAG | 9678 |
| rs186820467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085155 | AGGAAATGCAAATTA[C/T]CTGTCTTTGCCCTTT | 9678 |
| rs186846819 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11158787 | CATGTATGTCATAGT[C/T]GCTTACAGATTAGCC | 9678 |
| rs186871691 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11016891 | CCCCACCATTTCACC[C/G]TTTCCCTGCACTATC | 9678 |
| rs186912466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981662 | ATATAGTAGTTACTG[C/T]GTAGAAGTTTTGAAA | 9678 |
| rs186933666 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11080308 | TATTACACGTGCATA[C/G]TTGTTAACATCTCAC | 9678 |
| rs186940583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10987964 | GAGGTTGCGGTGAGC[C/T]GAGATCCCACCATTG | 9678 |
| rs186941135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087269 | CGATCTTGGCTCACT[A/G]CAACCTCTGCCTCCT | 9678 |
| rs186954155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068007 | TTGTAGGTGACAGGT[A/G]TCCAAACCATAGCAT | 9678 |
| rs186954904 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117608 | TTATATGTATAAATA[C/T]AAATATGTATTTGTA | 9678 |
| rs186956276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11050349 | CATTTTTATTAAGAG[A/G]ATACTATCAAACTTT | 9678 |
| rs186965350 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11125306 | CCACACTCAATCCCT[G/T]TGCAAAGATAGTTTA | 9678 |
| rs186969808 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058323 | TCAAGTACACTACTT[G/T]CAAGATAACTTGTCT | 9678 |
| rs186972204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11043322 | GCATATCGAATCACT[A/G]CATTTGATAAAGGTT | 9678 |
| rs186973105 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143414 | GCATGAGCCACCATG[C/T]CCAGCCAATTTTTTT | 9678 |
| rs186974424 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106650 | TATTCAATGAAAGAA[C/T]TCATCGCTACCTGTT | 9678 |
| rs186974875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002508 | CAATGGAGCAATCTC[C/G]ACTCACTGCAACCTC | 9678 |
| rs186981599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022039 | TTTAAATTTCAAAGT[C/T]AGTGATGCCACATTT | 9678 |
| rs186985134 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11137921 | CTTGTATTAAATAAA[A/G]AGGTAACCTTTATAC | 9678 |
| rs187012209 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160705 | ATATGTTTGTTGGCT[A/G]TTTGTATGTCTTCTG | 9678 |
| rs187060182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976806 | AACACACTAAAAATA[C/T]TTACTTTCTGTTCCC | 9678 |
| rs187101153 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11165113 | TATTTTTAGTAGAGA[C/G]GGGGTTTCACCATGT | 9678 |
| rs187114641 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10995815 | AGCCCCTCACTGCCC[A/G]GGGCTGGCAGTGCCC | 9678 |
| rs187116515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034146 | TTTTTAATATTAAGG[A/G]CACATTAGATTTTTT | 9678 |
| rs187133018 | snp | A/G | | | intron-variant, missense | PHF14 | GRCh38.p7 | 7:11062682 | TCAGACATAATGCTA[A/G]TCAGAAATCTTAGCT | 9678 |
| rs187141111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128068 | CATTGTAACTGCCCA[A/G]CTTCTCAAGATTCAC | 9678 |
| rs187156554 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164713 | TCCAGCTTCCTGTAG[G/T]GTTGCCATTTTATGT | 9678 |
| rs187167915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099652 | ATCATTTGGAAAGAC[C/T]GAGACTCTTACCACA | 9678 |
| rs187189620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959573 | ATGTGAGTGAGTGAG[C/T]GTGGGGTCTGGCCAC | 9678 |
| rs187206516 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11013655 | GTTTCATATCTTTTT[C/T]CTCATCTCTTTGCTA | 9678 |
| rs187224419 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11050010 | AGTTTTGCTAACCTA[A/T]TCTTAAATAATTGGA | 9678 |
| rs187224593 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963467 | GATTTCTATTCTTTT[A/C]CATTTGCTGAGGAGT | 9678 |
| rs187226690 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988582 | GTATTCCAAGGAAAG[C/T]CTTTTTTGGACTTAC | 9678 |
| rs187230040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032014 | AATCCCAGTACTTTG[A/G]GAGGCCAAGCCAAGG | 9678 |
| rs187232320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001726 | TAAGTTTGTATGCTG[C/T]AGTCTTGCTATAATT | 9678 |
| rs187236955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11024744 | ATTCCTTTCAAAAGA[C/T]TACTGCTTATCGACA | 9678 |
| rs187238650 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10979046 | TACCAGATCAATGAA[C/T]AGAATTAGATTGATG | 9678 |
| rs187246275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995158 | TACAAACCTTGAGCT[A/G]GACACAGAGTGCTGA | 9678 |
| rs187248563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956965 | TAGATTTCGGTATCA[C/G]AAGTGATTTGCTGCT | 9678 |
| rs187258867 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066783 | CATTGAGTTATGTAT[G/T]TATTCCTGTGCCAAG | 9678 |
| rs187259271 | snp | A/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 7:10970953 | TATTTAATAAAATTC[A/G]AAGCTCTTTCATGAT | 9678 |
| rs187296345 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10991363 | TTGTATTTTTAGTAG[A/G]GATGGAGTTTCACCA | 9678 |
| rs187296979 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11147362 | TTATGATTCGAAGAT[G/T]GCTGCTACAACTCCA | 9678 |
| rs187307660 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062235 | AAACAGATTTCATCC[A/G]CTTCTTAACCTCTCA | 9678 |
| rs187331830 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11109538 | AGAAATCTCAGCCTT[C/T]TCATAAACTCAGAAA | 9678 |
| rs187364756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129672 | AGTCTCATTTTTATT[A/G]GATAAAAATCTGTAT | 9678 |
| rs187371243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147687 | TCTCAGTCTTCTTAA[C/T]TGAATTCTCCATTTG | 9678 |
| rs187396992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065071 | TATATAATTTTGTCT[A/G]GAATCTAGGAGACAA | 9678 |
| rs187397939 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109887 | AGTCTTGAATCTACA[A/G]GGTTTTTGGAAAAGT | 9678 |
| rs187408489 | snp | C/G/T | 0.00438332 | 0.0466095 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974243 | CTTGTCTTCGCGGCC[C/G/T]CAGTCCCCGACCTCG | 9678 |
| rs187411469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098246 | AAAGCTGAAAATATC[A/T]GAATATTTTGGGAAC | 9678 |
| rs187414966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11115716 | ATGGCAAAAGGATTC[A/G]GTATAGAATCACAGG | 9678 |
| rs187419685 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11164940 | TGACATTCTTTTTTT[C/T]TTGAGACGGAGTCTC | 9678 |
| rs187453886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975602 | TTCTGTTCAGTGTAC[C/T]TTATGTATATATACA | 9678 |
| rs187467684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006043 | ATGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 9678 |
| rs187476005 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | PHF14 | GRCh38.p7 | 7:11073240 | AAGTTCCTTCCATCT[A/G]TGAGCCTGTAAAATC | 9678 |
| rs187498056 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008101 | ATATGTTAGTACTTG[A/T]CAGAAGTTAGGTAGT | 9678 |
| rs187499179 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11038225 | GAGACCATCCTAGGA[C/G]TTTGAGACCAGCCTG | 9678 |
| rs187501294 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079276 | TGTGAGATGGCTCGG[C/T]AGCTGGCTTTTGCCA | 9678 |
| rs187515450 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11110287 | CTTAATTGCAGATTT[C/G]TTGACATTTGAAGTT | 9678 |
| rs187524377 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11090728 | TCATATTAAAGATAC[G/T]GAAAGGCATTCACTT | 9678 |
| rs187524517 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11047664 | TGGTGATGGGGATTC[A/G]TAATCCCTGCTACTC | 9678 |
| rs187525903 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11072585 | AATACCGTACAAGTA[A/G]AGGGCTTGGCACAGT | 9678 |
| rs187528992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11028305 | TGTGGATTCTGCTGA[A/G]CGTGTATTGTTTTTG | 9678 |
| rs187562355 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11004887 | CTAAAAATACAAAAA[C/T]TAGCCTGTAATCCCA | 9678 |
| rs187575753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046575 | CATTAACCGCTAGTA[A/G]GAATTCCAGCATTAG | 9678 |
| rs187636040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11152204 | TTGTTTTGGAAAAGT[A/G]TGTGAAGCTTTTAAA | 9678 |
| rs187692868 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958438 | AGTTGCCAGCCATCC[A/G]GAGTTGTAGTTGAGA | 9678 |
| rs187715330 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:10992400 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 9678 |
| rs187730189 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11049424 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGG | 9678 |
| rs187740956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055176 | ATGTGGAAACTTTTA[C/G]TTACTTTTAGGCAAG | 9678 |
| rs187757607 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11130928 | TATGTAGCCTGTTCA[A/G]TTTGGCTTCTTTCCG | 9678 |
| rs187760860 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11013164 | TTTTTTATATTTTAT[A/C]TTTTTATTTTTTATG | 9678 |
| rs187766099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989266 | TCAAGTGTATTCAAG[C/T]GTCAGTTACAAATTG | 9678 |
| rs187766405 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11091247 | GCAGATAATTAATGA[A/C]AAATGGAAAGGCAAG | 9678 |
| rs187807078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997443 | CTTATTTTAGATGCT[A/G]TATTGATTATCTGCT | 9678 |
| rs187831363 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960480 | ACATTTTCTTTATCC[A/C]GTCTATTATTGATGG | 9678 |
| rs187840439 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965466 | GAGGGGCACCCACCT[C/G]TATGAGGTGTCTATC | 9678 |
| rs187844974 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11018362 | CATTTTAACAATATT[C/G]ATTCTTCCAGTTTGT | 9678 |
| rs187848626 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10983455 | TTCCATTCTCCTTTT[C/T]ATCCCTTTACTCCTT | 9678 |
| rs187850911 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960864 | CATTTTTTCATGTGT[C/T]TGTTGGCTGCATAAA | 9678 |
| rs187852652 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11155688 | TTGCAATGATACAGT[C/T]ACTTGAGTGATCAAT | 9678 |
| rs187864483 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11119479 | CCAGTTTTTATTTGT[C/T]GTGTGAGTGTGAGAG | 9678 |
| rs187868835 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138788 | TTCCTTGTTTTTACA[A/G]TTTGAAGACTTCTGT | 9678 |
| rs187887740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11032434 | TACAAGACCGAAGTT[A/G]TGTCTTCTTTCAGTT | 9678 |
| rs187889830 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11057648 | CAAAGTACTAAGATC[A/T]CAGGCCTGAGCCACT | 9678 |
| rs187899714 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169880 | GATTATCAATATAAA[C/G]AAAAACCAACATAGT | 9678 |
| rs187903886 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135650 | GAAGCAACAATTTCC[G/T]GCACTGGCAATGTTA | 9678 |
| rs187907769 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10995333 | ACAGAGTGCTGATTG[G/T]TGCATTTACAAGCCT | 9678 |
| rs187913160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11135441 | TCTGAAGCAGTGGAA[A/G]TAGCACATCTATTGT | 9678 |
| rs187930669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096897 | CTTCAAATGATTTCA[G/T]CCAATTCAGTACATT | 9678 |
| rs187934839 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11169262 | ACAGCACCTATTGCA[A/G]ATATTTAAATGTTAC | 9678 |
| rs187982471 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10995009 | ACAGAGAGCTGATTG[G/T]TCTGTTTTGACAGGG | 9678 |
| rs187988527 | snp | C/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10971718 | TAGTTTCTTAGTTTT[C/G]ATAAATGTATTATGG | 9678 |
| rs187999030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152382 | AATTTCCTCATTGGA[A/G]CATAGGAACAATAAT | 9678 |
| rs188015157 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135912 | AATTTTCAGCTGGCT[G/T]ACCAAGGTAAAGGAT | 9678 |
| rs188029172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083343 | CTTATTCCTCACTTA[C/T]ATTGTGCTTTACCTT | 9678 |
| rs188029806 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170125 | TGCAAGGTCCCACAC[A/G]CTATTCCTGGACATT | 9678 |
| rs188030419 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11030998 | AGATGGTTGTACTTA[C/T]GTACATAAGGATTTA | 9678 |
| rs188035260 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11040623 | GAGGAAAATGTTGCT[C/T]TTATTTCTTTCTTAA | 9678 |
| rs188036944 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963825 | ATCCCTTTACCGTTA[C/T]GTAATGGCCTTCTTT | 9678 |
| rs188042452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986836 | GAATTAATCCATGAC[C/T]GTAAATTATATCAAT | 9678 |
| rs188046381 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11020009 | ATGAAATATGGCTTT[G/T]AACTAAATTCCTTAA | 9678 |
| rs188046806 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065538 | GTCACAAAATATAAT[A/G]TTTGATGAAGGTATT | 9678 |
| rs188051384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047822 | AGGGAGGGCAGGAGG[A/G]AGGGAAAGAAGGAAG | 9678 |
| rs188053118 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000563 | AGGCTGGTCTCAAAC[G/T]CCAGACCTCAAGTGA | 9678 |
| rs188059720 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066634 | GAAGGTTTGTTTATT[A/G]TCTGCCCCATGTGGA | 9678 |
| rs188096931 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11147946 | GTTTCTTGATTCTTC[G/T]CTATTCCCATCACAA | 9678 |
| rs188157996 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11045866 | GTTGGTAACAACTTA[C/T]TGTGGAAAAATCAAA | 9678 |
| rs188165272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11024448 | CTATTGGAAGAAGAT[A/G]CCATCTAGGACTTAC | 9678 |
| rs188169592 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PHF14 | GRCh38.p7 | 7:11076063 | AGAATGGTGTGAACC[C/T]GGGAGGTGGAGCTTG | 9678 |
| rs188183899 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11041871 | TTTAAGTGTGTGTGT[G/T]TGTGTGTGACTTTTT | 9678 |
| rs188190587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078061 | GTATTTTAGTTCACA[C/T]TGTGGTATTTGAATA | 9678 |
| rs188192414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113690 | GATTCCCTTGAATAT[C/T]TGTGCTGCATCAGTG | 9678 |
| rs188194780 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061402 | AATGTGTGTAGTATG[A/T]TCCCAGGTTTAGCAT | 9678 |
| rs188200404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014653 | AGCCCCTCCGTTCTA[C/T]GAGACCTCCTGCCAT | 9678 |
| rs188207058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137058 | TATGGGGGCAAAAAT[A/G]CAAAATTAAAGTGGT | 9678 |
| rs188222365 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11099178 | ATTTTTTCTATAATT[A/G]AGTTGATTTGCTGAT | 9678 |
| rs188226408 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11116284 | TTCCTGGAATCAGCT[A/G]TTTCTCCAAGGAGCC | 9678 |
| rs188228344 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11161632 | ACATTTTTAAATATT[A/G]TTTTTGCCTAAATAT | 9678 |
| rs188235169 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11152102 | TGGATTTGAAAATTG[C/G]TTTTGATCAGTACTG | 9678 |
| rs188242997 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153931 | AAGCCTATGAAAGTG[G/T]TCCCTGTCTGTGTGT | 9678 |
| rs188255639 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11142799 | TGTGTTACTAGATTA[C/T]AGTTTTCTACTGTAA | 9678 |
| rs188265696 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11077193 | TGTCTTAAAGATCAA[C/T]ACATATTATTGCTCT | 9678 |
| rs188269845 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105950 | AAATACAAAGTTACA[C/T]GGAGCTTGAGCTCAG | 9678 |
| rs188346456 | snp | A/C/T | | | | | GRCh38.p7 | 7:10970568 | ACAAAGCAATACTCC[A/C/T]TCCCCCTACAGCTCC | 9678 |
| rs188383850 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11082532 | TTTTCCCTTGTTATT[C/G]AATCATTTATGCTTT | 9678 |
| rs188410661 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156234 | ACGTTATTTTTGACA[C/T]TGATAATAAAGTGCC | 9678 |
| rs188424152 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11119821 | AAAATTCGAAAAATG[A/G]ACTCTGGTAGTTAAT | 9678 |
| rs188436960 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10995533 | GTGGAGCTGCCCGCC[A/C]GTCCCATGCCGTGTG | 9678 |
| rs188450343 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11004193 | TCAAGGCTGCAGTGA[A/G]CCAAGATTGCACCAC | 9678 |
| rs188472424 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964395 | CTTTAAGAATGTTGA[A/C]TATTGGCCCCCACTA | 9678 |
| rs188475858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044571 | TATTAATTTTGGAGT[A/G]TGCAAGATTCAGAGA | 9678 |
| rs188477698 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958976 | AGGAATTCCTTTGGA[C/T]GATGTAGGAGTCTTT | 9678 |
| rs188478373 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10980868 | ACACATCTGGTTCTT[A/T]AAGTTTCAGATAGGG | 9678 |
| rs188483888 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973228 | GGCTGCTTTCTGCAA[C/T]CAATCAGACTGATTG | 9678 |
| rs188486099 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11023957 | AAGCTTAGTGAGGAA[A/G]GCATGTCGAAAGCCT | 9678 |
| rs188488010 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990743 | AAAACTGGAGCTCTC[A/C]AAAAATGGACCATAT | 9678 |
| rs188488669 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11163515 | AGAAGTATAGAAAAA[G/T]AAAAGGCCAAAGGTT | 9678 |
| rs188492921 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11127508 | GAAAGAACAGCCATT[C/T]CCACTGCAGCCATGC | 9678 |
| rs188495764 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10984373 | AAAAAATATTGCCTG[C/G]CTTCAATGTCATTCT | 9678 |
| rs188502688 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145151 | TAAAAAAAAACCCTC[A/G]GGAGGGGTTCAGGTG | 9678 |
| rs188517806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059809 | TAAATATACATTATG[C/T]AAATTAGATAATAGA | 9678 |
| rs188521839 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11086936 | CACTGAAATCTCTGC[A/G]TTATCTTTAATCTAA | 9678 |
| rs188536340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018799 | TAACAGTGGTGACAG[C/T]GGGCCTGCTTGTCGT | 9678 |
| rs188560628 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123421 | ATCTTCAAATTAAAT[A/T]TTCTGAAGATATGAT | 9678 |
| rs188574751 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11053660 | TAGTATTATCATCCT[C/T]AACTTTGGAGTTATC | 9678 |
| rs188610918 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956734 | AGACAGAGGCCGAGA[A/C]TGGAGTTATGCTACC | 9678 |
| rs188650873 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11139854 | GGTATGACTTAGTGT[A/G]CTATTCCTAATAATA | 9678 |
| rs188663178 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108504 | ACAAGCAAATTCTTT[C/T]TCCTTTGGAATGCAT | 9678 |
| rs188664944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120861 | TGAATAATAGGAAAA[A/G]ATCTAACTCATACGG | 9678 |
| rs188667637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089066 | GAGCCTCATTTTGAG[C/T]ACAGACAGACACAAA | 9678 |
| rs188668438 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11101770 | ACTTTTTCTGCGATG[C/T]GTGACTACTTGGCAT | 9678 |
| rs188670252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070365 | TTACAGGCATGAGCC[C/G]CTGTACCCAGCTAAG | 9678 |
| rs188684447 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139657 | AAAGTACTGGAGGTT[A/T]AAAAGGGAAGTCAAG | 9678 |
| rs188685977 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11157467 | ATTCAGTGTGTCCTA[C/G]ATCAAATGATGCTTC | 9678 |
| rs188691689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028124 | TACTGAGCACAGCTT[A/G]GTGTTGCCTACCTTT | 9678 |
| rs188701815 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PHF14 | GRCh38.p7 | 7:11100566 | CAGAAAAATACTACC[A/G]TAGTGTATGATAAAA | 9678 |
| rs188722164 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063621 | TTAATATGAGATTGA[C/T]TGAGGCCTTTTTGCT | 9678 |
| rs188754910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165795 | TCCTCTATCACAAAT[G/T]GATAGTGCAAGCTGA | 9678 |
| rs188764733 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11131967 | TTGTTGGGTTTTTTT[A/T]AAAATTTTTTATTGT | 9678 |
| rs188767278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965941 | GCCTGCTGTGAAGAC[C/T]GTGGGAAAAGTGCAG | 9678 |
| rs188790542 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958680 | TTAGCTGTTTGGCCA[A/G]CTGCTTACTTCTGTA | 9678 |
| rs188809503 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11038033 | TTAGTAAAAATGCCA[A/G]CAGAAAACAAAATGC | 9678 |
| rs188837838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998062 | AGTGGAAAGGGAGAA[C/T]TGGTGATATAAGGAA | 9678 |
| rs188839999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993320 | TTACAGCCCTTGTCC[C/G]AAGTAATTCTGGGAG | 9678 |
| rs188952869 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068937 | TAGGAATCTTGCATG[C/T]CTTTTATTACATGCA | 9678 |
| rs188954587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10981487 | GTAGTGTTGGGTTGA[A/G]AGGGACTGGGCTGCC | 9678 |
| rs188958923 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | PHF14 | GRCh38.p7 | 7:10995716 | GAGGCAGCTGAGGCC[C/T]GGCGAGAATTTGAGA | 9678 |
| rs188961808 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047515 | GAAAATTGAGAAAAG[A/G]CCAGACGCAGTGGCT | 9678 |
| rs188969500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016183 | CTTTTATATACTATT[A/T]GAACACTTGTGCTAA | 9678 |
| rs188969687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033875 | AAAGCAGCTGTTTGT[A/G]TGTGTTAATGTAGTC | 9678 |
| rs188987276 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976679 | TTTTATGATATCGAG[C/T]TAAGTAGAGATTTCT | 9678 |
| rs188994040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081933 | CTTTTCTCTATCTTC[A/T]TAGGTTTTTGATAGT | 9678 |
| rs189055646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148392 | TTTAGGACCGTTGCC[C/T]TTGTTCCCTGTGCCT | 9678 |
| rs189056871 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11010582 | TTTGTAACTATTAAT[A/G]TTAACTATATTTAGC | 9678 |
| rs189103952 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092901 | ACACACCAGTTAAAG[C/G]GTGTTTTTTTCCCCC | 9678 |
| rs189107973 | snp | A/G | 0.00177965 | 0.0297768 | intron-variant | PHF14 | GRCh38.p7 | 7:11111474 | TCTTCCAAGGTAAGG[A/G]GAGAAGTCTATAAGA | 9678 |
| rs189113365 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960965 | TTTAAGTTCTTTGTA[C/G]ATTCTGGATATTTGC | 9678 |
| rs189114113 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975928 | ATTATATTACTGTTG[A/C/G]TACTTTTAGTAGCAT | 9678 |
| rs189117504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976112 | GATCCAATGGATTTG[A/G]CTTCAGAATTTAGTC | 9678 |
| rs189122393 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11149015 | TGAAATAGGGTTTTT[G/T]TTTTGTTTTGTTTTG | 9678 |
| rs189129370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993691 | AGGGTGGTTGGGTGA[A/G]TTGCAGAAGTTTGTA | 9678 |
| rs189129793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006964 | TGGATCACCTGAAGT[C/T]AGGAGTTTGATACCA | 9678 |
| rs189132350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166765 | AGAAAGAGATTGGCT[C/T]TTATTTGTTATATAA | 9678 |
| rs189136251 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11132990 | GAAATTCTTAGGTAT[G/T]AATCTAACAAAATAT | 9678 |
| rs189153837 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11158342 | TGCTTAATATTTTCT[A/C]ATGATTAGATTGAGT | 9678 |
| rs189170056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160336 | TGATTACATGTCTTC[A/G]CTATTATGAACAGTG | 9678 |
| rs189190465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051152 | CTCAAGTGACTCTTT[C/T]ACTTCAGCTTCCTGA | 9678 |
| rs189199370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126006 | TCAAAGCACTTGTCA[A/G]CAATGTGTTCACTTT | 9678 |
| rs189217118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087903 | ATTTTTAAAGTGTAT[A/G]ACTTGAAACTAACAT | 9678 |
| rs189267055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961238 | AAGTCTTTAATCCAT[A/C]TTGAGTTAATTTTTG | 9678 |
| rs189309630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140045 | CCCTGTAACACCTTA[C/T]ACGTTCCTACACACT | 9678 |
| rs189324430 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959270 | GGAACAAGTCAGCTA[G/T]TCATTCCATATTGGA | 9678 |
| rs189335287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994168 | TCTCAGCCAAGCACA[A/G]TGGCCCACGCCTGTA | 9678 |
| rs189338915 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015395 | TCTTCTTCCTTATTG[A/T]CTATCCAAAAATAAA | 9678 |
| rs189347765 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10991212 | TTGAGATGATGTCTC[A/G]CACTGTTGCCCAGGC | 9678 |
| rs189370584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019000 | GTTGAAATGATCATA[C/T]GGTTTTTATCCTTCA | 9678 |
| rs189372464 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994593 | TTCCGGTACTGATTT[A/T]AGATTTTATTATTGT | 9678 |
| rs189396760 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11074179 | AACCACCTTGAATTC[C/G]TCTCCTGAAAATGCC | 9678 |
| rs189398802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11056034 | CTATTATCAGACTCA[A/G]GGTGACCTCTGAGGT | 9678 |
| rs189400698 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961392 | CAGATGGTTGTAGAT[A/G]TATGGTGTTATTTCT | 9678 |
| rs189408303 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:10999131 | CTTCTTGTTTCAGCT[C/T]CCTGAGTAGCTGTGA | 9678 |
| rs189408507 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11038613 | TAGTGAGCCGAAATC[A/G]TGTCACCGCACTCCA | 9678 |
| rs189417055 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10976849 | ATATCTAGTATGCTG[A/C]ACTCATAATTTACCT | 9678 |
| rs189419353 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11110813 | TTAGAAAGTTCACTT[A/G]CAATCTACTTTAACT | 9678 |
| rs189431044 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11092286 | TAAACATTAGGGTGC[A/T]TTTGAAGCACCTGAA | 9678 |
| rs189466160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068411 | ACCTTGAGAACGTTA[C/T]GCTAAGTAAAATAAA | 9678 |
| rs189488078 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11154292 | TGTGTGTGTCTGTAC[A/C]TTTGCATGTATAAAA | 9678 |
| rs189488975 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004587 | GTTCATGATGTTGAC[A/G]TATTGAAGAATCTTA | 9678 |
| rs189503347 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107176 | CATTCGATGAAATAA[A/G]TCAGCTGCTTCTTTT | 9678 |
| rs189519819 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11144172 | CATGATGAGATTTCT[C/T]ATCCCAGTTAGAATG | 9678 |
| rs189539290 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11060435 | TGAATGTAGAAATTA[C/T]TAGCCATAAGTTTTC | 9678 |
| rs189550278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136595 | CATGTCTTTTGCCAT[A/G]TTCTATTCTAACATC | 9678 |
| rs189586930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088755 | AATATATAACTCCCC[A/G]AATTAAAACAACTGA | 9678 |
| rs189602378 | snp | A/G | 0.00557542 | 0.0525036 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968891 | AAGTTTTATTCAGGA[A/G]AGAAATGCTATTTTC | 9678 |
| rs189623897 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973954 | GTGCAATTTCTGGTC[G/T]TTCGTTGCTTCTGGT | 9678 |
| rs189632811 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033507 | TGGCCAGAACTTAAT[C/T]ACATGGCCACATCTA | 9678 |
| rs189705898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11075007 | CAGTGGCATGATTTT[C/T]GTTTACTGCAACCCC | 9678 |
| rs189724423 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11150552 | TGGGAATTTTTATTT[A/C]TTTCTTCTCATTCTT | 9678 |
| rs189732539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112183 | GAATGAAGACATTCT[C/G]GTCAACTGTAGATTA | 9678 |
| rs189752056 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11155222 | AACTAGGTTCTAAAA[A/G]TTTAAGTGATTTCTT | 9678 |
| rs189752564 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10983333 | ACAGACTTTTATTAA[A/G]TATCTACTATTTGTC | 9678 |
| rs189758224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018052 | GTTCCTGGCACCTTT[A/G]TTAGGCACTAAGTTC | 9678 |
| rs189758512 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10997128 | TGTATTTAATGCATA[C/T]GTGCTTTACTTACTT | 9678 |
| rs189770199 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11138244 | GGCAGGGTTTCACCG[C/T]GTTAGCCAGGATGGT | 9678 |
| rs189793310 | snp | C/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972259 | TTTCTAGAGCAACTA[C/G]GTGTTATTTATTAAA | 9678 |
| rs189804179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051999 | ATATAAGGAACACAC[A/C]AGAGCATCCATCACC | 9678 |
| rs189813735 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11077668 | GTGAGTATGATTTGG[A/G]GAACAGATATACCTC | 9678 |
| rs189827513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153486 | GTTTATTGGAGACAA[A/G]TAGCAGTTGGAATAT | 9678 |
| rs189833830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11116181 | TTCAAGCTGCCTTCT[A/G]TATCCTTTTGACATG | 9678 |
| rs189853873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043990 | AGAGTTTCTGCAGCT[A/G]AAAAAAAACACACAC | 9678 |
| rs189902187 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063576 | TTGAACCTGTATGAG[C/T]ATCTACTGTGTCTTA | 9678 |
| rs189906707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047347 | TGCTGGATTACAGGC[A/G]TGAGCTACTGTGCCT | 9678 |
| rs189926915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100163 | TTGTATTGATTTTAT[A/G]TTTCTTTGGACATAT | 9678 |
| rs189928976 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11118867 | ATTTTGAAAATATGA[C/T]TTATTAAGATAAGTT | 9678 |
| rs189947184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081249 | AAACTTTTCTGGGGA[A/G]TAATTTAGCAATGTG | 9678 |
| rs189955937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093613 | CCCATTGCACTGTCT[A/T]TCCTCTTACTTAGCA | 9678 |
| rs189965546 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11056274 | AGTATGAAATAAAGA[C/T]AAGAATAGGTGGAGC | 9678 |
| rs189974985 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147739 | GCTTGGTCATTGTGT[A/C/G]CCTTCTCTATTTGTA | 9678 |
| rs189981467 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165003 | GATCTCCGCTCACTG[A/C]AGCCTCCACCTCCTG | 9678 |
| rs189988961 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11056143 | AACTCACTTTGGCTA[C/G]TTGGAAGAGATCTAC | 9678 |
| rs189989788 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11133443 | AAAGGCAATTCAGTA[A/C]AGAAAATATAGTCTT | 9678 |
| rs190008339 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167313 | GTTTTGGCTCATGTT[A/G]CTTCAAACATTTTTG | 9678 |
| rs190009267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019520 | TAGATTTTCTAATTT[A/G]TTGGCATATAGTTGC | 9678 |
| rs190049436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121909 | CGTACAGGTTTGTTC[C/T]GTAGGTATACATGTG | 9678 |
| rs190057505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989977 | ATTTATTACCAGTTT[A/T]CACTGGATATTTCTT | 9678 |
| rs190064013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158798 | TAGTTGCTTACAGAT[A/T]AGCCTGAAGTCCATC | 9678 |
| rs190065483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964827 | ATTTGATCTACAATC[A/G]CTGATATCCTTCCTT | 9678 |
| rs190111282 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11023414 | AACATGCCCTTAATA[G/T]ATGGTGAACTTAATT | 9678 |
| rs190150160 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986232 | CAAGCAGTCCTCCTG[A/C/G]TTCTGCCTTCCAAAG | 9678 |
| rs190163978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960413 | GTCCCTGCAAAGGAC[A/G]TGAACTCATCCTTTT | 9678 |
| rs190166461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975472 | AGATGTCTCTGAAGT[A/G]TAAGTCATGCATGCT | 9678 |
| rs190229714 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:10992142 | CACTGCAACCTCTGC[A/C]TCCCAGGTTCAAGCG | 9678 |
| rs190231527 | snp | G/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062850 | CTTTCAAAGGACAGT[G/T]TCACAAAAGTTCTTA | 9678 |
| rs190235424 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11005142 | ATAAATCTGTGGGGT[A/G]ATAACTTTGAGACTC | 9678 |
| rs190237305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047100 | TTGAGATGGAGTCTC[G/T]CTCTGTCACCCAGGC | 9678 |
| rs190255152 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039331 | TTTCAGCTGTATAAG[A/C]GATGGTTTTTTAAAC | 9678 |
| rs190306964 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104231 | CATCTTGCATTTTCA[G/T]TGGTGGTGGATATTC | 9678 |
| rs190312002 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029686 | GTAACTGTCTAAAAT[A/G]TAACTCACATAAACC | 9678 |
| rs190329354 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11140568 | AGATCTTTCATTGTT[C/G]AGCAATAATGAGCTA | 9678 |
| rs190343363 | snp | A/C/G | 0.00518109 | 0.0506754 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066043 | TTTATTTGAGTATAT[A/C/G]GCAAATTACATAGGT | 9678 |
| rs190348656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066537 | TCTTTGTTTTCTTCT[A/G]GAAGCTTTGTAGTTT | 9678 |
| rs190371594 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104665 | AGTAGTGGTTCTCAA[A/T]CGTTGTGCATTGGAA | 9678 |
| rs190383581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085588 | TTTGGCCTCGTTTCA[A/G]CATTTAACATTGGTG | 9678 |
| rs190383931 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103716 | GAGTAGGTAATGTTA[C/T]AGATAATCAAAAGCA | 9678 |
| rs190393749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967975 | TTAAATCCAAACTGG[A/G]TCAAATAATAAATAT | 9678 |
| rs190398989 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11159209 | TGTTATTTATTCTAA[A/G]GTGATGTTAAGATTG | 9678 |
| rs190399455 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168591 | TTGATGTTTATGCTT[C/T]AATTAACTCAGAAGA | 9678 |
| rs190407451 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000007 | AGGAAGAAAGTAGAG[A/G]AGGAGAGGGAAATTG | 9678 |
| rs190410361 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11122449 | TATATATACGTATAT[A/G]TATATATTGTGTGTG | 9678 |
| rs190415785 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11151840 | CCACTATATGAGTGT[A/G]TTTTAAGACATAAGA | 9678 |
| rs190419130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141562 | ATTGTTTTGATATAA[A/G]TTATTTTAAAATGTT | 9678 |
| rs190456665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966791 | TACACCCTTCTATCC[A/G]TAAACCTCCCCACAA | 9678 |
| rs190487897 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11107835 | ATTTTGTCCTATATT[A/G]TGTGCTGCATGTGTT | 9678 |
| rs190522105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959838 | CATCCATGGCACAGC[A/G]AGCCAGCCAGGAAAG | 9678 |
| rs190531050 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11144971 | GAGGTATTTTGTGTG[G/T]TATAAACGGGAACAG | 9678 |
| rs190534709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10975061 | AAAGCACGTAAACTT[C/T]ATTTATTTTGTCCAT | 9678 |
| rs190563516 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10985586 | ATATGCTTAATGGCC[G/T]TAACAACATGCTGCA | 9678 |
| rs190584522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134181 | TGAACTTTACAGTAG[C/G]CTTGTAGAATCTAAC | 9678 |
| rs190592253 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085101 | TAAAACCTAATTTGG[A/T]ATGTTATGAAATAGA | 9678 |
| rs190592905 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11113281 | GGGCATATTTTAGAT[C/T]TGTTTGAAACATTGC | 9678 |
| rs190607860 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11048699 | TTTACATATCTTAAA[G/T]GATATTTATAAGATG | 9678 |
| rs190612563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121465 | GCCTCCCCCCACTGC[C/T]TACTTAATTGCAGGG | 9678 |
| rs190637510 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10977384 | GGCTAACTGGATTCC[A/G]TGGATCAATTTCTTC | 9678 |
| rs190657594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012700 | TTTATTACATTAGCT[G/T]CCTAAATAATATGAT | 9678 |
| rs190664547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066257 | AAATATTAGTCTCTC[A/G]TTATTCTGATTATAA | 9678 |
| rs190666381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10977173 | GTCCTATCACTGGTT[C/T]CCAAACATGTTGAAG | 9678 |
| rs190673270 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:10994703 | TAAAGGCGGCGTGTC[C/T]GGAGTTTGCTCCTTC | 9678 |
| rs190674958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956929 | TGTAATGATTTTTAC[A/G]GCAGTCCTAGAAAAC | 9678 |
| rs190675398 | snp | C/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:10970604 | AAAATTCTGAGTTAA[C/G]AATGCCAAGAGTAAT | 9678 |
| rs190677127 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11049169 | TTAAGTAGACAAACA[A/G]CATATTTTAAAAGTA | 9678 |
| rs190681167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012167 | TTACCAAGATATTGT[C/T]AATGAAGTCCTGCCT | 9678 |
| rs190683587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030306 | ATACTTGGATCAGGG[A/C]ATCTATAGGATAAGG | 9678 |
| rs190696343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11164286 | GGAAATAGTTTGTTC[A/G]TATGGCCAAATTATA | 9678 |
| rs190703175 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133797 | ATTACATCATAAAAC[G/T]ATTCCTCCTGGATGC | 9678 |
| rs190708814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085317 | ATGTCATATTCTTCT[A/G]TTGATTTAAAACAAT | 9678 |
| rs190719876 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11113107 | CCCCCAGCAAACAAG[G/T]TAGGAAAACAATTTT | 9678 |
| rs190742521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126992 | CAAGGTACAAACAGA[A/G]ATGAGCTCGATTCCT | 9678 |
| rs190765478 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162444 | GTAGCTTTTCATGTT[G/T]ATGGAAATATATAAA | 9678 |
| rs190806199 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11052592 | TTCACACTCATACCA[A/G]CAATGGATAATGTTT | 9678 |
| rs190838217 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11089533 | CCATTCTCCACAAAA[A/G]GGAAAAAAAGGACAA | 9678 |
| rs190846004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013445 | GGGAATACAGGCATG[A/G]GCCACTGCACCCAGC | 9678 |
| rs190847908 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11041185 | TTGTAGGCAGTGGAT[A/C]ATGAAGATAAGTTTT | 9678 |
| rs190848520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026643 | AGCTGTGTTGTTTTT[C/G]TGTATGGGTATGATT | 9678 |
| rs190854205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021168 | TAATCTGTTAATAGT[C/T]TGTGCTAGGATGACA | 9678 |
| rs190869241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159954 | AGAGGTACATGGGCA[A/G]GTTTGTTACATAGGT | 9678 |
| rs190871705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093736 | TCCAAAGAATCACAA[C/G]CTTGGTTCTTGAGTG | 9678 |
| rs190876068 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11075648 | CACCTCCCACCAGGC[A/G]CACCTCCAACACTGG | 9678 |
| rs190877537 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10978743 | TACCTGCCCCAGCCT[C/G]ACCTCCACCTCCACT | 9678 |
| rs190878913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127660 | TTTAAAGTACCTCTT[C/T]TAAAGAAATCCTTAC | 9678 |
| rs190888626 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10995050 | TGTGTTTACAATCCC[C/T]GAGATAGACACAAAA | 9678 |
| rs190890594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057336 | TTAGAGAAATGTTTA[A/T]TTATTTGTTTTAGAT | 9678 |
| rs190928376 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962325 | TCAGCCTTTTCTGCA[G/T]CTATTGAGATAATCA | 9678 |
| rs190993178 | snp | G/T | 1.65993e-05 | 0.00288086 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036618 | CAATTCAGATACTAG[G/T]TCTAGTGTGGATGGA | 9678 |
| rs191001627 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018605 | CTTTTGTCTTTTGCA[A/G]CTTTACTGAATTTAT | 9678 |
| rs191003015 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11099873 | TGATTTATCTGCCTA[A/G]CATCACTACTAAGCA | 9678 |
| rs191013921 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11090316 | AGTGAATCAGGTTGA[C/G]AAAGATAGCTACACA | 9678 |
| rs191014121 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10997593 | CTCTCATGAAGTTGC[A/G]GGTCAAAGCCATAGC | 9678 |
| rs191018191 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11137806 | GTCCAGGCTGGTCTC[G/T]AACTCCTGACCTCAG | 9678 |
| rs191023627 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137947 | TATACCTAGCTCTTT[C/G]CTTGTATAAAGTACA | 9678 |
| rs191028098 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072026 | TTTATAACCATTCTG[A/C]TGAGTTGTATTAGTC | 9678 |
| rs191035828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11053338 | TAATTGAAACAGTTT[A/G]TTTTGGGTGCTCTAA | 9678 |
| rs191039872 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11128288 | TTCCCAGCAGACTTA[A/C]TTTTTCAAGATGATC | 9678 |
| rs191050426 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11109697 | AACTTAGCTTATATT[A/G]TTTATTATTCTTTCT | 9678 |
| rs191063396 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11035317 | TTTGGTATCCTTGGG[A/G]GGTCCTGGAACCAGT | 9678 |
| rs191086984 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109306 | AAGAATTCAAATAGA[A/C]CAGCTGACTCCTGGT | 9678 |
| rs191093360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071495 | GATAAATAGCAGATA[C/T]TTCCTTTTTAAAAAA | 9678 |
| rs191095704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10996234 | TAGGAAAATATTTAG[A/G]AGACCATTGCAATTA | 9678 |
| rs191109352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146320 | GGAATTTCTTTTTCA[A/G]TATTTTCATTGACAA | 9678 |
| rs191124998 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964937 | ATTTAAGCTCTTCTC[C/T]ACACTGGTTATTCTA | 9678 |
| rs191145911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11034605 | CCAGGCTGGAGTGCA[A/G]TGGCGCGATCTCGGT | 9678 |
| rs191212523 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120955 | TTAGACTATAAAGGC[A/T]TATTTTTTTCTTTGT | 9678 |
| rs191214685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139874 | TCCTAATAATATTCT[A/C]ATGCATCATTGTGAC | 9678 |
| rs191229895 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11117755 | ATTTAATTGAACTTG[G/T]TAATATTGGAAATTG | 9678 |
| rs191246044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080579 | AACATTAACTCTGCT[A/G]GTTTTTCTCCCTGAT | 9678 |
| rs191247741 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157639 | ATGGATCATATTACA[A/T]TTTTACCATATTACA | 9678 |
| rs191271721 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11154921 | AAATTAGAGTGACAT[A/G]GGTAGAATTGGCTTC | 9678 |
| rs191291558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049284 | TTGAGACCAGCTTGG[C/T]CAACATATAGTGAAA | 9678 |
| rs191294892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957557 | TCTCCAAAGCCTGCC[A/T]TTCATATGCACTGAA | 9678 |
| rs191304023 | snp | A/C | 0.00279162 | 0.0372561 | | | GRCh38.p7 | 7:10971030 | AAGGGCATCTTTGAA[A/C]AACTATAGATAACAT | 9678 |
| rs191315371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076369 | TTTGTTGTTCTTTGA[A/G]GCTTCAGTGCTATAA | 9678 |
| rs191330505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10982117 | TTAGTGCTTCTCTTT[C/T]TAAAGCATATTTTAA | 9678 |
| rs191335932 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:11114063 | ATGAAATGAAAAGCT[A/G]AAGGAGAAATACTTA | 9678 |
| rs191396670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017145 | TTCTTTATCGGATTC[A/G]TCTGTTGGTGGAAAC | 9678 |
| rs191443555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004892 | AATACAAAAATTAGC[C/T]TGTAATCCCAGCTGG | 9678 |
| rs191448029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10983818 | AACAGACATTTTTGT[C/T]ACAAAACTGCAGTAA | 9678 |
| rs191451329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966554 | GGACCTACCCTTTCC[C/T]GCGTAGGAACCTGTC | 9678 |
| rs191480392 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11047713 | ATTGCTTAAACCTGG[C/G]AGGCTGAGGCTACAA | 9678 |
| rs191481650 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11018991 | TCAGCATCAGTTGAA[A/C/G]TGATCATATGGTTTT | 9678 |
| rs191488722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028326 | ATTGTTTTTGCAACA[C/T]TGTAAAGTTAAAAAA | 9678 |
| rs191501834 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10985200 | ATGATTAAAGCTAGT[C/T]CTTGTTGCCTGTGGC | 9678 |
| rs191505082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129728 | TTCACTAGGTGCTTC[A/C]GATGTAGTAAGATGA | 9678 |
| rs191509193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008401 | AACTGGGCCTCACAG[C/T]AGGGGGTGAGCGGCT | 9678 |
| rs191509402 | snp | A/C | 0.0111196 | 0.0737302 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102718 | CTTGGACTAACAAGG[A/C]AGTAGATTTGCCTGT | 9678 |
| rs191511367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082785 | GCCTTCACACTCAGT[A/G]GAATTTTGGTTTCAT | 9678 |
| rs191511945 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999040 | GTTCTGGCGGCACTA[A/G]GGTTTTTTGCTGTTG | 9678 |
| rs191519263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065143 | GAAGGTTTACAGCAT[C/T]TCAGGCAATTTTATT | 9678 |
| rs191526316 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11109948 | GTTGTAGAGGAAGAA[A/G]TGCATAAACTTAGGA | 9678 |
| rs191540496 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11030948 | TATTAATGAAGTTTG[A/C]ATTTGACAGTAATCA | 9678 |
| rs191581682 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135468 | TTGTGTTTTTCATTT[A/C]TTTATTTGAAGACCA | 9678 |
| rs191585898 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11097101 | TCTCGTGCCTCAGCC[C/T]CCCAAGTAGCTGGGA | 9678 |
| rs191603302 | snp | A/G | 0.00248084 | 0.0351321 | nc-transcript-variant, missense, intron-variant | PHF14 | GRCh38.p7 | 7:11169420 | TTATTTCACAGGAAG[A/G]TGAAAATGAAGCTGA | 9678 |
| rs191613561 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11021741 | GTATTTGGGAGGTTG[C/G]ATTAAAACATTCTAT | 9678 |
| rs191646907 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976113 | ATCCAATGGATTTGA[C/G]TTCAGAATTTAGTCT | 9678 |
| rs191652276 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993865 | AGTACAAAAATTAAT[A/C]CGGCATGGTGGCACG | 9678 |
| rs191653977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057540 | CCACCACGTCCGGCT[A/G]AGTTTTGTATTTTAG | 9678 |
| rs191683770 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10991479 | CGCGCCCGGCCAATT[G/T]TTGTGTTCTTAGTAG | 9678 |
| rs191687531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096097 | GAATAAAGAGGTCTT[C/T]CTTAATCACATGGTT | 9678 |
| rs191693826 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965600 | AACCACTGCTCTCTT[C/T]AGAGCTGTCAGGCAG | 9678 |
| rs191699779 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161282 | TTTGATACAATGAGT[C/T]GAGTGTTGTATTAAA | 9678 |
| rs191715859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025406 | AAGGAAGTTCTACCA[C/T]GGGTAAAATGCTGTC | 9678 |
| rs191753202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962040 | GCAAACAGGGGCAAT[C/T]TGACTTCCTCTTTTC | 9678 |
| rs191793976 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105466 | CATGACTATTTCACC[A/G]AAATTTATTCAAGGA | 9678 |
| rs191810719 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066645 | TATTATCTGCCCCAT[A/G]TGGATTCCCAGTATC | 9678 |
| rs191813729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142311 | GTTCTTATAGTGATA[A/C]ACATAGCAATTATTC | 9678 |
| rs191829435 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167842 | AGACCATCCTGGCTA[A/G]CACGGTGAAACCCCG | 9678 |
| rs191842072 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087482 | GGCATGAGCCACTGC[A/G]CCTGGCCAGCACTGT | 9678 |
| rs191863016 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11021966 | TTAATATATTCACAG[G/T]GTTAATAGAGATTTG | 9678 |
| rs191864255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125425 | TTGCAGTACAAGTTT[C/G]TCTTCTTCAAAAGAA | 9678 |
| rs191869170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143698 | ATCTACTAAGCATCT[C/T]GTAAGTGTAACACCC | 9678 |
| rs191877686 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106975 | ATAAAAATGTACATC[C/T]TTGTTCAAGTCTATG | 9678 |
| rs191880825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001414 | AACTTTAGAGTCAGT[C/T]TGCAGTATCTACAAA | 9678 |
| rs191885246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10989024 | GATGAGTTTTCTTTA[A/G]GATGTTTTCAGTTTT | 9678 |
| rs191886955 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11057754 | TTGTCTCTAATACCA[C/T]GCCAATCTCTTCTAT | 9678 |
| rs191888500 | snp | C/T | | | | | GRCh38.p7 | 7:10969889 | GCTGTCTTTTGTATA[C/T]ATATTTGTTTCTTTT | 9678 |
| rs191891087 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001878 | TTCTTGTCTTATTAC[A/C]TGATGTTGAAAGCAG | 9678 |
| rs191897600 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11042578 | ACAGAAGAAATAGTA[A/T]GTTAAATCAAGATGA | 9678 |
| rs191927816 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11075806 | GAATTGATGAGGAAA[C/G]TGAAGAATAGAGCTT | 9678 |
| rs191947265 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000872 | ACATTTTAATGGAGT[C/G]CAACTTATAAATTAT | 9678 |
| rs191950773 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041430 | CTGGTGTTTTTGTGT[A/G]TGTGTGTGTGTGTAT | 9678 |
| rs191955915 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031700 | TTGAGGCTGCATTGA[A/G]CTATGTTCTCACCAC | 9678 |
| rs192004052 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106013 | TGAGCAGATGGAAAT[C/G]AGTTTATTAAAGAAC | 9678 |
| rs192045742 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11079644 | AAGTGTAGGGGAAGA[A/G]TGACCAAGCACTAAA | 9678 |
| rs192059393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11046694 | TACAAGTTGAGTTAA[A/G]TGTTGTTTTCTGCCC | 9678 |
| rs192065504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117241 | TTGTGAGAAGCCATG[A/G]AGTATACATGACAGG | 9678 |
| rs192087156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152580 | TCATATATCCAATAA[C/T]TATTCATAAGAACTA | 9678 |
| rs192092943 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147515 | TAATGTCACTTACAA[A/T]CTCTTTCTTATCAGA | 9678 |
| rs192096145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086387 | TTCTTTCTAAAACTA[A/G]CCTGTTGCTTTTATG | 9678 |
| rs192097189 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11151071 | AAAATAGAATCTTAG[A/C]CAAAAAAACCTGTCA | 9678 |
| rs192101829 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11136058 | ATAAGTAACATTGTT[A/G]AAAATAGTTTACACT | 9678 |
| rs192116204 | snp | A/G | 0.00636936 | 0.0560724 | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10958894 | TTTTGTAGAGATGGG[A/G]TCTCACTATGTTGCC | 9678 |
| rs192118327 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10995175 | ACACAGAGTGCTGAT[G/T]GGTGTATTTACAATC | 9678 |
| rs192122636 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170145 | TCCTGGACATTTCAA[A/G]AATAGTTCTTTTATG | 9678 |
| rs192125425 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122936 | AAATTCAGTTTGTCA[A/G]AATCAAGAATCTTCC | 9678 |
| rs192153762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11032111 | CTCTACACAAAATGT[A/G]AAAATTAGCCAGGTG | 9678 |
| rs192173616 | snp | A/G | 0.00279162 | 0.0372561 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972833 | GAGGCAGGAGAATAG[A/G]GTGTGGAGGCAGGGA | 9678 |
| rs192180151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014048 | ATAAATGACCAGTGG[G/T]ATACAGATGGAGAAG | 9678 |
| rs192185794 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11086989 | TTTGCTAATTTTTAC[A/G]TGGGGTAATATCAAG | 9678 |
| rs192185821 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990463 | CTAGAGGAGAGAGAA[G/T]ACGAAGCTTGCAGAG | 9678 |
| rs192188072 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11067251 | GTAAATCGAAACCAC[A/C]GTGAGATACCACCTC | 9678 |
| rs192189446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956611 | ATACGTAATTAATCC[A/G]GTGAGTTCATACTGG | 9678 |
| rs192196892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050288 | TTCAAAGATACTGAT[A/G]TAAACATATAAACTA | 9678 |
| rs192206016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987879 | GATCTAGCTGGGCGT[A/G]GTGGTACATACCTGT | 9678 |
| rs192229484 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11131144 | ACGCTACTATAAACA[C/T]TCAGGTACAAGTTTT | 9678 |
| rs192243938 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11091533 | GGCCAAGGTAGGCAG[A/C]TCAGTTGAGCCCAGG | 9678 |
| rs192245210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11165345 | CAGAGGTGATGTGCC[A/G]TTTTTAATACATCGT | 9678 |
| rs192270563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049672 | TTTATTATTAGTTAA[A/C]TAACAATATCTAACA | 9678 |
| rs192330374 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:10992603 | AGGAGGTGGAGGTTG[A/C]AGTGAGCCGAGATGG | 9678 |
| rs192348443 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11058635 | TACTCTTTATTGGGT[A/G]TAATTCTCTAACTTC | 9678 |
| rs192360353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043754 | TGGAATGTATTTATT[A/T]TGGTTTTTATGTGCT | 9678 |
| rs192372232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960794 | TGTAACTGGCATGAG[A/G]TTGTATCTCCTTGTG | 9678 |
| rs192381095 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11114458 | TTTTATAGAAATTCC[A/G]TAAGTCTAATAAGAT | 9678 |
| rs192389271 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11098235 | TATATAATTTGAAAG[C/G]TGAAAATATCAGAAT | 9678 |
| rs192397771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152274 | TATTGAAAAGGGAAT[A/G]CTTTTTATAGTCAGA | 9678 |
| rs192402791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055337 | TTTTGCTTTCTTTGC[A/G]CTCTAAGTCATGTAG | 9678 |
| rs192411202 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11062583 | TTACGAAATAAAGAA[A/G]GGTGAAAAGATGGCC | 9678 |
| rs192443624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099595 | TGCAGGGTGTTAATA[C/T]TGTTAAATTATACAA | 9678 |
| rs192475475 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962810 | GTTTAGTCTTGGGAG[G/T]GGTATGTTTCCAGGA | 9678 |
| rs192507107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164739 | TATGTAACCATAGTA[C/T]AATTATTGAAACCAA | 9678 |
| rs192535856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072993 | CTGCCCCTGTGGTCC[A/G]AACACCTCCCACCAG | 9678 |
| rs192536161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148646 | GCCATGAGGACGATA[C/T]GCTGTTGTTCACCAC | 9678 |
| rs192575134 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11139676 | AGGGAAGTCAAGTGT[A/G]TATTGTGTGTCAGTC | 9678 |
| rs192614557 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019309 | GTTTGAGTAAGATTG[G/T]TATTAGTTCTTCTTT | 9678 |
| rs192637539 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110356 | AGATTGGTTGAGAAA[A/G]TATTATTGTTTAATT | 9678 |
| rs192639157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975944 | TACTTTTAGTAGCAT[C/T]AACAGCAGAATTTGC | 9678 |
| rs192647482 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993396 | AATGCTCTGATCTTC[A/T]TGTGGAGCTGCCCTT | 9678 |
| rs192652259 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056087 | TATCTGTCATAGATT[C/G]TTAGAAGAAACCCTG | 9678 |
| rs192666945 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039197 | TTAGCAGTTTTAGAT[A/T]CCCTGCCACATTTTT | 9678 |
| rs192673606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147990 | CAGTCTTTCCTACCT[C/T]AGTCTCATCATTTTT | 9678 |
| rs192675074 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10998804 | TTGGTGATTCTCTTA[G/T]GATGCTGAGGGCACT | 9678 |
| rs192676102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111168 | TTGTTTTTGCTAAAA[C/T]ATTTATTTCAGGTTT | 9678 |
| rs192680585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11156007 | AATAGAAACCATTGG[C/T]TAAATGAATGCATTT | 9678 |
| rs192690180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038040 | AAATGCCAGCAGAAA[A/G]CAAAATGCTTACAGC | 9678 |
| rs192692597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092762 | CTTTACTCGCTGAAC[C/T]TGATCATTGACTCTT | 9678 |
| rs192698482 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11074310 | CTGCCTCCCGGGTTC[A/G]TACCATTCTCCTGCC | 9678 |
| rs192701747 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966105 | TGGGCTGCACCCACT[A/G]TCCAACCAGTTCCAG | 9678 |
| rs192714667 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10975665 | TATGTTTAATTTAAA[C/T]GTTTTATGGGAAAAA | 9678 |
| rs192721798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006090 | TAAAATTTCTTAGTC[A/G]AAAGATAAGTGTATT | 9678 |
| rs192753795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073817 | GATTTTTTCACTCTC[C/G]CATTCTGTGCACCTG | 9678 |
| rs192760880 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11014760 | ATTATTGCAGAGTAG[A/G]TATTGAAGCATGCGT | 9678 |
| rs192777028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980780 | TACCATGGACTTCAC[A/T]GGGGGTATTAGTGTA | 9678 |
| rs192789411 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11050427 | GTAAAAATTTACTTT[C/T]AACAACTGGTTTTAA | 9678 |
| rs192823359 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11054264 | GTATAGACTTTGGAC[A/C]CATTCTGGAATTAAT | 9678 |
| rs192836798 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11090921 | GTAGCAGTCATTCAA[G/T]GGAATAAACAGACAC | 9678 |
| rs192851440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120102 | CTTATAATTGGATGC[A/G]TCGTATAGTAGGAAG | 9678 |
| rs192855042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11098277 | AGTTTTCTATTAAAA[C/T]ATTTCTTGATCCATT | 9678 |
| rs192858670 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11156529 | GCCGGGCGTGGTGGC[G/T]CATGCCTGTAATCTC | 9678 |
| rs192863305 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11123867 | AAGTTGCAGTGAGCC[A/G]AGATCGTGCCACTAC | 9678 |
| rs192873515 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11160521 | TCCCACCAATAGTGT[A/G]TAAGCATTCCTTTTT | 9678 |
| rs192889560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960966 | TTAAGTTCTTTGTAG[A/T]TTCTGGATATTTGCC | 9678 |
| rs192905568 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11018813 | GTGGGCCTGCTTGTC[A/G]TGTTCCAGATCTTAG | 9678 |
| rs192908326 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963703 | CATTATTATTGTGTA[A/G]GACTCTAAGTCTCTT | 9678 |
| rs192912104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10984389 | CTTCAATGTCATTCT[A/G]ATTCTTACCTTTAAA | 9678 |
| rs192941982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059948 | TGATCATGTCTCACT[A/G]CAGCCTAGATCTCCT | 9678 |
| rs192949043 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11023596 | CTTCGGGAGGCCAAG[G/T]TGGGCAGATCACCTG | 9678 |
| rs192964117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995373 | CACAGAGTGCTGATT[C/G]GTGTATTTACAAACC | 9678 |
| rs192977149 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | PHF14 | GRCh38.p7 | 7:11032484 | ATGTCAGTTTTACCC[A/G]GGGAGCTTTGTTTAA | 9678 |
| rs192979217 | snp | A/C/T | 0.00358779 | 0.0422022 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964054 | GTCTGTGTTTTTTAA[A/C/T]TGGGGCATTTAGCCC | 9678 |
| rs192990481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11068192 | CGTCTCTACTAAAAA[A/G]TACAAAAAATTAGTC | 9678 |
| rs193015533 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068625 | GGGATGGTTGCACAA[C/T]AGTGTGAATGTGAAT | 9678 |
| rs193032327 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169946 | GGTTAAAACCAGTCA[A/G]TGCCACAAGGAGAAA | 9678 |
| rs193036858 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107186 | AATAAATCAGCTGCT[G/T]CTTTTTACTTGTTTG | 9678 |
| rs193048776 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11144337 | TAAAAGTAGAACTAA[C/T]TTATAACCCAGCAAT | 9678 |
| rs193064087 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142862 | CATTGATAAAACTCC[A/G]TTAATGACTTAATGG | 9678 |
| rs193067247 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11077326 | GCCAGATTCAGCCGG[A/G]CGCAGTGGGGCTCAT | 9678 |
| rs193079136 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972012 | GTGATCTCTGCTCAC[G/T]GCAACCTCTGCCTCC | 9678 |
| rs193081358 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116061 | TGTAAAAATATCCTA[C/T]TCCTCATCAAACCTT | 9678 |
| rs193086029 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11002990 | TCTCGCTCTGTCACC[A/G]GGCTGGAGTGCAGTG | 9678 |
| rs193125172 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11007312 | GTTGCAAATATTTTC[C/T]ATCCTTGCAAATGTT | 9678 |
| rs193134069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047566 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCACTTGA | 9678 |
| rs193142733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082424 | AGTCAATTCTCTTTT[C/T]GTTTGTCTATCCTAA | 9678 |
| rs193149886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119495 | GTGTGAGTGTGAGAG[A/C]CATGTTCATTGTGAA | 9678 |
| rs193157735 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PHF14 | GRCh38.p7 | 7:10979555 | TTCCTTTCTCTCTCT[C/T]TTTTTTTTTTTTTTG | 9678 |
| rs193175114 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11044536 | GATCAACTTAGCTTT[A/G]GTTAGCAGTTAACTG | 9678 |
| rs193178916 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003759 | TTCTTAATTATAAGT[G/T]ACATATGAGTAGATA | 9678 |
| rs193209889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11023183 | CTTAATTTAGAGTAA[C/T]GTATGAGGTAAAATG | 9678 |
| rs193219010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126580 | TAGCTGTTTCAAAAT[C/T]CCTAACTTTTGTCTT | 9678 |
| rs193221827 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088395 | TGTGTGTTGTTCACA[C/T]ACACACAAACACACA | 9678 |
| rs193223025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161928 | ATTAGTAGTTTACTA[A/C]CTGAAGGAAAATTTT | 9678 |
| rs193243914 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10989670 | GGGTCTTGTGCTGTC[C/T]CCCAGGCTGAAGTGC | 9678 |
| rs193250553 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958606 | ATGAACTACAGCAAG[A/G]TAAAATGAGCCATTC | 9678 |
| rs193255114 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165908 | ATAACTCAGTCTCAT[A/T]TTGCCACCTGGAGTA | 9678 |
| rs193282395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999566 | CCTTGGACTCTTAAC[C/T]TAGGATGAGTTCTTT | 9678 |
| rs193287979 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11028159 | TGCTTGGAACATTTA[A/C]ATTAGCCTACACTTG | 9678 |
| rs193293513 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11100904 | AAGTAGATACTTCCT[C/T]TTAACAGGCAATTCT | 9678 |
| rs193295482 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063657 | ACTTAGAGGTTTTTA[G/T]TAGGTTTTTTGTTTT | 9678 |
| rs193302215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139018 | CTAAGGCTGTGGAGA[C/T]ATTATAAAAATCTAA | 9678 |
| rs199497476 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122398 | CATACATACACACAC[-/AT]ATATATATATACACG | 9678 |
| rs199498346 | in-del | -/CG/CGCACC | 0.102014 | 0.201495 | intron-variant | PHF14 | GRCh38.p7 | 7:11088420 | ACACACACACACGCA[-/CG/CGCACC]CACACACACACAGTC | 9678 |
| rs199509477 | in-del | -/AAG | 0.0314385 | 0.121371 | intron-variant | PHF14 | GRCh38.p7 | 7:11081867 | TCTCAAAAAAAAAAA[-/AAG]AGATTTATGATCTTA | 9678 |
| rs199526779 | in-del | -/GGGCATGGTCT | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11033461 | GCAGCTTCCTTTCAA[-/GGGCATGGTCT]GGGCATTTCATACAA | 9678 |
| rs199535251 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988842 | AGATATTATTTTTAT[C/T]GCCATTTTGCAGATA | 9678 |
| rs199544005 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089095 | AAGATTAATTAGATA[A/T]AAAAAAAAAAAACCG | 9678 |
| rs199557830 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11117237 | TGTTTTGTGAGAAGC[A/G]ATGGAGTATACATGA | 9678 |
| rs199620281 | in-del | -/TACA | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11124370 | GTTGTTAAATACTCT[-/TACA]TAATCTATTTTTAAG | 9678 |
| rs199649673 | in-del | -/A | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10998343 | GGACAGTGGGGAGTT[-/A]AGAGATTTGGGGAGG | 9678 |
| rs199666860 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031361 | TACTTTGTGAATATT[C/T]CAGATTTATTAAGAA | 9678 |
| rs199667189 | in-del | -/TTAA | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11010536 | TGTTAATTAAAAATG[-/TTAA]TTAAATGAAATTAAT | 9678 |
| rs199671035 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11008067 | TTGTAGTGTGTCTGA[A/G]TTCAGGAGAATGTCA | 9678 |
| rs199691367 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055851 | ATATTTTTTAGATGT[A/T]AGTTTAGGAAAAATG | 9678 |
| rs199699774 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039541 | TCGCAAATATTTTTT[A/T]TTTTTTAAGGATGAT | 9678 |
| rs199706094 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145959 | TAAAGCAATGGCAGA[G/T]AACTCTTGAATATGT | 9678 |
| rs199711875 | snp | A/G | | | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982629 | AAGGAAAAAGAAAAG[A/G]AAAAGGAGAAAGAGA | 9678 |
| rs199736776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061876 | TTTTACACAGTCTTA[A/G]CTTTGAGAAATTTTC | 9678 |
| rs199753935 | in-del | -/A | 0.0410537 | 0.137264 | intron-variant | PHF14 | GRCh38.p7 | 7:11068227 | ATGGTGGTGGGCACC[-/A]GTAGTCCCAGCTACT | 9678 |
| rs199762530 | snp | A/C | 4.20601e-05 | 0.00458566 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982510 | AACAACTTAAAAATT[A/C]TGCAGAGGAAGAAGT | 9678 |
| rs199792165 | in-del | -/GGT | 0.495445 | 0.0475058 | intron-variant | PHF14 | GRCh38.p7 | 7:11015011 | CAATATAAGAGGGGG[-/GGT]GGGTACTTAAATTTT | 9678 |
| rs199802671 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132303 | TCTGTATAATTGAGA[-/TT]TTTTTTTTTTTTTTA | 9678 |
| rs199836922 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132088 | ATAATTACCATTTTT[C/T]TGGGAGGGAAGGTTT | 9678 |
| rs199857872 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961841 | TGTAGTAATTGTGAA[C/T]GGGAGTTCACTTGTG | 9678 |
| rs199877911 | in-del | -/A | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:10992936 | AGTCCAGTTTTTTTT[-/A]ATTTTGGTTTGTTTT | 9678 |
| rs199886253 | snp | C/T | 0.000100524 | 0.00708887 | intron-variant | PHF14 | GRCh38.p7 | 7:11035637 | TGTGCTTTCTTTGTA[C/T]AGGATATAGCAGATC | 9678 |
| rs199906960 | in-del | -/CTAA | 0.0138799 | 0.0821421 | intron-variant | PHF14 | GRCh38.p7 | 7:11079741 | CTTTTACATTGTATG[-/CTAA]CTGTGATATACAAAA | 9678 |
| rs199909426 | in-del | -/AAAA | 0.0126979 | 0.078662 | intron-variant | PHF14 | GRCh38.p7 | 7:11135990 | AAGTTAACTGGTATT[-/AAAA]AAAGAAAGAGAAGAA | 9678 |
| rs199916334 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145958 | TTAAAGCAATGGCAG[-/AT]AACTCTTGAATATGT | 9678 |
| rs199921487 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138055 | TCTTTTTTTTTTTTT[G/T]AGACGGAGTCTTTGC | 9678 |
| rs199939290 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069856 | TCTATTATTTATTTA[-/T]TTTATTTTTTTCTGG | 9678 |
| rs199941704 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098527 | TATGTCTCACTTCCC[A/C]CAACCTTCTGGCTCG | 9678 |
| rs199973155 | in-del | -/AA | 0.0528381 | 0.153711 | intron-variant | PHF14 | GRCh38.p7 | 7:11058936 | TTATATTTTTATAAT[-/AA]GTTTATTTTTGTAGA | 9678 |
| rs200004791 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004270 | AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAGAAAA | 9678 |
| rs200008518 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064073 | TTTATTGGTACTATA[C/T]TTTAATATTTCTTAG | 9678 |
| rs200011297 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | PHF14 | GRCh38.p7 | 7:10991732 | TACTGTTTCTTGTTT[G/T]TTTTTTTTTAATTTT | 9678 |
| rs200014344 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127258 | CCTTTTTTTTTTTTG[A/T]CTCATTGCTAGAGCT | 9678 |
| rs200053748 | in-del | -/A/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085891 | AAAACATAATAGTTT[-/A/AA]AAAAAAAAAACTGTG | 9678 |
| rs200058512 | in-del | -/TGAAGATA | 0.0221141 | 0.102801 | intron-variant | PHF14 | GRCh38.p7 | 7:11123425 | TCAAATTAAATATTC[-/TGAAGATA]TGATTAAATATGCTA | 9678 |
| rs200060412 | snp | A/T | 4.83688e-05 | 0.00491752 | intron-variant | PHF14 | GRCh38.p7 | 7:11022835 | GAATTTTATTAAAAG[A/T]TTTGATAGCAAAATC | 9678 |
| rs200080755 | in-del | -/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960929 | TGCCCACTTTTTGAT[-/G]GGTTTTTTTTTTCTT | 9678 |
| rs200083467 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129786 | AGATGCTAGTAGGAT[A/G]GATAAAGCATGTATG | 9678 |
| rs200084763 | in-del | -/TACACTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029359 | TAAAACTATTTTCAT[-/TACACTA]TAAAAATGTTACTTA | 9678 |
| rs200115142 | in-del | -/TTTTTT | 0.487809 | 0.0771174 | intron-variant | PHF14 | GRCh38.p7 | 7:11075565 | TGGGAAGGAAAGAGG[-/TTTTTT]TTTTTTTTTTTTTTT | 9678 |
| rs200148868 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057885 | AGTTCTTAAAAAAAA[A/G]AAAAACAAAAAATTG | 9678 |
| rs200154401 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048893 | TGATTTTTTGAGTTG[G/T]TCCGTGTTTTGTGGT | 9678 |
| rs200159816 | in-del | -/ATT | 0.0174175 | 0.0916809 | intron-variant | PHF14 | GRCh38.p7 | 7:11130096 | AGAGCAGCTCTGCTC[-/ATT]ATAGTCACTTGGGGA | 9678 |
| rs200165072 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122350 | ATATATATATATATA[C/T]ATACACACACACACA | 9678 |
| rs200174701 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977526 | ATAAAATAGAAACAA[-/A]TCAACATTGGTAAAG | 9678 |
| rs200200118 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104891 | TTTTTTTAAAACATC[A/G]TTGTGTTGTGCTTAA | 9678 |
| rs200202333 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153950 | CTGTCTGTGTGTGCG[C/T]GTGTGTGTGTGTGTG | 9678 |
| rs200205094 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960455 | TAGTATTCCACGGTG[C/T]ATATGTGCCACATTT | 9678 |
| rs200241568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051802 | TATTTTTTATTTATC[A/G]TAAGCATCATACAAT | 9678 |
| rs200262183 | in-del | -/ACT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987750 | ACTTTCTCTGAAACC[-/ACT]TTGAAAGATGATATA | 9678 |
| rs200277240 | snp | G/T | 0.000810355 | 0.0201127 | intron-variant | PHF14 | GRCh38.p7 | 7:11038862 | ACAGGGCAGGTTAGT[G/T]TCTTTCCAATTGCTG | 9678 |
| rs200309073 | in-del | -/TTAT | 0.495095 | 0.0492773 | intron-variant | PHF14 | GRCh38.p7 | 7:11056401 | TCATTAGACCCATAG[-/TTAT]TTCAGTTTATAGTAG | 9678 |
| rs200363777 | in-del | -/TTAC | 0.031825 | 0.122064 | intron-variant | PHF14 | GRCh38.p7 | 7:11029374 | TACACTATAAAAATG[-/TTAC]TTACTTTTCTGAACT | 9678 |
| rs200385519 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038180 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 9678 |
| rs200394435 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088422 | CACACACACACGCAC[A/G]CACACACACAGTCCT | 9678 |
| rs200403399 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11022663 | CTGCTGGAAAAGTAA[-/T]TTTCAGTCCCCTTTT | 9678 |
| rs200446052 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051294 | GTGCTGGGATTATGG[C/G]AGTGAGCCACTGCAG | 9678 |
| rs200472048 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055852 | TATTTTTTAGATGTT[A/T]GTTTAGGAAAAATGT | 9678 |
| rs200509461 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11010480 | ATATGACTTTCAGAT[A/T]GTGTGCGTATATATG | 9678 |
| rs200516226 | in-del | -/T | 0.0349115 | 0.127424 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107710 | TTTATTACATAGACA[-/T]TTGTGTTATTTAATA | 9678 |
| rs200519414 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046645 | CTGCTATTAAAGTTT[A/T]TACAGGTATTATAAC | 9678 |
| rs200521353 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960157 | CAGGTTTGTTACATA[G/T]GTATACATGTGCCAT | 9678 |
| rs200552769 | snp | A/G | 0.000268488 | 0.0115833 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982766 | TTCTGTTCCCACTAC[A/G]ACAACCGCTACAGAG | 9678 |
| rs200587514 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001612 | TCTTGGCAATATTAT[G/T]TTATTTTTTGGGGGG | 9678 |
| rs200596586 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120058 | ATAGTTATTTTTTCC[A/C]AAAAAATTGCCATTA | 9678 |
| rs200630564 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014889 | TTGCCATCTTCCATG[-/T]TTTTTTTTTTTTTAC | 9678 |
| rs200659450 | snp | A/C/G | 0.000422833 | 0.0145343 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982715 | TGCTGCTGCCACCAC[A/C/G]CCAGCCACAAGTCCT | 9678 |
| rs200694956 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089102 | ATTAGATATAAAAAA[A/G]AAAAACCGTAGCCCT | 9678 |
| rs200697724 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111908 | TAGAATCTGTTCCTT[A/T]AAAAAAAAAACAAAA | 9678 |
| rs200723969 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073245 | CCTTCCATCTATGAG[C/T]CTGTAAAATCAAAAA | 9678 |
| rs200754100 | in-del | -/T | 0.0225045 | 0.103662 | intron-variant | PHF14 | GRCh38.p7 | 7:11124594 | TTAAGGTGGTTATTG[-/T]TTTTTTTTTATCTCC | 9678 |
| rs200757397 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984594 | TACTTTTGACCACAT[C/T]ACTTTCTTCATTTTT | 9678 |
| rs200785973 | in-del | -/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11053802 | CCTTTACTGGTCTGC[-/T]TTTTTTTATCCTAGA | 9678 |
| rs200786334 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023776 | GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCACGG | 9678 |
| rs200795184 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069715 | CTTTCTTGTCTTTCC[-/C]TTTTTTTTTGGTTGG | 9678 |
| rs200805558 | in-del | -/TG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122457 | CGTATATATATATAT[-/TG]TGTGTGTGTGTGTGT | 9678 |
| rs200808469 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048879 | AGTTACATTTGTTTT[G/T]ATTTTTTGAGTTGTT | 9678 |
| rs200820924 | in-del | -/AC | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11084201 | AACTTCAAAATATGT[-/AC]ACACACACACAATCT | 9678 |
| rs200862420 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988017 | GCGAAACTCCTTCTC[-/A]AAAAAAAAAAAAAAA | 9678 |
| rs200869700 | in-del | -/A | 0.0279526 | 0.114869 | intron-variant | PHF14 | GRCh38.p7 | 7:11025794 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAGAAAAA | 9678 |
| rs200882340 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087470 | GCTGGGGTTACAGGC[A/G]TGAGCCACTGCGCCT | 9678 |
| rs200885524 | snp | A/G | 9.21701e-05 | 0.00678797 | intron-variant | PHF14 | GRCh38.p7 | 7:11037138 | TGATAGATCTTACTG[A/G]TGATTTCTTTTGTGA | 9678 |
| rs200885729 | in-del | -/ATTTCCC | 0.0217236 | 0.101931 | intron-variant | PHF14 | GRCh38.p7 | 7:11164680 | AAAAATAGTGTAGAA[-/ATTTCCC]ATTTGCCTTTATCCA | 9678 |
| rs200930490 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015822 | TAGCTCATGCATAGA[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs200941334 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048895 | ATTTTTTGAGTTGTT[C/T]CGTGTTTTGTGGTGT | 9678 |
| rs201014921 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996480 | ACCCAGAGAAAACTG[-/T]TTCAAAAAGAGAGTC | 9678 |
| rs201033449 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065624 | TTTTCCTCTGCTGTA[C/T]TTTAAGTAAGGAAAT | 9678 |
| rs201054935 | in-del | -/TCT | 0.0256215 | 0.110247 | intron-variant | PHF14 | GRCh38.p7 | 7:11081478 | CGTAAATTTTCATCC[-/TCT]TATTTGACCCCTTAT | 9678 |
| rs201065056 | snp | G/T | 0.000287102 | 0.0119778 | intron-variant | PHF14 | GRCh38.p7 | 7:11035796 | GCACAGGTATGGGAT[G/T]CATGTCAAAACCCGT | 9678 |
| rs201073448 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124095 | AAAGTTGGTATCAGG[-/A]AAAAAAAAATACACT | 9678 |
| rs201088701 | snp | A/G | | | | | GRCh38.p7 | 7:10971018 | CTCCACCTGAAAAAG[A/G]GCATCTTTGAAAAAC | 9678 |
| rs201123246 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068072 | AATGAAATTCTGGGC[C/T]GGGTGCGGTGGCTCA | 9678 |
| rs201125751 | in-del | -/ATAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072697 | TCTGTTTACATTGCT[-/ATAA]ATAAATACCTGAGGC | 9678 |
| rs201153054 | in-del | -/TTC | 0.0271762 | 0.113356 | | | GRCh38.p7 | 7:10970140 | ATAATTATTATATAA[-/TTC]TTCTTCTTCTTTGTG | 9678 |
| rs201216743 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055850 | AATATTTTTTAGATG[G/T]TAGTTTAGGAAAAAT | 9678 |
| rs201225188 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087207 | TCTTTCTTTTTTTTT[-/G]TTAAGATGGAGTCTC | 9678 |
| rs201233738 | in-del | -/G | 0.0178098 | 0.0926698 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149255 | TTTTTTAACATGCTT[-/G]ATTTGCCATCATTTA | 9678 |
| rs201245092 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959655 | TGCCAGCATAGGCAC[C/T]GGCTCTCTGTGAGGC | 9678 |
| rs201339391 | in-del | -/AATGA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009492 | ACTGAGCACATATGA[-/AATGA]GTTTTATGTGTTTAT | 9678 |
| rs201345870 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128689 | TTAGATGTAAATCAG[-/TC]TCTCTCTCTCCCCCC | 9678 |
| rs201370974 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137591 | TTAACTTAAAAATTC[-/TT]TTTTTTTTTTTTTTT | 9678 |
| rs201371373 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127493 | GCCTTAACAAGCTCA[A/G]AAAGAACAGCCATTC | 9678 |
| rs201396026 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990865 | AATGTTGCTTTCTTT[-/TC]TCTCTTTTTAGAAAT | 9678 |
| rs201423764 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168035 | AAAAAAAAAAAAAAA[C/T]AAATGTCATCTGTAG | 9678 |
| rs201467297 | in-del | -/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11134215 | TTAGAAACTGAGTAC[-/T]TGCCTGTATTTTCAA | 9678 |
| rs201489548 | in-del | -/TTTC | 0.0166325 | 0.0896639 | intron-variant | PHF14 | GRCh38.p7 | 7:11156320 | TTGAAGCAAATTCAA[-/TTTC]TTTTTAACCCATGAA | 9678 |
| rs201508531 | snp | A/G | 3.05106e-05 | 0.00390568 | intron-variant | PHF14 | GRCh38.p7 | 7:11051582 | AAGATAATAATAAAT[A/G]CATGACTTAAATTTT | 9678 |
| rs201516181 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127257 | TCCTTTTTTTTTTTT[G/T]ACTCATTGCTAGAGC | 9678 |
| rs201535136 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157914 | CAAATGTACTTCTAA[A/G]TCATCTAACAAAAAT | 9678 |
| rs201539409 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159300 | ACTATTTTTTTTAAG[-/T]TCTGGGGTGCAGAAT | 9678 |
| rs201553206 | in-del | -/AAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027725 | GTCTTAAAGATATTT[-/AAAA]CATGCATGATTTCTA | 9678 |
| rs201555495 | snp | G/T | 0.000192234 | 0.00980204 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982980 | AATGAGGATGATGAA[G/T]ATGAGGGAAGCGGGA | 9678 |
| rs201565420 | in-del | -/GGGT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015010 | CCAATATAAGAGGGG[-/GGGT]GGGTACTTAAATTTT | 9678 |
| rs201570666 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958677 | ATGTTAGCTGTTTGG[A/C]CAACTGCTTACTTCT | 9678 |
| rs201573304 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11023877 | TTCTACAGTGGCCTC[-/T]TAAGTGTTCAAGTGA | 9678 |
| rs201577689 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148831 | CGCTTTCACCAACTG[C/T]GCATCTGAGCTCAAC | 9678 |
| rs201582151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121039 | CAGTAAAATGTAAAC[A/G]TAACAAACCACTGAA | 9678 |
| rs201588691 | in-del | -/GATTTT | 0.0197687 | 0.0974348 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960086 | CAGTAGTTACAAGTG[-/GATTTT]AAAAAAATTATTATT | 9678 |
| rs201611627 | snp | A/G | 0.000757264 | 0.0194437 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061993 | AGAGAGAAGACAAAG[A/G]CAGTCTGTGTTGCAA | 9678 |
| rs201633412 | snp | A/G | 8.74929e-05 | 0.00661353 | intron-variant | PHF14 | GRCh38.p7 | 7:11037117 | TACAAAATATGCAAC[A/G]TAATGTGATAGATCT | 9678 |
| rs201639181 | in-del | -/AGA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145956 | TTTTAAAGCAATGGC[-/AGA]TAACTCTTGAATATG | 9678 |
| rs201639778 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153948 | CCCTGTCTGTGTGTG[C/T]GTGTGTGTGTGTGTG | 9678 |
| rs201649515 | in-del | -/TAT | 0.02016 | 0.0983543 | intron-variant | PHF14 | GRCh38.p7 | 7:11154169 | TGCTATGACTTGGAC[-/TAT]TATTTACTAAATAAT | 9678 |
| rs201677864 | snp | C/T | 0.00055016 | 0.0165764 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051767 | AACCCAAGAAGATTC[C/T]GATAAGAAACACGGT | 9678 |
| rs201679712 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122348 | ATATATATATATATA[C/T]ATATACACACACACA | 9678 |
| rs201688116 | snp | C/T | 0.00144895 | 0.026877 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982468 | TTTTAGAAGAAGAAC[C/T]GAATGAAGATATTAA | 9678 |
| rs201706743 | snp | A/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064011 | GAAGATAATATCGTA[A/T]ATTGTCTGCAAAGTT | 9678 |
| rs201723432 | in-del | -/CCTT | 0.171704 | 0.237423 | intron-variant | PHF14 | GRCh38.p7 | 7:11069680 | CGTCCCCTCCCTTTC[-/CCTT]CCTTCCTTCCTTCCT | 9678 |
| rs201729948 | in-del | -/TATGTATAAA | 0.0252524 | 0.109492 | intron-variant | PHF14 | GRCh38.p7 | 7:11117622 | ACAAATATGTATTTG[-/TATGTATAAA]TATGTATAAATATAT | 9678 |
| rs201732828 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145956 | TTTTAAAGCAATGGC[-/A]GATAACTCTTGAATA | 9678 |
| rs201744143 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076554 | GCTTATCTTGGATAT[-/G]TTTTTTCTTTTTCTT | 9678 |
| rs201799459 | snp | G/T | 0.00299548 | 0.0385846 | intron-variant | PHF14 | GRCh38.p7 | 7:11040833 | TTTTTAAACTGATAC[G/T]TATTAGAAAGAAGAT | 9678 |
| rs201862196 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047049 | TACACGAATAAAATT[C/G]TCTAAATTAGTCCAC | 9678 |
| rs201865390 | in-del | -/ATAAATTAATGTAATATATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144582 | TATAATATATAAAAT[-/ATAAATTAATGTAATATATT]TATATAATAATATAT | 9678 |
| rs201874434 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157389 | CTGTCAATGGGTTAC[A/C]AAAAAAAAAAAATAG | 9678 |
| rs201887845 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074180 | ACCACCTTGAATTCC[C/T]CTCCTGAAAATGCCT | 9678 |
| rs201917441 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083663 | AGACAGGGTTTCACC[A/G/T]TCTTGGCCAGGCTGG | 9678 |
| rs201923929 | snp | C/G | 0.000182492 | 0.00955054 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982828 | TTCGACGAAACCGAC[C/G]ACTTCTGGATTTTGT | 9678 |
| rs201953862 | in-del | -/G | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:10987893 | TGGTGGTACATACCT[-/G]TAATCCCAGCTACTC | 9678 |
| rs201971731 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091394 | ATATAATAGGTGAAT[A/G]GAGGGTTTTTTTTAA | 9678 |
| rs201981853 | in-del | -/C | 0.0460142 | 0.144533 | intron-variant | PHF14 | GRCh38.p7 | 7:11031361 | TACTTTGTGAATATT[-/C]CAGATTTATTAAGAA | 9678 |
| rs202042887 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11123116 | GTTGGTTTCACAGTC[-/T]TTTTTTTCTCGCTGC | 9678 |
| rs202055293 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979554 | TTTCCTTTCTCTCTC[-/TT]TTTTTTTTTTTTTTG | 9678 |
| rs202056727 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046867 | TAAGAAAAAAAAAAA[-/A]CTCTGGTGTGGGATC | 9678 |
| rs202058514 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130907 | CCTTTTCTGAATGTC[A/G]TATAGTATGTAGCCT | 9678 |
| rs202135801 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034155 | TAAGGACACATTAGA[-/T]TTTTTTTTTCTTTCT | 9678 |
| rs202136511 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962511 | AGGATTTTTGCATCA[A/G]TGTTCATTGGGGATA | 9678 |
| rs202147228 | snp | A/T | 3.55e-05 | 0.00421293 | intron-variant | PHF14 | GRCh38.p7 | 7:11071268 | ATATTCCATGTTCCC[A/T]AGTCCATGTTACCTG | 9678 |
| rs202213418 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153971 | TGTGTGTGTGTGTGT[G/T]TTTTAAGAATAAGGA | 9678 |
| rs202215163 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088412 | CACACAAACACACAC[A/G]CACACGCACACACAC | 9678 |
| rs202232633 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038110 | GTGGTATTGTGGCTT[G/T]AATATATTAAAAATA | 9678 |
| rs202237372 | snp | A/G | 9.35789e-05 | 0.00683964 | intron-variant | PHF14 | GRCh38.p7 | 7:11051576 | AGCCAGAAGATAATA[A/G]TAAATGCATGACTTA | 9678 |
| rs367545692 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11038621 | CGAAATCGTGTCACC[A/G]CACTCCAGCCTGGTG | 9678 |
| rs367589743 | snp | C/G | 0.000369222 | 0.0135821 | intron-variant | PHF14 | GRCh38.p7 | 7:11042634 | ATAAGTAAACTGTTT[C/G]ACTATGATAATTATT | 9678 |
| rs367597428 | snp | A/G | 9.01754e-05 | 0.00671413 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974876 | GTGAAGCCTTTGGCA[A/G]CTTCTCTGCTGGAAG | 9678 |
| rs367631778 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:10994946 | TGGGGCAGCTTGCTC[G/T]TATCCCCTTCTCTGG | 9678 |
| rs367668916 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083393 | CTCTCTTTCTCCCCG[C/T]ACTCCCACCCCGTAT | 9678 |
| rs367672289 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067691 | ATGTTTATTTGGCTC[A/G]CAATTCTCATTGTTG | 9678 |
| rs367675084 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049354 | GTGGCACACACCTGT[A/G]GTCCCAGCTACTTAG | 9678 |
| rs367684036 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026867 | CATCACTGGGAAACT[A/G]AGTTGAAAATTAGGT | 9678 |
| rs367702725 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979487 | TTTATTGTAGACTTG[A/C]AATTAACTCTTTCTG | 9678 |
| rs367709801 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964579 | CTCTTCTCAAGGAGT[A/T]TCTTTGTGGTGTTCT | 9678 |
| rs367727047 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962358 | TGGTTTTTGCCATTG[A/G]TTCTGTTTATGTGAT | 9678 |
| rs367748567 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997747 | GCATGGACCTCCCTC[A/G]TAAGCTGCATGAATG | 9678 |
| rs367756255 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118663 | TTTCTGAAACCTATT[C/T]CTAGACAATGTTTTT | 9678 |
| rs367757665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033242 | AACGAGTTGCTTAAA[C/T]GAAGAAGTTGAATTC | 9678 |
| rs367827659 | snp | A/C | 1.75167e-05 | 0.0029594 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983097 | GTTCTTAGCAGAAAC[A/C]GTGCTGATGATGAGG | 9678 |
| rs367829932 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072305 | TCACCATCATGAGAA[C/G]AGCACCAAGAGGATG | 9678 |
| rs367843700 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116638 | CCCACATGGATACCT[A/C]CTTTGCTTGTCATTT | 9678 |
| rs367847437 | snp | C/T | 0.000165986 | 0.00910854 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036508 | GTTCCAAGGGAAAAA[C/T]TGCCCAGACCACTCA | 9678 |
| rs367855064 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094338 | TTCTTCTAGAGTGTT[C/T]GGGGGTAGAACCCAT | 9678 |
| rs367901814 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012472 | TGTGTTGTGTTGAAA[G/T]AAATCTGCATATAAG | 9678 |
| rs367913646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995517 | CGCACCAGGGCCACA[C/T]GTGGAGCTGCCCGCC | 9678 |
| rs367914130 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11102154 | AAAATATTTATTGAT[C/T]AAATATTTCCTTTTA | 9678 |
| rs367931871 | in-del | -/AATG | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11168146 | ATAAAATAAGGAAAA[-/AATG]AAATGACAAACAGTG | 9678 |
| rs367949894 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137502 | TTTTAATAGTTTTGA[A/G]TGGTTTTTTTAAAAC | 9678 |
| rs367954143 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083622 | CCCGCCACTACGCCC[A/G]GCTAACTTCTTTGTA | 9678 |
| rs367962180 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980014 | GGCATGGTTATAAAT[C/G]AAAAACAGAATCAAG | 9678 |
| rs367972044 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168865 | ATTCACCATGTTCCA[C/G]AGGAACCTGCTATGA | 9678 |
| rs367972495 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108333 | ACTATTGACTTCAAG[A/G]TTGGATTCTTTTCTT | 9678 |
| rs367976974 | in-del | -/ATTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165252 | GAAGACTACTGTTTA[-/ATTA]TATTGTAGAGGGTTT | 9678 |
| rs367995457 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052583 | CCAAACCAGTTCACA[C/T]TCATACCAGCAATGG | 9678 |
| rs367997202 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161836 | TAAATAAAAATATTA[C/T]AAATGAAGGAAAGTT | 9678 |
| rs368000281 | snp | G/T | 0.000129893 | 0.00805788 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022892 | TATTGTTTGTGCCCT[G/T]TATGTTCCTGGAGTA | 9678 |
| rs368008865 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068407 | ATGAACCTTGAGAAC[A/G]TTATGCTAAGTAAAA | 9678 |
| rs368009113 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122398 | ACATACATACACACA[C/T]ATATATATATACACG | 9678 |
| rs368026241 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073538 | TTGGCTGCTCTCATG[G/T]GTTGGAGTTAAATGC | 9678 |
| rs368026676 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127901 | TCATGATTTTTTTTT[-/T]CATAATTATCACTTC | 9678 |
| rs368037808 | snp | A/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117717 | CTTCAGGAGTATCTT[A/G/T]CCACAATACATTAAA | 9678 |
| rs368038117 | snp | C/G | | | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108238 | ATTCTAAGATAGAAA[C/G]AACAGATTTTTTTCA | 9678 |
| rs368048250 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095443 | TGATGGGTCTTTATT[C/G]TGTAATTAACTCAAT | 9678 |
| rs368052787 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097827 | TGTTTGTCCCTTCCT[C/G]TATTCTATCTTCTCC | 9678 |
| rs368076168 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129300 | CCATGACCCAAATAT[G/T]CAAAAAAGACCAAGA | 9678 |
| rs368102377 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143134 | TAATTGGCTTTTTCA[A/G]CAATGGAAAAACAAA | 9678 |
| rs368120919 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101622 | TTTTACTTTCTTTGG[A/C]GGTTATTCAGTTTGG | 9678 |
| rs368153168 | snp | A/T | | | | | GRCh38.p7 | 7:10969572 | ACTGTATTAAATCCC[A/T]CAATCTCAGTGTTGA | 9678 |
| rs368159069 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086147 | CCATCACCTTCTCTA[C/G]TTTGAGTACCTCTAG | 9678 |
| rs368175957 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997710 | TTTGATGGCTGTTGG[C/T]CAGAGACCTCAGTTT | 9678 |
| rs368177997 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041861 | ATTTTGGCTTTTTAA[-/GT]GTGTGTGTGTGTGTG | 9678 |
| rs368201905 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167972 | CGGAGCTTGCAGTGA[A/G]CAGAGATCGCGCCAC | 9678 |
| rs368214242 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109005 | TTTGATTATTAGCAA[A/T]CTGAACTCTGGCGCA | 9678 |
| rs368261488 | snp | C/T | 0.000157988 | 0.00888645 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983012 | TGATGAAGACGAGAA[C/T]GATGAAGGCAATGAT | 9678 |
| rs368264098 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016796 | TTTAGTTTTTCTTGA[C/T]TGTAGTCACCCTGTT | 9678 |
| rs368265289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995805 | CCAGGTGCTAAGCCC[C/T]TCACTGCCCGGGGCT | 9678 |
| rs368312525 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028886 | ACTCTATGTCCTATA[A/T]TAAGTGTAAATAATA | 9678 |
| rs368347506 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050851 | AATATGACCTTTTTT[C/T]TCCCCCAACACTTCT | 9678 |
| rs368347508 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091049 | GTCCAATGGAGATTT[A/G]TTGAAGACAAGGGAT | 9678 |
| rs368350980 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960702 | GTTTACAGTCTCACC[A/G]ACAGTATAAAAGCGT | 9678 |
| rs368351182 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076728 | GCACACCACCACACC[C/T]GACTAATTTTTGTAT | 9678 |
| rs368353159 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058427 | TCCCATAGCTTTCAA[C/T]ATTTTCTTGGTTGGA | 9678 |
| rs368371971 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11162250 | CACGCCACCATACCC[A/G]GCTAATTTTTTGTAT | 9678 |
| rs368382038 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143605 | AATAAAAGTCATGAC[A/C]TACCTTCGAGAGATT | 9678 |
| rs368400972 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PHF14 | GRCh38.p7 | 7:11135469 | TGTGTTTTTCATTTC[C/T]TTATTTGAAGACCAT | 9678 |
| rs368431765 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112720 | AGGTTGCAGTGAACC[A/G]AGATCACGCCATTGC | 9678 |
| rs368442921 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073931 | GCTCTGTGCATCAGC[C/T]GGAGCTGGAGCAGCC | 9678 |
| rs368456290 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10976209 | CTAATTGAATTCATC[C/T]GCAGCAATCAAAAAT | 9678 |
| rs368462578 | snp | A/T | 4.27506e-05 | 0.00462314 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042798 | AGGATGCCAAGAAAG[A/T]CCAAAAACAGTTATT | 9678 |
| rs368464311 | snp | C/T | 1.87327e-05 | 0.00306039 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982385 | AGATTCTGAAGGGAG[C/T]GGTAATGGAAGTGAA | 9678 |
| rs368477993 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133278 | AACAAAGTCAGAGGA[-/C]TGACACTACCCAACT | 9678 |
| rs368481563 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023253 | ATGCCTAATACATAG[A/G]CCAAAACCTTATTTA | 9678 |
| rs368496401 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129423 | CTGTTCACAGATTTC[C/T]TTGGAATAGACACAG | 9678 |
| rs368499299 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103406 | ATTATTGACTATACA[A/G]CCTACCAGCTGAAAG | 9678 |
| rs368508445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068109 | TAATCCCAGCACTTC[A/G]GAAGGCCAAGGCAGG | 9678 |
| rs368514627 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045363 | CTGTGCCTTAGTCTG[C/T]AGCTTGAACTTCCAC | 9678 |
| rs368522194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961893 | TTCTTGGTGTATAGG[A/G]ATGCTTGTCATTTTT | 9678 |
| rs368548757 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009548 | TGAAAAAGAAAATAT[C/G]TTTCCCATACTCATG | 9678 |
| rs368553355 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997155 | ACTTTTTATCTATAC[A/G]TACACATATAAGTTT | 9678 |
| rs368570207 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964905 | TCTTGTGCTGTGGTT[G/T]TCAGCTCCATTAGGT | 9678 |
| rs368575058 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985563 | TTACTGCTCTTAATG[A/G]CCTTAACATATGCTT | 9678 |
| rs368585732 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090538 | CATGGTCTGTAAATG[C/T]AGATCTTTTTTTAAA | 9678 |
| rs368598730 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11055823 | CTGAAAATATGAAAT[-/A]TGTTTCATATAAATA | 9678 |
| rs368635924 | in-del | -/T/TT | 0.499295 | 0.0187567 | intron-variant | PHF14 | GRCh38.p7 | 7:10991759 | TTTTTAATTTTTTAA[-/T/TT]TTTTTTTTTTTTTTT | 9678 |
| rs368640277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11019183 | TCATCAGAGATACTG[A/G]CCTGTAGTTTTCTTT | 9678 |
| rs368647078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11148868 | CCACAATTTTTGGAA[A/G]TATATTTTAAACTTT | 9678 |
| rs368647375 | snp | A/G | 5.588e-05 | 0.00528553 | intron-variant | PHF14 | GRCh38.p7 | 7:11061915 | AATTGTTTCCCTCAT[A/G]TCCTTATTTTGTTTG | 9678 |
| rs368648414 | in-del | -/CTAAT | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966605 | ACCTTGAAAGCCCAT[-/CTAAT]TGGTGGAATCTAAAT | 9678 |
| rs368650881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988166 | GTTTTCCCTATTTCC[C/T]TCTTTGCGTTACATT | 9678 |
| rs368654816 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170012 | CGATACTCTAGGACT[A/G]CAGGGAAAGACTAAA | 9678 |
| rs368656912 | snp | C/G | 1.6577e-05 | 0.00287893 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036576 | AGCAGAACTCATGGG[C/G]ATCAGTACAGATATC | 9678 |
| rs368658260 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124486 | TCATACTAATAATAA[C/T]AATAGAAGTTAACAT | 9678 |
| rs368659921 | in-del | -/C/CA/T | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11026109 | AGTGTGAGACTCCAT[-/C/CA/T]AAAAAAAAAAAAAAA | 9678 |
| rs368675415 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100797 | ATAATTTGAGTCTAG[G/T]CAGTCTTAACCATAC | 9678 |
| rs368681801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145076 | CCTCTGAACTGTATA[C/T]TTAAAATGGTTAAGA | 9678 |
| rs368691763 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119664 | TGGTTCCTCTAATTT[A/T]TTAAACATTTTAATT | 9678 |
| rs368723287 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11140102 | TCTATACACATTTCT[A/G]TACATGACTACACAT | 9678 |
| rs368743718 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032090 | GGCAACATAGCAAGA[C/T]CCAATCTCTACACAA | 9678 |
| rs368750971 | snp | C/T | 0.000163987 | 0.00905352 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051620 | TATGTAGGCAGTGCT[C/T]GGAATGTGACCAGGC | 9678 |
| rs368811307 | in-del | -/TTTCCCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164681 | AAAATAGTGTAGAAA[-/TTTCCCA]TTTGCCTTTATCCAG | 9678 |
| rs368826482 | in-del | -/TCTT | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106296 | GAATATTTTTGTCTT[-/TCTT]ACTACCCATTCATTC | 9678 |
| rs368858100 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113888 | AAGCTGTATATTATT[A/G]ACATCCAAGTCAAGA | 9678 |
| rs368865433 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077086 | CTTAGGAAATTCATA[G/T]TATGTTACCATCTAC | 9678 |
| rs368919839 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162818 | AGCCTCCCGAGTGGC[C/T]GGGATTACAGGCACA | 9678 |
| rs368928621 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075199 | CTGCCTCATCCTCCC[A/G]AAGTGCTGGGATTAC | 9678 |
| rs368946548 | snp | A/G | 0 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965352 | CTGCTGGAGTTTGCT[A/G]GAGGTCCTCTCCAGA | 9678 |
| rs368971708 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11005683 | AACCATAATGTACTT[-/A]TTTTTTTGTTTCAAG | 9678 |
| rs368973689 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11157332 | TAAATGTATTCCATA[C/T]TCTTCTAAAATGAGA | 9678 |
| rs368974079 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097130 | GATTACAGGCATGCA[C/T]CACCATGCCCGGCTA | 9678 |
| rs368979585 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082081 | GAGTGCAGTGGCTCA[C/T]GCTTGTAATCCCAGC | 9678 |
| rs368993978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11025590 | CGAGATCAGGAGATC[A/G]AGACCATCCCGGGTA | 9678 |
| rs369035176 | in-del | -/CAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151072 | AAATAGAATCTTAGA[-/CAAA]AAAACCTGTCATAAT | 9678 |
| rs369059306 | snp | A/G | | | | | GRCh38.p7 | 7:10969488 | ATCTCTTTACCCCCT[A/G]CATCTTGGATTTGGT | 9678 |
| rs369064696 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986530 | AGAGTTCACTGGACC[A/G]CACCTTGAGAACTGC | 9678 |
| rs369069246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000709 | ATTTTTAAAAATTGG[A/T]TTGTTTTCTTATTGT | 9678 |
| rs369082948 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10989193 | ATTGTTTTACAAATC[C/T]GCCGCAATTTTAGAT | 9678 |
| rs369089698 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965666 | TTTTGTTCAGATATG[A/C]CCTGCCCTAAGAGGT | 9678 |
| rs369094205 | snp | A/C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981646 | TCTTCCATTCTAGAG[A/C/T]ATATAGTAGTTACTG | 9678 |
| rs369098196 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007124 | CTTGAACCCAGGAGG[C/T]GGAGATTGCAGTGAG | 9678 |
| rs369111804 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109535 | TTTAGAAATCTCAGC[C/T]TTCTCATAAACTCAG | 9678 |
| rs369124365 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074398 | TGTATTTTTAGTAGA[C/G]GCAGGGTTTCGCCGT | 9678 |
| rs369124427 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978458 | TTTAGATAAACAGCA[A/G]TCTTGGTGAGGCAAA | 9678 |
| rs369140808 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021301 | ACAAGGAAGATTTTT[C/T]TTTAAATTGTAGATT | 9678 |
| rs369171482 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170015 | TACTCTAGGACTGCA[A/G]GGAAAGACTAAAAAG | 9678 |
| rs369183041 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091584 | AAAATGGTGAAACCC[A/G]TCTCTACTAAAAATA | 9678 |
| rs369183265 | in-del | -/TTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075565 | TGGGAAGGAAAGAGG[-/TTT]TTTTTTTTTTTTTTT | 9678 |
| rs369185806 | in-del | -/T | 0.371582 | 0.218444 | intron-variant | PHF14 | GRCh38.p7 | 7:11129549 | TTGTGTGTATGTTTC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs369188657 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109301 | AATACAAGAATTCAA[A/G]TAGAACAGCTGACTC | 9678 |
| rs369207304 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956958 | ACAAATGTAGATTTC[G/T]GTATCAGAAGTGATT | 9678 |
| rs369222548 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007692 | AATATTAAATAAAAT[A/G]TGGAAAATATAGAAC | 9678 |
| rs369242285 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074453 | CTGACCTCGTGATCC[A/G]CCTGCTTCAGCCTCC | 9678 |
| rs369243742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056902 | GCATTTATTCCCCAG[A/C]ATAAATCTAATGCTA | 9678 |
| rs369248875 | in-del | -/TTTTCTCCTTACTTTTTCCTTTTCTTTTTTCTAACTCCAC | 0.0681886 | 0.171594 | intron-variant | PHF14 | GRCh38.p7 | 7:11124031 | CATGCCTCTCACTGT[lengthTooLong]TTTTCTGAAGAAAGT | 9678 |
| rs369250837 | in-del | -/T | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11145516 | GAATTGAGCATTTTC[-/T]TAATTCTTATAATAT | 9678 |
| rs369252666 | in-del | -/ACCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084140 | TTCAAAGTATTTACA[-/ACCA]TTACTATTTGTTTAA | 9678 |
| rs369254700 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032877 | GAAATCTCCTTAAAT[G/T]AATCTGATGACAGTC | 9678 |
| rs369280793 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044584 | GTGTGCAAGATTCAG[A/T]GAATTGTTTTTTCTT | 9678 |
| rs369288953 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076146 | TTGCGTAACTAGAAA[A/G]TGTTGGAACTGAGAT | 9678 |
| rs369297521 | snp | A/C/G | 6.92357e-05 | 0.00588335 | intron-variant | PHF14 | GRCh38.p7 | 7:11035615 | GTACAAATGTTCACT[A/C/G]TTTTTCTGTGCTTTC | 9678 |
| rs369303920 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089819 | CTTGTTGCCCAGGCT[A/G]GAGTGCATTGGCGTG | 9678 |
| rs369306657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993458 | CTCCAGTTACTGTTA[C/T]TCATTTATATTTTTA | 9678 |
| rs369309709 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056117 | GGCAAACAGTTTTTG[C/T]AGTGAACTAGAACTC | 9678 |
| rs369318529 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065035 | ATACTTGTTATGTCA[A/G]AAAATGTACATGTCC | 9678 |
| rs369326766 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995947 | GGGAGCTGGCTCCAC[C/T]CTCGGCCAGCCCAGA | 9678 |
| rs369330279 | snp | C/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973247 | TCAGACTGATTGCGC[C/G]TTACTTCATTTACAT | 9678 |
| rs369355330 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004270 | AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAGAAAA | 9678 |
| rs369358446 | snp | A/G | 0.000337943 | 0.0129945 | intron-variant | PHF14 | GRCh38.p7 | 7:11051570 | AGCTAAAGCCAGAAG[A/G]TAATAATAAATGCAT | 9678 |
| rs369365864 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985026 | ATTTTCCCCTCAATT[C/G]TATTATTCAAGCTCT | 9678 |
| rs369384008 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157517 | TACCTCTTTTTCCCT[A/G]TATAGTAGACATTGT | 9678 |
| rs369391817 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104461 | GTCCAACTACTATAA[G/T]GAGAAAATTGATGTG | 9678 |
| rs369407608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137749 | TGCCACCACGCCTGG[C/T]TAATTTTTGTATTTT | 9678 |
| rs369413654 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161911 | ATGCGTATTTCCCAG[A/T]TATTAGTAGTTTACT | 9678 |
| rs369420458 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084841 | AATGTTTATTCACTC[A/T]TATATTGATGAACCA | 9678 |
| rs369429837 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026952 | AGCCTTCTAGACCTC[A/G]TTGTCTACTCATTTT | 9678 |
| rs369479117 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038981 | TCAGGGCCTAATCCT[C/T]TGGGATAATGATTTC | 9678 |
| rs369493765 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986911 | TCACAGAAAATATTT[A/G]AAATTAGAGACAGTT | 9678 |
| rs369505434 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001608 | GAGATCTTGGCAATA[G/T]TATTTTATTTTTTGG | 9678 |
| rs369508864 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962514 | ATTTTTGCATCAATG[C/T]TCATTGGGGATATTG | 9678 |
| rs369532575 | snp | G/T | 0.000113033 | 0.00751688 | intron-variant | PHF14 | GRCh38.p7 | 7:10990860 | AAGGTAATGTTGCTT[G/T]CTTTTCTCTCTTTTT | 9678 |
| rs369551936 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048297 | TTTGATTTCAGCTGG[A/G]CGTGGTGGCTCACGC | 9678 |
| rs369623193 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057818 | ATCACGGACAGATTA[C/T]GAGCAAGGTGATTTA | 9678 |
| rs369680789 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005615 | TCTGTAATTCTTCTC[A/G]TGTCAGTGTATGTGG | 9678 |
| rs369687744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11012922 | TACTCTGAACTTTTC[A/G]AACTGTTCTATAGCT | 9678 |
| rs369705160 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153364 | AACAACTGAGTCTTA[C/T]AGACCAAGTGAGGTA | 9678 |
| rs369714267 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980233 | AAGTTTTGATTGATA[A/G]AAAGCCTTCTAGAAG | 9678 |
| rs369715148 | snp | C/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977778 | AAATGTTAGGTTGAA[C/G/T]TATATGGAATTACCA | 9678 |
| rs369777859 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984302 | GTGGAGATGAGACAG[C/T]AGTTTATATTTGGAT | 9678 |
| rs369790575 | snp | C/T | 0.000159987 | 0.00894249 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982846 | TTCTGGATTTTGTGT[C/T]CATGGAAGAGCTGAA | 9678 |
| rs369798911 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11088817 | TAACAAATCAGTATT[-/A]AAAAATTATGTATCT | 9678 |
| rs369824563 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031066 | TAAACTAAAATAGAT[C/T]TATGTTTGTGAGCAT | 9678 |
| rs369831952 | snp | G/T | | | | | GRCh38.p7 | 7:10969613 | CAATTAATTCTAACT[G/T]ATTTTCTTTTTCTCT | 9678 |
| rs369834087 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962608 | AAATGAGTTAGGGAG[G/T]ATTCCCTCTTTTTCT | 9678 |
| rs369858488 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081653 | TGAAGTCAGGAGATC[A/G]AGACCATCCCGGCTA | 9678 |
| rs369860286 | in-del | -/TTCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008068 | TGTAGTGTGTCTGAA[-/TTCA]GGAGAATGTCAGGTA | 9678 |
| rs369861089 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155774 | AATGTTTTTTTTTTG[-/T]TTTTTTTTAGCAACT | 9678 |
| rs369873426 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036317 | GTGTGAGAAGTTCTG[A/G]TTATCTTTCTGTGAA | 9678 |
| rs369907209 | in-del | -/CGTATATATATATACACGTATATATATATACG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122412 | ACATATATATATACA[lengthTooLong]TATATATATATATTG | 9678 |
| rs369925204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10989927 | GTGAGCCACTGTGCC[C/T]ATCCTCTCTTTTTAT | 9678 |
| rs369938538 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068889 | AGATACTCAGATAGT[C/G]TTTATTTTTTCTCAC | 9678 |
| rs369951569 | snp | A/T | 0.000177984 | 0.00943189 | intron-variant | PHF14 | GRCh38.p7 | 7:11040624 | AGGAAAATGTTGCTT[A/T]TATTTCTTTCTTAAA | 9678 |
| rs369992704 | in-del | -/TAAATGAGT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077779 | TTCAGTTAAATGAGT[-/TAAATGAGT]GGAGCAATACAAGGT | 9678 |
| rs370005938 | snp | A/C | 6.9752e-05 | 0.00590518 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990745 | AACTGGAGCTCTCAA[A/C]AAATGGACCATATTC | 9678 |
| rs370013561 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124861 | TATTATAAATAAACA[C/T]GACTTCTAATCGGAA | 9678 |
| rs370021494 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067695 | TTATTTGGCTCACAA[A/T]TCTCATTGTTGGGAA | 9678 |
| rs370037590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096362 | TGACAATTTCACTTA[C/T]AGGAGAAAGGGAATT | 9678 |
| rs370052450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956607 | TTGCATACGTAATTA[A/G]TCCGGTGAGTTCATA | 9678 |
| rs370059828 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039309 | TTCATTTTTATGTTA[A/G]TTTGGTTTTCAGCTG | 9678 |
| rs370061997 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058436 | TTTCAACATTTTCTT[C/G]GTTGGAGGACTTGGT | 9678 |
| rs370063505 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023981 | AAAGCCTAGGTAGGC[C/G]AAAAGCTGGGCCTCT | 9678 |
| rs370070699 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168781 | TATACTTTGAAGGTT[A/G]CCATTTAATACTGAA | 9678 |
| rs370083035 | in-del | -/GT | | | | | GRCh38.p7 | 7:10969612 | CAATTAATTCTAACT[-/GT]TATTTTCTTTTTCTC | 9678 |
| rs370083834 | in-del | -/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964406 | TTGACTATTGGCCCC[-/C]ACTATCTTCTGGCTT | 9678 |
| rs370105877 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054109 | AAAAAAGCATTTTTT[-/T]AAGACACTTTTTTTT | 9678 |
| rs370124583 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012998 | ATTATAATCTGCCAC[C/T]TCCAAAATTAGATCA | 9678 |
| rs370132642 | snp | C/T | 0.00017298 | 0.0092984 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061821 | AAACGAAGCTTCGTT[C/T]CTGAGGAAGAAAAAC | 9678 |
| rs370133904 | snp | A/C | 0.000167986 | 0.00916323 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035648 | TGTATAGGATATAGC[A/C]GATCCATTCTTTGCT | 9678 |
| rs370134131 | snp | A/G | 0.000164294 | 0.009062 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982952 | GTCTCAGAAAGAGGG[A/G]AGTGATGGAGACAAT | 9678 |
| rs370143387 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017557 | TATATGTCTTTTTTT[-/T]GAGAAATGTCTATTC | 9678 |
| rs370158275 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997161 | TATCTATACATACAC[A/G]TATAAGTTTTATTGA | 9678 |
| rs370160888 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078211 | ACCCTTATTTTTCCC[C/T]TAATATTGTTGACAT | 9678 |
| rs370166339 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008764 | TTTTTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 9678 |
| rs370195255 | in-del | -/AAAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031198 | ATAGGCTGTTAAAAA[-/AAAAA]GGTTGAAAAATAGAA | 9678 |
| rs370245298 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111244 | AGGATAAAATTAACA[A/G]TGTTGAAGTTGAAAT | 9678 |
| rs370272407 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027016 | TGCTTAGTTCACTAG[C/T]ATTTTAAATGATTCA | 9678 |
| rs370273254 | in-del | -/ATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11154173 | ATGACTTGGACTATT[-/ATT]TACTAAATAATTACT | 9678 |
| rs370278752 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973882 | TTTTCACTTCCTTTT[C/T]AGAGCTGTATCCGGG | 9678 |
| rs370327251 | snp | A/G | 1.75891e-05 | 0.00296551 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013831 | GGTTTTGTGATGCCT[A/G]TAAATGTGGTGTTTC | 9678 |
| rs370366640 | snp | A/G | 0.000165986 | 0.00910854 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974837 | TTTCTCTTCACAGTG[A/G]ATCGCAGCTCCAAGA | 9678 |
| rs370384251 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068283 | TGAACCCGGAGGCAG[-/A]GGCTTGCAGTGAGCC | 9678 |
| rs370387020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990291 | ATAAGCTCCTAAAGT[A/G]TAAGAATCATGTCTT | 9678 |
| rs370392657 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987877 | CAGATCTAGCTGGGC[A/G]TGGTGGTACATACCT | 9678 |
| rs370436467 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009035 | AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 9678 |
| rs370439873 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11054903 | TCAAAGTATAATTTG[G/T]TTTCATGTTAGTCTT | 9678 |
| rs370455642 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002642 | GAGACGGGATTTCTC[A/C]ATGTTGGTCAGGCTG | 9678 |
| rs370469851 | snp | G/T | 0.00517822 | 0.0506191 | | | GRCh38.p7 | 7:10970463 | TAATCCCAGTTACCA[G/T]GGAGGCTGAGGCAGG | 9678 |
| rs370474181 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151937 | ATATACATTTTTCCT[C/G]TTCTATTTCTGTATC | 9678 |
| rs370481655 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128715 | CCCCCCGCCCCCACT[C/G]CTTTCCTCCCGTTCT | 9678 |
| rs370485690 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963922 | TTTTTTTCTTTCCAT[A/T]TGCTTGGTAGATCTT | 9678 |
| rs370492144 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162459 | TATGGAAATATATAA[A/G]TTTATAGAATTGGGA | 9678 |
| rs370529509 | in-del | -/ATATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161726 | TTTATTTAAATAAAA[-/ATATT]ATATTTTATTTAAAT | 9678 |
| rs370551121 | snp | A/G | 0.000167986 | 0.00916323 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051778 | ATTCCGATAAGAAAC[A/G]CGGTAGTTTATTTTT | 9678 |
| rs370553685 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099893 | ACTACTAAGCAGCAG[A/G]GAATGAGCTTTGTCA | 9678 |
| rs370564240 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070255 | GCTGATTTTTTAATC[A/G]TTTGTAGAAATGGGG | 9678 |
| rs370568945 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141927 | AAATACTAGCATATC[A/T]TCCTCAAATTATCAA | 9678 |
| rs370572126 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078583 | CAGAAGTTAAGAAGA[A/G]AAAGAAATTCAGAAA | 9678 |
| rs370591060 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043306 | TTTTTTATTAACTTA[A/G]GCATATCGAATCACT | 9678 |
| rs370606676 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959922 | ATGAGGTTATGTGGA[C/T]AACTGGAGGGTGAGC | 9678 |
| rs370638008 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105021 | ATTTTTTTTAATTTT[A/T]TAAAATTTAGTTAAA | 9678 |
| rs370643822 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115453 | AGAACAGGTACATAA[A/G]ACGTCACACATACAT | 9678 |
| rs370649757 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138680 | CACTTGCATATCATT[C/T]GTGCAAGTTCTTTAA | 9678 |
| rs370651975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11003175 | TGATCTCCTGACCTC[A/G]TGGTCCGCCCGCCTT | 9678 |
| rs370674951 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079218 | TATGTCTCTAGACTG[A/T]CCTCATGTATTATTA | 9678 |
| rs370691574 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161753 | ATTTAAATAAAAATA[-/T]TTAGATTTTAGATAA | 9678 |
| rs370694399 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090999 | AAGAGAATAGGTAGA[C/T]TGGGGCCTTGAGTGC | 9678 |
| rs370696246 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145848 | TACTTCTATCGTATA[C/T]GTTATACATTACCAT | 9678 |
| rs370710582 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988016 | AGCGAAACTCCTTCT[A/C]AAAAAAAAAAAAAAA | 9678 |
| rs370759765 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11010678 | ATCTGAAAAAATATA[C/T]ATACTTTTTTGAGAC | 9678 |
| rs370760663 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994371 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 9678 |
| rs370766341 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11167407 | AATCTTAATTTACGA[C/T]AGTTAAGAACAATAT | 9678 |
| rs370774069 | snp | C/T | 0.000139747 | 0.00835787 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036432 | GGCAAGGATCAATGC[C/T]CGGCTTCAGCAGTAT | 9678 |
| rs370777256 | snp | A/G | 0.000286515 | 0.0119656 | intron-variant | PHF14 | GRCh38.p7 | 7:11022851 | TTTGATAGCAAAATC[A/G]TATCTTCTCTTCTTA | 9678 |
| rs370810427 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082476 | ATTTTCTTCCCTCAC[A/G]TTTTCAATGTCTATT | 9678 |
| rs370831148 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111905 | TTATAGAATCTGTTC[C/T]TTTAAAAAAAAAACA | 9678 |
| rs370838802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11115799 | CTTTCCTTAACTTTC[A/G]TTAGCTTGTGACTTT | 9678 |
| rs370866789 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159562 | ATCATAGTAAAGATG[A/T]TTACCACAATAGAAA | 9678 |
| rs370877850 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966787 | CAGATACACCCTTCT[A/G]TCCGTAAACCTCCCC | 9678 |
| rs370892598 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070739 | TTGTCCACGAGGTGA[A/G]TATAGCATCTGGACC | 9678 |
| rs370909588 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964467 | GTCTGATGGGCTTCC[C/G]TTTGTGGGTAACCAG | 9678 |
| rs370916871 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11045006 | AGCACTTCAGATTTT[A/G]GATTTTTGGATTTGG | 9678 |
| rs370917419 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:10979315 | TTTTAAAAATTCTGT[A/G]ATGGTAAAAAATTTC | 9678 |
| rs370949166 | snp | C/T | 0.000140908 | 0.0083925 | intron-variant | PHF14 | GRCh38.p7 | 7:11061956 | TTTTATTATCCCTTG[C/T]ATGGCAGGAAAGAGT | 9678 |
| rs370955142 | snp | C/T | 0.000101408 | 0.00711995 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982991 | TGAAGATGAGGGAAG[C/T]GGGAGTGATGAAGAC | 9678 |
| rs370968113 | in-del | -/TT | 0.0505692 | 0.150756 | intron-variant | PHF14 | GRCh38.p7 | 7:11099531 | GTTCTCATTTTACAC[-/TT]TTATATTTCTGTAAG | 9678 |
| rs370973342 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049198 | TAAATTAGAGCCTGG[C/T]GCGGTGGCTCACACC | 9678 |
| rs370988656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018553 | TTCAGATTATTCACT[A/G]TTGTCACGTAGACAT | 9678 |
| rs371006629 | in-del | -/TGTGTCCTCACATTAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153887 | AGAGTCTCGAAGTAT[-/TGTGTCCTCACATTAT]AATACATAGAGGCAA | 9678 |
| rs371009517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062795 | GATGGGGGAGTGAGT[G/T]TGTGAACAAAAAGAG | 9678 |
| rs371024741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038460 | AAAAATAGATCGAGA[C/G]CATCCTGGCCAACAT | 9678 |
| rs371034221 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054374 | AATGGTGATTACCTT[C/T]CCTTTTTCCCTCTCA | 9678 |
| rs371048768 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988033 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAAAAG | 9678 |
| rs371066475 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11128039 | GTGCACTTTTTAAAA[C/G]CATTAGAGTCCTCCA | 9678 |
| rs371074725 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071481 | CACCCACTTCCTTTG[A/G]TAAATAGCAGATATT | 9678 |
| rs371075014 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11168440 | TTGGTTTGCTTTTAC[G/T]TTATAAAGTCAATTC | 9678 |
| rs371086514 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11053852 | ATTTGCTAATATAAT[A/C]CCATTCCTTTCATCT | 9678 |
| rs371122029 | snp | G/T | 6.05547e-05 | 0.00550215 | nc-transcript-variant, missense, intron-variant | PHF14 | GRCh38.p7 | 7:11169431 | GAAGATGAAAATGAA[G/T]CTGAAAGAAAAAATA | 9678 |
| rs371159617 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997623 | CCTGGGCTGTAGTCA[A/T]TTTAAGATTTGGCTG | 9678 |
| rs371186221 | snp | C/G | 0.000373176 | 0.0136546 | intron-variant | PHF14 | GRCh38.p7 | 7:11036722 | ACATGCACATTTTCA[C/G]TGAGAACAATTTGTT | 9678 |
| rs371206420 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010892 | ACTCCTGGGCTCAAG[C/T]GATCATCCTGCCTCA | 9678 |
| rs371218532 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083509 | GCCCTTGCTCTGTCG[C/T]CCAGGCTGCAGTGCA | 9678 |
| rs371256129 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068233 | GTGGGCACCAGTAGT[A/C]CCAGCTACTTGGGAG | 9678 |
| rs371273610 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097586 | GACTTTTGAACTTCA[C/T]CAGCAGTATCCCCAC | 9678 |
| rs371289638 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118198 | AAATCTGCGGTGTTT[C/T]GTAGACTTACTAAAA | 9678 |
| rs371298295 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11161195 | TTTTTTAATGGCAGT[A/G]TAGAAGTTTGGTAAA | 9678 |
| rs371299877 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975691 | AAAAATACTGATAAA[C/G]ATGAACAATGAAAAT | 9678 |
| rs371338357 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981935 | TCTTGTTTTGGTTTT[A/G]ACTCAATACTTACAA | 9678 |
| rs371367280 | snp | A/G/T | 3.3193e-05 | 0.00407377 | synonymous-codon, missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036510 | TCCAAGGGAAAAATT[A/G/T]CCCAGACCACTCACC | 9678 |
| rs371434080 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989088 | TTATTTGGTTTTATA[A/G]CACAGAGAAGCAAAA | 9678 |
| rs371435682 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004379 | TTTGGTTGCTTGCTC[A/T]TACATATACACAAAT | 9678 |
| rs371461794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11033925 | TTAATTTTTAAAGCT[A/G]TATGAAGTAATTGTA | 9678 |
| rs371463566 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129548 | TTTGTGTGTATGTTT[C/T]TTTTTTTTTTTTTTT | 9678 |
| rs371492078 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147904 | AAAGATTGGCTCAAA[C/T]TTAATGTTACCAAAA | 9678 |
| rs371514694 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165573 | CTACAAGGTAAACAA[-/A]GTTATCTGTACTCAT | 9678 |
| rs371524517 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063394 | CATAAGCGTAACATA[A/G]TGGAGTAAATGAAAC | 9678 |
| rs371541846 | snp | G/T | 5.10174e-05 | 0.00505035 | intron-variant | PHF14 | GRCh38.p7 | 7:11013917 | GGAAGGTTAATGTCC[G/T]AATTATGTTGGTTCA | 9678 |
| rs371548531 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136373 | TTTTGCCTTTGGCTG[G/T]TTTTATCTCTTTATT | 9678 |
| rs371559740 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150077 | TACATTGCAAGTCAC[A/G]GAAGATTTACATAGC | 9678 |
| rs371588027 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11072533 | AAATAGCAATAAACA[A/G]TAGTACCTACTCCAT | 9678 |
| rs371588747 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163944 | AGGTTGAGTGTCTAC[A/G]TGTTTTTTCCCTAAA | 9678 |
| rs371589920 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117417 | ATAGGAGATTTTCTA[A/G]AACTACAAATGCGTG | 9678 |
| rs371592423 | in-del | -/AG | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10976048 | CATTTTACAGGTAAC[-/AG]GGGTATTGAGTTTAA | 9678 |
| rs371618422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11045661 | CCAGAGTTCTGTGGA[C/T]TGTGCTGGGCAGGTT | 9678 |
| rs371670051 | snp | A/G | 0.000392027 | 0.013995 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102530 | AGCTCATCCTCGGAG[A/G]CAATCCCGGAAACCT | 9678 |
| rs371675860 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102665 | AAGTTGCCTTTTGCT[C/T]GTCAGGTTTGGATAG | 9678 |
| rs371689041 | snp | A/C | 1.77735e-05 | 0.00298101 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983154 | TCTCAAAGCAAGAGT[A/C]ATGAGGTAGATCAAC | 9678 |
| rs371709359 | snp | A/C/G | 0.000156525 | 0.00884536 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038783 | ATCTTTAGAAGAACT[A/C/G]CAAAACCTGAATGGA | 9678 |
| rs371710148 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114418 | TATGAGGGCAAAAAT[C/T]TCTATCTTTACCCCT | 9678 |
| rs371712934 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137656 | GCTAGAGTGCAATGG[C/T]ACAATCTCGGCTCCC | 9678 |
| rs371735614 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122333 | CTGTTTGTACTTTTT[A/T]TATATATATATATAT | 9678 |
| rs371741311 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037737 | ACGGGTATTGACTTA[C/T]TGTTAGAAAACATTT | 9678 |
| rs371793909 | snp | C/G/T | 0.00113547 | 0.0238004 | intron-variant | PHF14 | GRCh38.p7 | 7:11071309 | TTTGATCACAAGCTC[C/G/T]TGTGTAACATACTCA | 9678 |
| rs371800252 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102974 | CTGTTGTGATTGAAC[A/G]ATACAAATAACAAAC | 9678 |
| rs371804763 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086842 | GCTTTTATTGTTCTA[G/T]GTGTATGATACCTAT | 9678 |
| rs371825439 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143173 | GAACTATGGTTTATA[A/G]TACTAAAATGTGTAC | 9678 |
| rs371825757 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157484 | TCAAATGATGCTTCT[A/G]TGGAGAAATTTCTTA | 9678 |
| rs371859217 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035874 | TCCAGTGACATGTGA[C/T]GTATAATAGGAAGTT | 9678 |
| rs371887412 | in-del | -/AAATAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117628 | TGTATTTGTATGTAT[-/AAATAC]AAATATGTATAAATA | 9678 |
| rs371921162 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104970 | TTAGATTTCCTCTAG[A/T]TAAAAGAATTAGTAA | 9678 |
| rs371922148 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968141 | TAAAATCATTTAAAA[A/G]ACTGAAGGAGTGAAA | 9678 |
| rs371934303 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092744 | GAGACCAAGAGCTCC[A/G]TTCTTTACTCGCTGA | 9678 |
| rs371973677 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038656 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 9678 |
| rs371973949 | snp | G/T | 0.000424854 | 0.0145687 | intron-variant | PHF14 | GRCh38.p7 | 7:11023023 | GAAAGAGAAAGGTTT[G/T]ACTTGTTAGTTTACC | 9678 |
| rs372006818 | in-del | -/TCCGCCT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143365 | GGGTCAAGTGATTCT[-/TCCGCCT]CTGCCTCCGAAAATG | 9678 |
| rs372011487 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088402 | TGTTCACATACACAC[-/AA]ACACACACACACACG | 9678 |
| rs372026673 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008273 | AAGATATCCTTAGGA[A/G]TGTTCACTGGATAGT | 9678 |
| rs372028912 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124655 | CAGAGAAGTTAAGGA[C/T]TACACAGCTAATAAG | 9678 |
| rs372029234 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979680 | ATTATTACCCAGCTA[C/T]GGTTGTAAATAAATA | 9678 |
| rs372152961 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050812 | GTATATTTCTTCTTT[C/T]AGAAGTAGTAGGGGC | 9678 |
| rs372214081 | snp | A/G | 0.000100082 | 0.00707325 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983013 | GATGAAGACGAGAAT[A/G]ATGAAGGCAATGATG | 9678 |
| rs372224460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086780 | ATGGTAGTTTTTGTC[A/G]TCATTTGAATATAAT | 9678 |
| rs372228055 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991452 | AGGTGTTGGATTACA[G/T]GCGTGAACTACCGCG | 9678 |
| rs372239231 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073582 | AGGCTCAGGGTGCAA[A/G]CTGCTGGTGGCTCTA | 9678 |
| rs372241731 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055358 | AGTCATGTAGTGACT[G/T]TTCATCTTTTGTAGA | 9678 |
| rs372270930 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161875 | AGGAGCCTCTTAATA[C/T]AGATTTCTAGCATAC | 9678 |
| rs372284209 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157816 | TAATGAGCTGAAATC[A/T]TAGAAATACTGAAAC | 9678 |
| rs372290299 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023423 | TTAATAGATGGTGAA[C/G]TTAATTGATATATGT | 9678 |
| rs372291776 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962163 | CCTTGTGTTGTGCAG[A/C]TTTTCAAAGGGAATG | 9678 |
| rs372296233 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024411 | ATTCAACAAAGATTT[G/T]CAATGTAGATGAAAC | 9678 |
| rs372307413 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015013 | ATATAAGAGGGGGGG[-/T]GGGTACTTAAATTTT | 9678 |
| rs372325845 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992693 | ACAAAAAAAGGCATT[C/T]TCTTACATAACCACA | 9678 |
| rs372329463 | snp | A/G | 7.27008e-05 | 0.00602869 | intron-variant | PHF14 | GRCh38.p7 | 7:11042647 | TTCACTATGATAATT[A/G]TTATTGAAATCTTTA | 9678 |
| rs372335318 | snp | G/T | 4.58873e-05 | 0.00478974 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974900 | CTGGAAGCTCTTGAT[G/T]ATGATAGTTCAGATG | 9678 |
| rs372405961 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074081 | TCTCCAAAATGCGTT[A/C]AATGCCTTTCCCCCA | 9678 |
| rs372429179 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022533 | ATGAAAATGATGTTT[C/T]GTTTCATTTGAATAG | 9678 |
| rs372432370 | in-del | -/CCCATTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164684 | ATAGTGTAGAAATTT[-/CCCATTT]GCCTTTATCCAGCTT | 9678 |
| rs372471473 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988113 | CCAGTTGAAACATTG[C/T]CTGCTAGCCATTTAG | 9678 |
| rs372480526 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150712 | AATCAGCATACTATT[A/T]GGTATTTATTGTGCT | 9678 |
| rs372511157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962530 | TCATTGGGGATATTG[A/G]CCTGCAATTCTTTTT | 9678 |
| rs372515728 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999838 | AGGATGTTGTGTCTA[C/T]ATAAAGTCATGTAAC | 9678 |
| rs372522731 | snp | A/T | 3.34644e-05 | 0.00409036 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013880 | TCCTAATCAGGATGG[A/T]ATTTTCAAGGAGACA | 9678 |
| rs372587045 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11138263 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT | 9678 |
| rs372609599 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066738 | TGGCTTTTTCAATGT[A/G]GGCTTATTTCTAGAC | 9678 |
| rs372620083 | snp | G/T | 0.000167986 | 0.00916323 | intron-variant | PHF14 | GRCh38.p7 | 7:11038884 | CAATTGCTGTCTCCT[G/T]CAGTTCTTGCTCCCT | 9678 |
| rs372707085 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135890 | AAAGCTAATTTATAG[C/G]TTACATAATTTTCAG | 9678 |
| rs372710656 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158680 | TTTCATACAAACAAT[G/T]GGGATTTAAATAAGA | 9678 |
| rs372726769 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11003374 | CTTTTACCCAGATTC[C/T]TCTTGTTCCACAAAT | 9678 |
| rs372727689 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961212 | TTTTTATGGTTTTAG[A/G]TGTTACATTTAAGTC | 9678 |
| rs372733900 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11050881 | TTGGAGTCTGTTTGT[A/C]TAGTTTCTTTAAGTA | 9678 |
| rs372740552 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995630 | GGAGGCTCAGGCCAC[G/T]CAGGAGCCCATGGCG | 9678 |
| rs372766227 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000787 | GATAGGTCTTTTGCA[A/G]ATACTTTCTCCCAGT | 9678 |
| rs372772837 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965078 | TTCTGTCAACTCTCA[A/T]ACTCATTCTCCATCC | 9678 |
| rs372787251 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076774 | GGTTTTGCAATGTTG[G/T]CCAGGCTCATCTCTA | 9678 |
| rs372812709 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993652 | AAATGAAGTAGGACA[A/G]GGAGTATAGGAATGC | 9678 |
| rs372836398 | in-del | -/GTAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122443 | CGTATATATATATAC[-/GTAT]ATATATATATTGTGT | 9678 |
| rs372843547 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11025600 | AGATCAAGACCATCC[C/T]GGGTAACACGGTGAA | 9678 |
| rs372849343 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056136 | GAACTAGAACTCACT[C/T]TGGCTACTTGGAAGA | 9678 |
| rs372869167 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168238 | CATTCCTGGTGTTCT[A/G]CATATCTATAATGAT | 9678 |
| rs372873525 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10982180 | CTATACTGAACTAAA[A/G]CCATTGTATCAACTT | 9678 |
| rs372882423 | snp | A/G | 0.000149126 | 0.00863371 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028803 | AGGTCTGCTTTCAGA[A/G]GCAGCGGCGGAAGAG | 9678 |
| rs372883049 | snp | C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973578 | CGTTTACTCAGTAAA[C/T]CCTTAAAAAACAGAT | 9678 |
| rs372896968 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139631 | GAATGTATCTATTTC[-/A]CACTAACCCTAAAGT | 9678 |
| rs372899815 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055675 | TGAGCCACTAGCCAG[C/T]TCTAAGTGGCAGTCT | 9678 |
| rs372941540 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013491 | TTTAAATTAAAAATT[G/T]ATTGTTTTCCCACCT | 9678 |
| rs372948537 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996396 | TAAATGCTTGTAACA[A/G]AGTCATCCTAGTACT | 9678 |
| rs372949454 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11069864 | TTTATTTATTTATTT[A/T]TTTCTGGTAGAAGTA | 9678 |
| rs372969091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053987 | GCAGTGTGATTATTT[A/T]CTTACTTGTAGAAAT | 9678 |
| rs372971181 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965547 | CCACTTGAGGAGGCC[A/G]TCTGTCTGTTAATGG | 9678 |
| rs372984990 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995824 | CTGCCCGGGGCTGGC[A/T]GTGCCCGCCAAGCCC | 9678 |
| rs372990079 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996447 | ATGGCCAGTGAGATA[C/T]GAGGACCATGGGTGA | 9678 |
| rs372993821 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152226 | GCTTTTAAAATTTAT[C/T]GATCATGAGCAATTC | 9678 |
| rs372994020 | snp | A/T | 3.79168e-05 | 0.00435396 | intron-variant | PHF14 | GRCh38.p7 | 7:11111476 | TTCCAAGGTAAGGGG[A/T]GAAGTCTATAAGAAA | 9678 |
| rs372996785 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104516 | GATTCATATTTCACA[A/G]ACCTACATAAGAAAA | 9678 |
| rs373003305 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980391 | CTGTGTCTTAGAAGT[A/G]TTGAGTCAACTCTGG | 9678 |
| rs373004825 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030679 | CATTAGGATGTGAGA[A/G]TTAGCCCTGAGGCAT | 9678 |
| rs373025398 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131224 | TGGGATCATATGGTA[A/G]GAGTGTGTTTGGCTG | 9678 |
| rs373032687 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089856 | GCTCACCACAAACTC[C/T]ACCTCCTGGCTTCAA | 9678 |
| rs373035212 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138277 | CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC | 9678 |
| rs373036263 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110152 | TAAAGTCAATTGTTT[C/T]TCTTTGTGTGTTGTT | 9678 |
| rs373038057 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11074651 | ACTCTTAAGTTCAAA[A/C]TTCCATAGATCCCAA | 9678 |
| rs373039518 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11082548 | AATCATTTATGCTTT[A/C]TGATTTATAAATTCA | 9678 |
| rs373093481 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061298 | TAGGATTTTGGATAT[C/G]TGAGAACTTTTCCTT | 9678 |
| rs373097187 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104450 | GTCCATAATCGGTCC[A/T]ACTACTATAAGGAGA | 9678 |
| rs373098665 | in-del | -/TTTATTAAAAGACTT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11040026 | TAAAAGACATTTTCA[-/TTTATTAAAAGACTT]TTAACAGAGGTTTGC | 9678 |
| rs373115349 | snp | A/C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093851 | TCCTTCTGACTCTCA[A/C/G]GGGTAGGAGACCTTT | 9678 |
| rs373129906 | in-del | -/T | 0.495927 | 0.0449436 | intron-variant | PHF14 | GRCh38.p7 | 7:11162701 | GGGAAATCCAAAGTC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs373143445 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137904 | GTTGAGTCATTCTTA[A/G]TCTTGTATTAAATAA | 9678 |
| rs373150504 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105891 | ATTGTAAAATCAGGA[C/T]CTACACTATTGATTA | 9678 |
| rs373150602 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162052 | CCCCTTCAGATCAGC[A/C]GGATATCTTAAAAAT | 9678 |
| rs373157702 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11070959 | TTTTTGAAAATATAA[A/G]AACTTTTAAAATTAC | 9678 |
| rs373159951 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052193 | TACTTATAAATAATA[C/G]ATGGTTTATTTTTGT | 9678 |
| rs373161301 | snp | A/G | 0.000165986 | 0.00910854 | intron-variant | PHF14 | GRCh38.p7 | 7:11028827 | GGAAGAGGTAGGTTT[A/G]TTTAAACCCATAGTT | 9678 |
| rs373197545 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965402 | ACCAGCGGAGGCTGC[A/G]GAACAGCAAATATTG | 9678 |
| rs373211361 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018737 | TGCCCTTTTTATCTT[C/T]CTGTTGTCTGATTGC | 9678 |
| rs373233668 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145331 | CATTTCAGTGAGGCT[C/T]TAGGAGGAAAAACAG | 9678 |
| rs373236835 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140155 | ATACCCCTGCACACA[C/G]CTGTACATACATCTC | 9678 |
| rs373272599 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002459 | TTATTTATTTTTGAG[A/G]CGGAGTTTTGCTCTT | 9678 |
| rs373295949 | snp | A/T | | | | | GRCh38.p7 | 7:10969614 | AATTAATTCTAACTT[A/T]TTTTCTTTTTCTCTT | 9678 |
| rs373331105 | snp | C/G | 0.000233618 | 0.0108053 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990770 | ATATTCTGATTTGCT[C/G]TGTTTGTCTGGGAGA | 9678 |
| rs373355026 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957447 | CTTATTTGTCTGTCT[A/G]ATATATAATATTGTA | 9678 |
| rs373366735 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076879 | AGCTTTCAAATATGG[-/T]TTTTTTTTTTTTTGG | 9678 |
| rs373370999 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989248 | AATTATTAATTGTGA[C/T]CTTCAAGTGTATTCA | 9678 |
| rs373386472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989589 | CAAGCAGACCCTCTT[C/T]TGAAATTTTATCTTT | 9678 |
| rs373391714 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010715 | TTGCTCTGTTGCCCA[A/G]GCTGGTTCACTGGCA | 9678 |
| rs373401340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11029425 | TTAGTGGAGACTTCC[A/G]GAGATTACATACAGT | 9678 |
| rs373425466 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988534 | ATTAGTTTCTAGTCT[G/T]TTTTTTTTTTTTTTT | 9678 |
| rs373433324 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051481 | TTTTCATTATGTACC[C/T]TATAATCACATTACC | 9678 |
| rs373462005 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11037221 | GCTCTTCCCTATAAC[G/T]CCTACTCCTCATTAG | 9678 |
| rs373499489 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069245 | CACACATACCCTTGT[A/G]CTTAGAGGAGAAATT | 9678 |
| rs373504024 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033927 | AATTTTTAAAGCTAT[A/G]TGAAGTAATTGTAAG | 9678 |
| rs373551248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984397 | TCATTCTAATTCTTA[A/C]CTTTAAAGGAAAGTT | 9678 |
| rs373570852 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111150 | TTTTATTGCTGTTGT[A/T]TTTTGTTTTTGCTAA | 9678 |
| rs373588595 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099223 | GGAATGGCTAACCTG[-/TC]TAACACATTTAGTAT | 9678 |
| rs373590650 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115448 | ACTATAGAACAGGTA[C/T]ATAAAACGTCACACA | 9678 |
| rs373592108 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147000 | TACAGGTGTGTGCCA[C/T]GACACCTGGCTAATT | 9678 |
| rs373608544 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016477 | ATGATGTGATTTAAT[A/G]TAAGAAAACCAGTAC | 9678 |
| rs373619933 | snp | A/G | 8.56274e-05 | 0.00654266 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061831 | TCGTTCCTGAGGAAG[A/G]AAAACATGAGGTTGG | 9678 |
| rs373644634 | snp | A/G | 1.69e-05 | 0.00290684 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982884 | GATGACTATGACAGT[A/G]AGGATGACAATGATT | 9678 |
| rs373650645 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053609 | ATGAAACATTATTTT[C/T]CCAGTTTCTTTATTG | 9678 |
| rs373672469 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142261 | TCAGGTATCTTCACA[G/T]TTAAAGCTGGTAGAA | 9678 |
| rs373694918 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045425 | CGGTTTATTTTTGCT[G/T]TCTTTATGTTTTGCA | 9678 |
| rs373703371 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090613 | ATTTGACTTTTTCCA[A/G]AGCTTGTAACTGTAA | 9678 |
| rs373706841 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027034 | TTTAAATGATTCAGG[C/T]GATTGAGGAAGATTC | 9678 |
| rs373716449 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076194 | GGCTACAGAGTCCAT[A/G]GTTTTAACCTCTATA | 9678 |
| rs373727440 | in-del | -/TTAA | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11168590 | ATTGATGTTTATGCT[-/TTAA]TTAACTCAGAAGAGT | 9678 |
| rs373779137 | snp | C/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149682 | ATAAATAAAAGAATG[C/G]TGATACAGAATTTAA | 9678 |
| rs373797547 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083621 | GCCCGCCACTACGCC[C/T]GGCTAACTTCTTTGT | 9678 |
| rs373802740 | snp | A/G | 7.67332e-05 | 0.0061936 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111429 | AAACAGACAGGCTAC[A/G]GATGGATATGTCAGG | 9678 |
| rs373805359 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011633 | GTGTCTCAGGAGACT[A/G]GAGAAATGCCCAAAC | 9678 |
| rs373820769 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039064 | TAATTTGGTTGTTTC[A/G]ACAGCTATCTTGTGT | 9678 |
| rs373823566 | in-del | -/GA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152663 | GTAATAAGAAAAACA[-/GA]AAATCTGCTGTCGTG | 9678 |
| rs373834240 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024435 | ATGAAACAGTCTTCT[A/G]TTGGAAGAAGATGCC | 9678 |
| rs373868701 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063304 | AGTAGTAAGTAGTTC[C/T]AAGTTCAGGAGATAC | 9678 |
| rs373873886 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074360 | GGACTACAGGCGCCT[A/G]CCACCACGCCCAGCT | 9678 |
| rs373901636 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084510 | GTTTTTTTTTTTTTT[A/T]AACTTCACAATGCAT | 9678 |
| rs373917896 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091652 | AGTTCCAGCTACTCC[A/G]GAGGCTGAGGTGGAA | 9678 |
| rs373936968 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162524 | TATCATCCATCATTC[A/C]TTTCCTTTCCTTTCT | 9678 |
| rs373937733 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143093 | TGCCTTACTTTGGGT[A/G]TCTATATTTCTTGAA | 9678 |
| rs373939483 | snp | C/T | 1.95486e-05 | 0.00312633 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982936 | GAAAAGGGAGATCTG[C/T]GTCTCAGAAAGAGGG | 9678 |
| rs373950707 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139234 | TTTATTAAAAAACAT[A/T]TTGAGAGAAAATGTT | 9678 |
| rs374001912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057522 | TGGGATTACAGGTGT[A/G]CACCACCACGTCCGG | 9678 |
| rs374024429 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074827 | CACTTAACAATACTC[-/T]TAAGAAGTTCCAAAT | 9678 |
| rs374032573 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11074871 | CTGTCTTCTTCTCAG[C/T]CCTCTAAACTCTTCC | 9678 |
| rs374071167 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156627 | GGTGAAACCCTATCT[C/T]TACTAAAAAATACAA | 9678 |
| rs374102578 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089977 | GGTTTCTCCATGTTG[G/T]TCAGGCTGGTCTCGA | 9678 |
| rs374112332 | snp | C/T | 0.000167986 | 0.00916323 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974307 | TCTTCTCCAAACGAC[C/T]ACCTCACGGATTCCT | 9678 |
| rs374137086 | snp | A/G | 8.29277e-05 | 0.00643871 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036519 | AAAATTGCCCAGACC[A/G]CTCACCAGCAGTGCT | 9678 |
| rs374147032 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147099 | GAGATCTGCCCACCT[C/T]GGCTTCCCAAAGTGC | 9678 |
| rs374170436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071925 | AAGCCTGCTAAATTT[A/G]TATTAAGAGCCTAGA | 9678 |
| rs374200554 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964027 | GGTCTTGACTCTTTA[A/T]CCAATTTTCCAGTCT | 9678 |
| rs374213180 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994622 | GTGTCCGGAATTGGT[C/G]GGTTCTTGGTTTCAC | 9678 |
| rs374221044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967180 | GCCTAAAACCTGCAA[C/T]TTGTGTATTCAGATT | 9678 |
| rs374227170 | in-del | -/AGATATGA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123428 | AATTAAATATTCTGA[-/AGATATGA]TTAAATATGCTATAA | 9678 |
| rs374231440 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140614 | CTTGTTTTTCTTATA[C/G]AAAGAAATAATATAA | 9678 |
| rs374240301 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11094284 | AAGACATAAGTCCAA[A/T]ACCAGTTTCATTTGG | 9678 |
| rs374242270 | in-del | -/CTGT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983944 | TTTGTGTCTCTTTGT[-/CTGT]GTGTTTTTGTATATG | 9678 |
| rs374242715 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070618 | ATGTGGCCCCATATT[A/G]ATCGTCTTACATTGA | 9678 |
| rs374261675 | snp | G/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169661 | TTTTAGAGTAATTTC[G/T]ACTTTTTTATTCAAA | 9678 |
| rs374269960 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040393 | TTTTTAAACCTCCTA[C/T]GTATGTGTCTTTGTC | 9678 |
| rs374285263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062934 | GTCTTCTGGTAAAGC[C/T]CTGTTAAATTAACTG | 9678 |
| rs374318335 | in-del | -/AAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071902 | TTAATTTTGGATATT[-/AAA]AAAGTAAGCCTGCTA | 9678 |
| rs374331487 | in-del | -/GT | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11041860 | ATTTTGGCTTTTTAA[-/GT]GTGTGTGTGTGTGTG | 9678 |
| rs374339821 | in-del | -/GAA | 0.00100123 | 0.022352 | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10982566 | AAAATGGAAAAGAAG[-/GAA]GAAGAAGAAAATGGA | 9678 |
| rs374351619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112406 | CTGCAAAAGTTTATT[C/T]ATTAAAAACTGCAAA | 9678 |
| rs374356828 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049639 | TTTCTCTAGTCATCT[G/T]TTTTGAAGGCTGTTG | 9678 |
| rs374406203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159250 | ATTTATATAAATTCT[A/G]TTTGTTTTTGGTTTT | 9678 |
| rs374418290 | snp | C/T | 9.12534e-05 | 0.00675414 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974870 | AGGCAGGTGAAGCCT[C/T]TGGCAGCTTCTCTGC | 9678 |
| rs374457982 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089438 | GCTCATACCTGTAAT[C/T]CCAGCACCTAGGGAG | 9678 |
| rs374458038 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089417 | GAAATTCAGCTGGGC[A/G]TGGTGGCTCATACCT | 9678 |
| rs374468111 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974611 | CTGGTCTGAGTTGGC[C/G]TTGGCAGCATCAGGG | 9678 |
| rs374488027 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962916 | TTTCTGTGGGATCAG[C/T]GGTGATATCCCCTTT | 9678 |
| rs374488424 | snp | C/G | 6.58913e-05 | 0.00573945 | intron-variant | PHF14 | GRCh38.p7 | 7:10974962 | TAAATATTTCCTTCT[C/G]TCTTCCCCTTTCCCA | 9678 |
| rs374514822 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966946 | CATTTATAGGGATGC[A/C]GTGAGAGAGATGGGC | 9678 |
| rs374530838 | snp | A/G | 5.14708e-05 | 0.00507274 | intron-variant | PHF14 | GRCh38.p7 | 7:11013932 | TAATTATGTTGGTTC[A/G]TATGTTTGCTTTATA | 9678 |
| rs374575711 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128764 | CTCCCTCCTCTCTCC[C/T]TCTCTTTTTCTCTTC | 9678 |
| rs374593297 | snp | G/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065801 | TTTATCTTAACTTTA[G/T]AGACTCAATGTGGCA | 9678 |
| rs374602064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047127 | AGGCTGGGGTGCAGT[A/G]GCACAATCGCAACTC | 9678 |
| rs374621276 | snp | A/G | 6.18487e-05 | 0.00556062 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982972 | ATGGAGACAATGAGG[A/G]TGATGAAGATGAGGG | 9678 |
| rs374625547 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979349 | ACTGTCTGTTAGTTG[A/G]AATAGCTGTTGCTTG | 9678 |
| rs374639835 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049244 | TTGGAAGGCTGAGGC[A/G]GGAGGATCACCTGAG | 9678 |
| rs374649933 | in-del | -/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11005149 | GTGGGGTAATAACTT[-/G]TGAGACTCTGTTAAT | 9678 |
| rs374664759 | snp | A/G | 6.69344e-05 | 0.0057847 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982770 | GTTCCCACTACGACA[A/G]CCGCTACAGAGGAAC | 9678 |
| rs374664932 | snp | C/G | 1.66087e-05 | 0.00288168 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051719 | GGCAGATTAAGGAAC[C/G]AGTGAAATTTGTTCC | 9678 |
| rs374731275 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11148642 | GAAGGCCATGAGGAC[G/T]ATACGCTGTTGTTCA | 9678 |
| rs374750118 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161757 | AAATAAAAATATTTA[G/T]ATTTTAGATAACATT | 9678 |
| rs374784102 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077558 | GTGAGCCCAGATCGC[A/G]CCACTGCACTCCGGC | 9678 |
| rs374786183 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058854 | TACCTCAGAAACTTA[C/G]CAGCTGTGTGACATC | 9678 |
| rs374790837 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036888 | TAAAAGTTTTAAACT[A/G]TGTAGGTTTATCAAT | 9678 |
| rs374806213 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960247 | CCTTCTCCAGCACCC[C/T]ACCCCCCTACAGGCC | 9678 |
| rs374833261 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033198 | GCATTAATTAGGACA[C/T]TATTTTGACTGGTTT | 9678 |
| rs374850904 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141777 | AAAGCTAGTCTGAAC[A/G]TGTGTCTAACAGCTG | 9678 |
| rs374855578 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164988 | GCAGTGCAGTGGCGC[A/G]ATCTCCGCTCACTGC | 9678 |
| rs374866138 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056485 | AACCCTGTTAACATA[A/G]GCTAAATTAGATAAA | 9678 |
| rs374869859 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094443 | CACATCTATTTATCT[C/T]TCTGATTCTGACTCC | 9678 |
| rs374871633 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11055911 | GTGACTAAAGGTTAC[G/T]GTACATTATGTTCAT | 9678 |
| rs374878136 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055396 | AAGGACTTGTTGGGA[C/T]CTCTCTTTCCATTGT | 9678 |
| rs374890621 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11034213 | TTGTCATTTCTCTTT[A/G]GGTTGTAAAACTCTA | 9678 |
| rs374916021 | snp | A/C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992867 | ATGTCTGTTTAGTCA[A/C/T]CTTTAATGTAGAACA | 9678 |
| rs374927878 | in-del | -/CAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145043 | GTGATGGTTTCACAA[-/CAA]TATAAATATTTAATA | 9678 |
| rs374955648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990383 | CGTTTTTCCTAGTTT[A/G]AGGGGCAAAGCAGAA | 9678 |
| rs374988340 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136884 | TTAATTACTTAAAAA[A/C]AATTATGAACTAGCA | 9678 |
| rs374994231 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11069032 | TTAGAGTTTAGAGCT[G/T]CCAGGTGGTCAGTTA | 9678 |
| rs374996070 | snp | C/T | | | | | GRCh38.p7 | 7:10971413 | GTATTGGGAAACAAC[C/T]AGCAGTTCTTTCCAT | 9678 |
| rs375014979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10986804 | TTTCAAGATTTTGAA[A/G]CTAAAGTTTTGCATG | 9678 |
| rs375028179 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032573 | CTAAACTTAATCCAT[A/T]GATGGATTTTGTTTG | 9678 |
| rs375043415 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127463 | TTTTGTCCTAGGGGA[-/AA]CACACAACCCCTTGC | 9678 |
| rs375063509 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11003185 | ACCTCGTGGTCCGCC[C/T]GCCTTGGCCTCCCAA | 9678 |
| rs375067112 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025939 | CAAAGTGGCAAAACC[A/C]TGTATCTACTAAAAA | 9678 |
| rs375095035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090600 | ACGTTGACTGAAGAT[C/T]TGACTTTTTCCAAAG | 9678 |
| rs375126190 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11069145 | CTGGCTCCTGAGTAT[G/T]ACATTGTTTCCCACT | 9678 |
| rs375136985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11074452 | CCTGACCTCGTGATC[C/T]GCCTGCTTCAGCCTC | 9678 |
| rs375139951 | in-del | -/CTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990870 | TGCTTTCTTTTCTCT[-/CTTT]TTAGAAATGGCTGAC | 9678 |
| rs375166963 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150202 | GGGAGGAGAATGGGA[C/T]GGGGAAAGAACATCC | 9678 |
| rs375173354 | snp | A/G | 3.4132e-05 | 0.00413096 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036462 | TCGTGCCAAAGCAGA[A/G]CTAGCTCGATCTACC | 9678 |
| rs375177927 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079430 | AGGAAAAAGCCATTC[C/G]TAGTACCTGCACAGT | 9678 |
| rs375195304 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045352 | TTATTTCATGACTGT[A/G]CCTTAGTCTGCAGCT | 9678 |
| rs375212286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007664 | GAAAACTATTTGCCT[A/G]TCATAATACATGAAT | 9678 |
| rs375226428 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155992 | TAGTAGCTAATAGGT[A/C]ATAGAAACCATTGGC | 9678 |
| rs375250561 | snp | A/G | 3.37081e-05 | 0.00410523 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983005 | GCGGGAGTGATGAAG[A/G]CGAGAATGATGAAGG | 9678 |
| rs375256340 | snp | A/G | 2.30317e-05 | 0.00339342 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983065 | GTGAAGGGGGTTGCA[A/G]GAAGAAGAAGAGTAA | 9678 |
| rs375265500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11028099 | TCAGTAAGTTAGGTG[C/T]ATTAAATTAATCTCA | 9678 |
| rs375298832 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026940 | CATGACTGGGACAGC[C/T]TTCTAGACCTCATTG | 9678 |
| rs375312904 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978139 | GTCAGCCTGAGACTT[C/T]GGTGGTATTTTGTGC | 9678 |
| rs375327516 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162207 | GATTCTTGTGCCTCA[A/G]CCTCCCAAGTAGCTG | 9678 |
| rs375346613 | in-del | -/ATAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122351 | TATATATATATATAT[-/ATAC]ACACACACACACACA | 9678 |
| rs375369454 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039244 | TGCTGTATTTTTTTT[-/T]CTATTCTTTGGATGT | 9678 |
| rs375400100 | snp | A/G | 6.9365e-05 | 0.00588877 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040697 | TACCGGCAATTTTGC[A/G]AGCACCCAAGGAGAG | 9678 |
| rs375426210 | snp | A/G | 0.000171985 | 0.00927163 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982515 | CTTAAAAATTCTGCA[A/G]AGGAAGAAGTACTAT | 9678 |
| rs375431663 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957645 | CAAAAATTGAAGTAC[C/T]CACTTGCCACTTTTG | 9678 |
| rs375432757 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984651 | CTAGCTAATGATAGA[A/G]GCAGTGTCGATTAGA | 9678 |
| rs375443864 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999120 | GCTCAAACAATCTTC[C/T]TGTTTCAGCTTCCTG | 9678 |
| rs375444319 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030665 | CAGGGAAACAGATAC[A/G]TTAGGATGTGAGAAT | 9678 |
| rs375447884 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062444 | AAAGTTACTAAGCTC[G/T]GTTAGCATATTCTAA | 9678 |
| rs375451434 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016739 | GTCTTTTGAGTTACA[A/G]ACAATCCAGTTACCC | 9678 |
| rs375453331 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137590 | TTTAACTTAAAAATT[-/C]TTTTTTTTTTTTTTT | 9678 |
| rs375464888 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983283 | GGCTGTGGGATGAAT[G/T]AGCACCCTAACTGTA | 9678 |
| rs375464982 | snp | A/G | 0.000204915 | 0.0101201 | nc-transcript-variant, synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:11169436 | TGAAAATGAAGCTGA[A/G]AGAAAAAATATATCT | 9678 |
| rs375511691 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127514 | ACAGCCATTCCCACT[A/G]CAGCCATGCATCTTT | 9678 |
| rs375539840 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058937 | ATATTTTTATAATAA[-/T]GTTTATTTTTGTAGA | 9678 |
| rs375557501 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080572 | TTAAATAAACATTAA[C/T]TCTGCTGGTTTTTCT | 9678 |
| rs375578088 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986148 | TGCTTTTATTTTTGA[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs375582276 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113583 | ATGTATTTGTATTTT[C/T]GTTATACTTATATGA | 9678 |
| rs375596326 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999871 | CTCTTCTTGTGTAAT[A/T]GATTTAACTGACTTT | 9678 |
| rs375615224 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024414 | CAACAAAGATTTTCA[A/G]TGTAGATGAAACAGT | 9678 |
| rs375628395 | snp | A/G | 0.000165986 | 0.00910855 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013889 | GGATGGAATTTTCAA[A/G]GAGACAGATGCTGGA | 9678 |
| rs375633106 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983267 | AATCCTATTTATAGA[C/T]GGCTGTGGGATGAAT | 9678 |
| rs375647312 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062389 | AATTTGATCTAAACA[C/T]TGTGTACTAAGATTA | 9678 |
| rs375651412 | snp | G/T | 2.70757e-05 | 0.00367928 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111443 | CGGATGGATATGTCA[G/T]GAATGTGATTCTTCA | 9678 |
| rs375656884 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964566 | TGTCTTGGGGTTGCT[C/G/T]TTCTCAAGGAGTATC | 9678 |
| rs375676438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058634 | TTACTCTTTATTGGG[C/T]ATAATTCTCTAACTT | 9678 |
| rs375720530 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129376 | TTTTCTTATGTAGTT[C/G]ACTCAGCATTTCTGT | 9678 |
| rs375735210 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058179 | GTTATATATACTTCT[A/G]TTCATCTGAGATGGG | 9678 |
| rs375744392 | snp | C/G | 5.08738e-05 | 0.00504324 | intron-variant | PHF14 | GRCh38.p7 | 7:11035802 | GTATGGGATTCATGT[C/G]AAAACCCGTATGTTT | 9678 |
| rs375755952 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11128643 | CTGACATTCAAGGCC[A/G]TATATAATCTAGACT | 9678 |
| rs375759262 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990456 | TCATATCCTAGAGGA[G/T]AGAGAATACGAAGCT | 9678 |
| rs375782328 | in-del | -/TATTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027309 | TTATTAGAGAAATTA[-/TATTA]ACTAGGCAGTAGGAT | 9678 |
| rs375818397 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000190 | TGACTTAAAAAATTA[C/T]GCTACTACTTTCATC | 9678 |
| rs375820637 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11153785 | TTGGGTGGTTATAGG[A/T]TTAATTAAAGAAGAC | 9678 |
| rs375842099 | snp | C/T | 1.65737e-05 | 0.00287864 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028811 | TTTCAGAGGCAGCGG[C/T]GGAAGAGGTAGGTTT | 9678 |
| rs375850380 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964128 | TCATTATGATGCTAG[C/G]TGGTTATTTCACCTG | 9678 |
| rs375853170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029610 | ACTTCGGTAATGGAC[C/G]CATTATTTAAAATAA | 9678 |
| rs375885668 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084624 | GTAATATTTCCCTAT[A/T]GAAAATTTATTTTTT | 9678 |
| rs375888068 | snp | C/G | 1.9989e-05 | 0.00316135 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982728 | ACACCAGCCACAAGT[C/G]CTCCTGCTGTTAACA | 9678 |
| rs375902128 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118238 | TTAAAACTGTGGTAT[C/G]TGGTTATCCTCAAAG | 9678 |
| rs375916496 | in-del | -/ATTG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005392 | ATAATCTATTAACTG[-/ATTG]CTGTTTCTGTTACTT | 9678 |
| rs375934934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160671 | TTCGCTGACAATTAG[C/T]GATGTTGAGCATTTT | 9678 |
| rs375942822 | snp | C/G | 0.000167986 | 0.00916323 | intron-variant | PHF14 | GRCh38.p7 | 7:10990896 | TGGCTGACTGTGGCT[C/G]TTTTACATTTGTACT | 9678 |
| rs375989572 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086851 | GTTCTATGTGTATGA[C/T]ACCTATTAAATTCTT | 9678 |
| rs376013618 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003925 | AGATATATGTCCTCT[A/G]TGGAAAACATCAGTA | 9678 |
| rs376032540 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048600 | AATAATTATTTGATT[C/T]CATTGAATTAGACAG | 9678 |
| rs376049311 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963013 | ATCTATTTTGTTGAT[A/C]TTTTAAAAAAACAGC | 9678 |
| rs376051955 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092351 | GAAGTGGTGACCAAG[A/G]ATTTGTATTTCTAAC | 9678 |
| rs376114217 | in-del | -/CCCCCCCC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026143 | AGAGAGAAATTGCCA[-/CCCCCCCC]CAGCCACTCCAACTT | 9678 |
| rs376152633 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988465 | CAGAGAAATTACCAC[A/G]CAGTCCATAAAGACA | 9678 |
| rs376162344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11057637 | CCTCGGCCTCCCAAA[A/G]TACTAAGATCACAGG | 9678 |
| rs376197216 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11169366 | GTCAAGTATAGCTGA[C/T]AAATGCTCTAAAGTT | 9678 |
| rs376200243 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966460 | AACTTCTCACTCCTG[C/G]TCATGGACTCTACCC | 9678 |
| rs376208688 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973333 | TTCTGTATCCGGGCC[C/T]TTGAGCCGCTGCTCA | 9678 |
| rs376209903 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996414 | TCATCCTAGTACTTT[A/G]GAGGAGATGGGGAAC | 9678 |
| rs376221866 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991889 | AGGCATGAACCAGTG[G/T]GCCAGGCCTTATTTC | 9678 |
| rs376227930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964119 | GTGATCCTGTCATTA[C/T]GATGCTAGCTGGTTA | 9678 |
| rs376254780 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094319 | GGTGTTCAGCAAGGC[C/T]GGTTTCTTCTAGAGT | 9678 |
| rs376254931 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995898 | GCCCCGGTTCCCACC[C/T]GTGCCTCTCCCTCCA | 9678 |
| rs376259335 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106742 | CAAGACTAATTTTTT[C/T]GAACATTCTTGTGAT | 9678 |
| rs376262553 | snp | A/T | 8.69225e-05 | 0.00659194 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061815 | GGACGAAAACGAAGC[A/T]TCGTTCCTGAGGAAG | 9678 |
| rs376285078 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158522 | CTCCACTATGAAGCT[A/C]CTTTTTTTATTTTGC | 9678 |
| rs376296159 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11131805 | TTTTGTGAAAGGTGT[G/T]AGACCTGTGCCTACG | 9678 |
| rs376313422 | snp | A/T | 0.000169986 | 0.00921758 | intron-variant | PHF14 | GRCh38.p7 | 7:11042823 | GTTATTGGTGAGTAA[A/T]ATAGAGGAGATTTAG | 9678 |
| rs376334388 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | PHF14 | GRCh38.p7 | 7:11070984 | AATTACTGAGTACAA[A/C]CTTAAAAATCGTGTA | 9678 |
| rs376336711 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974423 | GGAGAGTCCTGCGGG[A/G]AAGCAGGATTGGTGG | 9678 |
| rs376338755 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11053352 | TATTTTGGGTGCTCT[A/G]AGTAGATCAACTTGA | 9678 |
| rs376341885 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030073 | TTCCAATCTCTTCAT[G/T]TATATAGCTGTTCCA | 9678 |
| rs376347694 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091672 | CTGAGGTGGAAGAAT[C/T]ACCTGAACCCGGGAG | 9678 |
| rs376360985 | snp | C/T | 8.52522e-05 | 0.00652831 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102537 | CCTCGGAGGCAATCC[C/T]GGAAACCTCTTTTAT | 9678 |
| rs376374036 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003053 | TCAAGGAATTCTCCT[A/G]CCTCAGCCTCCCAAG | 9678 |
| rs376380502 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105961 | TACATGGAGCTTGAG[C/T]TCAGCAGGTTGTACT | 9678 |
| rs376383472 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103044 | CCTTCAACTTCATAC[A/G]TAGATTCATATATGA | 9678 |
| rs376387201 | snp | A/G | 0.000160591 | 0.00895934 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990722 | CGCTGATTCTTGAGA[A/G]GAGTCAAAACTGGAG | 9678 |
| rs376402803 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037840 | AATTAGATTCAGAGG[A/T]CCTGGGGATTCTTGC | 9678 |
| rs376409700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068086 | CCGGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 9678 |
| rs376428725 | in-del | -/TA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109542 | ATCTCAGCCTTCTCA[-/TA]AACTCAGAAATACTT | 9678 |
| rs376454768 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018551 | TTTTCAGATTATTCA[C/G]TGTTGTCACGTAGAC | 9678 |
| rs376456659 | in-del | -/GTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140345 | TTTAAAACAAATGTT[-/GTT]CACAGCTCAGTAAAT | 9678 |
| rs376458906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158998 | GTTTAAACTATTTAC[A/G]GTTTATCTGGCCTCA | 9678 |
| rs376483081 | in-del | -/AAAGATGAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024306 | CATCTCCGTAATATA[-/AAAGATGAA]GAAGATGCAGCAGGT | 9678 |
| rs376524888 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049343 | AACTGTGCGTGGTGG[C/G]ACACACCTGTAGTCC | 9678 |
| rs376530532 | snp | C/T | 0.000169986 | 0.00921759 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040750 | GGCACACAAAAGACA[C/T]CTACTCTTCCTGCAG | 9678 |
| rs376531837 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985347 | TGTTTTCAGAAACTA[C/G]TTTGTAGTAGAGTTA | 9678 |
| rs376534335 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081432 | CAAATGCCTGGTATT[A/T]CAAGAGTGGTTAAAT | 9678 |
| rs376540949 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114176 | TTGTTAAGTCCAACA[A/T]GTCTTCACTTTTATT | 9678 |
| rs376549304 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046241 | AAGACACATTTGGTA[A/G]GATACAAATGGTAAG | 9678 |
| rs376561081 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157260 | ATTCTAGGAATAGAC[A/G]TGACTTCAAGAGTTA | 9678 |
| rs376562531 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11097116 | TCCCAAGTAGCTGGG[A/T]TTACAGGCATGCACC | 9678 |
| rs376569735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081764 | GGGAGGCTGAGGCAG[G/T]AGAATCACTTGAGCC | 9678 |
| rs376579519 | snp | A/G | 0.000164894 | 0.00907854 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990780 | TTGCTGTGTTTGTCT[A/G]GGAGATAATAGTGAG | 9678 |
| rs376617625 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003544 | ATACATATAGATAGT[A/G]AAAAGGTTACTGTAG | 9678 |
| rs376626470 | snp | A/C | 0.000198952 | 0.00997179 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028743 | CATTAGCTGTGATGC[A/C]GGGATGTGCAGAGCC | 9678 |
| rs376635488 | in-del | -/GTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147207 | CATATGTGTTGTTTG[-/GTT]GTACAGGATATATTT | 9678 |
| rs376661251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988217 | ATGAGGATCAGAGGG[C/T]CAGAAACATTAGTTA | 9678 |
| rs376666006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11138128 | TCACTGCAGGCTCTG[C/T]CTCCTGGATTCACGC | 9678 |
| rs376684531 | snp | A/C | 9.28997e-05 | 0.00681478 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982925 | TGTAGTAAAGAGAAA[A/C]GGGAGATCTGCGTCT | 9678 |
| rs376714902 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076207 | ATGGTTTTAACCTCT[A/G]TAGTCTCAGCATAAT | 9678 |
| rs376735580 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11085314 | AGAATGTCATATTCT[C/T]CTGTTGATTTAAAAC | 9678 |
| rs376741300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990416 | GCAAAGCAGATCAAC[A/G]GTAGTTAGTTGCATG | 9678 |
| rs376790808 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10969777 | ATTTCCAGATTCTGG[A/G]TGATGAATCAGAGGC | 9678 |
| rs376793719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965222 | TCTTCCTTTGTCTTT[G/T]ATGTTGGTGACCTAC | 9678 |
| rs376799493 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147697 | CTTAACTGAATTCTC[A/C]ATTTGTGCTCAAGTT | 9678 |
| rs376818123 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073097 | ACTCCTTGCCCCCCC[-/C]TCCCCAGTTTTATCT | 9678 |
| rs376821126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11067249 | GAGTAAATCGAAACC[A/G]CAGTGAGATACCACC | 9678 |
| rs376848968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10988947 | AGTCAACTTTGAAGC[A/G]TGGCTAGTAGTATGA | 9678 |
| rs376871223 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040095 | TACACAGCAGAAGTA[G/T]AATTCATTTATACTG | 9678 |
| rs376884879 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963613 | GTGCAGAGCTGAGTC[C/G]AAGTCCTGGTTATCC | 9678 |
| rs376949955 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11066809 | CCAAGACCAACTCTT[C/G]ATTACTCAGGCTGTG | 9678 |
| rs376953948 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11045416 | TGAATGGCCGGTTTA[-/T]TTTTTGCTGTCTTTA | 9678 |
| rs376960154 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150284 | AGTTATGGTTATTGT[C/T]GTGCAGGAAACATTT | 9678 |
| rs376963600 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11075531 | TTTGTGTGAATTAAC[A/G]AGAACTCACTCATTC | 9678 |
| rs376971538 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168519 | CATCAGATACAGAGA[C/T]AGAGTGGTATGTTTG | 9678 |
| rs376978360 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965008 | CTTTGCGATGGGTTA[C/G]AACATGCTCCTTTAG | 9678 |
| rs376983515 | snp | A/G | 8.32272e-05 | 0.00645032 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035759 | GTCTTTGCAAGAGAG[A/G]GAGAAGCAACTATCA | 9678 |
| rs376988301 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027723 | TTGTCTTAAAGATAT[A/T]TAAAACATGCATGAT | 9678 |
| rs376995766 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11012787 | ATATTGTTTTCATCC[A/G]TTTCAGTTATAGACA | 9678 |
| rs377028517 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005787 | CTAGAAGTAAAAATT[-/C]TTTTTTTTTTTTTTT | 9678 |
| rs377088686 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017064 | GTTCCACCCAAGTTG[A/T]TGCAAATGACTGGCT | 9678 |
| rs377110279 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962568 | CTCTGCCAGGCTTTG[A/G]TATCAGGATGATGCT | 9678 |
| rs377111466 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10978089 | AAAGTTAGTTTAGTT[A/T]GGCCATATTGCCAGG | 9678 |
| rs377115549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10993030 | TTATATAGTGTTCTT[A/G]GTGCATCGTATTAGG | 9678 |
| rs377127753 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090717 | TTGAATTTATTTCAT[A/G]TTAAAGATACTGAAA | 9678 |
| rs377154146 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116060 | ATGTAAAAATATCCT[A/G]TTCCTCATCAAACCT | 9678 |
| rs377159216 | snp | A/G | 4.02115e-05 | 0.00448376 | intron-variant | PHF14 | GRCh38.p7 | 7:11111480 | AAGGTAAGGGGAGAA[A/G]TCTATAAGAAAAGGT | 9678 |
| rs377167095 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124761 | AAATAGGTATTTTCT[A/C]TTTCTTATTGTAAGA | 9678 |
| rs377175156 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104017 | GCTGCTTTTAAGCAA[A/G]ATGACAGATTGCCAT | 9678 |
| rs377179495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11068828 | TAACATTTTAACCAT[A/G]TTGCATCTTTCAATT | 9678 |
| rs377180278 | in-del | -/AGTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055852 | TATTTTTTAGATGTT[-/AGTT]TAGGAAAAATGTTGA | 9678 |
| rs377182242 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026703 | ATGTCTAGTTGGCTG[C/T]TGTGGTTAGTTGAAG | 9678 |
| rs377185814 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957409 | TTCAGTTGATGACAT[-/G]AAACCTCCTGTTCCT | 9678 |
| rs377195132 | snp | A/C | 0.00020632 | 0.0101547 | intron-variant | PHF14 | GRCh38.p7 | 7:10974816 | TATGAATGACAATGT[A/C]ATTTTTTTCTCTTCA | 9678 |
| rs377206349 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016879 | CTCCCACCTCCCCCC[-/C]ACCATTTCACCCTTT | 9678 |
| rs377235565 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993966 | GTGAGCCAAGATTGC[A/G]CCAGTGCACTTTGGC | 9678 |
| rs377269708 | in-del | -/GTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011245 | TCTCGTGGGTGATTT[-/GTTT]AACTCAGTATTCATT | 9678 |
| rs377278132 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956792 | AGGAACTGGAAGATA[C/G]AAAGAAGAATTCCCC | 9678 |
| rs377286215 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995695 | TTCCGAGCCCTGCCC[C/T]GCAGGGAGGCAGCTG | 9678 |
| rs377304441 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027476 | TCTTTTATGAAGATT[G/T]CTGTTACCAGAGTAG | 9678 |
| rs377320596 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152750 | CATTTTATTGTAATA[A/G]ATGTTATGGAAAACA | 9678 |
| rs377335699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007241 | TTATTAGGTTCTCTT[C/T]TTTTCTCATTGACTT | 9678 |
| rs377354061 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972231 | GTGAGCCACCGCACC[C/T]GGCAGTACAGTTTTT | 9678 |
| rs377362398 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047150 | CGCAACTCACCGCAA[C/T]TTCTGCCTCCTGGGT | 9678 |
| rs377386314 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122222 | CTGCATAGTGTTCCA[A/T]GGTATTCTGGAACTT | 9678 |
| rs377390793 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987868 | CTGTTAAAACAGATC[C/T]AGCTGGGCGTGGTGG | 9678 |
| rs377392342 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11082641 | TATATCACAATTACT[A/G]GAAGATAAAGAGTTG | 9678 |
| rs377403092 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990257 | GTATATGTGCGTCTT[C/G]TCTTCTCTAGGTAGG | 9678 |
| rs377404583 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162700 | TGGGAAATCCAAAGT[-/C]TTTTTTTTTTTTTTT | 9678 |
| rs377414813 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11168202 | ATCAAAGTTACATTG[C/G]CAAAATGATATTCAA | 9678 |
| rs377419288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061656 | TCCAATATAGTATTA[A/G]TTAGAAATAACTAAT | 9678 |
| rs377428329 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11061161 | ATGTAGTTACAGTTC[A/T]TTTAAACGTTTGTAT | 9678 |
| rs377428461 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11006711 | CTGGGCTGCCTCCAG[A/G]GTCTCAGTGTCTTGG | 9678 |
| rs377446959 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973806 | GGAAGGGTGCGCGGG[A/G]GCGAGTCCTGCGCAT | 9678 |
| rs377478018 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082287 | GGACATATTGAGGCT[A/G]CAGTGAGCCATGATC | 9678 |
| rs377480173 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034667 | AATTCTCCTACCTCA[A/G]CCTCCTGAGTAGCTG | 9678 |
| rs377515269 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120151 | TATAGAAAGTTAAGT[A/T]TGCAATTTGGTGTAG | 9678 |
| rs377555764 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966956 | GATGCAGTGAGAGAG[A/C]TGGGCATGAGGAGAA | 9678 |
| rs377567574 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139288 | TAAAAATTAGGCATT[C/G]ATCTATCTTTCACCA | 9678 |
| rs377621969 | snp | C/T | 1.72252e-05 | 0.00293467 | intron-variant | PHF14 | GRCh38.p7 | 7:11035824 | CGTATGTTTTTGTTT[C/T]AAGGTTATGTAAGGA | 9678 |
| rs377657481 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054251 | CACCCTAGAGCTAGT[A/G]TAGACTTTGGACCCA | 9678 |
| rs377750398 | in-del | -/CG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088414 | ACAAACACACACACA[-/CG]CACGCACACACACAC | 9678 |
| rs377752922 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975265 | TATCCCGAAGTAGAA[A/G]AGTATCCTGAGAGGT | 9678 |
| rs386409506 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988553 | TTTTTTTTTTTTTTT[-/TT]TAACCTAGATGTGGT | 9678 |
| rs386409507 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031607 | AAAAAAAAAAAAAAA[-/AA]ATTAGCTGGGTGTGA | 9678 |
| rs386409508 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149206 | ATCACAGTTGTTTTA[-/A]AAAGATGTATTCATA | 9678 |
| rs386710272 | multinucleotide-polymorphism | CTG/TTA | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961133 | ATTGCTTTTGGTGTT[CTG/TTA]GTCATGAAGTCTTTG | 9678 |
| rs386710273 | multinucleotide-polymorphism | CAGG/TAGC | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964631 | GTTGGCCTGTCTTGC[CAGG/TAGC]TTGGGGAAGATCTCC | 9678 |
| rs386710274 | multinucleotide-polymorphism | CTC/GTT | | | | | GRCh38.p7 | 7:10970106 | TTGAGGCAGTTTGTG[CTC/GTT]GCTGTTTTTTGGAAA | 9678 |
| rs386710275 | multinucleotide-polymorphism | CAG/TAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019685 | ACCTTTTCAAAATAC[CAG/TAA]CATTTTGTTTCATTG | 9678 |
| rs386710276 | multinucleotide-polymorphism | AC/CA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021897 | ATGCACCACAAAAAC[AC/CA]GAACCATGTAGCATG | 9678 |
| rs386710277 | in-del | AAATG/CACTATAAAAATGTTAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029361 | AAACTATTTTCATTA[AAATG/CACTATAAAAATGTTAC]TTACTTTTCTGAACT | 9678 |
| rs386710278 | multinucleotide-polymorphism | AG/TA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073239 | CAAGTTCCTTCCATC[AG/TA]TGAGCCTGTAAAATC | 9678 |
| rs386710279 | multinucleotide-polymorphism | AA/GG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085700 | CCAGGCTGGAGTGCG[AA/GG]AACTGCAGGTGTGTG | 9678 |
| rs386710280 | multinucleotide-polymorphism | CT/TG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098461 | CCTCTCTGTCTGCCT[CT/TG]CCTCTCCTCATTTTT | 9678 |
| rs386710281 | multinucleotide-polymorphism | AG/GA | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107143 | ACCCTTTGGAATACT[AG/GA]CTTTTGGCCTCTTAG | 9678 |
| rs386710282 | multinucleotide-polymorphism | AC/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116320 | TCCTTTTAGTGGAAA[AC/GT]GATATTTAGAAACCA | 9678 |
| rs397688987 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042982 | CTATAACAGCTTTTT[-/T]TGAGAAATGAGTTTT | 9678 |
| rs397721746 | in-del | -/A | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11168034 | AAAAAAAAAAAAAAA[-/A]GAAATGTCATCTGTA | 9678 |
| rs397758874 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149208 | CACAGTTGTTTTAAA[-/A]AGATGTATTCATAGG | 9678 |
| rs397759475 | in-del | -/T | 0.375 | 0.216506 | intron-variant | PHF14 | GRCh38.p7 | 7:11120055 | ATAATAGTTATTTTT[-/T]CCCAAAAAATTGCCA | 9678 |
| rs397798089 | in-del | -/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063054 | CAAATGATTTAATCT[-/T]ATTTTGGTCATTAAA | 9678 |
| rs397823884 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111918 | CCTTTAAAAAAAAAA[-/A]CAAAATAGTTTTCAT | 9678 |
| rs397824239 | in-del | -/A | 0.5 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11110673 | GAAAGTGACAGGTAA[-/A]TTTGTGAGAATAAAA | 9678 |
| rs397940425 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102774 | CTTTTTGCTTTTTTT[-/T]GCACTTATCAGAAAT | 9678 |
| rs397956350 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131843 | CTGTCTCTCTCTCTC[-/TC]ATTCTTTCTTTTTGA | 9678 |
| rs397963858 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149209 | ACAGTTGTTTTAAAA[-/A]GATGTATTCATAGGA | 9678 |
| rs397973264 | in-del | -/AAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077621 | AAAAAAAAAAAAAAA[-/AAA]GACAGATTCAAGCAC | 9678 |
| rs397975862 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057884 | AGTTCTTAAAAAAAA[-/A]GAAAAACAAAAAATT | 9678 |
| rs398003652 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11004366 | CTTTTTTTTTTTTTT[-/T]GGTTGCTTGCTCATA | 9678 |
| rs398003653 | in-del | -/A | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11049493 | AAAAAAAAAAAAAAA[-/A]GTGTAAATTAGAACT | 9678 |
| rs398003654 | in-del | -/AA | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11068373 | AAAAAAAAAAAAAAA[-/AA]TCTGATACTGCAACA | 9678 |
| rs398003656 | in-del | -/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11076585 | TTTTTTTTTTTTTTT[-/T]GAGGCAGAGTCTCAC | 9678 |
| rs398003658 | in-del | -/T | 0 | 0 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149819 | AGTTGATTTTTTTTT[-/T]ATATTTCTAAGTATA | 9678 |
| rs398085574 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120054 | GATAATAGTTATTTT[-/T]TCCCAAAAAATTGCC | 9678 |
| rs527244344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151273 | TAAATTTATAACTTC[A/T]GGCCAGGCACAGTGT | 9678 |
| rs527254897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157812 | TCTGTAATGAGCTGA[A/C]ATCATAGAAATACTG | 9678 |
| rs527254940 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128710 | TCTCTCCCCCCGCCC[C/G]CACTGCTTTCCTCCC | 9678 |
| rs527256218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111262 | TTGAAGTTGAAATAT[A/G]CAATAGTTTGTCTTT | 9678 |
| rs527257986 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973647 | GAGGTGAATTAGGCG[C/T]GGAGAGGGCGGAGCC | 9678 |
| rs527259151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073097 | CACTCCTTGCCCCCC[C/G]TCCCCAGTTTTATCT | 9678 |
| rs527300551 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060246 | ATTTAACCACTTATA[A/C]ATTTATTTTATTAAA | 9678 |
| rs527305337 | snp | A/T | | | | | GRCh38.p7 | 7:10970921 | TCACATGATCATCTC[A/T]ATAGACAGAGAAAGA | 9678 |
| rs527316601 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022605 | CAGTGAGTGAATTTT[A/C]AGTGAAAGGCAATTA | 9678 |
| rs527337482 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104432 | AGTATAAAATTATTC[C/T]GTGTCCATAATCGGT | 9678 |
| rs527349865 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993348 | GAGTCTGCTGGACTT[G/T]TGGGACTTTGCATGA | 9678 |
| rs527356959 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145176 | CAGGTGGCAGAGGAA[C/G]TCACCTGGTTTGAAA | 9678 |
| rs527381596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984563 | CAGTTAATACTCTAT[A/G]TATAATGAATAAGTT | 9678 |
| rs527395152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977450 | AAACTTTTTATATTT[C/T]TGTTTGGTTTTAAGA | 9678 |
| rs527402997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017149 | TTATCGGATTCGTCT[A/G]TTGGTGGAAACTTAG | 9678 |
| rs527418173 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11097268 | ACAGGCGCGAGCCAC[C/T]GTGCCCAGCCAGGAC | 9678 |
| rs527420712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145967 | TGGCAGATAACTCTT[C/G]AATATGTTGAGCCTA | 9678 |
| rs527441544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966052 | CCTTGAGCTTTCTGG[A/G]TGAGGTGACACCCCA | 9678 |
| rs527449438 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170237 | AGTAACCAGCCTCTT[C/T]ACTCTCCCCGGTTCT | 9678 |
| rs527462835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10999514 | TTTCAAAATGACCCT[C/T]GCTCTCTATTTTGTT | 9678 |
| rs527467695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083836 | ATTGTAAAAATGAGC[A/G]GTTGCCAGTAAAACC | 9678 |
| rs527476340 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017371 | CAACAGTGTACAAGG[C/G]TTCCCTTTTCTCCAC | 9678 |
| rs527504266 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11077552 | GTTGTAGTGAGCCCA[C/G]ATCGCGCCACTGCAC | 9678 |
| rs527504862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961553 | TTGTCTTGGCTATGC[A/G]GGCTGTTTTTGGTGC | 9678 |
| rs527510666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11163995 | ACTTTTAAAAGAAAC[A/G]TTATTAAAGTATAGA | 9678 |
| rs527514837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11015155 | AACATAAAAACTAGG[A/G]TATATTATGTCCTAA | 9678 |
| rs527526536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000117 | ATTTGAATTCTGTGA[A/G]CTTTATATATGTTCC | 9678 |
| rs527527073 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000443 | CTCCCAGGTTCCTGC[A/G]ATTCTCGTGCCTCAG | 9678 |
| rs527544297 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11074582 | TAAGCAGCCAGGCCA[A/C]ATCTTAACTGCTTCA | 9678 |
| rs527549172 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043013 | TCATTAATTGTGGCT[A/G]TTATCTTAGCAATAG | 9678 |
| rs527561551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034364 | ACTTTTTTGTACTAC[A/G]TCTTTACAAGTTGTT | 9678 |
| rs527572515 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11157218 | AATCATTGTTCAATA[A/C]ATTTTTGAGGGAGGA | 9678 |
| rs527584425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024683 | GTACCGCATGGTTTA[C/G]TGGATATTTTAAGCC | 9678 |
| rs527597754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117899 | TTTTAAATATTTTAA[C/G]TATTCATTTGACCTC | 9678 |
| rs527601662 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11110651 | TTTGTAAAACCAAAC[A/G]GTCTGAAGAAAGTGA | 9678 |
| rs527608260 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10989893 | GCTTCAACCTCCCAC[G/T]GTATTTGGGATTACC | 9678 |
| rs527644156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009536 | TGTTTACCCATATGA[A/G]AAAGAAAATATGTTT | 9678 |
| rs527645732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11016103 | TTACTGAGGGATTTT[G/T]TTTTGGATACTGTGG | 9678 |
| rs527647398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095828 | TATGAGATAAAACCT[C/T]AACTGGATTCTGTAG | 9678 |
| rs527660153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976457 | CTTTGACAAACATAG[C/T]TGGGTCGTGGAAGTT | 9678 |
| rs527679122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136697 | AAATGTTTTGAATAT[A/G]TAGGGTAAAGAAAAA | 9678 |
| rs527679772 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11007412 | GTTAACACCTGTAGA[-/T]TTTTTTTTCCCCCTT | 9678 |
| rs527701607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052407 | GATGGGCAGTTAGGT[G/T]TTTTTCATGTTTTTC | 9678 |
| rs527738705 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11046273 | GCTTGATTTATTAGA[A/G]TAGTTCAAATAGTTA | 9678 |
| rs527750333 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11130117 | GTCACTTGGGGACCC[G/T]AGCTGATGGAGGTTT | 9678 |
| rs527761714 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125146 | CTATTGAACTTGGAG[G/T]GAGGTAAAGGAAAGG | 9678 |
| rs527768048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005030 | TCAAAAAAAAAATGT[A/G]TAATGTCAATTTATT | 9678 |
| rs527816768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123064 | TTTGCCTTTTCTTAG[C/T]GGACCATTTCTTTGG | 9678 |
| rs527859372 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966703 | TAATACAGAGGAAGA[A/G]GTGAGAATGAAAGTC | 9678 |
| rs527864391 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11108988 | AATACTTCATCAAGA[A/G]CTTTGATTATTAGCA | 9678 |
| rs527894918 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988662 | TCTTTTGGGGGTACA[A/G]GGAAGATCCTCAGTG | 9678 |
| rs527899819 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149829 | TTTTTTATATTTCTA[A/G]GTATATAGCAGGTAA | 9678 |
| rs527913569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10988625 | ATTTAAAGTAGTAGT[A/G]CTCATTGGAGCTTGC | 9678 |
| rs527940974 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986100 | CAGCCTTTGGAGTAG[A/C]TGAGACTACAGGTGT | 9678 |
| rs527954433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143072 | TTTAGTTTTGTCAGA[A/C]ATATTTGCCTTACTT | 9678 |
| rs527955897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11150485 | ATAAGAATTCACGAC[A/G]TAACTACTGAATGAA | 9678 |
| rs527986639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981890 | GGGTAAAGAGTAAAA[C/T]AAATGAAGCAGTTTT | 9678 |
| rs528014432 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094886 | CCTCTGACATCAGCT[C/G]TCTCATGGCTTGAAA | 9678 |
| rs528017879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144004 | CTCTGTAGAACATAC[C/T]TGGAACTCTAACAAC | 9678 |
| rs528035030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007125 | TTGAACCCAGGAGGC[A/G]GAGATTGCAGTGAGC | 9678 |
| rs528039101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967948 | CCACTGGTAATCAAG[A/G]TATCATTGCCTTTAA | 9678 |
| rs528052284 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11102369 | ATCTATCTCTTTGGA[C/G]CAGATCATATGTTAT | 9678 |
| rs528056932 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10973851 | TGCTGCTCTCAGGGC[G/T]GCGCTCAGCCTCGTG | 9678 |
| rs528085889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133841 | ACAACAATTGCAGTA[C/T]GCAGTGATAGAAAAG | 9678 |
| rs528139060 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11134344 | TAATATGGACCTGAA[A/G]TATCATTTAGAGAGA | 9678 |
| rs528141755 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084622 | CTGTAATATTTCCCT[A/G]TTGAAAATTTATTTT | 9678 |
| rs528142577 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043577 | CTCAAATACATTAGG[A/C/T]ATATTTTTTGACCTC | 9678 |
| rs528147506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127149 | CCAGTCCAGTTTAAT[A/G]TCAAATCTTCTATTC | 9678 |
| rs528168429 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122397 | CACATACATACACAC[A/G]CATATATATATACAC | 9678 |
| rs528174374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166706 | TTTTTCACCCCTTCA[C/T]AATGCTTTTCTGCAC | 9678 |
| rs528177260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037223 | TCTTCCCTATAACTC[C/T]TACTCCTCATTAGCT | 9678 |
| rs528180589 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110848 | GAAAGAGAGAAATCG[A/G]GTCCAAATTGTATAG | 9678 |
| rs528180624 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087066 | ATAAAATAAATAAGG[G/T]TATACTTTGTTTGTA | 9678 |
| rs528198379 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140691 | CCATTTCAAGCAAGG[A/T]AGTTGAAATAATAGG | 9678 |
| rs528202382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120173 | TTGGTGTAGATGAAA[C/G]TGTTTTTCTGAGCTT | 9678 |
| rs528215274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044031 | AAATCATGTTCTTTG[C/T]AGCAACAAGGAGGCA | 9678 |
| rs528217545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127786 | GTATTTTATCAGTGC[A/G]TATCTTTAAAAATGA | 9678 |
| rs528227744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964258 | CTTCAGGAGCTCTGG[G/T]AATGCAGGCCTGGTG | 9678 |
| rs528249744 | snp | A/C | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105941 | TGAACAGGGAAATAC[A/C]AAGTTACATGGAGCT | 9678 |
| rs528250963 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138039 | AACAGGGAAAAATAC[C/T]TCTTTTTTTTTTTTT | 9678 |
| rs528269287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024063 | TGAAAGTGCTACTCC[A/G]GCAAACACATGAATG | 9678 |
| rs528269975 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099608 | TATTGTTAAATTATA[C/T]AAGGGAAGGATTATA | 9678 |
| rs528299236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146996 | GGAATACAGGTGTGT[A/G]CCACGACACCTGGCT | 9678 |
| rs528307970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11018509 | TTATGTGTGGCTATT[A/G]TAAATGCCATTACTT | 9678 |
| rs528312034 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106396 | TTATATTTGTGAAAT[A/G]ATTAAAAACCATTTT | 9678 |
| rs528317007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11062549 | GCTTATCAAAACAAA[C/T]GTGTTAAATGCTTCT | 9678 |
| rs528330524 | in-del | -/TTC | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11082893 | CCCTCCCCTTCCCTT[-/TTC]TTCTCTTTTTCTTTC | 9678 |
| rs528353835 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063124 | ATTTTATGAGTTTTT[A/T]ATGCTATCAATGAGA | 9678 |
| rs528384698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10979013 | CTATTGTGTATATTT[A/G]TAGTACTAACACTGT | 9678 |
| rs528399324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012764 | ATAAGAGGAAAAAAG[A/G]GAATGACATATTGTT | 9678 |
| rs528410809 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163175 | AAAGAGCTCTATTCT[A/G]CTTAATGATATATGT | 9678 |
| rs528449744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079086 | ACTAAGATGAATTAA[A/G]GTTATCAGTTTTTGA | 9678 |
| rs528456658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962858 | AGATTTTCTAGTTTA[C/T]TTGCACAGAGGTGTT | 9678 |
| rs528459537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035505 | CATTATGTACAAAAA[C/T]TATTTTTGTAATTTA | 9678 |
| rs528474764 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126043 | CTTGAGGGCTGGACC[A/G]TTCTCTCAATTTTTA | 9678 |
| rs528484000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073979 | GTCCTGAGGCTGAGC[A/G]AGGAAGCAGAGCCCC | 9678 |
| rs528496852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079854 | TTTTCTTCTTAGTAA[A/C]CTTTGATCATAAATG | 9678 |
| rs528518293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111926 | AAAAAAAACAAAATA[A/G]TTTTCATATCCTAAA | 9678 |
| rs528522086 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10995856 | TGCCCACCCGGAACT[C/T]GCGCTGGCCCGCAAG | 9678 |
| rs528523132 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11165956 | GGTCCATCTGTGCCT[A/G]GAAATTACCATTCTC | 9678 |
| rs528529111 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11055548 | CAAAATACTTTTTAG[C/T]AGCTTTGACTGAAAA | 9678 |
| rs528537586 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008489 | ATTCTCCTGGAAGCG[C/T]GAACACTATTGTGAA | 9678 |
| rs528565667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035960 | TGGCTGAATACAGTA[C/T]TCCTCATTTAGTCAA | 9678 |
| rs528582376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112586 | ACCAGCCTGGCCAAC[A/G]TGGCGAAACCCCATC | 9678 |
| rs528583720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074320 | GGTTCATACCATTCT[C/T]CTGCCTCAGCCTCCT | 9678 |
| rs528590316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068011 | AGGTGACAGGTATCC[A/C]AACCATAGCATACAT | 9678 |
| rs528629981 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11068417 | AGAACGTTATGCTAA[A/G]TAAAATAAACCAGTT | 9678 |
| rs528649938 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11097948 | ATGTGTGTGTGTAGA[C/T]AGGAGGGAGTGTATT | 9678 |
| rs528651867 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067106 | TATATAAAGAACTTG[A/G]ACAACTCAGCAATAA | 9678 |
| rs528696108 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138653 | AAATATTTTAATTTC[A/T]GATATTTATCTCACT | 9678 |
| rs528701672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054631 | AAAAATGAGGTGTTC[C/T]AATTGTGTTTCTTAG | 9678 |
| rs528707326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091400 | TAGGTGAATAGAGGG[G/T]TTTTTTTAAAGGTCT | 9678 |
| rs528716144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047521 | TGAGAAAAGGCCAGA[C/G]GCAGTGGCTCATGTC | 9678 |
| rs528719117 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077214 | TTATTGCTCTAATTA[C/T]AAATTGAAGAAACCT | 9678 |
| rs528753129 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047800 | CACAAAAAGACAGAA[G/T]AAGAGGAGGGAGGGC | 9678 |
| rs528761083 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11132352 | AGACCATTTAATATT[A/T]TTCTTTTTGTGCCTG | 9678 |
| rs528766665 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006588 | TCAGTGAACACAAGC[A/G]TGTTGTTGTCTTCTA | 9678 |
| rs528783003 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131481 | CAGATCTTTGGCCTG[G/T]TTTTTAAATTGGGTT | 9678 |
| rs528789838 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033956 | AGTAAACCCTGTTTT[A/T]CTAATGTGGTAACTG | 9678 |
| rs528830386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967002 | AAAGTAATGAACTCA[A/G]TTGAGTCCATTCATT | 9678 |
| rs528834394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018433 | TTTCTTTCATCAGTG[C/T]TTTATAGTTGTTATT | 9678 |
| rs528837474 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11145699 | TAACTATGCTTTGTT[C/T]GTACCACAAGGAAAT | 9678 |
| rs528838880 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11041870 | TTTTAAGTGTGTGTG[A/T]GTGTGTGTGACTTTT | 9678 |
| rs528839324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012217 | TGATAAATAATCTAC[C/T]CTTTTAAACTCAAAA | 9678 |
| rs528897073 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123507 | AGAAAGTTGGCTGGG[C/T]GCAGTGGCTCACACC | 9678 |
| rs528897159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055496 | CTGGTTGTGTTTTAT[A/G]TATTTTCTTTTTTGC | 9678 |
| rs528915806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048823 | TGCAACAATCATGTG[A/G]CGGTTGTCTTGAAAT | 9678 |
| rs528923920 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140143 | ATAAACCTTCTCATA[A/C]CCCTGCACACACCTG | 9678 |
| rs528926174 | snp | C/T | | | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108168 | AGAGTTCACTTGTGT[C/T]CAGTAAGATGTTTCT | 9678 |
| rs528936843 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996003 | GGCTGAAGGCTCCTC[A/C]AGTGCGGCCAGAGTG | 9678 |
| rs528943781 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977929 | TTGGTTATCTGCTAC[A/G]TTAATTGAATGTTTT | 9678 |
| rs528963890 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973509 | TCCTCTACCGGTGAC[A/T]ATATCATTTAAATAT | 9678 |
| rs528977088 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007039 | AAAATTTGCCAGGTG[A/T]GGTAGTGGGCACCTG | 9678 |
| rs528992631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085888 | TAGCAAAACATAATA[A/G]TTTAAAAAAAAAACT | 9678 |
| rs528994141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11049269 | CCTGAGGTCAGGAGT[C/T]TGAGACCAGCTTGGC | 9678 |
| rs529009179 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126349 | GAATGAAGTACATAT[G/T]TTTAGGATACATTAT | 9678 |
| rs529012353 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134567 | CGCTTTATTTTACAG[A/G]TGAGGAAAGTGAGAC | 9678 |
| rs529012354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092719 | TTTTGTTCTAATGTG[A/G]GGATGTCATGAGACC | 9678 |
| rs529013580 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11133762 | CAACCACAAACACAT[C/G]TTTATATTATATTGC | 9678 |
| rs529049553 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019690 | TTCAAAATACTAACA[C/T]TTTGTTTCATTGATC | 9678 |
| rs529052057 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11163013 | TGAAATTAGAAATTT[C/G]TTACTGCCCTTTTTC | 9678 |
| rs529061543 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976605 | AATATTCACAGGTAT[C/G]ACTTCTTTTTCAAGT | 9678 |
| rs529062190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073823 | TTCACTCTCGCATTC[C/T]GTGCACCTGGAGGCT | 9678 |
| rs529075733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111875 | TTATTTTAAAATATA[A/G]TATATTGTAATATCT | 9678 |
| rs529079505 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11067936 | GATTCATCTTCATGA[C/T]GTAAACACCTCCCAT | 9678 |
| rs529079916 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083705 | TGACCTCGTGACCCA[C/G]CCCCTTGGCCTCCCA | 9678 |
| rs529107658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159087 | TCTTAATGCAAATTA[C/T]AGTTTTCACTCTGAA | 9678 |
| rs529126573 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995388 | GGTGTATTTACAAAC[A/C]TTGAGCTAGACACAG | 9678 |
| rs529130292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11146335 | ATATTTTCATTGACA[A/G]ATGTTTTAACAGCTT | 9678 |
| rs529138237 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10991052 | CTGGAGTGCAGTGGC[A/C]CAATCTCGGTTCACT | 9678 |
| rs529152886 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021563 | ACATTTTAAGAAGGT[C/G]AGTATGAAGCAAGCA | 9678 |
| rs529171145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153147 | TATACAATTATAAAA[C/G]CAAAGCAAGGAGGCT | 9678 |
| rs529193358 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11146935 | CACTGCAGCCTCAAC[G/T]TCCTGGGCTCAAGCA | 9678 |
| rs529202593 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10985305 | TATTTGATTATATTT[C/G]AAGTTTGATTTTCCC | 9678 |
| rs529215637 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006021 | TTGGTCTCGATCTCC[A/G]GACCTCATGATCTGC | 9678 |
| rs529223964 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110267 | ATAAATTTTCCCCTT[A/G]GTTTCTTAATTGCAG | 9678 |
| rs529224574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084576 | AGTTTTTAAGTAGCT[A/G]CAAAATATAATTTGG | 9678 |
| rs529261293 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019709 | GTTTCATTGATCTTT[A/T]GTATATGTTTTTTAT | 9678 |
| rs529262560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966547 | TCACTGGGGACCTAC[C/G]CTTTCCCGCGTAGGA | 9678 |
| rs529296063 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053313 | ATGAGGCAAATCTTT[A/G]TCTCTTAGATAATTG | 9678 |
| rs529297594 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132265 | CCCATTTTCTTCCCA[C/G/T]TGATAACCAGGGTTT | 9678 |
| rs529319750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125294 | AACTACAGCCAGCCA[C/T]ACTCAATCCCTTTGC | 9678 |
| rs529324324 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164961 | ACGGAGTCTCGCTCA[A/C/G]TTGCCCAGGCTGCAG | 9678 |
| rs529342808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035081 | ATTACACATTCTTAG[A/T]TTCAACCAACTGCAG | 9678 |
| rs529355983 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076730 | ACACCACCACACCCG[A/G]CTAATTTTTGTATTT | 9678 |
| rs529382074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118744 | ATAGTATTAATAGAA[C/T]TGGAATCAGTATTGA | 9678 |
| rs529387339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073223 | TACTGGGGACTCAAG[A/G]CAAGTTCCTTCCATC | 9678 |
| rs529392669 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101310 | TCATCTCTATTATTT[A/G]TGCATGTAATTAAGA | 9678 |
| rs529401519 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165202 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTAGC | 9678 |
| rs529412167 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075038 | CATCTCCCAGGTTCA[A/G]GCAATTTTCCTGCCT | 9678 |
| rs529422847 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989504 | TAAGCACAATCTATT[A/T]AATATGCAAGAATCA | 9678 |
| rs529423331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016720 | ATCCATTTCTCAAAC[A/G]CTTGTCTTTTGAGTT | 9678 |
| rs529436143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096547 | AGTTCATTTACGGGT[A/G]TTTCATATCGTATGT | 9678 |
| rs529442801 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062170 | AATGAAAAAACAATT[G/T]CAGGATAAGACCTTT | 9678 |
| rs529473392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097162 | TTTTATATTTGTAGT[A/G]GAGATGGGGTTTCAC | 9678 |
| rs529475018 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104341 | CCTGCAAAAAGTATA[G/T]TTGAAGTAAGAAAAC | 9678 |
| rs529493950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137688 | GTACCCAGGTTCAAG[C/T]GATTCTCCTACCTCA | 9678 |
| rs529504113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060869 | CTAGGAACAGATTAA[A/C]TGGTAAGTAGTTAGC | 9678 |
| rs529522634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11005679 | GCTCAACCATAATGT[A/G]CTTATTTTTTTGTTT | 9678 |
| rs529522697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011406 | TTGGATATATATAAA[C/G]TTACCCATATGGTGA | 9678 |
| rs529528031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138166 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 9678 |
| rs529539846 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128506 | TTAAGCCATTCTACA[C/T]ACTTTTTCCCAGTCA | 9678 |
| rs529545960 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971512 | TCTTCCTTTTTCCCT[A/C]CCTCTCTTCCTTCCC | 9678 |
| rs529558351 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089171 | CTTTTATCAGGAGCA[A/G]CCATTGAGTAGGGCA | 9678 |
| rs529560796 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156575 | CGAGGCGGCGGATCA[C/T]CTAAGGTCGGGAGTT | 9678 |
| rs529573013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047066 | CTAAATTAGTCCACT[C/T]TCTTTTTTTTTTCTT | 9678 |
| rs529573014 | snp | C/T | | | | | GRCh38.p7 | 7:10970800 | CTATAAAAAGATTTA[C/T]ACAACATGACTAAGT | 9678 |
| rs529576126 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977299 | AACTTCTAGAAATGA[C/G]TCATTGAATGAACTA | 9678 |
| rs529589907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131818 | GTTAGACCTGTGCCT[A/C]CGTTCTCTCTCTGTC | 9678 |
| rs529590813 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014124 | ATCCATAATCTTAAT[G/T]AATCTTAATAATTGA | 9678 |
| rs529610988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003880 | TTGTACCTTGTGTAC[C/T]AGGGGTTTTTTAACT | 9678 |
| rs529629226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121883 | ATAAGTTCTGGGGTA[C/T]GTGTCCAGAACGTAC | 9678 |
| rs529650298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129269 | AAATGATGTTTGGAA[C/T]ATAAATTTCTGGCAG | 9678 |
| rs529658096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966185 | TGCATCGATCTTGCA[C/G]GGAGCTGTAGACCGG | 9678 |
| rs529664021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047480 | TAGTTGTATGGTGCT[A/G]GAAACATATAGAAGG | 9678 |
| rs529672542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965045 | GAAGTTTGTTATTAC[C/T]GACCTTCTGAAGCCT | 9678 |
| rs529686954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167613 | GGACAAATTCAGTGC[C/T]ACATATCAAAAATTT | 9678 |
| rs529692007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114829 | GCTATGCTTCAAAGC[C/T]ATTGATTAAGACAGC | 9678 |
| rs529695607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082508 | TGCATTATTTGCAGA[G/T]AAGCTTAATTTTCCC | 9678 |
| rs529698157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998540 | AATATATTCATATGA[A/G]TATGATATTAGTGGT | 9678 |
| rs529705366 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008066 | ATTGTAGTGTGTCTG[A/G]ATTCAGGAGAATGTC | 9678 |
| rs529717936 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065721 | ATGAAAAGGAAGTGG[A/G]CCTGTCTTTCAGTCT | 9678 |
| rs529730181 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960021 | GGCCAAGCTTGCAGA[C/T]TGCAATGCAGGAGCA | 9678 |
| rs529745532 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035903 | TTTGGTTAGTTACCT[A/G]GGAAATGGATTGTGA | 9678 |
| rs529752474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993880 | CCGGCATGGTGGCAC[A/G]TGCCTGTAATCCCAG | 9678 |
| rs529764796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032977 | GGCTTTCAGTTTTCT[A/G]TCCATAAAATTGATA | 9678 |
| rs529771074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994324 | TGTGCCTGTAGTCCT[A/G]GTTACTCAGGAGTCT | 9678 |
| rs529792978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070671 | ATCCCATGTCATGCT[G/T]TGATCCATTTTGCTT | 9678 |
| rs529800375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093339 | ACAGTAGAATACTTA[C/T]GCCTGAAAAGGGCAC | 9678 |
| rs529802481 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063675 | GGTTTTTTGTTTTGC[C/T]TTTGTCATATATTGG | 9678 |
| rs529836149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11100720 | TTCATTACTATTTTA[C/T]GGGTGAGGAAAATGA | 9678 |
| rs529836211 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10988114 | CAGTTGAAACATTGT[A/C]TGCTAGCCATTTAGT | 9678 |
| rs529850145 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11134417 | CTATATAATTTAAAG[A/G]TTTCATGGAGTAAAG | 9678 |
| rs529873064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974432 | TGCGGGAAAGCAGGA[A/T]TGGTGGACCCTCGCC | 9678 |
| rs529884298 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026077 | AGATTGCACCACTGC[A/C]CTCCAGCCTGGGTGA | 9678 |
| rs529918766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142058 | GGGGTTTTTTAAATT[C/T]CTTAGGGGTTTTTGT | 9678 |
| rs529927282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008602 | AATAATCCCCCTGTC[C/T]CATCCATGGAAAAAT | 9678 |
| rs529929335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975149 | CCTCAGAGATAATTA[A/G]CAGTCAGGGGAAGGA | 9678 |
| rs529930854 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11050221 | AATTTTGATGGAACG[A/T]AATCAAATCATAAAT | 9678 |
| rs529938765 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005118 | TTTTTTTTCTATTTG[C/T]AATTAATGATAAATC | 9678 |
| rs529944775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008120 | AAGTTAGGTAGTGTA[C/T]TTACCAGCAGTTGCC | 9678 |
| rs529951701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11087708 | CTTAATAATCTCTGT[A/G]TGTTTTCATTTGGCC | 9678 |
| rs529975766 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11044276 | TCATGCAGTATACCC[A/G]TGTAACAAACCTGTG | 9678 |
| rs530000075 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075080 | GTAGCTGGGACTACA[C/G]ACACATGCCATCACA | 9678 |
| rs530003330 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979364 | AAATAGCTGTTGCTT[A/G]GAGAGATTCTGATAT | 9678 |
| rs530003489 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11153704 | ATTGTCATTGGTAAG[G/T]ATTCTTTAACAGAAA | 9678 |
| rs530004152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069401 | TTCAAGTCTCCTTAA[C/T]AAGGAGGACGATAAG | 9678 |
| rs530034196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128419 | CCTGTCTCAGAAAAT[A/G]AAAGTGCCACTACCT | 9678 |
| rs530039351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11031325 | GTGAGAATCCATGTG[A/G]CATTTCTATTCTTTT | 9678 |
| rs530052292 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959837 | CCATCCATGGCACAG[C/T]GAGCCAGCCAGGAAA | 9678 |
| rs530053590 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11005554 | AAACTGGATAAATCC[C/G]TAAGATATTTTTCTA | 9678 |
| rs530064149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044947 | CTCCAATGAACATTT[C/T]CTTTGACTGTAATGT | 9678 |
| rs530064281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964687 | TTTCTAACTTGGTTC[C/T]ATTCTCCCCATCACT | 9678 |
| rs530068761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10986859 | ATATCAATAGAATTG[A/G]CATTTTTGTTTTGTA | 9678 |
| rs530071612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992933 | ATATAGTCCAGTTTT[A/T]TTTATTTTGGTTTGT | 9678 |
| rs530073603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019129 | CGTATTGTTAAATTC[A/G]GTTTGCTGGTATTTT | 9678 |
| rs530104765 | in-del | -/A | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11015618 | TGATGTAACCTTTTT[-/A]ATGCCTCAGTTTCCT | 9678 |
| rs530129007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987250 | TTTCTAAAAATGTAG[A/G]GGAAGTATGATTGGT | 9678 |
| rs530130014 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154238 | CCATTTATGTATACA[G/T]AGTTCCTCAATTTAA | 9678 |
| rs530145780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980452 | GTCAAGAGATTACTA[C/T]TATTGTTATTTTTAC | 9678 |
| rs530151391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025251 | CATGGATGAGTGAAG[A/G]AAGTGGTTTCTCGAG | 9678 |
| rs530161042 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003265 | TTAAAATAAAGTTCA[C/T]GCTAATAGCAGGACT | 9678 |
| rs530186668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080044 | TCTTGTCAACTTTAA[A/G]AGGATACATTTTTAC | 9678 |
| rs530191049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963533 | GTGCAATGTGGTGCT[A/G]AGAAGAATGTATATT | 9678 |
| rs530195734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11148298 | TAACCGTTATGGGCT[A/G]TGTAGTCAACTTAAC | 9678 |
| rs530199420 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168720 | CATGTATGATGAGAT[A/G]GGTTACAAATTGTAA | 9678 |
| rs530203495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064061 | GAAATTAAATGTTTT[A/G]TTGGTACTATATTTT | 9678 |
| rs530209338 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004408 | ATATATATTTTTAAT[G/T]TAATAGCCAATAATA | 9678 |
| rs530218986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11043392 | CTCCAAGAAAGGGAC[A/G]GATGTTCAGATTTTA | 9678 |
| rs530228937 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11057014 | TGTTCTATTTTTACA[A/T]ATAAGTTGCAGAGGG | 9678 |
| rs530231187 | in-del | -/TA | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063827 | TGAATAGTATTACTC[-/TA]TGTTATTTATTTCTT | 9678 |
| rs530239124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019426 | TCTCGTTACTTGTTA[C/T]TGGTCTGTACAGGCT | 9678 |
| rs530248366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957878 | GATTATCAAGGTCTA[C/T]GTGTAGGGGAAATGA | 9678 |
| rs530256948 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026010 | CCAGCTACTCAGGAA[A/G]CTGAGGCAGGAGAAT | 9678 |
| rs530256957 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11059324 | AAAACTACATGATAC[A/G]TTTGCTAGTTCATTA | 9678 |
| rs530257887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141294 | TAATTAAGAAATCCG[C/G]AGTTCAGAAGGATTG | 9678 |
| rs530258131 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11148974 | TACATAATCATTTTT[A/G]TTTATTTAAACCCAA | 9678 |
| rs530265628 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121103 | TCAAGGTGTATGCAG[C/T]TTCTGATAACAAAAG | 9678 |
| rs530274910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995957 | TCCACCCTCGGCCAG[C/T]CCAGAGAGGGGCTCC | 9678 |
| rs530284460 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007366 | GTATCCTTTAACTTT[A/G]TGATTTTTTATTGTT | 9678 |
| rs530306002 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074689 | CACAAAATATAGCCA[A/C]GTTCTTTGCTAGGGC | 9678 |
| rs530326831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167004 | TTATCCATATATTTA[A/G]AACATATTCAAATTA | 9678 |
| rs530364050 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11002714 | CTCCCAAAGTGCTGG[C/G]ATTACAGACGTGAGC | 9678 |
| rs530368598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120103 | TTATAATTGGATGCG[C/T]CGTATAGTAGGAAGA | 9678 |
| rs530376520 | in-del | -/GAA | | | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10983028 | GATGAAGGCAATGAT[-/GAA]GATCATAGTAGCCCT | 9678 |
| rs530383009 | in-del | -/GTTAACA | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11168297 | CTCTACTTTCCCAGT[-/GTTAACA]AAGTCTAAATCACAG | 9678 |
| rs530389109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11008076 | GTCTGAATTCAGGAG[A/G]ATGTCAGGTATATGT | 9678 |
| rs530394407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037209 | TGGAGCTCTTTGGCT[C/G]TTCCCTATAACTCCT | 9678 |
| rs530430805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134939 | TGTAATATGAATACT[G/T]GCACATAAACATGCT | 9678 |
| rs530433143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120977 | TTTCTTTGTCAAGGT[C/G]ATTAAAACTGTAAAC | 9678 |
| rs530453842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958655 | TGATCTCTTTAAGTG[A/G]TCATAAATGTTAGCT | 9678 |
| rs530483419 | snp | A/T | 0.00318978 | 0.0398085 | | | GRCh38.p7 | 7:10969334 | TGAACCAGCACTATT[A/T]TCCTTAGATTTACAG | 9678 |
| rs530510042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003820 | TCTACTTCTCTTTGC[A/G]TAGGGAATCACTGTT | 9678 |
| rs530515967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161048 | TCTTATAGTTTGAGG[C/T]CTTACATTTAAATCT | 9678 |
| rs530520895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031535 | AGGCCAGAGGATTGC[C/T]TGAGGCCAGGAGTTT | 9678 |
| rs530529643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003342 | CCAGTGTTTGGGGGC[C/T]TTCATATATGCTTTT | 9678 |
| rs530541170 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113149 | TTCCCACCTTTTTTA[A/C]ATATACCTTTTTGCA | 9678 |
| rs530562579 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11081430 | CACAAATGCCTGGTA[G/T]TACAAGAGTGGTTAA | 9678 |
| rs530568773 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063143 | CTATCAATGAGAAAG[A/G]TAAAGTAAAAATTAC | 9678 |
| rs530568852 | snp | A/C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045127 | CATAGTTAGGAGTAT[A/C/T]TGTACTGTAGAAATT | 9678 |
| rs530569471 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031193 | TTTATATAGGCTGTT[-/A]AAAAAAAAAGGTTGA | 9678 |
| rs530571904 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106713 | GAGATTTTTATTTAA[G/T]TAATGACAGTATTCA | 9678 |
| rs530589699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10997275 | TAGTAACATGAGGGT[C/T]ATTGGCCATCTTGAC | 9678 |
| rs530601816 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11075194 | TCCTTCTGCCTCATC[C/T]TCCCAAAGTGCTGGG | 9678 |
| rs530603024 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107212 | GTTTGCATATTCTCA[A/G]TAGTCAGGTAAACAC | 9678 |
| rs530637655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140287 | TTTTTTTATCCTTAC[A/T]ATGTGCGATATACCC | 9678 |
| rs530639818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063958 | TACTCTAAAATAATG[C/G]ATATGCAAAGTCCCC | 9678 |
| rs530643542 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085154 | CAGGAAATGCAAATT[A/G]TCTGTCTTTGCCCTT | 9678 |
| rs530647754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092795 | GGCTTTTAGGGAGGA[C/G]ATACAGTTGTCTTGG | 9678 |
| rs530656157 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019399 | TACCGGGAGACTTTA[C/T]TATGGCTTCAATCTC | 9678 |
| rs530677283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049439 | GAGATCGTGCCACTG[G/T]ACTCCAGCCTGGGCG | 9678 |
| rs530706828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980294 | CATCTTCATCTCCTA[A/G]CTCTCTTAATTATGG | 9678 |
| rs530720821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974384 | ATTCTAGAAGTCAGG[A/G]CCGGTGGGAGCAGGG | 9678 |
| rs530745415 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168224 | GATATTCAAAACCCC[A/C]TTCCTGGTGTTCTAC | 9678 |
| rs530775079 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104004 | TTGCTGAACTCTGGC[C/T]GCTTTTAAGCAAAAT | 9678 |
| rs530791609 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11042128 | TTTTAATTTTTTTAC[-/T]TTTGAATTTAATTAG | 9678 |
| rs530806322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112639 | AGCCAGACATGGTGG[C/T]GAGTGCCTCTAATCC | 9678 |
| rs530806445 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002793 | TTAGGGCAAACACAG[C/G]AAAGAAGAGGCAAAA | 9678 |
| rs530814277 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135724 | ACAGCCTGCTGTAAG[A/C]GATAAACCTATTGCA | 9678 |
| rs530818434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141154 | TTTAGGAAAATATCA[A/G]TCCAGTTACACCTTA | 9678 |
| rs530820240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068694 | AATGCTATGTATATT[C/T]TACCACAATTGATTT | 9678 |
| rs530828522 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008447 | CTGCCTGAACTCCAC[A/C]TCCTGTCGGATCAGT | 9678 |
| rs530831904 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968728 | TCTTCTTTATGATTT[A/G]TGAGTAGTTTCTATG | 9678 |
| rs530848378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10996317 | CTGTTTATGTAAGAT[A/G]TTAGGACTAGAAATT | 9678 |
| rs530853199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991691 | TGTTTCTTTAAAGGT[C/T]GGTGTTCTGGTATTG | 9678 |
| rs530861961 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10986180 | GTAGAGATGGTATAT[C/T]ACTATGTTGCCCAGG | 9678 |
| rs530865688 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10992179 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC | 9678 |
| rs530875721 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11050131 | TTTAACTCTTGTTGG[A/C]GTTCAAAATTTAAAG | 9678 |
| rs530883766 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11029833 | ATGGCTTTATGGTAA[G/T]AGTCTAAGCCTCTCC | 9678 |
| rs530893899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957611 | TCTAGGAGATCTGTC[C/T]AATAAACTGCTATTG | 9678 |
| rs530901783 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11166580 | AAAAAGACTTCCCTA[A/G/T]AGCTTTATTAGATCA | 9678 |
| rs530921636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11030187 | AGTTATAATTATACG[A/G]TAAAGGTAGTCTGGA | 9678 |
| rs530928365 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120002 | TGACATTTCTGAAAT[G/T]AGATTGTGTATCTAT | 9678 |
| rs530958831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153351 | GAGTTTGTGTTTGAA[C/T]AACTGAGTCTTATAG | 9678 |
| rs530966681 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11160093 | TTCTAGTAGTCTCCA[C/G]TGTCTATTATTGCCA | 9678 |
| rs530975824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006641 | GGTCAGCAGAAACTT[A/G]ATGATGGTATAGTAG | 9678 |
| rs530989593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041910 | TATTTAAAAAAAAAA[C/T]CTAACCATCATTGCT | 9678 |
| rs530992640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113110 | CCAGCAAACAAGTTA[C/G]GAAAACAATTTTTGA | 9678 |
| rs531019801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153616 | GACTATTATCAAAGG[A/T]TAGCAGAGTTCTAAG | 9678 |
| rs531056214 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010453 | CCTTTTAAATCTGTT[C/T]TTTGACATTTTATAT | 9678 |
| rs531057915 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11054198 | TTACTTGCATTAGGA[-/C]CCATCTTGGGTATTT | 9678 |
| rs531061244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001406 | TCCATGTAAACTTTA[A/G]AGTCAGTTTGCAGTA | 9678 |
| rs531089011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091931 | AGCAGGAAATCATGC[G/T]CTGTAAGAATGGAAC | 9678 |
| rs531089906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962937 | TATCCCCTTTATAAT[A/T]TTTTATTGCATCTAT | 9678 |
| rs531091337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012683 | GAGAATCTTTAAGGA[C/T]TTTTATTACATTAGC | 9678 |
| rs531092343 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079401 | TAATCTTTCAAATGC[C/T]ACATTAAACCTAGAG | 9678 |
| rs531115795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166106 | TCTGCAAAGTTGTTA[C/T]AGTCAGTGTATTTTT | 9678 |
| rs531134527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125437 | TTTCTCTTCTTCAAA[A/G]GAATACTTGCTTCTA | 9678 |
| rs531134962 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007036 | CAAAAAATTTGCCAG[G/T]TGTGGTAGTGGGCAC | 9678 |
| rs531167316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163967 | TCCCTAAAAGCTATA[G/T]ATGTATTCTTACACT | 9678 |
| rs531171678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072142 | TAAGGGAAGCATAGC[A/G]GTTTCTGCTTCTGGG | 9678 |
| rs531175557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077429 | AACGTGGTAAAACCC[C/T]GTCTCTACTACAAAT | 9678 |
| rs531175564 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155792 | TTTTTTAGCAACTAG[A/C]ACAGTGCCTGACACA | 9678 |
| rs531205872 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126280 | AATTTATCCTAGTAT[C/G]CAGTCATTTGCTTAA | 9678 |
| rs531244655 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991136 | GCTGGGACTACAGGC[A/G]CCCACCACCACACCT | 9678 |
| rs531268437 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11126941 | ACTCTTACGTTTTTA[C/T]TGTGATTTAAGTAAA | 9678 |
| rs531271250 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968880 | AGCTGTATTTGAAGT[C/T]TTATTCAGGAGAGAA | 9678 |
| rs531277226 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963496 | GTGTTTTACTTGCAA[C/T]TATGTGGTCAATTTA | 9678 |
| rs531302240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989836 | GGATCTCACTGTGTT[G/T]CCCAGGCTGGTCTCA | 9678 |
| rs531304987 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117732 | GCCACAATACATTAA[A/G]CAAGCACATTTAATT | 9678 |
| rs531320903 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034284 | GCTTATGTTTACTGT[G/T]CCTTTTTGGGACAGA | 9678 |
| rs531322924 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11027516 | TTAGACTAGCTAATT[C/G]CCCCTTTTTCTTTTA | 9678 |
| rs531336735 | snp | A/G | | | | | GRCh38.p7 | 7:10970973 | TCTTTCATGATAAAA[A/G]CAGTTGGCAAACTAG | 9678 |
| rs531336795 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993035 | TAGTGTTCTTAGTGC[A/G]TCGTATTAGGAAGCA | 9678 |
| rs531338531 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066332 | TGGCACTTTCTTGAC[G/T]CAGTACAGCCTCTGC | 9678 |
| rs531372392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017060 | TCTAGTTCCACCCAA[A/G]TTGTTGCAAATGACT | 9678 |
| rs531374442 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995049 | GTGTGTTTACAATCC[A/C]TGAGATAGACACAAA | 9678 |
| rs531385770 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024318 | ATAAAAGATGAAGAA[A/G]ATGCAGCAGGTACTG | 9678 |
| rs531414829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151191 | TATTTTTATTGAACA[A/G]TGTGGTTGCCACATA | 9678 |
| rs531466675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999362 | CTTTGAGGGTACTGT[C/G]TCTTGTTGCTGATAT | 9678 |
| rs531482493 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11076827 | CCTGCCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 9678 |
| rs531484378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965771 | TTACACTGTGAGCAT[A/G]GAACTGCCTACTCAA | 9678 |
| rs531489802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082784 | AGCCTTCACACTCAG[C/T]AGAATTTTGGTTTCA | 9678 |
| rs531497847 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170180 | TCTTTGGCTTAGAAA[A/T]TTTTCAAAATTCACC | 9678 |
| rs531510437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039008 | TTTCTGCTTGAAATA[C/T]ACCTAGAGCATTGGA | 9678 |
| rs531511395 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11053588 | GTCTACAAAGATTAT[A/C]CTCTTATGAAACATT | 9678 |
| rs531530467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994714 | TGTCCGGAGTTTGCT[C/T]CTTCTGATGTTCGGA | 9678 |
| rs531542684 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11130063 | TCTCATTCATGTAAC[G/T]TATCAGTACAGGTTG | 9678 |
| rs531557581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020587 | TTTCACCATGTTGCG[C/T]AGGCTGGTCTCAAAC | 9678 |
| rs531615053 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960703 | TTTACAGTCTCACCA[A/G]CAGTATAAAAGCGTT | 9678 |
| rs531622507 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972994 | GGGAAATTGGCTGTG[A/G]GCAGCAAATCAGACT | 9678 |
| rs531630643 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163075 | ATAAATAATGAATGA[A/C]ATGTTGCAGTATTAA | 9678 |
| rs531636339 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981750 | TAATTTCTCTTGCAA[A/C]TTCCTTTTTCTGTGC | 9678 |
| rs531639954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11033800 | ATTTGGGCTGAGGTT[C/T]GGTATAATCTTTATT | 9678 |
| rs531654576 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988296 | GCGTAGAGATATGAT[G/T]TAGGCATTTATGGTT | 9678 |
| rs531658557 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964587 | AAGGAGTATCTTTGT[A/G]GTGTTCTCTGTATTT | 9678 |
| rs531666409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116362 | TGGTCATTGTTACTG[A/G]GATATTGCTTTTCCC | 9678 |
| rs531687848 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147744 | GTCATTGTGTCCCTT[C/T]TCTATTTGTATGTCC | 9678 |
| rs531693837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143807 | GTATCTAGACAAGTG[A/G]CATGAAAACTGGAAG | 9678 |
| rs531721511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101618 | TTGTTTTTACTTTCT[C/T]TGGAGGTTATTCAGT | 9678 |
| rs531749859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142861 | ACATTGATAAAACTC[C/T]GTTAATGACTTAATG | 9678 |
| rs531757877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136601 | TTTTGCCATGTTCTA[G/T]TCTAACATCCTAGAA | 9678 |
| rs531767862 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094849 | GGGTCTATCTTTCTT[C/G]TATTTCAGGCCACTT | 9678 |
| rs531771400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959920 | GAATGAGGTTATGTG[A/G]ACAACTGGAGGGTGA | 9678 |
| rs531786302 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986000 | TTGAGACAGATTCTC[A/C/G]CTTTGTTTCCTGGAC | 9678 |
| rs531811615 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111056 | GGTTGTTTTGAACAC[A/G]TGATTATACATATAC | 9678 |
| rs531813242 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117429 | CTAGAACTACAAATG[C/T]GTGACAGACTAGCTA | 9678 |
| rs531828690 | in-del | -/ACTT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11147274 | CATATAAAATATAAC[-/ACTT]AAGAAGTCCAGAGAT | 9678 |
| rs531842543 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959094 | ATATAAACTCAATGT[C/T]TAACCTGGAGAAGAA | 9678 |
| rs531848490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11088709 | AGACATTTATAGCTA[C/T]AGTTATAGTAGGAAA | 9678 |
| rs531873078 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992907 | TTTCTGTCTCATAGA[A/C]ATTTTTAAATATATA | 9678 |
| rs531876890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155741 | CCATAAGGCAGGGAC[A/G]GTGTCTGTCTTATAT | 9678 |
| rs531887994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129574 | TTTTTTTGCCTTTAC[A/G]TAAAATTTAAGAGAC | 9678 |
| rs531891522 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11161637 | TTTAAATATTATTTT[G/T]GCCTAAATATTTCAA | 9678 |
| rs531901025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026792 | TTCACCTTGTGTAAA[A/G]TTCCATGTACAGAAA | 9678 |
| rs531908591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057831 | TACGAGCAAGGTGAT[C/T]TAAGCAGCTCAGGTT | 9678 |
| rs531914459 | in-del | -/TTTG | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11092977 | GCTCTGAAATAGCAC[-/TTTG]TCTGTTGTCTCCCTG | 9678 |
| rs531931212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114769 | CACACATACAAATAC[A/G]CAGAGACACATACAC | 9678 |
| rs531932271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108836 | GGTGATAAATAATGA[A/G]TTATGATACACATGC | 9678 |
| rs531935806 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070523 | GACTTTCCTGCTTTC[A/C/T]GTAATGTATTTGGGC | 9678 |
| rs531947401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065404 | TTTCGACAGTTCATG[A/G]CACATTTAATGATCA | 9678 |
| rs531979011 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10993768 | AATCCCAGCACTTTG[C/G]GAGGCCAAGGCAAGC | 9678 |
| rs531980082 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11169294 | TAATTTTACCATTTG[A/T]GTTTAGGATTATTAG | 9678 |
| rs531993203 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108193 | GTTTCTGTGATTAGC[A/G]CATAGAGCTATGGAT | 9678 |
| rs532007444 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006294 | GTGGCCATTTGCCAC[A/T]TTTTGTTTTCTGTTA | 9678 |
| rs532008329 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122931 | GCTGTAAATTCAGTT[A/T]GTCAAAATCAAGAAT | 9678 |
| rs532019010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994378 | CAGGAGGCAGAGGTT[A/G]CAGTGAGCTGAGGTC | 9678 |
| rs532041482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981092 | TGTTTTTGTTAGCAG[A/T]CATTTGTATGTGACT | 9678 |
| rs532049724 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11020061 | TTGCAATAGAAGGCA[A/G]CATTGAAATCTTTAT | 9678 |
| rs532059186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988484 | TCCATAAAGACATGT[A/G]GCATCCTAATTTTCA | 9678 |
| rs532102547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076230 | AGCATAATTTACATT[G/T]GAACAGTGTGGTTGG | 9678 |
| rs532108617 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072059 | TTCTTGCATAGCTGT[A/T]AAGAAATACCCAAGA | 9678 |
| rs532118987 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068573 | GGGTACAGAGTTTCA[C/G]CTGGGAAAGATGAAA | 9678 |
| rs532128519 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115555 | TGTAGTTATCATACC[A/T]CTGCTTGAAATCTGT | 9678 |
| rs532129611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995587 | GGTCGATGGGACCGC[A/G]CCACAGAGCGGGGGC | 9678 |
| rs532133081 | in-del | -/AGAA | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10997806 | TAAGTGATCAAAGAG[-/AGAA]AGAGACGGAAGCAGT | 9678 |
| rs532137994 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969870 | TCTCCAGACTCTTAA[A/G]TTTGCTGTCTTTTGT | 9678 |
| rs532139093 | in-del | -/AAAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988857 | CGCCATTTTGCAGAT[-/AAAG]AAATTACAGCTTCGA | 9678 |
| rs532140002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975919 | ATGAACGAAATTATA[C/T]TACTGTTGCTACTTT | 9678 |
| rs532173619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155829 | GCTAGTTGATGTTCA[A/G]TCAGGAAGGAATGAA | 9678 |
| rs532173936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163036 | CCTTTTTCTATCTTG[A/C]TATTTAAAAAATATT | 9678 |
| rs532208478 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10973845 | AATTCCTGCTGCTCT[C/G]AGGGCTGCGCTCAGC | 9678 |
| rs532218699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082165 | CCTAGGCAATGTATC[A/G]AGACCTTGTCTCTAA | 9678 |
| rs532220764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088672 | TAAGGAAATAGTCAA[A/G]GAAAGAAATGCTAAT | 9678 |
| rs532239132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997884 | CATACAACCATTTCT[A/G]CCATATTCCGCTGTT | 9678 |
| rs532247692 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981988 | GTTTAAGGGAGGAAG[A/C]ATTTTGTCTGTATTA | 9678 |
| rs532249728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020718 | AATTCTAGATTTAGT[A/G]AGTCTTAGTTCTGTC | 9678 |
| rs532251520 | snp | A/G | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:10970339 | ACTTTGAGAGGCTGA[A/G]GTGGGCGATCAGTTG | 9678 |
| rs532290793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004524 | GCACTTGTGTTATAT[A/C]TCTTTAGTCTCCATT | 9678 |
| rs532295477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008718 | GTAGGTACTGTCTTT[C/G]TCGTAAACAATATTA | 9678 |
| rs532324240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155066 | TGATTAAAAACTGTC[A/G]TAAAGTTAAGCCTAG | 9678 |
| rs532341071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965398 | TATCACCAGCGGAGG[C/T]TGCAGAACAGCAAAT | 9678 |
| rs532362409 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147912 | GCTCAAACTTAATGT[A/T]ACCAAAATAGAATTA | 9678 |
| rs532364199 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148445 | AGTACATGACTGTTT[C/G]CTTCAAGTCATTCAG | 9678 |
| rs532382300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100184 | TTGGACATATGAAAT[A/G]GACATTTGAAATAGA | 9678 |
| rs532385713 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065984 | TAAGCTATTTCACTT[C/T]TATAGCTAATTCTAC | 9678 |
| rs532386284 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005469 | CCCTTGTGTATACAC[A/T]AACACTTCTCTCTCT | 9678 |
| rs532389031 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985401 | ACATAATAGAAATAT[A/G]TAATTATACCATATT | 9678 |
| rs532392865 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11057460 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGATCGA | 9678 |
| rs532396602 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964076 | ATTTAGCCCATTTAC[A/G]TGTTGGCTAATATTG | 9678 |
| rs532412235 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965119 | CCTTGCTGGAGAGGA[C/G]CTGTGTTCCTTTGGA | 9678 |
| rs532429162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11057727 | ATTTTACACCTTTTC[A/G]GTTTAAATACATTGT | 9678 |
| rs532453517 | snp | A/C/G | 2.67448e-05 | 0.00365673 | intron-variant | PHF14 | GRCh38.p7 | 7:11038898 | TTCAGTTCTTGCTCC[A/C/G]TATATGATTTTCAAA | 9678 |
| rs532471465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975310 | TAGTCCCTGAGCAGG[A/G]TTCTTCTTTTTTCAG | 9678 |
| rs532492932 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10981016 | TGATAATGATTTCAT[A/G]GGGTCAGTCAGTATC | 9678 |
| rs532496934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960138 | GGTACATGTACACAA[C/T]GTGCAGGTTTGTTAC | 9678 |
| rs532520134 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958789 | TGTCCTCAAACACCT[G/T]GGCTCAAGTGACCTT | 9678 |
| rs532549736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019460 | GATTTCTTCATGGTT[C/T]AATCTTGGTAGGTTG | 9678 |
| rs532572750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074802 | ATTGCTATCAGCATT[C/T]GGCCACAACCACTTA | 9678 |
| rs532576748 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11003262 | CCCTTAAAATAAAGT[G/T]CACGCTAATAGCAGG | 9678 |
| rs532581004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11030808 | TGTGCTGTTGTTTTG[C/G]GGGGAAATGATTTAA | 9678 |
| rs532581354 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959228 | ACCATAACCACCTAA[C/T]AGCCACAACACTCAT | 9678 |
| rs532586423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014221 | TTTAAATAACTTATT[C/T]GTTCAAGACCACAAA | 9678 |
| rs532594023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160968 | ATTGCTTTTGAGGAC[A/G]TAGTCATAAATTCTT | 9678 |
| rs532636291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11145261 | ATTTCAGTACTATTA[C/T]AGGTGTATGTCCTCA | 9678 |
| rs532639097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992385 | TAAGAGCAAAGGGCC[A/G]GGTGCAGTGGCTCAC | 9678 |
| rs532657972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154423 | ATAAAAATGCTTTGT[A/G]TTTGTAAGAATATGG | 9678 |
| rs532658694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094076 | AGACTTTGGGTCTTT[C/T]CCACTGTGGTGGCCG | 9678 |
| rs532659708 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027391 | CCTTCTTATGTAGTT[C/G]ACTTTGAATACTTAT | 9678 |
| rs532666797 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062886 | CTTACAGGGACTTTG[C/T]AAGGGAATCCATTCT | 9678 |
| rs532674745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014898 | TCCATGTTTTTTTTT[C/T]TTTTACAGGAGACTA | 9678 |
| rs532674936 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121357 | TACAGCATTTATGCA[A/G]AAGAAAACCTTACAC | 9678 |
| rs532694413 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092652 | TTTTTTGCATATGCC[C/T]ACATATCACTCATCT | 9678 |
| rs532698253 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064195 | TCTTGGGTTAAAGAA[C/T]TTTTATATAAAATTT | 9678 |
| rs532700444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135085 | CTGAGAAGTTAGTTT[C/T]TTAGATGTACTCAAT | 9678 |
| rs532711709 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064306 | ATTGTTTGAAAATCA[-/C]CCCCCAAAAGTCTAC | 9678 |
| rs532720630 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11152424 | CTGGCTTTTGTGAGG[A/T]TTATAAATAACGAAC | 9678 |
| rs532726582 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103534 | TATGTTGAATATTTC[A/G]TCACTCAATCTTGAA | 9678 |
| rs532731385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996748 | ACCTAAATAAATCCT[A/G]GGGTACATAGTGTTG | 9678 |
| rs532753075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075138 | GAGACAGAGTTTCAC[C/T]GTGTTGCCCAGGCTG | 9678 |
| rs532784553 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976248 | TATCTTGATTAACTG[-/T]TTTTTTTATCCTTTG | 9678 |
| rs532808924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114103 | GAAAGGAAGTAATCA[A/G]TTGCAAATAAATTTA | 9678 |
| rs532826487 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10975922 | AACGAAATTATATTA[-/C]TGTTGCTACTTTTAG | 9678 |
| rs532833824 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098182 | TATTCAGACATTTTG[A/C]TGATTCTGTTCAAAA | 9678 |
| rs532834941 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11069891 | AGTATCACATTTTAT[C/T]AGATAATACTGGCCT | 9678 |
| rs532849300 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025326 | TACAACAAAAGACTT[A/C]GGATATTACATAAAC | 9678 |
| rs532869078 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973021 | GACTGATTGCAGGAG[A/G]GTCTTCCTTTGCATA | 9678 |
| rs532869823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138694 | TCGTGCAAGTTCTTT[A/G]AAGAGAAAAGAGATC | 9678 |
| rs532872695 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114608 | TTTATTATACCCATA[A/C/T]CCATGAAGTATAGCA | 9678 |
| rs532874629 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11122054 | GTGTGTTGCTTCTCT[-/C]CCTGTGTCCATGTGT | 9678 |
| rs532899091 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134289 | TGCCGCTTTTAAAAG[A/G]TATATCTTTAAATAT | 9678 |
| rs532909977 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017230 | GTGCAGATATCTCTT[A/T]AATGTACTGATTTCC | 9678 |
| rs532934159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097364 | ATAATATTTTATCAA[C/T]AAAAGCTAATGTTGA | 9678 |
| rs532939547 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104870 | AGAACCATTCATAGG[C/T]AGTATTTTTTTTAAA | 9678 |
| rs532955412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034989 | TTAATGATTATTTCT[A/G]CTTAAGATTATTAAA | 9678 |
| rs532957223 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995203 | ATCCCTTAGCTAGAC[A/T]TAAAGGTTCTCCAAG | 9678 |
| rs532983567 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956248 | TTTCCGTCTGGGAAG[C/T]GGGGAGCGCCTCGGC | 9678 |
| rs532993287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073185 | ACTCCATCGTTGATT[C/T]AAAAGTCCAAAATCC | 9678 |
| rs532999495 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019277 | AAATATTCCCTCTTC[C/T]TCTGTTTTTTGGAAT | 9678 |
| rs533010012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11028586 | CATTATTTGTATTTA[A/G]CATTTTAAATATTTA | 9678 |
| rs533035734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012103 | ATCAATGCTGACTGA[C/G]TTCACAGACAAAATT | 9678 |
| rs533039557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978228 | CCTTTGCTAGATGTT[A/G]TGGTGAATTTACAAA | 9678 |
| rs533048590 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017609 | TCAGATTATTAGATT[C/T]TTTCCTGTGGAGTTA | 9678 |
| rs533048864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158443 | CATGATGTCAGTATA[C/T]ATACTATACATTACT | 9678 |
| rs533090821 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984596 | CTTTTGACCACATCA[C/G]TTTCTTCATTTTTAT | 9678 |
| rs533090971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022729 | TTTTTAATGATGTGC[C/T]TGAGATTGCGAGATT | 9678 |
| rs533092107 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159503 | ATATATATTTAATAC[A/C/G]TATGAAATGATTTTC | 9678 |
| rs533101174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962060 | TTCCTCTTTTCCTAA[C/T]TGAATACCTTTTATT | 9678 |
| rs533106125 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11132418 | TCCATGTTGTGGCAG[A/G]TGGCGAGATCTCATT | 9678 |
| rs533122284 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11072717 | ATACCTGAGGCTAGC[G/T]AATTTATAAAGAAAG | 9678 |
| rs533126299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000667 | GTATATCTTCTTGGA[G/T]GAGGTGTCTATTCAG | 9678 |
| rs533127646 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104406 | AATCTCTTAAATGCT[C/T]TCATATCCACAGTAT | 9678 |
| rs533163711 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136217 | GACTTCCGCAGTGCC[A/G]AATCTATTGTATGCC | 9678 |
| rs533165773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131021 | TCACTGAGTAATGTT[C/T]TATTGTATGGATATG | 9678 |
| rs533218783 | snp | A/G | 0.000125102 | 0.00790792 | intron-variant | PHF14 | GRCh38.p7 | 7:11111308 | GTAGATGGTTTTTAT[A/G]TTATTTAGATACACC | 9678 |
| rs533219427 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005567 | CCCTAAGATATTTTT[C/G]TACAACTTGCTTTGT | 9678 |
| rs533219821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11040477 | TTGATGAAAGTCTGT[A/G]ATTATAGATTTCTAA | 9678 |
| rs533232703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000152 | AAAGATGCAAAAGAT[A/G]CAAAAAGGTCAAAAA | 9678 |
| rs533243086 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147332 | ATTTTTACTGTGATT[A/C]TTTTGGTCTTTCCAT | 9678 |
| rs533246370 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966112 | CACCCACTGTCCAAC[C/G/T]AGTTCCAGTGGGATG | 9678 |
| rs533255854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073683 | TGTGTGAGGGTTCCA[A/G]CTCCACATTTCCCTT | 9678 |
| rs533273673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029180 | CCTTGCTCTATTTTT[C/G]TTTAAATAAAATCAT | 9678 |
| rs533285196 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104445 | TCCGTGTCCATAATC[A/G]GTCCAACTACTATAA | 9678 |
| rs533304193 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961630 | GTGGTAGCTTTATGG[G/T]GATAGCATTGAATCT | 9678 |
| rs533305297 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11119906 | GATGGAATCTTTCCT[A/G]GGTGTGATAAGTTGT | 9678 |
| rs533318139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11021246 | CTTTCCCCAGTCAGC[A/G]TCTGTCATAATAGCT | 9678 |
| rs533321428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005064 | TTATTGGTGATAGTT[C/T]AGGTGATGTCAACCA | 9678 |
| rs533328326 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971412 | GGTATTGGGAAACAA[A/C]CAGCAGTTCTTTCCA | 9678 |
| rs533365557 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098716 | TCCAAGGCTGTCTTG[A/G]ACATTTACTGAACAA | 9678 |
| rs533384195 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11151112 | GTGAAATATAAATTT[A/C]AATTTTCTGAGTAAT | 9678 |
| rs533393383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11039618 | GTGAAGGAGCTTTTC[A/G]AACAGATATTTTTCA | 9678 |
| rs533435394 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | PHF14 | GRCh38.p7 | 7:11123797 | GAGGCTGGAATGAGC[A/C]GAGATCGTGCCACTA | 9678 |
| rs533454728 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153697 | GGCCAATATTGTCAT[C/T]GGTAAGGATTCTTTA | 9678 |
| rs533467828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016629 | GGTACATAGTAGATA[C/T]GTATATTCATGGGGT | 9678 |
| rs533470295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164058 | TAATAACTGTTCCTT[C/T]TCTGGTTAGTAAAAG | 9678 |
| rs533494240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137639 | TTGCTCTTGTTGCCC[A/G]GGCTAGAGTGCAATG | 9678 |
| rs533504584 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095268 | TTATTTACATTTATA[A/G]GTGAGAAAACTGAGG | 9678 |
| rs533505626 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057903 | AAACAAAAAATTGGA[A/G]TGTGTCAAGATTTGG | 9678 |
| rs533528113 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11150592 | TCATTAAATTTTTAA[A/G]TAAAGCTTACTTTAA | 9678 |
| rs533549580 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096152 | TGGTTCTTTTATTCT[A/T]TTTCGGTGTCTGAGT | 9678 |
| rs533569916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976771 | AGTTTTGTTAGGTTG[A/G]TATATCTATATATCC | 9678 |
| rs533571540 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11052630 | TTCACAAAGTTTTGT[C/T]CAGTGTTTTAATGCT | 9678 |
| rs533597227 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144035 | TCAACAGCAAAAAAA[A/C]CCCAAATAGTCCGAT | 9678 |
| rs533605681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095934 | GATATATCTCTACCT[A/G]TATATAGAAGGTCAG | 9678 |
| rs533609637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021792 | GGCTTTTTTCCCCAA[C/T]AAAAAAGATAATTTT | 9678 |
| rs533624515 | snp | C/G | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990727 | ATTCTTGAGAAGAGT[C/G]AAAACTGGAGCTCTC | 9678 |
| rs533624645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11059991 | TCTTCCCACCACAGC[C/T]TCCTGAGTAGCTGGG | 9678 |
| rs533634677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052494 | CAAGGAGTTTGTGTA[C/T]GTATTAAGGTGTAGA | 9678 |
| rs533640802 | snp | G/T | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:10970976 | TTCATGATAAAAACA[G/T]TTGGCAAACTAGGAA | 9678 |
| rs533660860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083674 | CACCATCTTGGCCAG[G/T]CTGGTCTCAAACTCC | 9678 |
| rs533664668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005238 | ATTACAATTACACTG[A/G]TTACATATGTAGGCT | 9678 |
| rs533664746 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11090353 | ACAGGCCTACAAAGG[A/T]CTAAATCAATGGGAT | 9678 |
| rs533668246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976915 | TGGTCTCAGGTCACA[A/G]ATTTGTATGTATAGT | 9678 |
| rs533668539 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970811 | TTTATACAACATGAC[G/T]AAGTAGAATTTATAC | 9678 |
| rs533701876 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11163275 | TTAAATATGCAACTT[G/T]TATCATACAAAAAAA | 9678 |
| rs533721217 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152638 | AATAAGACTAACTTA[C/T]AAGGATATCGTAATA | 9678 |
| rs533728840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994511 | AGTTTGTATGGCTAG[A/T]ACTGGGTGAGCAAGC | 9678 |
| rs533730390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144214 | AAAGACAAAAAATAG[C/G]AAATGGTAGCAAGCA | 9678 |
| rs533740955 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967765 | CAGAACTGCCACCTC[A/C]GCCCACCCCAGTCCA | 9678 |
| rs533745830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072193 | ATCATGGCAGAAAGC[A/T]AAGGGGGTAAAGGCA | 9678 |
| rs533778597 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989335 | TGGTTGAGTTTAAAA[G/T]AATATAAAAATATAA | 9678 |
| rs533784942 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966113 | ACCCACTGTCCAACC[A/G]GTTCCAGTGGGATGA | 9678 |
| rs533791573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10982237 | GGAATGTCTACCATT[C/T]TTTGACTTAAATTTG | 9678 |
| rs533792733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137073 | GCAAAATTAAAGTGG[C/T]TTGTGACTCCACGGC | 9678 |
| rs533794581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11144660 | TTTATATCACTGTAG[G/T]TTGACTATGGTTAAC | 9678 |
| rs533811816 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065827 | TGGCACATTTATTAC[-/T]TAATCAGAGATAGGA | 9678 |
| rs533817877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096615 | ACTATTAAAAGCTCT[A/G]TTTGGTTGTTGCCAA | 9678 |
| rs533827459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046659 | TTTACAGGTATTATA[A/G]CTACAAAAAGAATAA | 9678 |
| rs533840988 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039700 | TTAAATATTTTAAGA[A/G]GTGATACATACTGAT | 9678 |
| rs533850972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983270 | CCTATTTATAGACGG[C/T]TGTGGGATGAATGAG | 9678 |
| rs533870213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130762 | TAATAATGACACATG[C/T]CCACCATTACAGTGT | 9678 |
| rs533879522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053165 | AATTTTTTCCTTAAA[A/G]TAACAGTTTTCTCAA | 9678 |
| rs533895867 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994718 | CGGAGTTTGCTCCTT[A/C]TGATGTTCGGATGTG | 9678 |
| rs533908142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168056 | TCATCTGTAGGAACT[G/T]TTTTCTAAAAGTGGA | 9678 |
| rs533923628 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11154319 | AAAAGAAAAACAAAA[A/T]GTAAACATCATTTCA | 9678 |
| rs533952417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155933 | TTTGTCCTTATGTTT[A/T]ATAGCCTATATTATG | 9678 |
| rs533969093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116419 | GACTGGATGTAGGTA[C/T]ACGTATTCATACACA | 9678 |
| rs533985536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082951 | CATGCCACAGCACCA[A/G]TGGCTTATCAGTACC | 9678 |
| rs534006081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960285 | GAGATGTTCCCCATC[C/T]TGTGTCCATGTGTTC | 9678 |
| rs534012593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151987 | ATACCACAATAAATC[C/G]TAAATATTTTCAGAA | 9678 |
| rs534020534 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | PHF14 | GRCh38.p7 | 7:11128431 | AATAAAAGTGCCACT[A/G]CCTCCTCTGTTCTTT | 9678 |
| rs534020604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076425 | TAGTTGTATTTAATA[C/T]TATTTTTTTAAAATG | 9678 |
| rs534028805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150236 | AGAGCTACAATACGC[A/T]TTAGAATGCTTATGG | 9678 |
| rs534028964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162732 | TTGATATGGAGTTTC[A/G]GTCTTGTCGCCCAGG | 9678 |
| rs534047481 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11102360 | GTTTAGAGTATCTAT[C/G]TCTTTGGACCAGATC | 9678 |
| rs534064759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027596 | GTAATTTCAACAGTT[C/G]ATACCTTGGTTTTAT | 9678 |
| rs534077998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033304 | ACTGAGGGGAGTTTG[A/G]TTCCAGGGATCAGTT | 9678 |
| rs534099808 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964446 | CTGTTGAGAGATCCA[C/G]TCTTGGTCTGATGGG | 9678 |
| rs534105916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015507 | AGAGTGGCCTAGTAT[C/T]AGGGAGTTTAGTAAG | 9678 |
| rs534134941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11057990 | AATCAGTTTGGAATT[A/G]CACCCTTGCTTGATT | 9678 |
| rs534137926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142422 | TTCCTGGACTAGGAA[A/G]TACAAATAGAATAAG | 9678 |
| rs534142024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004060 | TGAGACCAGCCTGGG[C/T]AATGTGGTGAAACCC | 9678 |
| rs534159782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082304 | AGTGAGCCATGATCA[C/T]GTCACTGTACTCCAG | 9678 |
| rs534197911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960789 | GCCATTGTAACTGGC[A/G]TGAGGTTGTATCTCC | 9678 |
| rs534200635 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11135323 | CAGTGAACCTGACCA[A/C]TACCTAATTCATTCT | 9678 |
| rs534217943 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11051222 | ATTTTCTTTTTTTTT[G/T]TGTGAAGACAGTCTC | 9678 |
| rs534224785 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11093443 | TTCTTGTTGCTCTGC[-/T]TTACCTCAGTGTACC | 9678 |
| rs534230633 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11004756 | AGACGTATAATGTGG[C/T]TGGGTGCGGTGGCTC | 9678 |
| rs534235488 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969995 | ATATAGAACTCTGCT[G/T]TTCATAATTATTACT | 9678 |
| rs534246062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008818 | AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCGA | 9678 |
| rs534298383 | snp | C/T | 0.000509857 | 0.0159583 | intron-variant | PHF14 | GRCh38.p7 | 7:11035809 | ATTCATGTCAAAACC[C/T]GTATGTTTTTGTTTT | 9678 |
| rs534298733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042914 | TAATAAAGTATTTGG[A/C]ACATTTTAAAATTGA | 9678 |
| rs534340393 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11074658 | AGTTCAAACTTCCAT[A/G]GATCCCAAGAACATG | 9678 |
| rs534358874 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166286 | CATGTAGCCAGGGTC[G/T]TCTTTCATTGGGAAA | 9678 |
| rs534360834 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023806 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 9678 |
| rs534367278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11057413 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 9678 |
| rs534370166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057562 | GTATTTTAGTAGAGA[A/T]GAGATTTCGCCATGT | 9678 |
| rs534383467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10991369 | TTTTAGTAGAGATGG[A/G]GTTTCACCATATTGG | 9678 |
| rs534387005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11029719 | TTGGAGTCCTCAGTA[A/G]TTTTTAAGAATGTTA | 9678 |
| rs534395253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963574 | GGGGTGGGGAGTTCT[A/G]TAGATGTGTTTTAGG | 9678 |
| rs534399701 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957231 | CTTATTTGTTTTTCA[C/T]TTTTTTCTGTTATAT | 9678 |
| rs534399957 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11014457 | CTACCCTAGGTTGGG[G/T]TTCAGGCTTTGTTGG | 9678 |
| rs534402640 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111689 | CTGGAATATTTAGTT[A/G]TTTTACGTATTCTCT | 9678 |
| rs534439983 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10974730 | GAGAACTCAGTTAGA[C/G]AAAAATTCCTTGTGC | 9678 |
| rs534454603 | in-del | -/GATGTGGA | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11000301 | GACTTTCTGTTGTAT[-/GATGTGGA]GATGTGGAGTATCTT | 9678 |
| rs534534527 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146418 | CATTTCTGGACTATG[A/G]CAAAATTTCTAAATA | 9678 |
| rs534552110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006172 | TACCAACAATGCACA[A/G]ACTACTTGATAACAT | 9678 |
| rs534574539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963000 | TTGCTAGCAGTCTAT[C/T]TATTTTGTTGATCTT | 9678 |
| rs534589817 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132757 | TCTCCACCCCCTCAC[C/G]AACATTTGTTATCTT | 9678 |
| rs534591680 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11046431 | ATATATCCTTTTATT[C/G]CTTGGATATGTCTTT | 9678 |
| rs534603407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966832 | AATAAAACCACTACC[A/G]CCAAACATAAGGTAA | 9678 |
| rs534604499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002261 | TGGTTTAGAAGAAAG[A/T]AAAAATGGGGGGATA | 9678 |
| rs534620645 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126527 | ACTACATATGAATCT[A/G]ATTTTTGCAGTGAAA | 9678 |
| rs534669457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996022 | GCGGCCAGAGTGGGC[A/G]CCAAGGCCGAGGAGG | 9678 |
| rs534677415 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10995502 | TCACCCAGTGGATCC[C/T]GCACCAGGGCCACAT | 9678 |
| rs534686410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119568 | AATATCGCCTAAATA[A/G]TAGAAAAGGCTTAAA | 9678 |
| rs534697583 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11074488 | GTGCTGGGATTACAG[A/C/G]CATGAGCCACCGTGC | 9678 |
| rs534718648 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11030257 | GAGAGGGCAATACAG[G/T]TAAGAGTTAGAGGAC | 9678 |
| rs534739962 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972639 | TATGGAAGGATGAGT[C/G]GTTTTCATTTGAGAG | 9678 |
| rs534767217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023017 | TTGCTTGAAAGAGAA[A/G]GGTTTTACTTGTTAG | 9678 |
| rs534805762 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091111 | ATTGTGGTGACATAC[C/G]TGATGAACACATGGG | 9678 |
| rs534822884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11097254 | GAAGTGCTGGGATTA[C/T]AGGCGCGAGCCACCG | 9678 |
| rs534841018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978510 | GAATTGTTTTTTTAT[A/G]TTTGGGGATCAGTGT | 9678 |
| rs534850416 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084192 | ACAGAACTTAAACTT[C/G]AAAATATGTACACAC | 9678 |
| rs534874162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048268 | AGATAATCATGATTT[C/T]CCTTAAAATATTATT | 9678 |
| rs534879836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999821 | ATGCCAATTAAGTCA[A/G]CAGGATGTTGTGTCT | 9678 |
| rs534892300 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11000322 | GGAGTATCTTTTCAT[A/T]TGCTTATTTGCCTTT | 9678 |
| rs534906847 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973161 | TGATTGCTTTTTGCA[C/T]CAATGTTTGCACAGG | 9678 |
| rs534908813 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11123860 | GAGGCGGAAGTTGCA[A/G]TGAGCCGAGATCGTG | 9678 |
| rs534913172 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135902 | TAGCTTACATAATTT[C/T]CAGCTGGCTGACCAA | 9678 |
| rs534938248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085508 | TTGTTTCTATTGTAG[A/G]TGTCAGTGGTGAACA | 9678 |
| rs534953406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117546 | TATCTTTTCTGCATT[G/T]AAATAAATTCTATAA | 9678 |
| rs534953499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995174 | GACACAGAGTGCTGA[C/T]TGGTGTATTTACAAT | 9678 |
| rs534956935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077773 | AGGCAGGTTCAGTTA[A/G]ATGAGTGGAGCAATA | 9678 |
| rs534965191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034752 | CAGGCTTTTGCCGTG[C/T]TGGCCAGGCTAGTCT | 9678 |
| rs534967099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956439 | GTGCACGGACTTTCA[C/G]TTTCAGAATTGACAG | 9678 |
| rs534985892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067091 | TTAAGGGATTGAGAA[C/T]ATATAAAGAACTTGG | 9678 |
| rs534986796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073279 | GTTATTTACTTCCAA[A/G]ATACAATGGTGGTAC | 9678 |
| rs534989248 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072940 | CAGCAAGAATTTGCT[A/T]ATTCCCATGGGTTTA | 9678 |
| rs535008377 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097888 | ACAGCCCATGGTGGG[A/C]AAATGAAGACTTTAA | 9678 |
| rs535011712 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975381 | GTATTAGCTCTTTTA[C/G]TAGAATAAAATTGAC | 9678 |
| rs535014055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118311 | GGTGGGTGGGATAAA[A/G]CCCACAGATTTCCAG | 9678 |
| rs535062070 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10984346 | TAACTTCTGAAACCA[A/G]TATTTTATATGAAAA | 9678 |
| rs535072082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984892 | TTAGGTTAATAGTCC[C/G]AAACACAAACACATT | 9678 |
| rs535088256 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019909 | TGCTGTATCCCATAG[A/T]TTTTGGTATGTTGTG | 9678 |
| rs535093801 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084975 | ATAAGTTGCAAATAT[A/T]TTCTTTAAGGTTGTT | 9678 |
| rs535102978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048100 | AAGATTATCTTCAGT[A/G]TTGTCCATGGGAATT | 9678 |
| rs535122927 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973193 | GCATGACCTTTGTAA[C/T]TTCACTTCAGCCTCT | 9678 |
| rs535127815 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11041456 | TGTATGTATGTGTGT[A/G]TATATTTATCTATGT | 9678 |
| rs535135157 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105104 | ATCAATAAACATAGC[C/G]TGTGTTCACAATTCA | 9678 |
| rs535135689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977912 | AGGAGACTTATTTAC[A/T]TTTGGTTATCTGCTA | 9678 |
| rs535141868 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079971 | TTGTTGCATATTGCT[A/G]GAGCTGATTATACAA | 9678 |
| rs535161721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967101 | CTCTGAGATTTTGAG[A/G]CTTGGTTTTCAATTC | 9678 |
| rs535164074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035290 | ACATAAGACGCTTGA[A/G]CATCCACAGATTTTG | 9678 |
| rs535171318 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995536 | GAGCTGCCCGCCAGT[C/G]CCATGCCGTGTGCCC | 9678 |
| rs535185892 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11012443 | TTTTGTATCCCACAA[G/T]TGTATTTTCACTCTG | 9678 |
| rs535194105 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966202 | GAGCTGTAGACCGGA[A/G]CTGTTTCTATTGGGC | 9678 |
| rs535219800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962994 | TTAATCTTGCTAGCA[A/G]TCTATCTATTTTGTT | 9678 |
| rs535255833 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984036 | ACATGTAGAACTGTA[A/G]TAATTCTGTGATTTC | 9678 |
| rs535268055 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048518 | GGAGGTTACAGTGAG[C/T]CTTAGATCATGCCAC | 9678 |
| rs535272104 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11164291 | TAGTTTGTTCATATG[A/G]CCAAATTATAAAGGG | 9678 |
| rs535277000 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963097 | CAGTTCTGCTCTGAT[-/C]TTAGTTATTTCTTGT | 9678 |
| rs535286929 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016912 | CTGCACTATCCTTCC[C/G]AACGTCTAGTAACCA | 9678 |
| rs535312676 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075088 | GACTACAGACACATG[C/G]CATCACACCTGGCTA | 9678 |
| rs535312931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078451 | AGAGGCTGTATAACC[A/G]TGAGAAATGCAAATA | 9678 |
| rs535316502 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972177 | CCAACCTCAAGTGAT[C/T]CACCCGCCTCAGCCT | 9678 |
| rs535322210 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011211 | AATTATTTACTAATT[G/T]TATATGGCTCTTTTC | 9678 |
| rs535323440 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961810 | TAAGTTGCATTCCTA[C/G]GTATTTTATTCTCTT | 9678 |
| rs535338906 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11157642 | GATCATATTACATTT[G/T]TACCATATTACAGTT | 9678 |
| rs535363226 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11108627 | AATGGCATGTATTTG[C/T]TATCTTCTGATAAGC | 9678 |
| rs535363412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138341 | CCACTGCGCCTGGCC[A/G]GAAAAATATTTCTAA | 9678 |
| rs535375455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11035123 | TTGAAAAAAAAAAAG[C/T]GTAATAAAAAAGAAT | 9678 |
| rs535394856 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047642 | AAATACAAAAATTAG[C/G]TAGGAATGGTGATGG | 9678 |
| rs535396699 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046289 | TAGTTCAAATAGTTA[A/G]TCATCTCTTAATTTT | 9678 |
| rs535425396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132044 | GTAAAAAGTTACTAT[A/G]GTTCAAGTTAGCATA | 9678 |
| rs535431219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091517 | CCCCAGCACTTTGGG[C/T]GGCCAAGGTAGGCAG | 9678 |
| rs535443519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027729 | TAAAGATATTTAAAA[C/T]ATGCATGATTTCTAG | 9678 |
| rs535447784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117352 | TGCTACATTTTTTGA[A/G]TAGTAATAATTTTTG | 9678 |
| rs535459853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11085424 | CATTGATGTAACCTT[C/T]TGTGTAATGTATTGG | 9678 |
| rs535463050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994881 | CAAAGAGCGAAAGAA[C/G]AAAGCTTCCACAGTG | 9678 |
| rs535484902 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963393 | TAGTTGTTTTGAGTG[A/C]GTTTCTTAATCCTGA | 9678 |
| rs535494671 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11042074 | TAGCAATCACAAAAT[G/T]CCACAATCTTTGCAA | 9678 |
| rs535511308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001461 | TTGATTGGGATTTTA[C/T]TGAATCTATAGATCA | 9678 |
| rs535529775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028273 | GGAAAACAGAATGGT[C/T]GTATGGGTACTGAAA | 9678 |
| rs535530833 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11110999 | TAAAATGATTTAATG[A/G]GCAAATGATTAATTC | 9678 |
| rs535532032 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104705 | GGATTTGTAAAAACA[C/T]AGGTGACTACCCTAT | 9678 |
| rs535551232 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103712 | AATAGAGTAGGTAAT[A/G]TTATAGATAATCAAA | 9678 |
| rs535558698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11066995 | AAGTTAAAAACTTTT[A/G]TGTGTGAAAGGACAC | 9678 |
| rs535562977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022110 | AAAAAAGGTTCAGAG[C/T]AGTTTTTAAAAAATG | 9678 |
| rs535570150 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11119027 | AGCCACTTTCTAAAT[G/T]ACGCTTACTACAAAC | 9678 |
| rs535598406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132925 | GAAATGTCTATTCAA[G/T]TCTGAAATTTAAAAC | 9678 |
| rs535606168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067393 | AATTGTGCAGCTACT[A/G]GGGAAAACAGTATTT | 9678 |
| rs535643382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061266 | TTATGTGGCATTTTA[A/G]TTAGTTTTATGTTAA | 9678 |
| rs535659475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089748 | GACTTTAGTGTAGAA[C/T]TGTTCATGCATTCTT | 9678 |
| rs535673551 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11017275 | ATACCCAACAGTGCA[A/G]TTGCTGGATTATATG | 9678 |
| rs535677071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130642 | CATGTGGTACATTTG[C/T]TAAAAATTGATGAGC | 9678 |
| rs535678418 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10984836 | TTTAGTTTTTTTTCC[A/C]CACTAGAAGACACTT | 9678 |
| rs535684354 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11097430 | TATCAGAGTCTCCTC[A/C]GTTTTCTAAATTATG | 9678 |
| rs535685496 | snp | A/T | 0.00067874 | 0.0184095 | intron-variant | PHF14 | GRCh38.p7 | 7:11036388 | TTTCATTTTATTATC[A/T]TTTAAAATTTGAATA | 9678 |
| rs535698449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11083609 | GGGATTACAGGTGCC[C/T]GCCACTACGCCCGGC | 9678 |
| rs535739603 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977715 | TAAAATAGGATATAT[A/T]TGCATTATTAGAATT | 9678 |
| rs535743687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999777 | GTCTGAATCAAGGCA[G/T]ACAAATGAGATGATC | 9678 |
| rs535748531 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985017 | GCTTGAGTCATTTTC[C/T]CCTCAATTCTATTAT | 9678 |
| rs535772776 | snp | A/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11123853 | AACCCAGGAGGCGGA[A/G]GTTGCAGTGAGCCGA | 9678 |
| rs535772905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116668 | TGATAACTTTTAAAC[G/T]GAATTGTTCAGGAAG | 9678 |
| rs535773493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091039 | ATGTTAAGGGGTCCA[A/G]TGGAGATTTATTGAA | 9678 |
| rs535779314 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11078517 | GAGCAATGCATTAGA[G/T]TGATTTAAAAATCCC | 9678 |
| rs535790820 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092636 | TTTAAGGGCATATGC[C/G]TTTTTTGCATATGCC | 9678 |
| rs535806722 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961757 | TTTGTTGAGCAGTGG[C/T]TTGTAGTTCTCCATG | 9678 |
| rs535824738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11000259 | TGGAGTTTCTGTTGT[A/G]TGATTGATTTTGTAT | 9678 |
| rs535844775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075282 | CTTCTTGGTACCAAT[A/T]TTCTCTGTTAGTTGA | 9678 |
| rs535852425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997349 | AAGTGACCAAATGCA[A/T]TTCCTGTGATGAGTT | 9678 |
| rs535890054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995127 | TGAGCTAGACACAGG[A/G]TGCAGATTGGTGTGT | 9678 |
| rs535894665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072853 | GGTGAGCCAGTATAT[C/G]ACATAGAGTGAACAA | 9678 |
| rs535916203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048162 | TGCTAAGTAAAAATA[C/T]ATAGAATTAAGGTGA | 9678 |
| rs535942515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157935 | TAACAAAAATTAGAT[A/G]TTTGTCTGGTTTTAT | 9678 |
| rs535954299 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044095 | GGAAAAGAAAACCAA[A/G]TACTGCATGTTCTCA | 9678 |
| rs535959141 | snp | C/T | 0.000126725 | 0.00795905 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111428 | TAAACAGACAGGCTA[C/T]GGATGGATATGTCAG | 9678 |
| rs535965658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155315 | TGACAACAAAGCCCA[A/G]ATTTCCTCCACTACA | 9678 |
| rs535974317 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10984202 | ACAAGTTTTACATAG[A/C]AGTGATTATCTATTT | 9678 |
| rs535978478 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11042940 | ATTGACTGTCATCAA[-/TATT]TATTATAGCATTATG | 9678 |
| rs535999699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007837 | ATAAGGATCTTTAAG[C/T]TGAGATTTTGCTAAA | 9678 |
| rs536007008 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088082 | ATTGATTCCAGGACC[A/G]CTCTCGGATATCAAA | 9678 |
| rs536029838 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965606 | TGCTCTCTTCAGAGC[C/T]GTCAGGCAGGATGTT | 9678 |
| rs536030809 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11002376 | GAATGAAGTATGGTT[C/T]CTGGTATAAGGCAAA | 9678 |
| rs536078533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046440 | TTTATTCCTTGGATA[C/T]GTCTTTATTTTATGA | 9678 |
| rs536098837 | in-del | -/GAGG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072971 | GTGCCAAGCATTCAT[-/GAGG]GATCTGCCCCTGTGG | 9678 |
| rs536110059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120729 | TTTAAATATAGGATT[A/G]TGGTCCTATGTGAAT | 9678 |
| rs536120465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127979 | ACCTCCAGGCCACCA[C/T]TTACTCTCCTCCACC | 9678 |
| rs536126436 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094840 | TCTTTTATGGGGTCT[A/G]TCTTTCTTGTATTTC | 9678 |
| rs536137482 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070775 | TTTATTTCTAATGAC[C/T]GTGATAGTCTAATGC | 9678 |
| rs536139630 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965895 | TGTGTTGGCCTTGCC[A/G]AGCCAGGCACGGGAG | 9678 |
| rs536141325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11081638 | GAGGTGGGCGGATCA[C/T]GAAGTCAGGAGATCG | 9678 |
| rs536159165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084036 | AGTATAACATTACAT[A/G]AGGATATGAGAAGAT | 9678 |
| rs536163167 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125813 | ATATTTTCTCTGAAG[G/T]TTTCTTAAAGGTTTA | 9678 |
| rs536170358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077048 | ACTACATTTAATACT[A/G]TCTATATTTATGAAA | 9678 |
| rs536170982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113637 | TGAAAAATGAAATTT[A/C]ATATAATATTTAAGC | 9678 |
| rs536172679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121253 | CACATTCCTTGTTGA[A/G]TCTGGAAGTTAAGGT | 9678 |
| rs536217888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161151 | AGCCAGTTGCCAGCA[C/T]CATTTATTGAATGGA | 9678 |
| rs536222648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992526 | AAATTAGCCGGGCGT[G/T]GTGGCTTATACCTGT | 9678 |
| rs536273667 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981552 | TACAGTCCTGTGAGC[C/T]CTTTAATGTCTTCAG | 9678 |
| rs536294793 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070124 | GTGTTTCTCTTTTTG[A/G/T]TTGAGACAAGGTCTC | 9678 |
| rs536319698 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032519 | AAAAAAAAGATTTTA[A/G]GATTCTAGACCAAAT | 9678 |
| rs536322466 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11017865 | GTCCTGGATTCCCCA[A/G]TGTTTTCTTGTAGTA | 9678 |
| rs536324939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133600 | TTAGGGATCAGAAGA[A/G]GACAGGAAAAGCTAA | 9678 |
| rs536332927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148704 | TGACACATAATAGAC[A/T]CACATTTGTAGGTTA | 9678 |
| rs536334361 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138234 | TTTTAGTAGAGGCAG[G/T]GTTTCACCGCGTTAG | 9678 |
| rs536358469 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029813 | ATTTTTATTGCACAT[G/T]CATGATGGCTTTATG | 9678 |
| rs536359493 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973997 | AGTTTTTCTTTCTTT[A/C]ATTTTTTTTCTTCTA | 9678 |
| rs536366905 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007189 | CAAGAGCGAAACTCC[A/G]TCTCACAAAAAAAAA | 9678 |
| rs536371737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11086121 | AACTCTCTCCTGGAC[C/T]GTTGCAATAACCATC | 9678 |
| rs536376638 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11012001 | ACAAACTTTTAGGCA[-/T]CTTGATGCTGAGAAA | 9678 |
| rs536403044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074104 | TTCCCCCATGTCTTG[A/G]CTATTATCATTTGTC | 9678 |
| rs536408821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086696 | GTTATAATTGTCAGA[A/T]ATTAATGGGATCTTG | 9678 |
| rs536411353 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11163822 | TACATATCTAGCATA[A/T]GTTTTTAAATGAATA | 9678 |
| rs536419784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166183 | TACTTTCCAGTAGCC[C/T]CAAAGGATACATTTT | 9678 |
| rs536420169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158795 | TCATAGTTGCTTACA[G/T]ATTAGCCTGAAGTCC | 9678 |
| rs536434049 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000220 | CCTCTAGTTTAAATA[A/G]TTTCCCATTTCCCTT | 9678 |
| rs536447275 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11127237 | TAGATTTTGATTCTT[G/T]CCCCTCCTTTTTTTT | 9678 |
| rs536488376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068108 | GTAATCCCAGCACTT[C/G]GGAAGGCCAAGGCAG | 9678 |
| rs536490591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166853 | GGTGTGAAACAGTTA[C/T]GTACCTGTCCTGAAC | 9678 |
| rs536505918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037464 | AGTTGGTGTGAGGCC[A/G]ACTCATGTGACTCTG | 9678 |
| rs536506463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985581 | TTAACATATGCTTAA[A/T]GGCCTTAACAACATG | 9678 |
| rs536525886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062254 | CTTAACCTCTCACAC[A/G]TGGTTATACTCTGGA | 9678 |
| rs536527483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068799 | CAGGGAAAGGGGCTG[A/G]GGCAGGGGGACATTA | 9678 |
| rs536535340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074897 | CTTCCAACCTCTGCC[C/T]ATTACCCAGTTCCCA | 9678 |
| rs536548018 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054511 | GTGATCAGTCATTTT[G/T]GTCTTGATCTTACCA | 9678 |
| rs536610672 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964368 | ATGAAATTCTGGGTT[G/T]AAAATTCTTTTCTTT | 9678 |
| rs536614347 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062728 | CTTTTCCCAACGGTC[C/T]AGAGGCTGCTAATTT | 9678 |
| rs536625907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037296 | GCATAATTTTGATCT[A/C]TTTACATGTATTATT | 9678 |
| rs536628120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030301 | CGTAAATACTTGGAT[C/T]AGGGAATCTATAGGA | 9678 |
| rs536654173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056051 | GTGACCTCTGAGGTA[C/T]GAGTCAGATTATAAA | 9678 |
| rs536659767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147939 | ATTATTGGTTTCTTG[A/G]TTCTTCTCTATTCCC | 9678 |
| rs536692967 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014251 | ACTGGTGAATGGTCA[A/G]TTTTGAACCTAGATC | 9678 |
| rs536695076 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10996816 | CGGTTGTGAGAACCA[A/G]AGCCCACAAGATAGG | 9678 |
| rs536727817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069681 | CGTCCCCTCCCTTTC[C/T]CTTCCTTCCTTCCTT | 9678 |
| rs536730398 | snp | C/G | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10958892 | TTTTTTGTAGAGATG[C/G]GGTCTCACTATGTTG | 9678 |
| rs536736788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049097 | ACAATGATTTATCTG[A/G]AAAGGTACCTGCTTC | 9678 |
| rs536744730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153954 | CTGTGTGTGCGTGTG[C/T]GTGTGTGTGTGTGTG | 9678 |
| rs536749854 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973700 | GCACAGGGTTTGGCG[C/G]GGATCTCTGCTCCGC | 9678 |
| rs536760121 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968111 | ATTTCATGTAGAAAA[A/T]TATTTTGGTATGTAT | 9678 |
| rs536790830 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11044022 | AAAAAAGGGAAATCA[C/T]GTTCTTTGTAGCAAC | 9678 |
| rs536803630 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006880 | TGTCTTGTGAAAAGC[A/G]TAGTCATTTCTTGTC | 9678 |
| rs536806215 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957165 | GGTGTTGATGTGGAT[C/G]GTGTTTATAAGGGTG | 9678 |
| rs536814564 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053876 | TTCATCTTGTTCTTT[A/G]TCTCTAGTTTTCTTG | 9678 |
| rs536827087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029601 | AAAGTGTATACTTCG[A/G]TAATGGACCCATTAT | 9678 |
| rs536829540 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11020700 | TTCTTTTTTTTTCTT[C/T]AAAATTCTAGATTTA | 9678 |
| rs536830248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119554 | CTCACAATTGTGAAA[A/G]TATCGCCTAAATAAT | 9678 |
| rs536835730 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10995765 | CACTGCTGGGGGACC[C/T]GGTGCACCCTCCACA | 9678 |
| rs536843242 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977015 | AAATTGAATCATATT[A/T]TTGACTCTTGTTTTA | 9678 |
| rs536873906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11042245 | TTTACAACTAATGGT[A/G]GGAAATAAACTACCT | 9678 |
| rs536876643 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997900 | CCATATTCCGCTGTT[C/G]ACACAAGCCAACCCT | 9678 |
| rs536882317 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085120 | TTATGAAATAGACAA[C/T]AGATATATATTATTT | 9678 |
| rs536901102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112695 | AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG | 9678 |
| rs536930854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126563 | TTTCTCTCTTCGTTA[C/T]TTAGCTGTTTCAAAA | 9678 |
| rs536952865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024292 | TTAAGGAAAGAAGCC[A/G]TCTCCGTAATATAAA | 9678 |
| rs536953696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166351 | AAAAACCCTCCTGTA[C/T]ATCAGAAGAAATTTT | 9678 |
| rs536961562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086586 | ATTCCAGGTCCGAAG[C/G]CAATGCTTATCACAT | 9678 |
| rs536963493 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138142 | GCCTCCTGGATTCAC[A/G]CCATTCTCCTGCCTC | 9678 |
| rs536968217 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106028 | CAGTTTATTAAAGAA[A/C]AAAGCAGACATGTTT | 9678 |
| rs536985609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043660 | TTTTTCACTATTTTC[A/T]CATGATTGCTTTTTT | 9678 |
| rs536988434 | snp | A/G | 0.000145112 | 0.00851673 | intron-variant | PHF14 | GRCh38.p7 | 7:11036707 | AGTATAGACACTGGT[A/G]CATGCACATTTTCAC | 9678 |
| rs537019302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166735 | ACCTAGGTTACAGCT[A/G]TCCTTCTAAAAGGAA | 9678 |
| rs537033837 | in-del | -/CAAC | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11084138 | ACTTCAAAGTATTTA[-/CAAC]CATTACTATTTGTTT | 9678 |
| rs537044107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017451 | AACTGGGGTGAGATG[A/G]TATTTCATGATAGTT | 9678 |
| rs537060091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120544 | ATGCAGAAAAATGTC[A/C]ATTTGTTATAATTTC | 9678 |
| rs537063713 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169664 | TAGAGTAATTTCGAC[C/T]TTTTTATTCAAAAGC | 9678 |
| rs537084258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160393 | TCTTTTTGGTAGAAT[C/G]ATTTATTTTCTTCTG | 9678 |
| rs537105837 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992484 | CCTGGCCAACATGGC[A/G]AAACCCCATCTCTAC | 9678 |
| rs537114889 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11026680 | AAAGTGTCCAGTTAC[A/G]TTATCTGATGTCTAG | 9678 |
| rs537125883 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11069606 | TGAACGTATTCCCTC[C/T]CTCCCTCCCTCCCTC | 9678 |
| rs537128352 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059819 | TTATGCAAATTAGAT[A/G]ATAGAGTACCAAATT | 9678 |
| rs537139120 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163978 | TATATATGTATTCTT[A/G]CACTTTTAAAAGAAA | 9678 |
| rs537141157 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163467 | TAATTGTGGTCTTCA[A/G]TTGCTCATTCAATGC | 9678 |
| rs537141919 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133452 | TCAGTAAAGAAAATA[C/T]AGTCTTTTCAGTTAA | 9678 |
| rs537151891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091618 | GAATTAGCCGAGTGT[G/T]GTGGTGGTGCATGCC | 9678 |
| rs537152274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024799 | CTCTGATGAAGTACA[A/T]GGAGATTAATGTGTT | 9678 |
| rs537164347 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10979154 | GGGAGAACATTGGAT[A/G]TAATGGTATTGATGG | 9678 |
| rs537167257 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10987098 | AAATTTATAAATATC[C/T]ACTTCTATTTGGGAC | 9678 |
| rs537178001 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160417 | TCTTCTGGCTATATA[C/T]CCAGTAATGGGATTG | 9678 |
| rs537186536 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11048465 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA | 9678 |
| rs537213608 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967279 | TTGGAGGGCTGAGTG[A/G]TGGTGGTGCCACTGT | 9678 |
| rs537219451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165068 | TAGCTGGGACTATAG[G/T]CGCCCGCCACCACAC | 9678 |
| rs537222219 | in-del | -/TTAAGT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11156833 | ATTAACTTTCTACAC[-/TTAAGT]TTATTTCCAAAGCAT | 9678 |
| rs537232650 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995297 | TAAAGGTTCTCCAAG[G/T]CCCCACCAGATTAGC | 9678 |
| rs537258376 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118436 | AATGTCTTTTAATCC[C/G]TTAGTTTCTAATTGA | 9678 |
| rs537284577 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083041 | CTTCTACCCCCTCTC[C/G]CCTCTCTCCCTTATG | 9678 |
| rs537303505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043059 | ATGAATTCTGTCCAT[A/T]GCTTATAATTCTCTT | 9678 |
| rs537319025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111634 | TCTTGCTCTTAAATT[A/G]AGGAAAAAACAACTC | 9678 |
| rs537321842 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080531 | GCTCTTTATGGAACT[C/T]TGCAGGTATAGATTA | 9678 |
| rs537336240 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967987 | TGGGTCAAATAATAA[A/C]TATCAAATTCCCAGT | 9678 |
| rs537338528 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11068964 | TGCATTTTTAAGAAT[A/G]TAATGTTTTTGATGC | 9678 |
| rs537349630 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023107 | TATTTAGCACTAAAT[A/C]ATTTATTATTGATAG | 9678 |
| rs537360826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080161 | AGAGGAAGTAACTTG[C/T]CAAAATAGACTTTGT | 9678 |
| rs537367662 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106630 | TAATCAAAATAATTG[A/G]CCACTATTCAATGAA | 9678 |
| rs537367907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985023 | GTCATTTTCCCCTCA[A/G]TTCTATTATTCAAGC | 9678 |
| rs537368760 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077537 | ACCCAGGAGGCAAAG[C/G]TTGTAGTGAGCCCAG | 9678 |
| rs537370708 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991150 | CGCCCACCACCACAC[C/G]TAATTTTTGTGTTCT | 9678 |
| rs537398611 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122941 | CAGTTTGTCAAAATC[A/C/G]AGAATCTTCCTCTAT | 9678 |
| rs537399238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152723 | CAATCTGTAAATAAC[C/G]AAGTGGATGTTCATT | 9678 |
| rs537404991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061533 | AATTTTGGAGAATTC[A/G]TTTTTTTTCTATCAG | 9678 |
| rs537409223 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136233 | AATCTATTGTATGCC[A/C/G]TGGTGGGATGCTGTT | 9678 |
| rs537417517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068027 | AACCATAGCATACAT[A/G]CAGTAGAATATTATC | 9678 |
| rs537434379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020762 | GTTATATTTGAAAAT[C/G]AGTTAATTTTTCTGA | 9678 |
| rs537443704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062172 | TGAAAAAACAATTGC[A/C]GGATAAGACCTTTCT | 9678 |
| rs537444803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058747 | TTCTGAATGATTTAG[C/G]TCATTTCTATTTGGG | 9678 |
| rs537473238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015488 | TTACTCTAAGTTGGG[A/C]CTGAGAGTGGCCTAG | 9678 |
| rs537479710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10982167 | ATCTTCATTAGCACT[A/G]TACTGAACTAAAACC | 9678 |
| rs537488088 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10985450 | ACATTTTTCTTAGCT[G/T]CTAAGTTCATTTGTA | 9678 |
| rs537509151 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102995 | AATAACAAACAAGAA[A/G]GACAATGCATTCCAT | 9678 |
| rs537549460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978616 | TTCTCAACCTTGGCG[C/T]TATTGGCATTTTGTG | 9678 |
| rs537550171 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973238 | TGCAACCAATCAGAC[A/T]GATTGCGCGTTACTT | 9678 |
| rs537566659 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009673 | CTCAGTAAACCCAAC[A/C]GGTATGACAGAGAAA | 9678 |
| rs537578603 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11055853 | ATTTTTTAGATGTTA[C/G]TTTAGGAAAAATGTT | 9678 |
| rs537587271 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11136966 | TATTCAAGAAATAAC[C/T]ACTACTAACATTTCG | 9678 |
| rs537599645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960245 | TCCCTTCTCCAGCAC[C/T]CCACCCCCCTACAGG | 9678 |
| rs537619648 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168711 | TTGAAAGAACATGTA[A/T]GATGAGATGGGTTAC | 9678 |
| rs537630286 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963975 | CTATGTGTGTCTTTG[C/T]AAATGAGATGGGTCT | 9678 |
| rs537634057 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986961 | TTATAAATGTAACTT[G/T]ATGTTCTTTGCTGAG | 9678 |
| rs537673992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158180 | CCAAGATTCAATCCA[A/G]GATCTCCTGTTTCAT | 9678 |
| rs537677475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11162569 | CACTGTCACTTTTCA[C/T]TCACTGATCTTTGTT | 9678 |
| rs537685712 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11165374 | GTATCAGGGTGTTAA[C/T]ATATATTATTGGTGA | 9678 |
| rs537694002 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10994116 | TAAATATATTGGGAA[C/T]GAGCACTGCAAGTGG | 9678 |
| rs537703448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035575 | GTAATATTCTTTTGT[A/G]TTAGGTCTTTTATGA | 9678 |
| rs537705091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028911 | ATAATAAAAGAAATT[G/T]TAACATTTATTCTTA | 9678 |
| rs537711922 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037421 | GGTTCACACAAGTAG[A/T]CAAGTCACAGACTTG | 9678 |
| rs537724077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071703 | CAGCGTCAGGCAACC[A/G]CTGCAAATGTTCTTT | 9678 |
| rs537729516 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10981353 | CCTACTGCTCCCTGT[C/T]CTCTTTCCCTCCTCC | 9678 |
| rs537740289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029509 | TTATGTCAGTTATCT[A/G]GACATTAGTATGTAA | 9678 |
| rs537771962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988822 | TTCTTATAACCTCCT[C/G]AAGTAGATATTATTT | 9678 |
| rs537784627 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11112131 | TAGCCAGACTCCTAA[C/T]GTTTTGACTGATTTG | 9678 |
| rs537795260 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150199 | GAAGGGAGGAGAATG[G/T]GATGGGGAAAGAACA | 9678 |
| rs537816966 | snp | A/T | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10969549 | TTTGCATATCCTTGC[A/T]TAATAAAACTGTATT | 9678 |
| rs537853459 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967365 | GTTGTCACAATTTGG[G/T]TTAGGGAGAGCTGTT | 9678 |
| rs537856943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135196 | GGCAAGTGGCATAAT[A/G]GCTCTGTGCCTCAGT | 9678 |
| rs537857579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11150809 | CAGGCTACTTAGATT[A/C]TAAGAGTTCAGACTG | 9678 |
| rs537879479 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11088041 | GAGTTATCATTATTA[C/T]AGTCATCCCTCCATA | 9678 |
| rs537891311 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064447 | CTTACTCAGACATAC[A/G]TGTATGTCTGTTAGG | 9678 |
| rs537892106 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965255 | ATGTGGTTTTGGTGT[G/T]GATGTCCTTTTTGTT | 9678 |
| rs537897101 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989070 | GTCAGCCCCAGACCT[A/G]TTTTATTTGGTTTTA | 9678 |
| rs537902161 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11167338 | TTTTTGCTTATTTTT[A/T]TTTTCACTGTTGTTA | 9678 |
| rs537914454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045162 | AATACTACATAACAG[A/G]GCTTTCCCCCAGAGG | 9678 |
| rs537930900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003986 | GGCTTGGTGGCTCAC[A/G]CTTGTAATCCCAGCA | 9678 |
| rs537932072 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964933 | GGTCATTTAAGCTCT[A/T]CTCTACACTGGTTAT | 9678 |
| rs537937643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059574 | TTAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA | 9678 |
| rs537948347 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11077688 | AGATATACCTCGTAC[A/G]TAGTCTCTTGTTTGC | 9678 |
| rs537961187 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11167848 | TCCTGGCTAACACGG[A/T]GAAACCCCGTCTCTA | 9678 |
| rs537966990 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11082216 | CTGGGCATAGTGACA[C/T]GTGCCTATAGTCCCA | 9678 |
| rs537969140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114222 | CTATTTGTTTTGCCT[A/G]GAAGTTTAGATAATA | 9678 |
| rs537970391 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965735 | GGGCTCTGCCTAGTT[C/T]GAGCCTCCCTGCCTC | 9678 |
| rs537987726 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155440 | CAACCTTTCTGTGTT[A/G]TTTTCCACTACTTTG | 9678 |
| rs538006985 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11154577 | ATATTGGTCCTACCT[A/G]GATTCCCAATATTGT | 9678 |
| rs538017677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162160 | GTGGTGCAATCCTGG[C/T]TCACTGCAACCTCCA | 9678 |
| rs538019978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070025 | CATCTGAACCTAGAG[C/T]TTTCATTGTGGAAAT | 9678 |
| rs538024596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032343 | ACACATCAATTTTAC[C/T]ATTAAGATACCAGTA | 9678 |
| rs538033894 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012014 | CATCTTGATGCTGAG[A/G]AAGTTATTTATGATT | 9678 |
| rs538044599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025521 | CTTGCCAGCCGGGCA[C/T]GGTGGCTCACACCTG | 9678 |
| rs538052336 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107496 | TTGCTTTTATCTTAT[A/G]ATTGGGATTCCTTTA | 9678 |
| rs538067601 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11148703 | TGACACATAATAGAC[-/A]ACACATTTGTAGGTT | 9678 |
| rs538072510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140700 | GCAAGGAAGTTGAAA[C/T]AATAGGATTTTAAAC | 9678 |
| rs538086337 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983709 | TTTATGTGTATGGGA[A/C]ATACACATAAGTATG | 9678 |
| rs538086859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019653 | TCAGCCTGGCTAAAG[G/T]TTTGTCAGTGTTGTT | 9678 |
| rs538087487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070871 | TATATTTTTGCAACT[C/T]TATACAATTAAAATA | 9678 |
| rs538088849 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958000 | ACTAAAAATCACTGA[A/G]TTGTAAACCATGAAA | 9678 |
| rs538104032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994430 | GGCAACAGAGTGAGA[C/G]TCCGTCTCAAAAAAA | 9678 |
| rs538119418 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093085 | AGATTCTAAACTTCT[A/C]ATTTCCCTTAGGACT | 9678 |
| rs538124192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065280 | AATGCTAAAGGTCAA[C/G]TTGAAACTATTTCAT | 9678 |
| rs538151074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020280 | TTTTCTGTAGAGACG[A/C]GGTTTCAACCTGTTG | 9678 |
| rs538173338 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11050294 | GATACTGATATAAAC[A/T]TATAAACTAAATATC | 9678 |
| rs538195513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008277 | TATCCTTAGGAGTGT[C/T]CACTGGATAGTAGAA | 9678 |
| rs538198891 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11142332 | GCAATTATTCACTGC[A/G]CCATAATGGATCATT | 9678 |
| rs538228974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087411 | TGGCCATACTGGTCT[C/G]GAACTCCTGACCTTG | 9678 |
| rs538229839 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11070735 | TACTTTGTCCACGAG[G/T]TGAGTATAGCATCTG | 9678 |
| rs538232351 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11094111 | CCTTCTCCAGGTCTA[C/T]ACTGCCAACCAGTGA | 9678 |
| rs538240960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108453 | CTTTTGAGTGAGCTA[A/G]AACCTCAGAGAACTT | 9678 |
| rs538246711 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128161 | AGTTCACTACAAATT[C/G]ATGCCTTCTAATTTA | 9678 |
| rs538247635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026387 | ATACATGGAGAAACT[A/G]AAAAATTCTCGTGAT | 9678 |
| rs538262124 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044516 | ACATTTCCTTTGGCC[G/T]CTAAGATCAACTTAG | 9678 |
| rs538278854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003538 | TATGGGATACATATA[G/T]ATAGTAAAAAGGTTA | 9678 |
| rs538283514 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11008758 | AAATCTTTTTTGGCC[G/T]GGCGCGGTGGCTCAC | 9678 |
| rs538299170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038114 | TATTGTGGCTTGAAT[A/G]TATTAAAAATATATG | 9678 |
| rs538304392 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11101317 | TATTATTTGTGCATG[C/T]AATTAAGAGTTAATT | 9678 |
| rs538306866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981478 | AGTTACTAAGTAGTG[C/T]TGGGTTGAGAGGGAC | 9678 |
| rs538308013 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128704 | TCTCTCTCTCTCCCC[C/G]CGCCCCCACTGCTTT | 9678 |
| rs538350960 | in-del | -/CACACG/CACG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088412 | ACACAAACACACACA[-/CACACG/CACG]CACACGCACACACAC | 9678 |
| rs538351773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11149906 | TTTTCTGCTTGTGTT[A/G]GCTAACATCTCTAAA | 9678 |
| rs538365500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11102016 | CCCCGAGTCTCTGTA[C/T]TTGAGTATAACCAGC | 9678 |
| rs538369324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122021 | TCCCCTTGCCCTACC[C/T]CCCGACAGGCCTCTG | 9678 |
| rs538391129 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112187 | GAAGACATTCTGGTC[A/G]ACTGTAGATTAATCC | 9678 |
| rs538398517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063609 | AATTTTTTTTTTTTA[A/G]TATGAGATTGATTGA | 9678 |
| rs538406263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081652 | ATGAAGTCAGGAGAT[C/T]GAGACCATCCCGGCT | 9678 |
| rs538417519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003458 | TTTGGAGATTTGAAA[A/C]ATCTTACTTTTAATT | 9678 |
| rs538440489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099804 | GATTTCAAAACAAAT[A/G]TACAGTTTCAAAAAA | 9678 |
| rs538447449 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997412 | GATGTGAAATTGAGG[A/G/T]AGGGTTTTTTTCTTT | 9678 |
| rs538471563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013602 | ATATAAAATGAGTTT[A/C]TTTCTGTATTTTAAT | 9678 |
| rs538476752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987418 | TCATTTACAGTCATA[C/T]GTGGAATATATATAT | 9678 |
| rs538501189 | snp | A/C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032840 | AGAATTTGCAGAGTT[A/C/G]GGCTCTAGTTACCTC | 9678 |
| rs538512561 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141586 | AAATGTTCCTGGCAT[G/T]GTGTTATATAATAGC | 9678 |
| rs538514287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114271 | ATATTTGCTGGAAAA[A/G]TGAATTGCACTTTAA | 9678 |
| rs538527948 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11121953 | CTGCACCTGTCAACC[A/C]GTCAGACGTTTTAAG | 9678 |
| rs538531133 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142201 | ACCACAAACACATAT[C/T]ATCCCAACATATAAA | 9678 |
| rs538540107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075814 | GAGGAAACTGAAGAA[C/T]AGAGCTTAAGTAACT | 9678 |
| rs538570030 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087378 | TATATTTTTAGTAGA[G/T]ACGGGGTATCACCAT | 9678 |
| rs538581175 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11107811 | TTTATTCACTATTTA[C/T]TTTGATAAATTTTGT | 9678 |
| rs538589043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11114993 | CTGGAAAAGAAATGT[A/G]TTTTCTTCTTTCTTA | 9678 |
| rs538605537 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085570 | TTCTAAATACTCATC[C/G]TATTTGGCCTCGTTT | 9678 |
| rs538610346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064450 | ACTCAGACATACGTG[C/T]ATGTCTGTTAGGTTC | 9678 |
| rs538635234 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146821 | CTTTTGTGCAAATCA[A/G]CGATGCAGCTTTTTT | 9678 |
| rs538671233 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986280 | TGAGCCACCACACAT[A/G]GCCCCTTTACAGTTT | 9678 |
| rs538674004 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974137 | GGCCAGGCGAGGCCG[A/G]GGGGGCGGGGGGTTA | 9678 |
| rs538705587 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008367 | CCAACCAGGTGGTAC[A/T]GGTCCTTGGCCTGTT | 9678 |
| rs538709293 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984660 | GATAGAGGCAGTGTC[A/G]ATTAGATTTATGCTA | 9678 |
| rs538716258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050276 | TTATAAGCTACATTC[A/G]AAGATACTGATATAA | 9678 |
| rs538720513 | snp | A/C | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065472 | CTGAGTATTCTTTTG[A/C]TGAATTAATAAAAAC | 9678 |
| rs538724530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142489 | AATGCCTTATTCTGA[C/T]ATCATGTAGAAAACT | 9678 |
| rs538732812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094385 | GCACTAGAGTTGTTC[G/T]GCACTCCTTGGTTCA | 9678 |
| rs538741791 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111842 | GAATAACCAATTAAA[C/T]AGAATTTTATAGATG | 9678 |
| rs538747162 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006777 | TTTGGTGGCTGTGGA[C/T]ACCTTTCAACACTGC | 9678 |
| rs538768614 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080874 | TAATATTACTAATCC[A/T]TGTGTTAATTGCGCT | 9678 |
| rs538782325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008189 | TACTAAGAGATGTTT[C/T]CCCCTATTTATTTTT | 9678 |
| rs538790553 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141776 | TAAAGCTAGTCTGAA[C/T]GTGTGTCTAACAGCT | 9678 |
| rs538809102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958983 | CCTTTGGACGATGTA[A/G]GAGTCTTTTTAAAAC | 9678 |
| rs538812615 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064150 | TATAATGTGATCTTT[-/A]AAAAAAATACATTGT | 9678 |
| rs538823779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11153452 | TTGTACATGGTATGT[C/T]TGAGGTCCTTATTAA | 9678 |
| rs538835053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11121370 | CAAAAGAAAACCTTA[C/T]ACTTAAGTAAGGAAA | 9678 |
| rs538842166 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980804 | TAGTGTAATATATGG[G/T]GCATGTTCCATGTTA | 9678 |
| rs538854528 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11069492 | CAAAATCAACCTTGC[A/T]AATCTGGGATAAACC | 9678 |
| rs538858678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062863 | GTGTCACAAAAGTTC[C/T]TACAGTTCTTACAGG | 9678 |
| rs538894340 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11031723 | CTCACCACTGCACTC[A/T]GCCTGGAGAATAGAG | 9678 |
| rs538896776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147500 | TACAATGACTCTTGT[A/T]AATGTCACTTACAAT | 9678 |
| rs538902575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979481 | GAAAGGTTTATTGTA[G/T]ACTTGAAATTAACTC | 9678 |
| rs538920446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099008 | TTTAAAAGTTCATTT[A/C]AAAAATGCTTTTCTA | 9678 |
| rs538921273 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959611 | AGCCAGGCGCACCAA[A/C]TGCTGCATGTGGGGT | 9678 |
| rs538929964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025652 | TACAAAAAATTAGCC[A/G]GGCATGGTAGCAGGT | 9678 |
| rs538933802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11157259 | GATTCTAGGAATAGA[C/T]GTGACTTCAAGAGTT | 9678 |
| rs538939154 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11032232 | CATATATGGCTGAGG[G/T]GGGGTGGACAAGAAT | 9678 |
| rs538956119 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026397 | AAACTAAAAAATTCT[C/T]GTGATTTGTTTTATT | 9678 |
| rs538961478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056071 | CAGATTATAAAACCT[C/G]TATCTGTCATAGATT | 9678 |
| rs538964503 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973713 | CGGGGATCTCTGCTC[C/T]GCCTTGGCACTACTC | 9678 |
| rs539007655 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972468 | CTATCAGTCCATGAT[A/G]TGGTTGGTGTTTAAA | 9678 |
| rs539033485 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11013453 | AGGCATGAGCCACTG[C/T]ACCCAGCCTAATTTT | 9678 |
| rs539053551 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11090496 | GAACTGCAAAATTGC[A/C]TGATTATATCAAGGA | 9678 |
| rs539069393 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003514 | TATTTCAGGTATACA[A/G]TATGTTGTTATGGGA | 9678 |
| rs539074330 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971746 | TGGTTATATAAGATA[C/T]TGATATTAGTGGTAG | 9678 |
| rs539075942 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11047145 | ACAATCGCAACTCAC[C/T]GCAACTTCTGCCTCC | 9678 |
| rs539089062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043910 | TTATGCAGTTCTCTC[C/T]TTAAATGAAGTTATG | 9678 |
| rs539102170 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11005824 | TTTGAGACGGAGTCT[C/T]GTTCTTTCACCAGGC | 9678 |
| rs539112202 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968877 | TAGAGCTGTATTTGA[A/C]GTTTTATTCAGGAGA | 9678 |
| rs539132760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000426 | CTCACTGCAACCTCT[G/T]TCTCCCAGGTTCCTG | 9678 |
| rs539142303 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11098525 | ACTATGTCTCACTTC[C/T]CCCAACCTTCTGGCT | 9678 |
| rs539150519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966686 | TATTCTAACATGATC[G/T]GTAATACAGAGGAAG | 9678 |
| rs539162697 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084915 | CGCTTTATCTTTGGA[G/T]ATTTTTTTTTCTTTT | 9678 |
| rs539176729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037509 | TCAATAAACATTGCT[A/G]TAGAGCTTCACTTTC | 9678 |
| rs539178313 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11044343 | AAAAAAAAAGAAAAG[A/C]AGTAATGTACATAGC | 9678 |
| rs539184748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128077 | TGCCCAACTTCTCAA[C/G]ATTCACTGTATTGGT | 9678 |
| rs539212883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024319 | TAAAAGATGAAGAAG[A/G]TGCAGCAGGTACTGA | 9678 |
| rs539213692 | in-del | -/AAAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126459 | ACCTGTTTACAGCAT[-/AAAG]ACTCTGTTAAGTACA | 9678 |
| rs539215898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151001 | ACTACACTGTCTTAA[A/T]GGGTTTTCTGTTTAC | 9678 |
| rs539245229 | snp | G/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11021565 | ATTTTAAGAAGGTCA[G/T]TATGAAGCAAGCAGC | 9678 |
| rs539254528 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978929 | TGTCTTCAAGACATA[C/T]ACGGTTTTGGTCAAA | 9678 |
| rs539278578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151434 | TGTGGTGGTGCACAC[C/T]TATAGTTCCAACTAC | 9678 |
| rs539294489 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106966 | AACTTGATCATAAAA[A/G]TGTACATCCTTGTTC | 9678 |
| rs539332858 | in-del | -/TAC | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11004448 | TTCTTATAATCTGTA[-/TAC]CTCTATTGTCACTAT | 9678 |
| rs539337147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099653 | TCATTTGGAAAGACT[A/G]AGACTCTTACCACAG | 9678 |
| rs539358278 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989924 | GGTGTGAGCCACTGT[C/G]CCCATCCTCTCTTTT | 9678 |
| rs539364677 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971077 | CTGAAAGTTTTCTTC[A/C]TAAAGTCAGAAACAA | 9678 |
| rs539381897 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11148441 | ATCAGTACATGACTG[-/T]TTTCCTTCAAGTCAT | 9678 |
| rs539423919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033465 | CTTCCTTTCAAGGGC[A/G]TGGTCTGGGCATTTC | 9678 |
| rs539425594 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11042370 | AAATGGGTTTTAAGT[-/A]ATAACTAAAATTAAA | 9678 |
| rs539427704 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11039786 | CTTGTATCCTAAAGA[A/G]TGTTTTAAAAGGTGA | 9678 |
| rs539429558 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169717 | AGGAGAAAAATTCTT[A/G]ACTCAAATTTGAGAA | 9678 |
| rs539450654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091020 | CCTTGAGTGCAAGCT[A/G]ATGATGTTAAGGGGT | 9678 |
| rs539465070 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137994 | TAAACAGACCAGCAG[C/T]ATATCTGTGGCATTA | 9678 |
| rs539471770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11047596 | AGGTCAGGAGTTCAA[A/G]ACCAACATGATGAAA | 9678 |
| rs539481483 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990966 | TAATGCTAAATCATC[A/C]AAGTATGGATGCTAT | 9678 |
| rs539496246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006108 | AGATAAGTGTATTTA[A/G]ACTTCTAAAAACCAT | 9678 |
| rs539519164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116608 | AAACCAATCTCTTAT[C/G]ACCCTCTACTCCTGC | 9678 |
| rs539522749 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131994 | TTGTGTATATTTAAG[G/T]TATACAACATGGTGT | 9678 |
| rs539526310 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988174 | TATTTCCCTCTTTGC[A/G]TTACATTTCTATTAA | 9678 |
| rs539526860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123873 | CAGTGAGCCGAGATC[A/G]TGCCACTACACTCCA | 9678 |
| rs539535642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072297 | CTAAGAACTCACCAT[C/G]ATGAGAACAGCACCA | 9678 |
| rs539535873 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040179 | CACTGAGAAATGACT[C/T]TGATAGATGGTTGCT | 9678 |
| rs539551651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156643 | TACTAAAAAATACAA[A/G]AATTAGCCGGGTGTA | 9678 |
| rs539586057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124719 | GACTCTAGAGCCTGT[A/G]TTTTAGAAACTAGAT | 9678 |
| rs539588592 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157418 | AGGTGTTGATTGCCA[A/C]ATATTTTTACTTTGT | 9678 |
| rs539597508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015467 | TCTGTATCATAGGCA[C/T]AGGCATTACTCTAAG | 9678 |
| rs539602319 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11124740 | GAAACTAGATTTTAT[A/G]TATTAAAATAGGTAT | 9678 |
| rs539603812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11143269 | GCATAAATGTTTTCT[A/G]TCAATAACCATGAAA | 9678 |
| rs539620518 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10989573 | AAGGTTTAAATGCAA[A/G]CAAGCAGACCCTCTT | 9678 |
| rs539628921 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11066946 | GCATAGGTAATAACA[G/T]CAACAAAAAATTAGC | 9678 |
| rs539641342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110827 | TACAATCTACTTTAA[C/T]TTGAAGAAAGAGAGA | 9678 |
| rs539641367 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103247 | CATGAATAAAGATAT[A/G]TCTGTGTTGATCTCT | 9678 |
| rs539664904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136213 | TTGTGACTTCCGCAG[C/T]GCCAAATCTATTGTA | 9678 |
| rs539665845 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115436 | AAATAAGCTAGTACT[A/G]TAGAACAGGTACATA | 9678 |
| rs539670176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016246 | TTATAGGCCTTCACA[A/G]TATTTCCAAGGACGT | 9678 |
| rs539672547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984118 | TTTTTCCATATCACT[A/G]AAGTAAGTTAAACGG | 9678 |
| rs539683495 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11009595 | GAAAGATTTTAGAAC[A/G]TATTTAGTCACTAAT | 9678 |
| rs539685794 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11096200 | TTTGCATGTAAACTT[C/T]AAGTGGGATTAAAAC | 9678 |
| rs539703157 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103875 | AAAGATCTCATAACA[C/T]TGGAGGAAAAATATT | 9678 |
| rs539721026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11004813 | GGCCGAGGTGGGTGG[A/G]TTACTTGAAGTCAGG | 9678 |
| rs539737188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977147 | GGAGTCTTGTAGAGA[A/G]TAAGACATTAGTCCT | 9678 |
| rs539747987 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965584 | AACACCATGCTGGGG[A/G]AACCACTGCTCTCTT | 9678 |
| rs539775164 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073162 | ACAGTCCTCCAAAGT[A/C]TTTACTCACTCCATC | 9678 |
| rs539776051 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11119212 | GCAAACCTCATACTG[C/T]CCTGTAGTTTAAAAT | 9678 |
| rs539785454 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965867 | CTGCACTAGCAACGA[A/G]CAAGGCTCTGTGTGT | 9678 |
| rs539791521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162884 | TGCCACAAAGAAGTA[A/G]AAAGTTACAGGAGGA | 9678 |
| rs539793189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130367 | AATCCTTGGAGAGAG[A/G]GAGAACGTATATACA | 9678 |
| rs539797073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076467 | TTTTAACTTTAGATG[C/T]CATTGGATTTTTTAT | 9678 |
| rs539802228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083529 | GCTGCAGTGCAGTCT[C/T]GGCTCACTGGAAACT | 9678 |
| rs539832954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115990 | TGTTATATCTTAGGA[A/G]TTGTCTGCTAGTTTT | 9678 |
| rs539839636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11089154 | AAAAACCTAAGACAA[A/G]CCTTTTATCAGGAGC | 9678 |
| rs539871347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129952 | AATAGAATTATAAAG[A/G]CTAGTAGGATTTGAC | 9678 |
| rs539875423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965392 | CCTGGGTATCACCAG[C/T]GGAGGCTGCAGAACA | 9678 |
| rs539887474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076992 | ACTTATGTTGTATGT[A/G]CACATATTAAAATGC | 9678 |
| rs539905030 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11169231 | ACATACAGAAAATTT[G/T]AATGTGTTCTATAAA | 9678 |
| rs539916034 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11143403 | TAGGATTATAGGCAT[C/G]AGCCACCATGCCCAG | 9678 |
| rs539934895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122838 | CAGTAGTGTTTTCTT[C/G]GTCACCAATAAAACA | 9678 |
| rs539951661 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068279 | TGGCATGAACCCGGA[A/G]GCAGGGCTTGCAGTG | 9678 |
| rs539966964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999271 | CCAGTTCACTCCAGT[C/T]CTCTCTCAAACCACT | 9678 |
| rs539971866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11109991 | TTTTAAACTTCTTTA[C/T]ATCTGAGTAACTTAA | 9678 |
| rs539972776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008840 | GGAGATCGAGACCAT[C/G]CTGACTAACATGGTG | 9678 |
| rs539973644 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076610 | TCTCACTGTGTAGCC[C/T]AGGCTGGAGTGCAGT | 9678 |
| rs540011072 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120154 | AGAAAGTTAAGTATG[A/C]AATTTGGTGTAGATG | 9678 |
| rs540019187 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10980882 | TAAAGTTTCAGATAG[A/G]GAATTGCTGACCCGT | 9678 |
| rs540037645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045407 | ATAATATTTCTGAAT[A/G]GCCGGTTTATTTTTG | 9678 |
| rs540046429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101405 | AAACTACAGACAAAG[C/T]AGTTCTCAGAGTATC | 9678 |
| rs540069751 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976116 | CAATGGATTTGACTT[A/C]AGAATTTAGTCTGTT | 9678 |
| rs540079074 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10981660 | GCATATAGTAGTTAC[A/T]GCGTAGAAGTTTTGA | 9678 |
| rs540088898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975872 | CTTCTGGTTTTCCCT[A/T]GTCTTTTTCCTGCTA | 9678 |
| rs540107357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094488 | TACAAGAGCTCTTTC[A/C]TGTGATTATATCAGG | 9678 |
| rs540128929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015329 | TCTACCATTGAATCT[C/T]GGAGAATCCCATGTG | 9678 |
| rs540130038 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10970505 | AACCTGGGAGGCGGA[A/G]GTTGCAGTGAGCTGA | 9678 |
| rs540143777 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11088502 | AAAATAACAGAGTAT[G/T]TTTGTTTTCATCCAT | 9678 |
| rs540154419 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11083098 | AAATGTTCAGAGAAT[C/G/T]GGGTCTAGCTTAGAT | 9678 |
| rs540169405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009271 | AAGATGGAAGACTGA[A/T]AGTCCACTGGCCCCT | 9678 |
| rs540188658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995831 | GGGCTGGCAGTGCCC[A/G]CCAAGCCCATGCCCA | 9678 |
| rs540225346 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11075537 | TGAATTAACAAGAAC[C/T]CACTCATTCCCATGG | 9678 |
| rs540250249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046033 | TGTGAAAAGCTAGTA[A/G]AGAATATTATTAATA | 9678 |
| rs540250622 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970595 | CTCCCCCAAAAAATT[C/G]TGAGTTAAGAATGCC | 9678 |
| rs540270220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162225 | TCCCAAGTAGCTGGG[A/T]CTACAGGCACACGCC | 9678 |
| rs540271342 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083496 | TTTTTGATACAGAGC[C/T]CTTGCTCTGTCGCCC | 9678 |
| rs540274158 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11070252 | CCAGCTGATTTTTTA[A/G]TCGTTTGTAGAAATG | 9678 |
| rs540276023 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007180 | CCCGGGTAACAAGAG[C/T]GAAACTCCGTCTCAC | 9678 |
| rs540286790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039503 | TTTTTAGTACTGTGT[A/C]TATAATTGATAAATT | 9678 |
| rs540312365 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064559 | ACTGATGTTTATATC[A/C]CACTAGAATCTGCTC | 9678 |
| rs540319689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960536 | GCTATTGTGAATAGT[A/G]CTGCAATAAACACAC | 9678 |
| rs540325029 | in-del | -/T | 0.00755907 | 0.0610114 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973394 | TCAATAAGTCCCTGC[-/T]TTTTGTTGTTTTGTT | 9678 |
| rs540335587 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10987909 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 9678 |
| rs540393632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057706 | AGTTGCCTGCTAGAT[A/T]AGATAATTTTACACC | 9678 |
| rs540407477 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014856 | TAACACATTTGAGCA[C/G]TTGTCATCATAACGG | 9678 |
| rs540432073 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150233 | AAGAGAGCTACAATA[C/T]GCATTAGAATGCTTA | 9678 |
| rs540445287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044007 | AAAAAAACACACACA[A/G]AAAAAGGGAAATCAT | 9678 |
| rs540467749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008010 | AGATCTTCTAATATT[A/G]GGGTACCTCTGACCG | 9678 |
| rs540482385 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11054103 | TTTATCAAAAAAGCA[-/T]TTTTTTAAGACACTT | 9678 |
| rs540496539 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969057 | AACTCACTTTAGTGA[A/T]TCTTCTCTTTGATGA | 9678 |
| rs540533541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143430 | CCAGCCAATTTTTTT[C/T]ATATTGTTCCTTATC | 9678 |
| rs540533603 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11135727 | GCCTGCTGTAAGAGA[G/T]AAACCTATTGCAAAT | 9678 |
| rs540545916 | in-del | -/GTT | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11094962 | GGAGTGTTATTTCCA[-/GTT]GTTGTTGTTGTTGTT | 9678 |
| rs540562381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045624 | CACTAGTTCTAGATT[A/T]GGATGCTTTCTTCAG | 9678 |
| rs540594088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081810 | GCAGTGAGCTGAGAT[C/T]GCGCCACCACACTCC | 9678 |
| rs540605583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158440 | GAACATGATGTCAGT[A/G]TACATACTATACATT | 9678 |
| rs540611225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992970 | AGAATGTTCCTAATA[A/T]GATTAGATTTGGGTT | 9678 |
| rs540622999 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10997607 | CAGGTCAAAGCCATA[G/T]CCTGGGCTGTAGTCA | 9678 |
| rs540662585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155052 | CAGTATGTCATTAAT[A/G]ATTAAAAACTGTCGT | 9678 |
| rs540671973 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995837 | GCAGTGCCCGCCAAG[C/T]CCATGCCCACCCGGA | 9678 |
| rs540696367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115113 | TCCTTATCTCACATA[A/G]CAAATCACTTCCTGA | 9678 |
| rs540707115 | in-del | -/TA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021107 | GAGTCTTTTGAGAAG[-/TA]TATCACTCTACTTAG | 9678 |
| rs540712932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068184 | TGAAACCCCGTCTCT[A/G]CTAAAAAATACAAAA | 9678 |
| rs540712973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061710 | ATAACATTTAACAGA[A/G]GAAATTTATATTTAT | 9678 |
| rs540730927 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148986 | TTTGTTTATTTAAAC[A/C]CAAAGTCATTCCTTG | 9678 |
| rs540767903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117140 | GTATTCACAGACGCC[A/G]CTGAGGATTTAAATA | 9678 |
| rs540777362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019937 | GTGTTTCCATTACTA[G/T]TCGTCATACTCTTCT | 9678 |
| rs540781957 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11134324 | GAATTATAGAATTTA[A/G]TAGCTAATATGGACC | 9678 |
| rs540801106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098099 | TAATTATAAAAATTT[A/G]TATACAAAAATATAA | 9678 |
| rs540836272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997484 | AAATTATCCCAAAAC[A/G]TAGCAGCTTAAAACA | 9678 |
| rs540844268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041021 | CTGGAAAATTACTTT[A/G]GATAACATTATAGTT | 9678 |
| rs540852376 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11132173 | TTGCATACCTGTAGC[C/T]CTCATATTGTATATT | 9678 |
| rs540853692 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11081156 | TGCAAGAAATGTGTC[A/G]TTCTAGTTTGGAAAA | 9678 |
| rs540865244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087441 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 9678 |
| rs540876196 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037693 | AAATGTGGTTAAAAT[C/G]TTATACCAAGTATAA | 9678 |
| rs540881120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041486 | TATATGCATACATAT[A/G]TGTTATGCATGTGTA | 9678 |
| rs540881198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164806 | CCATTTTTAAATTTT[A/T]CCAGTTTTCTCACTA | 9678 |
| rs540903018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078084 | TTTGAATAGAAATGC[C/T]TTCACATTTTTGTTT | 9678 |
| rs540912357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121012 | AACTGAAATGAAAAT[A/G]CAAAGTAAATCCAGT | 9678 |
| rs540917814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962027 | AATCATGTCATCTGC[A/C]AACAGGGGCAATTTG | 9678 |
| rs540923613 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034902 | GTTAGCCAGTTAGAA[A/T]TGCCACACTTATCTT | 9678 |
| rs540936478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956167 | TTGCAGCAGTTTTAT[C/T]AAATAAATATCAGAT | 9678 |
| rs540941073 | in-del | -/GTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983986 | CAAAAGAAAGATTGA[-/GTT]GTTGTCTTACATGTA | 9678 |
| rs540949187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003714 | CATACACAGTACAAG[C/T]TTATTACCTTGAATT | 9678 |
| rs540950272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117968 | TGGATTTTATATGGC[C/T]GACAGAGACATCATT | 9678 |
| rs540963785 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11031340 | ACATTTCTATTCTTT[G/T]TCATCTACTTTGTGA | 9678 |
| rs540975161 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11024894 | AGTCTGATTATTTAA[A/G]AAATACATTTCATAA | 9678 |
| rs540990893 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073124 | ATCTTCTCCACATTG[C/G]AAAATACAATTGTCC | 9678 |
| rs541001013 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029153 | CGAGAAGCTGAAACT[G/T]TATTTGGGTAACCTT | 9678 |
| rs541016150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016611 | ATAGTTTTACTATTT[A/G]TGGGTACATAGTAGA | 9678 |
| rs541016391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995562 | TGCCCGCATTCCTCA[C/G]CCCTTGGGTGGTCGA | 9678 |
| rs541025051 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990910 | TCTTTTACATTTGTA[C/G]TAAGGTGGTTCTACA | 9678 |
| rs541034780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111740 | AGTGCTCCGAAAGCC[C/T]AAACAGATCACTCTC | 9678 |
| rs541038011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144414 | AGAGATACCTGCACC[C/G]CCATGTTTATTGCAG | 9678 |
| rs541040095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059957 | CTCACTGCAGCCTAG[A/C]TCTCCTGGGCTCAAG | 9678 |
| rs541093186 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010592 | TTAATATTAACTATA[G/T]TTAGCATAACTATTA | 9678 |
| rs541098484 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104800 | TAGTAGAAAATTTGC[A/G]TTTCTAACAAGTTCC | 9678 |
| rs541098528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112261 | TGTATTATGGACATC[C/G]AGCCATCTTTCTTCA | 9678 |
| rs541099963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016972 | GTTGTTTGGTTTTTA[C/G]ATCCCACAAATAAGT | 9678 |
| rs541121761 | snp | A/G | 0.0023933 | 0.0345097 | | | GRCh38.p7 | 7:10971365 | CCAGTTAAAATTTGG[A/G]GCTTCCATTTTTGAA | 9678 |
| rs541124614 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138072 | GACGGAGTCTTTGCT[C/G]TGTCACCCAGCAGGC | 9678 |
| rs541125359 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152964 | GAGCAGATCGGAGAA[C/G]TCAGTGAGGCCGGAA | 9678 |
| rs541128826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017656 | ATTCTGGTTATTTAT[A/C]CCTTGTTAGTTGGGT | 9678 |
| rs541174909 | snp | C/T | | | | | GRCh38.p7 | 7:10969376 | TACTTTCTTGGTTTC[C/T]TAAAAAATTAATCAG | 9678 |
| rs541176711 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050296 | TACTGATATAAACAT[A/G]TAAACTAAATATCAA | 9678 |
| rs541179953 | in-del | -/TTCTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131949 | GACTACTGGAATTTT[-/TTCTT]GTTGGGTTTTTTTAA | 9678 |
| rs541181176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966103 | CATGGGCTGCACCCA[C/T]TGTCCAACCAGTTCC | 9678 |
| rs541223176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084501 | TACTCTTGTGTTTTT[C/T]TTTTTTTTTAACTTC | 9678 |
| rs541233531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109637 | GTTGTACTGAGAAAG[A/G]GCATAAAATTATGTG | 9678 |
| rs541241306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000654 | TTATTTACCTTTTGT[A/G]TATCTTCTTGGATGA | 9678 |
| rs541244684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027405 | TCACTTTGAATACTT[A/G]TATTAAACAATTCTT | 9678 |
| rs541266305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989206 | TCTGCCGCAATTTTA[A/G]ATGTTATACACAAAG | 9678 |
| rs541291442 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11021211 | TTTTGGTGGTTTTAT[G/T]TGATGCTTATTTCCT | 9678 |
| rs541293365 | snp | C/T | | | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10968416 | ATGCCCATGGGATAC[C/T]TAATACATCTGAGTT | 9678 |
| rs541296415 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11110261 | TGTTCTATAAATTTT[C/T]CCCTTGGTTTCTTAA | 9678 |
| rs541304388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11125036 | CTCAACTCCTCAGGG[C/T]CCTTTCTTCATGAAA | 9678 |
| rs541307451 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10990270 | TTGTCTTCTCTAGGT[A/G]GGATTATAAGCTCCT | 9678 |
| rs541361802 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11118615 | CCTGGTCAAGTAGGT[A/G]GTTTTATTAATACTT | 9678 |
| rs541363249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11001085 | TTACGAGTATACGGT[C/T]TGTCTCGGAATTCAT | 9678 |
| rs541398184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961990 | GATTTTGGGCTGAGA[C/T]GATGGGGTTTTCTAA | 9678 |
| rs541402341 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164508 | ATTTCAGTGTAGAGG[C/G]TACAGGTGCCTTGCA | 9678 |
| rs541406242 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096542 | TTTCCAGTTCATTTA[C/T]GGGTATTTCATATCG | 9678 |
| rs541438614 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088783 | TGAAAACACTGTATA[A/G]GAGGGGAGTGATAAA | 9678 |
| rs541444952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060657 | GAGAAGCAAGTCTCA[A/G]TATTGTTCTTTGGAA | 9678 |
| rs541449968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145045 | GATGGTTTCACAACA[A/G]TATAAATATTTAATA | 9678 |
| rs541470056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073075 | AAACATCCAAACTAT[A/G]TACTTTCACTCCTTG | 9678 |
| rs541472141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165074 | GGACTATAGGCGCCC[A/G]CCACCACACCCAGCG | 9678 |
| rs541484632 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11097066 | CTCACTGCAACCTCT[A/G]CCTCCCAGGTTCAGG | 9678 |
| rs541484791 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970387 | CCAGCCTGGCCAACA[G/T]GGTGAAACCCTGTCT | 9678 |
| rs541487737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977207 | TGGATTCCCAGCCCT[A/G]CTTACGAATAGGAGA | 9678 |
| rs541499576 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11157758 | GAATGACTGTATGAT[C/T]CTACTAGCTGGCAGT | 9678 |
| rs541502659 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017253 | TGATTTCCTTTCTTT[C/T]GGATGTATACCCAAC | 9678 |
| rs541511390 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11053474 | CCTTTGTTAAATAAG[C/T]CGGCTAGTTTCTATT | 9678 |
| rs541525800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011274 | TCATTCATTTATATA[C/T]TGTAGTTATTTATTT | 9678 |
| rs541540098 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073569 | CTGTGGCTTTTCCAG[C/G]CTCAGGGTGCAAGCT | 9678 |
| rs541541632 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155262 | TTTGGGTAGTGTAGG[C/T]ATCAAAGTTAGGATT | 9678 |
| rs541541793 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046153 | ATGCATTTTGTCTCA[C/T]TTTTAGTTTATGTTA | 9678 |
| rs541544320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11067179 | TCTCCAAAGAAGATA[C/T]ACAGTAGCCAACAAG | 9678 |
| rs541544840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10991803 | GGGTTTTGCTATGTT[A/G]CCCAGGCTGATCTTG | 9678 |
| rs541545061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090771 | GATTTTTATGTAGAG[A/G]GTTTATAAGAGACAG | 9678 |
| rs541559759 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156024 | AAATGAATGCATTTT[C/G]AGACAAGCTTTATAA | 9678 |
| rs541589443 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138464 | TAGTAAACATTAAAA[A/T]TTATTTTTAAGCAAA | 9678 |
| rs541593015 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156376 | GTGTTACTTAGATAT[A/C]TAATGAGCTATTACG | 9678 |
| rs541593051 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034168 | AGATTTTTTTTTCTT[G/T]CTGTTCTTATATGTC | 9678 |
| rs541600102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072047 | TGTATTAGTCCATTC[C/T]TGCATAGCTGTAAAG | 9678 |
| rs541602289 | snp | A/G | | | | | GRCh38.p7 | 7:10970344 | GAGAGGCTGAGGTGG[A/G]CGATCAGTTGAGGTC | 9678 |
| rs541630548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046833 | ACTTTCCTCTAAATA[C/T]AGGAGAAAACATGGC | 9678 |
| rs541665561 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050470 | GTCCTTTATGATTGA[C/T]AATATAAAGATTTCC | 9678 |
| rs541674568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989764 | GCCACCTGAGTACCT[A/G]GGACTAAGGGCATGC | 9678 |
| rs541693237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11083767 | ACCTGGCCTGCTTTC[C/T]CTAATTTTACCTAAT | 9678 |
| rs541694872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066292 | TTTGTTGTTTGTTTT[C/T]GTTGTCACTCAGGCT | 9678 |
| rs541709095 | snp | A/C/G | 4.97767e-05 | 0.00498862 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982833 | CGAAACCGACCACTT[A/C/G]TGGATTTTGTGTCCA | 9678 |
| rs541718135 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11047290 | AGCCAGAATGGTCTC[C/G]ATCTCCTGACCTCAT | 9678 |
| rs541730746 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041529 | TTCTTCTCAAAATTT[C/G]TTTCTCAGAAATAGT | 9678 |
| rs541732479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966329 | TAGTCCTGAAATGTG[C/T]CTGAGTCTGGCTGAG | 9678 |
| rs541744882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077430 | ACGTGGTAAAACCCC[A/G]TCTCTACTACAAATA | 9678 |
| rs541767826 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044797 | AAAAAAATGATAAAC[A/G]CAGGTTGAGTATCCC | 9678 |
| rs541769718 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078003 | ATAACCTTAGACTGA[G/T]CTTTTTCAAGTATTA | 9678 |
| rs541791088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034292 | TTACTGTTCCTTTTT[A/G]GGACAGACATAAAGA | 9678 |
| rs541814769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995338 | GTGCTGATTGGTGCA[C/T]TTACAAGCCTTGCGC | 9678 |
| rs541840541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021101 | CTTAAATGAGTCTTT[A/T]GAGAAGTATCACTCT | 9678 |
| rs541848789 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11151040 | ATATATCAATGATTT[A/T]AAAAATAAGAAAAGC | 9678 |
| rs541868302 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076203 | GTCCATGGTTTTAAC[C/T]TCTATAGTCTCAGCA | 9678 |
| rs541901577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059288 | GAACTTGCAGCATTA[A/G]AATACATACTTGAAA | 9678 |
| rs541909492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118507 | ATCCCACTAATTATA[C/G]TTGGTACTTTGCTTT | 9678 |
| rs541910479 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144395 | AAATAAATTAGTATA[G/T]TGAAGAGATACCTGC | 9678 |
| rs541919859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976446 | GTGGTTGTAAACTTT[G/T]ACAAACATAGTTGGG | 9678 |
| rs541976570 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103788 | ACAGTGAGGAACGCT[A/G]TGATTGGATGAGATG | 9678 |
| rs541995270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028956 | ATCACTGTTCTAAAA[C/G]TTTAAGAGTAAATGC | 9678 |
| rs541995369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022547 | TTGTTTCATTTGAAT[A/G]GTAGTTTTATGCAAA | 9678 |
| rs542021219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137987 | ATAAACATAAACAGA[A/C]CAGCAGTATATCTGT | 9678 |
| rs542029858 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957540 | GCCCCTTGTGAAAAA[C/T]GTCTCCAAAGCCTGC | 9678 |
| rs542043029 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11032710 | TGCTTCTCATCATTC[A/G]TTTTTGTCTTATATT | 9678 |
| rs542045608 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10971288 | CCAGAACTTAACTGC[A/G]TAACTCCAAGCAACA | 9678 |
| rs542052682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998471 | ACACACACATACACA[A/G]CAATAAGACCACTTG | 9678 |
| rs542082600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11131392 | TTCATTTGCAGTTTC[A/G]TAAGGACATGTAGTG | 9678 |
| rs542123211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163979 | ATATATGTATTCTTA[A/C]ACTTTTAAAAGAAAC | 9678 |
| rs542129789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084401 | TATATCATCATCCAT[A/G]CTTCTTTCCTCTAAG | 9678 |
| rs542139909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040929 | TCAAAAGATGCATTC[C/T]AGTTTGAATGATAGA | 9678 |
| rs542164676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005866 | GGTGAGATCTCGGCT[C/T]ACTGCAACCTCTGCC | 9678 |
| rs542170040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156222 | ATGAAAATAGGGACG[A/T]TATTTTTGACACTGA | 9678 |
| rs542170932 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126688 | TATGTTCTTTTATCA[A/G]TGAAAAGCTTCCCTA | 9678 |
| rs542180463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11156687 | GTAATCCCAGCTACT[C/T]GGGAAGCTGAGGCAG | 9678 |
| rs542186232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109540 | AAATCTCAGCCTTCT[C/T]ATAAACTCAGAAATA | 9678 |
| rs542187553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11124073 | TTTCTAACTCCACTT[C/T]TCTGAAGAAAGTTGG | 9678 |
| rs542194820 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11110102 | ATTTCTACTAAAAAT[G/T]TAGATTTACAGTCCC | 9678 |
| rs542199913 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958671 | TCATAAATGTTAGCT[C/G]TTTGGCCAACTGCTT | 9678 |
| rs542209603 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155636 | TCTACTAAAAGTCAC[A/G]TAGCACTATGTTTTT | 9678 |
| rs542221281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154051 | AATCAGTTCATGTCG[C/T]CGGTAGGGTCTACCA | 9678 |
| rs542245089 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11010420 | TCCTTTGCTTATCTT[G/T]TGTGTTATAGTCTAA | 9678 |
| rs542249845 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107101 | AGTAGTTGTAGTTTA[C/T]TCCTCTAATGAAATT | 9678 |
| rs542259464 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103442 | TCTTCATCAACATCT[G/T]TATCTTTCCAGAGGT | 9678 |
| rs542277553 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11026132 | AAAAAAAAAAAGAGA[G/T]AGAAATTGCCACAGC | 9678 |
| rs542279831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11021602 | TTAGGTTTATCAGAG[A/G]TAAACTCCTACAGAG | 9678 |
| rs542287915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059879 | ATTTTTATTTTATTT[C/T]ATTTTTTTGAGACAA | 9678 |
| rs542301172 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10983414 | GAAATATTTTTATAT[A/C]CATAGACTTGGGAAA | 9678 |
| rs542309824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049276 | TCAGGAGTTTGAGAC[C/T]AGCTTGGCCAACATA | 9678 |
| rs542313796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140893 | TATATGGTCAGTTTC[G/T]TCATGTAAATGTCCA | 9678 |
| rs542354031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11023785 | GTGAGCTGAGATTGC[A/G]CCACGGCACTCCAGC | 9678 |
| rs542354455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096247 | TGTATTTTGTAAAGA[A/G]GATCATCCTGCATAA | 9678 |
| rs542391320 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151393 | AGACCACCCTCTCTA[C/T]AAAAAATAAAAACAA | 9678 |
| rs542396851 | snp | A/G | 0.000440001 | 0.0148259 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990799 | GATAATAGTGAGGAC[A/G]CTGATGAAATAATTC | 9678 |
| rs542410638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115430 | TGATTTAAATAAGCT[A/G]GTACTATAGAACAGG | 9678 |
| rs542416463 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11112427 | AAACTGCAAAAAGAC[A/G]TTTGGTTATAGAAAG | 9678 |
| rs542417384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080217 | AGTTTTAGCTTTGAT[A/G]TGGAGTACCTAGGTG | 9678 |
| rs542432239 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11076003 | AATTAGCCGGGCATG[G/T]TGGCGGGCGCCTGTA | 9678 |
| rs542435564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159108 | TCACTCTGAATCTTA[G/T]AAACTTGAGTCAGTG | 9678 |
| rs542459526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155767 | TATATACAATGTTTT[C/T]TTTTTGTTTTTTTTT | 9678 |
| rs542462466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996181 | TCACTCAGACTGCTG[G/T]GTTGGGAGTAGACTG | 9678 |
| rs542473664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024047 | AGCTCTTGAAGGAAA[C/T]TGAAAGTGCTACTCC | 9678 |
| rs542474033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108881 | CTCAAGTTATACACT[A/G]GAAATCATAATTTGA | 9678 |
| rs542476429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11036862 | TAGGTTCATTTATTT[A/G]TAAATATACTTAAAA | 9678 |
| rs542479293 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040817 | AATAATGTTGTGTAT[G/T]TTTTTAAACTGATAC | 9678 |
| rs542481814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112997 | ATTTTATTTAAATGT[A/G]AAAATAATGAAACAC | 9678 |
| rs542485476 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11032548 | ATCATGGCATCTAGA[-/G]GACCACAAGCTAAAC | 9678 |
| rs542515151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11030356 | AAACTTTGAGCTTTG[C/T]GGTTAGTAGGGTGCT | 9678 |
| rs542522008 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11038210 | CGAGGTCAAGAGATC[A/G]AGACCATCCTAGGAG | 9678 |
| rs542523476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992046 | AATTTTTTGTAGCTT[C/T]TTCTTTCATAGTTGT | 9678 |
| rs542556503 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11035329 | GGGGGGTCCTGGAAC[C/T]AGTCCCCCATGGATA | 9678 |
| rs542607558 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970055 | TAATTAGACAGAATT[C/G]TGGACATTAAGAATA | 9678 |
| rs542608098 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080695 | TAGATCAAAAGTACT[A/G]TTCAGGACATTCTGC | 9678 |
| rs542608853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006468 | TCGAACATATGCCTT[C/G]TTTTCTCCATCAGGC | 9678 |
| rs542610734 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091747 | TGGGTGACGGAGCGA[G/T]ACCCTTTCTCAAAAA | 9678 |
| rs542624008 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11055313 | AACTTGAAAGCTTTC[A/C]GATTTTCTTTTTGCT | 9678 |
| rs542652704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012557 | TCCAGAGATGTATCT[A/C]AGGCAACTTTGCTTT | 9678 |
| rs542660446 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10973839 | GCCCTCAATTCCTGC[C/T]GCTCTCAGGGCTGCG | 9678 |
| rs542663075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041695 | GCACATTCTCAGGCC[A/G]GCTTTTTCAAACACG | 9678 |
| rs542714780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092724 | TTCTAATGTGAGGAT[A/G]TCATGAGACCAAGAG | 9678 |
| rs542719857 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968569 | ATGGCCAGAATTGAT[A/G]TACTTTGTCCAAATA | 9678 |
| rs542729770 | in-del | -/TGTC | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10983941 | ACATTTGTGTCTCTT[-/TGTC]TGTGTGTTTTTGTAT | 9678 |
| rs542741818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001685 | TGTTCATTGCTTTCA[G/T]AAGAAAGCAATTGGC | 9678 |
| rs542744701 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106920 | AGTAAAATGTTCCAT[C/T]GGCATAAAAGATAAT | 9678 |
| rs542753368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093148 | ATTTTATTTCCAAAT[A/G]TTCGGAGGATTTTCC | 9678 |
| rs542754092 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119306 | GATAAAGGACATTTT[A/T]TTACGGCTTTACAAA | 9678 |
| rs542766495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11067730 | AAGATTGGGCATCTG[C/T]ATCTGGTGAGGACCT | 9678 |
| rs542770971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957531 | TTGGGACTTGCCCCT[C/T]GTGAAAAACGTCTCC | 9678 |
| rs542786915 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992607 | GGTGGAGGTTGCAGT[A/G]AGCCGAGATGGTGCC | 9678 |
| rs542793119 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165344 | CCAGAGGTGATGTGC[C/T]GTTTTTAATACATCG | 9678 |
| rs542813786 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10991470 | GTGAACTACCGCGCC[C/T]GGCCAATTTTTGTGT | 9678 |
| rs542839052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017120 | TCCATTGTGTATTGT[G/T]TACCACAATTTCTTT | 9678 |
| rs542850419 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999094 | GCCCCAGGCTTGCCT[C/T]AAACTCCTGGGCTCA | 9678 |
| rs542888345 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11068313 | CAAGATCGCACCACT[A/G]CACTCCAGCCTGGGT | 9678 |
| rs542899421 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115647 | TGCTATATTATTACT[A/G]TCTGATCCTCAGATT | 9678 |
| rs542918510 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995739 | ATTTGAGAGCAGCGC[C/T]GGCGGGCCAGCACTG | 9678 |
| rs542919301 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958378 | ATAATTTGAAAACAG[A/T]TTATCAATGAACTCT | 9678 |
| rs542927125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069250 | ATACCCTTGTACTTA[C/G]AGGAGAAATTTAGTC | 9678 |
| rs542959876 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056090 | CTGTCATAGATTCTT[A/C]GAAGAAACCCTGGCA | 9678 |
| rs542962719 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158785 | TCCATGTATGTCATA[C/G]TTGCTTACAGATTAG | 9678 |
| rs543002813 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053390 | TTTATTTGTAGTTTC[A/G]ACTGTTTATAACTCT | 9678 |
| rs543020502 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11084341 | ACCAAGTGTTATTTT[-/C]TTCTTACATCCTCTA | 9678 |
| rs543032844 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985303 | TATATTTGATTATAT[G/T]TGAAGTTTGATTTTC | 9678 |
| rs543036128 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023569 | TGGGTGCTCACGCCT[C/G]TTATCCCAGCACTTC | 9678 |
| rs543039973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977515 | TTAACTCTATCATAA[A/G]ATAGAAACAAATCAA | 9678 |
| rs543042748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085660 | TTTTTTTCCTTTTTT[C/T]TGAGACAGTGTCTCA | 9678 |
| rs543077208 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976349 | GGGAAAGGAGGTAAA[A/G]TTTAAATCTTAGTTC | 9678 |
| rs543080614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966969 | AGATGGGCATGAGGA[A/G]AATCAGCATCCCTTT | 9678 |
| rs543105853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078585 | GAAGTTAAGAAGAGA[A/G]AGAAATTCAGAAATG | 9678 |
| rs543114612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998591 | AAAGTAAACATGGTT[C/G]AATATATGTGTATTT | 9678 |
| rs543134047 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973383 | GTGCTTTAATTTTCA[A/G]TAAGTCCCTGCTTTT | 9678 |
| rs543141034 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035898 | GGAAGTTTGGTTAGT[A/G/T]ACCTAGGAAATGGAT | 9678 |
| rs543143030 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104905 | CGTTGTGTTGTGCTT[A/G]ACATTGATTGATAAA | 9678 |
| rs543143357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962643 | ATTGGAATAGTTTCA[A/G]AAGGAATGGTACCAG | 9678 |
| rs543144342 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139669 | GTTTAAAAGGGAAGT[C/G]AAGTGTGTATTGTGT | 9678 |
| rs543154859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11018888 | GGGTCTGTCATATAT[C/T]GCTTTTATTATGTTG | 9678 |
| rs543172162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979695 | TGGTTGTAAATAAAT[A/G]TGGTTTATCTCCATT | 9678 |
| rs543180818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152247 | TGAGCAATTCTAACT[A/G]TACATACGGTATATT | 9678 |
| rs543190595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091981 | GTGTCCTTGGTTTAG[C/T]TGAGTCACAGGCTAA | 9678 |
| rs543211190 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11159925 | AAAGGTTTTCAACTT[C/T]TATTTTAGATTCAAG | 9678 |
| rs543216128 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11125863 | CATTGAAATTAAGTC[A/G]GTTTTTTGTTAAGGG | 9678 |
| rs543224733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023156 | AATAATGCATAAATT[C/T]TTCTATACATTCTTA | 9678 |
| rs543239375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165174 | GTGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC | 9678 |
| rs543255656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118710 | CAGTAAAACATAGAT[A/T]GTTTATTAGTCATTC | 9678 |
| rs543261785 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11154273 | ACATCCACTTGAGTA[-/TG]TGTGTGTGTGTCTGT | 9678 |
| rs543261819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001651 | TAAATGGAATTTTGT[C/T]TTTAATTTCAATTCT | 9678 |
| rs543265022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035846 | ATGTAAGGATTTTAC[A/G]TCTCGTGTGGCTTCC | 9678 |
| rs543272607 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973541 | GGTAGTGGCTTAAGG[C/T]AGCAAACATCCCTTT | 9678 |
| rs543273207 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029210 | TTACTGTGTCTTTAG[A/T]ATCTCTGTTACTATC | 9678 |
| rs543287369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054613 | TCAATAGGTGGTATG[A/G]TGAAAAATGAGGTGT | 9678 |
| rs543295370 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992788 | ATTCAGATGTTGCCA[A/G]TTGTCCCAACAATGT | 9678 |
| rs543300709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11158542 | TTTTATTTTGCTTTA[A/G]CAAAGTAGTTTTAAA | 9678 |
| rs543317020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111816 | GTCATAATAAATTAT[A/G]TTAGCTAACAGAATA | 9678 |
| rs543332746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138497 | CAGTTTTGTGCCCTG[C/T]GCACAATTACCATAC | 9678 |
| rs543332873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146717 | ACATACATTCAGCTC[C/T]GCATGGTCATTTCCA | 9678 |
| rs543333573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963066 | CTTGAAGAGTTTTTT[A/G]TGTCTCTATCTTCTT | 9678 |
| rs543358222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957270 | AAATTTTTAAAAACT[A/G]TTGTATAGATTTAGA | 9678 |
| rs543369925 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11137506 | AATAGTTTTGAATGG[-/T]TTTTTTAAAACTTGA | 9678 |
| rs543384118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023789 | GCTGAGATTGCGCCA[C/T]GGCACTCCAGCCTGG | 9678 |
| rs543389217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097646 | CTTTCCCTTACCACA[A/G]TTAATGCTAGAGGCA | 9678 |
| rs543389384 | in-del | -/TT | 0.0148984 | 0.0850131 | intron-variant | PHF14 | GRCh38.p7 | 7:10990648 | ATTTTAGTGATTAAG[-/TT]TTTTTTTTACTTTAA | 9678 |
| rs543403368 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11011328 | GTGAGAGGTCACGCT[C/G]CAATTTAGGCTCCTG | 9678 |
| rs543405191 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104444 | TTCCGTGTCCATAAT[C/T]GGTCCAACTACTATA | 9678 |
| rs543428029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131803 | ATTTTTGTGAAAGGT[A/G]TTAGACCTGTGCCTA | 9678 |
| rs543428555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991412 | TGAACTCCTGACCTC[A/G]TGATCCACCCGCCTT | 9678 |
| rs543429708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090854 | ATAAACCAAGGTGAC[A/C]GGTGAATTGAATCTT | 9678 |
| rs543444903 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11164955 | TTTGAGACGGAGTCT[C/T]GCTCAATTGCCCAGG | 9678 |
| rs543445191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062388 | TAATTTGATCTAAAC[A/G]CTGTGTACTAAGATT | 9678 |
| rs543452645 | in-del | -/AG | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11026502 | TATTTGAGCATTAAC[-/AG]ATGTATTTATTGGGC | 9678 |
| rs543453187 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105560 | AATGGCAATTGAAAC[C/T]TGTTTAAGAGACTCA | 9678 |
| rs543461727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978909 | AGTTGTGTTGACTGA[C/T]TGGCTGTCTTCAAGA | 9678 |
| rs543481951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006005 | CACCATGTTGGCCAG[G/T]TTGGTCTCGATCTCC | 9678 |
| rs543491284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132214 | ACCTTTTTCATCTTA[C/T]ATATCTGCTGCTTTA | 9678 |
| rs543492911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985857 | GGGGTTTCACCATGT[C/T]GGCCAGGCTGTTCTC | 9678 |
| rs543504403 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995872 | GCGCTGGCCCGCAAG[C/T]GCCTTGCACAGCCCC | 9678 |
| rs543518047 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098503 | TATAATTGGGTTCTA[A/C]AGCTCTACTATGTCT | 9678 |
| rs543518055 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106305 | TGTCTTTCTTACTAC[C/T]CATTCATTCATTATT | 9678 |
| rs543547983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012693 | AAGGATTTTTATTAC[A/G]TTAGCTGCCTAAATA | 9678 |
| rs543550889 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11125225 | CTCAGTCAAATCTTA[C/G]TTTTTAATGTTTGTC | 9678 |
| rs543577043 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158553 | TTTAACAAAGTAGTT[C/T]TAAATCATTTGAGTT | 9678 |
| rs543578921 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099030 | GCTTTTCTATTAGTA[A/T]AAATCAGGGAAGAGA | 9678 |
| rs543586240 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000675 | TCTTGGATGAGGTGT[C/G]TATTCAGATCTTTTG | 9678 |
| rs543597514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10989815 | TTAAAATATTTTGTA[A/G]AGACAGGATCTCACT | 9678 |
| rs543602845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066661 | TGGATTCCCAGTATC[A/G]TTTGTTGAAAATACT | 9678 |
| rs543613838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156391 | CTAATGAGCTATTAC[A/G]TTCCAATAAAACTGA | 9678 |
| rs543633062 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11021809 | AAAAAGATAATTTTT[A/T]AAAAAGATTTAGAAC | 9678 |
| rs543646823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165803 | CACAAATTGATAGTG[A/C]AAGCTGACTAACATT | 9678 |
| rs543668100 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079755 | GCTAACTGTGATATA[C/G]AAAATCATTTAGCTG | 9678 |
| rs543681002 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104330 | AAGATATAGGTCCTG[C/T]AAAAAGTATAGTTGA | 9678 |
| rs543683426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956826 | AGAGCCTTTGGAGGG[A/C]GTGTGGTCCTGTTCA | 9678 |
| rs543687452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119255 | TTTTATTTTTTGTTA[C/T]TTTGTTATTTCAGCT | 9678 |
| rs543709468 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11159006 | TATTTACAGTTTATC[A/T]GGCCTCAGAAGTAAT | 9678 |
| rs543718106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11053092 | GGAGATACAAAGATA[C/T]TTTTAGGGTTAGTTG | 9678 |
| rs543747989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11112320 | AGAGTGAATTAAAAT[C/T]GATCATGTAATCAAA | 9678 |
| rs543752612 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11050911 | AGTATATTCAGCACA[A/G]GTTGTCACTGACTAC | 9678 |
| rs543754214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145788 | TTTTATTAAAACAGT[A/T]AATTAACATCATAGA | 9678 |
| rs543756516 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078302 | GTGATAGTGCATTTA[A/G]TATTTATCTTAGTGA | 9678 |
| rs543758565 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11074163 | CAAATGGTTGCTCCA[C/T]AACCACCTTGAATTC | 9678 |
| rs543794663 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076405 | ATTCTTATAAGTATG[C/G]TGTTTAGTTGTATTT | 9678 |
| rs543803045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053564 | GAAGAGTTATTACTT[C/T]GTATGTCTGTCTACA | 9678 |
| rs543816199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142551 | CAAGATAACATCAGC[A/G]TTTTCCTTCTTGAAA | 9678 |
| rs543817054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138433 | ACTTTTACCCACTTT[A/G]TCCCTTATTATTACA | 9678 |
| rs543818006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11128394 | TTATTTTCCCTACTT[C/T]ATTCTATTTCCTGTC | 9678 |
| rs543871614 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972172 | AACTCCCAACCTCAA[A/G]TGATCCACCCGCCTC | 9678 |
| rs543884369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129095 | ATATTTTTTCTAAGA[C/T]AGATTTAAGATTGTT | 9678 |
| rs543924574 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130294 | GTAAGTGTAATGCTA[C/T]CACCATATGCTACCA | 9678 |
| rs543930424 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972805 | ACATGGCAATGATAG[C/T]TTGGGTGAGAGTGAG | 9678 |
| rs543931078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11041603 | TTTGTTGGAGGCTCC[C/T]TCTACAAGTAATAGC | 9678 |
| rs543940793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966909 | TTGTCCTTGCCCCTT[C/G]GAACATACTGGGATC | 9678 |
| rs543947209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073014 | CTCCCACCAGGCCCA[C/T]CTCCAATATTGGAGA | 9678 |
| rs543951843 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079874 | GATCATAAATGACAT[A/G]TCAATAATCAGGAAA | 9678 |
| rs543960017 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088900 | TTATGTCATAAGTAT[A/G]TGCTACTAAATTGTT | 9678 |
| rs543963320 | in-del | -/ATA | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11070048 | GTGGAAATGTTTTTG[-/ATA]ATAAATTCAGTTTTT | 9678 |
| rs543970087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045567 | TTTTAAGCACTTGCT[A/G]TCCAGCCTTTTCTTC | 9678 |
| rs543974293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11082448 | ATCCTAAATTAGCAT[A/G]ACAAATTTATAAATT | 9678 |
| rs543985166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987232 | TTCATGAGAATTTAA[C/G]CTTTTCTAAAAATGT | 9678 |
| rs543986964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993427 | TTTTTGCTGCTAACA[C/G]TCACTGTGGGAATAT | 9678 |
| rs543990730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100049 | AACAAGTATGATCCA[A/G]CTTCTAGTTGAAAAG | 9678 |
| rs544002626 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144633 | ATTATATTTACTAAT[A/G]TTCCTAACGTTTTTA | 9678 |
| rs544003020 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157691 | TCTTAAACTGCAAGC[A/G/T]TTTAAAAACATGACA | 9678 |
| rs544007424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111090 | CATTCATATGCTCTT[A/C]ATATTTCTACTGTCA | 9678 |
| rs544011266 | snp | G/T | 2.11921e-05 | 0.00325508 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038804 | CCTGAATGGAAAACT[G/T]CGAAGTGAAGGACAA | 9678 |
| rs544032676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070226 | GTGACTACAAGTGCG[C/T]GCCACCATGCCCAGC | 9678 |
| rs544033792 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11067122 | ACAACTCAGCAATAA[A/G]AAACAACCCCATTAA | 9678 |
| rs544047274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987797 | CTAACAACAGTTGAT[A/T]ATAAATCAGGTTTTG | 9678 |
| rs544059773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11139753 | AGAAAATATAAGACA[A/G]ATAACTTTTGGTACT | 9678 |
| rs544062666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151827 | AGTATTGAGAAAGCC[A/T]CTATATGAGTGTATT | 9678 |
| rs544069009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060015 | AGCTGGGACTACCAG[C/T]ACTCACAACCATGCC | 9678 |
| rs544079134 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994726 | GCTCCTTCTGATGTT[C/T]GGATGTGTTCGGAGT | 9678 |
| rs544113078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094014 | TTTACAGCCTTTCTT[C/T]TAATGACATTATGGC | 9678 |
| rs544114774 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992523 | CAAAAATTAGCCGGG[C/T]GTGGTGGCTTATACC | 9678 |
| rs544118475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11016798 | TAGTTTTTCTTGACT[A/G]TAGTCACCCTGTTGT | 9678 |
| rs544137680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101371 | GTTGCTTCCTCTTGC[A/G]TTATACTTTTCCAGT | 9678 |
| rs544146469 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091399 | TAGGTGAATAGAGGG[-/T]TTTTTTTTAAAGGTC | 9678 |
| rs544170417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964553 | TCTGACAATTATGTG[C/T]CTTGGGGTTGCTCTT | 9678 |
| rs544184169 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052038 | AAGACAGACCATTCC[C/T]AAAGCTTTAGAAGTT | 9678 |
| rs544187726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014804 | TAAGTGGCACAAAGA[C/T]CTGTGTTCTTTTTAC | 9678 |
| rs544192412 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11058304 | CTTATGTTTTGGGAT[C/T]CATTCAAGTACACTA | 9678 |
| rs544203937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044937 | ATCTGCAATGCTCCA[A/G]TGAACATTTTCTTTG | 9678 |
| rs544208800 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992187 | GCCTCCCGAGTAGCT[A/G]GGATTACAGGTGCCT | 9678 |
| rs544213679 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082459 | GCATAACAAATTTAT[A/T]AATTTTCTTCCCTCA | 9678 |
| rs544230569 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051432 | AAATATTATATTCAT[A/T]GTAGTCACTCTTAGA | 9678 |
| rs544252685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988995 | TGTTTGCTTACTCTG[A/G]TACTGTAAAACCAGA | 9678 |
| rs544268680 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992823 | TCTAACAAAATCAAA[C/G]CCAGGATCATGTATT | 9678 |
| rs544275401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003157 | TGTTGGCCAGGATGG[C/T]CTTGATCTCCTGACC | 9678 |
| rs544289517 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997100 | CATCTTGGTCCTTCT[A/G]TCCCTTTCTGTCTGT | 9678 |
| rs544295083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043580 | AAATACATTAGGCAT[A/G]TTTTTTGACCTCATT | 9678 |
| rs544313393 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059130 | CCATTGTGTGATTGA[A/G]TCACTAATTGGCATT | 9678 |
| rs544313395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075460 | AAAGGGGGAGCTGGC[A/G]TATCACATAGAGCAA | 9678 |
| rs544317535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085628 | CCTCCTTAAAACACT[A/G]TCTTTTCTTGGTTTT | 9678 |
| rs544319280 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10970109 | AGGCAGTTTGTGCTC[A/G]CTGTTTTTTGGAAAT | 9678 |
| rs544321379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965002 | TACCTTCTTTGCGAT[G/T]GGTTAGAACATGCTC | 9678 |
| rs544333302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965273 | TGTCCTTTTTGTTGA[C/T]GTTGATGCTATTCCT | 9678 |
| rs544347613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168449 | TTTTACTTTATAAAG[C/T]CAATTCACAAAGTAG | 9678 |
| rs544351712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064002 | CCTTATTAAGAAGAT[A/G]ATATCGTAAATTGTC | 9678 |
| rs544360212 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113587 | ATTTGTATTTTCGTT[A/G]TACTTATATGACTTA | 9678 |
| rs544369345 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11167022 | CATATTCAAATTAAT[A/G]GAAGTTGCAAATTTT | 9678 |
| rs544372656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048712 | AAGGATATTTATAAG[A/G]TGAAGACTATAGTGT | 9678 |
| rs544386987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148259 | ATTCTTAAACCCTCC[A/T]GTGGCTTCTCACTGC | 9678 |
| rs544389803 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11161316 | TTCATTGTCCAGTGA[C/G]AAGGATAAACAAAAT | 9678 |
| rs544392843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155008 | GAGGATCCTTACTAT[C/T]TATCTGTAGGTACCT | 9678 |
| rs544406578 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963079 | TTGTGTCTCTATCTT[C/T]TTCAGTTCTGCTCTG | 9678 |
| rs544417748 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106924 | AAATGTTCCATTGGC[A/G]TAAAAGATAATGTGA | 9678 |
| rs544436580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967665 | CTTGGCAACGTAGCG[A/G]GGTCCCATGTCACAT | 9678 |
| rs544458109 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007031 | AAATACAAAAAATTT[A/G]CCAGGTGTGGTAGTG | 9678 |
| rs544483198 | snp | A/C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981882 | ATTTTACTGGGTAAA[A/C/G]AGTAAAATAAATGAA | 9678 |
| rs544483684 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071466 | TAAGTCAGTTTAAAA[C/T]ACCCACTTCCTTTGA | 9678 |
| rs544491894 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11081727 | GGGGTGTGGTGGCAC[A/G]TGCCTGTAGTCCCAG | 9678 |
| rs544492127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049817 | ACAAATGCAGGAGCA[A/G]TTTAATATATTCGTT | 9678 |
| rs544497634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057644 | CTCCCAAAGTACTAA[C/G]ATCACAGGCCTGAGC | 9678 |
| rs544510820 | snp | A/T | 0.00279162 | 0.0372561 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973756 | CTCCGCGCGGCTCCC[A/T]GGGCTTTCACTCGGC | 9678 |
| rs544512185 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963865 | GATCTTTGTTGGTTT[A/T]AAGTCTGTCTTATGA | 9678 |
| rs544516353 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979217 | ATTTGATATTGTAAA[C/G]GGATTCTTGAAGGTT | 9678 |
| rs544545634 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11119014 | AATTGAAAAACTAAG[C/T]CACTTTCTAAATTAC | 9678 |
| rs544572338 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102841 | TGTCTTGTCAGAATT[A/G]TCGTATTAAGTAATG | 9678 |
| rs544595210 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | PHF14 | GRCh38.p7 | 7:11133369 | GGTCAATGAAACAGA[A/G]TAGAGAGCCCAGAGA | 9678 |
| rs544620061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120899 | TTTTTTACTGACGAC[A/G]TATTTTAGTAACAAG | 9678 |
| rs544639055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11134346 | ATATGGACCTGAAAT[A/G]TCATTTAGAGAGATT | 9678 |
| rs544640787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030500 | GCAGCCATGTTTGGG[A/G]CAGTGGGGTGTAATG | 9678 |
| rs544657894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980238 | TTGATTGATAAAAAG[C/G]CTTCTAGAAGGTTGA | 9678 |
| rs544674243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100442 | TTTAGAAGAGAGGTA[A/G]CTGGGGTACATAGAC | 9678 |
| rs544717889 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107214 | TTGCATATTCTCAAT[A/T]GTCAGGTAAACACCT | 9678 |
| rs544744080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093947 | TTTTTTTTCCTCTTA[C/T]GTTTTTTTCTCTTCA | 9678 |
| rs544746145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140046 | CCTGTAACACCTTAC[A/G]CGTTCCTACACACTA | 9678 |
| rs544769221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092689 | AGTGAATTGCCTTTT[G/T]GAAGTCTCTTTTTTT | 9678 |
| rs544771719 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002591 | ACTACAGGCATATGC[A/G]CCACCACGCCCAGCT | 9678 |
| rs544790207 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992156 | CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTCA | 9678 |
| rs544791361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008413 | CAGCAGGGGGTGAGC[A/G]GCTGGTGAGGGAGCA | 9678 |
| rs544806481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992632 | GGTGCCACTGTACTC[C/T]AGCCTGGGCGACAGA | 9678 |
| rs544812033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013064 | TTTGATCTTTTATAT[A/G]TATATTTTAGTACCT | 9678 |
| rs544812052 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007037 | AAAAAATTTGCCAGG[A/T]GTGGTAGTGGGCACC | 9678 |
| rs544852395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086361 | AAATTTAGATCATCG[C/T]AGGTCATTTTTTCTT | 9678 |
| rs544855489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031213 | AAAAAGGTTGAAAAA[G/T]AGAATAAACATATCA | 9678 |
| rs544866577 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979455 | TAAAGATATATTTTT[-/TT]CAAACGTAAGAAAGG | 9678 |
| rs544867796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019019 | TTTTATCCTTCATCC[C/T]GTTGATGTGATATAT | 9678 |
| rs544887061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043347 | AAGGTTATAGTATCT[A/G]TAATGAGTTTTATCC | 9678 |
| rs544918208 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11089859 | CACCACAAACTCCAC[C/T]TCCTGGCTTCAAGCG | 9678 |
| rs544922142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002658 | ATGTTGGTCAGGCTG[C/G]TCTTGAACTCCCCCG | 9678 |
| rs544937555 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11007963 | AATTTGAGGGCTGCA[A/G]TGTGTCACTTAGTAT | 9678 |
| rs544940200 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:10987170 | TGAAACAAATTGCTC[C/T]GAGTCCTAAAAAAAG | 9678 |
| rs544990639 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11115053 | TTTCTTCTTCCATCC[A/G]TTCACCCAAGTCACA | 9678 |
| rs544994170 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11079912 | GACATAGAAATTACC[A/T]ATTGCATGTAACTCA | 9678 |
| rs544994667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057205 | CTTTTAGTTTTAAAT[G/T]TAGTTCATTTGCCAA | 9678 |
| rs544999161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027451 | AGTCTTTCATAATTT[A/G]ACATCTTTTTCTTTT | 9678 |
| rs545000026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11050050 | ATATTTAAATTAATA[C/T]GTTAAGGATTAATTT | 9678 |
| rs545012676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995857 | GCCCACCCGGAACTC[A/G]CGCTGGCCCGCAAGC | 9678 |
| rs545025292 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007278 | ATTCTTTTTTTAATG[C/G]TCTTTGTCTGTTATA | 9678 |
| rs545030294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080293 | AAACTTGATAACTTA[C/T]ATTACACGTGCATAC | 9678 |
| rs545073065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996246 | TAGGAGACCATTGCA[A/G]TTATCTAAGAGAGGA | 9678 |
| rs545076125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044036 | ATGTTCTTTGTAGCA[A/G]CAAGGAGGCAGCTGG | 9678 |
| rs545081421 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969277 | GTGTATTTTGGGGAG[A/G]GTAGTGAGGTAATTC | 9678 |
| rs545085318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002606 | GCCACCACGCCCAGC[C/T]AATTTTTTGTATTTT | 9678 |
| rs545095099 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115895 | TGGTTTAGATTCATT[A/G]TGCATCTTTGATAAG | 9678 |
| rs545112241 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967703 | TTTTTTTAAAAAGTT[A/G/T]AAACCCTGGGCTTGT | 9678 |
| rs545142586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113098 | TTTCTCCTACCCCCA[A/G]CAAACAAGTTAGGAA | 9678 |
| rs545156148 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140879 | GGAAGCGTCTTTGAT[A/T]TATGGTCAGTTTCTT | 9678 |
| rs545163643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963724 | TAAGTCTCTTTGTAG[G/T]TCTCTAAGGACTTGC | 9678 |
| rs545176985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978170 | TTAATCTGACTTTGA[A/G]TAAGTGGACCAAGAT | 9678 |
| rs545194826 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11167777 | CTCACGCCTGTAATC[C/T]CGGCACTTTGGGAGG | 9678 |
| rs545203434 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058345 | AACTTGTCTGTTGTG[A/G]TCTTAAGCAGTTATG | 9678 |
| rs545204190 | in-del | -/GG | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10988078 | AATTTTTTTTAAGGA[-/GG]ATGTGTTACTTAGAT | 9678 |
| rs545204237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160619 | TGGTATCAATGAGAT[A/G]CTATCACAAAAGAGA | 9678 |
| rs545209638 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120067 | TTTTCCCAAAAAATT[A/G]CCATTAAATTGGCGG | 9678 |
| rs545240427 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972978 | TTTCTGCAGGGCAGA[C/T]GGGAAATTGGCTGTG | 9678 |
| rs545252754 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973361 | TCAGGTCGCTTCCGT[A/G]CAGAGCGTGCTTTAA | 9678 |
| rs545267468 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11154105 | TGAAAGAAACTAATG[G/T]ATTTAACCAGGTTAT | 9678 |
| rs545271729 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063134 | TTTTTTATGCTATCA[A/G]TGAGAAAGATAAAGT | 9678 |
| rs545271733 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004881 | TCTCTACTAAAAATA[C/G]AAAAATTAGCCTGTA | 9678 |
| rs545308150 | in-del | -/TTAC | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:10977983 | AGATGCAGACATGTA[-/TTAC]TTCTATTAACCAGAC | 9678 |
| rs545308622 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002301 | CTGCAATGTGGACGA[C/T]GTCATGCTGGAGCTT | 9678 |
| rs545343398 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138243 | AGGCAGGGTTTCACC[A/G]CGTTAGCCAGGATGG | 9678 |
| rs545378579 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11133683 | AATATGGAGTTTAGG[A/G]CAGTGTCCTTACTGC | 9678 |
| rs545383572 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11092457 | TATGCTAAAGTCCTA[A/C]GATAGTGGTTCTCAA | 9678 |
| rs545386293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083706 | GACCTCGTGACCCAC[C/T]CCCTTGGCCTCCCAA | 9678 |
| rs545404856 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126928 | TTTTTAACAGACCAC[G/T]CTTACGTTTTTATTG | 9678 |
| rs545413406 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963431 | TTTGATTGCAGTGTG[G/T]TCTGAGAGACAGTTT | 9678 |
| rs545425779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077416 | GACCATCCTGGCCAA[C/T]GTGGTAAAACCCCGT | 9678 |
| rs545431413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166509 | TTAATCTGGAACTGC[A/G]TATAAATTCTTACAA | 9678 |
| rs545432224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035970 | CAGTACTCCTCATTT[A/G]GTCAAACAGAGCAGT | 9678 |
| rs545433649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043231 | TGGTATTTGTGCTAG[C/T]CATTTAAATTCAACC | 9678 |
| rs545466049 | in-del | -/T | 0.0980852 | 0.198549 | intron-variant | PHF14 | GRCh38.p7 | 7:11043286 | GATAAACATTTCTGA[-/T]TTTTTTTTTTATTAA | 9678 |
| rs545479994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999318 | TTGCCTAGTCCCTGG[A/G]GATATTTGAATATAT | 9678 |
| rs545487200 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967125 | TCAATTCTCAAGGTA[C/G]CATTCTATCCCAATA | 9678 |
| rs545490466 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073734 | CTTTCTGTGAAGGCT[C/G]TGTCTCTGTGACAGG | 9678 |
| rs545512445 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961070 | TTTTCTGTGCAGAAG[G/T]TCTTTAGTTTAATTA | 9678 |
| rs545515343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957564 | AGCCTGCCATTCATA[G/T]GCACTGAAACATGAG | 9678 |
| rs545520598 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013949 | ATGTTTGCTTTATAA[C/T]GTGTCTGCCTTTGAC | 9678 |
| rs545522215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030444 | GCATCATATGTCATC[A/G]TTTTTGGCAAGATGG | 9678 |
| rs545535955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160055 | GTTAGTTTTTCAACC[C/T]TTATTCCCTCCTTCC | 9678 |
| rs545543476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110325 | AGTGAAAGATAAACA[A/G]TAAAGAAAATCTGAC | 9678 |
| rs545548899 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998764 | TTGCTGATGTGTGAT[A/G]CAGTCATGATGAGTT | 9678 |
| rs545554689 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11146801 | CAATAAATGCAATTG[A/T]CTCACTTTTGTGCAA | 9678 |
| rs545559168 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042254 | AATGGTAGGAAATAA[A/G]CTACCTTCTGTTTGT | 9678 |
| rs545565379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116963 | TATTGTAATTTAAAA[A/G]GTAGGACATAGCTCA | 9678 |
| rs545579099 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098479 | CTCTCCTCATTTTTA[A/T]TGCTAGTGTATAATT | 9678 |
| rs545593885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11055401 | CTTGTTGGGACCTCT[C/T]TTTCCATTGTTTTTA | 9678 |
| rs545618861 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028088 | ATATTTTAAGTTGAG[A/C]TTAATTTAATACACC | 9678 |
| rs545627192 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970345 | AGAGGCTGAGGTGGG[C/T]GATCAGTTGAGGTCA | 9678 |
| rs545628719 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169997 | TATTTATATATTACA[C/T]GATACTCTAGGACTG | 9678 |
| rs545635067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11143685 | TTATTTAACAAATAT[C/G]TACTAAGCATCTTGT | 9678 |
| rs545647803 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970630 | GTAATTTATCACATA[C/T]GCCTTAAAGATGTTC | 9678 |
| rs545657647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095623 | AGGCATCCATTAAAT[A/G]TAGAGAATAAATGTT | 9678 |
| rs545666009 | snp | A/G | | | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10968407 | CATATCAAGATGCCC[A/G]TGGGATACCTAATAC | 9678 |
| rs545673409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048592 | AAAGAAAAAATAATT[A/G]TTTGATTTCATTGAA | 9678 |
| rs545711609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11140024 | CACAGTAAGAAATAC[A/G]TGTTACCCTGTAACA | 9678 |
| rs545728421 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11133978 | TATTAATCACTTAAG[-/T]TAGAAAGCTACTAAG | 9678 |
| rs545755565 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11156871 | GTCCTTGATGTTGAG[-/T]TTTATGTTAAAAGAG | 9678 |
| rs545767786 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11046161 | TGTCTCATTTTTAGT[G/T]TATGTTATTTTGATT | 9678 |
| rs545775138 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130782 | CATTACAGTGTCATA[C/G]AGAATAGTTCACTGC | 9678 |
| rs545810589 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120673 | TTTTCTAAATGTACT[A/G]TAGTTAGTACTTTTA | 9678 |
| rs545837751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123520 | GGCGCAGTGGCTCAC[A/T]CCTGTATTCCCAGTG | 9678 |
| rs545845660 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150573 | TCTCATTCTTTCATT[C/T]GCATCATTAAATTTT | 9678 |
| rs545866692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034221 | TCTCTTTGGGTTGTA[A/G]AACTCTACTTAGAGA | 9678 |
| rs545869286 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066188 | CTAAATTTGTTTGTG[C/T]CATAAATTATTAGGA | 9678 |
| rs545875821 | snp | A/G | 0.00160578 | 0.0282898 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961474 | CAAGCTGTTTTGGTT[A/G]CTGTAGGCTTGTGGT | 9678 |
| rs545876564 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134810 | AAAATAATTTTGCAA[A/G]AAAACATGAGTAAAC | 9678 |
| rs545879532 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11010209 | TAGATTGATGATACC[A/G]TTTCATTTTATGATT | 9678 |
| rs545887221 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150267 | TTATTGTTACTGGTT[A/G]TAGTTATGGTTATTG | 9678 |
| rs545915967 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007371 | CTTTAACTTTGTGAT[G/T]TTTTATTGTTTACAA | 9678 |
| rs545925408 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988468 | AGAAATTACCACACA[C/G]TCCATAAAGACATGT | 9678 |
| rs545937562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10981731 | TAATAAACAGGAAGA[C/T]TGATAATTTCTCTTG | 9678 |
| rs545948747 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128361 | TCTTTCTCCTCTCAG[C/G]CTTAAAAAAAGTCTT | 9678 |
| rs545963329 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166182 | CTACTTTCCAGTAGC[C/T]TCAAAGGATACATTT | 9678 |
| rs546002514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038222 | ATCGAGACCATCCTA[A/G]GAGTTTGAGACCAGC | 9678 |
| rs546031290 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11161616 | TTTTAGATTTTAGAT[A/G]ACATTTTTAAATATT | 9678 |
| rs546033403 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11003755 | AATATTCTTAATTAT[A/T]AGTGACATATGAGTA | 9678 |
| rs546039129 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031984 | ATAAAACCGGGTGTG[C/G]TGGCACACGCCTGTA | 9678 |
| rs546041161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038627 | CGTGTCACCGCACTC[C/T]AGCCTGGTGACAGAG | 9678 |
| rs546048208 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009827 | CTTTGAGCTTGCACA[A/C]CACCATTCTTCCAGA | 9678 |
| rs546049603 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161965 | TCAAGACCATAAGTT[C/T]GTCAGGGTTATCAAA | 9678 |
| rs546052731 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11136589 | GTTGAGCATGTCTTT[C/T]GCCATGTTCTATTCT | 9678 |
| rs546083516 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11089983 | TCCATGTTGGTCAGG[C/G]TGGTCTCGAACTCCT | 9678 |
| rs546098108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11169355 | AGTTAAAATCTGTCA[A/G]GTATAGCTGATAAAT | 9678 |
| rs546110095 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152787 | GTGATGGAGGAAGGG[C/T]AGATTTTGTGCATAA | 9678 |
| rs546125308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11032574 | TAAACTTAATCCATA[C/G]ATGGATTTTGTTTGT | 9678 |
| rs546127980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168266 | GATTCAGATTGGTTG[A/G]TAATATTGATAATTT | 9678 |
| rs546139890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997816 | AAGAGAGAAAGAGAC[A/G]GAAGCAGTTGTATCA | 9678 |
| rs546163520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987978 | CCGAGATCCCACCAT[C/T]GCACTCCAGCCTGGG | 9678 |
| rs546166822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11122242 | TTCTGGAACTTTTTA[A/T]TTACTATTTCCAGAT | 9678 |
| rs546171869 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034955 | TTTTGCAATATTAGT[C/T]TATGCATAACTTTAA | 9678 |
| rs546175383 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065257 | TTTATGCTATTTAAT[A/G]CAATCTAAATGCTAA | 9678 |
| rs546206734 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10994265 | CAACATGGTGAAACC[C/G]CATCTCTACTAAAAA | 9678 |
| rs546227975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115183 | TGCTCTTTGCTCCTT[C/T]TTTCCACTACTACTG | 9678 |
| rs546229459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108739 | GCAACAGATTGGAAC[C/T]GTGTTAGTGTAGCAA | 9678 |
| rs546250305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962999 | CTTGCTAGCAGTCTA[C/T]CTATTTTGTTGATCT | 9678 |
| rs546256834 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11066993 | CAAAGTTAAAAACTT[G/T]TGTGTGTGAAAGGAC | 9678 |
| rs546266532 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105014 | ACATACAATTTTTTT[A/T]AATTTTATAAAATTT | 9678 |
| rs546273651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115505 | TAAGATGTTTTTTCT[A/G]TTGATTTGCATCATC | 9678 |
| rs546285273 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021042 | GGCATTACTGATACA[C/G]AGCACTTCAAACTCC | 9678 |
| rs546291312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993896 | TGCCTGTAATCCCAG[C/T]TACTCTGGAGGCTAA | 9678 |
| rs546292435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101591 | TATTCTTTTGTGGGG[G/T]TGTTTACAGTTTTGT | 9678 |
| rs546300002 | snp | A/T | 0.00022498 | 0.0106038 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982648 | AGGAGAAAGAGAAGG[A/T]AAGAGAGAAGGAAAA | 9678 |
| rs546301745 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038058 | AAATGCTTACAGCAA[C/T]AAATACTGCTGAATA | 9678 |
| rs546302744 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080808 | AGCAAATGCATTAGA[A/G]GGCCATCAAGCACAA | 9678 |
| rs546318319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094710 | TCTGATATTAGCCAA[A/C]ATTTCACCTTTAGCA | 9678 |
| rs546325277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015354 | CATGTGTTGATGTTC[A/C]GGACAAATGACTAAA | 9678 |
| rs546328744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020140 | GTTCCCCAGGCTAAA[A/G]TGCAGTGGCACGATA | 9678 |
| rs546334031 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026154 | TGCCACAGCCACTCC[A/C]ACTTTCAGCAACCAC | 9678 |
| rs546354098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11102375 | CTCTTTGGACCAGAT[C/T]ATATGTTATTTGAAT | 9678 |
| rs546362961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167469 | CATACCTTTTATTCG[C/T]TCATTATTCCACTGT | 9678 |
| rs546364239 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052903 | AGGTACCTTGAAGGG[A/G]CCTCTACCAACTTGA | 9678 |
| rs546371984 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11087317 | CTGCCCCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 9678 |
| rs546377451 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:11118523 | TTGGTACTTTGCTTT[-/A]AAAAAAAAATTAGAG | 9678 |
| rs546401881 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121666 | ACAAGCCCTGCAGTA[C/G]TGTGATGGTCGATCT | 9678 |
| rs546405703 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10988119 | GAAACATTGTCTGCT[A/G]GCCATTTAGTTAGGG | 9678 |
| rs546411085 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11081845 | TGGGCGACAGAATGA[C/G]ACTCCGTCTCAAAAA | 9678 |
| rs546431631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997658 | TGGAGGATTTGCTTC[C/T]AAGCTAAGTCAAATA | 9678 |
| rs546450397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050247 | TAAATCTTTGAAAAT[A/G]CTTGCTATGAGAATT | 9678 |
| rs546454504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974441 | GCAGGATTGGTGGAC[C/T]CTCGCCCTCCATGGT | 9678 |
| rs546459599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087731 | ATTTGGCCCATGCTT[A/C]ATCTGTGTGTGTGGT | 9678 |
| rs546463431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11114626 | ATGAAGTATAGCATG[A/C]TAAGACTTTCTCTGT | 9678 |
| rs546464851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11008139 | CCAGCAGTTGCCCTC[A/G]GGTTTAGTTGCTATT | 9678 |
| rs546479902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960377 | TAGTTTGCTGAGAAT[A/G]ATGGTTCCAACTTCA | 9678 |
| rs546490121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070415 | TATTGATTTCATCTC[A/G]TTTGCCAGTTGCTTC | 9678 |
| rs546510498 | in-del | -/TACT | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063030 | TTGTATGTTTTTAAA[-/TACT]TACTTCCAAATGATT | 9678 |
| rs546512747 | in-del | -/AAAAC | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11049069 | AATATTTCAGTTTTT[-/AAAAC]AAAACAAAACAATGA | 9678 |
| rs546514599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025983 | TGGGCGTGGTGGCAC[A/G]TGCCTGTAACCCCAG | 9678 |
| rs546516222 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969442 | TCATTTTTTTCTTCA[C/T]TTATCTTATTTTACT | 9678 |
| rs546527381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997353 | GACCAAATGCAATTC[C/T]TGTGATGAGTTTTTA | 9678 |
| rs546534749 | in-del | -/T | 0.489837 | 0.0705577 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149810 | TAGTGTTTCAGTTGA[-/T]TTTTTTTTTATATTT | 9678 |
| rs546535509 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113880 | ACATTCGGAAGCTGT[A/G]TATTATTAACATCCA | 9678 |
| rs546551727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069867 | ATTTATTTATTTTTT[C/T]CTGGTAGAAGTATCA | 9678 |
| rs546594380 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11122445 | TATATATATATACGT[A/G]TATATATATATTGTG | 9678 |
| rs546629024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155400 | TGAGCACTGTGTAAT[A/G]CTAGAACCAGAAAAG | 9678 |
| rs546630811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033058 | AGTATATACAAAAGC[A/G]CATGTGCTTATTTCA | 9678 |
| rs546637730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064081 | TACTATATTTTAATA[C/T]TTCTTAGGACAAGAT | 9678 |
| rs546641949 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136221 | TCCGCAGTGCCAAAT[C/G]TATTGTATGCCGTGG | 9678 |
| rs546651871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980467 | TTATTGTTATTTTTA[C/T]CAGATGTGATTTTTC | 9678 |
| rs546652653 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993385 | ATTCTCTAGCTAATG[C/T]TCTGATCTTCATGTG | 9678 |
| rs546654291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960079 | CAACAAGCAGTAGTT[A/C]CAAGTGGATTTTAAA | 9678 |
| rs546654429 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070674 | CCATGTCATGCTGTG[A/T]TCCATTTTGCTTGTA | 9678 |
| rs546671055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162358 | GCCTTCCACAGTGCC[A/G]GGATTACAGGTGTGA | 9678 |
| rs546700529 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11123037 | CCTTCAGTGAACTTC[G/T]TCTCTCCTGCGTTTG | 9678 |
| rs546702663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994332 | TAGTCCTAGTTACTC[A/C]GGAGTCTGAGGCAGG | 9678 |
| rs546711931 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036082 | GTTTCAGTTTGTTCA[A/G]AGGATTTAGTCAGTT | 9678 |
| rs546737009 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168778 | GCTTATACTTTGAAG[G/T]TTACCATTTAATACT | 9678 |
| rs546741836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071505 | AGATATTTCCTTTTT[A/T]AAAAACAACTCTAGT | 9678 |
| rs546746818 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11100126 | TCTGTTTCATCTGTT[A/G]CTCCTGTATCAAGGT | 9678 |
| rs546749459 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028101 | AGATTAATTTAATAC[A/G]CCTAACTTACTGAGC | 9678 |
| rs546749486 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000605 | TGGTCTCCCAAAGTG[C/T]TGGGATTACAGGCGT | 9678 |
| rs546790749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142126 | AAGCAAATAGTTTTA[C/T]TGAGCTTTCTCCAAA | 9678 |
| rs546790961 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11134452 | CTGATAATTTTTGCT[C/G]TTTTATTTTTAGATT | 9678 |
| rs546804864 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013483 | TTATATTTTTTAAAT[C/T]AAAAATTTATTGTTT | 9678 |
| rs546816906 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964115 | GAATGTGATCCTGTC[A/G]TTATGATGCTAGCTG | 9678 |
| rs546821342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044298 | AAACCTGTGCATATA[C/T]CCCCTGATCTAAAAT | 9678 |
| rs546826853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11014191 | ATAGGTGTATAGTAC[C/T]CAGGGCTCAGATTAT | 9678 |
| rs546827052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957879 | ATTATCAAGGTCTAC[A/G]TGTAGGGGAAATGAG | 9678 |
| rs546839047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11127113 | TTAGGTATTAATAGT[C/T]TTTTTTTTAAATATC | 9678 |
| rs546843758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160299 | TTTCTTTATCCAGTC[C/T]ACCATTAATGGGCAC | 9678 |
| rs546844525 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11081639 | AGGTGGGCGGATCAT[A/G]AAGTCAGGAGATCGA | 9678 |
| rs546846657 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008658 | TGCCAAAAAGGTTGG[A/G]GACCAATGCTTTGGG | 9678 |
| rs546854132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135018 | AGACCCTTCTAAGGT[A/C]TCTAACTTCCTCTCA | 9678 |
| rs546887485 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965057 | TACCGACCTTCTGAA[G/T]CCTTTTTCTGTCAAC | 9678 |
| rs546896232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037211 | GAGCTCTTTGGCTCT[C/T]CCCTATAACTCCTAC | 9678 |
| rs546914861 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069429 | AAGGCACAGGTATTT[C/G]AACAGTGTTTGCTGG | 9678 |
| rs546922040 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075048 | GTTCAAGCAATTTTC[C/T]TGCCTCAGCCTCCTG | 9678 |
| rs546932853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030627 | CTGTGTATCTTACCT[A/G]TAAGCTAATTTGAGG | 9678 |
| rs546934522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063418 | ATGAAACAATAAAAA[C/T]AAAGAAAAAAAATAA | 9678 |
| rs546947963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067220 | GATGCTCAACATCAC[A/G]AATCATTCAGGAAGA | 9678 |
| rs546949909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060272 | TTAAAACAAGTTAAT[C/T]GAGTCTTTATGTCAT | 9678 |
| rs546994651 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128807 | CTCACTACTCTTTTG[C/G]AAAAAGCCTCATATA | 9678 |
| rs547004374 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10992311 | CACCCGACTCAGCTT[C/T]CCAAAGTGCTGGGAT | 9678 |
| rs547035526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11013406 | ACCTCAGGTGATCTG[C/T]CCACCTCGGCCTCCC | 9678 |
| rs547042507 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121615 | CTACTCTTGCACTTC[A/G]GGGTTGTTACTAAGT | 9678 |
| rs547059801 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131551 | TTTGAATGCCAGTCC[C/T]TTATCAGATATGTGG | 9678 |
| rs547059863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144728 | GGATTTTGAATGTTC[A/G]TAACACAAATGATAA | 9678 |
| rs547094244 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096642 | CCAATTATAAAGCAG[A/T]TGTGAAAAGAAAAAG | 9678 |
| rs547096512 | in-del | -/AGT | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11159016 | TTATCTGGCCTCAGA[-/AGT]AATAATATTAAAAGA | 9678 |
| rs547114155 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993766 | TAAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAA | 9678 |
| rs547123710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10996008 | AAGGCTCCTCAAGTG[C/T]GGCCAGAGTGGGCGC | 9678 |
| rs547124902 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10973856 | CTCTCAGGGCTGCGC[C/T]CAGCCTCGTGTTTTC | 9678 |
| rs547126170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141403 | TGGTCTTTCCCCTGT[A/G]TAGTATAGAATCTGG | 9678 |
| rs547127172 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11053167 | TTTTTTCCTTAAAGT[A/G]ACAGTTTTCTCAAAA | 9678 |
| rs547130875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090948 | ACACAAATAAAGACA[A/G]AGTGGGACCATATGA | 9678 |
| rs547141557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010937 | TGGGATTGCAGGCAT[A/G]AACTACACGCCTTGG | 9678 |
| rs547151269 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017374 | CAGTGTACAAGGGTT[C/G]CCTTTTCTCCACATT | 9678 |
| rs547170137 | in-del | -/AT | 0.0325453 | 0.123343 | intron-variant | PHF14 | GRCh38.p7 | 7:11122399 | CATACATACACACAC[-/AT]ATATATATACACGTA | 9678 |
| rs547181761 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164003 | AAGAAACATTATTAA[A/C]GTATAGAGATAATTC | 9678 |
| rs547224620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002978 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCAGGC | 9678 |
| rs547236647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11120124 | AGTAGGAAGATAGAG[C/T]AATTTAAATTATATA | 9678 |
| rs547237434 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058499 | TTTTATTTTTTTCTT[C/T]GGAAATATTAGTAAT | 9678 |
| rs547286808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027629 | ATTTTCTCTTTTTAT[A/G]CAGAAAGAATGTACA | 9678 |
| rs547288164 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11153705 | TTGTCATTGGTAAGG[A/C]TTCTTTAACAGAAAA | 9678 |
| rs547289149 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015264 | TGCCTCAATTGGTGG[A/G]CTGATCCTTGAGAAA | 9678 |
| rs547312390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11066820 | TCTTGATTACTCAGG[C/T]TGTGGAGTAAGCTGT | 9678 |
| rs547343717 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035206 | TATTAGGTATTATAA[A/G]TAATGTAGAGACTGC | 9678 |
| rs547357942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024738 | AAAAAGATTCCTTTC[A/G]AAAGATTACTGCTTA | 9678 |
| rs547389447 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11046282 | ATTAGAGTAGTTCAA[A/T]TAGTTAATCATCTCT | 9678 |
| rs547392345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016810 | ACTGTAGTCACCCTG[A/T]TGTGCTATTAAACAG | 9678 |
| rs547392390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022630 | CAATTATAGTTGTTA[C/G]CTCTCAGTTTTGGCT | 9678 |
| rs547421372 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103785 | GTTACAGTGAGGAAC[A/G]CTATGATTGGATGAG | 9678 |
| rs547424348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097323 | CATATTGCCACAATG[A/G]AGAATTATTATGACA | 9678 |
| rs547451901 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975004 | TTAGGCTTATTTTTA[C/G]ACTTTTTAAATCGGT | 9678 |
| rs547454445 | snp | A/G | | | | | GRCh38.p7 | 7:10971091 | CCTAAAGTCAGAAAC[A/G]AGACAAAGAAGTCTT | 9678 |
| rs547454928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053843 | AGCTTTAAAATTTGC[C/T]AATATAATCCCATTC | 9678 |
| rs547463474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004764 | AATGTGGCTGGGTGC[A/G]GTGGCTCATGCCTGT | 9678 |
| rs547471281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011491 | CATCAGTTTATTGCG[G/T]GTTACTTTGGATGCC | 9678 |
| rs547476452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039765 | ATGTGAAAAGAATGT[G/T]TGTGGCTTGTATCCT | 9678 |
| rs547477823 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11017154 | GGATTCGTCTGTTGG[G/T]GGAAACTTAGGTTGC | 9678 |
| rs547504998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130156 | CATATGTGGTCCACA[A/G]CATAGTAGCAGGAAA | 9678 |
| rs547512149 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156926 | TTTGTTTTAAAGATT[A/C]ACAATACTCACCTTT | 9678 |
| rs547515467 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965506 | TGGGAGATGTCTCCC[A/T]GTCAGGCTACTGGGG | 9678 |
| rs547522010 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138253 | TCACCGCGTTAGCCA[G/T]GATGGTCTCGATCTC | 9678 |
| rs547526693 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123774 | GAATCGCTTGAACCC[A/G]GGAAGCGGAGGCTGG | 9678 |
| rs547558603 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053809 | CTGGTCTGCTTTTTT[A/T]ATCCTAGAATTATAA | 9678 |
| rs547562126 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020698 | CTTTCTTTTTTTTTC[A/G/T]TTAAAATTCTAGATT | 9678 |
| rs547574766 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123090 | TTTGGTTTTTTTGAT[A/T]GGCTTCTCTAGGTTG | 9678 |
| rs547575440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116421 | CTGGATGTAGGTATA[C/T]GTATTCATACACAGC | 9678 |
| rs547613042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994816 | CGGTGAGTGTTACAG[C/T]TCATAAAGGCAGCGC | 9678 |
| rs547625854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028206 | ACAAAACTTTATTTT[A/G]TAATAAAATGTTAAC | 9678 |
| rs547632534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11117136 | ATATGTATTCACAGA[C/T]GCCACTGAGGATTTA | 9678 |
| rs547678873 | in-del | -/AG | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11097471 | ACCATTAGGCGTAGT[-/AG]TAGGCCTTTATCATT | 9678 |
| rs547680743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101812 | CTTCACAGATCTAAA[C/T]GTTTGAAGGAAATGA | 9678 |
| rs547687564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016120 | TTTGGATACTGTGGA[C/T]GTTACATAAGTAGAC | 9678 |
| rs547691682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11136178 | GTCAATGTAAGGCTG[C/T]AAGGTCAATGTGGTC | 9678 |
| rs547696630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989911 | ATTTGGGATTACCGG[C/T]GTGAGCCACTGTGCC | 9678 |
| rs547721166 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058695 | ATCACAATGTTACAG[A/T]TTAGTTTAAGTATTT | 9678 |
| rs547729088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094932 | GTTTATCTTTTTTTT[C/T]CTTGCTAGGATAGAA | 9678 |
| rs547731000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149258 | TTTAACATGCTTGAT[G/T]TGCCATCATTTAATC | 9678 |
| rs547740655 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11072620 | AAAAAATGGTAAAGG[-/C]TATATATATGCAAAT | 9678 |
| rs547742374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072546 | CAATAGTACCTACTC[C/T]ATAGATTGTCTGGAT | 9678 |
| rs547742708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052448 | AGCTTTGTTTAAAAT[A/G]TTCCTATAAATATCT | 9678 |
| rs547751960 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11021984 | TAATAGAGATTTGCT[G/T]CTGTGACCCTCTTTC | 9678 |
| rs547759097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010190 | GCATAGCACATGGAG[A/G]AAATAGATTGATGAT | 9678 |
| rs547759521 | snp | A/G | 3.48347e-05 | 0.00417326 | intron-variant | PHF14 | GRCh38.p7 | 7:11051795 | GGTAGTTTATTTTTT[A/G]TTTATCATAAGCATC | 9678 |
| rs547760267 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11111265 | AAGTTGAAATATACA[A/G]TAGTTTGTCTTTTTG | 9678 |
| rs547768919 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125842 | TATATTATAGTGTTA[C/T]ACCTTCATTGAAATT | 9678 |
| rs547769025 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156781 | CCTGGTCATAGAGCG[A/T]GACTGTCTCAGAAAA | 9678 |
| rs547776569 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10989388 | AAAAATATATATTGT[A/G]TATTGTATGAAACTA | 9678 |
| rs547786220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989868 | ACTCCTGGCCTCAAG[G/T]GATCCTCCTGCTTCA | 9678 |
| rs547786532 | snp | C/T | 5.81514e-05 | 0.00539187 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983043 | GAAGATCATAGTAGC[C/T]CTGCCAGTGAAGGGG | 9678 |
| rs547792100 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089691 | TAGAATGGTTGATTA[G/T]TGCCTCATGAATATA | 9678 |
| rs547795221 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986110 | AGTAGCTGAGACTAC[A/G]GGTGTACGACAACGA | 9678 |
| rs547804585 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11159777 | ACTTAATTTTTGAAA[-/G]TACAGAAAATTGAGG | 9678 |
| rs547813358 | snp | C/T | 0.00159617 | 0.0282053 | | | GRCh38.p7 | 7:10970730 | TCAAAATGTAATTTC[C/T]TTTATAAATATGGGT | 9678 |
| rs547840258 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096098 | AATAAAGAGGTCTTC[C/G]TTAATCACATGGTTT | 9678 |
| rs547868346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130942 | AATTTGGCTTCTTTC[C/T]GTAAGCAATACGCAT | 9678 |
| rs547878689 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11083485 | TTTTTTTTTTTTTTT[G/T]GATACAGAGCCCTTG | 9678 |
| rs547898795 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170243 | CAGCCTCTTTACTCT[C/T]CCCGGTTCTAATTTC | 9678 |
| rs547920575 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993143 | TTAGAATACTGGTGA[G/T]ATTTTGATCACTTGG | 9678 |
| rs547920806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059583 | GAGTTCGAGACCAGC[C/G]TGGCCAACATGGCAA | 9678 |
| rs547928227 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11096551 | CATTTACGGGTATTT[C/G]ATATCGTATGTTGCT | 9678 |
| rs547934681 | snp | C/G/T | 5.43198e-05 | 0.00521123 | intron-variant | PHF14 | GRCh38.p7 | 7:11042825 | TATTGGTGAGTAAAA[C/G/T]AGAGGAGATTTAGAT | 9678 |
| rs547940142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016154 | TCCTGTGATGGTGCA[A/G]TCTGGCAAAAATTCT | 9678 |
| rs547950999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046253 | GTAGGATACAAATGG[C/T]AAGGGCTTGATTTAT | 9678 |
| rs547957993 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125159 | AGGGAGGTAAAGGAA[A/G]GGGATCTAAAGGTGA | 9678 |
| rs547980854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076402 | TCTATTCTTATAAGT[A/G]TGCTGTTTAGTTGTA | 9678 |
| rs547991889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122039 | CGACAGGCCTCTGGT[A/G]TGTGTTGCTTCTCTC | 9678 |
| rs548009803 | in-del | -/TGAT | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11039105 | TTCATTTGCTCTAAC[-/TGAT]TGACCTGTCATTTGT | 9678 |
| rs548013772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071749 | ATAGCCCTGAGACAT[G/T]TTTCTGATTATGTAT | 9678 |
| rs548015325 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966834 | TAAAACCACTACCAC[C/T]AAACATAAGGTAACT | 9678 |
| rs548017877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076865 | GAGTCACTGTGCCTA[C/G]CTTTCAAATATGGTT | 9678 |
| rs548017914 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960734 | CCTATTTCTCCACAT[C/G]CTCTCCAGCATCTGT | 9678 |
| rs548018015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965811 | ATGGTGGACTCCCTT[C/T]CCCCCACCATGCTCC | 9678 |
| rs548050989 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11039071 | GTTGTTTCAACAGCT[A/G]TCTTGTGTGCAAAAT | 9678 |
| rs548071862 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039497 | ATGCCTTTTTTAGTA[C/G]TGTGTATATAATTGA | 9678 |
| rs548077256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961086 | TCTTTAGTTTAATTA[G/T]ATCCCATTTGTCAAT | 9678 |
| rs548092367 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11033279 | ATATACAATTCCAGG[C/T]GGATTGGATACTGAG | 9678 |
| rs548098798 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10994434 | ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAGA | 9678 |
| rs548099433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072163 | TGCTTCTGGGGAGGC[C/T]TCAGGAAACTTCTAA | 9678 |
| rs548129241 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011489 | GTCATCAGTTTATTG[C/T]GTGTTACTTTGGATG | 9678 |
| rs548137121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11163218 | TTTACTAAGAACATC[C/T]CAAGTGACTTTAATT | 9678 |
| rs548145949 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156994 | TGAACTCTGTAGCAT[A/G]GTAATCATAAAAATA | 9678 |
| rs548150776 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11066858 | TTCTGGATCCTTTGC[A/G]TTTTCATGTAAATAT | 9678 |
| rs548151440 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11088821 | AAATCAGTATTAAAA[A/C]ATTATGTATCTCCTA | 9678 |
| rs548171774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110512 | AATACAGATTTTTCT[C/T]CATTGTCAGCAGGAT | 9678 |
| rs548193336 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11150821 | ATTCTAAGAGTTCAG[A/G]CTGGTATCAAAGTCT | 9678 |
| rs548214648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066749 | ATGTGGGCTTATTTC[C/T]AGACTTTCTATTATA | 9678 |
| rs548221373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045171 | TAACAGGGCTTTCCC[C/T]CAGAGGGTCAAGTGT | 9678 |
| rs548228369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109789 | TGATATTGTCATAGT[A/G]AATAAAGTACTGTTG | 9678 |
| rs548228468 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166696 | GTGGAATGCCTTTTT[A/C]ACCCCTTCATAATGC | 9678 |
| rs548235176 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103664 | GACATCTTTTCGGGT[A/G]TAGTGACAATGGAAA | 9678 |
| rs548238730 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11043220 | CTTCTGGTATTTGGT[A/G]TTTGTGCTAGTCATT | 9678 |
| rs548256101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151231 | TGAAGTCACTGACTT[A/C]TGTGTATTTTCTCAT | 9678 |
| rs548282449 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014905 | TTTTTTTTTTTTTAC[A/T]GGAGACTACCATCTA | 9678 |
| rs548289493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052601 | ATACCAGCAATGGAT[A/G]ATGTTTCTGTTGCTT | 9678 |
| rs548299455 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965441 | TCTTTCCTCTAGAAG[A/C]TTTGTCCCAGAGGGG | 9678 |
| rs548301354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168712 | TGAAAGAACATGTAT[C/G]ATGAGATGGGTTACA | 9678 |
| rs548303052 | in-del | -/GCTGGGATTACAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090036 | TTAGCCTCCCAAAGT[-/GCTGGGATTACAG]GCGTGAGCCACCTCA | 9678 |
| rs548316978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130092 | TGACAGAGCAGCTCT[A/G]CTCATTATAGTCACT | 9678 |
| rs548330938 | in-del | -/ACTACACCTGACT | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11000492 | TTACAGGCACACACC[-/ACTACACCTGACT]AATTTTTTATTTTTA | 9678 |
| rs548350355 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072587 | TACCGTACAAGTAAA[A/G]GGCTTGGCACAGTGG | 9678 |
| rs548356105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162587 | ACTGATCTTTGTTGC[C/T]TTTAGTGTAAATATG | 9678 |
| rs548358760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122528 | CTATCTTTATGCCCT[A/G]CAATTATTTCCCTTT | 9678 |
| rs548366215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083397 | CTTTCTCCCCGCACT[C/T]CCACCCCGTATCATC | 9678 |
| rs548371380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039714 | AAGTGATACATACTG[A/G]TTTGTACTGTGCTAT | 9678 |
| rs548381665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999504 | TCCATGTACATTTCA[A/G]AATGACCCTCGCTCT | 9678 |
| rs548384080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129586 | TACATAAAATTTAAG[A/G]GACAGTAAACCCTTT | 9678 |
| rs548398190 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11084662 | ATTTCTATCCCAAAG[-/T]TAAGTGTGCTAGGCC | 9678 |
| rs548407240 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960583 | ATAGAATGATTTATA[A/G]TCCTTTGGGTATATA | 9678 |
| rs548420188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115701 | CCAGTAAGGTCATTT[A/G]TGGCAAAAGGATTCG | 9678 |
| rs548422001 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123027 | TTCTTTCTCGCCTTC[A/G]GTGAACTTCTTCTCT | 9678 |
| rs548423606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149177 | TGTGCTCATGTAGAT[A/G]TTTTAGGTAAGGCCA | 9678 |
| rs548459575 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11137455 | AAGACATTTATTTAA[-/T]TTTTTTTCATTTACT | 9678 |
| rs548470311 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155154 | CCTCATATTTTATTT[A/T]ATTTAATAATTTTAG | 9678 |
| rs548482879 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11116377 | GGATATTGCTTTTCC[C/T]GGTTCTTCTCAGTAG | 9678 |
| rs548502568 | snp | A/T | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108244 | AGATAGAAACAACAG[A/T]TTTTTTTCACATTGA | 9678 |
| rs548535159 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091859 | AGTATTCAATTCTAA[G/T]TTTCCGACCTTTGCT | 9678 |
| rs548545564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064872 | TACTTGCTTCATTAG[C/G]TACCTTATGGATAAT | 9678 |
| rs548546703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117032 | CAACAACTTGTATCT[C/G]CTGAAACACTTAAAA | 9678 |
| rs548549152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088081 | CATTGATTCCAGGAC[C/T]GCTCTCGGATATCAA | 9678 |
| rs548555427 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979986 | AATTTTTTAAAAAAT[C/T]GCTTTCTATTCAGGC | 9678 |
| rs548562908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020104 | TCTTTTTTTTTTTCC[A/G]ATCAGACGGGGCCTG | 9678 |
| rs548573738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048825 | CAACAATCATGTGGC[A/G]GTTGTCTTGAAATAG | 9678 |
| rs548574407 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121186 | CCTTTTTATTATATA[C/T]ATGTGGGATCTTTTA | 9678 |
| rs548586989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981851 | TATAAGTTGACTATC[A/G]TAAATATCTATGCTT | 9678 |
| rs548616803 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006491 | CATCAGGCCGAATTA[A/G]GGTGTTGACACCTTG | 9678 |
| rs548640069 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979813 | GTATTGCTGATCCCT[A/G]TAGAAAGATAAAATT | 9678 |
| rs548649549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015101 | AAGATTAACAGCAAA[A/G]CAACCTATATAAATT | 9678 |
| rs548661244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042888 | ATAAGATGAAATACT[A/G]TATTTGTTCATAATA | 9678 |
| rs548673710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089445 | CCTGTAATCCCAGCA[A/C]CTAGGGAGGCAGAGG | 9678 |
| rs548676243 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082374 | CAAACAAAAACATCA[A/G]TTTAATAAAACCATT | 9678 |
| rs548695586 | in-del | -/TTCTC | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11154358 | TAAATTACTTTTAAT[-/TTCTC]TTCCCATTCCAATAG | 9678 |
| rs548698166 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11043408 | GATGTTCAGATTTTA[A/G]TAGAATGATTTCTCA | 9678 |
| rs548709818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11004606 | TGAAGAATCTTAGTT[C/T]TTATAATGTCATATT | 9678 |
| rs548753344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967821 | TTCTATCATAACAAA[C/G]AATTGCTAACAGATC | 9678 |
| rs548759604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070559 | TTCTTCTTCCTTCTA[A/T]GCCTACATCAGTATT | 9678 |
| rs548766793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980650 | TTCACACAAACTTAC[C/T]TGATGGCAAAGCCTA | 9678 |
| rs548788667 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148696 | ACAGAACCTGACACA[C/T]AATAGACACACATTT | 9678 |
| rs548789391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019661 | GCTAAAGGTTTGTCA[A/G]TGTTGTTTACCTTTT | 9678 |
| rs548805092 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10988076 | CTAATTTTTTTTAAG[G/T]AGGATGTGTTACTTA | 9678 |
| rs548847855 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050506 | TTGTTGTTTAGATTT[A/C]TGCTGTCTAAATGTT | 9678 |
| rs548876215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146951 | TCCTGGGCTCAAGCA[A/C]CTCTCCCTTCTCAGC | 9678 |
| rs548927417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101678 | TTATTTGTCTGTGTG[C/T]CACTTTTCACTTTCT | 9678 |
| rs548938751 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973127 | TATACCACTTTGTAA[C/G]TTCACCCTAGCCTCT | 9678 |
| rs548945396 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11153154 | TTATAAAACCAAAGC[A/G]AGGAGGCTGATTAGG | 9678 |
| rs548949384 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976675 | AATATTTTATGATAT[A/C/T]GAGCTAAGTAGAGAT | 9678 |
| rs548981281 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118179 | TATTAGAATTAAATA[C/G]AACAAATCTGCGGTG | 9678 |
| rs548982342 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092042 | AGCCTCAAGATGAGA[G/T]TTTAATACTCTGCCA | 9678 |
| rs549003807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967133 | CAAGGTACCATTCTA[C/T]CCCAATAAATATCCT | 9678 |
| rs549034674 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11085892 | AAAACATAATAGTTT[A/T]AAAAAAAAACTGTGG | 9678 |
| rs549055173 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11018465 | TAGAAATCTTTTACT[A/T]CTTTAAGTTAATTCC | 9678 |
| rs549059495 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996075 | TGAGGGCTGCCAGCA[C/T]GCTGTCACCTATCAT | 9678 |
| rs549072484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007106 | CGCTTGAACCCAGGA[A/G]GGCTTGAACCCAGGA | 9678 |
| rs549076624 | in-del | -/ACAA | 0.0182019 | 0.0936463 | intron-variant | PHF14 | GRCh38.p7 | 7:11151071 | AAAATAGAATCTTAG[-/ACAA]AAAAACCTGTCATAA | 9678 |
| rs549099755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11029342 | TTCAAGTATTCTGAG[C/T]TTAAAACTATTTTCA | 9678 |
| rs549124486 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125299 | CAGCCAGCCACACTC[A/T]ATCCCTTTGCAAAGA | 9678 |
| rs549139223 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11152547 | GATTCCCATGCTTCT[A/G]TATAGTAAGGAATTC | 9678 |
| rs549150553 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11097181 | ATGGGGTTTCACCAT[A/G]TTGGTCCGGCTGGTC | 9678 |
| rs549156545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067937 | ATTCATCTTCATGAC[A/G]TAAACACCTCCCATT | 9678 |
| rs549159610 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11152647 | AACTTATAAGGATAT[C/T]GTAATAAGAAAAACA | 9678 |
| rs549184927 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134642 | TGACAGCTAGTTAAT[C/G]ACAGAGCTATGACCA | 9678 |
| rs549192924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984873 | ATAAAGGGACCTTTT[A/C]TGTTTAGGTTAATAG | 9678 |
| rs549205349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985313 | TATATTTGAAGTTTG[A/T]TTTTCCCTGCTTTTA | 9678 |
| rs549206259 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11035442 | AAAACGTTGTTGGTA[A/G]TTTGAAGTTGACATA | 9678 |
| rs549238482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005701 | TTTTTGTTTCAAGTT[G/T]TTCACTTATATATAG | 9678 |
| rs549241697 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974387 | CTAGAAGTCAGGGCC[A/G]GTGGGAGCAGGGCAG | 9678 |
| rs549255531 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141692 | TTGAAATTATTAATA[A/G]TTTCGTGTTGCATCA | 9678 |
| rs549262871 | snp | C/T | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11123855 | CCCAGGAGGCGGAAG[C/T]TGCAGTGAGCCGAGA | 9678 |
| rs549283914 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11102423 | TATGTTTCATAAGAC[A/G]TAGTGCAGAGCTGCT | 9678 |
| rs549309018 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012266 | AAATTTTAGGCAGAT[C/G]TGGAAGCCTAAATAG | 9678 |
| rs549320445 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11061760 | ATACTGTGGATTTTT[G/T]TTTTTTGTTTTTTTT | 9678 |
| rs549330772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146134 | ATATTTCACATATAT[G/T]TATATACATTACAAA | 9678 |
| rs549342523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091532 | CGGCCAAGGTAGGCA[A/G]ATCAGTTGAGCCCAG | 9678 |
| rs549345627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131123 | AAGTTTTGGCAGTTA[C/T]GAATAACGCTACTAT | 9678 |
| rs549356561 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019816 | TCTTTAAGATATGTC[A/G]TTGGATTGTTTATTT | 9678 |
| rs549358163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078424 | GAAATTTTGGTTAAG[C/T]CTCTGCCAGGGAGAG | 9678 |
| rs549363007 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11054117 | CATTTTTTAAGACAC[-/T]TTTTTTTTGGTAGCA | 9678 |
| rs549366405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035111 | GATCGAAAATGTTTG[A/G]AAAAAAAAAAGCGTA | 9678 |
| rs549384427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011429 | TATGGTGAAGTCTTT[A/T]AGGAGACGATCATGT | 9678 |
| rs549387707 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11164974 | CAATTGCCCAGGCTG[C/T]AGTGCAGTGGCGCGA | 9678 |
| rs549407607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054865 | ATTTTTGTCAGTTTT[C/T]CATTTTTCCTGCCAT | 9678 |
| rs549418817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077692 | ATACCTCGTACATAG[G/T]CTCTTGTTTGCCTGT | 9678 |
| rs549425970 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966750 | TATCTAGCCCAATTT[A/T]ATGCTTTGTCTACTC | 9678 |
| rs549444242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956423 | ACTTGATTTTAAAAC[C/T]GTGCACGGACTTTCA | 9678 |
| rs549449711 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11165253 | AAGACTACTGTTTAA[C/T]TATATTGTAGAGGGT | 9678 |
| rs549461449 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095002 | CCATTCTAGCCAGAG[G/T]CAGTTCAAAGAAACT | 9678 |
| rs549470615 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158639 | CTGGTGAAGAAACTG[A/T]TTTCATATTTTTGTC | 9678 |
| rs549475481 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105730 | GCCTCTTTCCCATAG[A/T]GCTCACTTTAAGGCT | 9678 |
| rs549475912 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11138333 | GGCGTGAGCCACTGC[A/G]CCTGGCCGGAAAAAT | 9678 |
| rs549494772 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051212 | GCCTAGTTAATTTTC[-/T]TTTTTTTTTTTGTGA | 9678 |
| rs549497216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111877 | ATTTTAAAATATAAT[A/G]TATTGTAATATCTTA | 9678 |
| rs549498404 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091027 | TGCAAGCTAATGATG[A/T]TAAGGGGTCCAATGG | 9678 |
| rs549518924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073895 | AGCTAGCTGTACCTG[C/G]TGATGTGAGCTGTAC | 9678 |
| rs549518987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067522 | CCTGTTTTCATAGCA[A/G]CATTATTCACAATAG | 9678 |
| rs549531629 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048329 | TGAAATCTCAGCACT[C/T]TGGGGAGGGCGGGGC | 9678 |
| rs549539955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010815 | CCACCATGCTTGGCT[A/G]AACTCTTTTTTGTAT | 9678 |
| rs549550574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11157875 | GCACATTATTTTGGC[A/G]GGTAACTTTATAGTA | 9678 |
| rs549561516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978320 | ATAATTAAATAAAAT[A/T]GTTGATACAAAGGAT | 9678 |
| rs549564487 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097717 | CCCTTCACATTCTCA[A/G]AGTTCATTGTTGATA | 9678 |
| rs549574098 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11145169 | AGGGGTTCAGGTGGC[A/C]GAGGAACTCACCTGG | 9678 |
| rs549650213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131876 | TTTGGAGGTCCATAT[C/G]GTCCAGCACTATTTG | 9678 |
| rs549658723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084665 | TTCTATCCCAAAGTA[A/G]GTGTGCTAGGCCAAA | 9678 |
| rs549677918 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956325 | CTGTGTGGGATCTTT[C/T]TGCCCTCCCTAAGTT | 9678 |
| rs549679795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061179 | TAAACGTTTGTATGC[A/G]TTCTTTCAAATGGTA | 9678 |
| rs549711465 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966548 | CACTGGGGACCTACC[C/G]TTTCCCGCGTAGGAA | 9678 |
| rs549720291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131035 | TCTATTGTATGGATA[C/T]GCTCCTATTAAAGGT | 9678 |
| rs549729703 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11022073 | TTTGTTGTAAGCAAG[A/C]AGAAAGAGTGCCTAA | 9678 |
| rs549775143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138710 | AAGAGAAAAGAGATC[A/G]TGAGAGATAAGTGCT | 9678 |
| rs549777962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123798 | AGGCTGGAATGAGCA[A/G]AGATCGTGCCACTAC | 9678 |
| rs549782737 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019329 | AGTTCTTCTTTAAGT[A/G]TTTGGTAAAATTCAG | 9678 |
| rs549852522 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973367 | CGCTTCCGTACAGAG[A/C]GTGCTTTAATTTTCA | 9678 |
| rs549858899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085349 | TATTAGTTTTCAGAG[G/T]CTCTATTTTGTTAAT | 9678 |
| rs549864434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10999600 | AGTAGATTCATTGTT[C/T]AGATAAACATAGATT | 9678 |
| rs549880776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039814 | TGAGAATTAGTAGTC[A/G]CCTCTGGGAGGATCA | 9678 |
| rs549886690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157380 | CAATAAAGTCTGTCA[A/C]TGGGTTACCAAAAAA | 9678 |
| rs549896836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035039 | GTGACTTTTTAAAAA[A/C]ATACAGCCGGCCCTC | 9678 |
| rs549898849 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028237 | TATCTCATGTAATTT[A/T]TTGAATACCCTACTG | 9678 |
| rs549908763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006653 | CTTGATGATGGTATA[A/G]TAGTCAAGCTTGTTT | 9678 |
| rs549940404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961257 | AGTTAATTTTTGTGT[A/C]AGTGTAAGGACAGGG | 9678 |
| rs549940748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073192 | CGTTGATTCAAAAGT[C/T]CAAAATCCAGTGTCT | 9678 |
| rs549948883 | snp | A/G | 0.000162588 | 0.00901486 | intron-variant | PHF14 | GRCh38.p7 | 7:11111329 | TAGATACACCTACCT[A/G]TAAATCTGTTTACCC | 9678 |
| rs549963166 | in-del | -/AT | 0.112157 | 0.208565 | intron-variant | PHF14 | GRCh38.p7 | 7:11122400 | TACATACACACACAT[-/AT]ATATATATACACGTA | 9678 |
| rs549966798 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11164142 | AGTGCCTGTCTGCAC[C/T]GTCTCCCTTCATTTT | 9678 |
| rs549978123 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159545 | AGAAAATATTCAAGC[A/C]AATCATAGTAAAGAT | 9678 |
| rs549983058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11117238 | GTTTTGTGAGAAGCC[A/G]TGGAGTATACATGAC | 9678 |
| rs549995357 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043652 | GCTGAAATTTTTTCA[C/T]TATTTTCACATGATT | 9678 |
| rs549997740 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10995383 | TGATTGGTGTATTTA[C/T]AAACCTTGAGCTAGA | 9678 |
| rs550007366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022739 | TGTGCCTGAGATTGC[A/G]AGATTTTAACATTTG | 9678 |
| rs550014361 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11157488 | ATGATGCTTCTATGG[A/G]GAAATTTCTTAAGTA | 9678 |
| rs550019357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984666 | GGCAGTGTCGATTAG[A/G]TTTATGCTAAAATGT | 9678 |
| rs550046706 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | PHF14 | GRCh38.p7 | 7:11110919 | TTTTAAAATTTTTTA[A/C]ATAATCAAAATGTAT | 9678 |
| rs550055594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130368 | ATCCTTGGAGAGAGA[A/G]AGAACGTATATACAA | 9678 |
| rs550062562 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11017712 | TGTGGGTTGTCTCTT[C/G]AGTTTGATGATGTAT | 9678 |
| rs550073195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144048 | AACCCCAAATAGTCC[A/G]ATTTTAAAAAGGATC | 9678 |
| rs550099140 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047283 | CCGTGTTAGCCAGAA[C/T]GGTCTCGATCTCCTG | 9678 |
| rs550111122 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11127898 | AAATCATGATTTTTT[C/T]TTTCATAATTATCAC | 9678 |
| rs550120569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095960 | GTCAGCTTTGGGGCT[A/C]TACTCTGAATTCATA | 9678 |
| rs550137128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136887 | ATTACTTAAAAAAAA[C/T]TATGAACTAGCACAT | 9678 |
| rs550140252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005612 | AATTCTGTAATTCTT[C/T]TCATGTCAGTGTATG | 9678 |
| rs550148583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097418 | CATAGGTATTGATAT[C/G]AGAGTCTCCTCAGTT | 9678 |
| rs550155774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003366 | TGCTTTTCCTTTTAC[A/C]CAGATTCCTCTTGTT | 9678 |
| rs550168608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000191 | GACTTAAAAAATTAC[A/G]CTACTACTTTCATCC | 9678 |
| rs550177222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083962 | GCAATAGGTAGATTC[A/G]AGCAAAGTTTATGGA | 9678 |
| rs550232570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966131 | TCCAGTGGGATGAAC[C/G]AGGTACCTCAGTTGG | 9678 |
| rs550241909 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11121815 | CATGCTCTTCAGAAT[G/T]GTATGCAATTTAAAA | 9678 |
| rs550244199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961705 | TTCCTATCCATGAGC[A/G]TGGAATGTTCTTCCA | 9678 |
| rs550277930 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044153 | AGTCATGGACATAAA[G/T]ATGGGGCCTACTAGA | 9678 |
| rs550278690 | in-del | -/CCCT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142946 | ACACAGAAATTGTAG[-/CCCT]ATAATTTACAACTGC | 9678 |
| rs550290191 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118120 | TTTTTACTAATACAG[A/G/T]TATGTAAAAAGTCTG | 9678 |
| rs550291188 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074824 | AACCACTTAACAATA[C/T]TCTAAGAAGTTCCAA | 9678 |
| rs550292927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032026 | TTGGGAGGCCAAGCC[A/G]AGGAGGATCTCTTGA | 9678 |
| rs550323818 | snp | A/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072778 | TGTTCAAGCAGCATG[A/G/T]CACTGACATCTGCTT | 9678 |
| rs550324395 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997292 | TTGGCCATCTTGACC[C/T]GAGAGAGTTCAAAGT | 9678 |
| rs550328010 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097023 | TTGCTCTTGTTGCCC[C/T]GGCTGGAGTGCAATG | 9678 |
| rs550329954 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995095 | CACAGAGCACTGATT[G/T]GTGCATTTACAAACC | 9678 |
| rs550346006 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11092807 | GGAGATACAGTTGTC[C/T]TGGCCAAAATGGTAT | 9678 |
| rs550351535 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125506 | TTGTGTTAATTCTTT[C/T]GCTGACAATTCTTTT | 9678 |
| rs550385053 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976129 | TTCAGAATTTAGTCT[C/G]TTTATCTGCTTGGAT | 9678 |
| rs550393939 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959414 | GGAAACCTCTATGGG[C/T]AGCGGCGATGCAACT | 9678 |
| rs550394311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976636 | GGTAAAACAATCTGA[A/T]ACAAACATAAAGTAC | 9678 |
| rs550400663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096343 | TTGAATGCTCATACA[C/G]ACCTGACAATTTCAC | 9678 |
| rs550416153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11086736 | TGTTATTTTTATATA[C/T]AAAACATTGAAATTT | 9678 |
| rs550418341 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11161692 | AATATTATATTTTAT[A/T]TAAATAAAAATATTA | 9678 |
| rs550431829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007729 | AAGAAAAAAACATTT[C/T]TAATTGTCCTCATAT | 9678 |
| rs550438258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052541 | CTATCTGCATCTTCA[A/G]TTTTGCTAGATAACT | 9678 |
| rs550443340 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137642 | CTCTTGTTGCCCAGG[C/G]TAGAGTGCAATGGCA | 9678 |
| rs550445316 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11114782 | ACACAGAGACACATA[C/T]ACTCATACACAAAAC | 9678 |
| rs550454747 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970853 | GGTTGATTAAACAAA[G/T]AAAAATCAAGCAATA | 9678 |
| rs550467246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11008081 | AATTCAGGAGAATGT[C/G]AGGTATATGTTAGTA | 9678 |
| rs550487916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980025 | AAATCAAAAACAGAA[C/T]CAAGGAGTCTCAATT | 9678 |
| rs550488854 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11090239 | TATTCTCTATGAATC[A/G]TAGCAAGAGGAGGAG | 9678 |
| rs550496594 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967031 | TTACAGTGTCTTCAA[A/C]AAGGCAGGTAGCTTC | 9678 |
| rs550496661 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990975 | ATCATCAAAGTATGG[A/T]TGCTATTTTTCAGGT | 9678 |
| rs550497005 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152629 | TATGATAGGAATAAG[A/G]CTAACTTATAAGGAT | 9678 |
| rs550499929 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141165 | ATCAATCCAGTTACA[C/T]CTTAAGTTTTACTTG | 9678 |
| rs550505516 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10996817 | GGTTGTGAGAACCAG[A/G]GCCCACAAGATAGGT | 9678 |
| rs550515233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965875 | GCAACGAGCAAGGCT[A/C]TGTGTGTGTTGGCCT | 9678 |
| rs550521942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037301 | ATTTTGATCTCTTTA[C/T]ATGTATTATTTAATT | 9678 |
| rs550559778 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104025 | TAAGCAAAATGACAG[A/G]TTGCCATTTTCTAAG | 9678 |
| rs550573531 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166171 | GGTAAGCCTGTCTAC[G/T]TTCCAGTAGCCTCAA | 9678 |
| rs550586414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167183 | CTAGAGAAAACTAGA[C/T]AGCCAAGCATGTTAA | 9678 |
| rs550605087 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11146446 | ATAGTTATCTAGACT[C/G]AGGACCTCCATTTCT | 9678 |
| rs550626344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098723 | CTGTCTTGGACATTT[A/G]CTGAACAATTTAGGG | 9678 |
| rs550631603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114150 | CAACTTCTTTCTCTG[C/T]GGTAGTCATGTTGTT | 9678 |
| rs550632018 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964672 | AATTCTGAAGAGTGT[A/T]TTCTAACTTGGTTCC | 9678 |
| rs550648389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167566 | GGAATGTATAAGATA[C/T]AGAAGATAAAACCTT | 9678 |
| rs550678017 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086401 | AACCTGTTGCTTTTA[G/T]GCCATCTTGCTTTTA | 9678 |
| rs550681982 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997705 | AGTTCTTTGATGGCT[G/T]TTGGCCAGAGACCTC | 9678 |
| rs550687440 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063313 | TAGTTCCAAGTTCAG[A/G]AGATACACCTGAATA | 9678 |
| rs550688693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11099473 | TGGGGTACACAATTT[C/T]AGAGTAATAAACATA | 9678 |
| rs550715478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070083 | AATAAATACTTCCTT[C/T]CATCTTGTGTCATTT | 9678 |
| rs550717425 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075758 | TATTAAGTCATTTAG[A/T]TACCCTATGAAATAA | 9678 |
| rs550723714 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10993171 | TGGTTGAGAGGGTGT[C/G]TTTCTGGTTTATCTG | 9678 |
| rs550728137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069380 | GAGTCCGCATGGAGA[A/G]GTGCCTTCAAGTCTC | 9678 |
| rs550735529 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973657 | AGGCGCGGAGAGGGC[A/G]GAGCCTTTGGGGTTT | 9678 |
| rs550737619 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11041082 | GATGAGCATTTATAT[C/T]TTATTTTACTTGAAT | 9678 |
| rs550759425 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11079273 | CTTTGTGAGATGGCT[C/G]GGTAGCTGGCTTTTG | 9678 |
| rs550777055 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000015 | AGTAGAGAAGGAGAG[A/G]GAAATTGATGCATAA | 9678 |
| rs550780072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133948 | GACCAGGTGACCCAA[A/G]TGAGGAATTTAAGGA | 9678 |
| rs550787579 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10983534 | TCACCTTTCTTTCAA[C/T]TTAGTTGTGTCCATA | 9678 |
| rs550796236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074064 | CTGCACTGCCTGGAA[A/G]ATCTCCAAAATGCGT | 9678 |
| rs550811961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063355 | AGTATAAATTTTGCA[A/G]TATGTCGAAAATGAA | 9678 |
| rs550813162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974395 | CAGGGCCGGTGGGAG[C/T]AGGGCAGGGGTGGGA | 9678 |
| rs550823821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086638 | CAAATTGAAAAAACA[A/G]TCTGTGGATTTTAAT | 9678 |
| rs550853967 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956287 | TGGCTGCCGTGCAAC[C/T]CTCTAGGTGTGAAGT | 9678 |
| rs550856088 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968739 | ATTTATGAGTAGTTT[C/T]TATGCTGGATCTTCC | 9678 |
| rs550859902 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072735 | TTTATAAAGAAAGTA[A/C]GTTTATTTGGCTCAT | 9678 |
| rs550864258 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11124199 | GAAGTATTTTAAATT[A/G]TCTGCAATTTAGCAC | 9678 |
| rs550865501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074412 | AGGCAGGGTTTCGCC[A/G]TGTTAGCCAGGATGG | 9678 |
| rs550871240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085793 | TCAACTCCTAGGTTC[A/G]GTCCTTCCACCTTGG | 9678 |
| rs550874080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050143 | TGGAGTTCAAAATTT[A/T]AAGCTGTCACTTTGA | 9678 |
| rs550883624 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165396 | TATTGGTGATATTAA[A/C]CTTGACCATTTGGTT | 9678 |
| rs550885613 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064438 | ATTTCAGCGCTTACT[C/G]AGACATACGTGTATG | 9678 |
| rs550895017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002817 | GGCAAAAATGAAATG[C/T]TGATGACAAAAATTA | 9678 |
| rs550903179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080586 | ACTCTGCTGGTTTTT[C/G]TCCCTGATGTCTCAA | 9678 |
| rs550918252 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11155762 | TGTCTTATATACAAT[-/G]TTTTTTTTTTGTTTT | 9678 |
| rs550933033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133870 | AGGAAGTTTTAGTTT[A/G]TAGAAGAGTTTGTAG | 9678 |
| rs550935352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042972 | TGTGACTAAATCTAT[A/G]ACAGCTTTTTTGAGA | 9678 |
| rs550944152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068738 | GAAGAACAAAAGTCT[A/G]CAGGGATTATAATAG | 9678 |
| rs550949203 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118004 | GTAAGATGTATACCA[C/T]TCAGCTGTCTAAATT | 9678 |
| rs550981269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, missense | PHF14 | GRCh38.p7 | 7:11062690 | AATGCTAATCAGAAA[A/T]CTTAGCTGATGCTGC | 9678 |
| rs550989544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963515 | GTGGTCAATTTAGAA[A/T]AAGTGCAATGTGGTG | 9678 |
| rs551042931 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059812 | ATATACATTATGCAA[A/G]TTAGATAATAGAGTA | 9678 |
| rs551065305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11049389 | CTGAGGCAGGAGAAT[C/T]GCTTGAATGGGGAAG | 9678 |
| rs551079807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007552 | CTTTTGTTTTTAAAT[A/G]TGGTTGCTTACAGTG | 9678 |
| rs551080392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958793 | CTCAAACACCTGGGC[G/T]CAAGTGACCTTCTCA | 9678 |
| rs551089619 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11157750 | GTGTTACTGAATGAC[-/TG]TATGATTCTACTAGC | 9678 |
| rs551112503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002739 | GTGAGCCACCGCGCC[C/T]GGCCAAAAATTAAGA | 9678 |
| rs551132812 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968654 | TGGTTCTGATGGTTG[C/T]GTGTTTGTTTGTAGG | 9678 |
| rs551141505 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11018522 | TTGTAAATGCCATTA[A/C/T]TTTTAAAATTTCTTT | 9678 |
| rs551145216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964322 | AATAATTTTATTTCT[A/C]CTTCACTTATGAAGC | 9678 |
| rs551145916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125456 | TACTTGCTTCTAAGT[C/G]TATTGAGTATAAATA | 9678 |
| rs551171592 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008919 | TGGGCGCCTGTAGTC[C/G]CAGCTACTCGGGAGG | 9678 |
| rs551206556 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11167118 | TACCTCCTAGTCCTT[A/G]GGGTTATTAAGTCTT | 9678 |
| rs551214250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126296 | CAGTCATTTGCTTAA[C/T]TATTAATTTTTACCA | 9678 |
| rs551216941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11166153 | CAAGTTTAAACATTA[A/G]GAGGTAAGCCTGTCT | 9678 |
| rs551238128 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022530 | CATATGAAAATGATG[A/C/T]TTTGTTTCATTTGAA | 9678 |
| rs551243341 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965800 | AAGTCTCAGCAATGG[C/T]GGACTCCCTTCCCCC | 9678 |
| rs551245951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957105 | TTAGATTCAAGATAA[G/T]GACTACCCTTAGGTA | 9678 |
| rs551264581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013242 | TCTTGGCTCACTGCA[A/G]CCTTTGCCTCCAGGG | 9678 |
| rs551295673 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11036049 | TACTCTATCAGTGCA[A/G]TATATTTATTACATC | 9678 |
| rs551296037 | in-del | -/A | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10996594 | TCCCAGAGGTTATTG[-/A]AAAAAAAAAACTAAT | 9678 |
| rs551315448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002276 | TAAAAATGGGGGGAT[A/G]AAAGGAACTCTGCAA | 9678 |
| rs551357861 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099386 | ATAGATGCAGTATAG[A/T]CAGGTAATTTGTATT | 9678 |
| rs551360826 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10995677 | GGCATGGTGGGCTGC[A/G]GGTTCCGAGCCCTGC | 9678 |
| rs551375548 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973886 | CACTTCCTTTTCAGA[C/G]CTGTATCCGGGTCGC | 9678 |
| rs551375593 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11086497 | CAATCACTTATACTT[A/T]GTCCATATGTCTTGG | 9678 |
| rs551385486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111986 | TAGAATGAAATTTCT[A/G]TAATCTAATGTTTAA | 9678 |
| rs551394506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140233 | TTATACGACCCTACC[A/G]TATATACACATGCAT | 9678 |
| rs551429193 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165734 | CAATTATTTGAACTA[C/T]CATGAGAACTAAATC | 9678 |
| rs551454087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11120392 | TACTCTGATTTTCAA[A/G]TGTTAAGAAATGTTT | 9678 |
| rs551480900 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11030830 | ATGATTTAAAGCATA[C/T]TTACATATATATGTT | 9678 |
| rs551491835 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084718 | TAATGGATAATATTA[A/T]CTTGTTACCCACTGG | 9678 |
| rs551509113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119393 | TTATATAATCAACCA[A/G]TATATCATAGATCGT | 9678 |
| rs551512364 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11097469 | TCACCATTAGGCGTA[-/G]TAGTAGGCCTTTATC | 9678 |
| rs551530427 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082781 | CTCAGCCTTCACACT[C/T]AGTAGAATTTTGGTT | 9678 |
| rs551535337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030120 | GAATTGTACTTTGAT[G/T]AAGGCTACTAGATGA | 9678 |
| rs551540925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091409 | AGAGGGTTTTTTTTA[A/G]AGGTCTACTGAATTA | 9678 |
| rs551540983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084837 | TTTCAATGTTTATTC[A/G]CTCATATATTGATGA | 9678 |
| rs551552994 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11062572 | ATGCTTCTCCCTTAC[A/G]AAATAAAGAAAGGTG | 9678 |
| rs551557069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10991611 | CACCGCACCTGGTCC[C/T]CCAGTCATCTTAATT | 9678 |
| rs551568714 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108878 | TGCCTCAAGTTATAC[A/G]CTAGAAATCATAATT | 9678 |
| rs551572061 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149438 | TTCTATCTACAGACT[-/A]AAAAAAAATGGATGA | 9678 |
| rs551604591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092200 | ATCTGTTTTGTATTT[G/T]CTTCTATTCCTTTTT | 9678 |
| rs551619131 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053945 | AAACACCAGGGAAAG[A/G]GTCCATGACCAGTAA | 9678 |
| rs551660484 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973619 | AACTGGCCTCCCAGG[A/G]ATTTGGACTCAGGAG | 9678 |
| rs551687490 | snp | A/G/T | 0.00199529 | 0.0315338 | intron-variant | PHF14 | GRCh38.p7 | 7:11056320 | TATTTTGTATATACC[A/G/T]TTATCTCTGAGAAGG | 9678 |
| rs551702295 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103267 | TGTTGATCTCTAGAT[A/G]TTTTTAGTAATACCC | 9678 |
| rs551713476 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118921 | TTTTGATATATTTAA[A/C]TATCAAATTCACAGA | 9678 |
| rs551720140 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124639 | AGAAAGAAATGAGAT[A/G/T]CAGAGAAGTTAAGGA | 9678 |
| rs551722367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10999518 | AAAATGACCCTCGCT[C/T]TCTATTTTGTTGTTT | 9678 |
| rs551731752 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163203 | TGTGTTTGAGCTGAG[G/T]TTACTAAGAACATCC | 9678 |
| rs551734624 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11148070 | TCCAAAGCATATCAT[A/G]CTTCTTTCCGTTCTG | 9678 |
| rs551741912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11074046 | CTCTGGGCCTGTGAT[A/G]GGCTGCACTGCCTGG | 9678 |
| rs551751579 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994402 | TGAGGTCGAGCCACT[C/G]CACTCCAGTCTGGGC | 9678 |
| rs551762196 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10991093 | CCTCCCAGGTTCAAG[C/T]GATTCTGCTGCCTCA | 9678 |
| rs551763227 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997180 | AAGTTTTATTGATCT[A/C]ATTTTGTTTCTCTAT | 9678 |
| rs551763754 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10988819 | TAATTCTTATAACCT[A/C]CTGAAGTAGATATTA | 9678 |
| rs551778473 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034452 | TTAGGCTATGAGAGA[A/G]CTGTAATTCCACTTG | 9678 |
| rs551819007 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11102035 | AGTATAACCAGCACT[A/G]TAACACACTGATCAG | 9678 |
| rs551825813 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:10985356 | AAACTACTTTGTAGT[A/G]GAGTTAGGTGAAAAT | 9678 |
| rs551826899 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11068019 | GGTATCCAAACCATA[A/G]CATACATACAGTAGA | 9678 |
| rs551829428 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100396 | CACATTCAGTTCTTA[C/G]AACAGTCCTATGAGG | 9678 |
| rs551841750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109724 | TTCTTAATGCCAGAA[C/T]AACAGGTATTTGAAC | 9678 |
| rs551878882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071692 | GCCCCCATTTCCAGC[A/G]TCAGGCAACCACTGC | 9678 |
| rs551906772 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068582 | GTTTCAGCTGGGAAA[C/G]ATGAAAAAGTTCTGG | 9678 |
| rs551911363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153194 | GATTAATCCACAGGC[A/C]AGAAACATGATAGCT | 9678 |
| rs551915794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065741 | TCTTTCAGTCTTTAT[C/T]GAACTATCAAATTAG | 9678 |
| rs551917413 | snp | C/T | 0.000217984 | 0.0104376 | intron-variant | PHF14 | GRCh38.p7 | 7:11061934 | TTATTTTGTTTGTTA[C/T]GTTTTATTTTATTAT | 9678 |
| rs551921105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068549 | AGGAATGGGCAGTTA[A/G]TGTTTAAGGGGTACA | 9678 |
| rs551954729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10982018 | ATCAGTAAAATTAAA[A/G]TCAAGTGCCCAATCT | 9678 |
| rs551974006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997934 | CAGATGTAGGTGGGG[A/G]CATTCTAAGAGTGTA | 9678 |
| rs551994105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966618 | ATCTAATTGGTGGAA[C/T]CTAAATCATATCTAT | 9678 |
| rs552004912 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041218 | TTTTGAGTTTCTACA[C/G]TTTTTTTCTCTTGAT | 9678 |
| rs552006088 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962178 | CTTTTCAAAGGGAAT[G/T]CTTCCAGTTTTTGCC | 9678 |
| rs552016864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075857 | CATAGCTAGGCTGGG[C/T]GCGGTGACTCATGCC | 9678 |
| rs552035758 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132363 | TATTTTTCTTTTTGT[G/T]CCTGGCTTGTTTCAC | 9678 |
| rs552038120 | snp | C/T | | | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11037025 | TCAGGAAAATATGGC[C/T]GAACAAAAGAATATA | 9678 |
| rs552046889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125407 | CCTAGTATCAGCATT[A/C]TTTTGCAGTACAAGT | 9678 |
| rs552060692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045063 | TACACACCCTTTTCC[C/T]CATCCTACATTCTGT | 9678 |
| rs552073494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165358 | CCGTTTTTAATACAT[C/T]GTATCAGGGTGTTAA | 9678 |
| rs552083864 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089896 | CTGCCTCAGCCTCCC[A/G]AGTAAACTGGGATTA | 9678 |
| rs552087709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993995 | GCCTGGGTGACAGAG[G/T]GTGACTCTGTCTCAA | 9678 |
| rs552093229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035203 | GTGTATTAGGTATTA[C/T]AAGTAATGTAGAGAC | 9678 |
| rs552106303 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064796 | TTTTTCTTGGGACTT[C/G]GGCAAGTAATTTAGC | 9678 |
| rs552120046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965138 | TGTTCCTTTGGAGGA[A/G]AAGAGGTGTTCTGGC | 9678 |
| rs552120531 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087380 | TATTTTTAGTAGAGA[C/T]GGGGTATCACCATGT | 9678 |
| rs552121876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956476 | TTATTCAAATGGTTC[A/G]GACCATGGTTTTTTG | 9678 |
| rs552148809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168664 | TAAATCAGAAATATT[A/G]GGAAAGCAAGACTGT | 9678 |
| rs552165289 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11122457 | CGTATATATATATAT[A/T]GTGTGTGTGTGTGTG | 9678 |
| rs552211942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162504 | AGTCTACCCTAACTC[A/G]TACTTATCATCCATC | 9678 |
| rs552212368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975412 | CAGAGTAAGAGTTGC[A/T]CTTCAAATTATAGTA | 9678 |
| rs552227428 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011737 | TGAAGGATGTTTTAC[A/T]TTAGGGCAGTGCCTT | 9678 |
| rs552228428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11115571 | CTGCTTGAAATCTGT[C/T]AGTGTTTTTTCATTC | 9678 |
| rs552240124 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988899 | AGGGAATAAGCGAGA[C/G]GTGAGAAAGAAACTT | 9678 |
| rs552248499 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11156411 | AATAAAACTGAAGAT[G/T]AATGGGTTCACTCTG | 9678 |
| rs552256858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | PHF14 | GRCh38.p7 | 7:11149060 | GTAAGAAAACTGAGA[A/G]TGAGGGGTCATATGC | 9678 |
| rs552262346 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066313 | CACTCAGGCTAGAGT[G/T]CAGTGGCACTTTCTT | 9678 |
| rs552264159 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039139 | GATGAAGCTTAAGAC[C/T]TGAAGCATGAGTTTT | 9678 |
| rs552271337 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980546 | TTCTTAATGCTTTAG[A/C]GACTGAAAAGAAGTC | 9678 |
| rs552274447 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096763 | TCTTCCCACAGGACA[A/G]TCATGGTGATTAATA | 9678 |
| rs552291195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11021283 | AAAATTAATGGTAAA[A/G]TAACAAGGAAGATTT | 9678 |
| rs552293682 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114126 | TAAATTTAGATGGTA[A/G]AATGTCTCCAACTTC | 9678 |
| rs552305111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11150630 | ATAGAGATTTATTTG[C/T]ATATTAGAATCCTCT | 9678 |
| rs552317511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058720 | GTATTTACGTGCAAT[A/G]AGAGATTTGCATTCT | 9678 |
| rs552341119 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094080 | TTTGGGTCTTTCCCA[C/T]TGTGGTGGCCGCTCC | 9678 |
| rs552348699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167717 | GTAAGATTTACTTTT[C/T]ATTATAATGTAGTTA | 9678 |
| rs552355961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135953 | AACTGATAAAGAATT[A/G]ATATTCAGACATTCC | 9678 |
| rs552356100 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11128680 | GCTAGTATTTTAGAT[A/G]TAAATCAGTCTCTCT | 9678 |
| rs552367264 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11051043 | CTTTCCAAAGGTAAA[A/T]TATTATTATTATTTA | 9678 |
| rs552386345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959259 | ATCTAGACACTGGAA[C/T]AAGTCAGCTAGTCAT | 9678 |
| rs552400503 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154461 | TCGTTTAAGCAACTA[G/T]ATGCCTAAAAAGGTC | 9678 |
| rs552413231 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11038484 | CCAACATGGTGAAAC[C/T]CTGTCTCTACTAAAA | 9678 |
| rs552430768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087913 | TGTATAACTTGAAAC[C/T]AACATAACAATTAAA | 9678 |
| rs552442094 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965414 | TGCAGAACAGCAAAT[A/G]TTGCTGACTGATCTT | 9678 |
| rs552451003 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125462 | CTTCTAAGTGTATTG[A/G]GTATAAATACAATTC | 9678 |
| rs552452642 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960678 | CTGTCTTCCACAATG[G/T]TTGAACTAGTTTACA | 9678 |
| rs552455905 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11121048 | GTAAACGTAACAAAC[C/G]ACTGAAGACAGTTGT | 9678 |
| rs552464464 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064202 | TTAAAGAATTTTTAT[A/G]TAAAATTTCATATGT | 9678 |
| rs552509388 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11114209 | AAATTTTGACTCCCT[A/C]TTTGTTTTGCCTAGA | 9678 |
| rs552510222 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141533 | ATATGCAGAAAAAGT[A/T]AAAATGTTTTCTCAT | 9678 |
| rs552519249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114117 | AATTGCAAATAAATT[C/T]AGATGGTAAAATGTC | 9678 |
| rs552523277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069902 | TTATTAGATAATACT[A/G]GCCTTCTGAATGGAG | 9678 |
| rs552524273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020049 | ATAAGCTTTATGTTG[C/T]AATAGAAGGCAGCAT | 9678 |
| rs552529336 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005100 | TCTTAATTTTAAAGG[-/T]TTTTTTTTTTCTATT | 9678 |
| rs552541721 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11016756 | AATCCAGTTACCCTC[-/T]TTTAAGTTATTTTTA | 9678 |
| rs552545483 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148319 | TCAACTTAACTTTTC[A/T]TCTTATGCTCGATTT | 9678 |
| rs552566896 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11019358 | AGCAGCGAAGCCATC[A/G]GGTCAAGCAGTCCCA | 9678 |
| rs552567659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964381 | TTGAAAATTCTTTTC[C/T]TTAAGAATGTTGACT | 9678 |
| rs552605216 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11072110 | ATATTTAATTGACTT[-/A]ACGGCTCTGCAGGCT | 9678 |
| rs552611491 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030061 | TACATATAGCTGTTC[C/T]AATCTCTTCATTTAT | 9678 |
| rs552615190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100913 | CTTCCTCTTAACAGG[A/C]AATTCTAACTATATA | 9678 |
| rs552659666 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958741 | CATTTTGTCACCCAG[C/G]CTGGAGTACAGTGGT | 9678 |
| rs552688249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154885 | TATTGTAATACCAAC[A/G]GTTGAAATTGCAAGA | 9678 |
| rs552707381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008721 | GGTACTGTCTTTCTC[A/G]TAAACAATATTACTC | 9678 |
| rs552712313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11002988 | AGTCTCGCTCTGTCA[C/T]CAGGCTGGAGTGCAG | 9678 |
| rs552714809 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107685 | TGTGCTATTCGTATA[A/G]TAATCTGTTTTTATT | 9678 |
| rs552724388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119828 | GAAAAATGAACTCTG[C/G]TAGTTAATGGAATTG | 9678 |
| rs552742096 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027751 | GATTTCTAGGTTGTA[A/G]TGCCTAGATTTTTTG | 9678 |
| rs552749890 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11148746 | TTTATATAAGTTTAA[C/T]TCTTAAAATATAACA | 9678 |
| rs552753148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11024759 | TTACTGCTTATCGAC[A/G]GTGCACCTGGTGGTC | 9678 |
| rs552764516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113358 | TTTAGTTTTGTTTTC[C/T]TCTCTACCACAGAAT | 9678 |
| rs552776405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11100379 | GTCTTTGACTCTACT[A/G]TCACATTCAGTTCTT | 9678 |
| rs552790761 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981634 | TATTCATCAATTTCT[C/T]CCATTCTAGAGCATA | 9678 |
| rs552801329 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997212 | GTAGAGTTTAATATC[C/T]TCAAGCAGAGCAAAA | 9678 |
| rs552839251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148509 | GGCTTCCTTGACTAC[C/G]TTGCCTAAGAGAACA | 9678 |
| rs552861866 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11127259 | CTTTTTTTTTTTTGA[C/T]TCATTGCTAGAGCTT | 9678 |
| rs552872081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080810 | CAAATGCATTAGAGG[A/G]CCATCAAGCACAAAG | 9678 |
| rs552878996 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010059 | GATAGCTCCTTAAGG[A/G]CTTTATTCTCTTGGT | 9678 |
| rs552885568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993254 | TAATCAGGGCTGTGA[C/T]TACCACAAAACAGTA | 9678 |
| rs552891217 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107424 | TTGTTATTTACATCT[A/G]TATCTGTTATTAATC | 9678 |
| rs552894594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037477 | CCAACTCATGTGACT[C/T]TGTTCTCTATTTCTA | 9678 |
| rs552914201 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146629 | TCTATGGTTGGGGAT[A/G]TAGGGCAACATATAT | 9678 |
| rs552914241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148130 | ATTCCTGATCTGTTT[A/G]CAGTAGACTGCTTCC | 9678 |
| rs552941443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979462 | ATATTTTTTTCAAAC[A/G]TAAGAAAGGTTTATT | 9678 |
| rs552948893 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987699 | TTTATGTAAAACCAT[A/C]TTTTAGAAATTTTAT | 9678 |
| rs552952655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100219 | ATAATGAAACGAGGT[A/G]AACTGAATTTGAAAA | 9678 |
| rs552967652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092420 | TAAACTATGGCAATC[A/C]CTGCCTTATGCATAA | 9678 |
| rs553002645 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100985 | GAAGCCCTTTGAAAA[C/T]AATTTTTTCTACATT | 9678 |
| rs553004913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086151 | CACCTTCTCTAGTTT[G/T]AGTACCTCTAGTCTG | 9678 |
| rs553006542 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11092865 | AAACTCAGAATTATT[A/G]AAAGCTCTTTTTGTA | 9678 |
| rs553006684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138242 | GAGGCAGGGTTTCAC[C/T]GCGTTAGCCAGGATG | 9678 |
| rs553008643 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106939 | ATAAAAGATAATGTG[A/G]TTATCACAATCAACT | 9678 |
| rs553011069 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11046786 | ATGATATTTGAGCCA[C/T]CTCTTAAAGTTTTAT | 9678 |
| rs553040147 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058402 | CTTCATTAAAACTAG[-/A]AAAAAAAAATCCCAT | 9678 |
| rs553053337 | in-del | -/CT | 0.0119185 | 0.0762706 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961474 | AAGCTGTTTTGGTTA[-/CT]CTGTAGGCTTGTGGT | 9678 |
| rs553096053 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11036871 | TTATTTGTAAATATA[C/G]TTAAAAGTTTTAAAC | 9678 |
| rs553099098 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973709 | TTGGCGGGGATCTCT[A/G]CTCCGCCTTGGCACT | 9678 |
| rs553100613 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11002396 | TATAAGGCAAATATC[A/C]GGTTGACAGTGAGGT | 9678 |
| rs553101848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006694 | AGCTCTTCCGAGGAT[A/G]TCTGGGCTGCCTCCA | 9678 |
| rs553132471 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10980736 | ATTTATACTTTTCTC[C/T]GCAGAAATAATGTTT | 9678 |
| rs553138642 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004630 | TCATATTGAATATCT[C/G]TCAGTCTGGATATAT | 9678 |
| rs553145822 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136617 | TCTAACATCCTAGAA[A/T]GTATCAAAATTTTAA | 9678 |
| rs553169204 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11043775 | TTTATGTGCTTCAGA[A/T]ACTGCTATAGCATAT | 9678 |
| rs553188181 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11075198 | TCTGCCTCATCCTCC[C/T]AAAGTGCTGGGATTA | 9678 |
| rs553199348 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11134059 | GACTATCCAGTGCCT[A/G]GGAAATTTTTCTTGT | 9678 |
| rs553200003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166863 | AGTTATGTACCTGTC[C/G]TGAACAGCAGGCAGT | 9678 |
| rs553241399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11075318 | CCATAAAGAAGTACC[A/G]AAGGCTTGCTAATTT | 9678 |
| rs553249177 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958380 | AATTTGAAAACAGAT[A/T]ATCAATGAACTCTTT | 9678 |
| rs553250466 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977023 | TCATATTTTTGACTC[C/T]TGTTTTAGGTGCATT | 9678 |
| rs553251451 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154064 | CGCCGGTAGGGTCTA[A/C]CATGATAATGATAGA | 9678 |
| rs553271222 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167228 | CGGTGGAGAAACTTA[C/G]TAGACTGTCCGTGTG | 9678 |
| rs553280599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091818 | ATAAATTTGATAACT[C/G]TTAAACACTTATTCT | 9678 |
| rs553291668 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012881 | TTGGCTCAGTTGTGC[A/G]TGGAACTCAGTCTGT | 9678 |
| rs553356051 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095914 | TAGTTGTTCTCTAGT[C/T]AGGGGATATATCTCT | 9678 |
| rs553386067 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997945 | GGGGGCATTCTAAGA[C/G]TGTAAATACCAGGAG | 9678 |
| rs553387891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10980209 | AATCTTACTTTTGCG[C/T]CTATCGTGAAGTTTT | 9678 |
| rs553403136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083678 | ATCTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC | 9678 |
| rs553405492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11090455 | TATTTTCCTTTTCAG[A/G]TTACTCATTTATGTC | 9678 |
| rs553433236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007850 | AGTTGAGATTTTGCT[A/G]AAAGATAGTATGCCA | 9678 |
| rs553434866 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098963 | TCTAAGGAAGGAATT[A/T]GAAAATTAAGTAAAT | 9678 |
| rs553439589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126745 | AATACAGTTAGCTGT[A/G]TTTTTTTAACCTCCT | 9678 |
| rs553451012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049117 | GTACCTGCTTCTATA[C/T]CTAGGGGATTTAGAT | 9678 |
| rs553472345 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080272 | AAAAACAATAAAATT[A/T]AAAAAAAACTTGATA | 9678 |
| rs553481573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043200 | GATTAGAGTCAAAGG[C/T]TTTACTTCTGGTATT | 9678 |
| rs553493328 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11084194 | AGAACTTAAACTTCA[A/T]AATATGTACACACAC | 9678 |
| rs553494999 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126380 | TTACTCTTTTATAAG[C/T]AGGCTAAGTGCTGTA | 9678 |
| rs553497327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999888 | ATTTAACTGACTTTG[A/G]TGGCAGTCCAAGTTA | 9678 |
| rs553527271 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166418 | TGGTAAAAAGCTTCC[C/T]TTGCAATTTTATTTA | 9678 |
| rs553532180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156592 | TAAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA | 9678 |
| rs553538577 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166464 | TCAATTATATTTTAT[G/T]TGCTGTCTGAGTTAC | 9678 |
| rs553552101 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105399 | TTAAACAAAGTTACT[A/T]ATTTCATAAAACTCA | 9678 |
| rs553561145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112228 | TCTCAAAAAAGATGA[C/T]GAAAATTAACTGTCT | 9678 |
| rs553561430 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170092 | AATTTATAAAACATT[C/T]ACTAAGGACCTGCTG | 9678 |
| rs553561750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047135 | GTGCAGTGGCACAAT[C/T]GCAACTCACCGCAAC | 9678 |
| rs553593640 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014324 | TAAAAAGAAGTTTAG[C/T]ATAAAGAATTTTTAA | 9678 |
| rs553608548 | snp | G/T | | | | | GRCh38.p7 | 7:10969836 | AAATTCAGTGGCCAA[G/T]CCTAGACCAAAATTC | 9678 |
| rs553618321 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023653 | CCAACATGGCGAAAC[C/G]TCGTCTCTACTAAAA | 9678 |
| rs553635046 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11162024 | CAGAAAAGGCTGTTT[A/G]CAGTATTCTTAGCCC | 9678 |
| rs553645083 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966248 | CCCCAAGGAGCTTTA[C/T]TGAGAGACAGAACAG | 9678 |
| rs553650831 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989497 | GTAATGTTAAGCACA[A/G]TCTATTAAATATGCA | 9678 |
| rs553653524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055324 | TTTCAGATTTTCTTT[C/T]TGCTTTCTTTGCACT | 9678 |
| rs553654370 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024298 | AAAGAAGCCATCTCC[G/T]TAATATAAAAGATGA | 9678 |
| rs553660249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11146718 | CATACATTCAGCTCC[A/G]CATGGTCATTTCCAG | 9678 |
| rs553665041 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11154857 | TTCTTGCTGTCTATG[A/C]ATAATACAATTATAT | 9678 |
| rs553666711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150260 | CTTATGGTTATTGTT[A/G]CTGGTTATAGTTATG | 9678 |
| rs553669834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012645 | AGCATTGCCAAGTTA[C/T]CTTGTCTGTTGGGTG | 9678 |
| rs553685579 | in-del | -/AGAA | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11012812 | TAGACAAATTTTCAC[-/AGAA]AGAATAATTTAAAAT | 9678 |
| rs553694610 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073732 | GGCTTTCTGTGAAGG[C/T]TCTGTCTCTGTGACA | 9678 |
| rs553707789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11102367 | GTATCTATCTCTTTG[G/T]ACCAGATCATATGTT | 9678 |
| rs553709803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059125 | CTATACCATTGTGTG[A/G]TTGAATCACTAATTG | 9678 |
| rs553722699 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009924 | AAAACTCTGTGCAAA[A/T]GTGCACGTTTGCTAT | 9678 |
| rs553753101 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11039221 | CATTTTTTTCTTTCC[A/T]GTCCTTATGCTGTAT | 9678 |
| rs553754860 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983294 | GAATGAGCACCCTAA[C/G]TGTAACATTTTTTCA | 9678 |
| rs553770507 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11137079 | TTAAAGTGGTTTGTG[A/G]CTCCACGGCTTAAAC | 9678 |
| rs553772959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095570 | GATCAGGTTTTCTCA[A/G]CCTGGGTTTCCTGGG | 9678 |
| rs553776178 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971022 | ACCTGAAAAAGGGCA[C/T]CTTTGAAAAACTATA | 9678 |
| rs553795681 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11052149 | CACTTCTTTTTCTTT[A/G]TAGAAGAGATTTACA | 9678 |
| rs553796601 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11005372 | TTACTGTGAGCTCAT[A/G]TGTTATAATCTATTA | 9678 |
| rs553804266 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960782 | AATGATTGCCATTGT[A/G/T]ACTGGCATGAGGTTG | 9678 |
| rs553806430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162811 | CTGCCTCAGCCTCCC[A/G]AGTGGCCGGGATTAC | 9678 |
| rs553832002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130767 | ATGACACATGTCCAC[C/T]ATTACAGTGTCATAC | 9678 |
| rs553838394 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964521 | ACATTTTTTTCCTTT[A/G]TTTCAACCTTGGTGA | 9678 |
| rs553854366 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10989348 | AAGAATATAAAAATA[G/T]AAAAAATAATAAAAC | 9678 |
| rs553854757 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122106 | TATGAGTGAGAACAT[A/G]GGGTGTTTGGTTTTC | 9678 |
| rs553860925 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11075947 | GCATCCTGGCTAATA[C/T]GATGAAACCCCGTCT | 9678 |
| rs553883342 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11032551 | ATGGCATCTAGAGGA[A/C]CACAAGCTAAACTTA | 9678 |
| rs553892436 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968077 | AAAATTAGTATAGCA[A/T]ATAGAAAACACTACA | 9678 |
| rs553893640 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018303 | GTCATTGGTATTTTG[A/G]TAGGGATTGCATTGA | 9678 |
| rs553923922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961417 | ATTTCTGAGGCTTCT[A/G]TTCTGTTCCATTTGT | 9678 |
| rs553929623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134862 | AATGAATAATTCAGT[A/G]GAGCAACATATAGAC | 9678 |
| rs553969057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109316 | ATAGAACAGCTGACT[C/G]CTGGTCCTCATTCCA | 9678 |
| rs553977388 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11150962 | AGTACAGTTTATTTT[C/G]TACTTTAAAAGAAAA | 9678 |
| rs553982424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044592 | GATTCAGAGAATTGT[C/T]TTTTCTTTAGTGTAC | 9678 |
| rs554019131 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103208 | ATATTATTAGCATGA[A/G]ATTTTTACTTCAGAT | 9678 |
| rs554025938 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11056387 | TATTTTATTATATAT[-/C]ATTAGACCCATAGTT | 9678 |
| rs554026334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020879 | TGAAGACAGTGAGCC[A/G]CACTCTGCTGTAAGC | 9678 |
| rs554039614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144251 | GGAAAGGGAAATCTT[G/T]TATACTGTTGGTGGT | 9678 |
| rs554056430 | in-del | -/TAGG | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064869 | TCATACTTGCTTCAT[-/TAGG]TACCTTATGGATAAT | 9678 |
| rs554061504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157266 | GGAATAGACGTGACT[C/T]CAAGAGTTAATATCT | 9678 |
| rs554064440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015509 | AGTGGCCTAGTATTA[A/G]GGAGTTTAGTAAGCA | 9678 |
| rs554077357 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969652 | TTTTTCATTGCATGT[A/C]CTCTAATTTCTTGGA | 9678 |
| rs554093445 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087872 | TTATTTTAAGAAGTC[A/G]AATGGGGGCAAAAAG | 9678 |
| rs554133438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168857 | TTTCATCTATTCACC[A/G]TGTTCCACAGGAACC | 9678 |
| rs554138683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964955 | ACTGGTTATTCTAGT[C/T]AGCCATTCATCTAAC | 9678 |
| rs554145884 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037918 | TTTTTTCATTGGGAA[A/G]ATAGTGGAAATACAT | 9678 |
| rs554150496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016197 | TTGAACACTTGTGCT[A/G]ATGTCTACACTTACC | 9678 |
| rs554163490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095436 | GAGGATATGATGGGT[C/G]TTTATTCTGTAATTA | 9678 |
| rs554163843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10980394 | TGTCTTAGAAGTGTT[A/G]AGTCAACTCTGGTTA | 9678 |
| rs554165837 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123048 | CTTCTTCTCTCCTGC[A/G]TTTGCCTTTTCTTAG | 9678 |
| rs554167643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009018 | TCCAGCCTGGGCGAC[A/G]GAGTGAGACTCTGTC | 9678 |
| rs554168792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998256 | ATGTGGTAGTTGGAG[C/G]ATGTGTAAGTTATTT | 9678 |
| rs554187180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083006 | GGAAGAAAACTAGCT[C/T]TCTAGCTTATCACAG | 9678 |
| rs554200510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089076 | TTGAGCACAGACAGA[C/G]ACAAAGATTAATTAG | 9678 |
| rs554206822 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11076435 | TAATATTATTTTTTT[A/T]AAATGTACTGTCTGC | 9678 |
| rs554211984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082328 | ACTCCAGCCTGGGCA[A/G]CAGAGCAAGACCCTG | 9678 |
| rs554227444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033320 | TTCCAGGGATCAGTT[C/T]CCTTCTTTCTTCTTG | 9678 |
| rs554232063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10998991 | AGACATTGGGAAATC[A/G]TACACATTTAGGATT | 9678 |
| rs554242450 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115126 | TAGCAAATCACTTCC[G/T]GAGTCCTATAAAAGT | 9678 |
| rs554255283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975827 | AATATACTTCCAGAG[A/C]GTTTGCCGTGGTTAG | 9678 |
| rs554266554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027290 | TACCATTTATGTTCT[A/G]CTGTTATTAGAGAAA | 9678 |
| rs554287806 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091412 | GGGTTTTTTTTAAAG[G/T]TCTACTGAATTAGAC | 9678 |
| rs554318375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136441 | TTACCAGAGTAAAGT[A/G]TCTGTACTATGAATG | 9678 |
| rs554337483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070883 | ACTCTATACAATTAA[A/C]ATAGTTTATAATTTG | 9678 |
| rs554339496 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149794 | AATTATCTTGTTTAT[A/G]ATAGTGTTTCAGTTG | 9678 |
| rs554399546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974745 | CAAAAATTCCTTGTG[C/G]GAGGTCATCTTTATG | 9678 |
| rs554400402 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019149 | GCTGGTATTTTGTTG[A/G]GGATCTTTGCGTCAG | 9678 |
| rs554411368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11008829 | TCACGAGGTCAGGAG[A/G]TCGAGACCATCCTGA | 9678 |
| rs554414540 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083142 | CCCAGCCAATGGGGA[A/T]AGGGCACAGGGGCAG | 9678 |
| rs554414681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010361 | TGAAGATGATGATTG[C/T]CAACCACAATTTAAT | 9678 |
| rs554424030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087459 | CCTCCCAAAGTGCTG[C/G]GGTTACAGGCATGAG | 9678 |
| rs554426332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118753 | ATAGAATTGGAATCA[C/G]TATTGATCTGTTTGG | 9678 |
| rs554459095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088128 | AGTCCCTTATGTAAA[A/G]TGCCATCATGTTTGC | 9678 |
| rs554500416 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065293 | AAGTTGAAACTATTT[C/G]ATGGAATTGGGAAGT | 9678 |
| rs554509451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058771 | ATTTGGGATTAAAGT[A/G]TTAATCTTGGATTAG | 9678 |
| rs554519301 | snp | G/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10969553 | CATATCCTTGCTTAA[G/T]AAAACTGTATTAAAT | 9678 |
| rs554544376 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10991060 | CAGTGGCACAATCTC[A/G]GTTCACTGCAACCTC | 9678 |
| rs554550595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976175 | ACGGAATCTTAAACA[C/G]AAACTGACTATTTGG | 9678 |
| rs554560128 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11074826 | CACTTAACAATACTC[-/T]TAAGAAGTTCCAAAT | 9678 |
| rs554563349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11051478 | GTTTTTTCATTATGT[A/G]CCCTATAATCACATT | 9678 |
| rs554563544 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985133 | TAATCAATTGTGATT[A/G]TTAGTTATATTTCTA | 9678 |
| rs554572750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015491 | CTCTAAGTTGGGCCT[C/G]AGAGTGGCCTAGTAT | 9678 |
| rs554580816 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964934 | GTCATTTAAGCTCTT[C/G]TCTACACTGGTTATT | 9678 |
| rs554607121 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11167885 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGTGGG | 9678 |
| rs554613113 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11075530 | TTTTGTGTGAATTAA[A/C]AAGAACTCACTCATT | 9678 |
| rs554651569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051896 | AAAAAGACATCTATT[C/G]GTTATTCTTAACAAT | 9678 |
| rs554688868 | snp | A/G | 0.000334253 | 0.0129234 | intron-variant | PHF14 | GRCh38.p7 | 7:11061886 | TCTTAACTTTGAGAA[A/G]TTTTCTTGCTTAAAA | 9678 |
| rs554699343 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056985 | GATTTTGGAATTTTG[A/C]CCATGAATAAGCATG | 9678 |
| rs554703813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994117 | AAATATATTGGGAAC[A/G]AGCACTGCAAGTGGA | 9678 |
| rs554724967 | in-del | -/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965453 | AAGCTTTGTCCCAGA[-/G]GGGCACCCACCTGTA | 9678 |
| rs554728620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959686 | TGTAGCTGGACCAGG[C/T]GTACTGCAAGTGGTT | 9678 |
| rs554743256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997576 | TTGTTCTGGCTTAGA[G/T]TCTCTCATGAAGTTG | 9678 |
| rs554745806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168936 | GTAAGCATTCTAAGC[C/T]GACATGCACATGCTT | 9678 |
| rs554787202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057536 | TGCACCACCACGTCC[A/G]GCTGAGTTTTGTATT | 9678 |
| rs554791149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141592 | TCCTGGCATTGTGTT[A/G]TATAATAGCCTAAGT | 9678 |
| rs554792172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162176 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGC | 9678 |
| rs554799979 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155903 | ATATTTTAAAATTTT[A/C]TTTTATAAAATAATT | 9678 |
| rs554813162 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026520 | TGTATTTATTGGGCA[A/G]CACTTAGAACTAGAA | 9678 |
| rs554830296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11109277 | GACCCTGAAAATCTA[C/T]AAAAATTGAATACAA | 9678 |
| rs554844567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009407 | TTGTGTACATTGCAT[A/G]TATTAGTCAAAGATT | 9678 |
| rs554867459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066010 | TCTACACTATCAAAT[A/G]CTTGCCAGATTCTCC | 9678 |
| rs554867624 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974200 | TGTCCGGCTGGCTGC[G/T]CGCCGGTTTTAAATA | 9678 |
| rs554886346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013627 | TTTAATACGTTTCTT[A/G]TAAACCATTGGTGTT | 9678 |
| rs554891562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11102271 | ATAATACAAGAGGAG[A/G]CAACTCAATGTTTCA | 9678 |
| rs554917648 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11020722 | CTAGATTTAGTAAGT[C/G]TTAGTTCTGTCCCTT | 9678 |
| rs554926519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142605 | AAAAAAGCAGTATTT[C/T]ATTAAAAATGCTTGT | 9678 |
| rs554946447 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11042087 | ATTCCACAATCTTTG[C/T]AATAAATATCAATTG | 9678 |
| rs554946630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11165101 | AGCGAATAATTGTAT[C/T]TTTAGTAGAGACGGG | 9678 |
| rs554954721 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052349 | AATGTATAGTTTTCT[A/C]TGGAAAGAATAGATT | 9678 |
| rs554973636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134747 | GTAATCTTGTCATTA[A/T]ATCTGTTCAGTACTT | 9678 |
| rs554974947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128259 | TTGACACATGCATCA[A/G]GGCTTCAGTTTTATT | 9678 |
| rs554976422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128705 | CTCTCTCTCTCCCCC[C/T]GCCCCCACTGCTTTC | 9678 |
| rs554984223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962406 | TTGTGTATGTTGAAC[C/T]AGCCTTGCATCCCAG | 9678 |
| rs555008533 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11087412 | GGCCATACTGGTCTC[A/G]AACTCCTGACCTTGT | 9678 |
| rs555014842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161318 | CATTGTCCAGTGAGA[A/C]GGATAAACAAAATGC | 9678 |
| rs555017397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073576 | TTTTCCAGGCTCAGG[A/G]TGCAAGCTGCTGGTG | 9678 |
| rs555091799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031829 | ACTACAACTTATGTT[A/C]CTATGTTTTACATTA | 9678 |
| rs555093070 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087593 | CCAATGATTGACTTC[C/T]AAGGAATCTTTACTC | 9678 |
| rs555105051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125630 | GTCTGTATGTAACTG[C/T]TTTTATTCTACTATA | 9678 |
| rs555128630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11025749 | GCAGTGAGCCGAGAT[C/T]GTGCCATTGCCCTCC | 9678 |
| rs555181891 | in-del | -/C | 0.0314385 | 0.121371 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964402 | AATGTTGACTATTGG[-/C]CCCCACTATCTTCTG | 9678 |
| rs555183874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047292 | CCAGAATGGTCTCGA[C/T]CTCCTGACCTCATGA | 9678 |
| rs555205694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014414 | AGGGAGATTATCCAA[A/G]GAATGACAAAATTGG | 9678 |
| rs555209064 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:10995766 | ACTGCTGGGGGACCC[A/G]GTGCACCCTCCACAG | 9678 |
| rs555209380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974672 | CTGTCCAGCCCTCCC[C/T]ACCCTGCTTCTGCAC | 9678 |
| rs555222179 | snp | A/G | | | | | GRCh38.p7 | 7:10970346 | GAGGCTGAGGTGGGC[A/G]ATCAGTTGAGGTCAG | 9678 |
| rs555223972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043993 | GTTTCTGCAGCTAAA[A/C]AAAAACACACACAAA | 9678 |
| rs555291142 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025999 | TGCCTGTAACCCCAG[C/G]TACTCAGGAAGCTGA | 9678 |
| rs555294633 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | PHF14 | GRCh38.p7 | 7:11017295 | TGGATTATATGGCAG[C/G]TCAATTTTTAGGAAC | 9678 |
| rs555304069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11003174 | TTGATCTCCTGACCT[C/T]GTGGTCCGCCCGCCT | 9678 |
| rs555317827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124879 | CTTCTAATCGGAAAG[A/G]GAAAAATATTATTAA | 9678 |
| rs555319143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054106 | TATCAAAAAAGCATT[C/T]TTTAAGACACTTTTT | 9678 |
| rs555327354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084416 | ACTTCTTTCCTCTAA[A/G]TACAAACAAAATATT | 9678 |
| rs555335180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011697 | GCAATGTGTTCATTA[C/T]TATATATGCTTTAGA | 9678 |
| rs555337419 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972573 | AATATCTGAAAGGCA[A/G]TGAGGAGTATTAAGC | 9678 |
| rs555356121 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11021604 | AGGTTTATCAGAGAT[A/C]AACTCCTACAGAGTA | 9678 |
| rs555394007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11079079 | ATCCTAAACTAAGAT[A/G]AATTAAGGTTATCAG | 9678 |
| rs555394937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11022192 | TTTGTTTTAGTCTTA[C/T]AGCATCATTCAAACT | 9678 |
| rs555399903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956691 | GAGGGACACACAGAC[A/T]CAGACACACACAGAG | 9678 |
| rs555431606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110128 | GTCCCTTTTATTATG[A/G]TGGTTTCTTAAAGTC | 9678 |
| rs555433136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118510 | CCACTAATTATAGTT[A/G]GTACTTTGCTTTAAA | 9678 |
| rs555454092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11117598 | AAATATGTATTTATA[C/T]GTATAAATACAAATA | 9678 |
| rs555463008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144978 | TTTGTGTGGTATAAA[C/T]GGGAACAGAGTTTTA | 9678 |
| rs555478817 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990887 | TTTTAGAAATGGCTG[A/C]CTGTGGCTCTTTTAC | 9678 |
| rs555490867 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990044 | TAGCAGCTAGTCAAT[A/C]TGGATCCTTTTTTAG | 9678 |
| rs555497021 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103454 | TCTGTATCTTTCCAG[A/C]GGTATACAGAATTAA | 9678 |
| rs555510317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122783 | GCCCTATAGTTCCAG[C/G]TTAGTCCAGTCCTGC | 9678 |
| rs555513079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059927 | CAGGCTTGGAATGCA[G/T]TGACTTGATCATGTC | 9678 |
| rs555513929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11011233 | GCTCTTTTCCTTTCT[C/T]GTGGGTGATTTGTTT | 9678 |
| rs555521600 | snp | C/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075995 | AAAGTAAAAATTAGC[C/G/T]GGGCATGGTGGCGGG | 9678 |
| rs555561166 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960198 | TGCACCCATCAACTC[A/G]TCATTTACATTAGGT | 9678 |
| rs555594002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977200 | GAAGTTGTGGATTCC[C/T]AGCCCTACTTACGAA | 9678 |
| rs555601988 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977806 | CCAGTTTTGTAGGTC[C/G/T]AAAACACACAGTCAA | 9678 |
| rs555617113 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999792 | GACAAATGAGATGAT[C/G]AAGCTGAGTGGTAAT | 9678 |
| rs555637325 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11116824 | TACAAAGTTTTGAAG[C/G]TAAAAATTAACTTTT | 9678 |
| rs555646267 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11039338 | TGTATAAGAGATGGT[C/T]TTTTAAACTTTAATG | 9678 |
| rs555663467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11005895 | CCTCCTGGGTTCAAG[C/T]GATTCTCCCGCCTCA | 9678 |
| rs555669810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027811 | TTCCAAGCAATTTTA[C/T]ATTGTTTAAGAATTA | 9678 |
| rs555679241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085014 | TGTTTGTTTTTGCTT[C/T]ATTGCTAATGGTATG | 9678 |
| rs555688322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033581 | TATGCCCAGTAAAAA[C/G]TCATAGGGGTCTAGT | 9678 |
| rs555691910 | snp | C/T | | | | | GRCh38.p7 | 7:10970175 | CATGCATAAATATCT[C/T]GAATTTGAATACCTG | 9678 |
| rs555694482 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072988 | GGGATCTGCCCCTGT[A/G]GTCCAAACACCTCCC | 9678 |
| rs555724671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157510 | TCTTAAGTACCTCTT[C/T]TTCCCTATATAGTAG | 9678 |
| rs555727663 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971852 | AGTTAAAAAAAAATG[A/C/G]TTGCTGATATCCAAT | 9678 |
| rs555727687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965954 | ACTGTGGGAAAAGTG[C/T]AGTATTTGGGCAGGA | 9678 |
| rs555748617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006163 | TGTACTAATTACCAA[A/C]AATGCACAAACTACT | 9678 |
| rs555759926 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10994630 | AATTGGTGGGTTCTT[C/G]GTTTCACTAACTTCA | 9678 |
| rs555784246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151615 | TAACTGTAGCATTGT[A/G]TCAGAGTTTTGTAGT | 9678 |
| rs555785418 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11164536 | GCATTTGTTTTCTTA[-/T]AAAATCTGTTCCCAT | 9678 |
| rs555787182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966256 | AGCTTTATTGAGAGA[A/C]AGAACAGCTCTCAGT | 9678 |
| rs555797886 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066484 | GTTATTTCCTATCTA[A/G]TAATTCTTTGCTTAG | 9678 |
| rs555812628 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104105 | GAAATTACTCGCAGT[A/T]GCTTTATTTTAGGTT | 9678 |
| rs555815165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034693 | AGCTGGGATTACAGG[C/T]ACATGCCACTGTGCC | 9678 |
| rs555815262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156780 | GCCTGGTCATAGAGC[A/G]AGACTGTCTCAGAAA | 9678 |
| rs555830435 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155773 | AATGTTTTTTTTTTG[-/T]TTTTTTTTTAGCAAC | 9678 |
| rs555846069 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131329 | TTTGCCAGCATTGAT[A/G]CTGTCAGTGTTTTAG | 9678 |
| rs555848434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073028 | ACCTCCAATATTGGA[C/G]ATCACATTTCAGCAT | 9678 |
| rs555883351 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10995316 | CACCAGATTAGCTAG[A/G]TACAGAGTGCTGATT | 9678 |
| rs555901203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130732 | TGTGGTACATTCTGT[A/G]GGTTTTGACAGTTGT | 9678 |
| rs555909386 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11083643 | CTTCTTTGTATTTTT[A/T]GTAGAGACAGGGTTT | 9678 |
| rs555922595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984215 | AGCAGTGATTATCTA[C/T]TTTAATTGCTTTGCT | 9678 |
| rs555928626 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016206 | TGTGCTAATGTCTAC[A/G]CTTACCTGTAGGCTG | 9678 |
| rs555957962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11084920 | TATCTTTGGAGATTT[C/T]TTTTTCTTTTTTAAA | 9678 |
| rs555967278 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044154 | GTCATGGACATAAAG[A/T]TGGGGCCTACTAGAA | 9678 |
| rs555968171 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11041300 | TTGCTCAATATTTTC[G/T]GTGTTCACCATTATA | 9678 |
| rs555978409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117691 | TTGTGTCTTTAAGAA[C/T]GGAACAATCTCTTCA | 9678 |
| rs556012050 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10971213 | GGAAAAGTTCAAGCC[C/T]CTTCATTTAATATCA | 9678 |
| rs556017969 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10969985 | CCATTTCTGAATATA[A/G]AACTCTGCTTTTCAT | 9678 |
| rs556034769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965905 | TTGCCGAGCCAGGCA[C/T]GGGAGGGAATCCCCT | 9678 |
| rs556035106 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960897 | TCTTCTTTTGAGAAG[G/T]GTCTGTTCATATCCT | 9678 |
| rs556054091 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991483 | CCCGGCCAATTTTTG[C/T]GTTCTTAGTAGAGAT | 9678 |
| rs556060069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144349 | TAACTTATAACCCAG[C/G]AATCACACTACTGGG | 9678 |
| rs556060133 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11129494 | AAGAACACTGGCATT[C/G]TCTAAGGGTATAAAA | 9678 |
| rs556061641 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11163709 | AACATTTTCATTATC[A/G]TCAGTATTTTCCAGT | 9678 |
| rs556065055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10994913 | GGAAGGGGACCCGAG[C/T]GGGTTGCCATTGCTG | 9678 |
| rs556083327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047179 | GTGCAAGCAATTCTC[C/T]TGCCTCAGCCTCCCG | 9678 |
| rs556089120 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123175 | ATACCACACCCATTT[C/T]GCAACAGGAAATCTT | 9678 |
| rs556108184 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11084348 | GTTATTTTCTTCTTA[A/C]ATCCTCTAAACCTGT | 9678 |
| rs556132168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11155857 | GAATAGATGGCTTAT[A/G]TAGCTTGCTGGAGAT | 9678 |
| rs556159480 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11131229 | TCATATGGTAAGAGT[G/T]TGTTTGGCTGCCAAA | 9678 |
| rs556171095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040858 | GAAGATCCTGCAAAT[A/G]TTTGAGAATGAATTA | 9678 |
| rs556185469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961964 | TGTCAGCAAACTTCA[A/G]CCCAAAAGGAGATTT | 9678 |
| rs556203238 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046752 | TAGGAGGGACTGAGG[C/T]ATTACTTGTCTGAGA | 9678 |
| rs556220698 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131996 | GTGTATATTTAAGGT[A/G]TACAACATGGTGTTC | 9678 |
| rs556225021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123939 | AAAAAAACTAGAAAG[C/T]AATAATTCAAAATAG | 9678 |
| rs556238176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027673 | TGTATATTACTACCA[A/T]TTTCACCTGATTATT | 9678 |
| rs556251537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165069 | AGCTGGGACTATAGG[C/T]GCCCGCCACCACACC | 9678 |
| rs556262342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071941 | TATTAAGAGCCTAGA[C/T]TCTATTACATTTCAA | 9678 |
| rs556275515 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11034801 | TGATCTGCTTGCCTC[A/G]GTCTCCCAAAGTGCT | 9678 |
| rs556295123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027322 | TATATTAACTAGGCA[A/G]TAGGATGTCAGGATT | 9678 |
| rs556301611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128973 | TTTTTTTGTCATGCT[A/T]TTGATCTTTTTATAT | 9678 |
| rs556321867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009616 | AGTCACTAATTAAAA[C/T]GAATTGGAGCAGATA | 9678 |
| rs556333559 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976819 | TATTTACTTTCTGTT[A/C]CCTCTTGTAATATAA | 9678 |
| rs556363751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144837 | TTTGCCAAGTAAAAT[A/G]GCCAGTCACAAAAAG | 9678 |
| rs556369217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129729 | TCACTAGGTGCTTCA[C/G]ATGTAGTAAGATGAG | 9678 |
| rs556376852 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11021047 | TACTGATACAGAGCA[C/T]TTCAAACTCCAATTT | 9678 |
| rs556385869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038709 | AAATGTAGATATTTC[C/T]TAAATTGTCAGATAT | 9678 |
| rs556396339 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11133390 | AGCCCAGAGATAGAC[C/T]CACATAAGTATAGTT | 9678 |
| rs556423254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11137946 | TTATACCTAGCTCTT[C/T]CCTTGTATAAAGTAC | 9678 |
| rs556439343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045451 | TTGCAAGCCTGTGGT[A/G]GCACCCTTACTACTA | 9678 |
| rs556448581 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155259 | ATTTTTGGGTAGTGT[A/G]GGTATCAAAGTTAGG | 9678 |
| rs556458859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096762 | ATCTTCCCACAGGAC[A/T]GTCATGGTGATTAAT | 9678 |
| rs556461837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004098 | ACAAAATACAGAAAA[A/G]TCAGCCAGGTGTGGT | 9678 |
| rs556470339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090501 | GCAAAATTGCCTGAT[G/T]ATATCAAGGACCTTG | 9678 |
| rs556486141 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021077 | TTATTGATTAATATA[C/G]TTTTCATTCTTAAAT | 9678 |
| rs556489349 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955931 | AAATAAATTAAATCA[A/G]TAATGGAAGAAATTG | 9678 |
| rs556495110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120553 | AATGTCCATTTGTTA[C/T]AATTTCTTGGTAGCA | 9678 |
| rs556528070 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153509 | TGGAATATGAGTTTA[A/C]AGCATGGTATAGATG | 9678 |
| rs556528849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965260 | GTTTTGGTGTGGATG[C/T]CCTTTTTGTTGATGT | 9678 |
| rs556533702 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116625 | CCCTCTACTCCTGCC[C/G]ACATGGATACCTACT | 9678 |
| rs556542577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011040 | TGCTTGAAGCAGCTT[A/G]TGTAAGTCATAGCTG | 9678 |
| rs556550295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024404 | TTTGTACATTCAACA[A/G]AGATTTTCAATGTAG | 9678 |
| rs556551730 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168879 | ACAGGAACCTGCTAT[A/G]AATTATGAGGCCACC | 9678 |
| rs556559910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998408 | GAATAAGGAAACATA[C/T]ACCTAAAATATATAT | 9678 |
| rs556575511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077016 | AAAATGCCATGTGTC[A/G]TGTTTAATTCATATA | 9678 |
| rs556611692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109463 | TGATTTTTAAATTTC[A/G]CATCAAAGATGATTA | 9678 |
| rs556615641 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10994872 | GATTTATTGCAAAGA[A/G]CGAAAGAACAAAGCT | 9678 |
| rs556616884 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10989046 | TTCAGTTTTATTTGC[C/T]AGCCATTTGTCAGCC | 9678 |
| rs556620455 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11162908 | AGGAGGAGCTAAAAA[C/G]TTACTCTACTCAATC | 9678 |
| rs556650284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021591 | GCAGCCAGCTGTTAG[A/G]TTTATCAGAGATAAA | 9678 |
| rs556671577 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160395 | TTTTTGGTAGAATGA[A/T]TTATTTTCTTCTGGC | 9678 |
| rs556702942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125906 | TGGCTGCAAAAGATT[A/G]TGTGCTTCACTGGTT | 9678 |
| rs556703457 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11088957 | GGAACAAAAAATGAG[C/T]ATGGTATTATTTTAG | 9678 |
| rs556721059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007167 | CATTGCACTCCAGCC[C/T]GGGTAACAAGAGCGA | 9678 |
| rs556728454 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989584 | GCAAACAAGCAGACC[C/G]TCTTCTGAAATTTTA | 9678 |
| rs556734335 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103291 | AATACCCAAATATAT[G/T]CAGTCCTTATTGTTT | 9678 |
| rs556759584 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107057 | TTTGCATAGGAGGTG[C/T]ACTTAATTGTTTCAG | 9678 |
| rs556773761 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001304 | TTACTGCAGCTTCAT[A/G]GTAAGTCTTGAAGTT | 9678 |
| rs556797570 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067680 | TAAAGAAGGAAATGT[G/T]TATTTGGCTCACAAT | 9678 |
| rs556816486 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019271 | GTTTGGAAATATTCC[C/G]TCTTCCTCTGTTTTT | 9678 |
| rs556818613 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011921 | TCTGAATGAAATACT[C/G]TCTCAGAACTTTTCA | 9678 |
| rs556829530 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11119795 | AAGAAAACTTTCAAA[A/T]CTAAGCCAAGAAAAT | 9678 |
| rs556844754 | snp | C/T | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10970546 | ACTACACACTCCAGC[C/T]GGGGCAACAAAGCAA | 9678 |
| rs556852370 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169746 | AACAGAGACAGAATG[C/T]TATTTTTTTTGTAAC | 9678 |
| rs556863613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086107 | TATTCTCCTTCATCA[A/G]CTCTCTCCTGGACCG | 9678 |
| rs556869017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112898 | AAGAATTATTTTCCA[A/G]GCATTTTATTAAGGC | 9678 |
| rs556871945 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079231 | TGACCTCATGTATTA[C/T]TAATAAAATATCCAG | 9678 |
| rs556920887 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043061 | GAATTCTGTCCATTG[C/T]TTATAATTCTCTTGT | 9678 |
| rs556926377 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082160 | AGTAGCCTAGGCAAT[A/G]TATCGAGACCTTGTC | 9678 |
| rs556939778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098411 | TCTTGCCGCCTTTCT[A/C]TGTTCCTCACTTCTG | 9678 |
| rs556988438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958170 | AGAATGAAAATTTCG[C/T]TTTCATGGTACTCTT | 9678 |
| rs556993269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012483 | GAAAGAAATCTGCAT[A/G]TAAGTGCACCTGACC | 9678 |
| rs556993694 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139360 | TTCTTCTGCTATTTG[G/T]AGAGTGTTTGATACA | 9678 |
| rs557011936 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992490 | CAACATGGCGAAACC[C/G]CATCTCTACTAAAAA | 9678 |
| rs557013891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10986532 | AGTTCACTGGACCAC[A/G]CCTTGAGAACTGCTG | 9678 |
| rs557016515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018891 | TCTGTCATATATCGC[C/T]TTTATTATGTTGAGG | 9678 |
| rs557045334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979698 | TTGTAAATAAATATG[A/G]TTTATCTCCATTCCT | 9678 |
| rs557045368 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:11162061 | TCAGCAGGATATCTT[-/A]AAAAATATGTCTTTT | 9678 |
| rs557057145 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169802 | CTAAAAAAAAAACCT[C/T]TGAAAGTCTTTTTTC | 9678 |
| rs557078894 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006922 | GCTCACACCTTTAAT[C/G]CCAGCATGTTGGGAG | 9678 |
| rs557086974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990190 | GTCCTTAAGTGTGCC[A/C]TCACATACATACTTG | 9678 |
| rs557096375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018078 | AGTTCACTTAGGTGC[A/G]TGGATTTGTTTCTGA | 9678 |
| rs557100334 | in-del | -/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11136254 | GGATGCTGTTAAATA[-/G]TTCTGGTCTGTCAGA | 9678 |
| rs557119303 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010177 | CCCATGTGGTATTGC[A/G]TAGCACATGGAGAAA | 9678 |
| rs557122292 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10987120 | ATTTGGGACTTCTAA[C/T]TTATTAATCAGTTGT | 9678 |
| rs557129739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073426 | AAAACAATGTCCTTC[A/G]ATGCCATATCCTGCA | 9678 |
| rs557147560 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973259 | CGCGTTACTTCATTT[A/T]CATGAGGTGAGCATT | 9678 |
| rs557150765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049070 | ATATTTCAGTTTTTA[A/C]AACAAAACAAAACAA | 9678 |
| rs557166230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035875 | CCAGTGACATGTGAC[A/G]TATAATAGGAAGTTT | 9678 |
| rs557170587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957278 | AAAAACTGTTGTATA[C/G]ATTTAGAACAATGTT | 9678 |
| rs557175860 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139871 | TATTCCTAATAATAT[G/T]CTAATGCATCATTGT | 9678 |
| rs557179460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967301 | TGCCACTGTTGTTGG[C/T]AGTGATTTGGCTCCC | 9678 |
| rs557179521 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079764 | GATATACAAAATCAT[A/T]TAGCTGTATTATCAA | 9678 |
| rs557195777 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037930 | GAAAATAGTGGAAAT[A/T]CATCTTGAGAGAGTC | 9678 |
| rs557200996 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995836 | GGCAGTGCCCGCCAA[G/T]CCCATGCCCACCCGG | 9678 |
| rs557202111 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055758 | TTTAACTAATTTTAC[A/G]CATATACAAAGTACC | 9678 |
| rs557209857 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104702 | GAAGGATTTGTAAAA[A/G]CACAGGTGACTACCC | 9678 |
| rs557222771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092226 | TTTTTCTTTGTGGTT[A/G]CCTTCATCCCAGCTA | 9678 |
| rs557242819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968053 | TATATACCAACTATT[A/G]TATCAGACAAAATTA | 9678 |
| rs557255932 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11112342 | GTAATCAAAAACATT[C/T]TTTTATCATTAACTA | 9678 |
| rs557265020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097714 | CTTCCCTTCACATTC[G/T]CAAAGTTCATTGTTG | 9678 |
| rs557271076 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105231 | TTATATTTATGCATT[A/G]TTTATAGATCATTGT | 9678 |
| rs557281313 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998366 | TGGGGAGGCAGAGTT[A/G]TATAAATTTATTTGG | 9678 |
| rs557303658 | snp | A/G | 1.70475e-05 | 0.0029195 | intron-variant | PHF14 | GRCh38.p7 | 7:11035814 | TGTCAAAACCCGTAT[A/G]TTTTTGTTTTAAGGT | 9678 |
| rs557304239 | snp | A/C/T | 0.00199529 | 0.0315338 | intron-variant | PHF14 | GRCh38.p7 | 7:11074567 | ATTCATAGGCTGTTA[A/C/T]AAGCAGCCAGGCCAC | 9678 |
| rs557313156 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10978052 | GGCAAAGTAAAATGG[G/T]GTTAACTTTAGATCT | 9678 |
| rs557318754 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069152 | CTGAGTATTACATTG[G/T]TTCCCACTGAACAGC | 9678 |
| rs557332048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158793 | TGTCATAGTTGCTTA[C/T]AGATTAGCCTGAAGT | 9678 |
| rs557362812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957232 | TTATTTGTTTTTCAT[A/T]TTTTTCTGTTATATT | 9678 |
| rs557364333 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020239 | GGTTATAGGTGTGCG[C/G]CACCACACCAGGCTA | 9678 |
| rs557381571 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114841 | AGCCATTGATTAAGA[C/T]AGCAGCCACCCAGAC | 9678 |
| rs557389073 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133481 | AATATATTTTTAATG[C/G]AAAATGGTTGGGCAT | 9678 |
| rs557422184 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055285 | GTGGACATATTTTCT[A/C]ATACTCTAATGTAAC | 9678 |
| rs557424838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957970 | ATAGTGGTGATGGTT[G/T]TACATTTTTTATATA | 9678 |
| rs557453347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153473 | TCCTTATTAAAAAGT[G/T]TATTGGAGACAAGTA | 9678 |
| rs557466432 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11166294 | CAGGGTCTTCTTTCA[C/T]TGGGAAACAAACAGA | 9678 |
| rs557484365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119619 | AGTGAGATTGCATGC[A/G]TTGTAGATGTAGATA | 9678 |
| rs557485302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118438 | TGTCTTTTAATCCCT[C/T]AGTTTCTAATTGAGT | 9678 |
| rs557498304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139129 | AGTTTCACTGAAATT[G/T]GCAGTAGAAAGCAAT | 9678 |
| rs557508690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11012379 | TCAAGTCCCACAGTC[A/G]GACCTGGGGAACTTG | 9678 |
| rs557549787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111639 | CTCTTAAATTAAGGA[A/T]AAAACAACTCTACTA | 9678 |
| rs557557816 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023819 | GGCGACAGAGTGAGA[C/G]TCCATCTCAAAAAAA | 9678 |
| rs557558744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028343 | GTAAAGTTAAAAAAT[C/T]AGAAGTGGAACTGTT | 9678 |
| rs557565739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030272 | GTAAGAGTTAGAGGA[C/T]CAGATAAATACTACG | 9678 |
| rs557579864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041492 | CATACATATATGTTA[C/T]GCATGTGTAAATACA | 9678 |
| rs557595389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028913 | AATAAAAGAAATTTT[A/G]ACATTTATTCTTAAA | 9678 |
| rs557602602 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024327 | GAAGAAGATGCAGCA[C/G]GTACTGATGGAGAAG | 9678 |
| rs557606802 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112696 | GAATCACTTGAACCC[A/G]GGAGGCAGAGGTTGC | 9678 |
| rs557618396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11042184 | TATTGAAAAGAGACT[C/T]ATGTATACTTGCAGT | 9678 |
| rs557662663 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018753 | CTGTTGTCTGATTGC[C/T]GGAAGCTAGGGCTTC | 9678 |
| rs557689009 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11119210 | TCGCAAACCTCATAC[A/T]GTCCTGTAGTTTAAA | 9678 |
| rs557715713 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11074158 | TTTAGCAAATGGTTG[C/G]TCCACAACCACCTTG | 9678 |
| rs557717039 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11048299 | TGATTTCAGCTGGGC[A/G]TGGTGGCTCACGCCT | 9678 |
| rs557724007 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164411 | GAAAATAAAAATCAA[C/T]AATATCAACATTATG | 9678 |
| rs557725594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967242 | GACATGGGATGAAAT[C/T]AATTTAGAGTAGTAG | 9678 |
| rs557735806 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | PHF14 | GRCh38.p7 | 7:11006851 | GGGACAGGAGCTTCC[G/T]TCACTTTCGGCACTG | 9678 |
| rs557743844 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11029756 | TGTGAGCAGGTTCAG[G/T]TCATTCCTTAAGCTT | 9678 |
| rs557753577 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104659 | ATAGCAAGTAGTGGT[A/T]CTCAAACGTTGTGCA | 9678 |
| rs557801921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112266 | TATGGACATCCAGCC[A/G]TCTTTCTTCAATGCT | 9678 |
| rs557806157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991375 | TAGAGATGGAGTTTC[A/G]CCATATTGGTCAGGC | 9678 |
| rs557813582 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001574 | TTTCTTTCATCAGAG[A/T]TTTGCAGTTTTCTTC | 9678 |
| rs557829809 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975582 | GTATGATTTTCCTTT[A/G]TATTTTCTGTTCAGT | 9678 |
| rs557866229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985738 | GCTCACTGCAACCTC[C/T]GCCTCATGGGTTCAA | 9678 |
| rs557890348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000396 | TCTGGCTGGAGTGCA[A/G]TGGTGGGATCTTGGC | 9678 |
| rs557897146 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053006 | GCTGGCTTACAGTTA[C/T]GAATTCTTAGGGCAT | 9678 |
| rs557913781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006272 | TAAGAATGAAGTTTG[A/G]CATCTTGTGGCCATT | 9678 |
| rs557925352 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106216 | CCACTCTTTAAGTGA[C/T]TATTAAATACAGATT | 9678 |
| rs557946974 | in-del | -/TTAAG | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11100516 | ATGATATTATGTAAA[-/TTAAG]TTATGTATTAGAATA | 9678 |
| rs557950565 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964351 | GCTTAGTTTGGCTGG[A/T]TATGAAATTCTGGGT | 9678 |
| rs557965534 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972675 | CAGGGTAACTGTTTC[G/T]ATTTCAGATGAGGAG | 9678 |
| rs557975461 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125010 | GAAGATGAATGTGGA[A/G]GATGAGGTAACTCAA | 9678 |
| rs557976017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146552 | TACCCCTGACTACAA[C/T]CATGTAGAGATAATT | 9678 |
| rs557977041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966879 | TGAAAACACTGTCTC[C/T]TTCAGGGTCAGAATT | 9678 |
| rs557989746 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078162 | TTTATCCTTATTCAC[A/T]TATTCTCTAGGTGGC | 9678 |
| rs557989989 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106438 | GTATAGAAACTGCTC[A/G]TGTAGGTAATTTGCA | 9678 |
| rs557996188 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11085116 | TATGTTATGAAATAG[A/G]CAACAGATATATATT | 9678 |
| rs558006203 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11151072 | AATAGAATCTTAGAC[-/A]AAAAAAACCTGTCAT | 9678 |
| rs558016352 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11001087 | ACGAGTATACGGTCT[G/T]TCTCGGAATTCATTA | 9678 |
| rs558032645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034177 | TTTCTTTCTGTTCTT[A/G]TATGTCTCTCCTCGG | 9678 |
| rs558069560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165784 | AACCGAGGGTCTCCT[C/G]TATCACAAATTGATA | 9678 |
| rs558111926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961862 | TTCACTTGTGATTTG[A/G]ATCTCTGTTTTTCTG | 9678 |
| rs558114918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152169 | ATAATCTGGTCAGTA[C/T]CCATTGAGCAAAAAT | 9678 |
| rs558127411 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104297 | TCACATGTTATACAT[A/T]TAGACTGCAAAATTC | 9678 |
| rs558127983 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044673 | TATTTTTGAAGTTAT[A/G]CTAAAGATAATAAAT | 9678 |
| rs558130101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101354 | CTATTATAAATGATT[C/T]GGTTGCTTCCTCTTG | 9678 |
| rs558142659 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105814 | GTAATTGGATGCACA[C/T]GCTGGGCTTTGTAAA | 9678 |
| rs558157229 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048605 | TTATTTGATTTCATT[A/G]AATTAGACAGGCCAT | 9678 |
| rs558165298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118346 | TCCTCTACTGTAGAA[C/G]AAGGTCCTCAACTAA | 9678 |
| rs558174281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11060689 | TCAGAATTGTAGATG[C/T]AGGATCTGCATTTAA | 9678 |
| rs558189145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015281 | TGATCCTTGAGAAAT[C/G]TTGCCATACAAGATT | 9678 |
| rs558190841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977208 | GGATTCCCAGCCCTA[C/T]TTACGAATAGGAGAT | 9678 |
| rs558194042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028879 | TCTTTTGACTCTATG[C/T]CCTATAATAAGTGTA | 9678 |
| rs558195835 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11075190 | GCAATCCTTCTGCCT[C/T]ATCCTCCCAAAGTGC | 9678 |
| rs558211300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061480 | GAGTAAATCATAATT[A/G]TGGACAATTATGAAG | 9678 |
| rs558217756 | snp | A/C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032541 | AGACCAAATCATGGC[A/C/G]TCTAGAGGACCACAA | 9678 |
| rs558221032 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11097511 | CAATTTAATTTCTTG[A/G]TGAATTAGGATTCAA | 9678 |
| rs558235872 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11115457 | CAGGTACATAAAACG[G/T]CACACATACATATTT | 9678 |
| rs558247366 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054304 | TTTAGGGGTTTGACT[A/C/T]AGCAGATTTCTTAGG | 9678 |
| rs558254012 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977940 | CTACATTAATTGAAT[C/G]TTTTAAAGAATGTTT | 9678 |
| rs558275352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008887 | AAAAATACAAAAAAA[C/T]TAGCCGGGCATGGTG | 9678 |
| rs558281596 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115195 | CTTTTTTCCACTACT[A/G]CTGTCTTGATTTAGT | 9678 |
| rs558287461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997432 | TTTTTTTCTTTCTTA[C/T]TTTAGATGCTGTATT | 9678 |
| rs558312705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077856 | GTAAGAACATTATCT[A/G]TCTCAGAATCTTCAT | 9678 |
| rs558347598 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040700 | CGGCAATTTTGCGAG[C/T]ACCCAAGGAGAGAAA | 9678 |
| rs558364791 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11046664 | AGGTATTATAACTAC[-/A]AAAAGAATAAAATTT | 9678 |
| rs558366484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11117574 | TAACTATGCCCAAAC[A/G]ATATATATAAATATG | 9678 |
| rs558385374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11051422 | AAATTGCCTTAAATA[C/T]TATATTCATAGTAGT | 9678 |
| rs558390124 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11024127 | GGAGAAAATTTTAAT[A/T]GTAGGGATAGATCAT | 9678 |
| rs558393232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072962 | ATGGGTTTAGTGCCA[A/G]GCATTCATGAGGGAT | 9678 |
| rs558416599 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065575 | GCTTGATAAAGGACA[A/G]TTGATTTTTTGTCAC | 9678 |
| rs558416687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088275 | TGTATTGCTATTTTT[C/T]ATTGGGTTTATTTTT | 9678 |
| rs558450549 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064084 | TATATTTTAATATTT[C/T]TTAGGACAAGATAAG | 9678 |
| rs558458438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022295 | AAAATGTGAATTGCT[C/T]ATTCTGTACCTTTTC | 9678 |
| rs558460246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108484 | GCCTATCACCCCTAA[C/T]TCTGACAAGCAAATT | 9678 |
| rs558479819 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016643 | ATGTATATTCATGGG[A/G]TACATGAGATGTTTT | 9678 |
| rs558490460 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067117 | CTTGGACAACTCAGC[A/T]ATAAGAAACAACCCC | 9678 |
| rs558503234 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119366 | CCCAGCATTTGAAAT[A/G]TTAAAATAAGGTTAT | 9678 |
| rs558508765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158052 | GTTAACATCTTATAT[A/G]AGCATAGAACAATTC | 9678 |
| rs558511219 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974138 | GCCAGGCGAGGCCGG[G/T]GGGGCGGGGGGTTAG | 9678 |
| rs558511329 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968289 | TGCCCTTATACCTTT[A/G]AATTAAGCTAGTGAA | 9678 |
| rs558516460 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073619 | TAAGGTCTGGAAGGC[-/A]ACAGCGCCCTTCCCA | 9678 |
| rs558518789 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988171 | CCCTATTTCCCTCTT[G/T]GCGTTACATTTCTAT | 9678 |
| rs558539521 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11070217 | TTAGTAGCTGTGACT[A/G]CAAGTGCGCGCCACC | 9678 |
| rs558544683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020238 | AGGTTATAGGTGTGC[A/G]CCACCACACCAGGCT | 9678 |
| rs558565650 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149351 | AACTTAGGAGACATA[A/G]ATTCAGATTCTAACT | 9678 |
| rs558578302 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11057634 | CCGCCTCGGCCTCCC[A/G]AAGTACTAAGATCAC | 9678 |
| rs558579796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065233 | AGTTCTCAACTAAAT[A/G]TATATTTCTTTATGC | 9678 |
| rs558597705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975033 | GTTTTGATTAAAATG[C/G]CAATTTTAAGTGAAA | 9678 |
| rs558611239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987780 | ACGTCTTCAGAAATA[C/T]ACTAACAACAGTTGA | 9678 |
| rs558621320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11143328 | GTCTCATTGTGTTGT[C/T]CAGGCTGATCTCAAG | 9678 |
| rs558631781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049788 | TTTGCCAGTCCTTGA[C/T]GTTTTCATATGGGAC | 9678 |
| rs558660644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007929 | GTGCTCACTTCATCT[A/G]AATCTCTTTTCTTTT | 9678 |
| rs558661054 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986725 | TAAGATTATCTTGCC[C/T]TTTAGTTTTCTGAGG | 9678 |
| rs558668209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11095126 | CAAATTGTAGTGATA[A/G]TAAGAGTGGTTGAGT | 9678 |
| rs558699794 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984718 | AGGAATTTGCCACGT[A/G]AAGTGTGTGTAGTAT | 9678 |
| rs558703213 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110061 | ATGAGTTTTTGGAAG[A/G]TTGGACTTTTGTATC | 9678 |
| rs558739761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964471 | GATGGGCTTCCCTTT[A/G]TGGGTAACCAGACCT | 9678 |
| rs558745448 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959640 | GTGGGCAGTTCCAGG[A/T]GCCAGCATAGGCACC | 9678 |
| rs558754221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056120 | AAACAGTTTTTGTAG[C/T]GAACTAGAACTCACT | 9678 |
| rs558775989 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11162043 | TATTCTTAGCCCCTT[C/G]AGATCAGCAGGATAT | 9678 |
| rs558781758 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161237 | GGGCCTGAGCAAAAA[A/C]AATATTTTTCTCTCA | 9678 |
| rs558795412 | snp | C/T | 0.00159808 | 0.0282221 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973716 | GGATCTCTGCTCCGC[C/T]TTGGCACTACTCGGC | 9678 |
| rs558800802 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978980 | AAATAACTAGTAGAA[C/T]AGTGATTGATCTGTT | 9678 |
| rs558801202 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958987 | TGGACGATGTAGGAG[A/T]CTTTTTAAAACGCGT | 9678 |
| rs558802176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033355 | ACCTTCCTTTAGTCT[A/G]TTGCACTCTCCTACA | 9678 |
| rs558819705 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11070776 | TTATTTCTAATGACC[A/G]TGATAGTCTAATGCA | 9678 |
| rs558828119 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11148851 | CTGAGCTCAACTTTG[A/T]ACCACAATTTTTGGA | 9678 |
| rs558838076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056917 | CATAAATCTAATGCT[A/G]TTTAGCTTAACAGAG | 9678 |
| rs558847539 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026413 | GTGATTTGTTTTATT[G/T]TGATACTTTATTGAA | 9678 |
| rs558878706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986426 | TCTGGAAAACTTCAT[C/G]GTACTCCCATGAGAG | 9678 |
| rs558886968 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998863 | TGCTGAGTACCATCT[C/G]TACTTCTTAAGTCAT | 9678 |
| rs558897809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064476 | GGTTCTCTTTTAAAA[C/T]TAAACTTCATGGGTC | 9678 |
| rs558903698 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11140217 | AGCCCTACATAGCCC[A/G]TTATACGACCCTACC | 9678 |
| rs558960473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134148 | ATTTTTTTGGGCAGC[A/G]TTCTAAGTTTAAAAT | 9678 |
| rs558970091 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119974 | GTTAATTGCCTTTTA[A/G]TATATTCATTTTTGA | 9678 |
| rs558995030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044396 | CTTCTAAAAGGGCGT[A/G]AACAACTTAGAGCCT | 9678 |
| rs558998995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120882 | ACTCATACGGAAACT[G/T]GTTTTTTACTGACGA | 9678 |
| rs559006528 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11088247 | AGTTGTTATACCATA[-/T]TTTTTTTATTGTTGT | 9678 |
| rs559013670 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11003529 | ATATGTTGTTATGGG[A/T]TACATATAGATAGTA | 9678 |
| rs559021410 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127443 | TGCTCTTTAACGGGC[C/G]CACATTTTGTCCTAG | 9678 |
| rs559035288 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957357 | GAGCAGAAGGTATCA[C/T]TGTGCATTTTTGTTT | 9678 |
| rs559042350 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11134330 | TAGAATTTAATAGCT[A/G]ATATGGACCTGAAAT | 9678 |
| rs559046405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043542 | TAAATGGTAATCTCT[A/G]CAAGAGGTTGTGTGT | 9678 |
| rs559047225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099205 | TGATCTTGTTAGACA[C/G]ATGGAATGGCTAACC | 9678 |
| rs559079412 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037519 | TTGCTATAGAGCTTC[A/T]CTTTCTAAGTTTGTA | 9678 |
| rs559086885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128129 | TGGCCAGAAATAACA[C/T]AAAATATATGTACTT | 9678 |
| rs559102164 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013204 | TTTGCTCTTGGCACC[A/C]AGGCTGGAGTGCAGT | 9678 |
| rs559127863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024055 | AAGGAAATTGAAAGT[A/G]CTACTCCAGCAAACA | 9678 |
| rs559158851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113037 | TAAATAGTTGTCTTA[C/T]GAGTCTCTTTAATAA | 9678 |
| rs559164663 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998130 | AAGGTTTTGAGTGCA[A/G]GATTAGAGGGGATGA | 9678 |
| rs559192636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11092504 | AAATATCACCTATAG[A/C]AGGAATTACAGAAAA | 9678 |
| rs559194369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955970 | CAAATAATGTTTAAG[A/G]GTATTTGTCAAAATG | 9678 |
| rs559210993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018868 | TTCAGTACGATACTA[A/G]CTGTGGGTCTGTCAT | 9678 |
| rs559216229 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11024471 | GGACTTACCATAGCT[A/G]GAGAGGAGAAGTCAC | 9678 |
| rs559216310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11018497 | AGGTATTTAATCTTA[C/T]GTGTGGCTATTGTAA | 9678 |
| rs559218925 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106974 | CATAAAAATGTACAT[A/C]CTTGTTCAAGTCTAT | 9678 |
| rs559219197 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049174 | TAGACAAACAACATA[G/T]TTTAAAAGTAAATTA | 9678 |
| rs559249510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019190 | AGATACTGGCCTGTA[A/G]TTTTCTTTTTTTGAT | 9678 |
| rs559313063 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165407 | TTAACCTTGACCATT[C/T]GGTTAAGGTGTTGTT | 9678 |
| rs559322981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099855 | CACCATTCATCTGAC[A/C]CTTGATTTATCTGCC | 9678 |
| rs559328789 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983229 | TAAATCACTCTACAC[A/G]TTGTATTAAGTGGCT | 9678 |
| rs559387050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979967 | ACAAACATAAAACAT[G/T]AAAAATTTTTTAAAA | 9678 |
| rs559393274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092733 | GAGGATGTCATGAGA[C/T]CAAGAGCTCCATTCT | 9678 |
| rs559403678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127121 | TAATAGTCTTTTTTT[A/T]AAATATCAAAGTCCA | 9678 |
| rs559406617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11001703 | GAAAGCAATTGGCTT[C/T]TGTATATTAAGTTTG | 9678 |
| rs559407321 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110711 | ATTGGGGTAGTGTCT[C/T]ACCTCTTTGTATATT | 9678 |
| rs559424556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080391 | CCCCCCTCAGAATTA[C/T]AGAATTTTTCATAAA | 9678 |
| rs559432896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11119343 | TAAAAGTATTTTTAC[C/G]TTATTAACCCAGCAT | 9678 |
| rs559446425 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140592 | TGAGCTATGGATTTA[C/T]AAATTTCTTGTTTTT | 9678 |
| rs559462462 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974251 | CGCGGCCCCAGTCCC[C/T]GACCTCGGCGCTGCC | 9678 |
| rs559473868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985168 | TCTTATTTGTATGAT[C/G]TTAATTTTGTGAAAA | 9678 |
| rs559474069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977445 | CTATAAAACTTTTTA[C/T]ATTTCTGTTTGGTTT | 9678 |
| rs559477735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074595 | CACATCTTAACTGCT[G/T]CACTGCTTAGAAATT | 9678 |
| rs559479382 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025872 | ATCCCGACACTTTGG[C/G]AGGCCGAGTTGGGTG | 9678 |
| rs559480843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086457 | CTGAAATAACCTCGT[C/T]TTTTTCTCTGGGATG | 9678 |
| rs559489890 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170046 | AAATGATAATTTGAC[A/G]GTCTCTGGCAGAAGT | 9678 |
| rs559491829 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167471 | TACCTTTTATTCGTT[C/T]ATTATTCCACTGTTT | 9678 |
| rs559494080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153174 | GGCTGATTAGGAAGC[C/T]ATTGGATTAATCCAC | 9678 |
| rs559497237 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099506 | TTCAAGCACCTACAG[C/T]AGTGAAATAGTTCTC | 9678 |
| rs559499534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11002733 | ACAGACGTGAGCCAC[C/T]GCGCCCGGCCAAAAA | 9678 |
| rs559516781 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104924 | TTGATTGATAAAGGA[A/G]TGTGCTTTTAACATC | 9678 |
| rs559519878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087051 | CCAGTTTTGGGTAGC[A/G]TAAAATAAATAAGGG | 9678 |
| rs559522268 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992071 | AGTTGTATTTTTATT[C/T]TTGAGACAGAGTCTT | 9678 |
| rs559525033 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11090932 | TCAAGGGAATAAACA[A/G]ACACAAATAAAGACA | 9678 |
| rs559534595 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105761 | TTCTGTAGGCCTGCC[A/G]ATAAGATTCACTGCT | 9678 |
| rs559537293 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10978110 | TATTGCCAGGAAATA[A/G]TTTAATGAGAAGTGT | 9678 |
| rs559546681 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078587 | AGTTAAGAAGAGAAA[G/T]AAATTCAGAAATGCA | 9678 |
| rs559555078 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146983 | TTCTGAGTAGCTGGG[A/G]ATACAGGTGTGTGCC | 9678 |
| rs559560529 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002055 | TTTTTTTTTTACTTG[-/T]TTGTTTTGAGACAGA | 9678 |
| rs559579097 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137951 | CCTAGCTCTTTCCTT[A/G]TATAAAGTACAGCTA | 9678 |
| rs559581373 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159970 | GTTTGTTACATAGGT[A/G]TATTGTGTGATGCTG | 9678 |
| rs559586228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127056 | AGCTTCCTTTTTCCC[C/T]CAGTTACTCTCAGAC | 9678 |
| rs559597477 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11098532 | CTCACTTCCCCCAAC[C/G]TTCTGGCTCGTTTCC | 9678 |
| rs559599721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055621 | TTTTAGAAGGAGATT[C/T]AAACACATCTAATCG | 9678 |
| rs559609025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091398 | AATAGGTGAATAGAG[A/G]GTTTTTTTTAAAGGT | 9678 |
| rs559610434 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10986079 | GCTCAGGCAATTCTC[A/C]CACCTCAGCCTTTGG | 9678 |
| rs559621842 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123699 | ACAGGAGAATCACTT[A/G]AACCCAGGAGGCAGA | 9678 |
| rs559625056 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067016 | GAAAGGACACCATCA[C/T]CAGATGGTAAAAAGG | 9678 |
| rs559639705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995854 | CATGCCCACCCGGAA[C/G]TCGCGCTGGCCCGCA | 9678 |
| rs559649481 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104732 | CTATTCCTCTCCTGG[A/G]TCTGCCCTCTGCCCA | 9678 |
| rs559650004 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062532 | ATTAGCACTTTCTTA[A/T]TGCTTATCAAAACAA | 9678 |
| rs559650737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085304 | TTGCTTTACCAGAAT[A/G]TCATATTCTTCTGTT | 9678 |
| rs559651753 | in-del | -/T | 0.173729 | 0.238081 | intron-variant | PHF14 | GRCh38.p7 | 7:10990649 | TTTTAGTGATTAAGT[-/T]TTTTTTTTACTTTAA | 9678 |
| rs559652193 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11069259 | TACTTAGAGGAGAAA[G/T]TTAGTCTTACTGCTA | 9678 |
| rs559675991 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11006965 | GGATCACCTGAAGTC[A/G]GGAGTTTGATACCAG | 9678 |
| rs559684167 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056159 | TTGGAAGAGATCTAC[C/T]CTGTGGGTGTCCTTA | 9678 |
| rs559691925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061668 | TTAATTAGAAATAAC[C/T]AATTTTGCAAGTGCC | 9678 |
| rs559696200 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11097925 | AATTTAAAGGAAGGG[A/G]TGTGTGTATGTGTGT | 9678 |
| rs559730137 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11083266 | AAATCCTTTGTCTGA[C/G]TGTTTGTTTTCCTTA | 9678 |
| rs559733299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054625 | ATGGTGAAAAATGAG[G/T]TGTTCTAATTGTGTT | 9678 |
| rs559734559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041769 | ACTTTTATGACTACA[A/G]TTCATTTTTGTTTCA | 9678 |
| rs559736457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11048532 | GCCTTAGATCATGCC[A/G]CTGCACTCCAGCCTT | 9678 |
| rs559768756 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021647 | ATACATCAGTGGAGC[A/T]TGAAAAAACTGAACA | 9678 |
| rs559775342 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11029378 | CTATAAAAATGTTAC[C/T]TACTTTTCTGAACTC | 9678 |
| rs559790460 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165255 | GACTACTGTTTAATT[A/C]TATTGTAGAGGGTTT | 9678 |
| rs559800284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994349 | GAGTCTGAGGCAGGA[A/G]AATGGCTTGAACCCA | 9678 |
| rs559800320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999283 | AGTCCTCTCTCAAAC[C/T]ACTTACTCATTTTTG | 9678 |
| rs559823480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042488 | AAGCTATTTTTAACA[G/T]TCTCAAAAGTATTTA | 9678 |
| rs559852118 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963235 | GGTTACAAATTTCCC[C/T]CTACACACTGCTTTA | 9678 |
| rs559856407 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11165915 | AGTCTCATATTGCCA[C/T]CTGGAGTATCAGCCC | 9678 |
| rs559858743 | in-del | -/AGT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11041610 | GAGGCTCCCTCTACA[-/AGT]AATAGCAAATAACTT | 9678 |
| rs559861684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994668 | AGCTGTGGATCCTCG[C/T]GGTGAGTGTTAACAG | 9678 |
| rs559897222 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11071753 | CCCTGAGACATGTTT[C/T]TGATTATGTATAAAT | 9678 |
| rs559914318 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972225 | ACAGGCGTGAGCCAC[C/T]GCACCCGGCAGTACA | 9678 |
| rs559924928 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975888 | GTCTTTTTCCTGCTA[C/G]GGATAGTAGGAAGGG | 9678 |
| rs559931416 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120393 | ACTCTGATTTTCAAA[C/T]GTTAAGAAATGTTTT | 9678 |
| rs559933282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089716 | AATATACTATTAAAA[A/G]TGTGACTTTATGATG | 9678 |
| rs559937854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965674 | AGATATGCCCTGCCC[C/T]AAGAGGTGGAATCTA | 9678 |
| rs559939829 | snp | C/G/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11033113 | TTCCCTTTCTGTCTT[C/G/T]CACTGGGAGTAGGAT | 9678 |
| rs559963377 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092755 | CTCCATTCTTTACTC[A/G]CTGAACCTGATCATT | 9678 |
| rs560001920 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11017577 | AATGTCTATTCAAAT[A/C]TTTTGTCTGTTTTTA | 9678 |
| rs560013938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047501 | ATATAGAAGGTATAG[A/G]AAATTGAGAAAAGGC | 9678 |
| rs560075881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965393 | CTGGGTATCACCAGC[A/G]GAGGCTGCAGAACAG | 9678 |
| rs560096896 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959785 | ATGGCAGAGCCCCAA[A/G]AGTTGGGGAGGGGAT | 9678 |
| rs560103241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047799 | TCACAAAAAGACAGA[A/C]GAAGAGGAGGGAGGG | 9678 |
| rs560108442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008711 | GCATGTTGTAGGTAC[C/T]GTCTTTCTCGTAAAC | 9678 |
| rs560122221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122926 | TCTGAGCTGTAAATT[C/T]AGTTTGTCAAAATCA | 9678 |
| rs560142840 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150276 | CTGGTTATAGTTATG[A/G]TTATTGTTGTGCAGG | 9678 |
| rs560144241 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11076693 | CTGCCTCAGCCTCCT[C/G]AGTAGCTGAGATTAC | 9678 |
| rs560153303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038881 | TTCCAATTGCTGTCT[C/G]CTTCAGTTCTTGCTC | 9678 |
| rs560153424 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011614 | ATTTTGAGATGTAAT[A/G]AATGTGTCTCAGGAG | 9678 |
| rs560176655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064586 | GCTCTTCAGCAGTTT[G/T]GATTTTTTAAACCAC | 9678 |
| rs560178313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033681 | TAAGTCAGAGTCTTG[A/G]TCCAAATGCTTAACT | 9678 |
| rs560191847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129400 | TTTCTGTTAACATTT[A/C]ATAGTACCTGTTCAC | 9678 |
| rs560236177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960614 | CCCAGTAATGGGATT[A/G]CTGTGTCAAATGGTA | 9678 |
| rs560236693 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068440 | AACCAGTTACAGAAG[G/T]GTACAAATAATGTAT | 9678 |
| rs560236846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072057 | CATTCTTGCATAGCT[A/G]TAAAGAAATACCCAA | 9678 |
| rs560238194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168547 | TTGATGATATTGATG[A/G]TTATTACTGTTGTCT | 9678 |
| rs560250426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987311 | TCTTCAGGGCAGTAG[A/G]ATTCTTTTAATTCTA | 9678 |
| rs560252721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025303 | GATGCTATGAACATT[A/G]TTAAAATTACAACAA | 9678 |
| rs560255108 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11101423 | TTCTCAGAGTATCAG[A/C]TTCAGAATGTGCTCA | 9678 |
| rs560262054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163016 | AATTAGAAATTTGTT[A/G]CTGCCCTTTTTCTAT | 9678 |
| rs560293788 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11139812 | ATGTTTATAGAATTG[A/T]TGAAAATTGAGTAAA | 9678 |
| rs560296310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094641 | GGTTCCTGGAAAAAA[A/G]TTTGTGAATGAAGGT | 9678 |
| rs560306978 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968276 | TGCTCCTCCATCTTG[C/T]CCTTATACCTTTGAA | 9678 |
| rs560320367 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11167027 | TCAAATTAATGGAAG[G/T]TGCAAATTTTTATTT | 9678 |
| rs560323411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156386 | GATATCTAATGAGCT[A/G]TTACGTTCCAATAAA | 9678 |
| rs560353391 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037699 | GGTTAAAATGTTATA[C/G]CAAGTATAACTTGAC | 9678 |
| rs560357610 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121702 | CTGAGACAGCTAAGT[A/G]ACTAACGAGCAGGTA | 9678 |
| rs560367137 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970311 | TGCAGTGGCTCACAC[G/T]TGTAATCCCAGTACT | 9678 |
| rs560370196 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142691 | TTTCATAGGGGAAAA[A/C]ATGATGATAAGATTT | 9678 |
| rs560370839 | snp | A/G/T | 8.26617e-05 | 0.00642838 | synonymous-codon, missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982616 | AAAGGAGAAAGAGAA[A/G/T]GAAAAAGAAAAGGAA | 9678 |
| rs560382812 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11100830 | TTCATGCACTAATTA[A/G]GCATACTGCCTCACC | 9678 |
| rs560383815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167459 | TTAATTCAGGCATAC[C/T]TTTTATTCGTTCATT | 9678 |
| rs560386850 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057721 | AAGATAATTTTACAC[A/C/G]TTTTCAGTTTAAATA | 9678 |
| rs560407190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11015340 | ATCTTGGAGAATCCC[A/G]TGTGTTGATGTTCAG | 9678 |
| rs560434709 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963991 | AAATGAGATGGGTCT[C/T]CTGAATACAGCACAC | 9678 |
| rs560438849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004482 | GTTTCTCCACACCCC[A/G]CAGGATCCATTCAGG | 9678 |
| rs560451390 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069874 | TATTTTTTTCTGGTA[G/T]AAGTATCACATTTTA | 9678 |
| rs560456774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993632 | GTGGCCCAGATTCTG[A/T]AGAAAAATGAAGTAG | 9678 |
| rs560466667 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136573 | TCTTAAAAAAGTGGA[G/T]GTTGAGCATGTCTTT | 9678 |
| rs560483509 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114589 | AAAAGTAGAAGAATG[A/T]CCATTTATTATACCC | 9678 |
| rs560483937 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107384 | ACATTTTGTTAATGG[A/G]TAAAAGACCATATAT | 9678 |
| rs560513635 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985351 | TTCAGAAACTACTTT[G/T]TAGTAGAGTTAGGTG | 9678 |
| rs560519675 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166329 | TATCTCAGCAGAGAG[-/A]AAAAAAAAAAACCCT | 9678 |
| rs560540601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025862 | CACGCCTGTAATCCC[A/G]ACACTTTGGGAGGCC | 9678 |
| rs560560155 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10987916 | AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATCG | 9678 |
| rs560569225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121038 | CCAGTAAAATGTAAA[C/T]GTAACAAACCACTGA | 9678 |
| rs560575093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003879 | GTTGTACCTTGTGTA[C/T]CAGGGGTTTTTTAAC | 9678 |
| rs560580253 | in-del | -/TTGGCACGGATCTCTGCTCCGCC | 0.00239521 | 0.0345234 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973716 | GATCTCTGCTCCGCC[-/TTGGCACGGATCTCTGCTCCGCC]TTGGCACTACTCGGC | 9678 |
| rs560580512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11075100 | ATGCCATCACACCTG[A/G]CTAATTTTTTGTATT | 9678 |
| rs560584305 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11142266 | TATCTTCACATTTAA[A/G]GCTGGTAGAAATACA | 9678 |
| rs560596713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014865 | TGAGCACTTGTCATC[A/G]TAACGGTGTTGCCAT | 9678 |
| rs560598638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020335 | GCTCAAGCAGTCCTC[C/T]CACCTCAGCCTTCCA | 9678 |
| rs560601031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031416 | CATGCTTTATTAGAA[A/G]GATATTTAAAACCAT | 9678 |
| rs560611802 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11004289 | AGAAAAAGAAAACAT[C/T]TCTCATAATCATACC | 9678 |
| rs560656824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122440 | ACACGTATATATATA[C/T]ACGTATATATATATA | 9678 |
| rs560670703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993018 | ATACCACGGAAGTTA[C/T]ATAGTGTTCTTAGTG | 9678 |
| rs560705693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980441 | AATTTTAAAATGTCA[A/G]GAGATTACTATTATT | 9678 |
| rs560749874 | in-del | -/ACAG | 0.00795532 | 0.062565 | intron-variant | PHF14 | GRCh38.p7 | 7:11101395 | TTCCAGTAGTAAACT[-/ACAG]ACAAAGTAGTTCTCA | 9678 |
| rs560752157 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997165 | TATACATACACATAT[A/T]AGTTTTATTGATCTC | 9678 |
| rs560766854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980813 | ATATGGTGCATGTTC[C/T]ATGTTACCCTTGAAA | 9678 |
| rs560766957 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100639 | TATATGCCAGTCAGT[G/T]TGCTAGTGCCTTCCA | 9678 |
| rs560778425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114072 | AAAGCTAAAGGAGAA[A/G]TACTTATTGCCATAA | 9678 |
| rs560781191 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147047 | AGACTGGATTTTGCA[A/G]TGTTGCCCAGGCTGG | 9678 |
| rs560793702 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081814 | TGAGCTGAGATCGCG[C/T]CACCACACTCCAGCC | 9678 |
| rs560801370 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032051 | TCTTGAGGCTGGCCT[C/G]AAGAGGATTTTGAGA | 9678 |
| rs560817228 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003085 | AGCTGGGATTACAGG[C/T]GTGTGCCACCACACC | 9678 |
| rs560821813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044943 | AATGCTCCAATGAAC[A/G]TTTTCTTTGACTGTA | 9678 |
| rs560843184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094047 | TCATTCCTTAAAGGA[A/G]AAGGGTCTGGGTGAG | 9678 |
| rs560848684 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068037 | TACATACAGTAGAAT[A/G]TTATCCAGCCTTAAA | 9678 |
| rs560862423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11162342 | TGATCCACCCACCTC[A/G]GCCTTCCACAGTGCC | 9678 |
| rs560881707 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11085846 | TACTGATAAGTACAG[-/T]TTTTTTTTAACCCTA | 9678 |
| rs560883519 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11167602 | GAGGAACAGATGGAC[A/G]AATTCAGTGCTACAT | 9678 |
| rs560883747 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11075641 | ACCCAAACACCTCCC[A/C]CCAGGCGCACCTCCA | 9678 |
| rs560886457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008593 | TTCATCCAAAATAAT[C/G]CCCCTGTCCCATCCA | 9678 |
| rs560887265 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065542 | CAAAATATAATGTTT[A/G]ATGAAGGTATTTAAA | 9678 |
| rs560905937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045573 | GCACTTGCTATCCAG[C/G]CTTTTCTTCCAGTAC | 9678 |
| rs560908962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992285 | TCTCGATTTCCTGGC[C/T]TCAAGTGATCCACCC | 9678 |
| rs560921373 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086416 | TGCCATCTTGCTTTT[A/G]TTATACTTTATGTTA | 9678 |
| rs560933409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069393 | GAAGTGCCTTCAAGT[C/T]TCCTTAATAAGGAGG | 9678 |
| rs560940140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014103 | AGTACCTGCATTTGC[C/T]TTTACATCCATAATC | 9678 |
| rs560943834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974425 | AGAGTCCTGCGGGAA[A/G]GCAGGATTGGTGGAC | 9678 |
| rs560953843 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030455 | CATCATTTTTGGCAA[C/G]ATGGCAGCTAATTAA | 9678 |
| rs560982974 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972215 | TGTTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 9678 |
| rs560996275 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088956 | GGGAACAAAAAATGA[A/G]CATGGTATTATTTTA | 9678 |
| rs560996345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11082483 | TCCCTCACATTTTCA[A/G]TGTCTATTTTGCATT | 9678 |
| rs561012025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076012 | GGCATGGTGGCGGGC[A/G]CCTGTAGTTCCAGCT | 9678 |
| rs561019917 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069861 | TTATTTATTTATTTA[A/T]TTTTTTCTGGTAGAA | 9678 |
| rs561058477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087655 | ATTATATTGTGGATT[A/T]TAACCACAACTATAT | 9678 |
| rs561059054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141292 | TGTAATTAAGAAATC[C/T]GGAGTTCAGAAGGAT | 9678 |
| rs561059291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11148883 | ATATATTTTAAACTT[C/T]ATAATAACTGTAGCT | 9678 |
| rs561078385 | in-del | -/TGTG | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10988081 | TTTTTTTAAGGAGGA[-/TGTG]TTACTTAGATTTTCC | 9678 |
| rs561090179 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028059 | CATCCTGATAAATCC[A/G]TTGTAAGTTTAAAAT | 9678 |
| rs561095210 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108028 | GATGAAGATTACAAA[A/G]TGGTATTTGTGTGTA | 9678 |
| rs561097671 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980257 | CTAGAAGGTTGATCC[A/G]GAAGAAAAGTACCTT | 9678 |
| rs561133450 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115636 | GAAGTTAACATTGCT[A/G]TATTATTACTGTCTG | 9678 |
| rs561134635 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003225 | GCATATCTGTTCATA[G/T]TATTTTCTGCTTAAA | 9678 |
| rs561135589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064518 | TTTATTTAATATACT[G/T]TGTTTACTTTCTCAA | 9678 |
| rs561137012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967694 | ATTTAGAAATTTTTT[A/T]AAAAAGTTAAAACCC | 9678 |
| rs561147637 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963523 | TTTAGAATAAGTGCA[A/C]TGTGGTGCTGAGAAG | 9678 |
| rs561152038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019876 | TATAGCTATAAACCT[C/T]CCTCTTAGTAGGGCT | 9678 |
| rs561188718 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014828 | TTTTTACTACATTCA[C/G]ACTCATGTTTGTTAA | 9678 |
| rs561195592 | snp | A/C | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10969428 | CAAAATAAGACAATT[A/C]ATTTTTTTCTTCATT | 9678 |
| rs561197612 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063362 | ATTTTGCAATATGTC[A/G]AAAATGAAATCCCAA | 9678 |
| rs561232460 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11030549 | AGTGCATCTCCGTCT[A/G]AAGGCATGCAAATTA | 9678 |
| rs561251392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019414 | TTATGGCTTCAATCT[C/T]GTTACTTGTTATTGG | 9678 |
| rs561266102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975144 | GTTTTCCTCAGAGAT[A/G]ATTAGCAGTCAGGGG | 9678 |
| rs561268058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981965 | AGTCCATATAGTTTA[C/T]AAAAGATGTTTAAGG | 9678 |
| rs561268954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024673 | GCACATCTGTGTACC[A/G]CATGGTTTACTGGAT | 9678 |
| rs561270866 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979553 | TTTCCTTTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs561300929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997108 | TCCTTCTATCCCTTT[C/T]TGTCTGTATTTAATG | 9678 |
| rs561325393 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073096 | TCACTCCTTGCCCCC[C/G]CTCCCCAGTTTTATC | 9678 |
| rs561325526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961996 | GGGCTGAGATGATGG[A/G]GTTTTCTAAATATAC | 9678 |
| rs561327015 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058882 | ATCAGCAAGTCATTT[C/T]TCTGGATTGCTTTTT | 9678 |
| rs561336475 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088990 | TGGTAGGAGTCTGAG[C/T]AAAGTAAAATCTTCA | 9678 |
| rs561357658 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018950 | TTTTTATGATGAAGG[A/G]ATGTTGAATTTTATT | 9678 |
| rs561358746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11025245 | ACTTCTCATGGATGA[A/G]TGAAGAAAGTGGTTT | 9678 |
| rs561364206 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11043367 | GAGTTTTATCCTTTT[C/G]TTAATTTTACTCCAA | 9678 |
| rs561382322 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080348 | TGTATTGGGTAGTGA[C/T]TGACTAAACACTACT | 9678 |
| rs561383304 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959175 | TGCAATCCAAATGTC[A/C]GAAAGCTGATGCTGT | 9678 |
| rs561384695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081782 | AATCACTTGAGCCCC[A/G]GAGGCAGAGGTTGCA | 9678 |
| rs561400427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037172 | TATGGCATTTCTTTT[A/T]TGTTTTGTTTTTAAT | 9678 |
| rs561401556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148291 | AATCAAATAACCGTT[A/G]TGGGCTATGTAGTCA | 9678 |
| rs561409928 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10992908 | TTCTGTCTCATAGAC[A/G]TTTTTAAATATATAG | 9678 |
| rs561424016 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996484 | AGAGAAAACTGTTTC[A/C]AAAAGAGAGTCAGTA | 9678 |
| rs561486548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042822 | AGTTATTGGTGAGTA[A/G]AATAGAGGAGATTTA | 9678 |
| rs561487301 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995351 | CATTTACAAGCCTTG[A/C/T]GCTAGACACAGAGTG | 9678 |
| rs561489514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11034869 | TTCTATTTTTATCCT[C/T]AGTAGAATCTGTCCA | 9678 |
| rs561498438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046852 | AGAAAACATGGCTAA[C/T]GGCTTAGACATAAGA | 9678 |
| rs561499461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110631 | TTAAATGTACTAGGA[A/G]GTACTTTGTAAAACC | 9678 |
| rs561499530 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995003 | CATTTTACAGAGAGC[C/T]GATTGGTCTGTTTTG | 9678 |
| rs561514030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127055 | GAGCTTCCTTTTTCC[C/G]CCAGTTACTCTCAGA | 9678 |
| rs561521350 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973780 | ACTCGGCTCTGTTCG[C/G]CTCCTGCTCGGGAAG | 9678 |
| rs561532569 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046168 | TTTTTAGTTTATGTT[A/G]TTTTGATTTTTGTTG | 9678 |
| rs561548619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966008 | TCATTCACAGCTTCC[C/G]TTGTTTAGAAAAGGG | 9678 |
| rs561554196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11002691 | TCTGGTGATCCACTC[A/G]CCTCTGCCTCCCAAA | 9678 |
| rs561554828 | in-del | -/AC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084202 | AACTTCAAAATATGT[-/AC]ACACACACAATCTGA | 9678 |
| rs561555218 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170210 | CTGTCCCCTGTCTTT[A/T]TCAGAGTTCTCAGTA | 9678 |
| rs561556133 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11002076 | TTGAGACAGAGTCTC[A/G]CTCTGCTGCCCAGGC | 9678 |
| rs561588590 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11166376 | AATTTTTGCTTACCT[A/G]TAATATCCAGTAGTA | 9678 |
| rs561591008 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11109139 | TGTCAGTTTACATAG[-/C]CTCAGTAAGTTTTAG | 9678 |
| rs561615482 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961552 | ATTGTCTTGGCTATG[C/T]GGGCTGTTTTTGGTG | 9678 |
| rs561619723 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163990 | CTTACACTTTTAAAA[C/G]AAACATTATTAAAGT | 9678 |
| rs561653267 | in-del | -/TATTGTGTCCTCACAT | 0.02016 | 0.0983543 | intron-variant | PHF14 | GRCh38.p7 | 7:11153884 | TACAGAGTCTCGAAG[-/TATTGTGTCCTCACAT]TATAATACATAGAGG | 9678 |
| rs561667025 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160135 | CTGTGTACCCAATGT[G/T]CTCCCACTTATGAGT | 9678 |
| rs561669223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081073 | TATATATGTGTGTGT[C/G]TATTTATATGTATAT | 9678 |
| rs561685715 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10989892 | TGCTTCAACCTCCCA[C/G]TGTATTTGGGATTAC | 9678 |
| rs561687951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072578 | ATTAAGTAATACCGT[A/G]CAAGTAAAGGGCTTG | 9678 |
| rs561697829 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970912 | GTACAAAAATCACAT[A/G]ATCATCTCAATAGAC | 9678 |
| rs561726040 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971297 | AACTGCATAACTCCA[A/G]GCAACATCAAGAAAG | 9678 |
| rs561730153 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104001 | CTGTTGCTGAACTCT[C/G]GCTGCTTTTAAGCAA | 9678 |
| rs561730265 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PHF14 | GRCh38.p7 | 7:11157790 | AATACTCATTTATAG[C/T]GTGGAGTCTGTAATG | 9678 |
| rs561743272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143922 | CAAAGGAAACAATCA[A/G]CAGAGTAAAGAGACA | 9678 |
| rs561791666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151906 | CCTCAGAAGCTGATC[C/T]TTGTACATTTTTCCA | 9678 |
| rs561798769 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11145170 | GGGGTTCAGGTGGCA[C/G]AGGAACTCACCTGGT | 9678 |
| rs561804828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144406 | TATATTGAAGAGATA[C/G]CTGCACCCCCATGTT | 9678 |
| rs561832639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060987 | GTTTAGAATTATTTG[A/G]TACCTACTCTAGCTT | 9678 |
| rs561839429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999512 | CATTTCAAAATGACC[C/T]TCGCTCTCTATTTTG | 9678 |
| rs561844794 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11143623 | CCTTCGAGAGATTAC[C/T]GCTGCTTGCATATTG | 9678 |
| rs561846739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124086 | TTTTCTGAAGAAAGT[C/T]GGTATCAGGAAAAAA | 9678 |
| rs561860929 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11046254 | TAGGATACAAATGGT[A/T]AGGGCTTGATTTATT | 9678 |
| rs561866288 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11157058 | TTATCACCTCCATGT[A/T]TACCTGATGCACTTT | 9678 |
| rs561866770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137361 | TTTTGTGTGTGACAG[C/T]TCTACACAATTCCCT | 9678 |
| rs561870790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052971 | ATTACATCAGGAGTG[C/T]AAATTTCAAACCTTT | 9678 |
| rs561881181 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966685 | TTATTCTAACATGAT[C/G]TGTAATACAGAGGAA | 9678 |
| rs561888410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976051 | TTTACAGGTAACAGG[G/T]GTATTGAGTTTAAAG | 9678 |
| rs561903019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130926 | AGTATGTAGCCTGTT[C/G]AATTTGGCTTCTTTC | 9678 |
| rs561914234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123731 | GCTGCAGTGAACCGA[A/G]ATCACACCACTACAC | 9678 |
| rs561915920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115456 | ACAGGTACATAAAAC[A/G]TCACACATACATATT | 9678 |
| rs561935630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083778 | TTTCCCTAATTTTAC[C/T]TAATGAGAATTCTTA | 9678 |
| rs561937862 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070420 | ATTTCATCTCATTTG[C/T]CAGTTGCTTCTTTCT | 9678 |
| rs561951541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026988 | CTGAATTATGTTCTC[C/T]TGTGTTCTCAGTTGC | 9678 |
| rs561958665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040387 | TTGTTTTTTTTAAAC[C/T]TCCTACGTATGTGTC | 9678 |
| rs561971186 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11077484 | CACGCGCCTGTAGTC[C/G]CAGCTACTCAGGAGG | 9678 |
| rs561993031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034298 | TTCCTTTTTGGGACA[A/G]ACATAAAGAATGAAC | 9678 |
| rs562012921 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11000530 | TTTTAGTAGAGATGG[A/G]GTTTTGCCATGTTGG | 9678 |
| rs562014619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149819 | CAGTTGATTTTTTTT[A/T]ATATTTCTAAGTATA | 9678 |
| rs562014939 | snp | A/G | 8.30668e-05 | 0.00644411 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982799 | ACAAGTCAGCGAGCC[A/G]AAAAAATGGAACCTT | 9678 |
| rs562033116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020623 | AGCTTAAGTGATCCT[C/T]CTACCTCTGCCTCCC | 9678 |
| rs562037083 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027393 | TTCTTATGTAGTTCA[C/T]TTTGAATACTTATAT | 9678 |
| rs562053359 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095924 | CTAGTCAGGGGATAT[A/G]TCTCTACCTGTATAT | 9678 |
| rs562069107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095819 | CAGCTAGAGTATGAG[A/G]TAAAACCTCAACTGG | 9678 |
| rs562069747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083405 | CCGCACTCCCACCCC[A/G]TATCATCGTGACTGG | 9678 |
| rs562069813 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035397 | TTATATTTGATTTCA[A/G]TATCTTTAAACCTGC | 9678 |
| rs562072427 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102569 | AGTGTGATTTTAAAA[A/G]TGTGGATTAAACTCT | 9678 |
| rs562097159 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125066 | ATTCAATTAAATAAG[A/G]TCTGTGTTAGGGGAG | 9678 |
| rs562110757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10994704 | AAAGGCGGCGTGTCC[A/G]GAGTTTGCTCCTTCT | 9678 |
| rs562129435 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016100 | GGTTTACTGAGGGAT[A/T]TTTTTTTGGATACTG | 9678 |
| rs562131569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10976453 | TAAACTTTGACAAAC[A/G]TAGTTGGGTCGTGGA | 9678 |
| rs562134192 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121694 | TCTAGTCACTGAGAC[A/G]GCTAAGTGACTAACG | 9678 |
| rs562156717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096248 | GTATTTTGTAAAGAA[G/T]ATCATCCTGCATAAT | 9678 |
| rs562163604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010083 | TCTTGGTAATTGCCT[A/T]CTTGTGTGGATGCAC | 9678 |
| rs562170845 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151579 | ATAAATTTATAACTT[C/G]ATTTTTGTTGTTGTT | 9678 |
| rs562177867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108980 | AAAATGTTAATACTT[C/T]ATCAAGAACTTTGAT | 9678 |
| rs562195373 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090052 | CTGGGATTACAGGCG[G/T]GAGCCACCTCACTTG | 9678 |
| rs562203434 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11005027 | GTCTCAAAAAAAAAA[A/T]GTATAATGTCAATTT | 9678 |
| rs562216599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065460 | CATAAGTAATGACTG[A/G]GTATTCTTTTGCTGA | 9678 |
| rs562223821 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10989364 | AAAAAATAATAAAAC[A/C]TATTTATGAAAAATA | 9678 |
| rs562239975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11101766 | GTGAACTTTTTCTGC[A/G]ATGTGTGACTACTTG | 9678 |
| rs562240629 | snp | A/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970715 | ATTCTTTATATGACA[A/T]CAAAATGTAATTTCC | 9678 |
| rs562252346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071488 | TTCCTTTGATAAATA[A/G]CAGATATTTCCTTTT | 9678 |
| rs562256024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058678 | AGAAATCTTCATTGG[A/G]CATCACAATGTTACA | 9678 |
| rs562265985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11061130 | GATATTTCTAACATA[C/T]TGGCTGCAAATACTA | 9678 |
| rs562270070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015413 | ATCCAAAAATAAAAT[A/G]TATAACAAATGATTT | 9678 |
| rs562273052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994322 | CATGTGCCTGTAGTC[C/G]TAGTTACTCAGGAGT | 9678 |
| rs562277118 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11032949 | GGTCTTGGTTCAGCA[A/G]CTTAACCTCTCTGGC | 9678 |
| rs562285508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989822 | ATTTTGTAGAGACAG[A/G]ATCTCACTGTGTTGC | 9678 |
| rs562294528 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007908 | TTACTGTAATTACTT[C/T]TCAGAGTGCTCACTT | 9678 |
| rs562299225 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033908 | CTAATTAATTTTTGT[A/G]TTTAATTTTTAAAGC | 9678 |
| rs562302057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040204 | GTTGCTGTCTGAGAA[C/G]CCAGCATACTACAGA | 9678 |
| rs562312387 | in-del | -/TAAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016983 | TTTAGATCCCACAAA[-/TAAG]TGAGAACATGTGATG | 9678 |
| rs562315549 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011144 | TAATGAAATACTTAC[A/G]TGTAACCACTGACAT | 9678 |
| rs562328692 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072184 | AAACTTCTAATCATG[A/G]CAGAAAGCAAAGGGG | 9678 |
| rs562332864 | snp | G/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970351 | TGAGGTGGGCGATCA[G/T]TTGAGGTCAGGAGTT | 9678 |
| rs562336861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052263 | TCTGGTAATTTGATA[C/T]TTTGACCAAAATTAT | 9678 |
| rs562343344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965418 | GAACAGCAAATATTG[C/G]TGACTGATCTTTCCT | 9678 |
| rs562347552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10988621 | TGATATTTAAAGTAG[C/T]AGTGCTCATTGGAGC | 9678 |
| rs562353380 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970632 | AATTTATCACATACG[C/T]CTTAAAGATGTTCAG | 9678 |
| rs562365516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068688 | ATGGTCAATGCTATG[C/T]ATATTTTACCACAAT | 9678 |
| rs562366588 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088188 | TTTCAGTTATCTCTA[C/G]ATACTTATTATAATA | 9678 |
| rs562374811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156316 | TTTCTTGAAGCAAAT[C/T]CAATTTCTTTTTAAC | 9678 |
| rs562392488 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961477 | GCTGTTTTGGTTACT[A/G]TAGGCTTGTGGTATA | 9678 |
| rs562401684 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11109583 | AGGTTTCTATATCCA[C/T]AGGTTTAATCGAAAT | 9678 |
| rs562417061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965759 | CTGCCTCTTTGTTTA[C/T]ACTGTGAGCATAGAA | 9678 |
| rs562435104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123541 | ATTCCCAGTGCTTTG[A/G]GAGGCCGAGACAGGC | 9678 |
| rs562435341 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10990981 | AAAGTATGGATGCTA[C/T]TTTTCAGGTTATCTT | 9678 |
| rs562451723 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167890 | AAAAATTAGCCGGGC[C/G]TGGTGGTGGGTGCCT | 9678 |
| rs562491455 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961077 | TGCAGAAGTTCTTTA[C/G]TTTAATTATATCCCA | 9678 |
| rs562492793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076810 | TGTTCTCAAGCAATC[C/T]GCCTGCCTTGGCCTC | 9678 |
| rs562496950 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966261 | TATTGAGAGACAGAA[C/T]AGCTCTCAGTGAAGA | 9678 |
| rs562507211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163898 | CTGTTTTTCTTTCTA[C/T]ACTTGTTCCGTAGCT | 9678 |
| rs562508352 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146871 | ATTTATTTAGAGACA[G/T]AGTCTCACTCTGATA | 9678 |
| rs562509167 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014542 | GCCATGGAAAAATGA[C/T]CTTCATGTTGGGCCA | 9678 |
| rs562515361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027481 | TATGAAGATTTCTGT[A/T]ACCAGAGTAGTTTAA | 9678 |
| rs562534670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156891 | TGTTAAAAGAGCAGT[A/G]TAAGTTACATTGAGC | 9678 |
| rs562539515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976301 | TTTAGTTGGTTTGCT[A/G]ATATTTGGTATTTCC | 9678 |
| rs562593198 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150332 | ATATGCTAAAGAAAC[A/G]TGAAGGTTTCTGTGT | 9678 |
| rs562601904 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124336 | GAAAAATATAATTGC[A/G]TGTATGGCAGTTTAC | 9678 |
| rs562606561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151136 | GAGTAATTGTTGAAC[A/G]TGTATATTATGAGAA | 9678 |
| rs562625235 | in-del | -/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964509 | TGGCTGCCCTTAACA[-/T]TTTTTTCCTTTATTT | 9678 |
| rs562647592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059270 | TAAAAGAATTGAAAA[C/T]ATGAACTTGCAGCAT | 9678 |
| rs562661963 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051631 | TGCTCGGAATGTGAC[C/G]AGGCAGGGAGCAGTG | 9678 |
| rs562672494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10985707 | GCCTAGGCTGGAGTA[C/T]AGTGGCATGATCTCG | 9678 |
| rs562680724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11163056 | TAAAAAATATTTACT[A/G]TTAATAAATAATGAA | 9678 |
| rs562682276 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962123 | TTTCAATACTATGTT[A/G]AATAGGAGAGGTGAG | 9678 |
| rs562693581 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11009836 | TGCACAACACCATTC[G/T]TCCAGATTACAAAGG | 9678 |
| rs562713664 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020056 | TTATGTTGCAATAGA[A/C]GGCAGCATTGAAATC | 9678 |
| rs562727665 | snp | A/C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093145 | TGTATTTTATTTCCA[A/C/G]ATATTCGGAGGATTT | 9678 |
| rs562735004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046165 | TCATTTTTAGTTTAT[A/G]TTATTTTGATTTTTG | 9678 |
| rs562761157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004967 | GGTTACAGTAAGCCA[A/G]GATTCTGTCACTGCA | 9678 |
| rs562774611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122955 | CAAGAATCTTCCTCT[A/G]TTATTCTGTGTCATG | 9678 |
| rs562778307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11111033 | AAGTTCACAATTGAA[A/G]TTGTTGTGGTTGTTT | 9678 |
| rs562786316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031993 | GGTGTGGTGGCACAC[A/G]CCTGTAATCCCAGTA | 9678 |
| rs562805402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10999336 | TATTTGAATATATAG[C/T]TCCTTATCTGCTTTG | 9678 |
| rs562816214 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148487 | AATGTCAGCTCTTTT[A/G]TAGCAGGGCTTCCTT | 9678 |
| rs562821767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11039572 | GGAGACCCACTGTTT[A/G]TGGTCCTTTCACTAA | 9678 |
| rs562825530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988472 | ATTACCACACAGTCC[A/G]TAAAGACATGTAGCA | 9678 |
| rs562825648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108785 | ATTAGCTGGAATTTC[A/G]TAGCTATATCAACAA | 9678 |
| rs562838753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094795 | CTCTCATGCTCTGCC[A/G]CAGGTGATCCAGAGC | 9678 |
| rs562865278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11136051 | GGTATACATAAGTAA[C/T]ATTGTTGAAAATAGT | 9678 |
| rs562866398 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11119707 | TATAAAATATTTGTT[A/G]AAAAATATTGTTTCC | 9678 |
| rs562871786 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010238 | TTTTTCTTTGAATAT[-/A]ATGTTTTGTTCTTTT | 9678 |
| rs562875475 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11088684 | CAAAGAAAGAAATGC[C/T]AATATAAAAAGACAT | 9678 |
| rs562886535 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:11101608 | GTTTACAGTTTTGTT[C/T]TTACTTTCTTTGGAG | 9678 |
| rs562899854 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120930 | TGAAGAAATATCCAA[G/T]AAATTTTTCTTAGAC | 9678 |
| rs562917076 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11023930 | ACTTTAAATTAAAAG[C/G]TAGAAATGATTAAGC | 9678 |
| rs562946003 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127891 | TGACTTAAATCATGA[-/T]TTTTTTTTTTCATAA | 9678 |
| rs563004206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015618 | GTGATGTAACCTTTT[C/T]ATGCCTCAGTTTCCT | 9678 |
| rs563006362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009436 | TTGATGCTAATTAAA[C/T]GGCCATAGAAACATG | 9678 |
| rs563010269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070455 | TGTCAGCACCATGGT[A/G]TTTTCTTTAGTCATG | 9678 |
| rs563048963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064836 | TCTTGGTTTTCCCCC[C/T]GTTGTACATGATCAC | 9678 |
| rs563057751 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075658 | CAGGCGCACCTCCAA[A/C]ACTGGAAGTCACATT | 9678 |
| rs563060962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048821 | ACTGCAACAATCATG[G/T]GGCGGTTGTCTTGAA | 9678 |
| rs563064256 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007421 | CTGTAGATTTTTTTT[A/C]CCCCTTAACTCTTTT | 9678 |
| rs563075332 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976474 | GGGTCGTGGAAGTTA[C/T]GAATTCTTTGAATAT | 9678 |
| rs563084004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964999 | TTCTACCTTCTTTGC[A/G]ATGGGTTAGAACATG | 9678 |
| rs563101868 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035257 | CATGTAAACTAGATG[C/G]AAATACCACACCATT | 9678 |
| rs563109873 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035414 | ATCTTTAAACCTGCA[C/G]GCCCTTTAAAGAAAA | 9678 |
| rs563133246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062393 | TGATCTAAACACTGT[A/G]TACTAAGATTATTAT | 9678 |
| rs563148490 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11075958 | AATACGATGAAACCC[C/T]GTCTCTACCAAAAAA | 9678 |
| rs563149790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978920 | CTGATTGGCTGTCTT[C/G]AAGACATATACGGTT | 9678 |
| rs563156621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993755 | GCTCATGCCTGTAAA[C/T]CCCAGCACTTTGGGA | 9678 |
| rs563161113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162279 | ATTTTTAGTGGAGAC[A/G]GGGTTTCTCCTTGCT | 9678 |
| rs563166756 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108142 | GTTTATTAATTCTTG[C/G]AAGTTCTGCTAGAGT | 9678 |
| rs563170725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11119266 | GTTATTTTGTTATTT[C/T]AGCTACTAAAATGCT | 9678 |
| rs563189709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115220 | TTTAGTGCCTCACTT[C/T]TTCTCATTCTGTTAT | 9678 |
| rs563205099 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049336 | CAAAATTAACTGTGC[A/G]TGGTGGCACACACCT | 9678 |
| rs563206209 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11071384 | TTATTTTTCTTGCTT[A/C]AATATCTTAGAATGG | 9678 |
| rs563215586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988003 | CCTGGGCAACAAGAG[C/T]GAAACTCCTTCTCAA | 9678 |
| rs563217626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994267 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 9678 |
| rs563271563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153120 | ATTACTGTCTCCTGT[A/G]TAAAGAATAGGTATA | 9678 |
| rs563303801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995597 | ACCGCGCCACAGAGC[A/G]GGGGCAGCACTCATA | 9678 |
| rs563308212 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10996116 | GTGGGAAGCCATAAC[A/G]TGGCTTTTCAGCAGA | 9678 |
| rs563314082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962545 | GCCTGCAATTCTTTT[C/T]GTTGTATCTCTGCCA | 9678 |
| rs563338767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165832 | TTTAAGCAAAATCTT[C/G]CAAGTTTTATTTAGT | 9678 |
| rs563343610 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134404 | TTTATATTGTTTGCT[A/G]TATAATTTAAAGATT | 9678 |
| rs563352064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099045 | AAAATCAGGGAAGAG[A/T]GGTTTAATTTAAAAA | 9678 |
| rs563364794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006013 | TGGCCAGGTTGGTCT[C/T]GATCTCCAGACCTCA | 9678 |
| rs563366277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091988 | TGGTTTAGTTGAGTC[A/G]CAGGCTAACTCCAGA | 9678 |
| rs563380660 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162614 | TATGCCCTCTTCAGA[G/T]GGCTGTGGCAATCCT | 9678 |
| rs563419997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035055 | ATACAGCCGGCCCTC[C/T]GTGTCTGTGGATTAC | 9678 |
| rs563429158 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11085838 | GGGATTTGCTACTGA[G/T]AAGTACAGTTTTTTT | 9678 |
| rs563429298 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998596 | AAACATGGTTGAATA[A/T]ATGTGTATTTTTCTT | 9678 |
| rs563443686 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11068275 | AGAATGGCATGAACC[C/T]GGAGGCAGGGCTTGC | 9678 |
| rs563530907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111826 | ATTATGTTAGCTAAC[A/G]GAATAACCAATTAAA | 9678 |
| rs563550739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991019 | ATTTTGAGATGGAGT[C/G]TCACTGTGTCGCCCA | 9678 |
| rs563556484 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104336 | TAGGTCCTGCAAAAA[C/G]TATAGTTGAAGTAAG | 9678 |
| rs563567189 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104937 | GAATGTGCTTTTAAC[A/C]TCTCCTTAAAAGGTC | 9678 |
| rs563611111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041675 | AGTGTACAATGTGAA[C/T]ATTAGCACATTCTCA | 9678 |
| rs563612180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985304 | ATATTTGATTATATT[C/T]GAAGTTTGATTTTCC | 9678 |
| rs563619750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11053298 | GGTCATATAAAATTT[A/G]TGAGGCAAATCTTTA | 9678 |
| rs563633583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001203 | AAAGATCAGTTGACT[A/G]TATTTCTTTGGGTCT | 9678 |
| rs563638707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010760 | GGCTCAAGTGATTCT[C/T]CCACCTCAGCCTTTC | 9678 |
| rs563647186 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019487 | GTTGTATGTGTCTAG[A/G]AGTTCATCCATTTCT | 9678 |
| rs563655142 | snp | A/C/G | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11027533 | CCCTTTTTCTTTTAA[A/C/G]AGATAGTTAAAGGAA | 9678 |
| rs563658201 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078348 | CCTCACTTGAAAATT[A/C]GGTCAATAACTAACT | 9678 |
| rs563660278 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030763 | GAATAATAAAATGCA[A/C]CTTTTCTCCCTATTC | 9678 |
| rs563691148 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976210 | TAATTGAATTCATCC[A/G]CAGCAATCAAAAATT | 9678 |
| rs563723521 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063769 | CATCATATTTTAGTC[A/G]TTTAATAAAAAAAGT | 9678 |
| rs563727105 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11067151 | AAAAATGGGCATAGG[A/C]CTTGAAAATATTTCT | 9678 |
| rs563729739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078318 | TATTTATCTTAGTGA[A/T]TAACAGAATATGAAC | 9678 |
| rs563741489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022419 | GAGTAATAAGAGAAA[C/T]TTTACCTAATTACTG | 9678 |
| rs563759149 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050821 | TTCTTTTAGAAGTAG[G/T]AGGGGCCACCAAATA | 9678 |
| rs563793730 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11000699 | TCTTTTGCCCATTTT[A/T]AAAAATTGGTTTGTT | 9678 |
| rs563798932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152976 | GAACTCAGTGAGGCC[A/G]GAAAGGTCAGAAGGG | 9678 |
| rs563816105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078935 | ATTATATTATCTACA[G/T]AAGTATTTTTAGCAT | 9678 |
| rs563826821 | snp | A/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973419 | TTTGTTGCTTCATTC[A/T]TTCTTTGCTTTGCTG | 9678 |
| rs563827836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10995849 | AAGCCCATGCCCACC[C/T]GGAACTCGCGCTGGC | 9678 |
| rs563827958 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11017104 | TTTTATGGCTTAGTA[C/T]TCCATTGTGTATTGT | 9678 |
| rs563842134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062331 | TTATTTTTCTCTTGA[C/T]AAGAGAAATTGACAG | 9678 |
| rs563854529 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10977289 | CTTTCAAAACAACTT[C/G]TAGAAATGACTCATT | 9678 |
| rs563879687 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11021883 | CTCTAAAACTCATAA[C/T]GCACCACAAAAACCA | 9678 |
| rs563883307 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990926 | TAAGGTGGTTCTACA[A/G]TATTTCATGGTGTTT | 9678 |
| rs563897354 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11041035 | TAGATAACATTATAG[G/T]TATTGTCTTAAATAA | 9678 |
| rs563905055 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11053089 | AAGGGAGATACAAAG[A/T]TATTTTTAGGGTTAG | 9678 |
| rs563913745 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11133981 | TTAATCACTTAAGTA[G/T]AAAGCTACTAAGTAG | 9678 |
| rs563916571 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11016684 | TGCAATGTGAAATAA[A/G]CACATCATGGAGAAT | 9678 |
| rs563920617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976928 | CAAATTTGTATGTAT[A/G]GTTCTTGGTATTTAT | 9678 |
| rs563945975 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10985226 | GTGGCCAATGTTTGG[G/T]TCTTAATCTTCCTGG | 9678 |
| rs563952308 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162248 | CACACGCCACCATAC[C/G]CAGCTAATTTTTTGT | 9678 |
| rs563964301 | snp | A/G | 0.00119737 | 0.0244387 | | | GRCh38.p7 | 7:10970686 | TATAGCCAGTTTACA[A/G]CCAATAAAGACAAAT | 9678 |
| rs563988306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11034914 | GAAATGCCACACTTA[C/T]CTTGTTGGCTAGTTG | 9678 |
| rs563994215 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956168 | TGCAGCAGTTTTATC[A/C]AATAAATATCAGATC | 9678 |
| rs563996729 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971509 | TCTTCTTCCTTTTTC[C/T]CTCCCTCTCTTCCTT | 9678 |
| rs564014512 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157846 | CCCCATTTTCCATAA[C/T]TCTGATTGCCTCTGC | 9678 |
| rs564023499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111744 | CTCCGAAAGCCCAAA[C/T]AGATCACTCTCTGCT | 9678 |
| rs564024673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035336 | CCTGGAACCAGTCCC[A/C]CATGGATATTGAAGG | 9678 |
| rs564034406 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11138165 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 9678 |
| rs564079675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11022674 | AGTAATTTCAGTCCC[C/G]TTTTTTGTAACTAAG | 9678 |
| rs564080267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067243 | CAGGAAGAGTAAATC[A/G]AAACCACAGTGAGAT | 9678 |
| rs564110373 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966430 | CACCATCTGATTGGC[C/T]AAAAGGCATCAAAGA | 9678 |
| rs564119126 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11137618 | TTTTTTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT | 9678 |
| rs564124559 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076765 | TAGAGATGGGGTTTT[C/G]CAATGTTGTCCAGGC | 9678 |
| rs564126526 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050397 | ATCATTCTTTTACAT[G/T]TGAAGAAAATATGAG | 9678 |
| rs564160755 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11146060 | GTGGTCAAGACATTC[A/T]ATTTTTTGACAGTTT | 9678 |
| rs564166999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017683 | GGGTAATTTGCAAAT[A/G]TTTTCTCCCATTCTG | 9678 |
| rs564180453 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11138091 | CACCCAGCAGGCTGG[A/G]GTGCAGTGGCACGAT | 9678 |
| rs564182534 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11131019 | AATCACTGAGTAATG[A/T]TCTATTGTATGGATA | 9678 |
| rs564184757 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11098152 | AATCTTACACTATCT[C/G]AATGTATTTACTTCT | 9678 |
| rs564199002 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973927 | ATTGTCTGAGGCAGC[A/C]GCCCTCGCGCTGTGC | 9678 |
| rs564199709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165166 | TTGACCTTGTGATCC[A/G]CCTGCCTCGGCCTCC | 9678 |
| rs564202754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018260 | CCGTATACATTTTAG[G/T]ATTATTTTTTCTATT | 9678 |
| rs564213318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054691 | ACAACAGCTTACTAA[A/C]TTGTATAAATACCTT | 9678 |
| rs564214144 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11118628 | GTGGTTTTATTAATA[C/T]TTTATTGTCCTAGAC | 9678 |
| rs564222210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138672 | ATTTATCTCACTTGC[A/G]TATCATTCGTGCAAG | 9678 |
| rs564244510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091416 | TTTTTTTAAAGGTCT[A/G]CTGAATTAGACATTT | 9678 |
| rs564264426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040454 | ATGTTTTAGTGTACC[A/T]CTGAAAATTGATGAA | 9678 |
| rs564266746 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11013306 | AGCTGGGATTCTGGG[C/T]GCCTGCCACCACGCC | 9678 |
| rs564271036 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11124179 | AAAAAAATTTTAAAC[A/G]TAAAGAAGTATTTTA | 9678 |
| rs564316112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164838 | TGTCCTTTTTATGTA[A/G]TCCAGGATTCCTCAC | 9678 |
| rs564323510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078767 | GGGAATTAATTATAA[C/T]GCAGTCACTTTTCAT | 9678 |
| rs564330698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118019 | CTCAGCTGTCTAAAT[A/T]CAGTACTCTTCTAGC | 9678 |
| rs564351206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11053487 | AGCCGGCTAGTTTCT[A/G]TTTCTAAAATATTTT | 9678 |
| rs564354080 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995369 | TAGACACAGAGTGCT[G/T]ATTGGTGTATTTACA | 9678 |
| rs564360972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073147 | AATTGTCCTTTATTA[A/G]CAGTCCTCCAAAGTC | 9678 |
| rs564362401 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111266 | AGTTGAAATATACAA[G/T]AGTTTGTCTTTTTGT | 9678 |
| rs564380905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011321 | GATGGTTGTGAGAGG[A/T]CACGCTCCAATTTAG | 9678 |
| rs564391993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028572 | GTACATAATTGGTTC[A/G]TTATTTGTATTTAGC | 9678 |
| rs564411356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090776 | TTATGTAGAGGGTTT[A/G]TAAGAGACAGAAGAA | 9678 |
| rs564448531 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046956 | AAATCATGAATTATT[A/T]GGAATATGGAATGTT | 9678 |
| rs564450843 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053031 | GGGCATACTTTCCTT[G/T]CTTGAGCTGAGGCAG | 9678 |
| rs564468676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016621 | TATTTGTGGGTACAT[A/G]GTAGATATGTATATT | 9678 |
| rs564469214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096337 | AAGTTTTTGAATGCT[C/T]ATACAGACCTGACAA | 9678 |
| rs564472719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11090141 | GCATGAAGCCTCAAG[C/T]GTGATTTAATTCATA | 9678 |
| rs564480499 | snp | A/G | 0.000798403 | 0.0199641 | | | GRCh38.p7 | 7:10971396 | GAAAAAGGAGATAAT[A/G]GGTATTGGGAAACAA | 9678 |
| rs564480628 | in-del | -/CTTCCGC | 0.00993419 | 0.0697739 | intron-variant | PHF14 | GRCh38.p7 | 7:11143363 | TGGGGTCAAGTGATT[-/CTTCCGC]CTCTGCCTCCGAAAA | 9678 |
| rs564494722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116894 | CAAATGTCAACAAAT[C/T]GACATTTTAATATTA | 9678 |
| rs564510054 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11030274 | AAGAGTTAGAGGACC[A/G]GATAAATACTACGTA | 9678 |
| rs564512892 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156152 | ATTTAATCATTCTTT[A/G]ATAAAAGCAAAGTAG | 9678 |
| rs564516448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134354 | CTGAAATATCATTTA[C/G]AGAGATTTGCAAACT | 9678 |
| rs564538366 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102838 | ACATGTCTTGTCAGA[A/G]TTGTCGTATTAAGTA | 9678 |
| rs564539774 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046884 | AAAAAAAAACTCTGG[A/T]GTGGGATCCTGAGTT | 9678 |
| rs564548664 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10989771 | GAGTACCTGGGACTA[A/G]GGGCATGCATCACCA | 9678 |
| rs564560314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005559 | GGATAAATCCCTAAG[A/T]TATTTTTCTACAACT | 9678 |
| rs564561897 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11083889 | CTAGATTTAAGCTAG[C/G]AGAAAATAAATAATG | 9678 |
| rs564575944 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11134917 | ACTGAATGCATTCTT[A/G]TGTGTGTGTAATATG | 9678 |
| rs564578193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000134 | TTTATATATGTTCCA[A/G]GTAAAGATGCAAAAG | 9678 |
| rs564586302 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | PHF14 | GRCh38.p7 | 7:11081085 | TGTGTATTTATATGT[A/T]TATATATGTGAGTGT | 9678 |
| rs564595436 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11008454 | AACTCCACCTCCTGT[C/G]GGATCAGTGGCAGCA | 9678 |
| rs564598807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084524 | TTAACTTCACAATGC[A/G]TAATGGACTTTTTCT | 9678 |
| rs564622795 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004618 | GTTTTTATAATGTCA[C/T]ATTGAATATCTCTCA | 9678 |
| rs564650664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066308 | GTTGTCACTCAGGCT[A/G]GAGTGCAGTGGCACT | 9678 |
| rs564657871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037865 | TCTTGCTAGTTCTGT[G/T]ATCTTGGCCAACTCA | 9678 |
| rs564660394 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125213 | ACTGTATTTTACCTC[A/G]GTCAAATCTTAGTTT | 9678 |
| rs564715133 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973711 | GGCGGGGATCTCTGC[C/T]CCGCCTTGGCACTAC | 9678 |
| rs564718556 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11050054 | TTAAATTAATACGTT[A/T]AGGATTAATTTGTAT | 9678 |
| rs564722712 | snp | G/T | 1.6593e-05 | 0.00288031 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982838 | CCGACCACTTCTGGA[G/T]TTTGTGTCCATGGAA | 9678 |
| rs564729095 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153660 | AGAGGGAAAAACTCA[C/T]AGAACTAGAAGAAAT | 9678 |
| rs564749367 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000115 | TAATTTGAATTCTGT[A/G]AACTTTATATATGTT | 9678 |
| rs564750021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087159 | TAATTTAGCTTCCTG[G/T]AGTGATTTTATGGTA | 9678 |
| rs564753443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099461 | GTGTGGTATTTCTGG[A/G]GTACACAATTTTAGA | 9678 |
| rs564755093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151095 | CCTGTCATAATGCAA[G/T]GGTGAAATATAAATT | 9678 |
| rs564758444 | in-del | -/ATA | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10990609 | CATTTGGAAATGCAT[-/ATA]ATAATGTTTAAGTAA | 9678 |
| rs564760324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044110 | ATACTGCATGTTCTC[A/T]CTTACAGGTGGAAGC | 9678 |
| rs564801886 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103555 | CAATCTTGAACTGAT[G/T]TAGAAGAGACTCTTT | 9678 |
| rs564807615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976497 | TTGAATATGGGAACA[A/G]TTCTAAAACTTACAT | 9678 |
| rs564814927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099906 | AGGGAATGAGCTTTG[C/T]CAAGGATAGAGCTGT | 9678 |
| rs564818389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144465 | AATTATGTACCTATA[A/C]CCCATGTTTATTGCA | 9678 |
| rs564821961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003319 | ATTTGAATGACTTGT[C/G]TTTTTCTCCAGTGTT | 9678 |
| rs564851640 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10995361 | CCTTGCGCTAGACAC[A/G]GAGTGCTGATTGGTG | 9678 |
| rs564871182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974379 | CAGCCATTCTAGAAG[C/T]CAGGGCCGGTGGGAG | 9678 |
| rs564871442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167513 | GAAAATATTGATTGG[A/G]CTACAACTATATACT | 9678 |
| rs564874851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141981 | AAATTTCAAATGGCC[A/G]TATTTTGAATATCTA | 9678 |
| rs564900216 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11024535 | TTTAGAGGTGAATGC[A/G]GCTGGTGACTTTAAG | 9678 |
| rs564919264 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093951 | TTTTCCTCTTATGTT[G/T]TTTTCTCTTCACAGT | 9678 |
| rs564930806 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111117 | GTCAGTGTTCTAAAT[A/G]TTTGTTTTGTTTGTT | 9678 |
| rs564935958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11081424 | AACCAACACAAATGC[C/T]TGGTATTACAAGAGT | 9678 |
| rs564946230 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969771 | AATATTATTTCCAGA[C/T]TCTGGGTGATGAATC | 9678 |
| rs564947047 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113011 | TAAAAATAATGAAAC[A/G]CTATGGAGTTTAAAT | 9678 |
| rs564950975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080298 | TGATAACTTATATTA[C/T]ACGTGCATACTTGTT | 9678 |
| rs564955740 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10979979 | CATTAAAAATTTTTT[A/T]AAAAATTGCTTTCTA | 9678 |
| rs564956707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087535 | TTTGTTGTTGTTTTA[C/G]ATATAGGTACTATGA | 9678 |
| rs564979343 | snp | C/T | | | | | GRCh38.p7 | 7:10971814 | GCACTTTTTGGTAAA[C/T]CTGAAATTACTTCAA | 9678 |
| rs564984530 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148197 | CATCTTTCTCTATAC[C/G]TCAACCAGAATAAGC | 9678 |
| rs564985561 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025795 | GCGAGACTCCGTCTC[-/A]AAAAAAAAGAAAAAG | 9678 |
| rs564998009 | in-del | -/TTTTTTTTTTTTTTTTTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162088 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTTTTTTT]GAGACAGAGCCTTGC | 9678 |
| rs565011829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044839 | GCTGGGGACCAGAAG[C/T]GATTTGGATTTTGTT | 9678 |
| rs565018295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991649 | AAATTTTAAATAATG[A/G]AAATAGAAATGCTAT | 9678 |
| rs565020584 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11081917 | TTATTTCATTTTAAA[A/G]CTTTTCTCTATCTTC | 9678 |
| rs565025111 | in-del | -/GTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981832 | TGGTATATTAGAGTT[-/GTA]GTATAAGTTGACTAT | 9678 |
| rs565036307 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11003786 | GATATGTAAAAATAG[A/T]TATGCTGTCTGTCTC | 9678 |
| rs565052155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063267 | CTATCCTGAAGGTTA[A/C]GTTTATTAAAATTTA | 9678 |
| rs565067978 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093194 | AATGATTTCTGGTTT[A/C]ATTGCATCTTTAATA | 9678 |
| rs565070779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069835 | CCACACCACCATGCC[C/T]AGCTGTTCTATTATT | 9678 |
| rs565072459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154112 | AACTAATGGATTTAA[C/T]CAGGTTATTTATATG | 9678 |
| rs565078947 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11147786 | CATGCAGTTGTACCT[A/G/T]TATTTGGGGGACTTT | 9678 |
| rs565079234 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144542 | CTATGTACCTGCACC[C/G]CATGTTTATTGTAGC | 9678 |
| rs565083110 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | PHF14 | GRCh38.p7 | 7:10992158 | TCCCAGGTTCAAGCG[A/G]TTCTCCTGCCTCAGC | 9678 |
| rs565128214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055440 | CATGCATCATCTACT[C/G]TCTTTGAAGTTCTGA | 9678 |
| rs565141375 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025672 | TGGTAGCAGGTGCCT[A/G]TAGTCTCAGCTACTT | 9678 |
| rs565145745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166527 | TAAATTCTTACAAAA[A/G]TTGACCTGCAATGTG | 9678 |
| rs565146415 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11153756 | ATACCCTGTATATTC[-/A]AAAATTGAGAAAATT | 9678 |
| rs565150560 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107107 | TGTAGTTTACTCCTC[C/T]AATGAAATTAGAGAT | 9678 |
| rs565177139 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10985688 | GACAGGGTCTCACTC[-/TG]TTGCCTAGGCTGGAG | 9678 |
| rs565191084 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105492 | AAGGAATTCAGAAGG[A/G]CTCTCCAGCAGAGCA | 9678 |
| rs565218721 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056303 | GCTTTCAAGACTTTC[C/T]TTATTTTGTATATAC | 9678 |
| rs565237804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11036015 | ATTTTCACATTGAAA[A/G]ATGTGACTGTGAGGA | 9678 |
| rs565246127 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999603 | AGATTCATTGTTCAG[A/G]TAAACATAGATTTCT | 9678 |
| rs565263903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086297 | CCAAACCCAGCCTCA[A/G]TCTGTCTTTTTGTTT | 9678 |
| rs565267178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074403 | TTTTAGTAGAGGCAG[C/G]GTTTCGCCGTGTTAG | 9678 |
| rs565284648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079913 | ACATAGAAATTACCA[A/C]TTGCATGTAACTCAA | 9678 |
| rs565315163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133286 | CAGAGGACTGACACT[A/C]CCCAACTTTAAAACT | 9678 |
| rs565333765 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11042131 | TAATTTTTTTACTTT[G/T]GAATTTAATTAGTAT | 9678 |
| rs565352785 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160075 | TCCCTCCTTCCCTCC[A/C]CATTCTAGTAGTCTC | 9678 |
| rs565363482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091912 | CAGTGGATATTGAAG[A/G]TACAGCAGGAAATCA | 9678 |
| rs565374358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042898 | ATACTATATTTGTTC[A/G]TAATAAAGTATTTGG | 9678 |
| rs565396260 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11007035 | ACAAAAAATTTGCCA[G/T]GTGTGGTAGTGGGCA | 9678 |
| rs565403696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957204 | ATGATGATTATTTGA[C/T]CTATACATTTACTTA | 9678 |
| rs565412671 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967565 | CAGTTAACGTCAGCT[G/T]GATGTAGTCACTCAC | 9678 |
| rs565414516 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11153605 | CATCTCCAGATGACT[A/G]TTATCAAAGGATAGC | 9678 |
| rs565414552 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160620 | GGTATCAATGAGATA[C/G]TATCACAAAAGAGAT | 9678 |
| rs565424093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166255 | ACTTGTCAGGGCTGT[C/T]ACTAAGAAAATGATC | 9678 |
| rs565472383 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11047961 | GGAGGGAGGGGGAGG[C/G]AGGAAGGGAAAAGAG | 9678 |
| rs565474227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978807 | TGCCAGTTGTCCTCT[A/G]GGGGAAAAAAATGTT | 9678 |
| rs565485679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159621 | CTTGACTTTATCAAT[A/G]TGGGTATCTTGGTTA | 9678 |
| rs565499552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012661 | CTTGTCTGTTGGGTG[C/T]GTTCATGAGAATCTT | 9678 |
| rs565517944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133148 | CTTAAACTATAGATT[C/G]AGTGCAATCCCAATC | 9678 |
| rs565531100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146466 | CCTCCATTTCTTCAC[C/T]TCCATGTCTCTCTTT | 9678 |
| rs565552896 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055027 | CAGACAGCAACTGCC[A/C]TGTTTACCACAGAAG | 9678 |
| rs565578596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126272 | CAATTTAAAATTTAT[C/T]CTAGTATCCAGTCAT | 9678 |
| rs565581409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11126430 | CCTTTCCTTGTGACA[A/G]TGTTGAAGCTTTAAC | 9678 |
| rs565592488 | snp | A/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11138860 | TTGCTTCATTGTGTT[A/T]CTTGGAACTCAAGTA | 9678 |
| rs565595116 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080259 | ACATCGTTATTTAAA[A/G]AACAATAAAATTTAA | 9678 |
| rs565606930 | in-del | -/AAAA | 0.00755907 | 0.0610114 | intron-variant | PHF14 | GRCh38.p7 | 7:11077300 | ACCAGTAGTGCAAAG[-/AAAA]AAAAAAAGCCAGATT | 9678 |
| rs565610589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166021 | AAGGAACCAAATTTT[G/T]TCATTTGATATTACA | 9678 |
| rs565626109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080065 | ACATTTTTACTACGA[A/G]TGAATGTCATAAAGT | 9678 |
| rs565650355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125697 | TGATTTCAGACTTTT[A/G]CAAGTTGTTTTATGT | 9678 |
| rs565655686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11139808 | GTAAATGTTTATAGA[A/G]TTGATGAAAATTGAG | 9678 |
| rs565657897 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067944 | TTCATGACGTAAACA[C/T]CTCCCATTAGGACCC | 9678 |
| rs565660175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11036340 | TCTGTGAACATGGGA[A/G]TAAAAATCAATGTAA | 9678 |
| rs565665743 | in-del | -/AA | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11127462 | ATTTTGTCCTAGGGG[-/AA]ACACACAACCCCTTG | 9678 |
| rs565687089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007114 | CCCAGGAGGGCTTGA[A/C]CCCAGGAGGCGGAGA | 9678 |
| rs565714842 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061817 | ACGAAAACGAAGCTT[C/T]GTTCCTGAGGAAGAA | 9678 |
| rs565744116 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10999442 | AGCAACTCTTTTACT[-/A]ATAGCTTTTACTTTA | 9678 |
| rs565775063 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:10995769 | GCTGGGGGACCCGGT[G/T]CACCCTCCACAGCTG | 9678 |
| rs565783039 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119559 | AATTGTGAAAATATC[C/G]CCTAAATAATAGAAA | 9678 |
| rs565789421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996012 | CTCCTCAAGTGCGGC[C/T]AGAGTGGGCGCCAAG | 9678 |
| rs565800325 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11055063 | GTCCCATTCTTCTTA[A/T]GTTTCATCAGTGAAA | 9678 |
| rs565815312 | snp | C/T | 0.000456113 | 0.0150946 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022973 | CTATTCCAAATATGG[C/T]GCCAAGGTGAGACAC | 9678 |
| rs565830600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11012329 | CCTAGGGAATTGGTT[C/T]CAGGACCCCTGCAGA | 9678 |
| rs565838979 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159891 | GAGAAGCAATTTTCC[A/G]CTTCTATCAACTTAA | 9678 |
| rs565839906 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10978947 | GGTTTTGGTCAAACA[C/T]AGCCCTGGGATAGCT | 9678 |
| rs565842297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985317 | TTTGAAGTTTGATTT[C/T]CCCTGCTTTTACTTT | 9678 |
| rs565845664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054113 | AAAGCATTTTTTAAG[A/T]CACTTTTTTTTTGGT | 9678 |
| rs565847069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111901 | TATCTTATAGAATCT[A/G]TTCCTTTAAAAAAAA | 9678 |
| rs565860007 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975306 | TTAATAGTCCCTGAG[C/T]AGGGTTCTTCTTTTT | 9678 |
| rs565867815 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973132 | CACTTTGTAACTTCA[C/G]CCTAGCCTCTGATTG | 9678 |
| rs565871894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011706 | TCATTATTATATATG[C/G]TTTAGATTGTTTCTT | 9678 |
| rs565887798 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972613 | CACTTCTGCACCTTG[A/T]GAAAATGAAGTATGG | 9678 |
| rs565898748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10995503 | CACCCAGTGGATCCC[G/T]CACCAGGGCCACATG | 9678 |
| rs565902339 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978488 | AAATTAAAAGTGTTG[A/G]GACTTGGAATTGTTT | 9678 |
| rs565912521 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103868 | CTTATTGAAAGATCT[C/T]ATAACATTGGAGGAA | 9678 |
| rs565931970 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163165 | AGGTTTTTAAAAAGA[G/T]CTCTATTCTACTTAA | 9678 |
| rs565948850 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005733 | GCTGACAAACATGTG[A/C]CATGTATATATATGT | 9678 |
| rs565992918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11012762 | TGATAAGAGGAAAAA[A/G]GAGAATGACATATTG | 9678 |
| rs566028357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990508 | ATAAGAGGGTGCTTA[C/T]AGGGTTCTTTGATAA | 9678 |
| rs566029104 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11000306 | TTCTGTTGTATGATG[G/T]GGAGTATCTTTTCAT | 9678 |
| rs566035141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117503 | TAAGTAGAGGACATA[A/C]GATATTTTTAATTTT | 9678 |
| rs566035531 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10990072 | TAGATTATTTTCTGT[A/G]TCTCTGTGTATTCAT | 9678 |
| rs566073665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152572 | GAATTCATTCATATA[C/T]CCAATAACTATTCAT | 9678 |
| rs566137427 | snp | C/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971591 | GCAAAAGATTAATAA[C/G]CTAAATGCAATATTG | 9678 |
| rs566149553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966198 | CAGGGAGCTGTAGAC[C/T]GGAGCTGTTTCTATT | 9678 |
| rs566159193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11108437 | CTGAAGCTTTTATTT[A/G]CTTTTGAGTGAGCTA | 9678 |
| rs566176848 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104609 | AATATCAGGAAGGAG[A/G]TGAAATGTCTCTGAA | 9678 |
| rs566196417 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097858 | TTCATCTTTTCTCTA[G/T]CTCTGAGCTGTCAAA | 9678 |
| rs566205107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061396 | GCAAACAATGTGTGT[A/G]GTATGATCCCAGGTT | 9678 |
| rs566213614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991070 | ATCTCGGTTCACTGC[A/G]ACCTCCACCTCCCAG | 9678 |
| rs566218130 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018055 | CCTGGCACCTTTGTT[A/G]GGCACTAAGTTCACT | 9678 |
| rs566218467 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109070 | ATAGTTAACAAACAA[A/G]ATTGAGCCCATTTAC | 9678 |
| rs566228166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984884 | TTTTATGTTTAGGTT[A/G]ATAGTCCCAAACACA | 9678 |
| rs566236338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084727 | ATATTATCTTGTTAC[C/G]CACTGGACATGAATG | 9678 |
| rs566254293 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PHF14 | GRCh38.p7 | 7:11048433 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCACCT | 9678 |
| rs566263835 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084156 | CCATTACTATTTGTT[G/T]AAAATAGAGTAAAAA | 9678 |
| rs566265128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124576 | GTAATCCTCACCACA[A/G]CCTTTAAGGTGGTTA | 9678 |
| rs566270770 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965916 | GGCACGGGAGGGAAT[C/T]CCCTGGTCTGCCTGC | 9678 |
| rs566294706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087352 | GCACACCACCATGCC[C/T]AGCTAATTTTTATAT | 9678 |
| rs566303841 | snp | C/G | 0.021333 | 0.101051 | intron-variant | PHF14 | GRCh38.p7 | 7:11123858 | AGGAGGCGGAAGTTG[C/G]AGTGAGCCGAGATCG | 9678 |
| rs566318067 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073497 | TGGGCAGCTCTGCTG[A/C]TGTGGCTTTCCAGGA | 9678 |
| rs566329732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087807 | TTTCTGGCATTGGAT[A/G]AACATTTTGAAATAT | 9678 |
| rs566331711 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11081641 | GTGGGCGGATCATGA[A/G]GTCAGGAGATCGAGA | 9678 |
| rs566346170 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961774 | TGTAGTTCTCCATGA[A/C]GAGGTCCTTCACATC | 9678 |
| rs566399210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071540 | TCTAATTTTCGTCCC[A/G]TTAAATTTTACCCAT | 9678 |
| rs566419079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082109 | AGCACTTTGGGAGGC[C/T]GAGGTGGGAGGATTG | 9678 |
| rs566423123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997356 | CAAATGCAATTCCTG[G/T]GATGAGTTTTTATAT | 9678 |
| rs566433878 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11101307 | TTCTCATCTCTATTA[G/T]TTGTGCATGTAATTA | 9678 |
| rs566447647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077557 | AGTGAGCCCAGATCG[C/T]GCCACTGCACTCCGG | 9678 |
| rs566476502 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11008279 | TCCTTAGGAGTGTTC[A/C/T]CTGGATAGTAGAATA | 9678 |
| rs566478483 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:10984591 | GTTTACTTTTGACCA[C/T]ATCACTTTCTTCATT | 9678 |
| rs566486289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155407 | TGTGTAATGCTAGAA[A/C]CAGAAAAGCAGAATT | 9678 |
| rs566486942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058086 | ATTCTTCCTTCTTCC[A/G]CATATTATTTTCATC | 9678 |
| rs566510778 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11026172 | TTTCAGCAACCACCA[C/G]CACCCCCATCCGTCA | 9678 |
| rs566514238 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PHF14 | GRCh38.p7 | 7:11148840 | CAACTGTGCATCTGA[C/G]CTCAACTTTGAACCA | 9678 |
| rs566529937 | snp | A/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065963 | TGAGGGTAGGAAATG[A/T]TCTATTAAGCTATTT | 9678 |
| rs566539123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092911 | TAAAGGGTGTTTTTT[C/T]CCCCCTAATAGTGAC | 9678 |
| rs566546585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155819 | CACATAGCTAGCTAG[C/T]TGATGTTCAATCAGG | 9678 |
| rs566551304 | snp | G/T | 0.0119091 | 0.0762411 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974100 | GCCAGGGAGCGCTGT[G/T]GGAAGGGGCTCGAGC | 9678 |
| rs566573636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167234 | AGAAACTTAGTAGAC[C/T]GTCCGTGTGATAAAG | 9678 |
| rs566588585 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11149884 | TTTTATACTTCATAT[C/G]TTTCTCTTTTCTGCT | 9678 |
| rs566603664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086768 | GGTTAGATTGGAATG[A/G]TAGTTTTTGTCATCA | 9678 |
| rs566604507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003942 | GGAAAACATCAGTAG[A/G]AATAAGCTAAGAAAA | 9678 |
| rs566604640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060825 | AATTTACTTTTTTTG[A/G]ATGACTAATTTAGTT | 9678 |
| rs566610953 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006696 | CTCTTCCGAGGATAT[C/T]TGGGCTGCCTCCAGA | 9678 |
| rs566614965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065660 | TGAGAATAAATGATT[A/G]ATCTATGAAAAGTAG | 9678 |
| rs566617036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10981440 | AGAATGATTACTGAG[C/T]ACTTACTGAGTAATG | 9678 |
| rs566625394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965102 | TCCATCCAGTTTTAT[A/G]CCCTTGCTGGAGAGG | 9678 |
| rs566626625 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138292 | GTGATCCACCCGCCT[C/T]GGCCCCCCAAAGTGC | 9678 |
| rs566635542 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032703 | TACTAACTGCTTCTC[A/G]TCATTCATTTTTGTC | 9678 |
| rs566657049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974538 | CTAAGTGGGGGATTA[C/T]GAGGAAGGTGCAGAA | 9678 |
| rs566661884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993305 | CCTGCTTTTCTGGTA[C/T]TACAGCCCTTGTCCC | 9678 |
| rs566677362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031719 | TGTTCTCACCACTGC[A/G]CTCAGCCTGGAGAAT | 9678 |
| rs566677934 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063841 | CTATGTTATTTATTT[A/C]TTTAGTTTCTGTTAT | 9678 |
| rs566688081 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127396 | CATCCCACCAACGCT[A/G]TCCTCTTTGGCTAGA | 9678 |
| rs566702344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128443 | ACTACCTCCTCTGTT[C/G]TTTATTCCAAACATC | 9678 |
| rs566704915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957897 | TAGGGGAAATGAGGA[A/G]TAACTGCGAATGGAT | 9678 |
| rs566709582 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11166476 | TATTTGCTGTCTGAG[-/T]TACTTTAATGATTTT | 9678 |
| rs566732520 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056798 | ACATATAATTTTATA[G/T]TCTTAGGAATTAAAT | 9678 |
| rs566740104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959603 | CTGCGCATAGCCAGG[A/C]GCACCAACTGCTGCA | 9678 |
| rs566744058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167638 | AAATTTCTTGCCATC[C/T]GTACCTGCTGATTTA | 9678 |
| rs566759863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121920 | GTTCCGTAGGTATAC[A/G]TGTGCCATGGTGGTT | 9678 |
| rs566760584 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161213 | GAAGTTTGGTAAAAC[A/T]TAATTTTAGGGCCTG | 9678 |
| rs566780281 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145149 | ATTAAAAAAAAACCC[C/T]CGGGAGGGGTTCAGG | 9678 |
| rs566780463 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069464 | TTCCATCCCCTCTGT[C/G]CCAGGGAGGCTTCAA | 9678 |
| rs566795324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038455 | AAAAAAAAAATAGAT[C/T]GAGACCATCCTGGCC | 9678 |
| rs566822129 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11161966 | CAAGACCATAAGTTC[A/G]TCAGGGTTATCAAAC | 9678 |
| rs566849314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148395 | AGGACCGTTGCCCTT[G/T]TTCCCTGTGCCTGTA | 9678 |
| rs566862331 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026076 | GAGATTGCACCACTG[C/G]ACTCCAGCCTGGGTG | 9678 |
| rs566875341 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11019457 | TTGGATTTCTTCATG[C/G]TTCAATCTTGGTAGG | 9678 |
| rs566881085 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11143951 | AACCTATAAAATGGG[-/A]AAAAAAAAGTAATTG | 9678 |
| rs566911242 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030241 | TGGTGGGCAAAAGTA[A/C]GAGAGGGCAATACAG | 9678 |
| rs566920930 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11057414 | GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 9678 |
| rs566921915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11134061 | CTATCCAGTGCCTGG[A/G]AAATTTTTCTTGTCT | 9678 |
| rs566922759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11141730 | TATGTAAATCTCTAC[A/G]TGATTATTGGTATTT | 9678 |
| rs566932826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093450 | TTGCTCTGCTTACCT[C/T]AGTGTACCACAAGGC | 9678 |
| rs566935509 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035110 | GATCGAAAATGTTTG[-/A]AAAAAAAAAAAGCGT | 9678 |
| rs566938255 | in-del | -/AA | 0.0283406 | 0.115616 | intron-variant | PHF14 | GRCh38.p7 | 7:11089096 | AGATTAATTAGATAT[-/AA]AAAAAAAAAACCGTA | 9678 |
| rs566942790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957010 | AAACATGAGTTGGTA[A/G]AAATATAAATGTTAA | 9678 |
| rs566948653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014197 | GTATAGTACCCAGGG[A/C]TCAGATTATTTAAAT | 9678 |
| rs566958950 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168812 | CACAAGATGCACTTC[A/G]TTTCTATGAAAGCAG | 9678 |
| rs566981247 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980772 | TAGGATAATACCATG[A/G]ACTTCACTGGGGGTA | 9678 |
| rs567035379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986369 | CACTTCAAATTAAAA[C/G]TGAGGAAGCACACAA | 9678 |
| rs567066557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074787 | TGGCCTTTGGTGTCA[A/G]TTGCTATCAGCATTC | 9678 |
| rs567078848 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106178 | TAATCTGGCTGCCAC[A/G]GATATAGCTAACTGA | 9678 |
| rs567091371 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11092824 | GGCCAAAATGGTATT[A/C]TAAAATGTTGAAGCC | 9678 |
| rs567096944 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11113305 | ACATTGCATACATTT[G/T]GTACATGCCATAGGT | 9678 |
| rs567102437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030645 | AGCTAATTTGAGGAA[A/G]TTTACAGGGAAACAG | 9678 |
| rs567115614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024302 | AAGCCATCTCCGTAA[C/T]ATAAAAGATGAAGAA | 9678 |
| rs567128517 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972124 | TATTTTTAGTAGACA[C/T]GGGGTTTCATCATGT | 9678 |
| rs567158206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161138 | TCTGCATATGGCTAG[C/T]CAGTTGCCAGCACCA | 9678 |
| rs567159443 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106892 | TGCTTTATATAAACT[C/T]ATAGGGGCTACAAGT | 9678 |
| rs567174918 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004102 | AATACAGAAAAATCA[C/G]CCAGGTGTGGTGGCT | 9678 |
| rs567181134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127230 | GGCATTCTAGATTTT[C/G]ATTCTTGCCCCTCCT | 9678 |
| rs567196913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986916 | GAAAATATTTAAAAT[C/T]AGAGACAGTTTGGAT | 9678 |
| rs567205026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037995 | ACAAACTGTAAAAGA[A/C]GGTATAAACGTAGTT | 9678 |
| rs567219632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11154817 | ATGTCTTTAAATGTA[A/G]TCATTCACCCACTTT | 9678 |
| rs567227438 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10997313 | AGTTCAAAGTGAGAA[C/T]AAAAGAAGGGAAAGT | 9678 |
| rs567230320 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141326 | TAATGAATTGTCTGA[A/T]GATATGTAATAAGTA | 9678 |
| rs567260374 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107588 | TCCAGTTTTTATTTT[A/G]TTAAAAAATCTTAGT | 9678 |
| rs567261610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964683 | GTGTTTTCTAACTTG[C/G]TTCCATTCTCCCCAT | 9678 |
| rs567287424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986258 | CAAAGTGTTGGGATT[A/C]CAGGTGTGAGCCACC | 9678 |
| rs567289074 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064395 | AAATAAGATATTTTA[A/C]ATAAGGATTTATTTT | 9678 |
| rs567322893 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070109 | CATTTTTGGTAAGCT[A/G]TGTTTCTCTTTTTGT | 9678 |
| rs567330417 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029644 | AATGAATATTGCAAA[A/G]AATTTTCAGTTTTAA | 9678 |
| rs567330683 | in-del | -/A | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063423 | ACAATAAAAATAAAG[-/A]AAAAAAATAACAATC | 9678 |
| rs567355575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098847 | AGAATGTTTCCTTTT[A/T]GCCTTAGACCAGGTT | 9678 |
| rs567367765 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138210 | CACACCTGGCTAATT[C/T]TTTGTATTTTTTAGT | 9678 |
| rs567404427 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166230 | GAACACTTCATGAAA[C/G]AAATGTCAAACTTGT | 9678 |
| rs567409954 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973967 | TCTTTCGTTGCTTCT[C/G]GTCCAGGCTAATAAA | 9678 |
| rs567447733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007175 | TCCAGCCCGGGTAAC[A/T]AGAGCGAAACTCCGT | 9678 |
| rs567460480 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10996921 | CAGTTAATCTACTCA[A/C]CAGCCGTAGGTTTTA | 9678 |
| rs567464165 | in-del | -/TGTCTG | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11003791 | TAAAAATAGTTATGC[-/TGTCTG]TGTCTGTCTCAACTC | 9678 |
| rs567464779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037320 | TATTATTTAATTCCC[A/C]GCTTAACTTTATAGT | 9678 |
| rs567467853 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060229 | ATCATTCATTAGTTC[C/T]GATTTAACCACTTAT | 9678 |
| rs567502348 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025973 | AAAAATTAGCTGGGC[A/G]TGGTGGCACGTGCCT | 9678 |
| rs567541234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079993 | ATTATACAAGGAAAC[A/G]AAATATGAATAGACT | 9678 |
| rs567542901 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074077 | AAGATCTCCAAAATG[A/C]GTTCAATGCCTTTCC | 9678 |
| rs567580909 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11081631 | GGAGGCCGAGGTGGG[C/T]GGATCATGAAGTCAG | 9678 |
| rs567582233 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054501 | ACAGAAGGGAGTGAT[C/G]AGTCATTTTGGTCTT | 9678 |
| rs567595744 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964392 | TTTCTTTAAGAATGT[G/T]GACTATTGGCCCCCA | 9678 |
| rs567610938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167210 | TTAAACCGGGAAGTC[A/T]TACGGTGGAGAAACT | 9678 |
| rs567621458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10991693 | TTTCTTTAAAGGTCG[A/G]TGTTCTGGTATTGTA | 9678 |
| rs567633952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10979274 | TTATTTTATTTTTTT[A/G]TCTGGCCATTACCAC | 9678 |
| rs567634233 | in-del | -/T | 0.256897 | 0.249905 | intron-variant | PHF14 | GRCh38.p7 | 7:10979554 | TTTCCTTTCTCTCTC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs567655240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153686 | GAAATTTAAGAGGCC[A/G]ATATTGTCATTGGTA | 9678 |
| rs567660981 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:10978729 | AGTAGCATCTTTCCT[A/G]CCTGCCCCAGCCTCA | 9678 |
| rs567678596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983215 | AGGGAATTCTTCTCT[A/C]AATCACTCTACACAT | 9678 |
| rs567695436 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973667 | AGGGCGGAGCCTTTG[A/G]GGTTTATGGGCGGAA | 9678 |
| rs567709587 | snp | C/G | 1.71864e-05 | 0.00293137 | intron-variant | PHF14 | GRCh38.p7 | 7:11035626 | CACTATTTTTCTGTG[C/G]TTTCTTTGTATAGGA | 9678 |
| rs567724002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063361 | AATTTTGCAATATGT[C/T]GAAAATGAAATCCCA | 9678 |
| rs567734126 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11147858 | AAATTCATATATTCA[A/C]ATGTTTGCCTGACAT | 9678 |
| rs567744949 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997863 | TATAATCTAATATTG[G/T]TAGTGCATACAACCA | 9678 |
| rs567745727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125975 | TTAAGAATCGCTTTG[A/G]AAAGTTCAAGCTGTA | 9678 |
| rs567756239 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11153177 | TGATTAGGAAGCTAT[A/T]GGATTAATCCACAGG | 9678 |
| rs567757847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096124 | GGTTTTCCCAGTCAT[A/G]CAAAGTTCATTTTGG | 9678 |
| rs567772958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013361 | GAGATGAGGTTTCAC[C/T]GTGTTGGCCAGGCTG | 9678 |
| rs567773853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957118 | AATGACTACCCTTAG[A/G]TAAGCAAGAGGGGCT | 9678 |
| rs567789548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10980046 | AGTCTCAATTTACCT[C/T]TCATTTGAAAAAATA | 9678 |
| rs567789615 | in-del | -/GTTTT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10977457 | TTATATTTCTGTTTG[-/GTTTT]AAGAATAAATATAGA | 9678 |
| rs567793117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096552 | ATTTACGGGTATTTC[A/G]TATCGTATGTTGCTT | 9678 |
| rs567793404 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000171 | AAAGGTCAAAAATAC[G/T]TTTTGACTTAAAAAA | 9678 |
| rs567794638 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11140416 | ACATTAGGGCTGATA[C/T]GTAGGTCTATATGTT | 9678 |
| rs567801826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165464 | CTTACATCAACATCT[A/G]TAAAGATATAAAGAA | 9678 |
| rs567819357 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152439 | ATTATAAATAACGAA[A/C]GTAAATACAAGCCTT | 9678 |
| rs567839490 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085024 | TGCTTTATTGCTAAT[A/G]GTATGTTTTGCTGAA | 9678 |
| rs567841640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119025 | TAAGCCACTTTCTAA[A/G]TTACGCTTACTACAA | 9678 |
| rs567844145 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11005213 | TTTAGCATCCTTGTC[A/G]AAGTCACTGATTACA | 9678 |
| rs567845058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11159499 | AAAAATATATATTTA[A/G]TACATATGAAATGAT | 9678 |
| rs567870767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112655 | GAGTGCCTCTAATCC[C/T]AGCTACTTGGGAGGC | 9678 |
| rs567891748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11036147 | AACCTATGGAGACAA[C/T]AGCAGTTATTAAGAA | 9678 |
| rs567898783 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014954 | AAGAGTAATTTTCAA[C/T]CTTTTGTATTTCGTG | 9678 |
| rs567902223 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11029576 | GTGTGTATGTGAATT[G/T]TATTTAGTAAAAGTG | 9678 |
| rs567909960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068101 | CACGCCTGTAATCCC[A/G]GCACTTCGGAAGGCC | 9678 |
| rs567912859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11068742 | AACAAAAGTCTACAG[A/G]GATTATAATAGGCTT | 9678 |
| rs567921615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163229 | CATCCCAAGTGACTT[C/T]AATTTCATAATATAG | 9678 |
| rs567936075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995950 | AGCTGGCTCCACCCT[C/T]GGCCAGCCCAGAGAG | 9678 |
| rs567937420 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012463 | TTTTCACTCTGTGTT[G/T]TGTTGAAAGAAATCT | 9678 |
| rs567939344 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165667 | CCATTGTTAGGAGTT[-/G]GTTACGTCCTAAGAG | 9678 |
| rs567940513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11030220 | CCTCATAGCTACAAC[C/T]CAGGATGGTGGGCAA | 9678 |
| rs567945440 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123258 | AGAGAGACTTTTTTG[A/C/G]CTTTTAAAATATCCT | 9678 |
| rs567957298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11151253 | TTTTCTCATTTTTAT[A/G]TATTTAAATTTATAA | 9678 |
| rs567964268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066016 | CTATCAAATGCTTGC[C/T]AGATTCTCCCCTTTA | 9678 |
| rs567975699 | snp | A/T | | | | | GRCh38.p7 | 7:10969758 | CAGACAGGTTATTAA[A/T]ATTATTTCCAGATTC | 9678 |
| rs567980391 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11039436 | CACCTTTAGTCTGTT[-/A]AAAGTTTTTGGTGTT | 9678 |
| rs568026665 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11021416 | GTTGTCTCGGCCATG[A/G]TTTTCATTGACTTTG | 9678 |
| rs568027111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060209 | AGTTTGTATTATATA[A/G]TATCATCATTCATTA | 9678 |
| rs568035974 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014178 | CGTTTCTCATTTTAT[A/G]GGTGTATAGTACCCA | 9678 |
| rs568041835 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095041 | TTTACTGAGCCTGAG[A/G]GAACACAAGTCAACT | 9678 |
| rs568054929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066353 | CAGCCTCTGCCTCCC[A/G]GGCTCAAGCAATCCT | 9678 |
| rs568062853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053098 | ACAAAGATATTTTTA[C/G]GGTTAGTTGTCATCA | 9678 |
| rs568091511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11010855 | AGACAGGGCCTTACT[A/G]TGTTGCCCAGGCTGA | 9678 |
| rs568092337 | snp | G/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105116 | AGCCTGTGTTCACAA[G/T]TCACTCATCCTTTTG | 9678 |
| rs568101998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045233 | TCTGCTTTAGACTCT[A/G]CCTTGTTCTTACTAG | 9678 |
| rs568111101 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052617 | ATGTTTCTGTTGCTT[A/C]ACAAAGTTTTGTCCA | 9678 |
| rs568111968 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991232 | GTTGCCCAGGCTGGA[G/T]TGCAGTGGTGCTATC | 9678 |
| rs568117492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144641 | TACTAATGTTCCTAA[C/T]GTTTTTATATCACTG | 9678 |
| rs568172373 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046621 | GTATATGAAATAACA[C/G]GTATATATCTGCTAT | 9678 |
| rs568196408 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967650 | GAGTTCAAGCCCAGC[C/G]TTGGCAACGTAGCGA | 9678 |
| rs568217819 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994503 | GGCACAGAAGTTTGT[A/T]TGGCTAGAACTGGGT | 9678 |
| rs568245891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965447 | CTCTAGAAGCTTTGT[C/T]CCAGAGGGGCACCCA | 9678 |
| rs568247649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960260 | CCCACCCCCCTACAG[A/G]CCTCAGTGTGAGATG | 9678 |
| rs568261948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162620 | CTCTTCAGATGGCTG[C/T]GGCAATCCTTAGGGC | 9678 |
| rs568300564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027158 | ATTACATGAAATTAT[C/T]CAGATAATCTAAACA | 9678 |
| rs568310773 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11116394 | GTTCTTCTCAGTAGA[A/C]AAAGCCAAGGACTGG | 9678 |
| rs568311500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989453 | CATAAATAAAAATGT[A/G]TGGACCCAAGTGCCA | 9678 |
| rs568322439 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149237 | GGATGCACACACACA[A/C]ATTTTTTTAACATGC | 9678 |
| rs568341724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020806 | TATGTAAATGAACAA[C/T]CTCCTACTCAACAGA | 9678 |
| rs568353678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109792 | TATTGTCATAGTAAA[G/T]AAAGTACTGTTGGTC | 9678 |
| rs568359976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069274 | TTTAGTCTTACTGCT[A/G]AAGGATTCCCAAACA | 9678 |
| rs568368185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11082302 | GCAGTGAGCCATGAT[C/T]ACGTCACTGTACTCC | 9678 |
| rs568373924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11150823 | TCTAAGAGTTCAGAC[G/T]GGTATCAAAGTCTCA | 9678 |
| rs568378495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11009489 | ACACACTGAGCACAT[A/G]TGAGTTTTATGTGTT | 9678 |
| rs568388302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038589 | CTTGAACCCCAGAGG[C/T]GGAGGTTGTAGTGAG | 9678 |
| rs568431595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094884 | GCCCTCTGACATCAG[C/T]TCTCTCATGGCTTGA | 9678 |
| rs568436665 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11128654 | GGCCATATATAATCT[-/A]GACTCATGCTGCTAG | 9678 |
| rs568437627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136128 | ATTTGCATTTCTTAC[A/G]TGGTAAAATCCTTCA | 9678 |
| rs568459237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998073 | AGAATTGGTGATATA[A/G]GGAAAATAGTGAGGA | 9678 |
| rs568496482 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11090215 | ACATGAAAGTAATTC[-/T]TTTAAGTATATTCTC | 9678 |
| rs568500499 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129588 | CATAAAATTTAAGAG[A/T]CAGTAAACCCTTTAT | 9678 |
| rs568519473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004710 | GTAAGAGTATTGTGC[C/T]GGTGTTTAGTTCCCA | 9678 |
| rs568543197 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11102076 | TTTCAGCACAGTTTT[A/G]TGTTTTCTCAAGCGA | 9678 |
| rs568553743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039108 | ATTTGCTCTAACTGA[G/T]TGACCTGTCATTTGT | 9678 |
| rs568559463 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152122 | GATCAGTACTGCAAG[A/G]TAGACTTAGGACCTT | 9678 |
| rs568577618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998940 | TTTTTAGGCCAGCAC[A/G]GTAGTTTTGAGTAAT | 9678 |
| rs568581138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974727 | GCTGAGAACTCAGTT[A/G]GACAAAAATTCCTTG | 9678 |
| rs568592144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122569 | CTGTCCTGATTCCCA[A/G]TAGAGGGAACCATTA | 9678 |
| rs568593607 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095254 | GGTGGTTACTGTTTT[A/T]ATTTACATTTATAAG | 9678 |
| rs568604056 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102983 | TTGAACAATACAAAT[A/G]ACAAACAAGAAAGAC | 9678 |
| rs568605680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017083 | AAATGACTGGCTCTC[A/G]TTCTTTTTTATGGCT | 9678 |
| rs568622656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035845 | TATGTAAGGATTTTA[C/T]GTCTCGTGTGGCTTC | 9678 |
| rs568634243 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10988085 | TTTAAGGAGGATGTG[C/T]TACTTAGATTTTCCA | 9678 |
| rs568642263 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11100347 | GATGCTTACTGTATC[C/T]CAGACTATGTTTTCT | 9678 |
| rs568672060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101157 | TAGGATGTAGGGATA[G/T]TAGCAATAGCTTTTT | 9678 |
| rs568693029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135271 | GGCTTTTGAGGGGGG[A/G]TTCTTTTGTCACTTT | 9678 |
| rs568731256 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11082779 | GTCTCAGCCTTCACA[C/G]TCAGTAGAATTTTGG | 9678 |
| rs568748195 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094219 | CTGTTAGAACAAATT[A/T]CTACAAATTTGGTAG | 9678 |
| rs568774053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076311 | CCTTCCGTGATCATA[A/C]CTGCTGTTTTATTTT | 9678 |
| rs568777060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10975571 | AAAACAGAAAAGTAT[A/G]ATTTTCCTTTGTATT | 9678 |
| rs568783397 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984354 | GAAACCAATATTTTA[C/T]ATGAAAAAATATTGC | 9678 |
| rs568797105 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11008771 | CCGGGCGCGGTGGCT[C/G]ACGCCTGTAATCCCA | 9678 |
| rs568800790 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994071 | GGATATTTGAGCAGT[G/T]ACCTGAAGGAAGTAA | 9678 |
| rs568812869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10988179 | CCCTCTTTGCGTTAC[A/G]TTTCTATTAAGAGCC | 9678 |
| rs568816814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994420 | CTCCAGTCTGGGCAA[C/G]AGAGTGAGACTCCGT | 9678 |
| rs568818078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065742 | CTTTCAGTCTTTATC[A/G]AACTATCAAATTAGG | 9678 |
| rs568828957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066331 | GTGGCACTTTCTTGA[C/T]GCAGTACAGCCTCTG | 9678 |
| rs568829888 | snp | A/G/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11027133 | GAAATCCCTTGCTCA[A/G/T]TTTCAACATATTACA | 9678 |
| rs568832835 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11143346 | GGCTGATCTCAAGCC[C/G]CTGGGGTCAAGTGAT | 9678 |
| rs568864681 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974650 | GCCTTTGAAACTGCC[C/T]GTGGAGCTGTCCAGC | 9678 |
| rs568888491 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047079 | CTTTCTTTTTTTTTT[C/G]TTTTTTTGAGATGGA | 9678 |
| rs568905058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057787 | ATTTTTTAATCACCT[C/T]TTTTCAAGTAAGTTG | 9678 |
| rs568909022 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089932 | ATGTGCCGTCACGAC[C/T]GGCTAATTTTGTATT | 9678 |
| rs568919403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015486 | CATTACTCTAAGTTG[A/G]GCCTGAGAGTGGCCT | 9678 |
| rs568923071 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969532 | AATTATGACCCCTCT[A/G]GTTTGCATATCCTTG | 9678 |
| rs568942803 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039358 | AAACTTTAATGTTAA[A/G]ATGTATTTTTCCCCT | 9678 |
| rs568946705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11150675 | GCAGAATGTTACCAA[C/G]TTTTCTATACAGCTT | 9678 |
| rs568968281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144067 | TTAAAAAGGATCTGA[A/G]TAGAAATTTCTCAAA | 9678 |
| rs568972239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976145 | TTTATCTGCTTGGAT[C/T]CCAAGAGTTGATGGA | 9678 |
| rs568973131 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11162133 | TTGCTCTGTCTCCCA[A/G]GCTGGAGTGCAGTGG | 9678 |
| rs568983488 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11051836 | GAGGCCAAAATTTAA[A/G]AGAGTGAGAAAGACA | 9678 |
| rs568988771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038522 | AATTAGCTGGATGTG[A/G]TGGTGCACACCTGTA | 9678 |
| rs569019836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960686 | CACAATGGTTGAACT[A/G]GTTTACAGTCTCACC | 9678 |
| rs569036940 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11114976 | TAATAAATGCCACAT[A/G]CCTGGAAAAGAAATG | 9678 |
| rs569041620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082200 | ATTTTTAAAAAATCA[C/G]CTGGGCATAGTGACA | 9678 |
| rs569046200 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168710 | GTTGAAAGAACATGT[A/T]TGATGAGATGGGTTA | 9678 |
| rs569054154 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037219 | TGGCTCTTCCCTATA[A/C]CTCCTACTCCTCATT | 9678 |
| rs569056569 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122019 | CCTCCCCTTGCCCTA[A/C]CCCCCGACAGGCCTC | 9678 |
| rs569062165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997978 | ACTGATTATTAAGGG[C/T]TATCTTAGAGGCTGC | 9678 |
| rs569067600 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11031488 | CTGGGTGCAGTGGCT[C/T]ATGCCTGTAATCTCA | 9678 |
| rs569075859 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983416 | AATATTTTTATATCC[A/G]TAGACTTGGGAAATG | 9678 |
| rs569086761 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019963 | CTTCTTCTTTATGTC[C/T]TTTGTTGGGTGTCCT | 9678 |
| rs569090172 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063595 | TACTGTGTCTTACTA[A/T]TTTTTTTTTTTTAAT | 9678 |
| rs569109585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162515 | ACTCATACTTATCAT[C/T]CATCATTCATTTCCT | 9678 |
| rs569113133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122499 | TGATTCATACATATA[A/G]ATTCTTCAGAACCCT | 9678 |
| rs569114378 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980886 | GTTTCAGATAGGGAA[C/T]TGCTGACCCGTATGA | 9678 |
| rs569115023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11032275 | TAATTAAGAAGATAA[C/G]TTTGATATGCCATTA | 9678 |
| rs569128278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093536 | TGCCAGAGTGCTTTT[C/T]GTCATTTGTACTCCC | 9678 |
| rs569174981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11124603 | GTTATTGTTTTTTTT[C/T]ATCTCCTTTCTGCAG | 9678 |
| rs569181949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148635 | TGAAATTGAAGGCCA[A/T]GAGGACGATACGCTG | 9678 |
| rs569182101 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11144894 | AGTAGTAAGAGTAGT[-/A]AAAAAATCATAGAGA | 9678 |
| rs569194644 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116715 | GGACTGACATTTGTA[G/T]TTTTTACAAGTTCCA | 9678 |
| rs569196482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033185 | CATGTCAACCAATGC[A/G]TTAATTAGGACATTA | 9678 |
| rs569214485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155838 | TGTTCAATCAGGAAG[A/G]AATGAATAGATGGCT | 9678 |
| rs569215150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11057484 | GGATCGAGCGATTCT[C/T]ATGCCTCAGCCTCCT | 9678 |
| rs569234698 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10987504 | CATTTTGGGGGTAAG[C/T]TTTAAATCCTGATGG | 9678 |
| rs569243051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11094089 | TTCCCACTGTGGTGG[C/T]CGCTCCCCTTCTCCA | 9678 |
| rs569246018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11149095 | CACAGAGTCAAACCA[A/G]TAGTTAAGTGCCAAA | 9678 |
| rs569250269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11014366 | AGAGTCACTATAAGG[C/T]ATAAAAAAACTCTAA | 9678 |
| rs569284516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008214 | ATTTTTCAGTTTACT[A/G]TTAGCCTAGCCCAAG | 9678 |
| rs569286510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015002 | CTTCCTCTCCAATAT[A/G]AGAGGGGGGGTGGGT | 9678 |
| rs569294459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135150 | GAATGCAGACTTGGA[A/G]TCAAATTATTTAGGT | 9678 |
| rs569299598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11047638 | CTAAAAATACAAAAA[C/T]TAGCTAGGAATGGTG | 9678 |
| rs569308324 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957693 | ACAAATACTGATGGC[A/G]TCTCACAGTATTGTG | 9678 |
| rs569320243 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10987074 | AATTAAAATGTAAAT[G/T]TTTTGCCAAAATTTA | 9678 |
| rs569327970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966769 | CTTTGTCTACTCAGC[A/G]ACCAGATACACCCTT | 9678 |
| rs569330919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088023 | ATAAAATATAACTTT[A/G]CAGAGTTATCATTAT | 9678 |
| rs569338384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048072 | TTAATTGGCTTGGAT[C/G]AATTAAAAGGTTAAG | 9678 |
| rs569344395 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145565 | TTTATAATTATGAAA[A/G]CATTTTTCCAGTTTT | 9678 |
| rs569352879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11045091 | TGTGATGCCATGTTG[A/G]TAATTTGAAATTGAA | 9678 |
| rs569369312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11003973 | CATCTCCCAGTTGGG[C/T]TTGGTGGCTCACGCT | 9678 |
| rs569372069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065470 | GACTGAGTATTCTTT[C/T]GCTGAATTAATAAAA | 9678 |
| rs569394638 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142258 | AACTCAGGTATCTTC[A/T]CATTTAAAGCTGGTA | 9678 |
| rs569396568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128689 | TTAGATGTAAATCAG[C/T]CTCTCTCTCTCCCCC | 9678 |
| rs569397462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019204 | AGTTTTCTTTTTTTG[A/G]TGTGCCTTTGGCTGG | 9678 |
| rs569397689 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141969 | TATTTACCTAGAAAA[G/T]TTCAAATGGCCATAT | 9678 |
| rs569399966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114124 | AATAAATTTAGATGG[C/T]AAAATGTCTCCAACT | 9678 |
| rs569425740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980150 | TAATAGCAAAGTTGG[A/C]TTGGTCTCAATTTTG | 9678 |
| rs569438652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967068 | AAAGAAGGGTCTAAT[A/T]CTACTAAGAAAATGA | 9678 |
| rs569440496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962268 | GTTCCATCAATACCT[A/G]GTTTACTGAGAATTT | 9678 |
| rs569444913 | in-del | -/ACTC | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11089629 | CTATATTCTTCAAAT[-/ACTC]AGGCAAGTTTGAGCA | 9678 |
| rs569477460 | snp | C/T | 3.31417e-05 | 0.00407059 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028767 | CAGAGCCTATTTCCA[C/T]GTGACCTGTGCTCAA | 9678 |
| rs569481502 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11069575 | TAATATTTTGATAAG[C/G]GTTATACATTCTCTG | 9678 |
| rs569483129 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974180 | GCTACTCTTGGGAGC[A/G]CCCCTGTCCGGCTGG | 9678 |
| rs569505029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064283 | CATATTTTGGAATTG[A/G]CACTGTTATTGTTTG | 9678 |
| rs569505579 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972504 | ATGGAAGTGAAATTC[A/C]CAGAGTGGAGTTTTT | 9678 |
| rs569514882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987406 | CTATTGTATATATCA[C/T]TTACAGTCATATGTG | 9678 |
| rs569521015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11019645 | TTTTTTCCTCAGCCT[A/G]GCTAAAGGTTTGTCA | 9678 |
| rs569572514 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10980570 | AGAAGTCACTTGTTT[C/G]TGAGTAATATTGGGT | 9678 |
| rs569586107 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | PHF14 | GRCh38.p7 | 7:11145517 | AATTGAGCATTTTCT[A/T]AATTCTTATAATATA | 9678 |
| rs569619905 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103646 | TTAATAAATGTGGTT[G/T]TGGACATCTTTTCGG | 9678 |
| rs569628880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132042 | TGGTAAAAAGTTACT[A/G]TAGTTCAAGTTAGCA | 9678 |
| rs569637375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11084938 | TTTCTTTTTTAAAAA[C/T]GAGTTTATTACATAT | 9678 |
| rs569647361 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973079 | TGCAAGAAATCAAAC[A/T]GATTGCAGGGGAAAT | 9678 |
| rs569654862 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043810 | ATCCCAACAATGTTA[A/G]TAAGCATCCTGGGTG | 9678 |
| rs569659355 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11132816 | TGAGTATGAGATGGT[A/T]TCTCATAGTGGTTTG | 9678 |
| rs569665749 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105842 | AAATAAAATGAGATT[A/G]ACACCCAGCAATTAT | 9678 |
| rs569667513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042009 | TTAAATTGCCTTTTT[A/G]CATAAGAGAAGTTAG | 9678 |
| rs569680870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11006136 | CATTTCCAGATTGAC[C/T]ACCAAAAGGACTGTA | 9678 |
| rs569697601 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PHF14 | GRCh38.p7 | 7:11123847 | CGCTTGAACCCAGGA[A/G]GCGGAAGTTGCAGTG | 9678 |
| rs569708872 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10990095 | GTATTCATATACCTA[A/C/T]GCAGGCTCTCATGGA | 9678 |
| rs569781706 | in-del | -/T | 0.447938 | 0.152711 | intron-variant | PHF14 | GRCh38.p7 | 7:11076567 | ATTTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs569792398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125496 | TTACACTCGTTTGTG[C/T]TAATTCTTTTGCTGA | 9678 |
| rs569823715 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11061227 | AGGATGTGAATTTTA[C/G]CTAAATTAGTTTAAA | 9678 |
| rs569831245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990433 | TAGTTAGTTGCATGC[A/G]TGCTTTTTCATATCC | 9678 |
| rs569831363 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10984172 | CTTTATTTGTTCTTT[C/G]ACATTTTTCTGCCTA | 9678 |
| rs569885372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096031 | CTGAGAATCCCAAGA[A/G]ATTTGTGTCTTTGTC | 9678 |
| rs569889523 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009656 | AGAACTTTGGTCTAG[A/G]GCTCAGTAAACCCAA | 9678 |
| rs569894904 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10977696 | GTTTGAAATGAGTAA[C/G]TCCTAAAATAGGATA | 9678 |
| rs569897311 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104570 | AGTTGTTTATCACAC[A/G]GTAGGGAAAGGAAGA | 9678 |
| rs569898602 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994225 | AGTGAATCACTTGAG[A/G]TCAGAAGTTCAAGGC | 9678 |
| rs569906545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040527 | AAAGCTCATTTTAAT[A/C]CTTTTTGCCAATGTA | 9678 |
| rs569941715 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10984716 | TTAGGAATTTGCCAC[G/T]TAAAGTGTGTGTAGT | 9678 |
| rs569946036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097426 | TTGATATCAGAGTCT[A/C]CTCAGTTTTCTAAAT | 9678 |
| rs569951613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961750 | CTTTTATTTTGTTGA[A/G]CAGTGGTTTGTAGTT | 9678 |
| rs569967179 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11138340 | GCCACTGCGCCTGGC[C/T]GGAAAAATATTTCTA | 9678 |
| rs569999472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980214 | TACTTTTGCGTCTAT[C/T]GTGAAGTTTTGATTG | 9678 |
| rs570014120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005082 | GTGATGTCAACCACA[A/G]ACCTCTTAATTTTAA | 9678 |
| rs570019338 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007793 | TATCTCCTTTTTTTT[A/G]AGAAATATGCTTATT | 9678 |
| rs570021726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961319 | AGTTTTCCCAGCAAC[A/G]TTTATTAAATAGGGA | 9678 |
| rs570034522 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123188 | TTTGCAACAGGAAAT[C/G]TTGGGATTTAGGATT | 9678 |
| rs570042512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10995110 | GGTGCATTTACAAAC[C/T]TTGAGCTAGACACAG | 9678 |
| rs570049177 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005671 | ATAGAATGGCTCAAC[A/C]ATAATGTACTTATTT | 9678 |
| rs570049836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164157 | CGTCTCCCTTCATTT[C/T]ACTGTTGTACCACCA | 9678 |
| rs570053651 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966150 | TACCTCAGTTGGAAA[A/T]GCAGAAATCACCCAT | 9678 |
| rs570058178 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:10994873 | ATTTATTGCAAAGAG[C/T]GAAAGAACAAAGCTT | 9678 |
| rs570060580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118123 | TTACTAATACAGATA[C/T]GTAAAAAGTCTGGAA | 9678 |
| rs570081757 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073133 | ACATTGCAAAATACA[A/G]TTGTCCTTTATTAAC | 9678 |
| rs570093005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157925 | CTAAATCATCTAACA[A/C]AAATTAGATGTTTGT | 9678 |
| rs570102531 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976662 | AGTACTTTCTCAAAA[G/T]ATTTTATGATATCGA | 9678 |
| rs570103146 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103398 | GTACAAAGATTATTG[A/G]CTATACAACCTACCA | 9678 |
| rs570105509 | in-del | -/ACA | 0.00597247 | 0.0543191 | intron-variant | PHF14 | GRCh38.p7 | 7:11145039 | GATGGTGATGGTTTC[-/ACA]ACAATATAAATATTT | 9678 |
| rs570123068 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11016126 | TACTGTGGACGTTAC[A/G]TAAGTAGACACCTCC | 9678 |
| rs570126044 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11072765 | TAGTTCTGCAGGCTG[G/T]TCAAGCAGCATGGCA | 9678 |
| rs570140216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11110923 | AAAATTTTTTAAATA[A/C]TCAAAATGTATTTTA | 9678 |
| rs570181067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11066981 | TTGGACTAAATTCAA[A/C]GTTAAAAACTTTTGT | 9678 |
| rs570213069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073215 | CAGTGTCTTACTGGG[G/T]ACTCAAGGCAAGTTC | 9678 |
| rs570218643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11101895 | TTCTCCACTGAAAAT[A/G]AAGACAAAAAGGTAA | 9678 |
| rs570247304 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972240 | CGCACCCGGCAGTAC[A/G]GTTTTTCTAGAGCAA | 9678 |
| rs570249040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090256 | AGCAAGAGGAGGAGA[A/G]GTTCTGCTTTGAATG | 9678 |
| rs570271155 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047048 | TTACACGAATAAAAT[G/T]CTCTAAATTAGTCCA | 9678 |
| rs570317910 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017411 | AACATTTGTTATTGC[C/T]TGTCTTTTGGATATA | 9678 |
| rs570324991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11083546 | GCTCACTGGAAACTC[C/T]GCCTCCCAGGTTCAA | 9678 |
| rs570326238 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054437 | GAAAACCAGACAATT[C/G]GTGCGAGGTATCATA | 9678 |
| rs570329546 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066378 | AATCCTCTCACCTCA[A/G]CCTCCCGAGTAGCTG | 9678 |
| rs570359903 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956590 | ATTTGGAAATAGGGT[A/C]TTTGCATACGTAATT | 9678 |
| rs570367568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11066824 | GATTACTCAGGCTGT[A/G]GAGTAAGCTGTTTCG | 9678 |
| rs570390548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965877 | AACGAGCAAGGCTCT[A/G]TGTGTGTTGGCCTTG | 9678 |
| rs570394518 | snp | C/T | | | | | GRCh38.p7 | 7:10969577 | ATTAAATCCCACAAT[C/T]TCAGTGTTGACAATT | 9678 |
| rs570401417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096664 | AAGAAAAAGAAAAAG[A/G]TAAAGCAGATTTGAA | 9678 |
| rs570407751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053208 | TAATCTGTATTAACC[G/T]CCTATATTATAATCA | 9678 |
| rs570415169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129006 | GGGTTATTTTTACCA[A/G]CTAGATTACAAACTC | 9678 |
| rs570432272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016828 | TGCTATTAAACAGTA[A/G]GTCTTAGTCTTTCCA | 9678 |
| rs570437735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11090489 | TATTAAAGAACTGCA[A/G]AATTGCCTGATTATA | 9678 |
| rs570455826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015398 | TCTTCCTTATTGTCT[A/G]TCCAAAAATAAAATA | 9678 |
| rs570455831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060308 | TTGTGTTAAGTTTAA[C/T]TGGGTGTAGAAAGAT | 9678 |
| rs570461490 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11047567 | TTGGGAGGCTGAGGC[A/G]GGCGGATCACTTGAG | 9678 |
| rs570469127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017167 | GGTGGAAACTTAGGT[A/T]GCTTCCAAATCTTAG | 9678 |
| rs570471184 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11010963 | CTTGGCTGACTTTCA[C/G]ATTTTATTAAAATTC | 9678 |
| rs570481775 | snp | A/G | | | | | GRCh38.p7 | 7:10971579 | AATACATGAATTGCA[A/G]AAGATTAATAACCTA | 9678 |
| rs570497262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047138 | CAGTGGCACAATCGC[A/C]ACTCACCGCAACTTC | 9678 |
| rs570508843 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039223 | TTTTTTTCTTTCCTG[A/T]CCTTATGCTGTATTT | 9678 |
| rs570523175 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11005818 | TTTTTTTTTGAGACG[G/T]AGTCTCGTTCTTTCA | 9678 |
| rs570536793 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017399 | CACATTCTTGCCAAC[A/G]TTTGTTATTGCCTGT | 9678 |
| rs570545143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11039770 | AAAAGAATGTGTGTG[A/G]CTTGTATCCTAAAGA | 9678 |
| rs570559028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11011558 | TAAACCTGGTCAAAA[A/G]GATGTTGGGATGGTT | 9678 |
| rs570577240 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131975 | TTTTTTTAAAAATTT[G/T]TTATTGTGTATATTT | 9678 |
| rs570604594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028220 | TATAATAAAATGTTA[A/C]CTATCTCATGTAATT | 9678 |
| rs570638447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989914 | TGGGATTACCGGTGT[A/G]AGCCACTGTGCCCAT | 9678 |
| rs570661531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156620 | CCAACATGGTGAAAC[A/C]CTATCTCTACTAAAA | 9678 |
| rs570683299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015185 | AAATAAAGGATAGGC[C/T]TTTAAATTTAATAAA | 9678 |
| rs570702752 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983998 | TGAGTTGTTGTCTTA[A/C/T]ATGTAGATGTATCTG | 9678 |
| rs570719611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015454 | CATGAATCTGTGGTC[C/T]GTATCATAGGCATAG | 9678 |
| rs570737568 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043199 | GGATTAGAGTCAAAG[A/G]CTTTACTTCTGGTAT | 9678 |
| rs570749377 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103874 | GAAAGATCTCATAAC[A/G]TTGGAGGAAAAATAT | 9678 |
| rs570749432 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144735 | GAATGTTCGTAACAC[A/C]AATGATAAATGTTTG | 9678 |
| rs570754317 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046296 | AATAGTTAATCATCT[A/C]TTAATTTTAGAAGAC | 9678 |
| rs570760982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136180 | CAATGTAAGGCTGTA[A/C]GGTCAATGTGGTCAC | 9678 |
| rs570767941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965864 | CTGCTGCACTAGCAA[C/T]GAGCAAGGCTCTGTG | 9678 |
| rs570776164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005058 | ATTGCATTATTGGTG[A/G]TAGTTTAGGTGATGT | 9678 |
| rs570821957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11129688 | GATAAAAATCTGTAT[A/G]GTATTCAGAAGGTGT | 9678 |
| rs570822216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965518 | CCCAGTCAGGCTACT[A/G]GGGGGTCAGGGACCC | 9678 |
| rs570823714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11136808 | GATATTTAGTTAGAC[A/G]TTAAGACCAAACATT | 9678 |
| rs570840437 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169575 | ATGTTAAATTGTAAA[A/G]TCTAATTTGCAAAAT | 9678 |
| rs570857895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11123781 | TTGAACCCAGGAAGC[A/G]GAGGCTGGAATGAGC | 9678 |
| rs570876697 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11069827 | TATTACCACCACACC[A/G]CCATGCCCAGCTGTT | 9678 |
| rs570884980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076978 | AATATATATGTTGTA[C/T]TTATGTTGTATGTGC | 9678 |
| rs570888136 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11127156 | AGTTTAATGTCAAAT[C/T]TTCTATTCTCAGCAG | 9678 |
| rs570971113 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072295 | TTCTAAGAACTCACC[A/T]TCATGAGAACAGCAC | 9678 |
| rs571009251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144034 | CTCAACAGCAAAAAA[A/T]CCCCAAATAGTCCGA | 9678 |
| rs571015737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143256 | TAAACTTCATTTAGC[A/G]TAAATGTTTTCTATC | 9678 |
| rs571021291 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152081 | AGCAGAACTGTCAAG[C/T]TGTTTTGGATTTGAA | 9678 |
| rs571026511 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10983640 | ATTCGTTTTAAATAT[A/T]AATTCCTTTACCAGT | 9678 |
| rs571029632 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009068 | GTCTTTTTTATTGAT[A/G]AGTTTCATAGTCAAA | 9678 |
| rs571036312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095111 | AGTAATAAACTAGAA[A/C]AAATTGTAGTGATAG | 9678 |
| rs571036581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11058709 | GTTTAGTTTAAGTAT[C/T]TACGTGCAATAAGAG | 9678 |
| rs571045115 | snp | A/C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092268 | CTTTAAGACAGTGGT[A/C/T]CTTAAACATTAGGGT | 9678 |
| rs571045594 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966977 | ATGAGGAGAATCAGC[A/G]TCCCTTTGCAAAGTA | 9678 |
| rs571049984 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11153887 | AGAGTCTCGAAGTAT[G/T]GTGTCCTCACATTAT | 9678 |
| rs571125746 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149358 | GAGACATAAATTCAG[A/G]TTCTAACTCTACCAA | 9678 |
| rs571131620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11045868 | TGGTAACAACTTACT[A/G]TGGAAAAATCAAACT | 9678 |
| rs571154527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963626 | TCCAAGTCCTGGTTA[A/T]CCTTGTTAATTTTCT | 9678 |
| rs571161808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088836 | AATTATGTATCTCCT[A/G]TAGATTTATAGATTA | 9678 |
| rs571161952 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11010684 | AAAAATATATATACT[C/T]TTTTGAGACGAGATT | 9678 |
| rs571175008 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026655 | TTTCTGTATGGGTAT[A/G]ATTTAGTAGAAAGTG | 9678 |
| rs571189639 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988802 | TTCTTGCCATATATT[A/G]TTAATTCTTATAACC | 9678 |
| rs571198033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089705 | ATTGCCTCATGAATA[C/T]ACTATTAAAAGTGTG | 9678 |
| rs571213326 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057857 | AGGTTGTAATTGTTC[C/T]CTAGCTAAATCAAGT | 9678 |
| rs571220095 | in-del | -/CTGA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165807 | AATTGATAGTGCAAG[-/CTGA]CTAACATTTAAGCAA | 9678 |
| rs571232965 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11160361 | ACAGTGCTGCAGTGA[A/G]CATACAAATGTGTGT | 9678 |
| rs571250389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002747 | CCGCGCCCGGCCAAA[A/C]ATTAAGACTTCTTAA | 9678 |
| rs571257767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113369 | TTTCTTCTCTACCAC[A/C]GAATGGGTCTTTGGA | 9678 |
| rs571262215 | snp | A/T | 0.000399281 | 0.0141238 | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968694 | GTTGGTGGTATAGGG[A/T]GGTTACATGTGAGTA | 9678 |
| rs571273412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10991108 | CGATTCTGCTGCCTC[A/G]GCCTCCTGGGTAGCT | 9678 |
| rs571285078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958862 | CACCATGCCCTGCTA[A/T]CTGATTTTTTTTCTT | 9678 |
| rs571296777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167177 | AGGTTGCTAGAGAAA[A/G]CTAGATAGCCAAGCA | 9678 |
| rs571337206 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105227 | GAAATTATATTTATG[C/G]ATTGTTTATAGATCA | 9678 |
| rs571359379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161047 | TTCTTATAGTTTGAG[G/T]TCTTACATTTAAATC | 9678 |
| rs571363733 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11092208 | TGTATTTGCTTCTAT[A/T]CCTTTTTCTTTGTGG | 9678 |
| rs571370974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10992428 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 9678 |
| rs571398292 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105954 | ACAAAGTTACATGGA[A/G]CTTGAGCTCAGCAGG | 9678 |
| rs571455613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11109018 | AATCTGAACTCTGGC[A/G]CACTACCCAAAAACC | 9678 |
| rs571458409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043027 | TATTATCTTAGCAAT[A/G]GATTCTTCTTTAAGG | 9678 |
| rs571464839 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082881 | AATCCACAGTACCCC[-/T]CCCCTTCCCTTTTCT | 9678 |
| rs571466707 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11002298 | ACTCTGCAATGTGGA[C/T]GATGTCATGCTGGAG | 9678 |
| rs571489634 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973642 | CTCAGGAGGTGAATT[A/G]GGCGCGGAGAGGGCG | 9678 |
| rs571509367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11029487 | TTGAGAATCCAGCTA[C/T]CTTTTTTTATGTCAG | 9678 |
| rs571515219 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11092768 | TCGCTGAACCTGATC[A/G]TTGACTCTTAGGGCT | 9678 |
| rs571530213 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11085326 | TCTTCTGTTGATTTA[A/T]AACAATTTATTAGTT | 9678 |
| rs571530324 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078484 | CTCTCTGCGAGCCAG[A/T]TTTCTCATTCATAGA | 9678 |
| rs571538582 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106545 | CAGAATTTTGTGCAA[A/G]CTTGTATTATTTGTA | 9678 |
| rs571551477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007598 | GTAATTCAGCCATGC[A/G]ATTTTTAAAAAACAT | 9678 |
| rs571553282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086582 | TAATATTCCAGGTCC[A/G]AAGCCAATGCTTATC | 9678 |
| rs571570113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11079204 | TTCTAATTCTGCTCT[A/G]TGTCTCTAGACTGAC | 9678 |
| rs571599618 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163232 | CCCAAGTGACTTTAA[C/T]TTCATAATATAGCCT | 9678 |
| rs571600664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10995516 | CCGCACCAGGGCCAC[A/G]TGTGGAGCTGCCCGC | 9678 |
| rs571600792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11023553 | TTTGGCCAATTAGGG[C/T]TGGGTGCTCACGCCT | 9678 |
| rs571604269 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11080128 | GCACCTGTGAGAACA[C/T]ACCAAGTGTAGTTGG | 9678 |
| rs571610324 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990756 | TCAAAAAATGGACCA[C/T]ATTCTGATTTGCTGT | 9678 |
| rs571614022 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10995704 | CTGCCCCGCAGGGAG[G/T]CAGCTGAGGCCCGGC | 9678 |
| rs571629416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985440 | AAGCAGGCAGACATT[G/T]TTCTTAGCTGCTAAG | 9678 |
| rs571644523 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112618 | CTACTAAAGATACAA[A/C]AAATTAGCCAGACAT | 9678 |
| rs571645466 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957027 | AATATAAATGTTAAC[A/G]TGCATCTGGGAAGGT | 9678 |
| rs571686805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147094 | CTCAAGAGATCTGCC[C/T]ACCTCGGCTTCCCAA | 9678 |
| rs571689429 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146627 | TATCTATGGTTGGGG[A/C]TATAGGGCAACATAT | 9678 |
| rs571690529 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:10976227 | AGCAATCAAAAATTG[-/A]TAAGTTTATCTTGAT | 9678 |
| rs571699871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956124 | AAGAATAGACAAACT[A/G]TGCTTTCTTTAATCT | 9678 |
| rs571704062 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962443 | AGCCAACTTGATCAT[C/G]GTGGATAAGCTTTTC | 9678 |
| rs571712380 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956729 | AGTGAAGACAGAGGC[C/T]GAGACTGGAGTTATG | 9678 |
| rs571721287 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020950 | GTGCTCTGTGCCTAG[G/T]AGACACTTATAATTG | 9678 |
| rs571726309 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020103 | TTCTTTTTTTTTTTC[C/G]AATCAGACGGGGCCT | 9678 |
| rs571730500 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078152 | TTTCCCCTTATTTAT[C/T]CTTATTCACTTATTC | 9678 |
| rs571732797 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153239 | AGCAGTGGAGATAGA[A/C]AGCACTAGACAGATT | 9678 |
| rs571758785 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962196 | TCCAGTTTTTGCCTA[C/T]TCAGTATGATATTGG | 9678 |
| rs571762044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11007003 | AATGTGGTGAAACTC[C/T]CTTCTCTACTAAAAA | 9678 |
| rs571777510 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000869 | TTTACATTTTAATGG[A/T]GTCCAACTTATAAAT | 9678 |
| rs571788995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11124714 | TCCCTGACTCTAGAG[A/C]CTGTGTTTTAGAAAC | 9678 |
| rs571792733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158886 | TATTGTACACTGAAG[A/T]CATATTAAACAGTTT | 9678 |
| rs571798853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067762 | AAGGTGCTTTCACTC[A/G]TGGTGAAAGGTAAAG | 9678 |
| rs571816889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985171 | TATTTGTATGATCTT[A/G]ATTTTGTGAAAAGAT | 9678 |
| rs571821485 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11051911 | GGTTATTCTTAACAA[-/T]TTTTTTTCTATATTA | 9678 |
| rs571827628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165016 | TGCAGCCTCCACCTC[C/T]TGGGTTCAAGCGATT | 9678 |
| rs571838839 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068117 | GCACTTCGGAAGGCC[A/T]AGGCAGGTGAATCAC | 9678 |
| rs571852343 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11118989 | CTTTCACTATATTGA[C/T]AATTTACAAAATTGA | 9678 |
| rs571882702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962934 | TGATATCCCCTTTAT[A/G]ATTTTTTATTGCATC | 9678 |
| rs571894317 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11047310 | CCTGACCTCATGATC[C/G]GCCTGCCTTGGCCTC | 9678 |
| rs571900603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138362 | ATATTTCTAAAGAGA[C/T]TCCTTACAAGGTGAT | 9678 |
| rs571903998 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11041888 | GTGTGTGACTTTTTT[C/T]TAGGAGTATTTAAAA | 9678 |
| rs571915799 | snp | A/G | | | | | GRCh38.p7 | 7:10969886 | TTTGCTGTCTTTTGT[A/G]TACATATTTGTTTCT | 9678 |
| rs571927706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028897 | TATAATAAGTGTAAA[A/T]AATAAAAGAAATTTT | 9678 |
| rs571934602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956536 | TGAATAGTGTCCTTC[C/T]AAAATTCATGAACAC | 9678 |
| rs571950508 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11073622 | GGTCTGGAAGGCAAC[A/G]GCGCCCTTCCCACAG | 9678 |
| rs571982081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047659 | AGGAATGGTGATGGG[A/G]ATTCGTAATCCCTGC | 9678 |
| rs571982976 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029144 | TATTTTATACGAGAA[C/G]CTGAAACTGTATTTG | 9678 |
| rs571985811 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143447 | TATTGTTCCTTATCT[A/G]TGATTTATTTAATAA | 9678 |
| rs571989796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11035529 | TAATTTATTAGATGT[A/G]ACTAGCACTAGTAGA | 9678 |
| rs572018925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11041483 | ATGTATATGCATACA[C/T]ATATGTTATGCATGT | 9678 |
| rs572043431 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962021 | ATATACAATCATGTC[A/T]TCTGCAAACAGGGGC | 9678 |
| rs572047184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11118531 | TTGCTTTAAAAAAAA[A/G]ATTAGAGTGTTTTAT | 9678 |
| rs572056530 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052366 | GGAAAGAATAGATTA[A/T]TACCTAGTTTTTCTT | 9678 |
| rs572068050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021636 | AGCGACATTTAATAC[A/G]TCAGTGGAGCATGAA | 9678 |
| rs572072321 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111009 | TAATGGGCAAATGAT[G/T]AATTCTTTAAGTTCA | 9678 |
| rs572094871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152939 | AGCCAGGTGAGGAAA[C/G]TGAACTTGTGAGCAG | 9678 |
| rs572099652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074117 | TGGCTATTATCATTT[G/T]TCTCTTTTTTAGTCA | 9678 |
| rs572103309 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971997 | CTGGAATGCAGTGGC[A/G]TGATCTCTGCTCACT | 9678 |
| rs572109898 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144408 | TATTGAAGAGATACC[G/T]GCACCCCCATGTTTA | 9678 |
| rs572113491 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10989626 | TTAGTTTATTAATAC[A/G]TCTTCCTATACTTTT | 9678 |
| rs572114477 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011234 | CTCTTTTCCTTTCTC[A/G/T]TGGGTGATTTGTTTA | 9678 |
| rs572129176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029652 | TTGCAAAAAATTTTC[A/T]GTTTTAATTTTTAAT | 9678 |
| rs572154757 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11022195 | GTTTTAGTCTTATAG[C/T]ATCATTCAAACTTTA | 9678 |
| rs572168602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966348 | AGTCTGGCTGAGTCT[A/G]AGGTTTTTATGGGCT | 9678 |
| rs572172822 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075996 | AAGTAAAAATTAGCC[A/G]GGCATGGTGGCGGGC | 9678 |
| rs572173428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11145014 | ATAAGATAGGGTTAT[A/G]GAGATGAATGATGGT | 9678 |
| rs572173969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11112229 | CTCAAAAAAGATGAC[A/G]AAAATTAACTGTCTG | 9678 |
| rs572187439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016940 | CCATCCTTCTCCTGT[C/G]TGTGTCCATGAGTTC | 9678 |
| rs572198859 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078106 | TTTTTGTTTTCTGAC[G/T]AAAGAGAAGAGAAGC | 9678 |
| rs572198874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131532 | TAAAGAGTTATTTGT[A/G]TATTTTGAATGCCAG | 9678 |
| rs572203419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132141 | CTCATTTTGCATGAA[C/T]TCCAAATACAGTACA | 9678 |
| rs572236846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138059 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTTGCTCTG | 9678 |
| rs572255060 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11124132 | TTTTAAAAATATTGT[A/G]AAAGTAGTAAATGGT | 9678 |
| rs572268777 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11124946 | ATAAAACACAAAGAT[A/G]TTTTAAAACAAATAA | 9678 |
| rs572276299 | snp | G/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11005911 | GATTCTCCCGCCTCA[G/T]CCTCCTGAGTAGCTG | 9678 |
| rs572297770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006165 | TACTAATTACCAACA[A/G]TGCACAAACTACTTG | 9678 |
| rs572309224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11091097 | TGTAAAAGGTTGATA[C/T]TGTGGTGACATACCT | 9678 |
| rs572316349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034894 | TGTCCATTGTTAGCC[A/G]GTTAGAAATGCCACA | 9678 |
| rs572325317 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11000610 | TCCCAAAGTGCTGGG[A/T]TTACAGGCGTGAGCC | 9678 |
| rs572338891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966828 | TAGCAATAAAACCAC[G/T]ACCACCAAACATAAG | 9678 |
| rs572368148 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103511 | CAGTTTTAAGTCAAC[A/G]GCAGAAGTATGTTGA | 9678 |
| rs572370983 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096484 | TGAATGCTAATACAG[A/G]CCTGACAGTTCCACT | 9678 |
| rs572399048 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104114 | CGCAGTTGCTTTATT[A/C/T]TAGGTTTTTTGAGAA | 9678 |
| rs572401183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11060596 | TTCTGCATTTCTAAT[A/G]GACACTCAGGTGATG | 9678 |
| rs572406441 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11110252 | AGTAATATATGTTCT[A/G]TAAATTTTCCCCTTG | 9678 |
| rs572441843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10983472 | TCCCTTTACTCCTTT[A/G]TTCACAGGACTGCTG | 9678 |
| rs572457228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052978 | CAGGAGTGTAAATTT[C/G]AAACCTTTAAGTGCT | 9678 |
| rs572460932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097056 | ACGATCTCGGCTCAC[C/T]GCAACCTCTGCCTCC | 9678 |
| rs572462568 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11019375 | GTCAAGCAGTCCCAG[G/T]CTTTTCTTTACCGGG | 9678 |
| rs572470837 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11107768 | TTTGTGGGTCAATGA[C/G]TGCTTCTGAAAAAGT | 9678 |
| rs572490259 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067075 | GCAAGTCATGTATCT[G/T]TTAAGGGATTGAGAA | 9678 |
| rs572512788 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127159 | TTAATGTCAAATCTT[C/G]TATTCTCAGCAGCTC | 9678 |
| rs572521674 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11158441 | AACATGATGTCAGTA[C/T]ACATACTATACATTA | 9678 |
| rs572522680 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11096261 | AAGATCATCCTGCAT[A/T]ATTACTCTTTATCAG | 9678 |
| rs572548614 | snp | C/T | 5.12133e-05 | 0.00506004 | intron-variant | PHF14 | GRCh38.p7 | 7:11013923 | TTAATGTCCTAATTA[C/T]GTTGGTTCATATGTT | 9678 |
| rs572549501 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971350 | TTTGAAAACTTATGC[C/T]CAGTTAAAATTTGGA | 9678 |
| rs572556065 | in-del | -/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11090067 | TGAGCCACCTCACTT[-/G]GCCTGTTCATGCCTT | 9678 |
| rs572558620 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PHF14 | GRCh38.p7 | 7:10976869 | ATAATTTACCTTCCT[G/T]GCCCCCTGGGGAGCT | 9678 |
| rs572566299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141747 | GATTATTGGTATTTT[G/T]GGGTTTCACTTTTTA | 9678 |
| rs572598371 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11033593 | AAACTCATAGGGGTC[A/T]AGTACTAATGGGAAG | 9678 |
| rs572617126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10977201 | AAGTTGTGGATTCCC[A/G]GCCCTACTTACGAAT | 9678 |
| rs572631681 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11163008 | ATACATGAAATTAGA[A/T]ATTTGTTACTGCCCT | 9678 |
| rs572634713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10994640 | TTCTTGGTTTCACTA[A/G]CTTCAAGAATGAAGC | 9678 |
| rs572636350 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141641 | TGGTAGCTGTTTCCC[A/G]CAGGGAAGTTTTATC | 9678 |
| rs572654487 | in-del | -/T | 0.0154538 | 0.0865337 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963012 | TATCTATTTTGTTGA[-/T]CTTTTAAAAAAACAG | 9678 |
| rs572655067 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016279 | TACTAGTTTGATTAA[A/T]GGTATAAAAAGCCAA | 9678 |
| rs572657733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989708 | AGATAATAGCTTGCT[A/G]CAGCATTGAATTCCT | 9678 |
| rs572681336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113040 | ATAGTTGTCTTACGA[A/G]TCTCTTTAATAAGTT | 9678 |
| rs572682681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072035 | ATTCTGCTGAGTTGT[A/C]TTAGTCCATTCTTGC | 9678 |
| rs572693758 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044234 | CTACCTGGGTGATAG[A/G]GATCATTCATATTCC | 9678 |
| rs572728437 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041331 | GTAATTTTATTATAG[G/T]CAAGACTTCTTTCCA | 9678 |
| rs572739326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11151050 | GATTTTAAAAATAAG[A/G]AAAGCAAAATAGAAT | 9678 |
| rs572740011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11113644 | TGAAATTTAATATAA[C/T]ATTTAAGCTGAAACT | 9678 |
| rs572767682 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11057138 | GTGACCTGGTCACAA[C/G]TGAATATGTGAAGCC | 9678 |
| rs572788095 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146806 | AATGCAATTGACTCA[A/C]TTTTGTGCAAATCAA | 9678 |
| rs572798113 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11148750 | TATAAGTTTAATTCT[G/T]AAAATATAACAACTT | 9678 |
| rs572798567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093180 | TATATATTTCTGCTA[A/G]TGATTTCTGGTTTAA | 9678 |
| rs572818512 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958829 | GTCTCCCTAGTAGCT[A/G]GGACTTCAGGTGAGC | 9678 |
| rs572822896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11100437 | TCCATTTTAGAAGAG[A/C]GGTAACTGGGGTACA | 9678 |
| rs572835601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008025 | AGGGTACCTCTGACC[A/G]TGATGTCACTTATCC | 9678 |
| rs572836178 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109218 | TTAAGCAAACACACC[A/G]AAAATATCAGGAAGC | 9678 |
| rs572841995 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076134 | ACAGCGAGAAAGTTG[C/T]GTAACTAGAAAGTGT | 9678 |
| rs572851438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11057621 | TCAGGTGATCTACCC[A/G]CCTCGGCCTCCCAAA | 9678 |
| rs572877275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11085674 | TTTGAGACAGTGTCT[C/T]ACTGTGTTACCCAGG | 9678 |
| rs572879935 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138300 | CCCGCCTCGGCCCCC[C/T]AAAGTGCTGGGATTA | 9678 |
| rs572881861 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143979 | TTGCAGAGTATTCAC[C/G]CAGTAAGTGCTCTGT | 9678 |
| rs572900970 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10969098 | GGATGAATTTATTAG[C/T]TCCTTAGTCTGTTGG | 9678 |
| rs572914057 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086178 | TCTGTATCCAGTTGT[C/G]TTACTAAAACATGAA | 9678 |
| rs572921465 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956780 | CCAGAAGCCAGTAGG[A/G]ACTGGAAGATAGAAA | 9678 |
| rs572923062 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135053 | TATCCCTCATTGCAT[C/G]TGTTACAAAATGTTT | 9678 |
| rs572932128 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10980065 | TTTGAAAAAATAATT[A/T]ATTAATTGGCATTGG | 9678 |
| rs572946478 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11030434 | CCTTTGCACAGCATC[A/G]TATGTCATCATTTTT | 9678 |
| rs572948536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964442 | GTTTCTGTTGAGAGA[C/T]CCACTCTTGGTCTGA | 9678 |
| rs572960331 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974266 | CGACCTCGGCGCTGC[C/T]TGGGCTCCTGCAGCC | 9678 |
| rs572997519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074996 | ATGCTGGAGTGCAGT[A/G]GCATGATTTTCGTTT | 9678 |
| rs573021262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10974760 | CGAGGTCATCTTTAT[C/G]TTCTCTTAGCACCAC | 9678 |
| rs573035260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166867 | ATGTACCTGTCCTGA[A/G]CAGCAGGCAGTGTTA | 9678 |
| rs573045177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986737 | GCCCTTTAGTTTTCT[C/G]AGGTAAGTTTTTTGG | 9678 |
| rs573060287 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098416 | CCGCCTTTCTCTGTT[C/G]CTCACTTCTGATTAT | 9678 |
| rs573074585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10978121 | AATAATTTAATGAGA[A/G]GTGTCAGCCTGAGAC | 9678 |
| rs573093885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11148147 | AGTAGACTGCTTCCT[C/T]ATCTCTGTATTTGTG | 9678 |
| rs573096495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069262 | TTAGAGGAGAAATTT[A/G]GTCTTACTGCTAAAG | 9678 |
| rs573098568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11160567 | AGCATCGTTGTTTTT[C/T]GACTTTTTAATAATA | 9678 |
| rs573101733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10987169 | ATGAAACAAATTGCT[C/G]TGAGTCCTAAAAAAA | 9678 |
| rs573130354 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986607 | CACCTGTTTTTGTCA[A/G]TAACCTTATGGCATT | 9678 |
| rs573160647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013044 | GTATCTTTGTTTTGC[A/C]TGAGTTTGATCTTTT | 9678 |
| rs573170565 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038410 | CACTCTAGCCTGGGC[A/G]ACAGAGTGAGACTCC | 9678 |
| rs573207105 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11126859 | AAAAAGAGACAAAAA[A/T]GTGGTTTTATTTGTT | 9678 |
| rs573211895 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968237 | AAAACTAGTGCAGCT[G/T]TTGCTGCTAACCCTC | 9678 |
| rs573215690 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083835 | AATTGTAAAAATGAG[C/T]GGTTGCCAGTAAAAC | 9678 |
| rs573221388 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080797 | ATGCCCTAATGAGCA[A/G]ATGCATTAGAGGGCC | 9678 |
| rs573241297 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998035 | CATGTTGTGTGCTCA[C/T]GGAAGTGACCCAGTG | 9678 |
| rs573245032 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081745 | CCTGTAGTCCCAGCT[A/G]CTTGGGAGGCTGAGG | 9678 |
| rs573251304 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973348 | CTTGAGCCGCTGCTC[A/G]GGTCGCTTCCGTACA | 9678 |
| rs573258973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042556 | ATGAAAGAAATTGTC[C/T]ATCTCAACAGAAGAA | 9678 |
| rs573275790 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11119857 | TGAGTTCTTTGAAAT[C/T]AAATATAGTTGAGCA | 9678 |
| rs573305639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11127313 | TGAGAGATGCCTTCT[A/G]TGGGTTACTTGTGAC | 9678 |
| rs573307188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147569 | AATCTTACTTGACCT[C/G]TCAATGTTATTTAAC | 9678 |
| rs573321905 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963714 | TGTAGGACTCTAAGT[A/C]TCTTTGTAGGTCTCT | 9678 |
| rs573356532 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10985630 | TCTCTAGCAGTGATT[C/G]TCAAACTGTTTTTTT | 9678 |
| rs573359244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11146719 | ATACATTCAGCTCCG[C/T]ATGGTCATTTCCAGC | 9678 |
| rs573364054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11166508 | ATTAATCTGGAACTG[C/T]GTATAAATTCTTACA | 9678 |
| rs573384695 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115715 | TATGGCAAAAGGATT[C/T]GGTATAGAATCACAG | 9678 |
| rs573425157 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087556 | GGTACTATGATATTG[A/G]GCCATAATCTTTGGC | 9678 |
| rs573433249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140710 | TGAAATAATAGGATT[C/T]TAAACATGGTCAAAT | 9678 |
| rs573448762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11147383 | TACAACTCCAGTTAT[C/T]ATCCATGTTCCTGAA | 9678 |
| rs573465229 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164980 | CCCAGGCTGCAGTGC[A/G]GTGGCGCGATCTCCG | 9678 |
| rs573471111 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098979 | GAAAATTAAGTAAAT[G/T]TTGTGCTATAATTTT | 9678 |
| rs573471726 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161896 | TCTAGCATACACTTC[A/C]TGCGTATTTCCCAGA | 9678 |
| rs573498511 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11119293 | TGCTGAGAGTTAAGA[C/T]AAAGGACATTTTATT | 9678 |
| rs573499642 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976020 | TTTCACAGTAACTTA[C/G]TGAAGGAGATACCAT | 9678 |
| rs573503947 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11048537 | AGATCATGCCACTGC[A/G]CTCCAGCCTTGGCAA | 9678 |
| rs573522517 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11056068 | AGTCAGATTATAAAA[C/T]CTCTATCTGTCATAG | 9678 |
| rs573523878 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018219 | TTGCTTAGGATAGCT[G/T]TGGCTCTTCTGGGTC | 9678 |
| rs573542476 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139616 | CTATATTTAAATGAA[G/T]AATGTATCTATTTCA | 9678 |
| rs573559278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11119812 | TAAGCCAAGAAAATT[C/T]GAAAAATGAACTCTG | 9678 |
| rs573571795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063021 | TTAGTGTTGTTGTAT[A/G]TTTTTAAATACTTAC | 9678 |
| rs573584801 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10988065 | AAACTGAGATCCTAA[-/T]TTTTTTTAAGGAGGA | 9678 |
| rs573588890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153983 | TGTGTTTTAAGAATA[A/C]GGAATACTTTCCCAG | 9678 |
| rs573598032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018895 | TCATATATCGCTTTT[A/T]TTATGTTGAGGTATG | 9678 |
| rs573605118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133019 | ATACACAAAACCTGT[A/G]TGAGAGAAACTACAA | 9678 |
| rs573606099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056202 | TTATTCAGAACCCTG[A/C]GACTCCTGTTTTGCT | 9678 |
| rs573613680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11030311 | TGGATCAGGGAATCT[A/G]TAGGATAAGGTTAGT | 9678 |
| rs573643368 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001450 | ATCCTGGAATTTTGA[C/T]TGGGATTTTATTGAA | 9678 |
| rs573653035 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11091352 | CAGAAAAAAGATGAG[C/T]TGGCTATATTTATTT | 9678 |
| rs573669652 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11098435 | ACTTCTGATTATCTC[A/T]CCCTTGGATCCCTCT | 9678 |
| rs573671934 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11166726 | CTTTTCTGCACCTAG[G/T]TTACAGCTATCCTTC | 9678 |
| rs573685961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964595 | TCTTTGTGGTGTTCT[C/T]TGTATTTCCTGAATT | 9678 |
| rs573693193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11069726 | TTTCCTTTTTTTTTG[A/G]TTGGTTGGTTGTTGC | 9678 |
| rs573701552 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973791 | TTCGGCTCCTGCTCG[G/T]GAAGGGTGCGCGGGG | 9678 |
| rs573719813 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139424 | TAATTTTACAAGTTC[C/T]GTTCTCAATTTGAAT | 9678 |
| rs573723976 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11079770 | CAAAATCATTTAGCT[A/G]TATTATCAAAAATGA | 9678 |
| rs573774582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957390 | TTGAAAGCTTCTCCA[A/C]CTTTTCAGTTGATGA | 9678 |
| rs573786280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11080194 | GAATTTTGTAGCATT[A/G]GATTTTCAGTTTTAG | 9678 |
| rs573787302 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11006948 | GGGAGGCTGAGGCAT[A/G]TGGATCACCTGAAGT | 9678 |
| rs573790252 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11099812 | AACAAATATACAGTT[G/T]CAAAAAAGATCCTAA | 9678 |
| rs573801707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133528 | CATAAAGGGTGGTAA[A/T]TATTATGTCATGAGT | 9678 |
| rs573818413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001683 | CTTGTTCATTGCTTT[C/T]ATAAGAAAGCAATTG | 9678 |
| rs573836988 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963128 | CTTCTGCTAGCTTTT[C/G]AGTTTGTTTGCTCTT | 9678 |
| rs573837210 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11165886 | TTTACTTAATTTCTC[A/T]GTTAGAATAACTCAG | 9678 |
| rs573869111 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10984511 | AAAATCTAATTGTTT[G/T]TATTTAATTGAGGCA | 9678 |
| rs573869354 | snp | C/T | 0.0010341 | 0.0227152 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990798 | AGATAATAGTGAGGA[C/T]GCTGATGAAATAATT | 9678 |
| rs573877005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10996158 | GTTTGATTCATGTTT[C/T]GGAAGGATCACTCAG | 9678 |
| rs573886659 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11074254 | CTTGCTCTGTTGCCC[A/C]GGCTGGAGTGCAGTG | 9678 |
| rs573887362 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080625 | GGTTTACATTTAGTC[A/T]GCAATTCTTTGTCTT | 9678 |
| rs573916237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011840 | TTAGGAGTCATGACT[A/G]TCATCAGTAGAGAAG | 9678 |
| rs573917226 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025038 | GGGAGGAGGTCAAAA[G/T]ATCCATATTAACAGG | 9678 |
| rs573918412 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972834 | AGGCAGGAGAATAGG[G/T]TGTGGAGGCAGGGAA | 9678 |
| rs573924635 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133094 | TCCATGTTCATTGAC[A/G]GGAGAAATAAATATT | 9678 |
| rs573939199 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160622 | TATCAATGAGATACT[A/G]TCACAAAAGAGATAA | 9678 |
| rs573945718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10978649 | GGATAATTTTTTGTT[A/G]TGGAGGCTTGTCCTG | 9678 |
| rs573951823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149314 | CAGTACTGACTCGTC[A/G]TGGCAAACAATTCCT | 9678 |
| rs573978811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078545 | CCCTTTTAATTTTCA[A/G]ATTTCATGATTTTGT | 9678 |
| rs573980358 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11012529 | TGTTCCATTGTCAAC[C/T]GTAACTTGTAATTCC | 9678 |
| rs574009110 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106918 | CAAGTAAAATGTTCC[A/C]TTGGCATAAAAGATA | 9678 |
| rs574009953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11097766 | CATCTTGTTTAATAT[C/T]ATTGTATTACATAAG | 9678 |
| rs574013625 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11118052 | TTGTGGGACAAGCTT[A/G]CAAAAGCTTACAAAA | 9678 |
| rs574016994 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104544 | AAAAAATGGCACATC[A/C]GGTAAATGATAGTTG | 9678 |
| rs574045063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088442 | CACACAGTCCTATTT[C/G]CCAACATGAGAAATT | 9678 |
| rs574045314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11095519 | AGTCAAGGGCATTTC[A/G]TTTAATCCTGTATCC | 9678 |
| rs574051790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042355 | AAATGAACTAATGTG[A/C]AATGGGTTTTAAGTA | 9678 |
| rs574058546 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973270 | ATTTACATGAGGTGA[C/G]CATTAGGTGGCCAAT | 9678 |
| rs574058723 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11047719 | TAAACCTGGGAGGCT[A/G]AGGCTACAATGAGCT | 9678 |
| rs574070940 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11055295 | TTTCTAATACTCTAA[C/T]GTAACTTGAAAGCTT | 9678 |
| rs574100203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004464 | ACCTCTATTGTCACT[A/T]TGGTTTCTCCACACC | 9678 |
| rs574112842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11133548 | ATGTCATGAGTTTAT[A/G]GCCACTGAAAATCTA | 9678 |
| rs574135536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11089130 | CCTGATCAGTTAACC[A/G]CAGCAAATAAAAACC | 9678 |
| rs574138522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11111710 | CGTATTCTCTATTAT[C/T]GTAACATATTAAATA | 9678 |
| rs574146052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11048528 | GTGAGCCTTAGATCA[C/T]GCCACTGCACTCCAG | 9678 |
| rs574162513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966923 | TCGAACATACTGGGA[C/T]CTGATTCCATTTATA | 9678 |
| rs574167166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11067729 | CAAGATTGGGCATCT[A/G]CATCTGGTGAGGACC | 9678 |
| rs574198617 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995657 | GGCGGGGTGGGTAAG[G/T]CTCAGGCATGGTGGG | 9678 |
| rs574209015 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | PHF14 | GRCh38.p7 | 7:11122797 | GCTTAGTCCAGTCCT[G/T]CTGTATATTAAATTA | 9678 |
| rs574211195 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994833 | CATAAAGGCAGCGCG[C/T]ACCCGAAGAGTGAGC | 9678 |
| rs574228029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967447 | TAGGACAGCCTTCCT[C/G]AGCCTTTTGCCACAG | 9678 |
| rs574231621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017487 | TTGCATTTCTCTGAT[A/G]ATCAAGGATTTTGAG | 9678 |
| rs574236201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028948 | TTGCCAAGATCACTG[C/T]TCTAAAACTTTAAGA | 9678 |
| rs574237182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020288 | AGAGACGAGGTTTCA[A/C]CCTGTTGCCCAGGCT | 9678 |
| rs574270225 | in-del | -/CTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975854 | TTAGTCACATCTCTC[-/CTT]CTTCTGGTTTTCCCT | 9678 |
| rs574290888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11152238 | TATTGATCATGAGCA[A/C]TTCTAACTGTACATA | 9678 |
| rs574318271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015500 | GGGCCTGAGAGTGGC[C/G]TAGTATTAGGGAGTT | 9678 |
| rs574324876 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11062241 | ATTTCATCCACTTCT[C/T]AACCTCTCACACATG | 9678 |
| rs574332526 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150065 | TAATGTTGAAAATAC[A/G]TTGCAAGTCACGGAA | 9678 |
| rs574344441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071455 | GGAGTAGAAAATAAG[C/T]CAGTTTAAAACACCC | 9678 |
| rs574352162 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009886 | ATTTCAGAATCATTC[C/T]TAAGATTAACTGTAG | 9678 |
| rs574355256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009729 | GGCAAGTAAAGAACT[A/C]TATAAAGGTAATGAC | 9678 |
| rs574367687 | snp | A/C | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10970587 | CCCTACAGCTCCCCC[A/C]AAAAATTCTGAGTTA | 9678 |
| rs574374273 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:10992420 | TAATCCCAGCACTTT[-/G]GGGAGGCCGAGGCGG | 9678 |
| rs574405273 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068276 | GAATGGCATGAACCC[A/G]GAGGCAGGGCTTGCA | 9678 |
| rs574406219 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11094462 | GATTCTGACTCCTCC[G/T]ACTTCTCTCTTACAA | 9678 |
| rs574424200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054572 | TTTTTACTTATTTCT[A/G]TTTGAGTTGTATTTA | 9678 |
| rs574430272 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11146712 | TTCATACATACATTC[A/G]GCTCCGCATGGTCAT | 9678 |
| rs574439640 | in-del | -/AAAAA | 0.0107246 | 0.0724382 | intron-variant | PHF14 | GRCh38.p7 | 7:11031193 | TTTATATAGGCTGTT[-/AAAAA]AAAAAGGTTGAAAAA | 9678 |
| rs574465567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130759 | TTGTAATAATGACAC[A/G]TGTCCACCATTACAG | 9678 |
| rs574506960 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034008 | TTTTTTGAAGTCCCA[G/T]AGCCTGTAAATGATA | 9678 |
| rs574513004 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167919 | CTGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG | 9678 |
| rs574533315 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965479 | CTGTATGAGGTGTCT[A/G]TCGGCCCCTACTGGG | 9678 |
| rs574549107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11047489 | GGTGCTAGAAACATA[C/T]AGAAGGTATAGAAAA | 9678 |
| rs574550835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034665 | GCAATTCTCCTACCT[C/T]AGCCTCCTGAGTAGC | 9678 |
| rs574576300 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11162218 | CTCAGCCTCCCAAGT[A/T]GCTGGGACTACAGGC | 9678 |
| rs574583429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11168955 | ATGCACATGCTTCCT[A/G]TTTTAGACCTCACTG | 9678 |
| rs574584119 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032936 | CATACTGGACATAGG[G/T]CTTGGTTCAGCAACT | 9678 |
| rs574584889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075910 | GCTGAGGCGGGTGGA[C/T]CACGAGGTCAGGAGA | 9678 |
| rs574624477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101399 | AGTAGTAAACTACAG[A/G]CAAAGTAGTTCTCAG | 9678 |
| rs574628535 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11058374 | TGAATTTTCGTAGTT[A/G]TAGTTGCTGCCACTT | 9678 |
| rs574638542 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11019903 | GGCTTTTGCTGTATC[C/T]CATAGATTTTGGTAT | 9678 |
| rs574655299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11102317 | CAATTTTAACCAATA[A/G]GAACCTACACAAGAT | 9678 |
| rs574655567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015313 | CTGGGATAGCGTAGA[A/G]TCTACCATTGAATCT | 9678 |
| rs574657089 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11075858 | ATAGCTAGGCTGGGC[A/G]CGGTGACTCATGCCT | 9678 |
| rs574668333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049877 | TGACAACCTAGGGGA[C/T]AACCTGCCAGCTATA | 9678 |
| rs574681019 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062510 | ACTTTTTATTGACAA[G/T]AACTTAATTAGCACT | 9678 |
| rs574684937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11141613 | TAGCCTAAGTTGCAT[C/G]AGGAGTATAATTTGG | 9678 |
| rs574689293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149583 | TTTTGAATGCAAATT[A/G]CTTATTTAATATATC | 9678 |
| rs574714797 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985337 | GCTTTTACTTTGTTT[G/T]CAGAAACTACTTTGT | 9678 |
| rs574727836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020291 | GACGAGGTTTCAACC[C/T]GTTGCCCAGGCTGGT | 9678 |
| rs574751584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11142616 | ATTTTATTAAAAATG[C/G]TTGTGACAACTTTAA | 9678 |
| rs574761004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161319 | ATTGTCCAGTGAGAA[A/G]GATAAACAAAATGCT | 9678 |
| rs574766793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11043997 | CTGCAGCTAAAAAAA[A/C]ACACACACAAAAAAA | 9678 |
| rs574775618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11038195 | AAGGCAGGTGGATCA[C/T]GAGGTCAAGAGATCG | 9678 |
| rs574803544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044543 | TTAGCTTTGGTTAGC[A/G]GTTAACTGGGTGTAT | 9678 |
| rs574804302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031853 | TACATTATATAGTCT[A/G]AAGTTACTTATAGTC | 9678 |
| rs574814194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11143406 | GATTATAGGCATGAG[C/T]CACCATGCCCAGCCA | 9678 |
| rs574820570 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958363 | AGTCAGTATTTTAAC[A/G]TAATTTGAAAACAGA | 9678 |
| rs574821465 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11155026 | TCTGTAGGTACCTAT[C/G]TTCACTACAGCAGTA | 9678 |
| rs574859737 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108037 | TACAAAGTGGTATTT[A/G]TGTGTAAAATTAATA | 9678 |
| rs574864002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11101360 | TAAATGATTTGGTTG[C/T]TTCCTCTTGCATTAT | 9678 |
| rs574883658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11121506 | AAGACCCCTAGAAGA[C/T]GCCTTAAACCAGTTA | 9678 |
| rs574895042 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11015291 | GAAATGTTGCCATAC[A/C]AGATTGCTGGGATAG | 9678 |
| rs574906023 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095844 | ACTGGATTCTGTAGA[-/T]TTTTTTTTTTTACCC | 9678 |
| rs574923863 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155550 | TTGACCAACTCTTTC[C/T]TATCCTTCATGTCTC | 9678 |
| rs574925133 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087640 | ACTGACTATTGCTAA[-/T]TTATATTGTGGATTA | 9678 |
| rs574926925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134240 | TTTCAATTCAAAAAA[C/G]ACCTTAAAATCTAAA | 9678 |
| rs574935762 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974238 | TCGGACTTGTCTTCG[C/T]GGCCCCAGTCCCCGA | 9678 |
| rs574943699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013634 | CGTTTCTTATAAACC[A/G]TTGGTGTTTCATATC | 9678 |
| rs574947039 | snp | A/G | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11114466 | AAATTCCGTAAGTCT[A/G]ATAAGATTCATCATA | 9678 |
| rs574977762 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149725 | ATAATCTGTAGTTTT[A/G]TTTTTTGTTATCTAC | 9678 |
| rs574983708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008946 | GAGGCTGAGGCAGGA[A/G]AATGGCTTGAACCTG | 9678 |
| rs575001750 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025758 | CGAGATCGTGCCATT[C/G]CCCTCCAGCCTAGGT | 9678 |
| rs575027458 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11004046 | TGAGCTCAGGAGTTT[C/G]AGACCAGCCTGGGCA | 9678 |
| rs575031347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11134751 | TCTTGTCATTAAATC[C/T]GTTCAGTACTTAAAA | 9678 |
| rs575051308 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10997123 | CTGTCTGTATTTAAT[A/G]CATACGTGCTTTACT | 9678 |
| rs575053885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11087423 | TCTCGAACTCCTGAC[C/T]TTGTGATCCACCTGC | 9678 |
| rs575063449 | snp | G/T | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 7:10969629 | ATTTTCTTTTTCTCT[G/T]ACATCATTTTTTCAT | 9678 |
| rs575085828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093983 | AGATTACTCTGTTCC[C/G]TGTGTGGCAGCAGGG | 9678 |
| rs575089199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007999 | TCTTTGTGGGAAGAT[C/T]TTCTAATATTAGGGT | 9678 |
| rs575093480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128277 | CTTCAGTTTTATTCC[A/C]AGCAGACTTACTTTT | 9678 |
| rs575122940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:10987204 | AGTTCTGTAACATTT[A/G]TAAATATCGAGATTC | 9678 |
| rs575124623 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10993420 | TGCCCTTTTTTTGCT[G/T]CTAACACTCACTGTG | 9678 |
| rs575179596 | in-del | -/G | 0.00398564 | 0.0444627 | | | GRCh38.p7 | 7:10969370 | TAATTTTACTTTCTT[-/G]GTTTCTTAAAAAATT | 9678 |
| rs575202331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008286 | GAGTGTTCACTGGAT[A/G]GTAGAATATGTTCAA | 9678 |
| rs575215484 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11142342 | ACTGCGCCATAATGG[A/G]TCATTTTTATCTGCA | 9678 |
| rs575267357 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11061373 | TGTATGCACATGCAT[A/G]TATGTAGGCAAACAA | 9678 |
| rs575269116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11135622 | TTTCCCATTGAAACT[A/C]CATCTTTGTTAAGAA | 9678 |
| rs575295185 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043521 | AAAGAGTGAACCCCA[A/G]ATTTTTAAATGGTAA | 9678 |
| rs575297360 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049423 | GAGGTTGCAGTGAGC[C/G]GAGATCGTGCCACTG | 9678 |
| rs575300291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11025194 | GTGACTGAACTGCTG[C/T]GATCTCATGATAAAA | 9678 |
| rs575312675 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109462 | GTGATTTTTAAATTT[C/T]GCATCAAAGATGATT | 9678 |
| rs575317065 | in-del | -/AG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146870 | TATTTATTTAGAGAC[-/AG]AGTCTCACTCTGATA | 9678 |
| rs575323057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11004119 | CAGGTGTGGTGGCTT[G/T]CGCCTGTAGTCCCAA | 9678 |
| rs575330296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075042 | TCCCAGGTTCAAGCA[A/G]TTTTCCTGCCTCAGC | 9678 |
| rs575340710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11084026 | TTTTTATTGGAGTAT[A/G]ACATTACATAAGGAT | 9678 |
| rs575349999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10992677 | AAATTTAAACAAACA[A/G]ACAAAAAAAGGCATT | 9678 |
| rs575350527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11161280 | AGTTTGATACAATGA[A/G]TCGAGTGTTGTATTA | 9678 |
| rs575370666 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006905 | CTTGTCCTGGCGCGG[C/T]GGCTCACACCTTTAA | 9678 |
| rs575379416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11114329 | GGAAACTCTAAAATA[C/T]TGCTATTTATACTGT | 9678 |
| rs575420038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070225 | TGTGACTACAAGTGC[A/G]CGCCACCATGCCCAG | 9678 |
| rs575457140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064487 | AAAATTAAACTTCAT[A/G]GGTCACAATTAGTCT | 9678 |
| rs575494228 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984789 | GTTGTAGACTAACAT[A/T]TATGATGCATTTAAA | 9678 |
| rs575495883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11141995 | CATATTTTGAATATC[C/T]AGAAATCAGAAAAAT | 9678 |
| rs575500679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10980791 | TCACTGGGGGTATTA[G/T]TGTAATATATGGTGC | 9678 |
| rs575505379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11056932 | ATTTAGCTTAACAGA[A/G]GTTTTCAAAGTTTGA | 9678 |
| rs575509127 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973726 | TCCGCCTTGGCACTA[C/G]TCGGCTCCGCTCGCC | 9678 |
| rs575525599 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11002655 | TCCATGTTGGTCAGG[C/G]TGGTCTTGAACTCCC | 9678 |
| rs575536534 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11080418 | TAAAAGTTGCAATTT[A/C]AATTAAGGGAATGGA | 9678 |
| rs575541393 | in-del | -/GTA | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11167905 | TGGTGGTGGGTGCCT[-/GTA]GTCCCAGCTACTCGG | 9678 |
| rs575562993 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11086870 | TATTAAATTCTTACT[A/T]GAGTTTTATTACTCT | 9678 |
| rs575570418 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974158 | CGGGGGGTTAGGGGA[C/T]CGCGGGGCTACTCTT | 9678 |
| rs575571099 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015786 | TTATTGCTCCACTTA[C/T]TTTAGGTAATCATGG | 9678 |
| rs575572461 | snp | C/T | 0.000798403 | 0.0199641 | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10968359 | GCTGTTACAGCTACA[C/T]GAACATGGCCTCTGC | 9678 |
| rs575584976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966258 | CTTTATTGAGAGACA[A/G]AACAGCTCTCAGTGA | 9678 |
| rs575609683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964535 | TATTTCAACCTTGGT[A/G]AATCTGACAATTATG | 9678 |
| rs575634085 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11003116 | CAGCTAATTTCTGTA[C/T]TTTTAGTAGAGATGG | 9678 |
| rs575657168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149380 | CTCTACCAATTGGCT[A/G]TGGGACCCTGGGGAA | 9678 |
| rs575660106 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112123 | TAAGTAAATAGCCAG[A/G]CTCCTAATGTTTTGA | 9678 |
| rs575666750 | in-del | -/TAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050075 | TAATTTGTATTTTAG[-/TAA]TAATATGTTTGCATT | 9678 |
| rs575668136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11113782 | TTTCTTCTGAAAGAT[A/G]TTTGCTAGTATTACA | 9678 |
| rs575683748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11007956 | TTTTTGAAATTTGAG[C/G]GCTGCAGTGTGTCAC | 9678 |
| rs575684339 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11069856 | TTCTATTATTTATTT[A/T]TTTATTTTTTTCTGG | 9678 |
| rs575686822 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11167337 | ATTTTTGCTTATTTT[A/T]ATTTTCACTGTTGTT | 9678 |
| rs575687788 | in-del | -/AGG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015005 | CCTCTCCAATATAAG[-/AGG]GGGGGTGGGTACTTA | 9678 |
| rs575701986 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075903 | TTGGGAGGCTGAGGC[A/G]GGTGGATCACGAGGT | 9678 |
| rs575713686 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11121461 | AGTAGCCTCCCCCCA[C/G]TGCCTACTTAATTGC | 9678 |
| rs575722092 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11073051 | TTCAGCATGTTATTT[G/T]AATGGGAGAAACATC | 9678 |
| rs575736684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11037523 | TATAGAGCTTCACTT[G/T]CTAAGTTTGTAGAAA | 9678 |
| rs575741093 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11074259 | TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCACG | 9678 |
| rs575768912 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11128144 | TAAAATATATGTACT[A/T]GAGTTCACTACAAAT | 9678 |
| rs575791731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11092555 | ATCTCACTCTTGAAG[A/G]TTCCAATCAGTAGGT | 9678 |
| rs575797241 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051093 | TTACCCAGGCTGGAG[G/T]GCAGTGTTGAGATCA | 9678 |
| rs575806351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11148089 | CTTTCCGTTCTGACT[A/G]CATTACAGTACTCCA | 9678 |
| rs575817340 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058266 | TTGCTTTTTTGTACC[A/G]TTTCTCCCTCTTTTA | 9678 |
| rs575819242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052902 | CAGGTACCTTGAAGG[A/G]GCCTCTACCAACTTG | 9678 |
| rs575826046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11031282 | TATGACTTTGTATAG[A/C]CTTCTGACATAGTCC | 9678 |
| rs575830487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11086359 | CTAAATTTAGATCAT[C/T]GCAGGTCATTTTTTC | 9678 |
| rs575867643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11140692 | CATTTCAAGCAAGGA[A/G]GTTGAAATAATAGGA | 9678 |
| rs575869490 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137053 | GTTCTTATGGGGGCA[A/G]AAATGCAAAATTAAA | 9678 |
| rs575876293 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11099017 | TCATTTCAAAAATGC[C/T]TTTCTATTAGTAAAA | 9678 |
| rs575877849 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11093003 | TCTCCCTGAGACAGT[G/T]ATCTGTTTTCACTAT | 9678 |
| rs575902155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11049814 | GGGACAAATGCAGGA[A/G]CAATTTAATATATTC | 9678 |
| rs575904682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11053280 | ATCAGTTTTGTGTTA[C/T]GGGGTCATATAAAAT | 9678 |
| rs575910575 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 7:10971250 | GGAAGTTGCACGTAC[C/T]GTTTCTGCTGACATG | 9678 |
| rs575937975 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11040879 | GAATGAATTATGTCC[A/G]TACCAGAATTTAAGT | 9678 |
| rs575940729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11099783 | ATGTAACTTTTATAA[C/G]TGAGAGATTTCAAAA | 9678 |
| rs575947466 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11004526 | ACTTGTGTTATATCT[C/T]TTTAGTCTCCATTAA | 9678 |
| rs575948355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961545 | GCTTAGGATTGTCTT[A/G]GCTATGCGGGCTGTT | 9678 |
| rs575958567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020724 | AGATTTAGTAAGTCT[C/T]AGTTCTGTCCCTTGC | 9678 |
| rs575964595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961966 | TCAGCAAACTTCAGC[C/G]CAAAAGGAGATTTTG | 9678 |
| rs575973656 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965970 | AGTATTTGGGCAGGA[G/T]TGTACAGTTCCTCCA | 9678 |
| rs575974416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034827 | GTGCTGGGATTACAG[A/G]CATGTGCCACCACGC | 9678 |
| rs575976952 | snp | A/T | | | | | GRCh38.p7 | 7:10970012 | TCATAATTATTACTG[A/T]TGCTTGTGCAGTCAT | 9678 |
| rs575981535 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:10992535 | GGGCGTGGTGGCTTA[C/T]ACCTGTAATCCCAGT | 9678 |
| rs575982660 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11133720 | CATCTGCTCACAGTT[C/T]TGCTAATTATACATT | 9678 |
| rs575982864 | in-del | -/TATC | 0.00438332 | 0.0466095 | intron-variant | PHF14 | GRCh38.p7 | 7:11041463 | ATGTGTGTGTATATT[-/TATC]TATGTATATGCATAC | 9678 |
| rs575995619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11013540 | GACTAAAACTATTTT[A/T]AAAATGTCATTTATT | 9678 |
| rs576012562 | snp | A/G | | | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968538 | TTGTGTTCATAGTAT[A/G]TAATACGTAGTGTTG | 9678 |
| rs576044131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11134167 | TAAGTTTAAAATGAT[C/G]AACTTTACAGTAGGC | 9678 |
| rs576049658 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002368 | GCAATGTAGAATGAA[A/G]TATGGTTCCTGGTAT | 9678 |
| rs576070251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11157707 | TTTAAAAACATGACA[A/G]TGAATTTCATGTGTT | 9678 |
| rs576071000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11027694 | CCTGATTATTAACCT[A/G]AAATTACTTTTAGTT | 9678 |
| rs576090093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955927 | GGTTAAATAAATTAA[A/G]TCAATAATGGAAGAA | 9678 |
| rs576101660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158216 | CATTATGTCTCCTCA[A/G]TCTCTTCCAGTCTGT | 9678 |
| rs576110819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11111148 | GATTTTATTGCTGTT[A/G]TATTTTGTTTTTGCT | 9678 |
| rs576120057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11016525 | TTTATTTTATATCTT[A/C]TGGAGAGTAAGACTT | 9678 |
| rs576162157 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964852 | TTCCTTCTGCTTGAT[C/T]GAATTGGTTATTGAA | 9678 |
| rs576162801 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PHF14 | GRCh38.p7 | 7:11124741 | AAACTAGATTTTATA[C/T]ATTAAAATAGGTATT | 9678 |
| rs576168818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11117692 | TGTGTCTTTAAGAAC[A/G]GAACAATCTCTTCAG | 9678 |
| rs576194572 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11137131 | CTTAAGATTTAATCT[C/G/T]TCAGGTTTTCTTGGG | 9678 |
| rs576204058 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096267 | ATCCTGCATAATTAC[C/T]CTTTATCAGTAACTA | 9678 |
| rs576218783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028345 | AAAGTTAAAAAATTA[A/G]AAGTGGAACTGTTGT | 9678 |
| rs576228484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11090013 | TGACCTCAGGTGATT[C/T]GCCCGCCTTAGCCTC | 9678 |
| rs576229145 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11118468 | TGCTGTACTTTGGGA[C/T]TATTAATAATTATTT | 9678 |
| rs576229412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122287 | GGTAACTGAAACCTG[A/G]GAAAGCAAAACCACA | 9678 |
| rs576229473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11129778 | AAAAACTTAGATGCT[A/G]GTAGGATAGATAAAG | 9678 |
| rs576238357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11090586 | GTAGAGCATTGAGCA[C/T]GTTGACTGAAGATTT | 9678 |
| rs576240220 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126643 | CCAAGCAGTATTTGG[A/T]AACATGACAATATAT | 9678 |
| rs576257330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11130841 | CACCACTCCCTCTCT[A/G]CCATCAAACCACTGG | 9678 |
| rs576259635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11096215 | CAAGTGGGATTAAAA[C/G]CATTTAGGGCCATCC | 9678 |
| rs576288113 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040231 | CAGATTAGTAGAAAC[A/C]CAAAGAGAATCTCAC | 9678 |
| rs576291411 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11131317 | TTGTTCCATATCTTT[A/G]CCAGCATTGATGCTG | 9678 |
| rs576291604 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063215 | ATAATAATTGGCTAA[-/T]TTTTTTTGAGGTAGT | 9678 |
| rs576307187 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PHF14 | GRCh38.p7 | 7:11010556 | TAAATGAAATTAATT[A/G]TATAGTTTAATTTGT | 9678 |
| rs576310218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000051 | GAAGCTGAATAGTCT[C/T]TGACCACTTTAGGTG | 9678 |
| rs576328858 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971877 | TCCAATGGCCACAGG[C/T]TTGGAAAACTAGAAA | 9678 |
| rs576342827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11156216 | GAAATAATGAAAATA[A/G]GGACGTTATTTTTGA | 9678 |
| rs576345646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11033490 | CATTTCATACAACTT[A/G]TTGGCCAGAACTTAA | 9678 |
| rs576346866 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11096813 | AAGTTGTTTCTTGAG[C/T]TTACCAATTTCTGTT | 9678 |
| rs576393038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11011172 | CATATAATGACGTCT[A/G]GTTAATTAATGTTGG | 9678 |
| rs576400279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11083337 | TGGAGTCTTATTCCT[C/T]ACTTATATTGTGCTT | 9678 |
| rs576407706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066228 | AGAATTCATATGTAT[C/T]ACATTTTAATTTCAA | 9678 |
| rs576419963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11021092 | GTTTTCATTCTTAAA[C/T]GAGTCTTTTGAGAAG | 9678 |
| rs576458469 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11015738 | ACTCTTACTACTGCC[A/G]TTACTGCTGCTACTA | 9678 |
| rs576459198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11045822 | AAGAGACCTGGGATG[A/G]TGATGGGCTCTTGAG | 9678 |
| rs576465094 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073733 | GCTTTCTGTGAAGGC[A/T]CTGTCTCTGTGACAG | 9678 |
| rs576485016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976400 | GATAAGAATATTCCT[G/T]GCTAGGATGTAGTTT | 9678 |
| rs576511029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11059863 | TTAAACTTTTTGTCA[A/G]ATTTTTATTTTATTT | 9678 |
| rs576528581 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11072348 | CATGAGAAATCTACC[C/T]CCGTGATCCAGTCAC | 9678 |
| rs576529217 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11084200 | TAAACTTCAAAATAT[A/G]TACACACACACAATC | 9678 |
| rs576551712 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11102416 | TTGTTAGTATGTTTC[A/G]TAAGACATAGTGCAG | 9678 |
| rs576565548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077869 | CTATCTCAGAATCTT[C/T]ATAAAATAAATGTCA | 9678 |
| rs576568844 | snp | A/G | 2.73706e-05 | 0.00369927 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038780 | TGAATCTTTAGAAGA[A/G]CTACAAAACCTGAAT | 9678 |
| rs576570262 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11083101 | TGTTCAGAGAATCGG[G/T]TCTAGCTTAGATTGT | 9678 |
| rs576572652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11004833 | TTGAAGTCAGGAGTT[C/T]GAGACCAGCTTGGTC | 9678 |
| rs576578957 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11010432 | CTTGTGTGTTATAGT[C/G/T]TAACTCCTTTTAAAT | 9678 |
| rs576593239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960418 | TGCAAAGGACATGAA[C/T]TCATCCTTTTTTATG | 9678 |
| rs576610907 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11059143 | GAATCACTAATTGGC[A/C/G]TTATACCATATGATG | 9678 |
| rs576612098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10998462 | TGTATATATACACAC[A/G]CATACACAGCAATAA | 9678 |
| rs576617691 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103358 | TTCTCAACCTTAAAT[A/G]TGAACTTAGGAAATA | 9678 |
| rs576666612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11162921 | AACTTACTCTACTCA[A/G]TCTGCTCCAGAATCA | 9678 |
| rs576692036 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960863 | GCATTTTTTCATGTG[A/T]CTGTTGGCTGCATAA | 9678 |
| rs576703994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976244 | AAGTTTATCTTGATT[A/G]ACTGTTTTTTTATCC | 9678 |
| rs576707651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11071980 | TTATTTTGAGAGGCA[A/G]TACTGTAAAATGAAT | 9678 |
| rs576709104 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040604 | TTGGCTTGAGTGGCA[A/G]TTAGAGGAAAATGTT | 9678 |
| rs576711755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11120463 | TGCCTTCACACACAT[A/C]AAATGAAAATCTTTC | 9678 |
| rs576713216 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075993 | AAAAAGTAAAAATTA[G/T]CCGGGCATGGTGGCG | 9678 |
| rs576718020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024763 | TGCTTATCGACAGTG[C/T]ACCTGGTGGTCACCC | 9678 |
| rs576720605 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103573 | GAAGAGACTCTTTGC[C/T]GAAATTGAATTGCAC | 9678 |
| rs576723807 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965730 | GTGGTGGGCTCTGCC[C/T]AGTTCGAGCCTCCCT | 9678 |
| rs576739580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11168900 | TGAGGCCACCACTTA[A/G]AATTGAAACTGTAGA | 9678 |
| rs576741695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11070230 | CTACAAGTGCGCGCC[A/G]CCATGCCCAGCTGAT | 9678 |
| rs576744714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11046730 | AGAGATACCCATAAT[A/G]CAGAAGTAGGAGGGA | 9678 |
| rs576759079 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045410 | ATATTTCTGAATGGC[C/T]GGTTTATTTTTGCTG | 9678 |
| rs576767906 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989634 | TTAATACGTCTTCCT[A/G]TACTTTTTCTTTTTG | 9678 |
| rs576773144 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11005394 | AATCTATTAACTGAT[A/T]GCTGTTTCTGTTACT | 9678 |
| rs576773972 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10976784 | TGATATATCTATATA[A/T]CCCTTAAACACACTA | 9678 |
| rs576788438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965933 | CCTGGTCTGCCTGCT[A/G]TGAAGACTGTGGGAA | 9678 |
| rs576805434 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042243 | GGTTTACAACTAATG[G/T]TAGGAAATAAACTAC | 9678 |
| rs576839489 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11162829 | TGGCCGGGATTACAG[A/G]CACACACCACCACTG | 9678 |
| rs576841163 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11155596 | TTTTGGAGAGTAGGG[C/G]ACTTTGCTGAAATTT | 9678 |
| rs576843252 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010194 | AGCACATGGAGAAAA[C/T]AGATTGATGATACCG | 9678 |
| rs576872297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11077396 | TCACAAGGTCAAGAG[A/G]TGAAGACCATCCTGG | 9678 |
| rs576882036 | in-del | -/T | 0.0189856 | 0.0955633 | intron-variant | PHF14 | GRCh38.p7 | 7:11007369 | CCTTTAACTTTGTGA[-/T]TTTTTTATTGTTTAC | 9678 |
| rs576882829 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126416 | TAGATATTTCTTTAC[C/G]TTTCCTTGTGACAAT | 9678 |
| rs576888331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11000417 | GGATCTTGGCTCACT[A/G]CAACCTCTGTCTCCC | 9678 |
| rs576902194 | snp | A/G | 0 | 0 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961461 | TTGGTACCAGTACCA[A/G]GCTGTTTTGGTTACT | 9678 |
| rs576902759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11072433 | AGTGGGACACGTATC[C/G]AAACTATATCAAGGT | 9678 |
| rs576964466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11131181 | GGCACCAGTCAACTT[A/G]GTCAGGAAATACCAA | 9678 |
| rs576969412 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968192 | TTCAGTTTCAAGATC[A/G]TATAACTGTAGCTAT | 9678 |
| rs576978119 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126585 | GTTTCAAAATCCCTA[A/G]CTTTTGTCTTCCTGT | 9678 |
| rs576982744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11040155 | TGAACAGATGTGGGC[C/G]CACCAGGCCACTGAG | 9678 |
| rs577006595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11044750 | ATCTATGCTCTAGAG[A/G]TTATTTAAGTCTATT | 9678 |
| rs577013913 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11123866 | GAAGTTGCAGTGAGC[C/T]GAGATCGTGCCACTA | 9678 |
| rs577014379 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11095572 | TCAGGTTTTCTCAAC[C/G]TGGGTTTCCTGGGAG | 9678 |
| rs577019568 | snp | A/G | 0.00111501 | 0.0235852 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040743 | AGAAGGAGGCACACA[A/G]AAGACATCTACTCTT | 9678 |
| rs577027648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11144257 | GGAAATCTTGTATAC[C/T]GTTGGTGGTAATGTA | 9678 |
| rs577049600 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152727 | CTGTAAATAACCAAG[A/T]GGATGTTCATTTTAT | 9678 |
| rs577053180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11009819 | TGGTTGTTCTTTGAG[C/T]TTGCACAACACCATT | 9678 |
| rs577073607 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PHF14 | GRCh38.p7 | 7:11046107 | TGTGATCTAGGTTCT[A/G]TTTTGTTTGTACCTC | 9678 |
| rs577074580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11128868 | GTCCAGTTTAAATTA[C/T]AGTTTTCTAGTTGCC | 9678 |
| rs577075247 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11020912 | TTCACATACATCTTT[A/C]TAACTTCCAAACTAC | 9678 |
| rs577090237 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11150365 | GCTGGTTATAAAGAC[A/G]AACAGAGGCATAAAC | 9678 |
| rs577091247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11038221 | GATCGAGACCATCCT[A/G]GGAGTTTGAGACCAG | 9678 |
| rs577106295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11052727 | TTTTGTTCATCTATT[C/T]ACATATTTTTGGTAA | 9678 |
| rs577110839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965830 | CCACCATGCTCCAGC[A/G]TCCCAGGTTGATCTC | 9678 |
| rs577111393 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012519 | AAACCTGTGTTGTTC[A/C]ATTGTCAACTGTAAC | 9678 |
| rs577138131 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103242 | AAGCTCATGAATAAA[A/G]ATATATCTGTGTTGA | 9678 |
| rs577171493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11029782 | AGCTTACATAGTAAT[G/T]AATGTTTATTTAGTA | 9678 |
| rs577176151 | in-del | -/CTTT | 0.00159617 | 0.0282053 | intron-variant | PHF14 | GRCh38.p7 | 7:11041279 | TATTTTTGTTTTTTA[-/CTTT]CTTTGCTCAATATTT | 9678 |
| rs577190326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11076445 | TTTTTAAAATGTACT[A/G]TCTGCTTTTTAACTT | 9678 |
| rs577201023 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11026672 | TTTAGTAGAAAGTGT[C/G]CAGTTACGTTATCTG | 9678 |
| rs577210302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115965 | TTTTGATTTGAATTA[C/T]AGATAATGATGTTAT | 9678 |
| rs577234202 | snp | C/T | 0 | 0 | intron-variant | PHF14 | GRCh38.p7 | 7:11159708 | TACAAGGGATCTCTG[C/T]ATTATTTCTTTCAAC | 9678 |
| rs577234420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11153111 | CTTACAAAGATTACT[A/G]TCTCCTGTATAAAGA | 9678 |
| rs577236917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11137085 | TGGTTTGTGACTCCA[C/T]GGCTTAAACCCTTCC | 9678 |
| rs577237873 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998565 | AGTGGTAATGAATAC[C/T]GTTACTGAGAAAAGT | 9678 |
| rs577240176 | in-del | -/A | 0.366473 | 0.221211 | intron-variant | PHF14 | GRCh38.p7 | 7:11031590 | GACCCCATCTCTACC[-/A]AAAAAAAAAAAAAAA | 9678 |
| rs577253587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149681 | GATAAATAAAAGAAT[A/G]CTGATACAGAATTTA | 9678 |
| rs577271814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10989014 | TGTAAAACCAGATGA[C/G]TTTTCTTTAGGATGT | 9678 |
| rs577279330 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11062348 | AGAGAAATTGACAGT[G/T]CTCTCTATTTAGAGG | 9678 |
| rs577284182 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PHF14 | GRCh38.p7 | 7:11094246 | GTAGCTTAAAACAAT[A/G]TAAAATTTTTTCATA | 9678 |
| rs577286285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11027300 | GTTCTACTGTTATTA[A/G]AGAAATTATATTAAC | 9678 |
| rs577290105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11115181 | TCTGCTCTTTGCTCC[C/T]TTTTTCCACTACTAC | 9678 |
| rs577293993 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033555 | TCAGATAGTTTCTAG[C/G]AGGGTAGCCATATGC | 9678 |
| rs577300752 | in-del | -/T | 0.188631 | 0.242351 | intron-variant | PHF14 | GRCh38.p7 | 7:11026723 | GTTAGTTGAAGCTTG[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs577301042 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11077850 | TAGCAAGTAAGAACA[-/T]TATCTATCTCAGAAT | 9678 |
| rs577339959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008412 | ACAGCAGGGGGTGAG[C/T]GGCTGGTGAGGGAGC | 9678 |
| rs577341104 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:10994209 | TTTGGGAGGCCGAGG[C/T]AGTGAATCACTTGAG | 9678 |
| rs577355556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11067586 | GGATTAAAGGATAAA[A/C]AAAATGTAGTGTATA | 9678 |
| rs577360206 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034704 | CAGGCACATGCCACT[A/G]TGCCTGGCTAATTTT | 9678 |
| rs577362148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062975 | AATTAAACATTTCAA[A/G]AAGAATAAACATATT | 9678 |
| rs577373165 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11008831 | ACGAGGTCAGGAGAT[C/G]GAGACCATCCTGACT | 9678 |
| rs577392916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964980 | TCTAACCTTTTTTCT[A/G]GGTTTCTACCTTCTT | 9678 |
| rs577413719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125119 | ATTTATGTAGACACA[A/G]CAGAAACTAATCTAT | 9678 |
| rs577413757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11132821 | ATGAGATGGTATCTC[A/G]TAGTGGTTTGGATTT | 9678 |
| rs577418804 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PHF14 | GRCh38.p7 | 7:11121662 | GGACACAAGCCCTGC[A/C]GTACTGTGATGGTCG | 9678 |
| rs577419416 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PHF14 | GRCh38.p7 | 7:11109333 | TGGTCCTCATTCCAA[A/G]GACAAAAGGCTGACA | 9678 |
| rs577467095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11075647 | ACACCTCCCACCAGG[C/T]GCACCTCCAACACTG | 9678 |
| rs577475810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11125862 | TCATTGAAATTAAGT[C/T]GGTTTTTTGTTAAGG | 9678 |
| rs577482817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11122221 | GCTGCATAGTGTTCC[A/G]TGGTATTCTGGAACT | 9678 |
| rs577501680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965245 | TGACCTACGGATGTG[A/G]TTTTGGTGTGGATGT | 9678 |
| rs577502373 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11075951 | CCTGGCTAATACGAT[A/G]AAACCCCGTCTCTAC | 9678 |
| rs577508173 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11129094 | CATATTTTTTCTAAG[-/AT]AGATTTAAGATTGTT | 9678 |
| rs577526326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11088156 | TGCATATAACCTATG[C/T]ATATGTTCCTGTATG | 9678 |
| rs577542992 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966557 | CCTACCCTTTCCCGC[A/G]TAGGAACCTGTCTGC | 9678 |
| rs577566059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957256 | TTATATTTTCCAATA[A/C]ATTTTTAAAAACTGT | 9678 |
| rs577567469 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10997632 | TAGTCATTTTAAGAT[A/T]TGGCTGGACCTGGAG | 9678 |
| rs577575270 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017067 | CCACCCAAGTTGTTG[C/G]AAATGACTGGCTCTC | 9678 |
| rs577590027 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11068230 | GTGGTGGGCACCAGT[A/T]GTCCCAGCTACTTGG | 9678 |
| rs577608849 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11112758 | CCTGGGCGACAGGGC[A/G]AGACTCCATCTCAAA | 9678 |
| rs577609445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11082364 | AAAAACAAAGCAAAC[A/G]AAAACATCAATTTAA | 9678 |
| rs577642434 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11018330 | TTGAATCTGTAGATT[G/T]CTTTGGGTAGTATGG | 9678 |
| rs577646934 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11156784 | GGTCATAGAGCGAGA[A/C]TGTCTCAGAAAAAAA | 9678 |
| rs577652777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10985748 | ACCTCCGCCTCATGG[A/G]TTCAAGCAATTCTTC | 9678 |
| rs577665315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11017375 | AGTGTACAAGGGTTC[C/T]CTTTTCTCCACATTC | 9678 |
| rs577670642 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164611 | AGCCATTTTTATTTT[A/C]TGTTTCTTTAATCAT | 9678 |
| rs577674014 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10986434 | ACTTCATGGTACTCC[A/C]ATGAGAGAAAGAGTG | 9678 |
| rs577690467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11024369 | TATTCAGAAGATTTA[C/G]CTAAGACAAATGATG | 9678 |
| rs577714051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966906 | AATTTGTCCTTGCCC[C/T]TTCGAACATACTGGG | 9678 |
| rs577736580 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006388 | TTTAGAATTAGCCAG[A/C]TGGACTCAGTTTAGA | 9678 |
| rs577736867 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PHF14 | GRCh38.p7 | 7:11047680 | TAATCCCTGCTACTC[A/G]GGAGGCTGAGGTAGA | 9678 |
| rs577739720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:10991380 | ATGGAGTTTCACCAT[A/G]TTGGTCAGGCTGGTC | 9678 |
| rs577749963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11132197 | GTATATTTTATCTCT[A/G]GACCTTTTTCATCTT | 9678 |
| rs577756276 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PHF14 | GRCh38.p7 | 7:11041523 | TAAATATTCTTCTCA[A/G]AATTTCTTTCTCAGA | 9678 |
| rs577757079 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105559 | AAATGGCAATTGAAA[A/C]TTGTTTAAGAGACTC | 9678 |
| rs577777478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11006859 | AGCTTCCTTCACTTT[C/T]GGCACTGTCTTGTGA | 9678 |
| rs577797937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11042198 | TCATGTATACTTGCA[A/G]TATATCTACATGTTG | 9678 |
| rs577798103 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11165168 | GACCTTGTGATCCGC[A/C]TGCCTCGGCCTCCCA | 9678 |
| rs577800834 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11001105 | TCGGAATTCATTATT[C/T]TGCATGTGTGTGTTC | 9678 |
| rs577817018 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106297 | AATATTTTTGTCTTT[A/C]TTACTACCCATTCAT | 9678 |
| rs577820568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11001614 | TTGGCAATATTATTT[C/T]ATTTTTTGGGGGGTG | 9678 |
| rs577893536 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963014 | TCTATTTTGTTGATC[C/T]TTTAAAAAAACAGCT | 9678 |
| rs577896922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11074160 | TAGCAAATGGTTGCT[C/T]CACAACCACCTTGAA | 9678 |
| rs577904270 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133839 | ACACAACAATTGCAG[C/T]ATGCAGTGATAGAAA | 9678 |
| rs577905585 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960915 | CTGTTCATATCCTTT[C/G]CCCACTTTTTGATGG | 9678 |
| rs577917440 | in-del | -/TTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985667 | TTTTTTTTTTTTTTT[-/TTT]GGAGACAGGGTCTCA | 9678 |
| rs577919196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11078798 | TTATTACTAATTGAG[A/G]TAAGTTTGTAAGAAA | 9678 |
| rs577922431 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104248 | GGTGGTGGATATTCT[A/G]TTCCACATTTGGTGC | 9678 |
| rs577930242 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11023049 | TTACCTGGCTTTTTA[G/T]TTGTATTATGTTGAC | 9678 |
| rs577936281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10984964 | TGTAGAAGAGATTAT[A/G]AAAAGGTACTTTTTC | 9678 |
| rs577947126 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080519 | GTAGATTTTATTGCT[C/G]TTTATGGAACTCTGC | 9678 |
| rs578006489 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133206 | TTTGACAAACTGATT[C/G]TCAAGTTTATATGGA | 9678 |
| rs578014707 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11138393 | AATGAAAAAAAAACA[C/G]AGTTGAGAAACACTG | 9678 |
| rs578038212 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160335 | TTGATTACATGTCTT[C/T]GCTATTATGAACAGT | 9678 |
| rs578050241 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158455 | ATACATACTATACAT[C/T]ACTAGTGATGTTAGC | 9678 |
| rs578074376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11164350 | ATTACGAAGGAAATC[A/T]ATGCTCACAGTGGGA | 9678 |
| rs578075259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11139260 | ATGTTTAAATAATTT[A/T]GTTTGTTGTTTCTAA | 9678 |
| rs578106390 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100855 | CTCACCGCACTACAC[G/T]GCTTTAGCATATTTG | 9678 |
| rs578121226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11028004 | GTGTTTAATGATTAC[A/G]TATATTTATACATAT | 9678 |
| rs578121753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11054399 | CTCTCATCTTTTCTG[C/G]CTGCCTTCCAACAAT | 9678 |
| rs578126211 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972147 | CATCATGTTGGGCAG[A/G]CTGGTCTCGAACTCC | 9678 |
| rs578146905 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PHF14 | GRCh38.p7 | 7:10989810 | TAATTTTAAAATATT[C/T]TGTAGAGACAGGATC | 9678 |
| rs578162748 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048800 | ACTCAGTGTGGACTC[-/T]TATCTACTGCAACAA | 9678 |
| rs578182474 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PHF14 | GRCh38.p7 | 7:11156823 | AAGAAAAGAAATTAA[C/T]TTTCTACACTTAAGT | 9678 |
| rs578183195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:10990134 | ACAGTAGTTTGATAA[A/T]GCTGGAATTTCTGAA | 9678 |
| rs578204773 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PHF14 | GRCh38.p7 | 7:11022296 | AAATGTGAATTGCTT[A/G]TTCTGTACCTTTTCC | 9678 |
| rs578214722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11034779 | GTCTCGAACTCCCAA[C/T]CTCAAGTGATCTGCT | 9678 |
| rs578229795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11145094 | AAAATGGTTAAGATG[A/G]TAATTTTTATGTCTA | 9678 |
| rs578243949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PHF14 | GRCh38.p7 | 7:11158154 | TTTGCCACTAGTGTT[C/T]TTTCTCTGGACCAAG | 9678 |
| rs745342983 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027068 | TTCTTTGATAGATTG[-/T]TTTTATAGTCTAAAA | 9678 |
| rs745357823 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043537 | ATTTTTAAATGGTAA[A/T]CTCTACAAGAGGTTG | 9678 |
| rs745358225 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019987 | GTGTCCTCCCAGCTG[C/T]TCTGAAATGAAATAT | 9678 |
| rs745368140 | snp | A/G/T | 4.19421e-05 | 0.00457926 | intron-variant | PHF14 | GRCh38.p7 | 7:11038859 | ATCACAGGGCAGGTT[A/G/T]GTTTCTTTCCAATTG | 9678 |
| rs745388101 | in-del | -/TTTAAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110223 | TATTGAATAGTAGTT[-/TTTAAC]TTTAATCAAGTAATA | 9678 |
| rs745393122 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973387 | TTTAATTTTCAATAA[A/G]TCCCTGCTTTTGTTG | 9678 |
| rs745393292 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962506 | TATTGAGGATTTTTG[C/G]ATCAATGTTCATTGG | 9678 |
| rs745410860 | in-del | -/CTC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016933 | CTAGTAACCATCCTT[-/CTC]CTGTCTGTGTCCATG | 9678 |
| rs745442915 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065057 | TACATGTCCTGTTGT[A/G]TATAATTTTGTCTAG | 9678 |
| rs745475876 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998808 | TGATTCTCTTATGAT[A/G]CTGAGGGCACTATCT | 9678 |
| rs745500807 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081309 | TTTGTAAAGTAACAG[C/T]ACTTGGAGGACTCTT | 9678 |
| rs745506853 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125055 | TTCTTCATGAAATTC[A/T]ATTAAATAAGATCTG | 9678 |
| rs745536490 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168659 | AATGATAAATCAGAA[A/T]TATTAGGAAAGCAAG | 9678 |
| rs745571406 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123804 | GAATGAGCAGAGATC[A/G]TGCCACTACACTCCA | 9678 |
| rs745573853 | snp | C/T | 1.6825e-05 | 0.00290038 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013901 | CAAGGAGACAGATGC[C/T]GGAAGGTTAATGTCC | 9678 |
| rs745575412 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983652 | TATTAATTCCTTTAC[C/G]AGTTGTAGCACTCAT | 9678 |
| rs745580490 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136971 | AAGAAATAACCACTA[C/G]TAACATTTCGTTAGG | 9678 |
| rs745587879 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148975 | ACATAATCATTTTTG[A/T]TTATTTAAACCCAAA | 9678 |
| rs745602564 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990046 | GCAGCTAGTCAATCT[A/G]GATCCTTTTTTAGAT | 9678 |
| rs745631524 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085901 | TAGTTTAAAAAAAAA[A/C]CTGTGGTTAAATGCT | 9678 |
| rs745637942 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043480 | ATGAATATTCTTTTT[A/G]TACAAGTTACCTTTC | 9678 |
| rs745646673 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058789 | AATCTTGGATTAGCC[A/G]TGCAAGAAAAGTCAC | 9678 |
| rs745660713 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014346 | AATTTTTAAGCTGTG[A/G]TAAAAGAGTCACTAT | 9678 |
| rs745670891 | snp | A/G | 1.73282e-05 | 0.00294343 | intron-variant | PHF14 | GRCh38.p7 | 7:11035612 | GGAGTACAAATGTTC[A/G]CTATTTTTCTGTGCT | 9678 |
| rs745673402 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955991 | TGTCAAAATGGTTTC[A/G]TAAGCAAAGTGCTGT | 9678 |
| rs745688502 | snp | A/G | 2.77704e-05 | 0.00372618 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982704 | GTGGCTGCTTCTGCT[A/G]CTGCCACCACACCAG | 9678 |
| rs745725841 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041510 | ATGTGTAAATACATA[A/G]ATATTCTTCTCAAAA | 9678 |
| rs745734771 | snp | G/T | 2.57384e-05 | 0.00358727 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111381 | CTCTGCTACCATTTT[G/T]GCTGTTTGGATCCTC | 9678 |
| rs745744611 | in-del | -/GTAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060872 | GGAACAGATTAAATG[-/GTAA]GTAGTTAGCCATGGT | 9678 |
| rs745749858 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030648 | TAATTTGAGGAAATT[C/T]ACAGGGAAACAGATA | 9678 |
| rs745769949 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977064 | ATAGCTGAGATATTC[A/G]CTTACTCTAGATTAC | 9678 |
| rs745777539 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116978 | AGTAGGACATAGCTC[A/G]TGCTTCAGTCTTTTC | 9678 |
| rs745778611 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993821 | TGATATCAGCCTGGC[C/G]AAAATGGTGAAACGA | 9678 |
| rs745795275 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120058 | TAGTTATTTTTTCCC[-/A]AAAAAATTGCCATTA | 9678 |
| rs745813267 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150788 | ATCATTTCTGTGACA[A/G]TGATTCAGGCTACTT | 9678 |
| rs745827747 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075871 | GCGCGGTGACTCATG[C/T]CTGTAATCCCAGCAC | 9678 |
| rs745846252 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148091 | TTCCGTTCTGACTAC[A/T]TTACAGTACTCCAAG | 9678 |
| rs745864970 | snp | C/T | 0.000283515 | 0.0119028 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982775 | CACTACGACAACCGC[C/T]ACAGAGGAACAAGTC | 9678 |
| rs745870257 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972346 | ATAAACACGAATGCC[A/G]GATTTTGAATTTCTC | 9678 |
| rs745876100 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167971 | GCGGAGCTTGCAGTG[A/G]GCAGAGATCGCGCCA | 9678 |
| rs745900375 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987023 | AGTACATTAGATGTC[A/G]TGTTGAGAAATGGCA | 9678 |
| rs745919690 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078187 | GGTGGCATGTGTGTC[A/G]TTAGCTTAACCCTTA | 9678 |
| rs745925484 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961890 | CTGTTCTTGGTGTAT[A/G]GGAATGCTTGTCATT | 9678 |
| rs745926248 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077451 | ACTACAAATACAAAA[A/T]TTAGCCGGGTGTGGT | 9678 |
| rs745940381 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005727 | TATAGTGCTGACAAA[C/T]ATGTGCCATGTATAT | 9678 |
| rs745942084 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047409 | ACTATTAAACATTTT[C/T]CTTTAGTAACTAAGA | 9678 |
| rs745951744 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164741 | TGTAACCATAGTACA[A/G]TTATTGAAACCAAGA | 9678 |
| rs745972406 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959736 | TCTGGATGAGGGGAA[A/C]ACGATGGTGCCCCAA | 9678 |
| rs746002227 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046372 | GCCTTTTCCAATTGT[C/T]TGAAGAATATTCTGA | 9678 |
| rs746059134 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107477 | AGTAAGAATCTAATT[A/G]GGTTTGCTTTTATCT | 9678 |
| rs746066232 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985537 | TTTATTTTAGCAGGG[C/G]CCTTTTATAATTACT | 9678 |
| rs746071580 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142537 | CGCAAGCTTATAACC[A/G]AGATAACATCAGCAT | 9678 |
| rs746090013 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079202 | TCTTCTAATTCTGCT[C/G]TATGTCTCTAGACTG | 9678 |
| rs746122368 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020729 | TAGTAAGTCTTAGTT[C/T]TGTCCCTTGCTAGAC | 9678 |
| rs746134561 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113483 | TACCAATATAAACAA[C/T]TAACATTTTCAAAAT | 9678 |
| rs746137710 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165761 | AATCACATTTATAAA[C/T]AAAGAAAAACCGAGG | 9678 |
| rs746147409 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120976 | TTTTCTTTGTCAAGG[A/T]CATTAAAACTGTAAA | 9678 |
| rs746152669 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995358 | AAGCCTTGCGCTAGA[C/T]ACAGAGTGCTGATTG | 9678 |
| rs746155093 | snp | A/C | 0.000152268 | 0.00872415 | intron-variant | PHF14 | GRCh38.p7 | 7:10983208 | GGGGAAAAGGGAATT[A/C]TTCTCTAAATCACTC | 9678 |
| rs746183451 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089095 | AGATTAATTAGATAT[-/A]AAAAAAAAAAAACCG | 9678 |
| rs746209816 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998576 | ATACTGTTACTGAGA[A/G]AAGTAAACATGGTTG | 9678 |
| rs746228014 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144081 | AGTAGAAATTTCTCA[A/G]AAGTCATACAAGCAG | 9678 |
| rs746274550 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071763 | TGTTTCTGATTATGT[A/G]TAAATTAGATTTTGT | 9678 |
| rs746319641 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017155 | GATTCGTCTGTTGGT[A/G]GAAACTTAGGTTGCT | 9678 |
| rs746331584 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979020 | GTATATTTATAGTAC[G/T]AACACTGTTGTACCA | 9678 |
| rs746336846 | snp | C/G | 1.70557e-05 | 0.0029202 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036463 | CGTGCCAAAGCAGAA[C/G]TAGCTCGATCTACCA | 9678 |
| rs746417227 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001761 | TTTAGTTCCAGGAAA[-/T]TTTTGGCTACTCTTC | 9678 |
| rs746435258 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990096 | TATTCATATACCTAC[A/G]CAGGCTCTCATGGAT | 9678 |
| rs746438844 | snp | A/C | 8.47206e-05 | 0.00650793 | intron-variant | PHF14 | GRCh38.p7 | 7:11061872 | GCACTTTTACACAGT[A/C]TTAACTTTGAGAAAT | 9678 |
| rs746460501 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082603 | TGACAATGAATTGTT[A/G]ACTTGTACTTCCCAG | 9678 |
| rs746466354 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053476 | TTTGTTAAATAAGCC[A/G]GCTAGTTTCTATTTC | 9678 |
| rs746470576 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170023 | GACTGCAGGGAAAGA[C/G]TAAAAAGAAATGATA | 9678 |
| rs746493873 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018247 | GTCTTTTGTGGTTCC[A/G]TATACATTTTAGGAT | 9678 |
| rs746524741 | snp | C/T | 1.7524e-05 | 0.00296002 | intron-variant | PHF14 | GRCh38.p7 | 7:11102481 | CTTATCACTTTACTG[C/T]GTAGATACCCTTCAT | 9678 |
| rs746569962 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093214 | CATCTTTAATATCTC[C/T]GTCATCCCAGAGTTT | 9678 |
| rs746575407 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081444 | ATTACAAGAGTGGTT[A/G]AATAAATTAATAATA | 9678 |
| rs746582820 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085439 | TTGTGTAATGTATTG[A/G]ATCTTAATGGTGTTG | 9678 |
| rs746596589 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026327 | AAAATACATAATGTT[A/G]TTATGCATTTAATAG | 9678 |
| rs746610634 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059238 | AAGTTATTATCAAAA[C/T]GGTAAATAAACATCC | 9678 |
| rs746623152 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145439 | GTTGCTAAAACTTAT[A/G]TAGACTGAAAATGAG | 9678 |
| rs746624028 | snp | A/T | 7.68728e-05 | 0.00619923 | intron-variant | PHF14 | GRCh38.p7 | 7:11013705 | TTATGTGACTTTAAC[A/T]AAATAAACCCTATTT | 9678 |
| rs746650464 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072660 | TCTGATATAACATAT[A/G]TAGTGCTTATTGTGT | 9678 |
| rs746653110 | snp | G/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973527 | ATCATTTAAATATTG[G/T]TAGTGGCTTAAGGTA | 9678 |
| rs746661007 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036370 | AAAATCTTAAGGAAC[A/T]TGTTTCATTTTATTA | 9678 |
| rs746696863 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151106 | GCAATGGTGAAATAT[A/T]AATTTAAATTTTCTG | 9678 |
| rs746707497 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974420 | GTGGGAGAGTCCTGC[A/G]GGAAAGCAGGATTGG | 9678 |
| rs746713057 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157923 | TTCTAAATCATCTAA[C/T]AAAAATTAGATGTTT | 9678 |
| rs746720079 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126391 | TAAGCAGGCTAAGTG[C/T]TGTAAAGGATAGATA | 9678 |
| rs746720375 | snp | A/G | | | | | GRCh38.p7 | 7:10970171 | TAGTCATGCATAAAT[A/G]TCTTGAATTTGAATA | 9678 |
| rs746726627 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963796 | TAGGACAGTTAGCTC[A/T]TCTTGTTGAATTGAT | 9678 |
| rs746744509 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065250 | ATATTTCTTTATGCT[A/G]TTTAATGCAATCTAA | 9678 |
| rs746768601 | in-del | -/AGAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168516 | TTTCATCAGATACAG[-/AGAT]AGAGTGGTATGTTTG | 9678 |
| rs746780635 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033627 | GGATATTGTAAGACA[A/G]TTAGTAGTTTCTGCC | 9678 |
| rs746789885 | snp | C/T | 3.49144e-05 | 0.00417803 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042758 | ACTACATTACCATCT[C/T]GGATGTCTGGATCCT | 9678 |
| rs746806815 | snp | A/C/T | 0.000123559 | 0.00785911 | intron-variant | PHF14 | GRCh38.p7 | 7:11028651 | TGGAAATAAGTTTGC[A/C/T]TTGAGAATTTTTCTG | 9678 |
| rs746813149 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993882 | GGCATGGTGGCACGT[A/G]CCTGTAATCCCAGCT | 9678 |
| rs746828977 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958581 | TTTTCTCTTGGATAT[C/G]TCTGAAAATATGAAC | 9678 |
| rs746842357 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044876 | TTTGTTTTGGAATAT[G/T]TGCATTGTACCTACT | 9678 |
| rs746847166 | in-del | -/TTTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075567 | GGAAGGAAAGAGGTT[-/TTTTT]TTTTTTTTTTTTTTT | 9678 |
| rs746865124 | snp | A/T | 2.21144e-05 | 0.00332516 | intron-variant | PHF14 | GRCh38.p7 | 7:11062091 | ATCTTGTCAGGTAAG[A/T]TGGATGCTAAAACCT | 9678 |
| rs746873034 | snp | G/T | 0.000117405 | 0.00766087 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982688 | AACAGTATCTGAGAA[G/T]GTGGCTGCTTCTGCT | 9678 |
| rs746881919 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020651 | CCCAAAGTGCTGGGA[C/T]TACAGGCATGAGCCA | 9678 |
| rs746891286 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967831 | ACAAACAATTGCTAA[C/G]AGATCTTGTGTTCAA | 9678 |
| rs746918815 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168797 | CCATTTAATACTGAA[C/T]ACAAGATGCACTTCA | 9678 |
| rs746920246 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095132 | GTAGTGATAGTAAGA[A/G]TGGTTGAGTTGAACT | 9678 |
| rs746933523 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983784 | AAATGGAATAAAAAC[C/G]CAAACATTTCCATCA | 9678 |
| rs746937571 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956238 | ATTACTTGATTTTCC[A/G]TCTGGGAAGTGGGGA | 9678 |
| rs746964457 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128326 | TTATTTTCACTGAGG[A/G]AAGGGGGGTGATATT | 9678 |
| rs746977258 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957120 | TGACTACCCTTAGGT[A/G]AGCAAGAGGGGCTCA | 9678 |
| rs746993295 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031833 | CAACTTATGTTACTA[C/T]GTTTTACATTATATA | 9678 |
| rs746997378 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165860 | AGTGATAAGATAAAC[A/G]TGGCAGTGTGTTTAC | 9678 |
| rs747004837 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994831 | CTCATAAAGGCAGCG[C/T]GTACCCGAAGAGTGA | 9678 |
| rs747018120 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124351 | ATGTATGGCAGTTTA[-/C]CATGTTGTTAAATAC | 9678 |
| rs747019859 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098562 | CTCACCTGATAAAAT[G/T]GCCAGAACTTGAACT | 9678 |
| rs747024875 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108930 | GTTATAAAGTAAATA[A/T]GCAGTAATTAGGTAG | 9678 |
| rs747025004 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095550 | CTAGAAGTAAATGGA[A/G]ATAAGATCAGGTTTT | 9678 |
| rs747059703 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025419 | CATGGGTAAAATGCT[A/G]TCAAATAGCATCACG | 9678 |
| rs747074799 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069734 | TTTTTTGGTTGGTTG[A/G]TTGTTGCCCAGGCTT | 9678 |
| rs747090379 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996051 | GGTGCCAAGAGTGAG[C/T]GAGGGCTGTGAGGGC | 9678 |
| rs747097203 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153522 | TAAAGCATGGTATAG[A/G]TGTGAGGGCTGAAGA | 9678 |
| rs747149608 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049932 | ACATAAAAGTTTTCT[A/G]AGTAATACATGATTA | 9678 |
| rs747161896 | in-del | -/TTTTTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075565 | TGGGAAGGAAAGAGG[-/TTTTTTT]TTTTTTTTTTTTTTT | 9678 |
| rs747169557 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959766 | AAACTTGGAGATGCC[A/G]GCAATGGCAGAGCCC | 9678 |
| rs747180790 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128154 | GTACTTGAGTTCACT[A/G]CAAATTCATGCCTTC | 9678 |
| rs747182864 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090484 | TCAATTATTAAAGAA[C/G]TGCAAAATTGCCTGA | 9678 |
| rs747188149 | snp | C/G | 5.28947e-05 | 0.00514242 | intron-variant | PHF14 | GRCh38.p7 | 7:11169398 | ATATTTTAATGTTTT[C/G]TAAAATTTATTTCAC | 9678 |
| rs747201228 | snp | C/T | | | | | GRCh38.p7 | 7:10970680 | TGCTATTATAGCCAG[C/T]TTACAACCAATAAAG | 9678 |
| rs747207586 | snp | G/T | 4.9666e-05 | 0.00498302 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983058 | CCTGCCAGTGAAGGG[G/T]GTTGCAAGAAGAAGA | 9678 |
| rs747231976 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070294 | TTTTGCCCAGGCTGG[C/T]GTAGAACTTGTGAAC | 9678 |
| rs747234960 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155014 | CCTTACTATCTATCT[C/G]TAGGTACCTATCTTC | 9678 |
| rs747269671 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102546 | CAATCCCGGAAACCT[C/G]TTTTATAAGTGTGAT | 9678 |
| rs747272623 | snp | A/C | 5.92376e-05 | 0.00544199 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036433 | GCAAGGATCAATGCC[A/C]GGCTTCAGCAGTATC | 9678 |
| rs747294606 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986696 | GCCGTTAATCTTGCA[A/G]CTTTGAGATTCCTTA | 9678 |
| rs747295419 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140553 | CAGGCTTTTGTGATG[A/C]GATCTTTCATTGTTC | 9678 |
| rs747328351 | in-del | -/AA | 5.30012e-05 | 0.0051476 | intron-variant | PHF14 | GRCh38.p7 | 7:11061942 | TTGTTATGTTTTATT[-/AA]TTATTATCCCTTGTA | 9678 |
| rs747388914 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979220 | TGATATTGTAAAGGG[A/G]TTCTTGAAGGTTGGT | 9678 |
| rs747389131 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147018 | CACCTGGCTAATTTT[A/G]TATTTTTTAGTAGAG | 9678 |
| rs747397461 | snp | A/G | | | | | GRCh38.p7 | 7:10969916 | TTTTTCTTACAGTAG[A/G]TGTCCACAACAAGCT | 9678 |
| rs747411936 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132145 | TTTTGCATGAATTCC[A/G]AATACAGTACAATTG | 9678 |
| rs747413596 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067940 | CATCTTCATGACGTA[A/C]ACACCTCCCATTAGG | 9678 |
| rs747418501 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100751 | GAAGAATTACTTGCC[C/T]AAGATTGTACAACTG | 9678 |
| rs747429125 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006582 | ACTTCCTCAGTGAAC[A/G]CAAGCATGTTGTTGT | 9678 |
| rs747439917 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060480 | TAAGTGTTGTTAAGG[A/T]CCTTTCTACACTGGT | 9678 |
| rs747450424 | snp | A/G | 1.66854e-05 | 0.00288833 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051769 | CCCAAGAAGATTCCG[A/G]TAAGAAACACGGTAG | 9678 |
| rs747457217 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015465 | GGTCTGTATCATAGG[-/C]ATAGGCATTACTCTA | 9678 |
| rs747457750 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162151 | TGGAGTGCAGTGGTG[C/G]AATCCTGGCTCACTG | 9678 |
| rs747467173 | in-del | -/ACAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122353 | TATATATATATATAT[-/ACAC]ACACACACACACACA | 9678 |
| rs747500143 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078322 | TATCTTAGTGAATAA[C/G]AGAATATGAACCTCA | 9678 |
| rs747509095 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134347 | TATGGACCTGAAATA[C/T]CATTTAGAGAGATTT | 9678 |
| rs747529577 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048439 | TAGCCAGGCATGGTG[A/G]CAGGCACCTGTAATC | 9678 |
| rs747538687 | snp | A/G | 1.77565e-05 | 0.00297958 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051636 | GGAATGTGACCAGGC[A/G]GGGAGCAGTGACATG | 9678 |
| rs747561191 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956612 | TACGTAATTAATCCG[C/G]TGAGTTCATACTGGA | 9678 |
| rs747564200 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105031 | ATTTTATAAAATTTA[-/G]TTAAATGTTTGTTTT | 9678 |
| rs747573966 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073909 | GGTGATGTGAGCTGT[A/C]CCTGGGGCTCTGTGC | 9678 |
| rs747581778 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980273 | GAAGAAAAGTACCTT[G/T]TCTTTCATCTTCATC | 9678 |
| rs747587064 | snp | A/G | 7.46519e-05 | 0.00610904 | intron-variant | PHF14 | GRCh38.p7 | 7:10974793 | CTCTCCCCTGTGTTT[A/G]GTGTGATTATGAATG | 9678 |
| rs747598856 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159059 | TGAAATATTTAAATC[A/C]GGCTATTTTATATCT | 9678 |
| rs747603503 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114646 | ACTTTCTCTGTCTCA[A/T]CAACTCTTCATAAAC | 9678 |
| rs747608687 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079524 | TTGATGTATGTATTT[C/T]CTATTACTTTTTTTG | 9678 |
| rs747627310 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994481 | TGCTTAAGAGTGTTT[G/T]TATAATGGCACAGAA | 9678 |
| rs747671820 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021400 | ATTAAAAGGGACCAT[A/G]GTTGTCTCGGCCATG | 9678 |
| rs747674000 | snp | A/C | 3.85527e-05 | 0.00439032 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982504 | AAGAAGAACAACTTA[A/C]AAATTCTGCAGAGGA | 9678 |
| rs747679444 | snp | A/G | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061976 | CAGGAAAGAGTTCCT[A/G]GAGAGAGAAGACAAA | 9678 |
| rs747690723 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113532 | TAATATTGGAATGTC[A/G]CAGCAGTTTACTGTA | 9678 |
| rs747694596 | in-del | -/AAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000882 | GGAGTCCAACTTATA[-/AAT]TATTTCTCTTGTTTA | 9678 |
| rs747700886 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085597 | GTTTCAACATTTAAC[A/G]TTGGTGACCAACCTT | 9678 |
| rs747710102 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083819 | AATCACTTAGTAAGA[G/T]AATTGTAAAAATGAG | 9678 |
| rs747722817 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980478 | TTTACCAGATGTGAT[G/T]TTTCTTGGTAGGTTG | 9678 |
| rs747749448 | in-del | -/TT | 0.000262502 | 0.0114535 | intron-variant | PHF14 | GRCh38.p7 | 7:11061768 | GATTTTTGTTTTTTG[-/TT]TTTTTTTTTGTTTTT | 9678 |
| rs747754836 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133171 | TCCCAATCGAACTCT[A/C]AGCAAGTTATTTTGT | 9678 |
| rs747757516 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062169 | AAATGAAAAAACAAT[A/T]GCAGGATAAGACCTT | 9678 |
| rs747758419 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039810 | AAGGTGAGAATTAGT[A/T]GTCGCCTCTGGGAGG | 9678 |
| rs747768340 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992999 | TTATATGCTTTTGGC[C/T]GGAATACCACGGAAG | 9678 |
| rs747789848 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153860 | TTACTCCCATGGCCA[C/T]AAGATGGCTACAGAG | 9678 |
| rs747791334 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147868 | ATTCAAATGTTTGCC[C/T]GACATTCCCACTAGA | 9678 |
| rs747796534 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147126 | GTGCTGGGATTACGG[A/G]CATAAGCCGCCACAC | 9678 |
| rs747796982 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102767 | TTTTTCTTCTTTTTG[C/G]TTTTTTTGCACTTAT | 9678 |
| rs747816700 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965544 | GACCCACTTGAGGAG[A/G]CCGTCTGTCTGTTAA | 9678 |
| rs747832896 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017460 | GAGATGATATTTCAT[G/T]ATAGTTTTGATTTGC | 9678 |
| rs747838972 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128509 | AGCCATTCTACACAC[A/T]TTTTCCCAGTCACTC | 9678 |
| rs747850121 | snp | A/C | 4.38126e-05 | 0.00468021 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11062073 | GAACTGGAGACAATG[A/C]AAATCTTGTCAGGTA | 9678 |
| rs747865274 | snp | C/G | 5.64191e-05 | 0.00531097 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982672 | AGGAAAAAGAAAAAG[C/G]AACAGTATCTGAGAA | 9678 |
| rs747908920 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137196 | AAAATACAGAAAATA[C/T]ATACAAAATTAATGC | 9678 |
| rs747927280 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106171 | AATCTTGTAATCTGG[A/C]TGCCACAGATATAGC | 9678 |
| rs747955606 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152101 | TTGGATTTGAAAATT[G/T]CTTTTGATCAGTACT | 9678 |
| rs747959583 | snp | A/C | 8.04667e-05 | 0.00634247 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040672 | TGTTCAAATCAATAG[A/C]AGTTGAATATACCGG | 9678 |
| rs747963826 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006147 | TGACTACCAAAAGGA[C/G]TGTACTAATTACCAA | 9678 |
| rs747999089 | snp | A/T | 1.77694e-05 | 0.00298067 | intron-variant | PHF14 | GRCh38.p7 | 7:11028644 | TTTAGTCTGGAAATA[A/T]GTTTGCTTTGAGAAT | 9678 |
| rs748046852 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000484 | AGCTGGGATTACAGG[A/C]ACACACCACTACACC | 9678 |
| rs748065124 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958738 | TCTCATTTTGTCACC[A/C]AGGCTGGAGTACAGT | 9678 |
| rs748074371 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095181 | GCACTTACCACAACC[A/G]TATGCCAAGCATTAT | 9678 |
| rs748076297 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082828 | TGTGGGATATGACAA[C/G]ATTTCTCTTCAAATA | 9678 |
| rs748077254 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168938 | AAGCATTCTAAGCCG[A/G]CATGCACATGCTTCC | 9678 |
| rs748086948 | snp | A/G | 9.01023e-05 | 0.00671141 | intron-variant | PHF14 | GRCh38.p7 | 7:11040805 | TAATAATGATAGAAT[A/G]ATGTTGTGTATTTTT | 9678 |
| rs748108325 | snp | C/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170116 | CCTGCTGTGTGCAAG[C/G]TCCCACACACTATTC | 9678 |
| rs748132594 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010694 | ATACTTTTTTGAGAC[A/G]AGATTTTGCTCTGTT | 9678 |
| rs748135754 | snp | A/C | 2.11647e-05 | 0.00325298 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022927 | TTGGAGATATTGACA[A/C]ATTACGACCAGTAAC | 9678 |
| rs748137996 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987393 | GATAAAATTTAGCCT[A/G]TTGTATATATCATTT | 9678 |
| rs748151575 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143703 | CTAAGCATCTTGTAA[A/G]TGTAACACCCACTAA | 9678 |
| rs748162837 | snp | C/T | 0.000131415 | 0.00810494 | intron-variant | PHF14 | GRCh38.p7 | 7:11051607 | AATTTTTCCCCTTTA[C/T]GTAGGCAGTGCTCGG | 9678 |
| rs748181126 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092177 | GTAATTTGTCTTTTA[C/T]CCCCTTTATCTGTTT | 9678 |
| rs748185064 | snp | A/G | 0.000215003 | 0.0103661 | intron-variant | PHF14 | GRCh38.p7 | 7:10974360 | TGCGGCGAGAGGTCC[A/G]TTTCAGCCATTCTAG | 9678 |
| rs748188064 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119675 | ATTTATTAAACATTT[C/T]AATTAGTTCATAATT | 9678 |
| rs748199443 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096469 | TTATCGTAAAGTTTT[C/T]GAATGCTAATACAGA | 9678 |
| rs748241569 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023647 | GCCTGGCCAACATGG[C/T]GAAACCTCGTCTCTA | 9678 |
| rs748261023 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072231 | TGGCAGGGGCCAGGG[A/G]CAAAGAGAGAGATGT | 9678 |
| rs748263319 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978223 | TTAGCCCTTTGCTAG[A/T]TGTTATGGTGAATTT | 9678 |
| rs748270640 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070711 | GTCATTATTGTCTGT[C/G]AATTAATTTACTTTG | 9678 |
| rs748280534 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110601 | GTGGCAAAGACACTA[C/T]CAAAACATAAGTTTT | 9678 |
| rs748299847 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159874 | GCAAATAAAAAGGGA[A/G]TGAGAAGCAATTTTC | 9678 |
| rs748395868 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091195 | AATGCAAAGGATTAG[A/G]AAGATCTCGGAAACA | 9678 |
| rs748437752 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162573 | GTCACTTTTCACTCA[C/G]TGATCTTTGTTGCCT | 9678 |
| rs748441266 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003840 | GAATCACTGTTAACA[A/G]TTTGGTATGTATCTA | 9678 |
| rs748445931 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014709 | GAGCTTAGTGTTATG[C/T]TCACTCTGAGAAGAA | 9678 |
| rs748474367 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128853 | TCTTCTTAATTAAAT[A/G]TCCAGTTTAAATTAT | 9678 |
| rs748482581 | snp | A/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079571 | AATGATTTAATGTTG[A/G/T]CATTTTGTTTTGCTG | 9678 |
| rs748491227 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047424 | TCTTTAGTAACTAAG[A/C]TTCTGAAATTCCATT | 9678 |
| rs748492461 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050113 | AACAAATGGTACTTG[A/G]TATTTAACTCTTGTT | 9678 |
| rs748512801 | snp | A/C | 8.61289e-05 | 0.00656179 | intron-variant | PHF14 | GRCh38.p7 | 7:11037113 | TAGCTACAAAATATG[A/C]AACATAATGTGATAG | 9678 |
| rs748519663 | in-del | -/GGATTGGT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974429 | TCCTGCGGGAAAGCA[-/GGATTGGT]GGACCCTCGCCCTCC | 9678 |
| rs748526976 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981387 | TTATTTCTCGCTTCA[A/T]AGATTTTAGATTGTT | 9678 |
| rs748530019 | snp | A/G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960716 | CAACAGTATAAAAGC[A/G/T]TTCCTATTTCTCCAC | 9678 |
| rs748544636 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044853 | GTGATTTGGATTTTG[-/T]TTTTGTATTTGTTTT | 9678 |
| rs748574744 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007724 | GAGAGAAGAAAAAAA[-/C]ATTTCTAATTGTCCT | 9678 |
| rs748576350 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048824 | GCAACAATCATGTGG[C/T]GGTTGTCTTGAAATA | 9678 |
| rs748592077 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080061 | GGATACATTTTTACT[A/G]CGAATGAATGTCATA | 9678 |
| rs748596443 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035955 | ATTTTTGGCTGAATA[C/T]AGTACTCCTCATTTA | 9678 |
| rs748603136 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063569 | TAATTATTTGAACCT[A/G]TATGAGTATCTACTG | 9678 |
| rs748623990 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123424 | TTCAAATTAAATATT[C/T]TGAAGATATGATTAA | 9678 |
| rs748625250 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986773 | GCAGTGTACTATTTT[C/T]AGAAATGGTTCCCAT | 9678 |
| rs748627444 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155172 | TTAATAATTTTAGTC[A/G]TCAAAAATAGTTACT | 9678 |
| rs748644313 | snp | C/T | 8.4285e-05 | 0.00649118 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974285 | GCTCCTGCAGCCTCT[C/T]CCTAAGTCTTCTCCA | 9678 |
| rs748646480 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069934 | TGGAAAAAGTGTTCC[C/G]TTATTCTTTGTTTTT | 9678 |
| rs748649367 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007384 | ATTTTTTATTGTTTA[C/T]AATTTTCTGTACAGT | 9678 |
| rs748682616 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034891 | ATCTGTCCATTGTTA[A/G]CCAGTTAGAAATGCC | 9678 |
| rs748726483 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097261 | TGGGATTACAGGCGC[A/G]AGCCACCGTGCCCAG | 9678 |
| rs748733899 | snp | C/G | 1.68275e-05 | 0.0029006 | intron-variant | PHF14 | GRCh38.p7 | 7:10990861 | AGGTAATGTTGCTTT[C/G]TTTTCTCTCTTTTTA | 9678 |
| rs748735326 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028351 | AAAAAATTAGAAGTG[C/G]AACTGTTGTAAACTG | 9678 |
| rs748736215 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996140 | CAGCAGAGGATTAAT[A/G]TGGTTTGATTCATGT | 9678 |
| rs748740578 | in-del | -/T | 0.000117647 | 0.00766875 | intron-variant | PHF14 | GRCh38.p7 | 7:11013736 | ATCATAGTGTTTTTG[-/T]TTTTTTTTAGGTTGT | 9678 |
| rs748752167 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103775 | GTGATCTCTAGTTAC[A/G]GTGAGGAACGCTATG | 9678 |
| rs748765556 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147965 | TTCCCATCACAATTT[A/G]CTTCTCCCACAGTCT | 9678 |
| rs748770999 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156731 | TCCAGGAGGCAGAGG[A/T]TGCAGTGAGCAGAAG | 9678 |
| rs748776032 | snp | C/T | | | | | GRCh38.p7 | 7:10970959 | ATAAAATTCGAAGCT[C/T]TTTCATGATAAAAAC | 9678 |
| rs748777005 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126776 | CATAGCAATAGGATG[-/A]AAAAAAAAAAAAAGC | 9678 |
| rs748777882 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115778 | GAATCTGGACAGTTC[C/T]TTAGTCTTTCCTTAA | 9678 |
| rs748815763 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018558 | ATTATTCACTGTTGT[C/G]ACGTAGACATGCTCC | 9678 |
| rs748817536 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993037 | GTGTTCTTAGTGCAT[C/T]GTATTAGGAAGCATA | 9678 |
| rs748866067 | snp | A/C | 9.81274e-05 | 0.00700386 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982497 | AAAGTAAAAGAAGAA[A/C]AACTTAAAAATTCTG | 9678 |
| rs748889970 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007619 | TAAAAAACATGGTTA[A/G]ATATGAACTTCATGA | 9678 |
| rs748920196 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135931 | AAGGTAAAGGATGAT[A/G]TATGAAAACTGATAA | 9678 |
| rs748921640 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981830 | TTTGGTATATTAGAG[G/T]TGTAGTATAAGTTGA | 9678 |
| rs748931383 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019070 | TGTTGAACCATGCTT[G/T]CAACCCAGGGATAAA | 9678 |
| rs748938774 | in-del | -/TC | 6.32011e-05 | 0.00562108 | intron-variant | PHF14 | GRCh38.p7 | 7:10974959 | AGGTAAATATTTCCT[-/TC]TCTCTTCCCCTTTCC | 9678 |
| rs748963229 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131661 | AGCTTAATTTTTTTC[G/T]CTTATGGATTATATT | 9678 |
| rs748996528 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989861 | GTCTCAAACTCCTGG[C/T]CTCAAGTGATCCTCC | 9678 |
| rs749011567 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981071 | TATGCAATTTTGCTT[G/T]CAGGATGTTTTTGTT | 9678 |
| rs749032753 | snp | C/T | 2.11423e-05 | 0.00325126 | intron-variant | PHF14 | GRCh38.p7 | 7:10982355 | GTGTGGTTTTTTTTT[C/T]CTCATATTTTCAACA | 9678 |
| rs749041239 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104482 | AATTGATGTGTGCTT[A/C]AGAAAATATGTACTA | 9678 |
| rs749048824 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096257 | AAAGAAGATCATCCT[A/G]CATAATTACTCTTTA | 9678 |
| rs749050110 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012423 | TGATGCTTTGTTTAT[G/T]TGAGTTTTGTATCCC | 9678 |
| rs749052159 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986409 | TCCCATTTCATGTAG[C/T]GTCTGGAAAACTTCA | 9678 |
| rs749094292 | in-del | -/TA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110959 | TTCATATCCTGGAAT[-/TA]TATATGTATCTTATT | 9678 |
| rs749096118 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069130 | AGTCAGGAAAGGTTG[C/G]TGGCTCCTGAGTATT | 9678 |
| rs749096287 | snp | A/G | 2.56098e-05 | 0.0035783 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982942 | GGAGATCTGCGTCTC[A/G]GAAAGAGGGAAGTGA | 9678 |
| rs749099453 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965613 | TTCAGAGCTGTCAGG[C/T]AGGATGTTTAAGTCT | 9678 |
| rs749101263 | snp | A/G | 4.96697e-05 | 0.00498321 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111422 | GTCTCCTAAACAGAC[A/G]GGCTACGGATGGATA | 9678 |
| rs749122023 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078141 | TAACCTCATTTTTTC[C/G]CCTTATTTATCCTTA | 9678 |
| rs749171367 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043102 | AGAATTTCTCAAATG[C/T]TTTATTGTTATTTTG | 9678 |
| rs749184100 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056565 | ACTGCCATTCCATTG[A/G]TTGTTTATTGGTAGC | 9678 |
| rs749197622 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128706 | TCTCTCTCTCCCCCC[A/G]CCCCCACTGCTTTCC | 9678 |
| rs749206003 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975102 | ATTTTGCCTTTAGAT[C/T]CTGTCACTAGACCTA | 9678 |
| rs749211655 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074087 | AAATGCGTTCAATGC[C/T]TTTCCCCCATGTCTT | 9678 |
| rs749225242 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114737 | CACGTATTTACATAC[A/G]TGGAGGCACAAATAT | 9678 |
| rs749226901 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145792 | ATTAAAACAGTAAAT[C/T]AACATCATAGATGCC | 9678 |
| rs749231874 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001911 | CTGACAGAGAACATC[C/G]TTGCCTCATACCTCA | 9678 |
| rs749237498 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085126 | AATAGACAACAGATA[C/T]ATATTATTTAGGCAG | 9678 |
| rs749263625 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041191 | GCAGTGGATAATGAA[A/G]ATAAGTTTTAGTTTT | 9678 |
| rs749271117 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967086 | ACTAAGAAAATGATG[A/C]TCTGAGATTTTGAGG | 9678 |
| rs749279875 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116992 | CATGCTTCAGTCTTT[C/T]CCAGGATATTCTTGA | 9678 |
| rs749291895 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159227 | GATGTTAAGATTGTT[A/G]TAATGCCATTTATAT | 9678 |
| rs749313293 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128005 | CCACCTTTTTAAAGT[C/T]GTAACTTGACATTTT | 9678 |
| rs749319852 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003625 | AAGTTTACCAAGTCC[A/G]TCCTTCTGCAGAAAT | 9678 |
| rs749330063 | snp | A/G | 4.66146e-05 | 0.00482754 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990824 | TAATTCAGTGTGACA[A/G]TTGTGGCATTACAGT | 9678 |
| rs749334317 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045039 | TGCTCAACCTATGAT[A/G]GTTGCTACTACACAC | 9678 |
| rs749337290 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094377 | CTTTTCTAGCACTAG[A/G]GTTGTTCTGCACTCC | 9678 |
| rs749347872 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981665 | TAGTAGTTACTGCGT[A/G]GAAGTTTTGAAAGTG | 9678 |
| rs749384661 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130028 | ATCCCAAATTTTTAG[G/T]TGATTAATATAAGTT | 9678 |
| rs749390504 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145158 | AAACCCTCGGGAGGG[A/G]TTCAGGTGGCAGAGG | 9678 |
| rs749391240 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033230 | ACAAAACCAAGTAAC[A/G]AGTTGCTTAAACGAA | 9678 |
| rs749394729 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957259 | TATTTTCCAATAAAT[G/T]TTTAAAAACTGTTGT | 9678 |
| rs749409938 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099102 | GCCCAGCTGCCACTG[A/C]ATTTTTCTTATTAAG | 9678 |
| rs749427948 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058872 | GCTGTGTGACATCAG[C/G]AAGTCATTTCTCTGG | 9678 |
| rs749449355 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118846 | GTAAATTATTCCTTA[A/G]GCATCATTTTGAAAA | 9678 |
| rs749453420 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978364 | TGTAGTTCAAGTCTT[C/T]AATAGGAAATGAGAT | 9678 |
| rs749475095 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164387 | GAAAATGTGGCAAAG[C/T]ACAGGTAAGAAAATA | 9678 |
| rs749475230 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150876 | TATTCCTGCTTTAAT[A/C]AGTCTTTTGAAATTC | 9678 |
| rs749478815 | snp | A/G | 1.65721e-05 | 0.0028785 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028809 | GCTTTCAGAGGCAGC[A/G]GCGGAAGAGGTAGGT | 9678 |
| rs749483493 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994914 | GAAGGGGACCCGAGC[A/G]GGTTGCCATTGCTGG | 9678 |
| rs749497357 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137249 | TGAGGGGAGGACTTT[C/T]GATCAATTGCTTGAT | 9678 |
| rs749511343 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077269 | AAAAATGTTAGAAAC[A/G]TAAGCATTTGAATTA | 9678 |
| rs749527158 | in-del | -/ATTAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007680 | TCATAATACATGAAT[-/ATTAA]ATAAAATGTGGAAAA | 9678 |
| rs749550834 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140256 | ACATGCATACACCCC[C/G]ACACGGAAATAAAAC | 9678 |
| rs749569642 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004763 | TAATGTGGCTGGGTG[C/T]GGTGGCTCATGCCTG | 9678 |
| rs749582063 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117958 | TTTAAGTTTCTGGAT[G/T]TTATATGGCCGACAG | 9678 |
| rs749591239 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967998 | ATAAATATCAAATTC[C/T]CAGTGTTGAAGTTTT | 9678 |
| rs749602680 | snp | C/T | 1.68165e-05 | 0.00289965 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036472 | GCAGAACTAGCTCGA[C/T]CTACCAGACCCCAGG | 9678 |
| rs749613783 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110624 | TAAGTTTTTAAATGT[A/G]CTAGGAAGTACTTTG | 9678 |
| rs749624801 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964317 | CTGTAAATAATTTTA[C/T]TTCTCCTTCACTTAT | 9678 |
| rs749627086 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070978 | TTTTAAAATTACTGA[A/G]TACAAACTTAAAAAT | 9678 |
| rs749653093 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997584 | GCTTAGAGTCTCTCA[C/T]GAAGTTGCAGGTCAA | 9678 |
| rs749653514 | snp | A/C | 2.50982e-05 | 0.00354238 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11062035 | GGCTGAAGATTTAAG[A/C]ACTGAATGTGCAACT | 9678 |
| rs749654238 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155353 | ATAGAAGAAACAGAA[C/G]AAATATGAAGTATGT | 9678 |
| rs749657082 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008762 | CTTTTTTGGCCGGGC[A/G]CGGTGGCTCACGCCT | 9678 |
| rs749675667 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961494 | AGGCTTGTGGTATAG[A/T]CTGAAGTCAGGTATG | 9678 |
| rs749686504 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071792 | GTTTCCACAACTAAT[C/T]TAATGCAATAAGAGA | 9678 |
| rs749702874 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087207 | CTTTCTTTTTTTTTG[-/T]TTAAGATGGAGTCTC | 9678 |
| rs749711699 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080132 | CTGTGAGAACATACC[A/G]AGTGTAGTTGGATAG | 9678 |
| rs749722903 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091895 | TAAATGACTGCGTCT[C/T]TCAGTGGATATTGAA | 9678 |
| rs749727642 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097851 | CTTCTCCTTCATCTT[C/T]TCTCTAGCTCTGAGC | 9678 |
| rs749730086 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051139 | TCCACCTCCTGGGCT[C/G]AAGTGACTCTTTCAC | 9678 |
| rs749732644 | in-del | -/AAAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163093 | GTTGCAGTATTAAAT[-/AAAG]GGAGATCTCTTTGAT | 9678 |
| rs749750656 | snp | A/G | 1.97299e-05 | 0.00314079 | intron-variant | PHF14 | GRCh38.p7 | 7:10990688 | TTCTGATATATGTTA[A/G]TATTTTAATATTAGG | 9678 |
| rs749751589 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014960 | AATTTTCAACCTTTT[A/G]TATTTCGTGGAGATC | 9678 |
| rs749757748 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024557 | GACTTTAAGTTGAAG[C/G]CAGTGCTCCTATACT | 9678 |
| rs749765416 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111696 | ATTTAGTTGTTTTAC[A/G]TATTCTCTATTATTG | 9678 |
| rs749774261 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071710 | AGGCAACCACTGCAA[A/G]TGTTCTTTTGTCACT | 9678 |
| rs749842219 | snp | C/T | 0.000126202 | 0.00794262 | intron-variant | PHF14 | GRCh38.p7 | 7:11036702 | TGGTCAGTATAGACA[C/T]TGGTACATGCACATT | 9678 |
| rs749847655 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023696 | AGCTGGGCGTGGTGG[C/T]GCGTGCCTGTAATCC | 9678 |
| rs749852279 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995694 | GTTCCGAGCCCTGCC[C/T]CGCAGGGAGGCAGCT | 9678 |
| rs749853460 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110846 | AAGAAAGAGAGAAAT[C/T]GGGTCCAAATTGTAT | 9678 |
| rs749862247 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988178 | TCCCTCTTTGCGTTA[A/C]ATTTCTATTAAGAGC | 9678 |
| rs749870593 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962297 | TTTTAGCATGAAAGG[C/T]TGTTGAATTTTGTCA | 9678 |
| rs749878976 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105820 | GGATGCACATGCTGG[A/G]CTTTGTAAATAAAAT | 9678 |
| rs749902770 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161628 | GATAACATTTTTAAA[C/T]ATTATTTTTGCCTAA | 9678 |
| rs749916319 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994752 | GGAGTTTCTTCTTTC[C/T]GGTGGGTTCGTGGTC | 9678 |
| rs749917924 | snp | A/G | 5.74036e-05 | 0.0053571 | intron-variant | PHF14 | GRCh38.p7 | 7:11111502 | AGAAAAGGTATTGGT[A/G]TCCTTCCGTTTGATA | 9678 |
| rs749923583 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077898 | CAGTTTGTTCCTCAG[C/T]TGAGAAGTTTTGCAC | 9678 |
| rs749925472 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119179 | GGTTGCCATACATAT[-/A]AATGTCTTTTAAAAG | 9678 |
| rs749934683 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959354 | TATTACCTCCCTCCT[A/T]TTTTCTAAATATCAC | 9678 |
| rs749950317 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003370 | TTTCCTTTTACCCAG[A/T]TTCCTCTTGTTCCAC | 9678 |
| rs749952694 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005284 | GCTAATTCCAATTCT[A/G]ATTCCTCCTACATTT | 9678 |
| rs749955691 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136392 | TATCTCTTTATTTTA[C/G]CATATTTAATCATTT | 9678 |
| rs749961103 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118474 | ACTTTGGGACTATTA[A/C]TAATTATTTGCTTAA | 9678 |
| rs749980412 | snp | A/G | 3.21466e-05 | 0.00400902 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983023 | AGAATGATGAAGGCA[A/G]TGATGAAGATCATAG | 9678 |
| rs750006246 | snp | A/G | | | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968673 | TTTGTTTGTAGGGTT[A/G]AGGAAGTTGGTGGTA | 9678 |
| rs750014212 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053184 | CAGTTTTCTCAAAAA[A/G]CATTTTCTTAATCTG | 9678 |
| rs750017443 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087598 | GATTGACTTCTAAGG[A/C]ATCTTTACTCACGCA | 9678 |
| rs750029054 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107010 | GGATTTTGCTTCTTT[C/G]TAAAGTTTAGCTTAC | 9678 |
| rs750046104 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010389 | AATGACATTAAAGAA[A/G]TTAATGAGTTTTGAT | 9678 |
| rs750078607 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153085 | TGGGTGGATTGTGAT[A/G]TGATGTGTGTCTTAC | 9678 |
| rs750112797 | snp | C/T | | | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982831 | GACGAAACCGACCAC[C/T]TCTGGATTTTGTGTC | 9678 |
| rs750119011 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959122 | GAAGTTAGGGAGCTG[C/T]TTCCTGAATTTTGGC | 9678 |
| rs750152199 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138294 | GATCCACCCGCCTCG[G/T]CCCCCCAAAGTGCTG | 9678 |
| rs750198140 | snp | A/T | 1.66012e-05 | 0.00288103 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051728 | AGGAACCAGTGAAAT[A/T]TGTTCCACAGGATGT | 9678 |
| rs750201051 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993409 | CATGTGGAGCTGCCC[-/T]TTTTTTTGCTGCTAA | 9678 |
| rs750253833 | snp | A/G | 5.08066e-05 | 0.00503991 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974850 | TGGATCGCAGCTCCA[A/G]GAGGAGGCAGGTGAA | 9678 |
| rs750257464 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045870 | GTAACAACTTACTGT[A/G]GAAAAATCAAACTGA | 9678 |
| rs750259192 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086132 | GGACCGTTGCAATAA[A/C]CATCACCTTCTCTAG | 9678 |
| rs750286162 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163348 | AAGTTCATTTCAGTA[A/T]CTGTCATGGCTCACT | 9678 |
| rs750290365 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071388 | TTTTCTTGCTTAAAT[A/G]TCTTAGAATGGAAGC | 9678 |
| rs750293850 | in-del | -/TTACTC | 6.59914e-05 | 0.00574381 | intron-variant | PHF14 | GRCh38.p7 | 7:11042853 | GATGTTTGAATTGAT[-/TTACTC]TTAGTTTCAGCAGTA | 9678 |
| rs750302120 | in-del | -/AAG | 0.000238729 | 0.0109228 | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10983064 | AGTGAAGGGGGTTGC[-/AAG]AAGAAGAAGAGTAAA | 9678 |
| rs750325250 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004121 | GGTGTGGTGGCTTGC[A/G]CCTGTAGTCCCAACT | 9678 |
| rs750327033 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974466 | CATGGTCCGCGGGAA[G/T]GAAGCCCGCTTGTTT | 9678 |
| rs750328681 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963111 | TCTTAGTTATTTCTT[A/G]TCTTCTGCTAGCTTT | 9678 |
| rs750360538 | snp | C/T | 7.47524e-05 | 0.00611315 | intron-variant | PHF14 | GRCh38.p7 | 7:11036409 | AATTTGAATACATTT[C/T]TTTTATAGGCAAGGA | 9678 |
| rs750393913 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044573 | TTAATTTTGGAGTGT[A/G]CAAGATTCAGAGAAT | 9678 |
| rs750397444 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100213 | GACATAATAATGAAA[C/T]GAGGTGAACTGAATT | 9678 |
| rs750413103 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015961 | TTTACTGTTTTTCTT[C/G]TTGATAATTTAAAAG | 9678 |
| rs750433090 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101273 | CAAAGTGAAATACAA[A/T]TACATATTTTCAGTT | 9678 |
| rs750437630 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980880 | CTTAAAGTTTCAGAT[A/G]GGGAATTGCTGACCC | 9678 |
| rs750448503 | snp | C/G | 1.67607e-05 | 0.00289483 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035778 | AAGCAACTATCACCA[C/G]AAGCACAGGTATGGG | 9678 |
| rs750460098 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103453 | ATCTGTATCTTTCCA[A/G]AGGTATACAGAATTA | 9678 |
| rs750462132 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089517 | GCAATAAAGTGAGAC[C/T]CCATTCTCCACAAAA | 9678 |
| rs750463816 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028160 | GCTTGGAACATTTAC[A/G]TTAGCCTACACTTGA | 9678 |
| rs750466368 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011547 | CCCTCTTAGAATAAA[A/C]CTGGTCAAAAGGATG | 9678 |
| rs750517181 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039501 | CTTTTTTAGTACTGT[G/T]TATATAATTGATAAA | 9678 |
| rs750520565 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115346 | GCCCCACAGTAGATA[C/T]ACAAAATGACTCATT | 9678 |
| rs750525357 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980153 | TAGCAAAGTTGGATT[A/G]GTCTCAATTTTGATC | 9678 |
| rs750525419 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992804 | TTGTCCCAACAATGT[A/C]ATTTCTAACAAAATC | 9678 |
| rs750525659 | snp | C/T | 1.77517e-05 | 0.00297919 | intron-variant | PHF14 | GRCh38.p7 | 7:11071254 | TATTCAAAGACTATA[C/T]ATTCCATGTTCCCAA | 9678 |
| rs750528057 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017909 | AGGTCTTAGATTTAA[C/G]TCTTTAATCCATTTT | 9678 |
| rs750549491 | snp | A/C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11102358 | AGGTTTAGAGTATCT[A/C/G]TCTCTTTGGACCAGA | 9678 |
| rs750585126 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061617 | TTTATTTCCTATGGC[A/G]TAAATGGTAACAAAG | 9678 |
| rs750602470 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990900 | TGACTGTGGCTCTTT[G/T]ACATTTGTACTAAGG | 9678 |
| rs750629944 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134867 | ATAATTCAGTAGAGC[A/G]ACATATAGACCACCA | 9678 |
| rs750638485 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121817 | TGCTCTTCAGAATGG[C/T]ATGCAATTTAAAACT | 9678 |
| rs750650071 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966555 | GACCTACCCTTTCCC[A/G]CGTAGGAACCTGTCT | 9678 |
| rs750653377 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090502 | CAAAATTGCCTGATT[A/G]TATCAAGGACCTTGT | 9678 |
| rs750662566 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018825 | GTCGTGTTCCAGATC[G/T]TAGAGGAAAAGCTTA | 9678 |
| rs750691328 | snp | A/G | | | | | GRCh38.p7 | 7:10969502 | TACATCTTGGATTTG[A/G]TTACCGTAATTTAGA | 9678 |
| rs750701346 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997974 | GGCACTGATTATTAA[-/GT]GGGCTATCTTAGAGG | 9678 |
| rs750702861 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988832 | CTCCTGAAGTAGATA[C/T]TATTTTTATCGCCAT | 9678 |
| rs750705615 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147806 | TGGGGGACTTTTAAA[C/T]GTGTAATACCATCCA | 9678 |
| rs750717965 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026832 | GCTAATTTCCTCTTG[A/C]TTATTTTGCTTTAAG | 9678 |
| rs750723466 | snp | C/T | 1.67245e-05 | 0.00289171 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11037024 | TTCAGGAAAATATGG[C/T]TGAACAAAAGAATAT | 9678 |
| rs750724665 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006453 | GTAATCAGGAGCCAG[C/T]CGAACATATGCCTTC | 9678 |
| rs750742302 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039406 | CGTAGTTATTAAAAA[A/G]AACTTTATTCATGAA | 9678 |
| rs750744492 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160790 | GCTTTTTGAATTAAG[-/T]TTCTTGTAGATTCTG | 9678 |
| rs750745923 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127522 | TCCCACTGCAGCCAT[G/T]CATCTTTGCTTTGCT | 9678 |
| rs750756416 | in-del | -/CT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047777 | GGTGACAGAGTGAGA[-/CT]CTGTCTCACAAAAAG | 9678 |
| rs750781111 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126356 | GTACATATTTTTAGG[A/G]TACATTATTTACTCT | 9678 |
| rs750783441 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985938 | GATTACAGGCATGAG[C/G]CACCACACCTGGTCT | 9678 |
| rs750790539 | snp | C/T | 0.000108021 | 0.00734837 | intron-variant | PHF14 | GRCh38.p7 | 7:11042651 | CTATGATAATTATTA[C/T]TGAAATCTTTACTTG | 9678 |
| rs750793338 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094506 | TGATTATATCAGGCC[C/T]CTCTTCTCAAAATTC | 9678 |
| rs750794682 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119260 | TTTTTTGTTATTTTG[C/T]TATTTCAGCTACTAA | 9678 |
| rs750803358 | snp | A/G | 3.08485e-05 | 0.00392725 | intron-variant | PHF14 | GRCh38.p7 | 7:11022990 | CCAAGGTGAGACACA[A/G]AGCATTTTTGATTGC | 9678 |
| rs750816011 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068503 | AGATTTATAGAGACA[A/G]AAGTAAAAATGGTGG | 9678 |
| rs750838976 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082028 | AACAGAAGACTCTGG[A/G]TATTAGATATCTCTT | 9678 |
| rs750852666 | snp | A/G | 3.21838e-05 | 0.00401134 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061996 | GAGAAGACAAAGACA[A/G]TCTGTGTTGCAAAAG | 9678 |
| rs750860479 | in-del | -/CGGTTTTTTTTTTTTTTTTTTTTTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985636 | CAGTGATTCTCAAAC[-/CGGTTTTTTTTTTTTTTTTTTTTTTT]TGTTTTTTTTTTTTT | 9678 |
| rs750929227 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049476 | CAAGACTGTCTCTCA[-/A]AAAAAAAAAAAAAAA | 9678 |
| rs750967239 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084202 | AACTTCAAAATATGT[A/G]CACACACACAATCTG | 9678 |
| rs750990149 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122284 | ATGGGTAACTGAAAC[C/G]TGGGAAAGCAAAACC | 9678 |
| rs750992764 | in-del | -/AAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037598 | TATAATGTTTGGAAT[-/AAA]AATTTCCAAATTTGA | 9678 |
| rs750994785 | snp | A/T | 0.000309358 | 0.0124332 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982486 | ATGAAGATATTAAAG[A/T]AAAAGAAGAACAACT | 9678 |
| rs751004489 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108331 | AAACTATTGACTTCA[A/T]GATTGGATTCTTTTC | 9678 |
| rs751027957 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094995 | TGTTTTTCCATTCTA[G/T]CCAGAGGCAGTTCAA | 9678 |
| rs751047005 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068841 | ATGTTGCATCTTTCA[A/G]TTTATGATCATGGTA | 9678 |
| rs751087994 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153231 | AAGATGGTAGCAGTG[C/G]AGATAGAAAGCACTA | 9678 |
| rs751093268 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074670 | CATAGATCCCAAGAA[C/T]ATGCACAAAATATAG | 9678 |
| rs751096128 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975881 | TTCCCTTGTCTTTTT[C/T]CTGCTAGGGATAGTA | 9678 |
| rs751100215 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046909 | TGAGTTCTTGATGAC[-/T]GAAAAAGATAAATTG | 9678 |
| rs751105281 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021410 | ACCATAGTTGTCTCG[G/T]CCATGATTTTCATTG | 9678 |
| rs751106493 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057360 | TTTAGATGAATAAAC[A/T]ATTTATTTACTTATT | 9678 |
| rs751119602 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141654 | CCACAGGGAAGTTTT[A/G]TCTTATTTACAGATT | 9678 |
| rs751126966 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959417 | AACCTCTATGGGCAG[C/T]GGCGATGCAACTCTG | 9678 |
| rs751201563 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096082 | TTTATTTTAAATAAG[G/T]AATAAAGAGGTCTTC | 9678 |
| rs751213249 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012434 | TTATGTGAGTTTTGT[A/C]TCCCACAAGTGTATT | 9678 |
| rs751222988 | snp | C/T | 2.90668e-05 | 0.00381216 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111366 | TGTGATGAATGCAGA[C/T]TCTGCTACCATTTTG | 9678 |
| rs751227465 | snp | A/G | 1.76027e-05 | 0.00296665 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982903 | ATGACAATGATTGGC[A/G]ACCTACTGTAGTAAA | 9678 |
| rs751231303 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021109 | AGTCTTTTGAGAAGT[A/G]TCACTCTACTTAGTC | 9678 |
| rs751231491 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069856 | TTCTATTATTTATTT[-/A]TTTATTTTTTTCTGG | 9678 |
| rs751245340 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055636 | TAAACACATCTAATC[A/G]TTTTTCCATCGCACT | 9678 |
| rs751257777 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132614 | AGTATATTCCTAGAA[C/G]AGGGAATCTGGGTCA | 9678 |
| rs751290414 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089129 | CCCTGATCAGTTAAC[C/T]GCAGCAAATAAAAAC | 9678 |
| rs751291502 | snp | G/T | 4.15757e-05 | 0.00455918 | intron-variant | PHF14 | GRCh38.p7 | 7:10974340 | GTAAGTGTATCCGAG[G/T]CCTCTGCGGCGAGAG | 9678 |
| rs751309745 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022459 | TTCACAGTTATTAAA[G/T]TAGTATCCTTAATTC | 9678 |
| rs751315590 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112451 | AGAAAGAAACTAAAC[-/T]TTTTTTTAAATATCA | 9678 |
| rs751338131 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980036 | AGAATCAAGGAGTCT[C/T]AATTTACCTCTCATT | 9678 |
| rs751362850 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087687 | TGACTCCCAGTGGTC[G/T]TCTCACTTAATAATC | 9678 |
| rs751367742 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074938 | ATATTTTCAGATATC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs751378132 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023085 | AAATGCTTACTAGGA[A/G]TCATTCTATTTAGCA | 9678 |
| rs751383664 | snp | A/C | 3.41384e-05 | 0.00413135 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013757 | TTTAGGTTGTTATGG[A/C]GTTGATGGAGAGAGT | 9678 |
| rs751390214 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966197 | GCAGGGAGCTGTAGA[C/T]CGGAGCTGTTTCTAT | 9678 |
| rs751392595 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032974 | TCTGGCTTTCAGTTT[C/T]CTATCCATAAAATTG | 9678 |
| rs751400595 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086685 | ATATTTTAAAAGTTA[C/T]AATTGTCAGATATTA | 9678 |
| rs751402385 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131089 | GTTTGTTTTGTACAC[A/G]ACAGTCTTGTTTGTT | 9678 |
| rs751407908 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995546 | CCAGTCCCATGCCGT[A/G]TGCCCGCATTCCTCA | 9678 |
| rs751434352 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146568 | CATGTAGAGATAATT[C/G]TTAGGACACTAAATT | 9678 |
| rs751480827 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047119 | TGTCACCCAGGCTGG[A/G]GTGCAGTGGCACAAT | 9678 |
| rs751491414 | snp | A/G | 1.67239e-05 | 0.00289166 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051695 | CAGATGGAACCAAAC[A/G]ATCAAGGAGGCAGAT | 9678 |
| rs751505045 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130374 | GGAGAGAGAGAGAAC[A/G]TATATACAATTTATA | 9678 |
| rs751515636 | in-del | -/GATTTTA | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960086 | CAGTAGTTACAAGTG[-/GATTTTA]AAAAAATTATTATTA | 9678 |
| rs751538173 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123138 | TCTCGCTGCAGTTGA[C/T]AGCATCTATACCCAA | 9678 |
| rs751539156 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164261 | AGTCTTGTAACTCTT[A/G]CTTATTTCTGGAAAT | 9678 |
| rs751551111 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158085 | AAACCTAAGAAATTA[A/G]TCTTAATACAATACT | 9678 |
| rs751551444 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005434 | GTCCAAGTTTGACCA[G/T]TGAGAGTCCTTTAAG | 9678 |
| rs751554572 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091788 | GTGAATATAAAGAGG[A/G]TTAGAACTCTGGAAA | 9678 |
| rs751558783 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078059 | GGGTATTTTAGTTCA[C/T]ACTGTGGTATTTGAA | 9678 |
| rs751586164 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11102127 | TGAAAAAATAGCAAA[-/T]TGAAATTTTTCAAAA | 9678 |
| rs751590109 | snp | C/T | 3.02311e-05 | 0.00388776 | intron-variant | PHF14 | GRCh38.p7 | 7:11051583 | AGATAATAATAAATG[C/T]ATGACTTAAATTTTT | 9678 |
| rs751597615 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014586 | ACTGAGGGACTGTGT[A/G]TATAGCTGGGGCAGA | 9678 |
| rs751607039 | in-del | -/TGAAA | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106390 | TTAGTCTTATATTTG[-/TGAAA]TGATTAAAAACCATT | 9678 |
| rs751608259 | snp | A/G | | | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968787 | CAACTGAAAGTCAGT[A/G]AGGTTACTATCAGTC | 9678 |
| rs751622363 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080301 | TAACTTATATTACAC[C/G]TGCATACTTGTTAAC | 9678 |
| rs751645942 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972868 | AAGGATGTGTCACTC[C/T]GACTTCCTAAGAACT | 9678 |
| rs751654144 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996604 | TATTGAAAAAAAAAA[-/G]CTAATTGATAAAATG | 9678 |
| rs751666719 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007269 | CTTATTGGAATTCTT[C/T]TTTTAATGGTCTTTG | 9678 |
| rs751667899 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166949 | AAAAAGACAAACATT[A/G]TATTAAGAATGTTAC | 9678 |
| rs751668111 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981529 | TGGAAGAAACCTGCT[A/G]GAAAGCTTACAGTCC | 9678 |
| rs751699438 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090817 | AATGGGATCATTCCT[A/G]AAAGGATAAAGAAGT | 9678 |
| rs751719113 | snp | A/G | 2.52369e-05 | 0.00355216 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982477 | AAGAACTGAATGAAG[A/G]TATTAAAGTAAAAGA | 9678 |
| rs751736515 | in-del | -/A | 2.98668e-05 | 0.00386426 | nc-transcript-variant, frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11169464 | TCTCAGGAGCTCAAC[-/A]TGGAACAGAAAAATC | 9678 |
| rs751742618 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11037506 | TAATCAATAAACATT[A/G]CTATAGAGCTTCACT | 9678 |
| rs751753648 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064407 | TTAAATAAGGATTTA[C/T]TTTCTCTACAGATAT | 9678 |
| rs751756726 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156379 | TTACTTAGATATCTA[A/G]TGAGCTATTACGTTC | 9678 |
| rs751796994 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080686 | ACTCTTTTCTAGATC[A/G]AAAGTACTATTCAGG | 9678 |
| rs751803773 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124238 | ACTACATTTCTGCTC[A/G]TGTTTTGGTGGTATG | 9678 |
| rs751805762 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148283 | TCACTGCAAATCAAA[C/T]AACCGTTATGGGCTA | 9678 |
| rs751823773 | snp | A/G | 0.000301575 | 0.0122758 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061965 | CCCTTGTATGGCAGG[A/G]AAGAGTTCCTAGAGA | 9678 |
| rs751857019 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119446 | GTGTGGAATATATTA[A/G]TTATGTAAATTTTTA | 9678 |
| rs751880334 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002481 | TTTGCTCTTGTTGTC[C/T]AGGCTGGAGTGCAAT | 9678 |
| rs751884362 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059934 | GGAATGCAGTGACTT[G/T]ATCATGTCTCACTGC | 9678 |
| rs751890042 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997137 | TGCATACGTGCTTTA[C/G]TTACTTTTTATCTAT | 9678 |
| rs751896863 | in-del | -/AGTC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114693 | AGTTTCATAAAAAAT[-/AGTC]AGTTACATGGACACA | 9678 |
| rs751903326 | in-del | -/TAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990490 | AGAGAAGTGAAAAAT[-/TAAA]TAAGAGGGTGCTTAC | 9678 |
| rs751906585 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115487 | TATGTTGAGGTGCAT[A/T]CTTAAGATGTTTTTT | 9678 |
| rs751911250 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084547 | CTTTTTCTCAGTAAA[C/T]ATAGAACTAAGCCAG | 9678 |
| rs751934234 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093527 | AGGTTGTAATGCCAG[A/T]GTGCTTTTCGTCATT | 9678 |
| rs751937016 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032354 | TTACTATTAAGATAC[C/T]AGTAAAGCGTAGGTA | 9678 |
| rs751953128 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046866 | CGGCTTAGACATAAG[-/A]AAAAAAAAAAACTCT | 9678 |
| rs751954656 | in-del | -/CA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026109 | AGTGTGAGACTCCAT[-/CA]AAAAAAAAAAAAAAA | 9678 |
| rs751996468 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128435 | AAAGTGCCACTACCT[C/G]CTCTGTTCTTTATTC | 9678 |
| rs752038739 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980899 | AATTGCTGACCCGTA[C/T]GATATTGCTCTTGTA | 9678 |
| rs752040709 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11149028 | TTTTTTTGTTTTGTT[C/T]TGTTTTCATTTTACA | 9678 |
| rs752044371 | in-del | -/CA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109514 | GAAGGAGTATGCTCT[-/CA]GTTATTTAGAAATCT | 9678 |
| rs752070457 | snp | A/G | 6.47312e-05 | 0.00568871 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040720 | AAGGAGAGAAAACCA[A/G]GTAAAAAAGAAGGAG | 9678 |
| rs752070507 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992885 | TTAATGTAGAACAGT[C/T]CTTGAGTTTCTGTCT | 9678 |
| rs752090130 | snp | A/G | 2.91864e-05 | 0.00382 | intron-variant | PHF14 | GRCh38.p7 | 7:11022982 | ATATGGTGCCAAGGT[A/G]AGACACAAAGCATTT | 9678 |
| rs752090533 | snp | A/G | 1.67806e-05 | 0.00289656 | intron-variant | PHF14 | GRCh38.p7 | 7:10974948 | GGAGATGCCTCAGGT[A/G]AATATTTCCTTCTCT | 9678 |
| rs752099791 | snp | C/G/T | 6.78317e-05 | 0.00582341 | missense, synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983006 | CGGGAGTGATGAAGA[C/G/T]GAGAATGATGAAGGC | 9678 |
| rs752107368 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144888 | TGTAAGAAGTAGTAA[A/G]AGTAGTAAAAAATCA | 9678 |
| rs752113872 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075267 | TATAGCAACACTACA[C/G]TTCTTGGTACCAATT | 9678 |
| rs752121185 | snp | C/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063256 | TGTGTTGGGAGCTAT[C/G]CTGAAGGTTAAGTTT | 9678 |
| rs752126751 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096889 | AAACTCATCTTCAAA[G/T]GATTTCAGCCAATTC | 9678 |
| rs752128625 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161285 | GATACAATGAGTCGA[C/G]TGTTGTATTAAAATT | 9678 |
| rs752163470 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084861 | TTGATGAACCATTTG[G/T]ATTTTCATATCTGTG | 9678 |
| rs752163976 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005346 | TCTTCCCCTTTTTTT[C/G]CTTTTCAGTATTACT | 9678 |
| rs752167422 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096866 | TTATCACTATATACT[A/G]GAAAAAAAAACTCAT | 9678 |
| rs752211753 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112658 | TGCCTCTAATCCCAG[C/T]TACTTGGGAGGCTGA | 9678 |
| rs752213726 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055800 | GTTTAAGCTTAAGTC[C/T]TGAGAATCTGAAAAT | 9678 |
| rs752220769 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051856 | TGAGAAAGACACAGG[A/G]CAAACATATACTCAG | 9678 |
| rs752230703 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987233 | TCATGAGAATTTAAC[C/G]TTTTCTAAAAATGTA | 9678 |
| rs752233987 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044030 | GAAATCATGTTCTTT[C/G]TAGCAACAAGGAGGC | 9678 |
| rs752246269 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161462 | ACAAACTTAGTTATC[A/G]CTGAGTAATTTTTAG | 9678 |
| rs752254662 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141250 | TGGCCAAATTCTTTT[A/G]GATCTTGTTTCTGTC | 9678 |
| rs752260478 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129629 | ATTTTCTTTCTGTTG[A/G]TGGACCTACCAATAT | 9678 |
| rs752326846 | snp | C/T | 8.40273e-05 | 0.00648125 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982765 | CTTCTGTTCCCACTA[C/T]GACAACCGCTACAGA | 9678 |
| rs752336912 | in-del | -/AA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049475 | GCAAGACTGTCTCTC[-/AA]AAAAAAAAAAAAAAA | 9678 |
| rs752360507 | snp | A/G | 1.65899e-05 | 0.00288005 | intron-variant | PHF14 | GRCh38.p7 | 7:11028861 | GAACATGTTCACAAG[A/G]TATCTTTTGACTCTA | 9678 |
| rs752366218 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003146 | GGGTTTCACCATGTT[G/T]GCCAGGATGGTCTTG | 9678 |
| rs752373643 | snp | A/G | 1.65784e-05 | 0.00287905 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035721 | AGAAAAAACTACTTG[A/G]CTCTACAGTCCTATT | 9678 |
| rs752389979 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000834 | TATTCTCTTGAAGGT[A/G]TCTCTCACAGAGCAG | 9678 |
| rs752396646 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026517 | AGATGTATTTATTGG[A/G]CAGCACTTAGAACTA | 9678 |
| rs752442183 | snp | A/G | 1.83829e-05 | 0.00303168 | intron-variant | PHF14 | GRCh38.p7 | 7:10983181 | CAACCCAATTTTTAT[A/G]TCTGTCTGTCTGGGG | 9678 |
| rs752450965 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014093 | CCATTTATTGAGTAC[C/T]TGCATTTGCCTTTAC | 9678 |
| rs752450996 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128610 | CTATACTATAGTATA[A/G]ACATCAGGGTTTTAT | 9678 |
| rs752454425 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002690 | CTCTGGTGATCCACT[C/T]GCCTCTGCCTCCCAA | 9678 |
| rs752476199 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049600 | AAGTGAAGCAGTGTG[C/G]CTTTTTGTAATATAA | 9678 |
| rs752488095 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078649 | ATTTATAGAATAAGC[C/G]TCTCACCCAACAGTG | 9678 |
| rs752494764 | snp | A/T | 1.68049e-05 | 0.00289865 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036993 | TAAATAGAGAGAAAT[A/T]TGCGCATGATTCAAA | 9678 |
| rs752510272 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040004 | CTGTTTAAAATACTA[C/T]CTACCATAAAAGACA | 9678 |
| rs752530237 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022690 | TTTTTTGTAACTAAG[C/T]GTTATTCTGTAGGTG | 9678 |
| rs752545452 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002853 | TGAGCACCAATAGAA[-/C]GGTTGAGGGTCAATG | 9678 |
| rs752548688 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996768 | ACATAGTGTTGATAT[A/G]TTTTGGCTTATCAAC | 9678 |
| rs752557051 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140124 | ACTACACATCCTTCT[A/G]TATATAAACCTTCTC | 9678 |
| rs752562693 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066647 | TTATCTGCCCCATGT[A/G]GATTCCCAGTATCAT | 9678 |
| rs752567447 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120336 | CTCAGTAAGTGACAA[A/G]CATTTTAGGCACAGA | 9678 |
| rs752571481 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980745 | TTTCTCCGCAGAAAT[A/G]ATGTTTGATTATAGG | 9678 |
| rs752578304 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11154276 | TCCACTTGAGTATGT[A/G]TGTGTGTGTCTGTAC | 9678 |
| rs752579689 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089322 | GTTCATTGAGGCACA[A/G]ACAATTCATTGACTT | 9678 |
| rs752641016 | snp | C/T | 2.9526e-05 | 0.00384215 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042722 | TGATCAGCATCTTCT[C/T]TTATTGTGTGATACC | 9678 |
| rs752661396 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111588 | AACATTTTAACCAGT[A/G]CACCTTAAGAATATA | 9678 |
| rs752670611 | in-del | -/A | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958229 | ATACATATTATCTAT[-/A]AAAATTAATTAACTT | 9678 |
| rs752688551 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135760 | AGACAGCCTTCATTT[C/T]CCTTCTACCTCAGGC | 9678 |
| rs752740641 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11169367 | TCAAGTATAGCTGAT[A/G]AATGCTCTAAAGTTT | 9678 |
| rs752743758 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097230 | GTGATCCGCCTGCCT[C/T]AGCCTCCCGAAGTGC | 9678 |
| rs752776487 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964227 | ATCAGTTATTCCTTT[C/G]CATGTTTAGTGCTTC | 9678 |
| rs752824284 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153285 | TGATAAAGATAACAG[A/G]AGTTGGCTATAGAGT | 9678 |
| rs752827419 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989638 | TACGTCTTCCTATAC[-/T]TTTTCTTTTTGAGAC | 9678 |
| rs752832905 | snp | A/G | 1.96887e-05 | 0.00313751 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982452 | GATTCTGAAGAAAAT[A/G]TTTTAGAAGAAGAAC | 9678 |
| rs752835339 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998420 | ATATACCTAAAATAT[A/G]TATGTATACACACAC | 9678 |
| rs752921915 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072398 | CCAACATTGGGGACT[A/G]TAATTCAACATGAGA | 9678 |
| rs752922427 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025583 | TGGATCACGAGATCA[A/G]GAGATCAAGACCATC | 9678 |
| rs752928882 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999703 | CAGATGAATAGCCTC[A/G]GTACTGGAAAATCTA | 9678 |
| rs752929359 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973112 | TCCTTTGCATAGAGG[C/T]ATACCACTTTGTAAC | 9678 |
| rs752948754 | in-del | -/TGT | 2.03172e-05 | 0.00318719 | intron-variant | PHF14 | GRCh38.p7 | 7:11040807 | ATAATGATAGAATAA[-/TGT]TGTGTATTTTTTTAA | 9678 |
| rs752958524 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973825 | AGTCCTGCGCATGCG[C/T]CCTCAATTCCTGCTG | 9678 |
| rs752971716 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097273 | CGCGAGCCACCGTGC[C/T]CAGCCAGGACTAGAA | 9678 |
| rs752972639 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963298 | TTTGTTCTTATTGGT[C/T]TCAAAGAACATCTTT | 9678 |
| rs752974944 | in-del | -/AG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025815 | AAAAGAAAAAGAAAA[-/AG]AAAGAAATTGCCAGG | 9678 |
| rs752980210 | in-del | -/GAGGG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015004 | TCCTCTCCAATATAA[-/GAGGG]GGGGTGGGTACTTAA | 9678 |
| rs752995719 | in-del | -/AAGGAGAAAGAG | 8.0551e-05 | 0.00634579 | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10982632 | GAAAAAGAAAAGGAA[-/AAGGAGAAAGAG]AAGGAAAGAGAGAAG | 9678 |
| rs753002744 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029926 | CATTTATTTCATTTC[C/G]AGAAAGTGAGCAAAG | 9678 |
| rs753010374 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039083 | GCTATCTTGTGTGCA[A/G]AATTTTTTCATTTGC | 9678 |
| rs753011959 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977278 | GATCATATCTTCTTT[A/C]AAAACAACTTCTAGA | 9678 |
| rs753014818 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035207 | ATTAGGTATTATAAG[C/T]AATGTAGAGACTGCT | 9678 |
| rs753020930 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972092 | AGGTATGTGCCACCA[C/T]GCCCAGCTAATTTTT | 9678 |
| rs753023524 | snp | C/G | 4.58411e-05 | 0.00478732 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974897 | CTGCTGGAAGCTCTT[C/G]ATTATGATAGTTCAG | 9678 |
| rs753026309 | in-del | -/CCTTTAAAGTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127643 | TTCTGAGAGGGACTT[-/CCTTTAAAGTA]CCTCTTCTAAAGAAA | 9678 |
| rs753052449 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018982 | AATGCTTTTTCAGCA[A/T]CAGTTGAAATGATCA | 9678 |
| rs753061497 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984493 | ATCTTAAACAGGCAT[A/G]GAAAAATCTAATTGT | 9678 |
| rs753091576 | snp | A/C | 1.65987e-05 | 0.00288082 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982848 | CTGGATTTTGTGTCC[A/C]TGGAAGAGCTGAATG | 9678 |
| rs753092881 | snp | A/G | 3.34253e-05 | 0.00408797 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111355 | TACCCTGCAGGTGTG[A/G]TGAATGCAGACTCTG | 9678 |
| rs753100570 | snp | C/T | 1.79564e-05 | 0.00299631 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013826 | ACCTTGGTTTTGTGA[C/T]GCCTGTAAATGTGGT | 9678 |
| rs753100661 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967061 | CACCAAGAAAGAAGG[G/T]TCTAATTCTACTAAG | 9678 |
| rs753125503 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100430 | ATATATCTCCATTTT[A/T]GAAGAGAGGTAACTG | 9678 |
| rs753186191 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051835 | TGAGGCCAAAATTTA[A/G]GAGAGTGAGAAAGAC | 9678 |
| rs753186398 | snp | A/G | 3.32895e-05 | 0.00407966 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111467 | TTCTTCATCTTCCAA[A/G]GTAAGGGGAGAAGTC | 9678 |
| rs753230072 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983277 | ATAGACGGCTGTGGG[A/T]TGAATGAGCACCCTA | 9678 |
| rs753234198 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091837 | AACACTTATTCTTTA[C/T]CCCTTAAGTATTCAA | 9678 |
| rs753244365 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963821 | ATTGATCCCTTTACC[A/G]TTATGTAATGGCCTT | 9678 |
| rs753253711 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119100 | CATTTACATAGCATG[C/T]TGTGGAATACCATAT | 9678 |
| rs753254939 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019659 | TGGCTAAAGGTTTGT[C/T]AGTGTTGTTTACCTT | 9678 |
| rs753268920 | snp | A/C | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065778 | CACCAAACTTCTAAA[A/C]CTCAAATTTTATCTT | 9678 |
| rs753277673 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051028 | TAAAGAAAAGTCATG[A/C]TTTCCAAAGGTAAAT | 9678 |
| rs753294558 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003186 | CCTCGTGGTCCGCCC[G/T]CCTTGGCCTCCCAAA | 9678 |
| rs753295141 | in-del | -/TGTCT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141869 | CTGCCTTTTTCTTAC[-/TGTCT]TATCTGTCACAATTG | 9678 |
| rs753298294 | snp | A/G | 6.28042e-05 | 0.00560341 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038806 | TGAATGGAAAACTTC[A/G]AAGTGAAGGACAAGG | 9678 |
| rs753306417 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986135 | CAACGACTGGCTAAT[C/G]CTTTTATTTTTGATT | 9678 |
| rs753306943 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091537 | AAGGTAGGCAGATCA[G/T]TTGAGCCCAGGAGTT | 9678 |
| rs753307760 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150106 | GCATCATACATTCAT[A/G]TGAAATATTGAGGTA | 9678 |
| rs753328089 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116775 | TTAGGAATAAGAACT[A/G]CTGTTATACCTAGTT | 9678 |
| rs753338399 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086502 | ACTTATACTTAGTCC[A/G]TATGTCTTGGTCAGT | 9678 |
| rs753347385 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956804 | ATAGAAAGAAGAATT[C/G]CCCTCTAGAGCCTTT | 9678 |
| rs753357776 | snp | C/T | 6.66556e-05 | 0.00577264 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040754 | CACAAAAGACATCTA[C/T]TCTTCCTGCAGTACT | 9678 |
| rs753378724 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150350 | AAGGTTTCTGTGTTT[A/G]CTGGTTATAAAGACG | 9678 |
| rs753423687 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118199 | AATCTGCGGTGTTTT[C/G]TAGACTTACTAAAAG | 9678 |
| rs753424174 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098451 | CCCTTGGATCCCTCT[A/C]TGTCTGCCTTGCCTC | 9678 |
| rs753482811 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133786 | ATATTGCACATATTA[C/T]ATCATAAAACGATTC | 9678 |
| rs753484941 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978570 | AAAATAGAATAAGGT[C/G]AAATTGTGGCTGTAT | 9678 |
| rs753490717 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076503 | ATTTTGAATGAAGAC[C/T]ATCGCACAGATTGGG | 9678 |
| rs753528405 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104550 | TGGCACATCAGGTAA[A/T]TGATAGTTGTTTATC | 9678 |
| rs753535409 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003115 | CCAGCTAATTTCTGT[A/G]TTTTTAGTAGAGATG | 9678 |
| rs753547518 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967201 | TATTCAGATTTATCA[A/G]TTGTTAATGATATCA | 9678 |
| rs753553371 | snp | A/T | 3.18041e-05 | 0.00398761 | intron-variant | PHF14 | GRCh38.p7 | 7:11042673 | CTTTACTTGCTGCCT[A/T]TATTAAAAGTTGTGG | 9678 |
| rs753584695 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004028 | TGAGGTGGGTGGATC[A/G]CTTGAGCTCAGGAGT | 9678 |
| rs753591764 | snp | A/G | 2.08409e-05 | 0.00322801 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036428 | TATAGGCAAGGATCA[A/G]TGCCCGGCTTCAGCA | 9678 |
| rs753599667 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167596 | TCCTTTGAGGAACAG[A/G]TGGACAAATTCAGTG | 9678 |
| rs753604669 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993572 | GGTGGAACTTAATGT[C/G]TGGACAGACAGGCAG | 9678 |
| rs753616624 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110027 | TTGCTTAACTTTTCT[A/G]GAACTCTTGATTCCC | 9678 |
| rs753623613 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118313 | TGGGTGGGATAAAGC[C/G]CACAGATTTCCAGTT | 9678 |
| rs753652356 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046333 | TATATTTCTGCCTCC[A/G]CTCATCTGATTGGAA | 9678 |
| rs753676660 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960414 | TCCCTGCAAAGGACA[C/T]GAACTCATCCTTTTT | 9678 |
| rs753677515 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11154660 | AGAGCATTAATTTAC[A/G]TTCTCTACAATGACA | 9678 |
| rs753698921 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988486 | CATAAAGACATGTAG[C/T]ATCCTAATTTTCAAA | 9678 |
| rs753703739 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072669 | ACATATATAGTGCTT[A/G]TTGTGTTTGTCAGTC | 9678 |
| rs753710746 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083082 | ATCTAAGAAAAAGTT[C/G]AAATGTTCAGAGAAT | 9678 |
| rs753711872 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122837 | TCAGTAGTGTTTTCT[A/T]GGTCACCAATAAAAC | 9678 |
| rs753732681 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079895 | AATCAGGAAAGCTTT[A/G]TGACATAGAAATTAC | 9678 |
| rs753750979 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157923 | TTCTAAATCATCTAA[-/C]AAAAATTAGATGTTT | 9678 |
| rs753751736 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143247 | TAAAATATATAAACT[G/T]CATTTAGCATAAATG | 9678 |
| rs753764759 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058367 | GCAGTTATGAATTTT[C/T]GTAGTTATAGTTGCT | 9678 |
| rs753769297 | snp | A/T | 1.69657e-05 | 0.00291248 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169527 | GAAAAGTTTGCAGCT[A/T]ATGTAATAGCAGATA | 9678 |
| rs753797733 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100467 | ATAGACACTAAGCAG[G/T]GTGAAATAGAAATTA | 9678 |
| rs753806676 | in-del | -/TTTTTTGTTTTT | 0.000105697 | 0.00726893 | intron-variant | PHF14 | GRCh38.p7 | 7:11061761 | TACTGTGGATTTTTG[-/TTTTTTGTTTTT]TTTTTTGTTTTTTTC | 9678 |
| rs753838701 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073351 | ACCAAAAGAAACAGG[C/G]AGTAGGCCCCCACAT | 9678 |
| rs753839486 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141447 | ATTAAATCTCTTACA[A/G]TGCCTACACAATTCC | 9678 |
| rs753853081 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057531 | AGGTGTGCACCACCA[C/T]GTCCGGCTGAGTTTT | 9678 |
| rs753864577 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961414 | GTTATTTCTGAGGCT[A/T]CTGTTCTGTTCCATT | 9678 |
| rs753884780 | snp | A/T | 1.65754e-05 | 0.00287879 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036553 | GCTATTCGTAAACTT[A/T]TGCGGAAAGCAGAAC | 9678 |
| rs753898264 | snp | C/T | 8.28626e-05 | 0.00643618 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983048 | TCATAGTAGCCCTGC[C/T]AGTGAAGGGGGTTGC | 9678 |
| rs753926940 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127735 | GAGTTACCATACCAA[A/C]TTTTGTGTAAGACTT | 9678 |
| rs753938130 | in-del | -/ATATATATATAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122343 | TTTTTATATATATAT[-/ATATATATATAC]ACACACACACACACA | 9678 |
| rs753939585 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113014 | AAATAATGAAACACT[A/G]TGGAGTTTAAATAGT | 9678 |
| rs753964207 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025681 | GTGCCTGTAGTCTCA[A/G]CTACTTGGGAGGCTG | 9678 |
| rs753969153 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990028 | AGTTCTCTGACCCTT[C/G]TAGCAGCTAGTCAAT | 9678 |
| rs753993806 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047323 | TCCGCCTGCCTTGGC[C/T]TCCCAAAGTGCTGGA | 9678 |
| rs754016699 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072507 | CCTGTGTTTTACCTT[C/T]ATTATCTATAAAATA | 9678 |
| rs754028063 | in-del | -/A | 0.00027329 | 0.0116863 | frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:10982599 | GAAAGACCTAGAAAG[-/A]AAAAGGAGAAAGAGA | 9678 |
| rs754029680 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061191 | TGCGTTCTTTCAAAT[A/G]GTAAATGTATTCTGA | 9678 |
| rs754041042 | snp | A/G | 4.19454e-05 | 0.00457941 | intron-variant | PHF14 | GRCh38.p7 | 7:10974346 | GTATCCGAGGCCTCT[A/G]CGGCGAGAGGTCCAT | 9678 |
| rs754048986 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101672 | AACGCTTTATTTGTC[C/T]GTGTGCCACTTTTCA | 9678 |
| rs754049768 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964501 | TTTCTCTCTGGCTGC[C/T]CTTAACATTTTTTTC | 9678 |
| rs754076838 | snp | A/C | 0.000286492 | 0.0119651 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990742 | CAAAACTGGAGCTCT[A/C]AAAAAATGGACCATA | 9678 |
| rs754087334 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147712 | CATTTGTGCTCAAGT[C/T]GTATTAGTAACGCTT | 9678 |
| rs754131653 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052152 | TTCTTTTTCTTTATA[A/G]AAGAGATTTACACTC | 9678 |
| rs754145388 | snp | A/G | 2.47571e-05 | 0.00351823 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013782 | GAGAGTGACTCTATT[A/G]TGAGTTCAGCTTCTG | 9678 |
| rs754158302 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020375 | GATTACTGTACCTGG[C/T]CAATTTTTTCTTTTT | 9678 |
| rs754162931 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027167 | AATTATCCAGATAAT[C/G]TAAACAATATGTCTC | 9678 |
| rs754175226 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100926 | GGCAATTCTAACTAT[A/G]TAAGATACAGAATAT | 9678 |
| rs754182696 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076780 | GCAATGTTGTCCAGG[-/C]TCATCTCTAACTCCT | 9678 |
| rs754199167 | snp | A/G | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061967 | CTTGTATGGCAGGAA[A/G]GAGTTCCTAGAGAGA | 9678 |
| rs754202445 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144956 | AGGAAAGGAGAGAAT[A/G]AGGTATTTTGTGTGG | 9678 |
| rs754208580 | snp | G/T | 1.65817e-05 | 0.00287933 | intron-variant | PHF14 | GRCh38.p7 | 7:11028846 | AAACCCATAGTTGGT[G/T]AACATGTTCACAAGA | 9678 |
| rs754246352 | snp | A/G | 6.95676e-05 | 0.00589737 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11037070 | GAATGAACAAGAAAA[A/G]CTTCATGTAGAATAT | 9678 |
| rs754279486 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983351 | TCTACTATTTGTCAC[C/T]GTTCTCAAGGAGCTC | 9678 |
| rs754292172 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957965 | ATTAGATAGTGGTGA[C/T]GGTTGTACATTTTTT | 9678 |
| rs754327340 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157615 | GAAACTACAGTTGAA[G/T]AAATAAAAATGGATC | 9678 |
| rs754338200 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038016 | AAACGTAGTTACCAT[C/T]ATTAGTAAAAATGCC | 9678 |
| rs754364821 | snp | C/T | 1.97939e-05 | 0.00314588 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982729 | CACCAGCCACAAGTC[C/T]TCCTGCTGTTAACAC | 9678 |
| rs754398719 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124738 | TAGAAACTAGATTTT[A/G]TATATTAAAATAGGT | 9678 |
| rs754408331 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082092 | CTCACGCTTGTAATC[C/T]CAGCACTTTGGGAGG | 9678 |
| rs754431759 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055653 | TTTTCCATCGCACTT[A/G]ACAATGTGAGCCACT | 9678 |
| rs754436719 | snp | C/T | 5.32496e-05 | 0.00515965 | intron-variant | PHF14 | GRCh38.p7 | 7:11071292 | TTACCTGTTTATTTA[C/T]ATTTGATCACAAGCT | 9678 |
| rs754437339 | in-del | -/T/TT | 0.266829 | 0.249521 | intron-variant | PHF14 | GRCh38.p7 | 7:11061767 | GATTTTTGTTTTTTG[-/T/TT]TTTTTTTTTTTGTTT | 9678 |
| rs754440957 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966376 | GCTCAGAATGTAGAA[A/G]GTGCATGCTGATTGG | 9678 |
| rs754451456 | snp | A/G | 0.000106366 | 0.00729189 | intron-variant | PHF14 | GRCh38.p7 | 7:11023024 | AAAGAGAAAGGTTTT[A/G]CTTGTTAGTTTACCT | 9678 |
| rs754478552 | in-del | -/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963739 | TCTCTAAGGACTTGC[-/T]TTTATGAATCTGGGT | 9678 |
| rs754491013 | snp | C/G | 5.81581e-05 | 0.00539219 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042689 | TATTAAAAGTTGTGG[C/G]ATTTGTAAGAAGAAC | 9678 |
| rs754491328 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965397 | GTATCACCAGCGGAG[C/G]CTGCAGAACAGCAAA | 9678 |
| rs754501932 | snp | C/T | 0.000292997 | 0.0121001 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040771 | CTTCCTGCAGTACTT[C/T]ATAGGCAAGTAATGA | 9678 |
| rs754502474 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011661 | AACCTAAAGGTGATA[C/T]TTCAGGACAAGAATT | 9678 |
| rs754520771 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999662 | ATGCTTACAGCTATT[-/G]AAAGTTCATAATACG | 9678 |
| rs754543816 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053630 | TTCTTTATTGTTTCA[A/G]GAAAGCCTTTTGACT | 9678 |
| rs754565423 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068851 | TTTCAATTTATGATC[A/G]TGGTATATCTCTCCA | 9678 |
| rs754570708 | snp | A/G | 0.00012451 | 0.00788919 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982666 | GAGAGAAGGAAAAAG[A/G]AAAAGCAACAGTATC | 9678 |
| rs754578454 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021417 | TTGTCTCGGCCATGA[A/T]TTTCATTGACTTTGA | 9678 |
| rs754611202 | in-del | -/CC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126971 | ATTTTGCTCTTAATT[-/CC]AAGACAAGGTACAAA | 9678 |
| rs754617696 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040788 | TAGGCAAGTAATGAA[A/C]TTAATAATGATAGAA | 9678 |
| rs754635332 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114523 | CACATGAAAGCGGAA[A/G]TACACCTAAATATTT | 9678 |
| rs754639145 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128455 | GTTCTTTATTCCAAA[C/T]ATCTCCTTTCTCTTC | 9678 |
| rs754657125 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083742 | TAGGAGTACAGGTGT[C/G]AGTCACCACACCTGG | 9678 |
| rs754658779 | snp | C/G | 4.97121e-05 | 0.00498534 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028773 | CTATTTCCATGTGAC[C/G]TGTGCTCAAAAGGAA | 9678 |
| rs754666059 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974460 | GCCCTCCATGGTCCG[C/T]GGGAATGAAGCCCGC | 9678 |
| rs754677673 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031864 | GTCTAAAGTTACTTA[C/T]AGTCCAAGTAAGCCA | 9678 |
| rs754684074 | in-del | -/ATATATATATACACAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122343 | TTTTTATATATATAT[-/ATATATATATACACAC]ACACACACACACACA | 9678 |
| rs754698326 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012549 | CTTGTAATTCCAGAG[A/G]TGTATCTAAGGCAAC | 9678 |
| rs754727115 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127798 | TGCATATCTTTAAAA[A/G]TGAATAGCTTAGACC | 9678 |
| rs754746712 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164281 | TTTCTGGAAATAGTT[A/T]GTTCATATGGCCAAA | 9678 |
| rs754767917 | snp | G/T | | | | | GRCh38.p7 | 7:10969626 | CTTATTTTCTTTTTC[G/T]CTTACATCATTTTTT | 9678 |
| rs754774521 | snp | C/G | 2.65284e-05 | 0.00364191 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983052 | AGTAGCCCTGCCAGT[C/G]AAGGGGGTTGCAAGA | 9678 |
| rs754785895 | snp | A/C | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064428 | CTACAGATATATTTC[A/C]GCGCTTACTCAGACA | 9678 |
| rs754794063 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017038 | TATTTCACCTAACAT[A/G]ATGATCTCTAGTTCC | 9678 |
| rs754805908 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046034 | GTGAAAAGCTAGTAA[A/G]GAATATTATTAATAG | 9678 |
| rs754830116 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156390 | TCTAATGAGCTATTA[C/T]GTTCCAATAAAACTG | 9678 |
| rs754847920 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975342 | TCACTTGACAATCTC[-/TT]AGGGGAGTTTTGCTT | 9678 |
| rs754850683 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985158 | TTTCTAGTTTTCTTA[C/T]TTGTATGATCTTAAT | 9678 |
| rs754864419 | snp | C/T | 2.06464e-05 | 0.00321291 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036429 | ATAGGCAAGGATCAA[C/T]GCCCGGCTTCAGCAG | 9678 |
| rs754866556 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004579 | TTTGTGGTGTTCATG[A/G]TGTTGACATATTGAA | 9678 |
| rs754875677 | snp | A/T | 1.69957e-05 | 0.00291506 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169528 | AAAAGTTTGCAGCTT[A/T]TGTAATAGCAGATAA | 9678 |
| rs754891086 | snp | A/C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138365 | TTTCTAAAGAGACTC[A/C/T]TTACAAGGTGATAAT | 9678 |
| rs754898052 | snp | G/T | 3.60004e-05 | 0.00424251 | intron-variant | PHF14 | GRCh38.p7 | 7:10983165 | GAGTAATGAGGTAGA[G/T]CAACCCAATTTTTAT | 9678 |
| rs754911991 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165369 | ACATCGTATCAGGGT[A/G]TTAATATATATTATT | 9678 |
| rs754939497 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984013 | CATGTAGATGTATCT[C/G]TTACATCACATGTAG | 9678 |
| rs754947953 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106111 | TTATTGTGTATTTTT[A/G]TATGAATTGTTTTGT | 9678 |
| rs754949400 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066414 | TGATTTTTTATTTTT[A/G]ATTAACTTTTCTGTT | 9678 |
| rs754951271 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033057 | TAGTATATACAAAAG[C/T]GCATGTGCTTATTTC | 9678 |
| rs754975785 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151946 | TTTCCTCTTCTATTT[A/C]TGTATCCTCATAAGA | 9678 |
| rs754985183 | snp | C/T | 2.45655e-05 | 0.00350459 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013783 | AGAGTGACTCTATTA[C/T]GAGTTCAGCTTCTGA | 9678 |
| rs754988802 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070362 | GGATTACAGGCATGA[A/G]CCGCTGTACCCAGCT | 9678 |
| rs754992131 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119998 | TTTTTGACATTTCTG[A/G]AATTAGATTGTGTAT | 9678 |
| rs755010771 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086388 | TCTTTCTAAAACTAA[C/T]CTGTTGCTTTTATGC | 9678 |
| rs755027342 | snp | G/T | | | | | GRCh38.p7 | 7:10969750 | TAAGTAACCAGACAG[G/T]TTATTAATATTATTT | 9678 |
| rs755032968 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035851 | AGGATTTTACGTCTC[A/G]TGTGGCTTCCAGTGA | 9678 |
| rs755072880 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082452 | TAAATTAGCATAACA[A/C]ATTTATAAATTTTCT | 9678 |
| rs755083261 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007280 | TCTTTTTTTAATGGT[C/G]TTTGTCTGTTATATG | 9678 |
| rs755084731 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963155 | TCTTGCTTCTCTAGT[G/T]CTTTTAATTGTGATG | 9678 |
| rs755088125 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997151 | ACTTACTTTTTATCT[A/G]TACATACACATATAA | 9678 |
| rs755092252 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091808 | AACTCTGGAAATAAA[C/T]TTGATAACTGTTAAA | 9678 |
| rs755094172 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168339 | GTTGAGTTTAGAGAA[A/G]CAAAGTATATAAAAA | 9678 |
| rs755099584 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143613 | TCATGACCTACCTTC[G/T]AGAGATTACCGCTGC | 9678 |
| rs755105822 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111571 | TTGGAATATGAAGAA[A/C]CAACATTTTAACCAG | 9678 |
| rs755118765 | in-del | -/GAGAAAGAGAAGGAAAAAGAAAAGGAAAA | 8.25866e-05 | 0.00642546 | frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:10982605 | CCTAGAAAGAAAAAG[lengthTooLong]GGAGAAAGAGAAGGA | 9678 |
| rs755126280 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119520 | GTGAAAAGATACTCC[-/T]TAGTGGAATTAAACT | 9678 |
| rs755145482 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056345 | AGAAGGTTTTTATAG[C/T]AGCACTTACTTGTCA | 9678 |
| rs755155191 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984782 | TAAGAGGTTGTAGAC[-/T]TAACATTTATGATGC | 9678 |
| rs755156684 | snp | A/T | 2.72187e-05 | 0.00368898 | intron-variant | PHF14 | GRCh38.p7 | 7:11051593 | AAATGCATGACTTAA[A/T]TTTTTCCCCTTTATG | 9678 |
| rs755169708 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148501 | TGTAGCAGGGCTTCC[C/T]TGACTACCTTGCCTA | 9678 |
| rs755181611 | snp | C/T | 4.2115e-05 | 0.00458865 | intron-variant | PHF14 | GRCh38.p7 | 7:10974350 | CCGAGGCCTCTGCGG[C/T]GAGAGGTCCATTTCA | 9678 |
| rs755184164 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132747 | TTCCCCTTTTCTCCA[-/C]CCCCCTCACCAACAT | 9678 |
| rs755189057 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960555 | CAATAAACACACATG[C/T]GCATGTGTCTTTATA | 9678 |
| rs755191281 | snp | C/G | | | | | GRCh38.p7 | 7:10971646 | GAAAAAAGGACATTA[C/G]TAGGAAAATTAGTGA | 9678 |
| rs755193966 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988786 | GTTTGTGCCAGGAAC[A/G]TTCTTGCCATATATT | 9678 |
| rs755206515 | in-del | -/ACTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030156 | AGCATCTTCTCAGCT[-/ACTA]ACTAGGTAGACATAG | 9678 |
| rs755231234 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023574 | GCTCACGCCTGTTAT[C/T]CCAGCACTTCGGGAG | 9678 |
| rs755249795 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123234 | CTTTCTCTGAGTTAA[C/T]GTCCCTCAAGAGAGA | 9678 |
| rs755282199 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156389 | ATCTAATGAGCTATT[A/G]CGTTCCAATAAAACT | 9678 |
| rs755334405 | snp | C/T | 1.74747e-05 | 0.00295585 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982748 | TGCTGTTAACACATC[C/T]CCTTCTGTTCCCACT | 9678 |
| rs755344034 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071096 | CTGCACTGAGAGTTA[C/G]GAGATCTCAACTAGT | 9678 |
| rs755356268 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992954 | TTTGGTTTGTTTTTA[C/T]AGAATGTTCCTAATA | 9678 |
| rs755371730 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983209 | GGGAAAAGGGAATTC[C/T]TCTCTAAATCACTCT | 9678 |
| rs755382942 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102737 | AGATTTGCCTGTGTG[A/G]AATTTTTTTTCCTAT | 9678 |
| rs755387983 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981564 | AGCTCTTTAATGTCT[G/T]CAGCCTAACTTTTTA | 9678 |
| rs755411845 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135034 | TCTAACTTCCTCTCA[G/T]CAATATCCCTCATTG | 9678 |
| rs755429841 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160110 | GTCTATTATTGCCAT[C/T]TTCATGTCCCTGTGT | 9678 |
| rs755437355 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003629 | TTACCAAGTCCATCC[G/T]TCTGCAGAAATTACC | 9678 |
| rs755450414 | snp | G/T | 5.11627e-05 | 0.00505754 | intron-variant | PHF14 | GRCh38.p7 | 7:10990852 | AGTCCATGAAGGTAA[G/T]GTTGCTTTCTTTTCT | 9678 |
| rs755460012 | snp | A/G | 2.25395e-05 | 0.00335697 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11062056 | ATGTGCAACTTGCAA[A/G]GGAACTGGAGACAAT | 9678 |
| rs755482475 | snp | A/G | 2.27105e-05 | 0.00336968 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038794 | AACTACAAAACCTGA[A/G]TGGAAAACTTCGAAG | 9678 |
| rs755493524 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018923 | ATGTCTTTCTATCCC[A/G]TTTTTGGGGAGTTTT | 9678 |
| rs755499456 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966259 | TTTATTGAGAGACAG[A/G]ACAGCTCTCAGTGAA | 9678 |
| rs755524529 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049952 | ATACATGATTATGTA[C/T]ATTTTTGTTTTGCTT | 9678 |
| rs755526471 | snp | C/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064489 | AATTAAACTTCATGG[C/G]TCACAATTAGTCTTT | 9678 |
| rs755537099 | snp | A/G | 7.65726e-05 | 0.00618712 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11037090 | ATGTAGAATATAATA[A/G]GGTAAGTTAGCTACA | 9678 |
| rs755547457 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980939 | AGGTTGTTTAGGATA[A/G]GAGTGTTTTTTTCAG | 9678 |
| rs755557778 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014120 | TTACATCCATAATCT[G/T]AATTAATCTTAATAA | 9678 |
| rs755574541 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128666 | TCTAGACTCATGCTG[A/C]TAGTATTTTAGATGT | 9678 |
| rs755586562 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096881 | GGAAAAAAAAACTCA[C/T]CTTCAAATGATTTCA | 9678 |
| rs755595331 | snp | A/G | 9.28807e-05 | 0.00681408 | intron-variant | PHF14 | GRCh38.p7 | 7:11040647 | TTCTTAAAACAATAT[A/G]TACTACATTTGTTCA | 9678 |
| rs755597437 | snp | A/T | 9.97307e-05 | 0.00706084 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169523 | TTTTGAAAAGTTTGC[A/T]GCTTATGTAATAGCA | 9678 |
| rs755639664 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086695 | AGTTATAATTGTCAG[A/T]TATTAATGGGATCTT | 9678 |
| rs755661504 | snp | C/T | 7.98945e-05 | 0.00631988 | intron-variant | PHF14 | GRCh38.p7 | 7:11023006 | AGCATTTTTGATTGC[C/T]TGAAAGAGAAAGGTT | 9678 |
| rs755685259 | snp | C/T | 5.93525e-05 | 0.00544727 | intron-variant | PHF14 | GRCh38.p7 | 7:11111503 | GAAAAGGTATTGGTG[C/T]CCTTCCGTTTGATAG | 9678 |
| rs755693701 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040986 | AAACTCTATGGAAAT[A/G]AGCAGTACCCTTTGG | 9678 |
| rs755714475 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012769 | AGGAAAAAAGAGAAT[A/G]ACATATTGTTTTCAT | 9678 |
| rs755727647 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057474 | CCGCCTCCCAGGATC[A/G]AGCGATTCTCATGCC | 9678 |
| rs755729087 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028340 | ATTGTAAAGTTAAAA[A/T]ATTAGAAGTGGAACT | 9678 |
| rs755736977 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149260 | TAACATGCTTGATTT[A/G]CCATCATTTAATCTA | 9678 |
| rs755749294 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116722 | CATTTGTATTTTTTA[C/G]AAGTTCCACAGGTGA | 9678 |
| rs755755042 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156566 | GTGGGAGGCCGAGGC[A/G]GCGGATCACCTAAGG | 9678 |
| rs755766591 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993497 | TGTTGAGTACCTTCT[A/G]TGTGCTTGGTATTCT | 9678 |
| rs755791164 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066700 | CACATTAAATTACTT[C/T]GGTGCCACTTTTAAA | 9678 |
| rs755792157 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965546 | CCCACTTGAGGAGGC[C/T]GTCTGTCTGTTAATG | 9678 |
| rs755822507 | snp | A/G | 2.61271e-05 | 0.00361426 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022872 | TCTCTTCTTAGATGG[A/G]TTCATATTGTTTGTG | 9678 |
| rs755824056 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085663 | TTTTCCTTTTTTTTG[A/G]GACAGTGTCTCACTG | 9678 |
| rs755827547 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021476 | TATCCTCACATGAGT[A/G]GTTGGGAGAATGATA | 9678 |
| rs755843668 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995866 | GAACTCGCGCTGGCC[C/T]GCAAGCGCCTTGCAC | 9678 |
| rs755845230 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064611 | AACCACACTTCTCTA[C/T]GTAATTCAGGCTATA | 9678 |
| rs755849690 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107254 | CTTGTTATATGGATC[A/G]TAGCACATATGAAGG | 9678 |
| rs755852903 | in-del | -/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972215 | GTTGGGATTACAGGC[-/G]GTGAGCCACCGCACC | 9678 |
| rs755858031 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012293 | ATAGAAACTTTAAAT[A/G]TACAGTCACCCCTCA | 9678 |
| rs755858827 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993017 | AATACCACGGAAGTT[A/G]TATAGTGTTCTTAGT | 9678 |
| rs755861054 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003180 | TCCTGACCTCGTGGT[C/G]CGCCCGCCTTGGCCT | 9678 |
| rs755863823 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034302 | TTTTTGGGACAGACA[A/T]AAAGAATGAACAGCC | 9678 |
| rs755876247 | in-del | -/TTTA | 1.70621e-05 | 0.00292074 | intron-variant | PHF14 | GRCh38.p7 | 7:11051785 | TAAGAAACACGGTAG[-/TTTA]TTTTTTATTTATCAT | 9678 |
| rs755877871 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153402 | TTTTTAGTGGGGGTA[A/G]GGGAAGTTTAGGGTT | 9678 |
| rs755907404 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165569 | CAGTCTACAAGGTAA[A/G]CAAAGTTATCTGTAC | 9678 |
| rs755914377 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960359 | GGTTTTCTGTCCTTG[C/T]GATAGTTTGCTGAGA | 9678 |
| rs755938681 | snp | A/G | 1.67984e-05 | 0.00289809 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035783 | ACTATCACCAGAAGC[A/G]CAGGTATGGGATTCA | 9678 |
| rs755955594 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033180 | TATTCCATGTCAACC[A/G]ATGCATTAATTAGGA | 9678 |
| rs755955768 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049647 | GTCATCTGTTTTGAA[G/T]GCTGTTGCATTTATT | 9678 |
| rs755957063 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121710 | GCTAAGTGACTAACG[A/T]GCAGGTAGCACATAC | 9678 |
| rs755957503 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976162 | CAAGAGTTGATGGAC[A/G]GAATCTTAAACAGAA | 9678 |
| rs755984303 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141377 | CTTTGACTTTCTGTC[A/T]CCAAGTCTAATGGTC | 9678 |
| rs756019619 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127980 | CCTCCAGGCCACCAT[G/T]TACTCTCCTCCACCT | 9678 |
| rs756033900 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096223 | ATTAAAACCATTTAG[A/G]GCCATCCATGTATTT | 9678 |
| rs756045096 | snp | A/G | 3.14056e-05 | 0.00396255 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983029 | ATGAAGGCAATGATG[A/G]AGATCATAGTAGCCC | 9678 |
| rs756079424 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986374 | CAAATTAAAACTGAG[A/G]AAGCACACAAGTTAT | 9678 |
| rs756083980 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145024 | GTTATGGAGATGAAT[-/G]ATGGTGATGGTTTCA | 9678 |
| rs756091650 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022714 | GTAGGTGTTTCATAT[G/T]TTTTAATGATGTGCC | 9678 |
| rs756105832 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140193 | AACTCTACACATACC[C/T]ATACACACAGCCCTA | 9678 |
| rs756108273 | in-del | -/AC | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988415 | TTCCCATATGGGTAA[-/AC]CTTTTTTCCAGGGCT | 9678 |
| rs756109263 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055831 | ATGAAATATGTTTCA[G/T]ATAAATATTTTTTAG | 9678 |
| rs756116442 | snp | A/G | 0.000129299 | 0.00803946 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11037031 | AAATATGGCTGAACA[A/G]AAGAATATAAAAGAT | 9678 |
| rs756131014 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988840 | GTAGATATTATTTTT[A/T]TCGCCATTTTGCAGA | 9678 |
| rs756140176 | snp | A/G | 3.00287e-05 | 0.00387472 | intron-variant | PHF14 | GRCh38.p7 | 7:11036414 | GAATACATTTCTTTT[A/G]TAGGCAAGGATCAAT | 9678 |
| rs756146576 | in-del | -/G | 1.87278e-05 | 0.00305999 | intron-variant | PHF14 | GRCh38.p7 | 7:10983192 | TATATCTGTCTGTCT[-/G]GGGGAAAAGGGAATT | 9678 |
| rs756153756 | snp | A/G | 9.7661e-05 | 0.0069872 | intron-variant | PHF14 | GRCh38.p7 | 7:10990667 | TTTTTTACTTTAAAT[A/G]TGATTTTCTGATATA | 9678 |
| rs756191939 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013349 | GTGTTTTTAGGAGAG[A/G]TGAGGTTTCACCGTG | 9678 |
| rs756204069 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999744 | AAAGTAGCTTTGATT[A/T]TCAGAAACATTTAAA | 9678 |
| rs756225720 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978295 | ACATGTAAGTAAAAT[A/G]AAAATTAGAATAATT | 9678 |
| rs756235935 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157505 | AAATTTCTTAAGTAC[A/C]TCTTTTTCCCTATAT | 9678 |
| rs756236006 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143980 | TGCAGAGTATTCACC[C/T]AGTAAGTGCTCTGTA | 9678 |
| rs756273594 | snp | C/T | 1.70755e-05 | 0.00292189 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036669 | AGCTCTCACTGCAGA[C/T]TTTGTGAATTATTAT | 9678 |
| rs756315392 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059832 | ATAATAGAGTACCAA[A/G]TTAGGGAAAAATAAT | 9678 |
| rs756321412 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963381 | TCAGTCTCCATGTAG[C/T]TGTTTTGAGTGAGTT | 9678 |
| rs756323892 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156504 | TAAAGTTTTAGAAAT[G/T]CACTTTCTGGCCGGG | 9678 |
| rs756350052 | snp | C/T | 4.8526e-05 | 0.00492551 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990800 | ATAATAGTGAGGACG[C/T]TGATGAAATAATTCA | 9678 |
| rs756352556 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978837 | TCCCGTTTGAGTACC[A/G]CTGGCTCATACAAAC | 9678 |
| rs756370377 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112914 | GCATTTTATTAAGGC[C/T]TAGATTTAAGAGAGA | 9678 |
| rs756376108 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065809 | AACTTTATAGACTCA[A/G]TGTGGCACATTTATT | 9678 |
| rs756379123 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127692 | CTCCAGTTTCACCTT[C/T]CCTCATTCTTCAGAC | 9678 |
| rs756387864 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097396 | AGATTTAAGGTGACT[-/A]ATCTATCATAGGTAT | 9678 |
| rs756400279 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098995 | TTGTGCTATAATTTT[C/T]AAAAGTTCATTTCAA | 9678 |
| rs756400467 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150127 | TATTGAGGTATAACA[A/G]TATGCCAGGGAGTGA | 9678 |
| rs756427316 | snp | A/G | 2.82068e-05 | 0.00375534 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982487 | TGAAGATATTAAAGT[A/G]AAAGAAGAACAACTT | 9678 |
| rs756468668 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135623 | TTCCCATTGAAACTC[C/T]ATCTTTGTTAAGAAG | 9678 |
| rs756489958 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961317 | CCAGTTTTCCCAGCA[A/C]CATTTATTAAATAGG | 9678 |
| rs756494181 | snp | A/G | 1.65745e-05 | 0.00287871 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028755 | TGCAGGGATGTGCAG[A/G]GCCTATTTCCATGTG | 9678 |
| rs756507009 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998542 | TATATTCATATGAAT[A/G]TGATATTAGTGGTAA | 9678 |
| rs756546310 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124613 | TTTTTTATCTCCTTT[C/T]TGCAGATGAAAGAAA | 9678 |
| rs756555575 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162701 | GGGAAATCCAAAGTC[-/TT]TTTTTTTTTTTTTTT | 9678 |
| rs756557502 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140179 | ACATCTCTACCAACA[A/G]CTCTACACATACCCA | 9678 |
| rs756561740 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075060 | TTCCTGCCTCAGCCT[A/C]CTGAGTAGCTGGGAC | 9678 |
| rs756563472 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030008 | GAATAAACAGATCTT[A/T]TAGGAATTGTATTTT | 9678 |
| rs756568597 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052308 | GACATGCTGATCCAT[C/G]TAGTTGTAGTTTATT | 9678 |
| rs756607267 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168448 | CTTTTACTTTATAAA[A/G]TCAATTCACAAAGTA | 9678 |
| rs756621876 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050309 | ATATAAACTAAATAT[A/C]AAATACAATTTTACA | 9678 |
| rs756623595 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10983322 | TCATTTGGCCAACAG[A/G]CTTTTATTAAATATC | 9678 |
| rs756624542 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963853 | TTTGTCTCTTTTGAT[A/C]TTTGTTGGTTTAAAG | 9678 |
| rs756634221 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136756 | AGATTAGATATATGA[C/G]ACCAAGAAATTCTGT | 9678 |
| rs756634394 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008712 | CATGTTGTAGGTACT[A/G]TCTTTCTCGTAAACA | 9678 |
| rs756647718 | snp | C/T | 9.58359e-05 | 0.00692162 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061997 | AGAAGACAAAGACAG[C/T]CTGTGTTGCAAAAGA | 9678 |
| rs756681855 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035994 | GAGCAGTCCTTTATA[A/C]AGTAAATTTTCACAT | 9678 |
| rs756695653 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956857 | CGCCTTTGTTTCAGA[C/T]TTCTGACTTCCAAAA | 9678 |
| rs756697474 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076510 | ATGAAGACCATCGCA[C/G]AGATTGGGAACTGAA | 9678 |
| rs756704769 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116784 | AGAACTACTGTTATA[C/T]CTAGTTGTTAAAAAC | 9678 |
| rs756744606 | snp | C/G | 2.84176e-05 | 0.00376935 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111368 | TGATGAATGCAGACT[C/G]TGCTACCATTTTGGC | 9678 |
| rs756749466 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086504 | TTATACTTAGTCCAT[A/G]TGTCTTGGTCAGTGT | 9678 |
| rs756773218 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993617 | AATATCTCTTAGTTG[G/T]TGGCCCAGATTCTGA | 9678 |
| rs756778278 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067487 | CACCCAAAGCAGAAA[C/G]TCAAACAGATAATTG | 9678 |
| rs756793312 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958155 | CTAGGGCACAAAGGT[A/G]GAATGAAAATTTCGC | 9678 |
| rs756834532 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985811 | GTGCATGCCACCATG[C/G]CCAGCACATTTTTGT | 9678 |
| rs756846559 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158764 | AAATATAAGAGAATA[A/C]GATGTTCCATGTATG | 9678 |
| rs756871282 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956086 | TCCAAATTCACATTA[C/G]AAAGGTCATAACAAA | 9678 |
| rs756871480 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136922 | ATTATAGAAAACTTG[A/G]AGAACAATTAATATG | 9678 |
| rs756879797 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044476 | GCACAGTGAAGCCTT[A/T]AATTTCTCCTTGTTT | 9678 |
| rs756881561 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105693 | AGGCATGCTTTGCAA[A/G]TATTTCTCTATAAAA | 9678 |
| rs756892064 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161920 | TCCCAGATATTAGTA[C/G]TTTACTACCTGAAGG | 9678 |
| rs756897261 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967327 | CTCCCCAGTGGATAT[A/T]TGGCAATGTATGTCC | 9678 |
| rs756911506 | snp | A/G | 8.33994e-05 | 0.00645699 | intron-variant | PHF14 | GRCh38.p7 | 7:11111484 | TAAGGGGAGAAGTCT[A/G]TAAGAAAAGGTATTG | 9678 |
| rs756920017 | in-del | -/TAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071965 | TTTCAAAGTGTCTAT[-/TAAA]TATTTTGAGAGGCAG | 9678 |
| rs756927117 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043391 | ACTCCAAGAAAGGGA[C/T]AGATGTTCAGATTTT | 9678 |
| rs756942636 | snp | A/G | 9.97277e-05 | 0.00706073 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038841 | TGGGCTTTACTAGGC[A/G]GAATCACAGGGCAGG | 9678 |
| rs756944645 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070202 | CCCACCTCAGCCTCC[-/T]TAGTAGCTGTGACTA | 9678 |
| rs756948082 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057549 | CCGGCTGAGTTTTGT[A/G]TTTTAGTAGAGATGA | 9678 |
| rs756950032 | in-del | -/CTA | 1.76561e-05 | 0.00297115 | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10982906 | ACAATGATTGGCGAC[-/CTA]CTGTAGTAAAGAGAA | 9678 |
| rs756973774 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031336 | TGTGACATTTCTATT[C/G]TTTTTCATCTACTTT | 9678 |
| rs756990801 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987347 | ACAGGAAATGTGCTG[A/G]AATTTCCTTGTATTA | 9678 |
| rs757006369 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071329 | TAACATACTCAGTAG[A/C]ATCTTCTTCCAAGCT | 9678 |
| rs757007494 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013010 | CACCTCCAAAATTAG[A/G]TCAAAGACTTTTTGG | 9678 |
| rs757014023 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141519 | GTTTATTGTTTGTTA[C/T]ATGCAGAAAAAGTAA | 9678 |
| rs757029444 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958683 | GCTGTTTGGCCAACT[A/G]CTTACTTCTGTAGTT | 9678 |
| rs757044561 | snp | C/T | 4.15291e-05 | 0.00455662 | intron-variant | PHF14 | GRCh38.p7 | 7:10974341 | TAAGTGTATCCGAGG[C/T]CTCTGCGGCGAGAGG | 9678 |
| rs757045080 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156318 | TCTTGAAGCAAATTC[A/C]ATTTCTTTTTAACCC | 9678 |
| rs757049948 | snp | A/C | | | splice-acceptor-variant | PHF14 | GRCh38.p7 | 7:11035638 | GTGCTTTCTTTGTAT[A/C]GGATATAGCAGATCC | 9678 |
| rs757085864 | in-del | -/TTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089763 | TTGTTCATGCATTCT[-/TTTT]TTTTTTTTTTTTTTT | 9678 |
| rs757094014 | snp | A/G/T | 5.96806e-05 | 0.00546236 | intron-variant | PHF14 | GRCh38.p7 | 7:11051584 | GATAATAATAAATGC[A/G/T]TGACTTAAATTTTTC | 9678 |
| rs757107656 | in-del | -/AAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142659 | ATAAACTTTAGTATA[-/AAG]AAGATCCTGTTAGGT | 9678 |
| rs757114217 | in-del | -/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060121 | AGCTCAAGCAGTCTT[-/C]CCCGCTTAGCCTCTC | 9678 |
| rs757116291 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129861 | AAGTATAGGTAAGGT[A/G]CAGTGGGAATTTTGA | 9678 |
| rs757129967 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961435 | CTGTTCCATTTGTCT[A/G]TTTATCTGTTTTGGT | 9678 |
| rs757149531 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115887 | TTTTCTTGTGGTTTA[G/T]ATTCATTATGCATCT | 9678 |
| rs757150678 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084962 | TACATATCTTTGTAT[A/G]AGTTGCAAATATTTT | 9678 |
| rs757159769 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993357 | GGACTTGTGGGACTT[C/T]GCATGATCTGTGATT | 9678 |
| rs757160922 | in-del | -/ATG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134162 | CGTTCTAAGTTTAAA[-/ATG]ATGAACTTTACAGTA | 9678 |
| rs757165551 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015062 | TGTTTTAGTATTTTA[C/T]TAAACATGCTTTATA | 9678 |
| rs757187981 | snp | A/T | 7.61702e-05 | 0.00617084 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042780 | CTGGATCCTCCTCTT[A/T]CAAGGATGCCAAGAA | 9678 |
| rs757194104 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10982023 | TAAAATTAAAATCAA[-/G]TGCCCAATCTTAAAA | 9678 |
| rs757199975 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014222 | TTAAATAACTTATTC[C/G]TTCAAGACCACAAAC | 9678 |
| rs757202445 | snp | A/G | 1.67119e-05 | 0.00289062 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035771 | GAGAGAGAAGCAACT[A/G]TCACCAGAAGCACAG | 9678 |
| rs757206204 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143310 | ATTTTTTGTAGTGAC[C/T]AGGTCTCATTGTGTT | 9678 |
| rs757218577 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148614 | CAGTTTGTTGCCTGT[C/G]TCTGTTGAAATTGAA | 9678 |
| rs757219041 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058409 | AAAACTAGAAAAAAA[A/G]AATCCCATAGCTTTC | 9678 |
| rs757257442 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043246 | TCATTTAAATTCAAC[C/G]ATTCTTTGACATCTA | 9678 |
| rs757270020 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150482 | ATTATAAGAATTCAC[A/G]ACATAACTACTGAAT | 9678 |
| rs757288114 | snp | A/G | 1.66521e-05 | 0.00288544 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051705 | CAAACGATCAAGGAG[A/G]CAGATTAAGGAACCA | 9678 |
| rs757290285 | snp | A/T | 0.000121995 | 0.00780913 | intron-variant | PHF14 | GRCh38.p7 | 7:11035599 | TTTATGACTCTTGGG[A/T]GTACAAATGTTCACT | 9678 |
| rs757306124 | snp | C/T | 1.78436e-05 | 0.00298688 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036447 | CCGGCTTCAGCAGTA[C/T]CGTGCCAAAGCAGAA | 9678 |
| rs757308090 | snp | A/G | 7.49822e-05 | 0.00612254 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061978 | GGAAAGAGTTCCTAG[A/G]GAGAGAAGACAAAGA | 9678 |
| rs757311413 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138382 | TACAAGGTGATAATG[-/A]AAAAAAAACACAGTT | 9678 |
| rs757313535 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143370 | AAGTGATTCTTCCGC[A/C]TCTGCCTCCGAAAAT | 9678 |
| rs757335429 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145161 | CCCTCGGGAGGGGTT[A/C]AGGTGGCAGAGGAAC | 9678 |
| rs757344664 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100582 | TAGTGTATGATAAAA[C/T]CTACTGACCTTCACA | 9678 |
| rs757372973 | snp | A/G | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035686 | AGCAACATGCAGATA[A/G]GTTAGACAGAAAGTG | 9678 |
| rs757379890 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017109 | TGGCTTAGTACTCCA[C/T]TGTGTATTGTGTACC | 9678 |
| rs757399516 | snp | A/C | 3.61709e-05 | 0.00425255 | intron-variant | PHF14 | GRCh38.p7 | 7:11061851 | CATGAGGTTGGAATA[A/C]GTTAAGCACTTTTAC | 9678 |
| rs757400727 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089365 | ATCTTTTAAAGCTTG[A/G]ATCGTATTTGAACAC | 9678 |
| rs757413479 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158626 | GCAGTTTTAAAATCT[C/G]GTGAAGAAACTGATT | 9678 |
| rs757438149 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011013 | ATAGCATAAGGATAA[A/C]AATTAAACAGTTGCT | 9678 |
| rs757443889 | snp | C/T | 1.86862e-05 | 0.00305659 | intron-variant | PHF14 | GRCh38.p7 | 7:10983190 | TTTTATATCTGTCTG[C/T]CTGGGGAAAAGGGAA | 9678 |
| rs757460259 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11168218 | CAAAATGATATTCAA[A/G]ACCCCATTCCTGGTG | 9678 |
| rs757466944 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047337 | CCTCCCAAAGTGCTG[A/G]ATTACAGGCGTGAGC | 9678 |
| rs757469860 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025706 | AGGCTGAGGCAGGAG[A/T]ATGGCGTGAACCCGG | 9678 |
| rs757479186 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164674 | ATTTGCAAAAATAGT[A/G]TAGAAATTTCCCATT | 9678 |
| rs757481765 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089587 | AGAACTCTGGAAATA[-/T]TTTTTAATGAGATAC | 9678 |
| rs757485974 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120566 | TATAATTTCTTGGTA[A/G]CAATGAAAGCTATCT | 9678 |
| rs757511531 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088660 | GGGAATTTATCATAA[A/G]GAAATAGTCAAAGAA | 9678 |
| rs757518649 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053085 | CCACAAGGGAGATAC[A/G]AAGATATTTTTAGGG | 9678 |
| rs757527441 | in-del | -/TCT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160714 | TTGGCTGTTTGTATG[-/TCT]TCTGAGAAGTGTCTG | 9678 |
| rs757531656 | in-del | -/AATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087922 | TGAAACTAACATAAC[-/AATT]AAAAGTTACCCAGGG | 9678 |
| rs757554536 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138135 | AGGCTCTGCCTCCTG[C/G]ATTCACGCCATTCTC | 9678 |
| rs757563632 | snp | A/C | | | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169566 | AATTGTAAAATGTTA[A/C]ATTGTAAAATCTAAT | 9678 |
| rs757574483 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132731 | CTAACAGTGTACATG[A/C]GTTCCCCTTTTCTCC | 9678 |
| rs757576239 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017833 | AGTTTCGCTCAAGAA[A/G]TTTTACCCAGAGCAA | 9678 |
| rs757582542 | in-del | -/TAAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152715 | CAGACAGACAATCTG[-/TAAA]TAACCAAGTGGATGT | 9678 |
| rs757601636 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964509 | TGGCTGCCCTTAACA[A/T]TTTTTTCCTTTATTT | 9678 |
| rs757634490 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124789 | AGAGATTCTCAAATT[A/C]GATTTTGTCCTAAAG | 9678 |
| rs757654864 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026685 | GTCCAGTTACGTTAT[C/T]TGATGTCTAGTTGGC | 9678 |
| rs757673133 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072521 | TCATTATCTATAAAA[C/T]AGCAATAAACAATAG | 9678 |
| rs757677339 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089948 | GGCTAATTTTGTATT[A/T]TTAGTAAAGACGGGG | 9678 |
| rs757682318 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145092 | TTAAAATGGTTAAGA[C/T]GGTAATTTTTATGTC | 9678 |
| rs757683876 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052249 | ATCAAATGTTTTTCT[C/T]TGGTAATTTGATATT | 9678 |
| rs757694669 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001047 | AAATTTGCATTTCAC[A/G]TTTGGGTCTGAATTT | 9678 |
| rs757695881 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052698 | TTATGTTGCATTTCT[C/G]TCAGTACTAATGATT | 9678 |
| rs757698033 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020422 | TGGCTTTGTCACCCT[G/T]ACTGGAGTGCAGTGG | 9678 |
| rs757698897 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093043 | GTGTGATACAGTCCT[A/G]CCAAGCAAAACTAGC | 9678 |
| rs757705535 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157633 | ATAAAAATGGATCAT[A/G]TTACATTTTTACCAT | 9678 |
| rs757705572 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055665 | CTTAACAATGTGAGC[C/T]ACTAGCCAGTTCTAA | 9678 |
| rs757709897 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039377 | TATTTTTCCCCTTTA[A/G]CAGTAGCTGTGATCG | 9678 |
| rs757715010 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026611 | AACCAAAGTAAGGAA[-/AT]TACTTAATTGACTAC | 9678 |
| rs757750844 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126252 | AGCAAATCATCTTAA[C/T]GACTCAATTTAAAAT | 9678 |
| rs757770713 | snp | A/T | 2.63891e-05 | 0.00363233 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982481 | ACTGAATGAAGATAT[A/T]AAAGTAAAAGAAGAA | 9678 |
| rs757784672 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000043 | TAAATAGGGAAGCTG[A/T]ATAGTCTTTGACCAC | 9678 |
| rs757786587 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119160 | AATTAATCAAAGTAC[A/G]GTAGGTTGCCATACA | 9678 |
| rs757802554 | snp | C/G | 2.99738e-05 | 0.00387117 | intron-variant | PHF14 | GRCh38.p7 | 7:11022986 | GGTGCCAAGGTGAGA[C/G]ACAAAGCATTTTTGA | 9678 |
| rs757807505 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083220 | CAAAGAGAAGCACCC[A/C]TCTGTGCAGAAGTAA | 9678 |
| rs757816324 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151850 | AGTGTATTTTAAGAC[A/G]TAAGAACAGTCATTC | 9678 |
| rs757832281 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995131 | CTAGACACAGGGTGC[A/T]GATTGGTGTGTTACA | 9678 |
| rs757842209 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973267 | TTCATTTACATGAGG[C/T]GAGCATTAGGTGGCC | 9678 |
| rs757862363 | snp | A/G | 1.6819e-05 | 0.00289987 | intron-variant | PHF14 | GRCh38.p7 | 7:10974950 | AGATGCCTCAGGTAA[A/G]TATTTCCTTCTCTCT | 9678 |
| rs757874460 | snp | A/G | 0.000107458 | 0.0073292 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982674 | GAAAAAGAAAAAGCA[A/G]CAGTATCTGAGAATG | 9678 |
| rs757878521 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959278 | TCAGCTAGTCATTCC[A/G]TATTGGAACTCATGC | 9678 |
| rs757881450 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077916 | AGAAGTTTTGCACCA[C/T]TAAGTTGCTTCTCTC | 9678 |
| rs757894432 | snp | G/T | 1.65987e-05 | 0.00288082 | intron-variant | PHF14 | GRCh38.p7 | 7:11028868 | TTCACAAGATATCTT[G/T]TGACTCTATGTCCTA | 9678 |
| rs757899904 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043953 | ACTGCTCAGCCTGCA[C/G]AGCTCTGGTTTCCAG | 9678 |
| rs757940218 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020506 | ACCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG | 9678 |
| rs757948373 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136986 | CTAACATTTCGTTAG[G/T]ACCTTAATATATAAG | 9678 |
| rs757982388 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073053 | CAGCATGTTATTTGA[A/G]TGGGAGAAACATCCA | 9678 |
| rs757988302 | snp | A/G | 3.10284e-05 | 0.00393869 | intron-variant | PHF14 | GRCh38.p7 | 7:11051578 | CCAGAAGATAATAAT[A/G]AATGCATGACTTAAA | 9678 |
| rs758001976 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010433 | TTGTGTGTTATAGTC[C/T]AACTCCTTTTAAATC | 9678 |
| rs758006540 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126360 | ATATTTTTAGGATAC[A/G]TTATTTACTCTTTTA | 9678 |
| rs758012245 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109873 | TAAGCATTTTTTAAA[A/G]TCTTGAATCTACAAG | 9678 |
| rs758021142 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058010 | CTTGCTTGATTAATC[-/AT]GTGGAATTTCCAGGT | 9678 |
| rs758026497 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984949 | TTCGAAAAGTGCCCA[G/T]GTAGAAGAGATTATA | 9678 |
| rs758030213 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031741 | CTGGAGAATAGAGTG[A/G]GACCCTACCTCTAAA | 9678 |
| rs758038389 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150447 | CCTCTATTCTCCTCC[C/T]TGTCCTGAACATATG | 9678 |
| rs758041502 | in-del | -/TC | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107689 | CTATTCGTATAATAA[-/TC]TGTTTTTATTACATA | 9678 |
| rs758043514 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083392 | TCTCTCTTTCTCCCC[A/G]CACTCCCACCCCGTA | 9678 |
| rs758055892 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958498 | CTGACTTTTCTTTCT[C/G]GGAGTACTTATGATT | 9678 |
| rs758058808 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139911 | GTCCATATAATAATG[A/T]TATTGACTTTGAGAT | 9678 |
| rs758067597 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044729 | ATTTTGTCACATTTT[A/C]CTATTATCTATGCTC | 9678 |
| rs758070691 | snp | A/G | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169929 | TGCTTGCACATGAAA[A/G]TGGTTAAAACCAGTC | 9678 |
| rs758071088 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018162 | TGTTTTGGCTACTGT[A/G]GGTTTGTGGTATAAT | 9678 |
| rs758072113 | in-del | -/ATA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132784 | TCTTTTGACTTTTTG[-/ATA]ATTAGCCATCCTAAT | 9678 |
| rs758075391 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001538 | TGAACATAATAAACA[-/T]TTATTTATTTAGTTC | 9678 |
| rs758084505 | snp | A/G | 1.91093e-05 | 0.003091 | intron-variant | PHF14 | GRCh38.p7 | 7:11102439 | TAGTGCAGAGCTGCT[A/G]TGATCTTTAAATGTT | 9678 |
| rs758089866 | in-del | -/TTTTTTTTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034540 | AATTTCTTAATTCTA[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 9678 |
| rs758109377 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960311 | TGTTCTCCTTGTTCA[A/G]CTCCCACTTATGACT | 9678 |
| rs758124695 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984702 | ACACCTGCATGTGTT[C/T]AGGAATTTGCCACGT | 9678 |
| rs758126632 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129890 | GAGAGTAGGATGATT[C/G]CTTTCAGCACCAAGC | 9678 |
| rs758162376 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003267 | AAAATAAAGTTCACG[C/T]TAATAGCAGGACTCT | 9678 |
| rs758177940 | in-del | -/A | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959217 | GGCTGCCCAAACCAT[-/A]AACCACCTAACAGCC | 9678 |
| rs758190346 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085417 | AAGCTATCATTGATG[C/T]AACCTTTTGTGTAAT | 9678 |
| rs758276217 | snp | C/T | 2.96555e-05 | 0.00385057 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042723 | GATCAGCATCTTCTT[C/T]TATTGTGTGATACCT | 9678 |
| rs758292820 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974508 | TTTTGCCGTTTTTAT[G/T]GACTGTTACGATGTC | 9678 |
| rs758304364 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993548 | ATAGAATGTACACAT[G/T]GTTGACCTGGTGGAA | 9678 |
| rs758321302 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076790 | CCAGGCTCATCTCTA[A/T]CTCCTGTTCTCAAGC | 9678 |
| rs758343550 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104323 | AATTCATAAGATATA[A/G]GTCCTGCAAAAAGTA | 9678 |
| rs758360254 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163425 | TTAAATGAAATAAGA[A/G]TCTCAAATATGCAAA | 9678 |
| rs758406583 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030286 | ACCAGATAAATACTA[C/T]GTAAATACTTGGATC | 9678 |
| rs758448826 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165779 | AGAAAAACCGAGGGT[C/T]TCCTCTATCACAAAT | 9678 |
| rs758455600 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988914 | GGTGAGAAAGAAACT[C/T]AGGAATGTTTGATTT | 9678 |
| rs758458753 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049870 | GGTAATCTGACAACC[C/T]AGGGGATAACCTGCC | 9678 |
| rs758464210 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086788 | TTTTGTCATCATTTG[A/C]ATATAATTTGTATAG | 9678 |
| rs758475475 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018826 | TCGTGTTCCAGATCT[C/T]AGAGGAAAAGCTTAC | 9678 |
| rs758480951 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966567 | CCCGCGTAGGAACCT[C/G]TCTGCCTCCCACCAC | 9678 |
| rs758508132 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103483 | AAAATTTGATCTTCA[A/C]GCTTTAATGATCCAG | 9678 |
| rs758544545 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960441 | TTTTTATGACTGCAT[A/G]GTATTCCACGGTGTA | 9678 |
| rs758556419 | snp | A/G | 1.69398e-05 | 0.00291026 | intron-variant | PHF14 | GRCh38.p7 | 7:11035800 | AGGTATGGGATTCAT[A/G]TCAAAACCCGTATGT | 9678 |
| rs758584939 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079955 | CTTTTGATTGTCACT[G/T]TTGTTGCATATTGCT | 9678 |
| rs758626017 | snp | A/G | 8.67115e-05 | 0.00658394 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061818 | CGAAAACGAAGCTTC[A/G]TTCCTGAGGAAGAAA | 9678 |
| rs758647626 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153467 | TTGAGGTCCTTATTA[A/G]AAAGTTTATTGGAGA | 9678 |
| rs758649231 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108847 | ATGAATTATGATACA[C/T]ATGCATCATGATAGT | 9678 |
| rs758652910 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056069 | GTCAGATTATAAAAC[C/T]TCTATCTGTCATAGA | 9678 |
| rs758653422 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034714 | CCACTGTGCCTGGCT[A/G]ATTTTTGTACTTTTA | 9678 |
| rs758657418 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122903 | CCAGCTGCATGTCCA[C/G]GAACTTCTCTGAGCT | 9678 |
| rs758660024 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148022 | ACAACCAGCAGCAGT[A/G]TAATCATTCCTAATT | 9678 |
| rs758663691 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986031 | TGGGGTGCAGTGGTG[-/T]GATCATGGCTAACTG | 9678 |
| rs758673502 | in-del | -/TTATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145770 | TGGAATATTATTATC[-/TTATT]TTATTAAAACAGTAA | 9678 |
| rs758706447 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080251 | GCCCTGTCACATCGT[C/T]ATTTAAAAAACAATA | 9678 |
| rs758720557 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996009 | AGGCTCCTCAAGTGC[A/G]GCCAGAGTGGGCGCC | 9678 |
| rs758739011 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121895 | GTACGTGTCCAGAAC[A/G]TACAGGTTTGTTCCG | 9678 |
| rs758758299 | snp | A/G | 1.65616e-05 | 0.00287759 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111358 | CCTGCAGGTGTGATG[A/G]ATGCAGACTCTGCTA | 9678 |
| rs758760465 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000235 | ATTTCCCATTTCCCT[G/T]TTTAATTTTGGAGTT | 9678 |
| rs758770831 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132865 | GATTAGTGATGTTGA[A/G]CACCTTTTCATATAC | 9678 |
| rs758772340 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113351 | ATAAGGTTTTAGTTT[C/T]GTTTTCTTCTCTACC | 9678 |
| rs758777975 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965265 | GGTGTGGATGTCCTT[G/T]TTGTTGATGTTGATG | 9678 |
| rs758814524 | snp | C/T | 1.99253e-05 | 0.0031563 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038824 | GTGAAGGACAAGGAA[C/T]ATGGGCTTTACTAGG | 9678 |
| rs758827864 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109423 | AAATTATATTTAATA[-/T]GTTTATTTGATGAAA | 9678 |
| rs758831982 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027325 | ATTAACTAGGCAGTA[G/T]GATGTCAGGATTTGA | 9678 |
| rs758832780 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028921 | AAATTTTAACATTTA[C/T]TCTTAAAGTTCTTGC | 9678 |
| rs758846578 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980177 | TTTGATCAGCTACCC[A/G]CACTTCTGCCCCAGT | 9678 |
| rs758848714 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978716 | TCTACTAGATGCCAG[G/T]AGCATCTTTCCTACC | 9678 |
| rs758849156 | in-del | -/CT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080572 | TTAAATAAACATTAA[-/CT]CTGCTGGTTTTTCTC | 9678 |
| rs758858573 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146896 | CTGATACCCAGGCTG[G/T]AGTCCAGTGGTGCGA | 9678 |
| rs758866555 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114276 | TGCTGGAAAAATGAA[C/T]TGCACTTTAACATTT | 9678 |
| rs758883429 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091890 | TTAAGTAAATGACTG[C/T]GTCTTTCAGTGGATA | 9678 |
| rs758884724 | snp | A/C | 4.34018e-05 | 0.00465822 | intron-variant | PHF14 | GRCh38.p7 | 7:10974365 | CGAGAGGTCCATTTC[A/C]GCCATTCTAGAAGTC | 9678 |
| rs758934762 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159897 | CAATTTTCCGCTTCT[A/G]TCAACTTAATAAAAA | 9678 |
| rs758934899 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991266 | GCTCACTTCATCCTC[C/T]GCCTCCTGGGTTCAA | 9678 |
| rs758940982 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100733 | TATGGGTGAGGAAAA[C/T]GAGAAGAATTACTTG | 9678 |
| rs758941314 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975862 | ATCTCTCCTTCTTCT[A/G]GTTTTCCCTTGTCTT | 9678 |
| rs758941869 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022573 | GCAAATATTTAAGAA[C/T]AGATAAGTGCAAAGT | 9678 |
| rs758956222 | snp | A/T | 7.25242e-05 | 0.00602137 | intron-variant | PHF14 | GRCh38.p7 | 7:11013717 | AACAAAATAAACCCT[A/T]TTTAATCATAGTGTT | 9678 |
| rs758964766 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061632 | ATAAATGGTAACAAA[C/G]TGCAGTAGTCCAATA | 9678 |
| rs758979353 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161785 | ATTTTTAGATATTAT[C/T]TTTGCCTAAATATTT | 9678 |
| rs759009649 | snp | A/G | 2.81456e-05 | 0.00375127 | intron-variant | PHF14 | GRCh38.p7 | 7:11038902 | GTTCTTGCTCCCTAT[A/G]TGATTTTCAAAGAAC | 9678 |
| rs759029550 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034111 | AGATATCACACTACA[C/G]AATTGCCTCATATGC | 9678 |
| rs759031831 | snp | C/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169660 | ATTTTAGAGTAATTT[C/T]GACTTTTTTATTCAA | 9678 |
| rs759039149 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996713 | AGGCTGGGGTTTAAG[C/T]AGGATAGAAGGACCA | 9678 |
| rs759041102 | snp | C/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087294 | CCTCCTGGGTTCAAG[C/G/T]GATTTTTCTGCCCCA | 9678 |
| rs759041927 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142877 | GTTAATGACTTAATG[G/T]TTAATTGGCTAATAT | 9678 |
| rs759043077 | snp | C/T | 1.69115e-05 | 0.00290782 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051779 | TTCCGATAAGAAACA[C/T]GGTAGTTTATTTTTT | 9678 |
| rs759045303 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078399 | GGCATAGAGCTAAAA[C/T]TAAGAGGTTGAAATT | 9678 |
| rs759047063 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167443 | TTTTCCAAATTATGT[A/G]TTAATTCAGGCATAC | 9678 |
| rs759058696 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070094 | CCTTTCATCTTGTGT[C/T]ATTTTTGGTAAGCTG | 9678 |
| rs759061293 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108478 | GAACTTGCCTATCAC[C/G]CCTAATTCTGACAAG | 9678 |
| rs759069593 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978025 | CATGCTCTCTACCCC[-/T]ATCCCCCACCAGGCA | 9678 |
| rs759086921 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144755 | ATAAATGTTTGTGGT[A/G]ATGTGGGGGGAAGAA | 9678 |
| rs759091091 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111039 | ACAATTGAAATTGTT[G/T]TGGTTGTTTTGAACA | 9678 |
| rs759094976 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960303 | TGTCCATGTGTTCTC[C/T]TTGTTCAACTCCCAC | 9678 |
| rs759098556 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122607 | ACTTCCTTAATCATA[C/G]CATATGTTTCTTTAT | 9678 |
| rs759126692 | in-del | -/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957258 | ATATTTTCCAATAAA[-/T]TTTTAAAAACTGTTG | 9678 |
| rs759129860 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155607 | AGGGGACTTTGCTGA[A/C]ATTTTTAGATCCTTC | 9678 |
| rs759135108 | snp | A/G | 6.63306e-05 | 0.00575855 | intron-variant | PHF14 | GRCh38.p7 | 7:11028850 | CCATAGTTGGTGAAC[A/G]TGTTCACAAGATATC | 9678 |
| rs759140431 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079662 | ACCAAGCACTAAATT[C/G]TATAATATGACTCTC | 9678 |
| rs759144019 | snp | A/C | 1.65817e-05 | 0.00287933 | intron-variant | PHF14 | GRCh38.p7 | 7:11051563 | AAACTATAGCTAAAG[A/C]CAGAAGATAATAATA | 9678 |
| rs759146952 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010295 | TAAAATTATATTTCC[C/T]TTTAATTTTATGATA | 9678 |
| rs759174349 | snp | A/G | 3.41425e-05 | 0.0041316 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051661 | GACATGGAAGCAGAT[A/G]TGGCCATGGAAACCC | 9678 |
| rs759224610 | snp | G/T | 1.65756e-05 | 0.00287881 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036554 | CTATTCGTAAACTTA[G/T]GCGGAAAGCAGAACT | 9678 |
| rs759229051 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997699 | GGCTTCAGTTCTTTG[A/G]TGGCTGTTGGCCAGA | 9678 |
| rs759231240 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987093 | TGCCAAAATTTATAA[A/G]TATCCACTTCTATTT | 9678 |
| rs759247444 | snp | A/G | | | | | GRCh38.p7 | 7:10971130 | CACATTTATTCAACA[A/G]TGTTCTGCAGGTTCT | 9678 |
| rs759258429 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023391 | TAATTGTTTTGGGGC[A/G]TGCCGTTAACATGCC | 9678 |
| rs759298762 | snp | C/T | 2.41304e-05 | 0.00347342 | intron-variant | PHF14 | GRCh38.p7 | 7:11062129 | AGGGGATGAAAGTTC[C/T]ATATTTATTTTCTCA | 9678 |
| rs759311149 | snp | A/G | 0.000292343 | 0.0120866 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974301 | CCTAAGTCTTCTCCA[A/G]ACGACCACCTCACGG | 9678 |
| rs759326593 | snp | C/T | 6.39161e-05 | 0.00565279 | intron-variant | PHF14 | GRCh38.p7 | 7:11038736 | ATATTTTAATGAAGT[C/T]TACTAATTTGGCTTA | 9678 |
| rs759327301 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114830 | CTATGCTTCAAAGCC[A/G]TTGATTAAGACAGCA | 9678 |
| rs759332522 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006911 | CTGGCGCGGTGGCTC[A/G]CACCTTTAATCCCAG | 9678 |
| rs759345032 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069124 | GAAGCCAGTCAGGAA[A/G]GGTTGCTGGCTCCTG | 9678 |
| rs759355188 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981177 | GTGCTTAGTTAATTA[C/T]AGAGGTTAAGCCTAG | 9678 |
| rs759363519 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090137 | TTATGCATGAAGCCT[C/T]AAGTGTGATTTAATT | 9678 |
| rs759384512 | snp | A/G | 4.53525e-05 | 0.00476174 | intron-variant | PHF14 | GRCh38.p7 | 7:11061960 | ATTATCCCTTGTATG[A/G]CAGGAAAGAGTTCCT | 9678 |
| rs759391437 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967850 | TCTTGTGTTCAACAG[A/G]CACCTTATTTCAGTT | 9678 |
| rs759398995 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147542 | CAGACCCAATAGTTA[G/T]GCCGCTGTCTGAATC | 9678 |
| rs759404470 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974284 | GGCTCCTGCAGCCTC[G/T]CCCTAAGTCTTCTCC | 9678 |
| rs759419617 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152785 | GAGTGATGGAGGAAG[C/G]GCAGATTTTGTGCAT | 9678 |
| rs759422545 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018673 | TCCAAATACAACATT[A/G]TATTACCTGCTAACA | 9678 |
| rs759424079 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074303 | GCAAGTTCTGCCTCC[C/T]GGGTTCATACCATTC | 9678 |
| rs759440081 | snp | C/T | | | | | GRCh38.p7 | 7:10970352 | GAGGTGGGCGATCAG[C/T]TGAGGTCAGGAGTTG | 9678 |
| rs759453561 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103148 | AGACTTGTGAAGCAT[A/G]TGACATTCTATTTTT | 9678 |
| rs759459270 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002864 | TAGAAGGTTGAGGGT[C/T]AATGCAGATGGAAGC | 9678 |
| rs759476223 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049292 | AGCTTGGCCAACATA[C/T]AGTGAAACCCTGTCT | 9678 |
| rs759485864 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11066819 | CTCTTGATTACTCAG[G/T]CTGTGGAGTAAGCTG | 9678 |
| rs759537075 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994981 | ACCCACATCCTGCTG[A/T]TAGGTCCATTTTACA | 9678 |
| rs759540775 | snp | C/G | 1.72124e-05 | 0.00293359 | intron-variant | PHF14 | GRCh38.p7 | 7:11036967 | ACTAAAGTAAAATTC[C/G]ATATTTCATTTAAAT | 9678 |
| rs759541154 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105296 | TATTTATGATGTTAA[A/G]AATAGACTGCTGACC | 9678 |
| rs759550512 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159211 | TTATTTATTCTAAAG[-/T]GATGTTAAGATTGTT | 9678 |
| rs759567726 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017128 | GTATTGTGTACCACA[A/T]TTTCTTTATCGGATT | 9678 |
| rs759599571 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980706 | AGTATTTATTTCTCA[C/T]ACTCTGTAAATAGGA | 9678 |
| rs759601185 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151152 | TGTATATTATGAGAA[A/G]TAGCACTTTGTAAAC | 9678 |
| rs759611857 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978016 | CAGATTAGCCATGCT[C/T]TCTACCCCTATCCCC | 9678 |
| rs759614650 | snp | A/G | 4.66038e-05 | 0.00482698 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022949 | ACCAGTAACACTAAC[A/G]GAAATGAACTATTCC | 9678 |
| rs759615037 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999553 | GTCATGTTTTGCTCC[C/T]TGGACTCTTAACTTA | 9678 |
| rs759646547 | in-del | -/ATCT | 6.59044e-05 | 0.00574002 | frameshift-variant, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040748 | AGGCACACAAAAGAC[-/ATCT]ATCTACTCTTCCTGC | 9678 |
| rs759647974 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973816 | GCGGGGGCGAGTCCT[A/G]CGCATGCGCCCTCAA | 9678 |
| rs759652104 | in-del | -/TTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113054 | AGTCTCTTTAATAAG[-/TTT]TTTTAAGTGCATTTT | 9678 |
| rs759682882 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019528 | CTAATTTATTGGCAT[A/G]TAGTTGCTCATAGTA | 9678 |
| rs759706629 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009917 | GAGGTTTAAAACTCT[A/G]TGCAAATGTGCACGT | 9678 |
| rs759715393 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106900 | ATAAACTTATAGGGG[-/C]TACAAGTAAAATGTT | 9678 |
| rs759730948 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984254 | TGGTGATTTCGTTAC[C/G]AAAATAATCTATAGC | 9678 |
| rs759747827 | snp | A/T | 2.76736e-05 | 0.00371968 | nc-transcript-variant, missense | PHF14 | GRCh38.p7 | 7:11111447 | TGGATATGTCAGGAA[A/T]GTGATTCTTCATCTT | 9678 |
| rs759751173 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127111 | CTTTAGGTATTAATA[-/GT]CTTTTTTTTAAATAT | 9678 |
| rs759758848 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060149 | CTCAAAGTGTTGAGA[-/T]TATGGCCGTGAGCCA | 9678 |
| rs759771864 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958292 | TATGTGGAAAGTTTT[C/T]ACTCATGTAATACCA | 9678 |
| rs759777267 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093788 | TGCCCTTTTTCCTAT[G/T]GCAGCTTTATTCTGG | 9678 |
| rs759790210 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161345 | ATGCTGTCATATTCT[A/G]TTAAAGAAGGCATTG | 9678 |
| rs759795414 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137424 | TAAAAAGTTAAAGTT[C/T]ACCAAGAATGATTTT | 9678 |
| rs759809034 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957344 | GATTGATTTAAAAGA[A/G]CAGAAGGTATCACTG | 9678 |
| rs759828141 | snp | A/T | 1.71717e-05 | 0.00293011 | intron-variant | PHF14 | GRCh38.p7 | 7:11013934 | ATTATGTTGGTTCAT[A/T]TGTTTGCTTTATAAT | 9678 |
| rs759841245 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052878 | GAAATCATTTATGTT[C/G]ATGTTTACCAGGTAC | 9678 |
| rs759841249 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11169295 | AATTTTACCATTTGT[C/G]TTTAGGATTATTAGA | 9678 |
| rs759857393 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152677 | AGAAAATCTGCTGTC[A/G]TGGAGCATGCACTCT | 9678 |
| rs759859799 | snp | A/G | 7.34511e-05 | 0.00605972 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040687 | AAGTTGAATATACCG[A/G]CAATTTTGCGAGCAC | 9678 |
| rs759864810 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976470 | AGTTGGGTCGTGGAA[G/T]TTACGAATTCTTTGA | 9678 |
| rs759868212 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058036 | CCAGGTAACGTATCT[A/G]TGTTACATTCTAAAG | 9678 |
| rs759891117 | snp | A/C | 1.65787e-05 | 0.00287907 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035697 | GATAGGTTAGACAGA[A/C]AGTGGAAGAGAAAAA | 9678 |
| rs759897138 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163881 | GAAGCCAAGTAGTGT[A/G]TCTGTTTTTCTTTCT | 9678 |
| rs759917610 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973673 | GAGCCTTTGGGGTTT[A/G]TGGGCGGAATTGCAC | 9678 |
| rs759946090 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097173 | TAGTAGAGATGGGGT[C/T]TCACCATGTTGGTCC | 9678 |
| rs759973263 | snp | A/G | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11150011 | AGATGAAAAGCATAT[A/G]TGTTAATATTAAGTA | 9678 |
| rs759975989 | in-del | -/CT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004351 | GTTTGTTCTTCCAGG[-/CT]TTTTTTTTTTTTTTG | 9678 |
| rs760008757 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956659 | ATCAAATGACTTGGT[A/G]TCCTTATAAGAAGAG | 9678 |
| rs760070107 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118112 | GGTTTGCCTTTTTAC[C/T]AATACAGATATGTAA | 9678 |
| rs760085891 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076263 | AAACTTTCTTTGATA[A/G]ATGTAATTTGTTAAA | 9678 |
| rs760101481 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988470 | AAATTACCACACAGT[A/C]CATAAAGACATGTAG | 9678 |
| rs760102202 | in-del | -/TAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139058 | GAAGTCTGCAAATGG[-/TAT]TATTGTTGTTTTCAT | 9678 |
| rs760102521 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045350 | TCTTATTTCATGACT[C/G]TGCCTTAGTCTGCAG | 9678 |
| rs760103118 | snp | C/T | 8.55688e-05 | 0.00654042 | intron-variant | PHF14 | GRCh38.p7 | 7:11036947 | TATGTCAGTTTTTAC[C/T]TCCTACTAAAGTAAA | 9678 |
| rs760114524 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162828 | GTGGCCGGGATTACA[A/G]GCACACACCACCACT | 9678 |
| rs760146668 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024009 | TCTTCTGCCGAATAG[C/T]CAGTATGTCAGTGCA | 9678 |
| rs760148381 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081555 | TAAGTTTAAGTTAGA[A/G]TCGTCCCATATTTGT | 9678 |
| rs760150007 | snp | A/G | 5.3049e-05 | 0.00514992 | intron-variant | PHF14 | GRCh38.p7 | 7:11111331 | GATACACCTACCTAT[A/G]AATCTGTTTACCCTG | 9678 |
| rs760166248 | in-del | -/TATT | 2.40151e-05 | 0.00346511 | intron-variant | PHF14 | GRCh38.p7 | 7:11062131 | GGGATGAAAGTTCTA[-/TATT]TATTTTCTCATCACA | 9678 |
| rs760169477 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143058 | GGAATATAAAGCATT[C/T]TAGTTTTGTCAGAAA | 9678 |
| rs760170760 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023458 | TGTGTTCTGACTGCT[G/T]CACCAACCTGGTGTT | 9678 |
| rs760211667 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099807 | TTCAAAACAAATATA[A/C]AGTTTCAAAAAAGAT | 9678 |
| rs760227882 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118590 | TTGAACTTATTAGTC[A/T]TCATTATTGCCTGGT | 9678 |
| rs760246906 | snp | C/T | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036467 | CCAAAGCAGAACTAG[C/T]TCGATCTACCAGACC | 9678 |
| rs760261483 | snp | A/T | 0.000103254 | 0.00718446 | intron-variant | PHF14 | GRCh38.p7 | 7:11042662 | ATTATTGAAATCTTT[A/T]CTTGCTGCCTTTATT | 9678 |
| rs760262059 | snp | A/G | 1.75847e-05 | 0.00296514 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983144 | CCTGACCCTATCTCA[A/G]AGCAAGAGTAATGAG | 9678 |
| rs760281914 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978574 | TAGAATAAGGTCAAA[C/T]TGTGGCTGTATATAC | 9678 |
| rs760309140 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071258 | CAAAGACTATATATT[C/G]CATGTTCCCAAGTCC | 9678 |
| rs760354638 | snp | C/T | 8.82418e-05 | 0.00664177 | stop-gained, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061803 | CAGAGAACCAGAGGA[C/T]GAAAACGAAGCTTCG | 9678 |
| rs760367759 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144254 | AAGGGAAATCTTGTA[A/T]ACTGTTGGTGGTAAT | 9678 |
| rs760377196 | snp | A/G | 1.78541e-05 | 0.00298776 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982425 | AAGGACAGTGGAGAA[A/G]GTTCCTGTAGTGATT | 9678 |
| rs760380594 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962708 | AATCTGTCTGGTCCT[A/G]GACTTTTTTTTGGTT | 9678 |
| rs760423342 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129653 | CCAATATATTAGCAA[C/T]AGGAGTCTCATTTTT | 9678 |
| rs760424938 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050347 | ATCATTTTTATTAAG[A/C]GAATACTATCAAACT | 9678 |
| rs760425294 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989411 | TGAAACTAATTTATT[A/T]AATTTATTTCTGAAT | 9678 |
| rs760431262 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098333 | TCCTTGAGACCTTTC[A/G]CAGTGTCTAGCCTCT | 9678 |
| rs760454650 | snp | C/T | 1.66225e-05 | 0.00288287 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990760 | AAAATGGACCATATT[C/T]TGATTTGCTGTGTTT | 9678 |
| rs760458190 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079872 | TTGATCATAAATGAC[A/G]TGTCAATAATCAGGA | 9678 |
| rs760460146 | snp | C/G | | | | | GRCh38.p7 | 7:10971527 | CCCTCTCTTCCTTCC[C/G]TCCTTTTCTCCTTCT | 9678 |
| rs760478561 | in-del | -/AAAT | 3.4712e-05 | 0.00416591 | nc-transcript-variant, frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11169485 | CAGAAAAATCCAAAG[-/AAAT]AAAAGATTTTCTGTA | 9678 |
| rs760492277 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003006 | GGCTGGAGTGCAGTG[G/T]CATGATCTCCGCTCA | 9678 |
| rs760498733 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979585 | GGAACATAGCACAGA[C/G]TCATTCTTTGATGAC | 9678 |
| rs760523570 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981265 | CATTACCTTTTTCTT[C/G]GCTATAGGTGCAAAA | 9678 |
| rs760530084 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134839 | ACTCAAACTATAGAA[A/G]GATACACAATGAATA | 9678 |
| rs760560263 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157441 | TACTTTGTTTTGACA[-/T]TTTATTCTTAATTCA | 9678 |
| rs760576878 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961151 | GTCATGAAGTCTTTG[C/T]CCATGCCTGGGTCCT | 9678 |
| rs760597723 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069860 | ATTATTTATTTATTT[-/A]TTTTTTTCTGGTAGA | 9678 |
| rs760605324 | snp | A/G | 1.65809e-05 | 0.00287926 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036529 | AGACCACTCACCAGC[A/G]GTGCTTCAGCTATTC | 9678 |
| rs760612233 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975677 | AAATGTTTTATGGGA[A/G]AAATACTGATAAACA | 9678 |
| rs760614064 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018783 | CCAGTACTATGTTGA[A/G]TAACAGTGGTGACAG | 9678 |
| rs760614517 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083042 | TTCTACCCCCTCTCC[C/T]CTCTCTCCCTTATGT | 9678 |
| rs760621059 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035537 | TAGATGTAACTAGCA[C/T]TAGTAGATTCTTTGA | 9678 |
| rs760633209 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137978 | GCTATGCATATAAAC[A/G]TAAACAGACCAGCAG | 9678 |
| rs760634810 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054524 | TTGGTCTTGATCTTA[C/T]CATTTATGCTGAGTT | 9678 |
| rs760659536 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103871 | ATTGAAAGATCTCAT[-/A]ACATTGGAGGAAAAA | 9678 |
| rs760663208 | snp | A/G | | | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170262 | GGTTCTAATTTCCAA[A/G]CTGCCATTTGCCAAT | 9678 |
| rs760686289 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964288 | GGTGACAAAATCTCT[C/G]AGCATTTGCTTCTCT | 9678 |
| rs760699334 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964978 | CATCTAACCTTTTTT[C/T]TAGGTTTCTACCTTC | 9678 |
| rs760699567 | snp | A/G | 0.000102333 | 0.00715235 | intron-variant | PHF14 | GRCh38.p7 | 7:11061948 | ATGTTTTATTTTATT[A/G]TCCCTTGTATGGCAG | 9678 |
| rs760709739 | snp | A/G | 4.56277e-05 | 0.00477617 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982514 | ACTTAAAAATTCTGC[A/G]GAGGAAGAAGTACTA | 9678 |
| rs760718614 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067985 | GGATCACATTTCAAC[A/G]TTAGGTTTGTAGGTG | 9678 |
| rs760729425 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011091 | TTGCTTACTATTAGG[C/T]TATTTTAGTTATGAT | 9678 |
| rs760732345 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136232 | AAATCTATTGTATGC[C/T]GTGGTGGGATGCTGT | 9678 |
| rs760740216 | snp | A/G | 4.55156e-05 | 0.0047703 | intron-variant | PHF14 | GRCh38.p7 | 7:11038877 | TTCTTTCCAATTGCT[A/G]TCTCCTTCAGTTCTT | 9678 |
| rs760756423 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990458 | ATATCCTAGAGGAGA[A/G]AGAATACGAAGCTTG | 9678 |
| rs760775796 | snp | C/G | 0.000117185 | 0.00765368 | intron-variant | PHF14 | GRCh38.p7 | 7:11111322 | TATTATTTAGATACA[C/G]CTACCTATAAATCTG | 9678 |
| rs760800082 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039164 | AGTTTTTCCTACTAC[A/T]TTCTTCTTTCCTTTA | 9678 |
| rs760800245 | snp | C/T | 1.65924e-05 | 0.00288027 | stop-gained, intron-variant | PHF14 | GRCh38.p7 | 7:10982818 | AAATGGAACCTTCGA[C/T]GAAACCGACCACTTC | 9678 |
| rs760803539 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073250 | CATCTATGAGCCTGT[A/T]AAATCAAAAACAAGT | 9678 |
| rs760817256 | snp | C/G | 2.66514e-05 | 0.00365034 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013775 | TGATGGAGAGAGTGA[C/G]TCTATTATGAGTTCA | 9678 |
| rs760829910 | snp | A/G | 2.5583e-05 | 0.00357643 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111431 | ACAGACAGGCTACGG[A/G]TGGATATGTCAGGAA | 9678 |
| rs760833698 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065614 | AGTGGATAGTTTTTC[C/T]TCTGCTGTATTTTAA | 9678 |
| rs760858338 | in-del | -/GTTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055848 | AAATATTTTTTAGAT[-/GTTA]GTTAGTTTAGGAAAA | 9678 |
| rs760871297 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093955 | CCTCTTATGTTTTTT[A/T]CTCTTCACAGTGAGA | 9678 |
| rs760878858 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957612 | CTAGGAGATCTGTCT[A/T]ATAAACTGCTATTGT | 9678 |
| rs760888741 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087932 | ATAACAATTAAAAGT[A/T]ACCCAGGGCAATTAT | 9678 |
| rs760900681 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035361 | TGAAGGGCTACTATA[C/T]AAGTACACCCAAATA | 9678 |
| rs760917761 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031271 | TCTGTATTTTTTATG[A/G]CTTTGTATAGCCTTC | 9678 |
| rs760919364 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012077 | TTGGTTTCTAAGATA[C/G]CGGCAGCCTCATCAA | 9678 |
| rs760932413 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010764 | CAAGTGATTCTCCCA[C/T]CTCAGCCTTTCTAGC | 9678 |
| rs760934422 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005014 | AGAGCGAGATTCCGT[C/T]TCAAAAAAAAAATGT | 9678 |
| rs760943575 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10973928 | TTGTCTGAGGCAGCC[G/T]CCCTCGCGCTGTGCA | 9678 |
| rs760945362 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083942 | AGATGGGATGCCCGT[C/G]TGGGGCAATAGGTAG | 9678 |
| rs760948090 | snp | A/G | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051614 | CCCCTTTATGTAGGC[A/G]GTGCTCGGAATGTGA | 9678 |
| rs760956941 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118153 | AAAAAAGTTGTTTCT[A/G]TTGTGTCCTATATTA | 9678 |
| rs760974014 | snp | C/T | 2.69887e-05 | 0.00367337 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038781 | GAATCTTTAGAAGAA[C/T]TACAAAACCTGAATG | 9678 |
| rs760990680 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040041 | TTTATTAAAAGACTT[C/T]TAACAGAGGTTTGCA | 9678 |
| rs761016715 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152821 | CAAAGAACTCACTCA[C/G]TGATACCTGCATGAC | 9678 |
| rs761021556 | snp | A/T | 6.38508e-05 | 0.0056499 | intron-variant | PHF14 | GRCh38.p7 | 7:11042846 | AGATTTAGATGTTTG[A/T]ATTGATTTACTCTTA | 9678 |
| rs761028422 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976687 | TATCGAGCTAAGTAG[A/C]GATTTCTGACCTTGT | 9678 |
| rs761043102 | snp | A/G | 2.13095e-05 | 0.00326409 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982722 | GCCACCACACCAGCC[A/G]CAAGTCCTCCTGCTG | 9678 |
| rs761048355 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087334 | GTAGCTGGGACTACA[A/G]GCGCACACCACCATG | 9678 |
| rs761048427 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076410 | TATAAGTATGCTGTT[C/T]AGTTGTATTTAATAT | 9678 |
| rs761060036 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132716 | CAACTTACATTCCTA[C/T]TAACAGTGTACATGA | 9678 |
| rs761073553 | in-del | -/T | 1.73285e-05 | 0.00294346 | intron-variant | PHF14 | GRCh38.p7 | 7:11035614 | AGTACAAATGTTCAC[-/T]ATTTTTCTGTGCTTT | 9678 |
| rs761095906 | in-del | -/AATTTTGC | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063346 | TCTGACCACAGTATA[-/AATTTTGC]AATATGTCGAAAATG | 9678 |
| rs761101353 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010098 | ACTTGTGTGGATGCA[C/T]ATTTTATCTAGTTTG | 9678 |
| rs761103559 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020904 | GTAAGCACTTCACAT[A/C]CATCTTTATAACTTC | 9678 |
| rs761179001 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153950 | TGTCTGTGTGTGCGT[-/GT]GTGTGTGTGTGTGTG | 9678 |
| rs761193506 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020296 | GGTTTCAACCTGTTG[C/T]CCAGGCTGGTCTTGA | 9678 |
| rs761241016 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11066953 | TAATAACAGCAACAA[A/C]AAATTAGCTAAGTTG | 9678 |
| rs761245812 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092913 | AAGGGTGTTTTTTTC[C/T]CCCTAATAGTGACCC | 9678 |
| rs761248638 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121714 | AGTGACTAACGAGCA[C/G]GTAGCACATACAGTA | 9678 |
| rs761256033 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103510 | CCAGTTTTAAGTCAA[C/T]GGCAGAAGTATGTTG | 9678 |
| rs761276098 | in-del | -/CACTGATTACAATTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005218 | CATCCTTGTCAAAGT[-/CACTGATTACAATTA]CACTGATTACATATG | 9678 |
| rs761280487 | in-del | -/ATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126197 | ATAAGGTATTTCAGC[-/ATT]ATTTCTTTATTTTAA | 9678 |
| rs761297480 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003208 | CCTCCCAAAGTGCTG[A/G]TGCATATCTGTTCAT | 9678 |
| rs761301816 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130648 | GTACATTTGTTAAAA[A/G]TTGATGAGCCAGTAT | 9678 |
| rs761308186 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119310 | AAGGACATTTTATTA[C/T]GGCTTTACAAAAGTT | 9678 |
| rs761333962 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105536 | ATTAAATTTTTAAAA[A/T]AATTTAAAAATGGCA | 9678 |
| rs761381429 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015601 | GCTATAATTTTAGGC[A/G]AGTGATGTAACCTTT | 9678 |
| rs761388221 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990279 | CTAGGTAGGATTATA[A/G]GCTCCTAAAGTGTAA | 9678 |
| rs761403749 | snp | A/G/T | 5.38808e-05 | 0.00519013 | intron-variant | PHF14 | GRCh38.p7 | 7:11061940 | TGTTTGTTATGTTTT[A/G/T]TTTTATTATCCCTTG | 9678 |
| rs761403761 | snp | C/T | 6.28358e-05 | 0.00560481 | intron-variant | PHF14 | GRCh38.p7 | 7:11036387 | GTTTCATTTTATTAT[C/T]TTTTAAAATTTGAAT | 9678 |
| rs761411463 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081538 | CTGTGTGGGAAAACA[-/T]TTAAGTTTAAGTTAG | 9678 |
| rs761438687 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100082 | AACTATATTGTTTTT[G/T]ATTTTTCTTTCATTT | 9678 |
| rs761446009 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126120 | AAATTTAGATGATTA[G/T]TTATTTGTAAATCAT | 9678 |
| rs761446903 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146752 | AACTAGGACATGTAA[A/G]TATAAAATAAGATGA | 9678 |
| rs761471844 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995077 | AAAAGTTCTCCAAGT[C/T]CGCACAGAGCACTGA | 9678 |
| rs761484075 | snp | C/T | 6.89513e-05 | 0.00587119 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983115 | GCTGATGATGAGGAA[C/T]TGACCAATGATAGCC | 9678 |
| rs761499308 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151792 | CTTGGAAAATAACTT[A/G]TTTTGTAAGTAGCTG | 9678 |
| rs761558774 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046892 | ACTCTGGTGTGGGAT[C/G]CTGAGTTCTTGATGA | 9678 |
| rs761561069 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985680 | TTTTTGGAGACAGGG[A/T]CTCACTCTGTTGCCT | 9678 |
| rs761561899 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005185 | ATTCTCTAGCAACTT[C/T]CCACTTAATAGTTTT | 9678 |
| rs761579769 | snp | C/T | 0.000119725 | 0.00773615 | intron-variant | PHF14 | GRCh38.p7 | 7:11013926 | ATGTCCTAATTATGT[C/T]GGTTCATATGTTTGC | 9678 |
| rs761600429 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138168 | GCCTCAGCCTCCCGA[G/T]TAGCTGGGATTACAT | 9678 |
| rs761607393 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989643 | CTTCCTATACTTTTT[C/G]TTTTTGAGACAGGGT | 9678 |
| rs761616433 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11080610 | GTCTCAAAATAGAAG[C/G]GTTTACATTTAGTCA | 9678 |
| rs761616453 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092584 | GTGAACAATTTAGCA[A/G]TAGTACCTCAGAGTT | 9678 |
| rs761636085 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141015 | AATATGTTCTGAGGA[A/G]CATAAGACAGACCTG | 9678 |
| rs761638106 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072341 | AACCATTCATGAGAA[A/G]TCTACCCCCGTGATC | 9678 |
| rs761668930 | in-del | -/CAGGAGAATGGCTTGAACC | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994344 | CTCAGGAGTCTGAGG[-/CAGGAGAATGGCTTGAACC]CAGGAGGCAGAGGTT | 9678 |
| rs761678549 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157082 | GCACTTTATTATATA[A/C]TTTCTCCATTGCATT | 9678 |
| rs761689260 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997893 | ATTTCTGCCATATTC[C/T]GCTGTTCACACAAGC | 9678 |
| rs761713212 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074476 | CAGCCTCCCAAAGTG[C/T]TGGGATTACAGGCAT | 9678 |
| rs761725566 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125436 | GTTTCTCTTCTTCAA[A/G]AGAATACTTGCTTCT | 9678 |
| rs761751336 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024207 | TAACTGTTCAATATT[G/T]TGAAGGCTGAGAGAG | 9678 |
| rs761756648 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041751 | AATATCACTATGCTT[C/G]TGACTTTTATGACTA | 9678 |
| rs761767411 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166172 | GTAAGCCTGTCTACT[C/T]TCCAGTAGCCTCAAA | 9678 |
| rs761775712 | snp | C/T | 0.000110675 | 0.00743808 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974840 | CTCTTCACAGTGGAT[C/T]GCAGCTCCAAGAGGA | 9678 |
| rs761781299 | snp | G/T | 0.000993048 | 0.0222607 | intron-variant | PHF14 | GRCh38.p7 | 7:11061768 | GATTTTTGTTTTTTG[G/T]TTTTTTTTTTGTTTT | 9678 |
| rs761815577 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128353 | TATTTTTATCTTTCT[C/T]CTCTCAGCCTTAAAA | 9678 |
| rs761817605 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976823 | TACTTTCTGTTCCCT[C/T]TTGTAATATAATATC | 9678 |
| rs761871984 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002101 | CCAGGCTGGAGTGCA[C/G]TGGCGCAATTTCGGC | 9678 |
| rs761883914 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999359 | CTGCTTTGAGGGTAC[C/T]GTCTCTTGTTGCTGA | 9678 |
| rs761923390 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027189 | ATATGTCTCTGTTCA[C/T]AGTGTGGACATCCTT | 9678 |
| rs761929332 | in-del | -/ATT | | | intron-variant, cds-indel | PHF14 | GRCh38.p7 | 7:11066108 | ATTTGGTCTGTAAAC[-/ATT]GTTGTTCGCACTTTT | 9678 |
| rs761935905 | snp | G/T | 3.31521e-05 | 0.00407123 | intron-variant | PHF14 | GRCh38.p7 | 7:11028825 | GCGGAAGAGGTAGGT[G/T]TATTTAAACCCATAG | 9678 |
| rs761940232 | snp | A/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062758 | TTAGCGGAAATGAAG[A/T]CATTGATCAAAGCTC | 9678 |
| rs761962913 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147718 | TGCTCAAGTTGTATT[A/G]GTAACGCTTGGTCAT | 9678 |
| rs761963841 | snp | C/T | 1.68023e-05 | 0.00289843 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036994 | AAATAGAGAGAAATA[C/T]GCGCATGATTCAAAT | 9678 |
| rs762002392 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084054 | GATATGAGAAGATAC[A/G]TTAAAGACACTATTT | 9678 |
| rs762013234 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040197 | ATAGATGGTTGCTGT[C/T]TGAGAAGCCAGCATA | 9678 |
| rs762027897 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148519 | ACTACCTTGCCTAAG[A/G]GAACATGTGCTCCCA | 9678 |
| rs762066964 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990326 | TTTTAAAACACATGT[A/G]TAGGATCAATGATTA | 9678 |
| rs762076773 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132830 | TATCTCATAGTGGTT[C/T]GGATTTGCATCTCCC | 9678 |
| rs762099309 | in-del | -/T | 0.0301243 | 0.118974 | intron-variant | PHF14 | GRCh38.p7 | 7:10982346 | TATACATATGTGTGG[-/T]TTTTTTTTTCTCATA | 9678 |
| rs762115365 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160796 | TGAATTAAGTTTCTT[A/G]TAGATTCTGGATGTT | 9678 |
| rs762146169 | in-del | -/AGGG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015005 | CCTCTCCAATATAAG[-/AGGG]GGGGTGGGTACTTAA | 9678 |
| rs762146249 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016492 | GTAAGAAAACCAGTA[C/T]ATTCTTGTCATTAAA | 9678 |
| rs762172832 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121157 | TTTTTAACAGGTAAA[C/T]ATCAGCAACACACCC | 9678 |
| rs762187958 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140671 | AGAAATATTTAAAGA[A/G]ACTACCATTTCAAGC | 9678 |
| rs762203275 | snp | A/G | 3.35008e-05 | 0.00409259 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040730 | AACCAAGTAAAAAAG[A/G]AGGAGGCACACAAAA | 9678 |
| rs762219756 | snp | A/G | 1.66313e-05 | 0.00288364 | nc-transcript-variant, synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:11169490 | AAATCCAAAGAAATA[A/G]AAGATTTTCTGTAGT | 9678 |
| rs762234045 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122442 | CGTATATATATATAC[-/AT]GTATATATATATATT | 9678 |
| rs762251165 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011331 | AGAGGTCACGCTCCA[A/G]TTTAGGCTCCTGGTT | 9678 |
| rs762265972 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984715 | TTTAGGAATTTGCCA[C/T]GTAAAGTGTGTGTAG | 9678 |
| rs762279169 | in-del | -/TTAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147576 | CTTGACCTCTCAATG[-/TTAT]TTAACAATGTCAACC | 9678 |
| rs762287227 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959297 | TGGAACTCATGCCTA[C/T]TGGAGTTTGTTTGTC | 9678 |
| rs762308706 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975802 | AGTTTCATCTCTTCA[A/G]CAGTTTTTAAATATA | 9678 |
| rs762315858 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054959 | AATTTTACCTTCATG[A/G]CATACGTAGGGCAAT | 9678 |
| rs762323060 | in-del | -/CTAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079109 | GTTTTTGAATGAGCT[-/CTAA]CTATTACAATGAACT | 9678 |
| rs762332076 | snp | A/C | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149656 | TTTAATCAGTCTTGA[A/C]ATTTAGGGAGATAAA | 9678 |
| rs762337936 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127414 | CTCTTTGGCTAGATT[C/G]CTTTCTAGAGTCTTG | 9678 |
| rs762341237 | snp | C/T | 1.69694e-05 | 0.0029128 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051668 | AAGCAGATATGGCCA[C/T]GGAAACCCTACCAGA | 9678 |
| rs762374434 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095773 | GATAATCCCTGCATG[A/C]TGTAAGTATCAAGCA | 9678 |
| rs762381739 | snp | C/G/T | 0.000183855 | 0.00958643 | intron-variant | PHF14 | GRCh38.p7 | 7:10974830 | TAATTTTTTTCTCTT[C/G/T]ACAGTGGATCGCAGC | 9678 |
| rs762403244 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022063 | CACATTTTGTTTTGT[G/T]GTAAGCAAGCAGAAA | 9678 |
| rs762412591 | in-del | -/TTGG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069722 | GTCTTTCCTTTTTTT[-/TTGG]TTGGTTGGTTGGTTG | 9678 |
| rs762418783 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047040 | TTTTTAACTTACACG[A/T]ATAAAATTCTCTAAA | 9678 |
| rs762429708 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139181 | TTTGCCACTATCATA[G/T]AAGTGAATTATTTAT | 9678 |
| rs762461772 | in-del | -/ATT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049136 | GGGGATTTAGATAAC[-/ATT]ATGTTTGCCTGTTAT | 9678 |
| rs762464206 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094252 | TAAAACAATATAAAA[C/T]TTTTTCATAATTTTG | 9678 |
| rs762465114 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119766 | TCTTTTGCTTATGAC[G/T]AAGAGACTTCTTCAA | 9678 |
| rs762474213 | snp | C/T | | | | | GRCh38.p7 | 7:10969160 | ACTGTCAAAATTCCT[C/T]CATAGCCCTCAAAAG | 9678 |
| rs762510892 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079607 | CTTTTTCTTCATTAA[A/C]AAGAAACCAAAGTTA | 9678 |
| rs762519723 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165278 | GAGGGTTTATCTGAT[A/G]TTTTCTCAGATTAGA | 9678 |
| rs762524875 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166181 | TCTACTTTCCAGTAG[A/C]CTCAAAGGATACATT | 9678 |
| rs762526621 | snp | G/T | 9.98436e-05 | 0.00706483 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982863 | ATGGAAGAGCTGAAT[G/T]ACATGGATGACTATG | 9678 |
| rs762537315 | snp | A/G | 4.97541e-05 | 0.00498744 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035734 | TGGCTCTACAGTCCT[A/G]TTGTAAAATGTCTTT | 9678 |
| rs762540106 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133337 | CAAGACAGTGTTGTA[C/T]TTGTAAAAGACAAAT | 9678 |
| rs762550355 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960207 | CAACTCGTCATTTAC[A/T]TTAGGTATTTCTCCC | 9678 |
| rs762560535 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005085 | ATGTCAACCACAGAC[C/G]TCTTAATTTTAAAGG | 9678 |
| rs762562386 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980604 | CACTCTTGAAATCCA[A/G]GAAGCTTAAAAATCC | 9678 |
| rs762586287 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089153 | TAAAAACCTAAGACA[A/T]ACCTTTTATCAGGAG | 9678 |
| rs762588143 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034313 | GACATAAAGAATGAA[C/G]AGCCTGTTGTTTTGT | 9678 |
| rs762597697 | snp | A/G | 1.73036e-05 | 0.00294134 | intron-variant | PHF14 | GRCh38.p7 | 7:11035835 | GTTTTAAGGTTATGT[A/G]AGGATTTTACGTCTC | 9678 |
| rs762615853 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985939 | ATTACAGGCATGAGC[C/T]ACCACACCTGGTCTC | 9678 |
| rs762640310 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962521 | CATCAATGTTCATTG[A/G]GGATATTGGCCTGCA | 9678 |
| rs762669504 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126712 | TTCCCTAAGATAGCA[A/G]TGTCCCTAATAGGGT | 9678 |
| rs762672407 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073098 | ACTCCTTGCCCCCCC[C/T]CCCCAGTTTTATCTT | 9678 |
| rs762691551 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153107 | GTGTCTTACAAAGAT[G/T]ACTGTCTCCTGTATA | 9678 |
| rs762706677 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033977 | GTGGTAACTGAGGCC[C/T]AGAGATGTTAAGCAA | 9678 |
| rs762713259 | snp | A/G | 0.000108627 | 0.00736896 | intron-variant | PHF14 | GRCh38.p7 | 7:11051815 | TCATAAGCATCATAC[A/G]ATTCTGAGGCCAAAA | 9678 |
| rs762721263 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141331 | AATTGTCTGAAGATA[C/T]GTAATAAGTAGGAGC | 9678 |
| rs762731714 | snp | A/G | 0.00010214 | 0.00714559 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038767 | CTTTGTAGCTATGTG[A/G]ATCTTTAGAAGAACT | 9678 |
| rs762736929 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025861 | TCACGCCTGTAATCC[C/T]GACACTTTGGGAGGC | 9678 |
| rs762759739 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132502 | TTGTCTGTTAATGGG[A/C]GGTTAGGTTGTTTTT | 9678 |
| rs762760438 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082964 | CAATGGCTTATCAGT[A/G]CCAGCTCACATTCCT | 9678 |
| rs762794215 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060848 | ATTTAGTTGACTCTT[A/G]GTTATCTAGGAACAG | 9678 |
| rs762805134 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978766 | CCTCCACTTCCACTG[-/T]TGTGGCAACTATTGT | 9678 |
| rs762836697 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989958 | AGTATCACTAGCTAG[A/T]TGTATTTATTACCAG | 9678 |
| rs762849280 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11051586 | TAATAATAAATGCAT[G/T]ACTTAAATTTTTCCC | 9678 |
| rs762851966 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146256 | AATATCAGATGGGAT[A/G]TATCTGCCACAGGAA | 9678 |
| rs762866344 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113662 | TTAAGCTGAAACTTC[C/T]GGAGACTTAATTGAT | 9678 |
| rs762900537 | snp | C/G | 4.11836e-05 | 0.00453763 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974320 | ACCACCTCACGGATT[C/G]CTTAGTAAGTGTATC | 9678 |
| rs762906982 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028874 | AGATATCTTTTGACT[C/T]TATGTCCTATAATAA | 9678 |
| rs762910696 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147388 | CTCCAGTTATTATCC[A/G]TGTTCCTGAAATTAA | 9678 |
| rs762926704 | snp | A/T | 0.000179461 | 0.00947091 | splice-acceptor-variant | PHF14 | GRCh38.p7 | 7:11013745 | GTTTTTGTTTTTTTT[A/T]GGTTGTTATGGAGTT | 9678 |
| rs762940647 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979971 | ACATAAAACATTAAA[A/C]ATTTTTTAAAAAATT | 9678 |
| rs762948032 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116383 | TGCTTTTCCCGGTTC[C/T]TCTCAGTAGAAAAAG | 9678 |
| rs762955417 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135388 | ATGGTTTTCATTAAG[A/C]TAAAGGTGAAAAATA | 9678 |
| rs762964700 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101182 | CTTTTTAGTTTTTAT[C/G]AAACTTATCAACTTG | 9678 |
| rs763018565 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11149006 | GTCATTCCTTGAAAT[A/G]GGGTTTTTTTTTTGT | 9678 |
| rs763029818 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990370 | TGGATTCATTTTTCG[G/T]TTTTCCTAGTTTAAG | 9678 |
| rs763044835 | snp | A/G | 7.59042e-05 | 0.00616006 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982541 | ACTATCATCAGAAAA[A/G]CAATTAATTAAAATG | 9678 |
| rs763062575 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076008 | GCCGGGCATGGTGGC[A/G]GGCGCCTGTAGTTCC | 9678 |
| rs763077239 | in-del | -/A | 5.81581e-05 | 0.00539219 | nc-transcript-variant, frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11169438 | AAATGAAGCTGAAAG[-/A]AAAAAATATATCTCA | 9678 |
| rs763079381 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050887 | TCTGTTTGTATAGTT[G/T]CTTTAAGTAGTATAT | 9678 |
| rs763080183 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045235 | TGCTTTAGACTCTAC[C/G]TTGTTCTTACTAGTC | 9678 |
| rs763084999 | in-del | -/TCTTT | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957661 | CACTTGCCACTTTTG[-/TCTTT]TCTCCATGCAGAACA | 9678 |
| rs763109989 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019335 | TCTTTAAGTGTTTGG[C/T]AAAATTCAGCAGCGA | 9678 |
| rs763119112 | in-del | -/CA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123110 | TCTCTAGGTTGGTTT[-/CA]CAGTCTTTTTTTCTC | 9678 |
| rs763121127 | snp | A/G | 0.000142602 | 0.0084428 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982655 | AGAGAAGGAAAGAGA[A/G]AAGGAAAAAGAAAAA | 9678 |
| rs763122045 | snp | C/G | 2.52032e-05 | 0.00354978 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022963 | CGGAAATGAACTATT[C/G]CAAATATGGTGCCAA | 9678 |
| rs763124471 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108708 | GATAATTTAATTGTA[C/T]GAGTAGTTGAAATCA | 9678 |
| rs763137020 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072412 | TATAATTCAACATGA[A/G]ATTTGAGTGGGACAC | 9678 |
| rs763147487 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028180 | CCTACACTTGAACAC[A/C]ATCATCTGACACAAA | 9678 |
| rs763150574 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075221 | TGGGATTACAGGTGT[C/G]GGCCACTGCACCTGG | 9678 |
| rs763150656 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010155 | TAAATAAAATATATA[-/T]TTTTTTCCCATGTGG | 9678 |
| rs763163979 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020129 | GGCCTGGCTCTGTTC[A/C]CCAGGCTAAAGTGCA | 9678 |
| rs763171524 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976829 | CTGTTCCCTCTTGTA[A/G]TATAATATCTAGTAT | 9678 |
| rs763173351 | in-del | -/AAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032265 | TGATAATGCATAATT[-/AAG]AAGATAAGTTTGATA | 9678 |
| rs763174236 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114458 | TTTATAGAAATTCCG[-/T]TAAGTCTAATAAGAT | 9678 |
| rs763194127 | snp | A/G | | | | | GRCh38.p7 | 7:10970780 | TAGCAAACTGAATCT[A/G]GCATCTATAAAAAGA | 9678 |
| rs763208316 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012340 | GGTTCCAGGACCCCT[A/G]CAGATACCAAAATTA | 9678 |
| rs763249651 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966932 | CTGGGATCTGATTCC[A/G]TTTATAGGGATGCAG | 9678 |
| rs763256581 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095982 | GAATTCATAACTAGT[A/T]ATTCTATTTCAAGGT | 9678 |
| rs763264901 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069959 | GTTTTTAAAGCATTT[C/G]TTTAAGATACTGTTT | 9678 |
| rs763273635 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994669 | GCTGTGGATCCTCGC[A/G]GTGAGTGTTAACAGT | 9678 |
| rs763278720 | in-del | -/A | 0.000207354 | 0.0101801 | intron-variant | PHF14 | GRCh38.p7 | 7:11042662 | ATTATTGAAATCTTT[-/A]CTTGCTGCCTTTATT | 9678 |
| rs763293279 | in-del | -/GAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002457 | TTTATTTATTTTTGA[-/GAC]GACGGAGTTTTGCTC | 9678 |
| rs763312012 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109392 | ATTCTTACTGATGAC[A/C]TGAGATGACAAATAT | 9678 |
| rs763317545 | snp | G/T | 1.72776e-05 | 0.00293913 | intron-variant | PHF14 | GRCh38.p7 | 7:11028665 | CTTTGAGAATTTTTC[G/T]GTTACTTTGTTGTAG | 9678 |
| rs763363414 | snp | A/G | 6.72269e-05 | 0.00579732 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982992 | GAAGATGAGGGAAGC[A/G]GGAGTGATGAAGACG | 9678 |
| rs763397057 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11141057 | CTACTTCTCCACTTA[A/G]CTGTGCCACTCTGGG | 9678 |
| rs763403117 | snp | A/G | 5.76735e-05 | 0.00536967 | nc-transcript-variant, missense, intron-variant | PHF14 | GRCh38.p7 | 7:11169448 | TGAAAGAAAAAATAT[A/G]TCTCAGGAGCTCAAC | 9678 |
| rs763407899 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059825 | AAATTAGATAATAGA[A/G]TACCAAATTAGGGAA | 9678 |
| rs763454725 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042113 | AATTGATGTGTGCGT[C/T]TTTAATTTTTTTACT | 9678 |
| rs763458266 | in-del | -/TATAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081387 | CTTTATGGTGCTCAT[-/TATAA]TAGTGAAAAATATTT | 9678 |
| rs763459968 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129781 | AACTTAGATGCTAGT[A/C]GGATAGATAAAGCAT | 9678 |
| rs763470009 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115414 | TTTGAGTCTATTTTC[A/G]TGATTTAAATAAGCT | 9678 |
| rs763489753 | in-del | -/GG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004367 | TTTTTTTTTTTTTTT[-/GG]TTGCTTGCTCATACA | 9678 |
| rs763499836 | snp | A/C/T | 0.000324526 | 0.0127346 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040717 | CCCAAGGAGAGAAAA[A/C/T]CAAGTAAAAAAGAAG | 9678 |
| rs763504986 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115015 | TCTTTCTTAACCTCA[A/G]CTTTTCTCTTATTTT | 9678 |
| rs763505164 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098374 | ATGTTATTCTGTTCA[C/T]CTTAGCTTCTTTGCT | 9678 |
| rs763505988 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129227 | TAGTTTTTGCCTTAG[A/C]GGCCCAAGGCTGTTT | 9678 |
| rs763525952 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026540 | TAGAACTAGAAAAGG[C/T]TCAGAGATGCCCACT | 9678 |
| rs763544428 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144259 | AAATCTTGTATACTG[C/T]TGGTGGTAATGTAAA | 9678 |
| rs763549340 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126394 | GCAGGCTAAGTGCTG[A/T]AAAGGATAGATATTT | 9678 |
| rs763572796 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967190 | TGCAACTTGTGTATT[A/C]AGATTTATCAATTGT | 9678 |
| rs763588869 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147081 | CGAACTCCTTGAGCT[C/G]AAGAGATCTGCCCAC | 9678 |
| rs763599415 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142527 | TCATTTCAGCCGCAA[A/G]CTTATAACCAAGATA | 9678 |
| rs763618798 | snp | C/T | 1.66067e-05 | 0.00288151 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035749 | ATTGTAAAATGTCTT[C/T]GCAAGAGAGAGAGAA | 9678 |
| rs763625591 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11024074 | CTCCAGCAAACACAT[A/G]AATGATAAGAAAGTG | 9678 |
| rs763633839 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143106 | GTATCTATATTTCTT[C/G]AATTTGGCTTGATAA | 9678 |
| rs763655455 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116730 | TTTTTTACAAGTTCC[A/G]CAGGTGATTTTATGA | 9678 |
| rs763658419 | snp | A/G | | | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968541 | TGTTCATAGTATATA[A/G]TACGTAGTGTTGATG | 9678 |
| rs763665627 | snp | A/G | 1.69792e-05 | 0.00291364 | intron-variant | PHF14 | GRCh38.p7 | 7:11036372 | AATCTTAAGGAACAT[A/G]TTTCATTTTATTATC | 9678 |
| rs763695340 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076413 | AAGTATGCTGTTTAG[A/T]TGTATTTAATATTAT | 9678 |
| rs763698956 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014156 | CCTATGATGAGGCAG[A/G]TGGTAACGTTTCTCA | 9678 |
| rs763706865 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118596 | TTATTAGTCATCATT[A/G]TTGCCTGGTCAAGTA | 9678 |
| rs763719219 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988483 | GTCCATAAAGACATG[C/T]AGCATCCTAATTTTC | 9678 |
| rs763742869 | snp | C/G | 1.6904e-05 | 0.00290719 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051674 | ATATGGCCATGGAAA[C/G]CCTACCAGATGGAAC | 9678 |
| rs763760344 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978586 | AAATTGTGGCTGTAT[A/G]TACGAGTTAATGGTT | 9678 |
| rs763766482 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977816 | AGGTCCAAAACACAC[A/C]GTCAAATATTAGCAA | 9678 |
| rs763780081 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160767 | TTTAATTGAGTCATT[A/T]GTTTTTTGCTTTTTG | 9678 |
| rs763782936 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142508 | TGTAGAAAACTATCT[-/A]AAATCATTTCAGCCG | 9678 |
| rs763783851 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079885 | ACATGTCAATAATCA[A/G]GAAAGCTTTATGACA | 9678 |
| rs763804844 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130422 | TAGTGTGAAATGTAA[C/T]GGTAGTAGTAATAGC | 9678 |
| rs763819023 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045475 | ACTACTAAATACCCT[C/G]TAAGCAAACTGTACC | 9678 |
| rs763826017 | snp | A/T | 3.67654e-05 | 0.00428735 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013753 | TTTTTTTAGGTTGTT[A/T]TGGAGTTGATGGAGA | 9678 |
| rs763829168 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069950 | TTATTCTTTGTTTTT[A/G]AAGCATTTGTTTAAG | 9678 |
| rs763831038 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163164 | AAGGTTTTTAAAAAG[A/G]GCTCTATTCTACTTA | 9678 |
| rs763860071 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134844 | AACTATAGAAGGATA[C/T]ACAATGAATAATTCA | 9678 |
| rs763862250 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981307 | CCTGTGGATTTTACT[A/G]GCTAAGACTTAACTG | 9678 |
| rs763910651 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044318 | TGATCTAAAATAAAA[C/G]TTGAAATTAAAAAAA | 9678 |
| rs763915970 | snp | A/G | 3.35284e-05 | 0.00409427 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11038768 | TTTGTAGCTATGTGA[A/G]TCTTTAGAAGAACTA | 9678 |
| rs763935529 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11008021 | TATTAGGGTACCTCT[A/G]ACCGTGATGTCACTT | 9678 |
| rs763943820 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958279 | TCCATTTGCTAAATA[C/T]GTGGAAAGTTTTTAC | 9678 |
| rs763947762 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961185 | TGGTATTGCCCATGT[G/T]TTCTTCTAAGGTTTT | 9678 |
| rs763954045 | snp | A/C | 4.13368e-05 | 0.00454606 | intron-variant | PHF14 | GRCh38.p7 | 7:10974335 | CCTTAGTAAGTGTAT[A/C]CGAGGCCTCTGCGGC | 9678 |
| rs763955850 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122820 | TTAAATTAGTAGTAG[C/T]TTCAGTAGTGTTTTC | 9678 |
| rs763960162 | snp | A/C/G | | | | | GRCh38.p7 | 7:10971568 | TACTTTCTTTCAATA[A/C/G]ATGAATTGCAAAAGA | 9678 |
| rs763988947 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070195 | TGATCTTCCCACCTC[A/T]GCCTCCTTAGTAGCT | 9678 |
| rs763989805 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163656 | AAAAACTCTAATTAA[-/T]TTCAGTCTGAAGCAT | 9678 |
| rs763995451 | snp | A/G | 6.63031e-05 | 0.00575736 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036541 | AGCAGTGCTTCAGCT[A/G]TTCGTAAACTTATGC | 9678 |
| rs764005957 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023479 | ACCTGGTGTTCCCCT[A/G]TCTTTCTCCCTGACT | 9678 |
| rs764020397 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109421 | ATAAATTATATTTAA[A/T]ATGTTTATTTGATGA | 9678 |
| rs764021169 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007141 | GAGATTGCAGTGAGC[C/T]GAGATCGCGCCATTG | 9678 |
| rs764041152 | snp | A/G | 5.32505e-05 | 0.00515969 | intron-variant | PHF14 | GRCh38.p7 | 7:11071304 | TTACATTTGATCACA[A/G]GCTCCTGTGTAACAT | 9678 |
| rs764041387 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962735 | GGTTGGTAGCTTATT[A/C]ATTATTGTGTCAATT | 9678 |
| rs764047454 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959971 | ATTTATTTTTTTTAA[G/T]TTTTATTTTTTAATA | 9678 |
| rs764062006 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111190 | TTCAGGTTTAGTTTG[C/G]CTTTATCATCATCAT | 9678 |
| rs764088768 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010656 | TATATACACACACAC[-/AT]GCATAATCTGAAAAA | 9678 |
| rs764100241 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981927 | TAGATTTATCTTGTT[C/T]TGGTTTTGACTCAAT | 9678 |
| rs764107545 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039198 | TAGCAGTTTTAGATT[C/G]CCTGCCACATTTTTT | 9678 |
| rs764134894 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127320 | TGCCTTCTGTGGGTT[A/G]CTTGTGACTTCCTTT | 9678 |
| rs764140257 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101875 | TTACTTCTAATCACT[A/G]AAATTTCTCCACTGA | 9678 |
| rs764152135 | in-del | -/AC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005414 | TTTCTGTTACTTATT[-/AC]ATTGTCCAAGTTTGA | 9678 |
| rs764162145 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123926 | CCATCTCAAAAAAAA[A/G]AAAACTAGAAAGTAA | 9678 |
| rs764168818 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040134 | ACACTTTTTTTTTCA[G/T]TTGGTTGAACAGATG | 9678 |
| rs764200389 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011168 | CTGACATATAATGAC[A/G]TCTAGTTAATTAATG | 9678 |
| rs764219494 | snp | C/T | 1.66754e-05 | 0.00288746 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028702 | AGCTTTTGTGAAGAC[C/T]CTCGCTTTGCTAGAA | 9678 |
| rs764221357 | snp | A/G | 2.26956e-05 | 0.00336857 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982469 | TTTAGAAGAAGAACT[A/G]AATGAAGATATTAAA | 9678 |
| rs764224894 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125845 | ATTATAGTGTTATAC[A/C]TTCATTGAAATTAAG | 9678 |
| rs764252449 | snp | A/G | | | utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170276 | AGCTGCCATTTGCCA[A/G]TGACAGGAAGAGCAA | 9678 |
| rs764253179 | in-del | -/GA | 0.00213915 | 0.0326343 | intron-variant | PHF14 | GRCh38.p7 | 7:11035598 | TTTTATGACTCTTGG[-/GA]GTACAAATGTTCACT | 9678 |
| rs764261811 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061178 | TTAAACGTTTGTATG[C/T]GTTCTTTCAAATGGT | 9678 |
| rs764274041 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046300 | TTAATCATCTCTTAA[-/T]TTTTAGAAGACTAAT | 9678 |
| rs764298903 | snp | C/G | 4.28183e-05 | 0.0046268 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061964 | TCCCTTGTATGGCAG[C/G]AAAGAGTTCCTAGAG | 9678 |
| rs764302259 | snp | A/G | 2.89758e-05 | 0.00380619 | intron-variant | PHF14 | GRCh38.p7 | 7:11038905 | CTTGCTCCCTATATG[A/G]TTTTCAAAGAACAGA | 9678 |
| rs764305399 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127696 | AGTTTCACCTTTCCT[C/G]ATTCTTCAGACTTCT | 9678 |
| rs764322596 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151611 | TTCTTAACTGTAGCA[C/T]TGTGTCAGAGTTTTG | 9678 |
| rs764323958 | in-del | -/G | 2.88106e-05 | 0.00379532 | nc-transcript-variant, frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11169444 | AGCTGAAAGAAAAAA[-/G]TATATCTCAGGAGCT | 9678 |
| rs764333619 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114023 | TAGGTAGCACTGGGT[A/G]TATTTGCCATGTTCA | 9678 |
| rs764354909 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038930 | AACAGATTTTTGATA[A/C]AACTGTCATTTGACT | 9678 |
| rs764395416 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146663 | CATTTTTACAAAAGC[A/G]TTTAGAGAACTCTAC | 9678 |
| rs764397856 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975734 | CACCTCTTTTGAAAA[C/T]TTTAATAAAGTGAGA | 9678 |
| rs764415575 | snp | A/G | 9.29152e-05 | 0.00681535 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982575 | AAGAAGGAAGAAGAA[A/G]AAAATGGAGAAAGAC | 9678 |
| rs764416347 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073347 | ATTAACCAAAAGAAA[C/T]AGGCAGTAGGCCCCC | 9678 |
| rs764443412 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082016 | ACGTAGAATTCTAAC[A/T]GAAGACTCTGGATAT | 9678 |
| rs764463020 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020302 | AACCTGTTGCCCAGG[C/G]TGGTCTTGAGCTCCT | 9678 |
| rs764492310 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055598 | GCATTATTTCTTTTA[G/T]ATCATTATTTTAGAA | 9678 |
| rs764494625 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020999 | GAAAATAACGTACTT[G/T]ACGTGAATTTGTTTT | 9678 |
| rs764523429 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144932 | TAGAATTATGGTTGC[C/T]AGGAGGTAAGGAAAG | 9678 |
| rs764526251 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105646 | AGCACTTTGTAAGTT[A/T]ACATAAAATTAAGGA | 9678 |
| rs764582426 | in-del | -/AG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139546 | AAATTAAAGACAAAC[-/AG]AAATCATCAGCCTTT | 9678 |
| rs764584226 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164159 | TCTCCCTTCATTTTA[C/T]TGTTGTACCACCATG | 9678 |
| rs764606017 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103541 | AATATTTCATCACTC[A/G]ATCTTGAACTGATTT | 9678 |
| rs764623247 | snp | C/T | | | | | GRCh38.p7 | 7:10969472 | TTTCCCTAGGCACTT[C/T]ATCTCTTTACCCCCT | 9678 |
| rs764637300 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087493 | CTGCGCCTGGCCAGC[A/G]CTGTTCTTCTTTCTT | 9678 |
| rs764645955 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11066997 | GTTAAAAACTTTTGT[A/G]TGTGAAAGGACACCA | 9678 |
| rs764651990 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091745 | CCTGGGTGACGGAGC[A/G]AGACCCTTTCTCAAA | 9678 |
| rs764659073 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990155 | AATTTCTGAATTTCC[C/T]GGTACTTAAGGAGTA | 9678 |
| rs764660747 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966307 | CTAGCTCCCATCCTC[A/T]GGCAGGTAGTCCTGA | 9678 |
| rs764664266 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060744 | AGTTTTCTGCCTAAT[A/T]ACTTCCATAATATAA | 9678 |
| rs764708942 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118390 | CTAATTGCTTCTAGC[A/G]TGTTCCTTGGCAAGT | 9678 |
| rs764727201 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122055 | TGTGTTGCTTCTCTC[A/C]CTGTGTCCATGTGTT | 9678 |
| rs764770258 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016709 | GAGAATGGGGTATCC[A/G]TTTCTCAAACACTTG | 9678 |
| rs764773832 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020473 | AACCCCCGCCTCCTA[C/G]GCTCAAGCAGTCCTC | 9678 |
| rs764774820 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025483 | GAATCTATGCAGCAA[-/A]CTTCATTGTTTTATT | 9678 |
| rs764786936 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959350 | TTGCTATTACCTCCC[A/T]CCTATTTTCTAAATA | 9678 |
| rs764788245 | snp | A/G | 1.70356e-05 | 0.00291848 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051663 | CATGGAAGCAGATAT[A/G]GCCATGGAAACCCTA | 9678 |
| rs764797295 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130761 | GTAATAATGACACAT[A/G]TCCACCATTACAGTG | 9678 |
| rs764825959 | snp | A/G | | | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982412 | TGAAGATGCTTCAAA[A/G]GACAGTGGAGAAGGT | 9678 |
| rs764832370 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067195 | ACAGTAGCCAACAAG[C/T]ATATGAAAAGATGCT | 9678 |
| rs764860677 | snp | C/T | 1.65864e-05 | 0.00287974 | intron-variant | PHF14 | GRCh38.p7 | 7:11028855 | GTTGGTGAACATGTT[C/T]ACAAGATATCTTTTG | 9678 |
| rs764866358 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031949 | TACTCTGTTCTGTAG[A/G]AAATTATATTTGAAA | 9678 |
| rs764882794 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106936 | GGCATAAAAGATAAT[A/G]TGATTATCACAATCA | 9678 |
| rs764898637 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11143316 | TGTAGTGACTAGGTC[C/T]CATTGTGTTGTCCAG | 9678 |
| rs764901528 | in-del | -/TT | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958184 | GCTTTCATGGTACTC[-/TT]TTGTGCATTTAAACA | 9678 |
| rs764921582 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978500 | TTGAGACTTGGAATT[-/G]TTTTTTTATATTTGG | 9678 |
| rs764927286 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10978001 | CTTCTATTAACCAGA[C/T]AGATTAGCCATGCTC | 9678 |
| rs764929497 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131832 | TACGTTCTCTCTCTG[-/TC]TCTCTCTCTCATTCT | 9678 |
| rs764951487 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071337 | TCAGTAGCATCTTCT[A/T]CCAAGCTATTCTGTG | 9678 |
| rs764952236 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004805 | CTTTGGGAGGCCGAG[C/G]TGGGTGGATTACTTG | 9678 |
| rs764959625 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032588 | AGATGGATTTTGTTT[C/G]TTAGGAGTAGAGTTA | 9678 |
| rs764964734 | snp | C/T | | | downstream-variant-500B | LOC107986767 | GRCh38.p7 | 7:10968648 | GTATACTGGTTCTGA[C/T]GGTTGTGTGTTTGTT | 9678 |
| rs764965665 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046548 | TTACATTTTTTTATT[A/G]CCTCTTCTTCCCATT | 9678 |
| rs764967707 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151830 | ATTGAGAAAGCCACT[A/C]TATGAGTGTATTTTA | 9678 |
| rs764977461 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072757 | TTGGCTCATAGTTCT[C/G]CAGGCTGTTCAAGCA | 9678 |
| rs764978234 | snp | C/G | 0.000163519 | 0.00904062 | intron-variant | PHF14 | GRCh38.p7 | 7:11036974 | TAAAATTCGATATTT[C/G]ATTTAAATAGAGAGA | 9678 |
| rs764986885 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009832 | AGCTTGCACAACACC[A/G]TTCTTCCAGATTACA | 9678 |
| rs765001238 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124228 | ACCTAAAGATACTAC[A/G]TTTCTGCTCATGTTT | 9678 |
| rs765042746 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157140 | ACTGGGGCATGAGAT[A/C]CTCTAGGCAATAAAA | 9678 |
| rs765042875 | snp | C/G | 1.80218e-05 | 0.00300176 | intron-variant | PHF14 | GRCh38.p7 | 7:10983166 | AGTAATGAGGTAGAT[C/G]AACCCAATTTTTATA | 9678 |
| rs765045389 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046939 | GTGGAGGAGAAAAAA[A/G]TAAATCATGAATTAT | 9678 |
| rs765047299 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031696 | GAGTTTGAGGCTGCA[C/T]TGAACTATGTTCTCA | 9678 |
| rs765062289 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960229 | ATTTCTCCCAACACT[A/G]TCCCTTCTCCAGCAC | 9678 |
| rs765068189 | snp | G/T | 1.77577e-05 | 0.00297969 | intron-variant | PHF14 | GRCh38.p7 | 7:11071237 | TAGTACACTAGCTCT[G/T]ATATTCAAAGACTAT | 9678 |
| rs765082007 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999418 | CAATGTCTCACATCT[A/G]TAATAGTAAAGCAAC | 9678 |
| rs765099588 | snp | A/T | 1.65954e-05 | 0.00288053 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990773 | TTCTGATTTGCTGTG[A/T]TTGTCTGGGAGATAA | 9678 |
| rs765148163 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11015714 | TAAGTGGTCAGTAAA[G/T]GTCTCCTTACTCTTA | 9678 |
| rs765148644 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058578 | AGTTAGTATGTAGTA[C/T]GGAGCTACCAAATTA | 9678 |
| rs765174179 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997894 | TTTCTGCCATATTCC[A/G]CTGTTCACACAAGCC | 9678 |
| rs765174940 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989364 | AAAAAATAATAAAAC[-/AT]ATTTATGAAAAATAT | 9678 |
| rs765177536 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059673 | CAGCTACTTGCAAGG[C/T]TGAGGTGTGAGAATC | 9678 |
| rs765182036 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11169170 | TCAGTGGCAGGTGTT[G/T]CCAAAGTAATTTTTA | 9678 |
| rs765195523 | snp | C/T | 5.20134e-05 | 0.00509941 | intron-variant | PHF14 | GRCh38.p7 | 7:11013944 | TTCATATGTTTGCTT[C/T]ATAATGTGTCTGCCT | 9678 |
| rs765198778 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100140 | TACTCCTGTATCAAG[A/G]TTTTCATTTGTATTG | 9678 |
| rs765231755 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039495 | GAATGCCTTTTTTAG[A/T]ACTGTGTATATAATT | 9678 |
| rs765254597 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027191 | ATGTCTCTGTTCACA[A/G]TGTGGACATCCTTTA | 9678 |
| rs765260547 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992692 | AACAAAAAAAGGCAT[C/T]CTCTTACATAACCAC | 9678 |
| rs765266596 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101962 | TTTTTAAAAGAAAGT[C/T]AGCTTAGGCACAGGA | 9678 |
| rs765269674 | in-del | -/GC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089317 | GATATGTTCATTGAG[-/GC]ACAAACAATTCATTG | 9678 |
| rs765287418 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114116 | CAATTGCAAATAAAT[G/T]TAGATGGTAAAATGT | 9678 |
| rs765288240 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098517 | ACAGCTCTACTATGT[C/G]TCACTTCCCCCAACC | 9678 |
| rs765330247 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103735 | TAATCAAAAGCAATT[C/G]TAATTGTAAAGCTGC | 9678 |
| rs765341663 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017878 | CAATGTTTTCTTGTA[C/G]TATTTTCATAGTTTG | 9678 |
| rs765350667 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988781 | GTCTAGTTTGTGCCA[-/G]GAACATTCTTGCCAT | 9678 |
| rs765350771 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064292 | GAATTGGCACTGTTA[C/T]TGTTTGAAAATCACC | 9678 |
| rs765373525 | in-del | -/G | 0.00014108 | 0.00839763 | intron-variant | PHF14 | GRCh38.p7 | 7:11023018 | TGCTTGAAAGAGAAA[-/G]GTTTTACTTGTTAGT | 9678 |
| rs765416948 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074431 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 9678 |
| rs765418237 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128354 | ATTTTTATCTTTCTC[C/T]TCTCAGCCTTAAAAA | 9678 |
| rs765426950 | in-del | -/TAA | 1.84708e-05 | 0.00303892 | intron-variant | PHF14 | GRCh38.p7 | 7:11040790 | GGCAAGTAATGAAAT[-/TAA]TAATGATAGAATAAT | 9678 |
| rs765453653 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977704 | TGAGTAAGTCCTAAA[A/G]TAGGATATATATGCA | 9678 |
| rs765457635 | snp | A/G | 8.15627e-05 | 0.00638551 | intron-variant | PHF14 | GRCh38.p7 | 7:11038900 | CAGTTCTTGCTCCCT[A/G]TATGATTTTCAAAGA | 9678 |
| rs765460133 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022101 | TAATATATTAAAAAA[A/G]GTTCAGAGCAGTTTT | 9678 |
| rs765487069 | in-del | -/AAGGAAAAAGAA | 8.29084e-05 | 0.00643796 | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10982614 | AAAAAGGAGAAAGAG[-/AAGGAAAAAGAA]AAGGAAAAGGAGAAA | 9678 |
| rs765491880 | in-del | -/GAG | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956516 | TTGGGAAAGTGTAAT[-/GAG]GAGTTGAATAGTGTC | 9678 |
| rs765510832 | snp | A/G | 4.72746e-05 | 0.00486159 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022952 | AGTAACACTAACGGA[A/G]ATGAACTATTCCAAA | 9678 |
| rs765555840 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11062986 | TCAAAAAGAATAAAC[A/G]TATTGATAAAACAAA | 9678 |
| rs765566785 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133588 | CATTAGAGGAAGTTA[A/G]GGATCAGAAGAGGAC | 9678 |
| rs765571287 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966070 | AGGTGACACCCCACC[A/C]TGCTTTGGCTTGTCC | 9678 |
| rs765580500 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011371 | GTGTTTACCAGTTCA[A/G]ATAATCACATGATCT | 9678 |
| rs765585985 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068487 | GATTCCTAGAGTAGT[C/T]AGATTTATAGAGACA | 9678 |
| rs765604795 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985886 | TCCAACTCCTGACCT[C/T]AAGTGATCCACCTGC | 9678 |
| rs765628391 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11040336 | GCTGAAGAAAATAAA[G/T]GGCCTCAATATTCTT | 9678 |
| rs765632919 | snp | C/G | 1.7074e-05 | 0.00292177 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982755 | AACACATCCCCTTCT[C/G]TTCCCACTACGACAA | 9678 |
| rs765636641 | snp | C/T | 1.66319e-05 | 0.00288369 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028712 | AAGACCCTCGCTTTG[C/T]TAGAACTGGGGTTTG | 9678 |
| rs765639713 | snp | C/T | 0.000129096 | 0.00803314 | intron-variant | PHF14 | GRCh38.p7 | 7:11111343 | TATAAATCTGTTTAC[C/T]CTGCAGGTGTGATGA | 9678 |
| rs765664337 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021313 | TTTTTTTAAATTGTA[C/G]ATTTGTCTTAATTAC | 9678 |
| rs765671030 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127438 | AGTCTTGCTCTTTAA[C/T]GGGCCCACATTTTGT | 9678 |
| rs765687172 | snp | A/T | 5.89223e-05 | 0.00542749 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990769 | CATATTCTGATTTGC[A/T]GTGTTTGTCTGGGAG | 9678 |
| rs765728975 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001073 | AATTTATTTTTGTTA[C/T]GAGTATACGGTCTGT | 9678 |
| rs765735726 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152991 | GGAAAGGTCAGAAGG[A/G]CCTGATGATGTACTT | 9678 |
| rs765755806 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984863 | ACTTTAGTAAATAAA[A/G]GGACCTTTTATGTTT | 9678 |
| rs765769130 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153130 | CCTGTATAAAGAATA[G/T]GTATACAATTATAAA | 9678 |
| rs765797097 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073407 | ATTAAACCTTAAAAG[A/C]TTCAAAACAATGTCC | 9678 |
| rs765837672 | snp | C/T | 3.09114e-05 | 0.00393125 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111461 | ATGTGATTCTTCATC[C/T]TCCAAGGTAAGGGGA | 9678 |
| rs765845329 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121371 | AAAAGAAAACCTTAC[A/G]CTTAAGTAAGGAAAT | 9678 |
| rs765919351 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006097 | TCTTAGTCAAAAGAT[A/G]AGTGTATTTAAACTT | 9678 |
| rs765921632 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10995138 | CAGGGTGCAGATTGG[C/T]GTGTTACAAACCTTG | 9678 |
| rs765931928 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119790 | TCTTCAAGAAAACTT[A/T]CAAATCTAAGCCAAG | 9678 |
| rs765934071 | in-del | -/TAAAT | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955919 | CATGGTGAGGTTAAA[-/TAAAT]TAAATCAATAATGGA | 9678 |
| rs765941476 | snp | C/T | 1.66156e-05 | 0.00288228 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10990764 | TGGACCATATTCTGA[C/T]TTGCTGTGTTTGTCT | 9678 |
| rs765959134 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985979 | TTTTTTAAATGTTTA[G/T]TTTTTTTGAGACAGA | 9678 |
| rs765964936 | snp | A/G | | | | | GRCh38.p7 | 7:10970333 | CCCAGTACTTTGAGA[A/G]GCTGAGGTGGGCGAT | 9678 |
| rs765973682 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006688 | TGGGGGAGCTCTTCC[A/G]AGGATATCTGGGCTG | 9678 |
| rs765976413 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078579 | GCTTCAGAAGTTAAG[A/G]AGAGAAAGAAATTCA | 9678 |
| rs765993776 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068833 | TTTTAACCATGTTGC[A/G]TCTTTCAATTTATGA | 9678 |
| rs766000421 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096076 | TAAAGGTTTATTTTA[A/G]ATAAGGAATAAAGAG | 9678 |
| rs766013629 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070001 | TTTGATAGAATTCTC[C/T]GGTGATACCATCTGA | 9678 |
| rs766022229 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138618 | AAATAAAACAATAAC[-/AT]ATAAATCATATACTT | 9678 |
| rs766022927 | snp | G/T | 5.07653e-05 | 0.00503786 | intron-variant | PHF14 | GRCh38.p7 | 7:11061949 | TGTTTTATTTTATTA[G/T]CCCTTGTATGGCAGG | 9678 |
| rs766030646 | snp | A/G | 1.76983e-05 | 0.0029747 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983150 | CCTATCTCAAAGCAA[A/G]AGTAATGAGGTAGAT | 9678 |
| rs766035630 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020803 | TCATATGTAAATGAA[C/T]AACCTCCTACTCAAC | 9678 |
| rs766042021 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108319 | TGTTTATCACCAAAA[C/G]TATTGACTTCAAGAT | 9678 |
| rs766044810 | in-del | -/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107712 | TATTACATAGACATT[-/T]GTGTTATTTAATAAA | 9678 |
| rs766050609 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076104 | AGATCGTGCCGCTGC[A/C]CTCCAGCCTGGGCAA | 9678 |
| rs766059393 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100243 | TTGAAAATAGGACTG[A/G]ACACAAATTTTGAAA | 9678 |
| rs766072232 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959405 | TCACCAGCTGGAAAC[C/T]TCTATGGGCAGCGGC | 9678 |
| rs766088860 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050029 | TAAATAATTGGAAAT[G/T]TTAAGATATTTAAAT | 9678 |
| rs766122744 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025574 | CGAGGTGGGTGGATC[A/G]CGAGATCAGGAGATC | 9678 |
| rs766143037 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140003 | CAGAGGTCTTTGACT[A/G]GAACTCACAGTAAGA | 9678 |
| rs766145449 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112798 | ATTATAAATATTTGT[A/G]TGAGGATTATTAAGA | 9678 |
| rs766157422 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023075 | TTGACTGCAGAAATG[C/G]TTACTAGGAATCATT | 9678 |
| rs766175764 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073199 | TCAAAAGTCCAAAAT[A/C]CAGTGTCTTACTGGG | 9678 |
| rs766185684 | in-del | -/T | 7.95007e-05 | 0.00630429 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169504 | AAAGATTTTCTGTAG[-/T]TGTTTTTGAAAAGTT | 9678 |
| rs766265213 | snp | C/T | 1.79686e-05 | 0.00299733 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982430 | CAGTGGAGAAGGTTC[C/T]TGTAGTGATTCTGAA | 9678 |
| rs766267807 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064212 | TTTATATAAAATTTC[A/G]TATGTTTAATAAAAG | 9678 |
| rs766274546 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112424 | TAAAAACTGCAAAAA[A/G]ACATTTGGTTATAGA | 9678 |
| rs766296399 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005432 | TTGTCCAAGTTTGAC[C/G]AGTGAGAGTCCTTTA | 9678 |
| rs766316879 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007235 | GCTTAGTTATTAGGT[C/T]CTCTTTTTTTCTCAT | 9678 |
| rs766324507 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11066220 | AACCAGCAAGAATTC[A/G]TATGTATTACATTTT | 9678 |
| rs766325966 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114229 | TTTTGCCTAGAAGTT[G/T]AGATAATACATAGCA | 9678 |
| rs766331871 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989965 | CTAGCTAGATGTATT[C/T]ATTACCAGTTTACAC | 9678 |
| rs766334418 | in-del | -/CT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086108 | ATTCTCCTTCATCAA[-/CT]CTCTCCTGGACCGTT | 9678 |
| rs766336502 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164239 | CATCTTCTCTTTGTA[C/T]TCATAGAGTCTTGTA | 9678 |
| rs766344759 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132541 | GCTATTGTGAATAAT[A/G]CTGCAGTGAACATGA | 9678 |
| rs766359586 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11061023 | TGTTCCTTGATCTCA[A/G]CTGTCAAAGTAATTT | 9678 |
| rs766362300 | in-del | -/AAAGAAAAAGGAGAAAGAGAAGGAA | 9.23489e-05 | 0.00679455 | frameshift-variant, intron-variant | PHF14 | GRCh38.p7 | 7:10982595 | TGGAGAAAGACCTAG[-/AAAGAAAAAGGAGAAAGAGAAGGAA]AAAGAAAAGGAAAAG | 9678 |
| rs766379366 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11088823 | ATCAGTATTAAAAAA[C/T]TATGTATCTCCTATA | 9678 |
| rs766389910 | in-del | -/TTTCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150566 | TCTTTCTTCTCATTC[-/TTTCA]TTTGCATCATTAAAT | 9678 |
| rs766398314 | snp | A/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11149870 | ACCTCTTTTACAATT[A/T]TTATACTTCATATCT | 9678 |
| rs766428429 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019348 | GGTAAAATTCAGCAG[C/T]GAAGCCATCAGGTCA | 9678 |
| rs766441109 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135689 | TATAGCTTTCAATTC[A/G]TTGCCGTGGTTATAT | 9678 |
| rs766441339 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090777 | TATGTAGAGGGTTTA[C/T]AAGAGACAGAAGAAT | 9678 |
| rs766444459 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087685 | TTTGACTCCCAGTGG[C/T]CTTCTCACTTAATAA | 9678 |
| rs766474452 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11029029 | AACATAATTTTTATA[A/G]TGAGATCTGACAGAT | 9678 |
| rs766475546 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104362 | GTAAGAAAACTTGAA[C/G]TAACTAGAATAGAAT | 9678 |
| rs766477462 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104387 | TAGAATACTTTCTCC[A/T]AATAATCTCTTAAAT | 9678 |
| rs766513555 | snp | C/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972863 | AACCTAAGGATGTGT[C/T]ACTCCGACTTCCTAA | 9678 |
| rs766515507 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11014423 | ATCCAAGGAATGACA[A/G]AATTGGAATGATGAC | 9678 |
| rs766519763 | snp | C/T | 2.58041e-05 | 0.00359185 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013778 | TGGAGAGAGTGACTC[C/T]ATTATGAGTTCAGCT | 9678 |
| rs766548988 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961551 | GATTGTCTTGGCTAT[A/G]CGGGCTGTTTTTGGT | 9678 |
| rs766549987 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992611 | GAGGTTGCAGTGAGC[C/T]GAGATGGTGCCACTG | 9678 |
| rs766550483 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082159 | GAGTAGCCTAGGCAA[G/T]GTATCGAGACCTTGT | 9678 |
| rs766592086 | snp | A/G | 1.65778e-05 | 0.002879 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035716 | GGAAGAGAAAAAACT[A/G]CTTGGCTCTACAGTC | 9678 |
| rs766599226 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991159 | CCACACCTAATTTTT[C/G]TGTTCTTTTTTATTT | 9678 |
| rs766599587 | snp | A/G | 6.96161e-05 | 0.00589942 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982657 | AGAAGGAAAGAGAGA[A/G]GGAAAAAGAAAAAGC | 9678 |
| rs766609232 | snp | G/T | | | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982835 | AAACCGACCACTTCT[G/T]GATTTTGTGTCCATG | 9678 |
| rs766612405 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084406 | CATCATCCATACTTC[C/T]TTCCTCTAAGTACAA | 9678 |
| rs766613005 | snp | C/T | 5.4799e-05 | 0.00523417 | intron-variant | PHF14 | GRCh38.p7 | 7:11111328 | TTAGATACACCTACC[C/T]ATAAATCTGTTTACC | 9678 |
| rs766617072 | snp | A/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957731 | AAAAACAAGTTGTAT[A/T]ACAACATGGATGAGC | 9678 |
| rs766635079 | snp | C/T | 2.33244e-05 | 0.00341492 | intron-variant | PHF14 | GRCh38.p7 | 7:11038883 | CCAATTGCTGTCTCC[C/T]TCAGTTCTTGCTCCC | 9678 |
| rs766693140 | snp | C/G | 1.65814e-05 | 0.00287931 | intron-variant | PHF14 | GRCh38.p7 | 7:11028844 | TTAAACCCATAGTTG[C/G]TGAACATGTTCACAA | 9678 |
| rs766730762 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975873 | TTCTGGTTTTCCCTT[G/T]TCTTTTTCCTGCTAG | 9678 |
| rs766742438 | snp | C/T | 6.4933e-05 | 0.00569757 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040737 | TAAAAAAGAAGGAGG[C/T]ACACAAAAGACATCT | 9678 |
| rs766747029 | snp | C/G/T | | | | | GRCh38.p7 | 7:10970992 | TTGGCAAACTAGGAA[C/G/T]AGGAAAGTTCCTCCA | 9678 |
| rs766766816 | snp | C/T | 1.6574e-05 | 0.00287867 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028757 | CAGGGATGTGCAGAG[C/T]CTATTTCCATGTGAC | 9678 |
| rs766767343 | in-del | -/TAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005122 | TTTTCTATTTGTAAT[-/TAA]TGATAAATCTGTGGG | 9678 |
| rs766781052 | snp | C/T | 6.7914e-05 | 0.00582687 | intron-variant | PHF14 | GRCh38.p7 | 7:11042856 | GTTTGAATTGATTTA[C/T]TCTTAGTTTCAGCAG | 9678 |
| rs766782854 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059900 | TTTGAGACAAAGTCT[C/T]GTCCTGTTGCTCAGG | 9678 |
| rs766797980 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003048 | CAGCTTCAAGGAATT[C/T]TCCTGCCTCAGCCTC | 9678 |
| rs766806784 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122828 | GTAGTAGCTTCAGTA[A/G]TGTTTTCTTGGTCAC | 9678 |
| rs766824353 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966199 | AGGGAGCTGTAGACC[A/G]GAGCTGTTTCTATTG | 9678 |
| rs766827749 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11115442 | GCTAGTACTATAGAA[C/T]AGGTACATAAAACGT | 9678 |
| rs766831139 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987056 | TGTCACCTGATTTTT[G/T]TGAATTAAAATGTAA | 9678 |
| rs766851752 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116446 | CACAGCCACACTTAC[A/G]TCTATATTTTTGCTT | 9678 |
| rs766858831 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161247 | AAAAAAAATATTTTT[A/C]TCTCAATACAAGTTT | 9678 |
| rs766872272 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162702 | GGAAATCCAAAGTCT[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs766882601 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023441 | AATTGATATATGTTA[C/T]GTGTGTTCTGACTGC | 9678 |
| rs766909167 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11109800 | TAGTAAATAAAGTAC[A/T]GTTGGTCCTATTGGT | 9678 |
| rs766912799 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992849 | GTATTGCATTTAATC[A/G]TCATGTCTGTTTAGT | 9678 |
| rs766920586 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127650 | AGGGACTTCCTTTAA[A/G]GTACCTCTTCTAAAG | 9678 |
| rs766934433 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042188 | GAAAAGAGACTCATG[A/T]ATACTTGCAGTATAT | 9678 |
| rs766934831 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041854 | TTTATTTATTTTGGC[-/T]TTTTAAGTGTGTGTG | 9678 |
| rs766957228 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075242 | CTGCACCTGGCCTTT[C/G]AGACATCTTTATAGC | 9678 |
| rs766968534 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035411 | AATATCTTTAAACCT[A/G]CAGGCCCTTTAAAGA | 9678 |
| rs766969396 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155664 | TTTCTTCCATTGAAT[A/G]TGTCATAATTGCAAT | 9678 |
| rs766983193 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963739 | GTCTCTAAGGACTTG[C/G]TTTATGAATCTGGGT | 9678 |
| rs766988009 | snp | A/G | 1.77502e-05 | 0.00297905 | intron-variant | PHF14 | GRCh38.p7 | 7:11071283 | AAGTCCATGTTACCT[A/G]TTTATTTACATTTGA | 9678 |
| rs767014613 | in-del | -/CT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048563 | GGCAATAGTGCAAGA[-/CT]CTGTCTGAAAACAAA | 9678 |
| rs767016640 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965384 | CTTGTTTGCCTGGGT[A/G]TCACCAGCGGAGGCT | 9678 |
| rs767016656 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131436 | ATATGCTTATTTGCC[-/AT]ATATATATATCTTTT | 9678 |
| rs767037749 | snp | A/T | | | downstream-variant-500B, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11170029 | AGGGAAAGACTAAAA[A/T]GAAATGATAATTTGA | 9678 |
| rs767048364 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042349 | GAGAAAAAATGAACT[A/G]ATGTGAAATGGGTTT | 9678 |
| rs767088541 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149318 | ACTGACTCGTCATGG[C/T]AAACAATTCCTGACT | 9678 |
| rs767089833 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085605 | ATTTAACATTGGTGA[A/C]CAACCTTCCTCCTTA | 9678 |
| rs767111057 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996731 | GATAGAAGGACCACA[C/T]TACCTAAATAAATCC | 9678 |
| rs767149253 | snp | G/T | 3.88267e-05 | 0.00440589 | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169501 | AATAAAAGATTTTCT[G/T]TAGTGTTTTTGAAAA | 9678 |
| rs767167134 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006173 | ACCAACAATGCACAA[A/C]CTACTTGATAACATT | 9678 |
| rs767168241 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11058115 | TCCTACAGTTTTATT[A/G]TTGCTAAAGTAGTTT | 9678 |
| rs767175335 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988430 | ACCTTTTTTCCAGGG[A/C]TGAATAATTTTAATT | 9678 |
| rs767181811 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055258 | GTTACTTTAAAATTG[G/T]TGTTTATACTTGTGG | 9678 |
| rs767189289 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980726 | TGTAAATAGGATTTA[G/T]ACTTTTCTCCGCAGA | 9678 |
| rs767194587 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988169 | TTCCCTATTTCCCTC[-/TT]TGCGTTACATTTCTA | 9678 |
| rs767205036 | in-del | -/CGTATATATATATACACGTATATATATATACG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122428 | ACATATATATATACA[lengthTooLong]TATATATATATATTG | 9678 |
| rs767209483 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142933 | GAATTTTCTTCCCAC[A/T]CAGAAATTGTAGCCC | 9678 |
| rs767213770 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089276 | TAATTTCAGTTAGTT[A/G]TGCAGTATACTAAAT | 9678 |
| rs767216081 | in-del | -/AA | 2.86611e-05 | 0.00378546 | frameshift-variant, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11042698 | TGTGGGATTTGTAAG[-/AA]AAGAACCATGATCAG | 9678 |
| rs767221796 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023514 | TGGGGCCTCTCTGTT[C/T]GCTGAGACACAGTGA | 9678 |
| rs767229355 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114786 | AGAGACACATACACT[C/T]ATACACAAAACATAC | 9678 |
| rs767273693 | snp | A/G | 1.65754e-05 | 0.00287879 | missense, nc-transcript-variant, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10974841 | TCTTCACAGTGGATC[A/G]CAGCTCCAAGAGGAG | 9678 |
| rs767275087 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000746 | TTAAGAGTTCCTTGT[A/G]TATTTTGGATATCAG | 9678 |
| rs767277374 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992347 | GCATGAGCCACCGTG[C/T]CTGGCTGACAGTATG | 9678 |
| rs767278428 | snp | A/G | 5.17621e-05 | 0.00508708 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983122 | ATGAGGAACTGACCA[A/G]TGATAGCCTGACCCT | 9678 |
| rs767314643 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047146 | CAATCGCAACTCACC[A/G]CAACTTCTGCCTCCT | 9678 |
| rs767333225 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158323 | ATGTCCCACAAGTTG[A/G]GTTTGCTTAATATTT | 9678 |
| rs767344177 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103156 | GAAGCATATGACATT[A/C]TATTTTTGACTTATT | 9678 |
| rs767345500 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071172 | AATCTCTTTCAATCT[C/T]ACTTTTCTTATTTTA | 9678 |
| rs767359106 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097828 | TTTGTCCCTTCCTCT[-/A]ATTCTATCTTCTCCT | 9678 |
| rs767361590 | snp | C/T | 0.000166227 | 0.00911514 | intron-variant | PHF14 | GRCh38.p7 | 7:10974342 | AAGTGTATCCGAGGC[C/T]TCTGCGGCGAGAGGT | 9678 |
| rs767372156 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018680 | ACAACATTATATTAC[C/G]TGCTAACAAGAATAA | 9678 |
| rs767395016 | snp | A/G | | | | | GRCh38.p7 | 7:10970360 | CGATCAGTTGAGGTC[A/G]GGAGTTGAAGGCCAG | 9678 |
| rs767400957 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002615 | CCCAGCTAATTTTTT[A/G]TATTTTTATTAGAGA | 9678 |
| rs767409695 | snp | G/T | 1.71155e-05 | 0.00292531 | intron-variant | PHF14 | GRCh38.p7 | 7:11013927 | TGTCCTAATTATGTT[G/T]GTTCATATGTTTGCT | 9678 |
| rs767416570 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166648 | ATTTTGATAATGTTA[C/T]AGCAATTTTAATATT | 9678 |
| rs767426652 | snp | C/T | 1.77533e-05 | 0.00297932 | intron-variant | PHF14 | GRCh38.p7 | 7:11071252 | GATATTCAAAGACTA[C/T]ATATTCCATGTTCCC | 9678 |
| rs767456204 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147546 | CCCAATAGTTATGCC[A/G]CTGTCTGAATCTTAC | 9678 |
| rs767459974 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11017791 | ATATCTTTCGTCTGT[A/T]TTTGCTTCGGTTGCT | 9678 |
| rs767471168 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034164 | CATTAGATTTTTTTT[C/T]CTTTCTGTTCTTATA | 9678 |
| rs767493185 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121472 | CCCACTGCCTACTTA[A/G]TTGCAGGGGTTATGT | 9678 |
| rs767493317 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006967 | ATCACCTGAAGTCAG[G/T]AGTTTGATACCAGCC | 9678 |
| rs767510817 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11049538 | CTACATTTCACTCAA[C/G]TGATAGAAATGATCA | 9678 |
| rs767519963 | in-del | -/AT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021252 | CAGTCAGCATCTGTC[-/AT]ATAATAGCTCCAAGC | 9678 |
| rs767523504 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079823 | ATTTTTTTTTCTTCA[C/T]TGTCGTCATCCTGTT | 9678 |
| rs767531141 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084717 | TTAATGGATAATATT[A/G]TCTTGTTACCCACTG | 9678 |
| rs767548090 | snp | G/T | 0.00151469 | 0.0274782 | intron-variant | PHF14 | GRCh38.p7 | 7:11061779 | TTTGTTTTTTTTTTT[G/T]TTTTTTTCCAGAGAA | 9678 |
| rs767548273 | snp | A/T | 1.672e-05 | 0.00289132 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035772 | AGAGAGAAGCAACTA[A/T]CACCAGAAGCACAGG | 9678 |
| rs767555878 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963180 | GTGATGTTAGGGTGT[C/T]GATATTAGATCTTTT | 9678 |
| rs767557169 | snp | A/G | | | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983152 | TATCTCAAAGCAAGA[A/G]TAATGAGGTAGATCA | 9678 |
| rs767581525 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009920 | GTTTAAAACTCTGTG[C/T]AAATGTGCACGTTTG | 9678 |
| rs767594294 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083011 | AAAACTAGCTCTCTA[A/G]CTTATCACAGATGAC | 9678 |
| rs767607967 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime | PHF14 | GRCh38.p7 | 7:10973838 | CGCCCTCAATTCCTG[C/G]TGCTCTCAGGGCTGC | 9678 |
| rs767612618 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032489 | AGTTTTACCCAGGGA[A/G]CTTTGTTTAAAAAAA | 9678 |
| rs767613882 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124380 | ACTCTTACATAATCT[A/G]TTTTTAAGTGCTGTA | 9678 |
| rs767642144 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099252 | TATTTATTGTATCAC[-/A]TTCTTTGACTTAAAA | 9678 |
| rs767647737 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964082 | CCCATTTACATGTTG[A/G]CTAATATTGTTATGT | 9678 |
| rs767651940 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11136696 | CAAATGTTTTGAATA[C/T]GTAGGGTAAAGAAAA | 9678 |
| rs767688682 | in-del | -/GGCACTACTC | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973719 | TCTCTGCTCCGCCTT[-/GGCACTACTC]GGCTCCGCTCGCCTC | 9678 |
| rs767711303 | snp | C/T | 7.35429e-05 | 0.0060635 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036996 | ATAGAGAGAAATATG[C/T]GCATGATTCAAATTC | 9678 |
| rs767717515 | snp | A/G | 3.55334e-05 | 0.00421491 | intron-variant | PHF14 | GRCh38.p7 | 7:11051806 | TTTTATTTATCATAA[A/G]CATCATACAATTCTG | 9678 |
| rs767733294 | snp | A/G | 3.01418e-05 | 0.00388201 | intron-variant | PHF14 | GRCh38.p7 | 7:11022987 | GTGCCAAGGTGAGAC[A/G]CAAAGCATTTTTGAT | 9678 |
| rs767737270 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162881 | AGCTGCCACAAAGAA[A/G]TAAAAAGTTACAGGA | 9678 |
| rs767739962 | snp | A/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10971915 | TATCCACTCTTGGTG[A/G]TATATATATTAGTAC | 9678 |
| rs767747204 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11100030 | AACACTTGGAGTCAT[A/G]CAAAACAAGTATGAT | 9678 |
| rs767755844 | in-del | -/CTTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997104 | TTGGTCCTTCTATCC[-/CTTT]CTGTCTGTATTTAAT | 9678 |
| rs767762040 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11085953 | TTGGGTTCAGATTTT[C/T]ACCCAGCATTTATTA | 9678 |
| rs767770715 | snp | A/G | 1.94169e-05 | 0.00311578 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982618 | AGGAGAAAGAGAAGG[A/G]AAAAGAAAAGGAAAA | 9678 |
| rs767779742 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999697 | CTGCTTCAGATGAAT[A/G]GCCTCGGTACTGGAA | 9678 |
| rs767812193 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111584 | AACCAACATTTTAAC[C/G]AGTACACCTTAAGAA | 9678 |
| rs767828750 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10957473 | TTGTATGCTTTACGA[C/T]GTTGCTCTACTGATG | 9678 |
| rs767832219 | snp | C/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149112 | AGTTAAGTGCCAAAG[C/G]AGGATTCAAAATAAG | 9678 |
| rs767832705 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038936 | TTTTTGATACAACTG[C/T]CATTTGACTAACCGA | 9678 |
| rs767833026 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081997 | TTTTAAAAGCTAATA[C/G]TGTACGTAGAATTCT | 9678 |
| rs767854372 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11091829 | AACTGTTAAACACTT[A/C]TTCTTTACCCCTTAA | 9678 |
| rs767856551 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131833 | CGTTCTCTCTCTGTC[-/TC]TCTCTCTCTCATTCT | 9678 |
| rs767856720 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086360 | TAAATTTAGATCATC[G/T]CAGGTCATTTTTTCT | 9678 |
| rs767878425 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993443 | TCACTGTGGGAATAT[C/T]TCCAGTTACTGTTAT | 9678 |
| rs767880024 | snp | C/T | 7.25111e-05 | 0.00602082 | intron-variant | PHF14 | GRCh38.p7 | 7:11042648 | TCACTATGATAATTA[C/T]TATTGAAATCTTTAC | 9678 |
| rs767890645 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956688 | AGGGAGGGACACACA[C/G]ACACAGACACACACA | 9678 |
| rs767900963 | in-del | -/TTTAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076328 | TGCTGTTTTATTTTC[-/TTTAT]TTTATGGTTTTCAAT | 9678 |
| rs767921401 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994318 | GTGGCATGTGCCTGT[A/T]GTCCTAGTTACTCAG | 9678 |
| rs767942364 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977718 | AATAGGATATATATG[A/C]ATTATTAGAATTATG | 9678 |
| rs767951404 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003757 | TATTCTTAATTATAA[C/G]TGACATATGAGTAGA | 9678 |
| rs767957705 | in-del | -/AGA | 0.000282395 | 0.0118793 | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10982457 | TGAAGAAAATATTTT[-/AGA]AGAAGAACTGAATGA | 9678 |
| rs767971514 | snp | A/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116671 | TAACTTTTAAACTGA[A/G/T]TTGTTCAGGAAGAGG | 9678 |
| rs767972374 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097269 | CAGGCGCGAGCCACC[G/T]TGCCCAGCCAGGACT | 9678 |
| rs767994498 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034800 | GTGATCTGCTTGCCT[C/T]GGTCTCCCAAAGTGC | 9678 |
| rs768001929 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11019537 | TGGCATATAGTTGCT[C/T]ATAGTAGCTGCTAAT | 9678 |
| rs768002015 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031140 | GGAACTTTTCAAAAG[A/G]CTATATCAAGTTGGA | 9678 |
| rs768017565 | snp | C/T | 2.02251e-05 | 0.00317996 | intron-variant | PHF14 | GRCh38.p7 | 7:10982363 | TTTTTTTTCTCATAT[C/T]TTCAACAGATTCTGA | 9678 |
| rs768019943 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989574 | AGGTTTAAATGCAAA[C/T]AAGCAGACCCTCTTC | 9678 |
| rs768050553 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994154 | AGTGAATGTAAAGAT[C/G]TCAGCCAAGCACAAT | 9678 |
| rs768068133 | in-del | -/AAAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11124956 | AAGATATTTTAAAAC[-/AAAT]AAGTTGATTAAAGAT | 9678 |
| rs768078737 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981610 | GCTCATTTTCAGGAT[A/G]GACTGCTTTATTCAT | 9678 |
| rs768081859 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11105482 | AAATTTATTCAAGGA[A/G]TTCAGAAGGACTCTC | 9678 |
| rs768082389 | snp | A/G | 3.32082e-05 | 0.00407468 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028722 | CTTTGCTAGAACTGG[A/G]GTTTGCATTAGCTGT | 9678 |
| rs768094111 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025010 | GATGTCATTAAGAAT[A/G]TTTATGATTCATGGG | 9678 |
| rs768100094 | in-del | -/TTTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11154830 | TAATCATTCACCCAC[-/TTTA]TTTATTTATTCTTGC | 9678 |
| rs768106549 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010314 | AATTTTATGATAGTG[C/T]ATTTAAAGTAATGTA | 9678 |
| rs768111920 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999327 | CCCTGGAGATATTTG[A/C]ATATATAGTTCCTTA | 9678 |
| rs768117406 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064515 | TCTTTTATTTAATAT[A/G]CTGTGTTTACTTTCT | 9678 |
| rs768150578 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121402 | GTTTACTAATTCTCC[A/G]ATGCTACTAATTCTT | 9678 |
| rs768151777 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006845 | TTAGGAGGGACAGGA[A/G]CTTCCTTCACTTTCG | 9678 |
| rs768159261 | in-del | -/T | 0.000117647 | 0.00766875 | intron-variant | PHF14 | GRCh38.p7 | 7:11013737 | ATCATAGTGTTTTTG[-/T]TTTTTTTAGGTTGTT | 9678 |
| rs768162362 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11157934 | CTAACAAAAATTAGA[C/T]GTTTGTCTGGTTTTA | 9678 |
| rs768184724 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000399 | GGCTGGAGTGCAGTG[G/T]TGGGATCTTGGCTCA | 9678 |
| rs768197833 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963874 | TGGTTTAAAGTCTGT[C/T]TTATGAGAGACAAGG | 9678 |
| rs768210462 | snp | C/T | 2.07493e-05 | 0.0032209 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022921 | TAGCCTTTGGAGATA[C/T]TGACAAATTACGACC | 9678 |
| rs768213450 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082635 | CTTCCTTATATCACA[A/G]TTACTAGAAGATAAA | 9678 |
| rs768230933 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979477 | GTAAGAAAGGTTTAT[C/T]GTAGACTTGAAATTA | 9678 |
| rs768239274 | snp | A/G | 1.86274e-05 | 0.00305177 | intron-variant | PHF14 | GRCh38.p7 | 7:11051829 | CAATTCTGAGGCCAA[A/G]ATTTAAGAGAGTGAG | 9678 |
| rs768290011 | in-del | -/TG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148892 | AAACTTTATAATAAC[-/TG]TAGCTAACATTGTTT | 9678 |
| rs768290145 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026418 | TTGTTTTATTGTGAT[A/G]CTTTATTGAAGTGGT | 9678 |
| rs768300262 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145560 | CACTTTTTATAATTA[C/T]GAAAGCATTTTTCCA | 9678 |
| rs768314071 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11150769 | CAAATTAATTATGGG[G/T]TATATCATTTCTGTG | 9678 |
| rs768314816 | snp | A/C | 6.65469e-05 | 0.00576793 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982498 | AAGTAAAAGAAGAAC[A/C]ACTTAAAAATTCTGC | 9678 |
| rs768323713 | in-del | -/T | 0.00352715 | 0.0418465 | intron-variant | PHF14 | GRCh38.p7 | 7:11061779 | TTGTTTTTTTTTTTG[-/T]TTTTTTTCCAGAGAA | 9678 |
| rs768348516 | in-del | -/ACAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101394 | TTCCAGTAGTAAACT[-/ACAG]ACAGACAAAGTAGTT | 9678 |
| rs768352269 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016570 | GGGAAATTTTTTGGC[A/G]TGCTCTCCTTTTTTA | 9678 |
| rs768357326 | in-del | -/CTTCCCCTTTCCCAG | 6.76933e-05 | 0.0058174 | intron-variant | PHF14 | GRCh38.p7 | 7:10974964 | AATATTTCCTTCTCT[-/CTTCCCCTTTCCCAG]CTTTCTGGAGTTAGG | 9678 |
| rs768362054 | snp | G/T | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972728 | AGGAAAAATGTTTAC[G/T]AAGTAGGTTATACAT | 9678 |
| rs768397724 | snp | A/G | 2.61544e-05 | 0.00361615 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982946 | ATCTGCGTCTCAGAA[A/G]GAGGGAAGTGATGGA | 9678 |
| rs768399562 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099978 | CTATTGACAATTTCT[C/T]TAAATGAGCTGATGA | 9678 |
| rs768405037 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060509 | GTGTCCTTAAACTTA[C/T]GTGTATTTGACCTAC | 9678 |
| rs768407855 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072715 | AAATACCTGAGGCTA[A/G]CTAATTTATAAAGAA | 9678 |
| rs768424516 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081663 | AGATCGAGACCATCC[C/T]GGCTAACAGGATGAA | 9678 |
| rs768433469 | snp | A/T | 0.000164803 | 0.00907604 | intron-variant | PHF14 | GRCh38.p7 | 7:11061933 | CTTATTTTGTTTGTT[A/T]TGTTTTATTTTATTA | 9678 |
| rs768449113 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098645 | ATATGTTGTCTTCCT[C/T]CTTTAATCCCCACTG | 9678 |
| rs768451254 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052528 | GCTAAGTTACAGACT[A/T]TCTGCATCTTCAGTT | 9678 |
| rs768467127 | snp | C/G | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10972593 | GAGTATTAAGCATGG[C/G]ATGCCACTTCTGCAC | 9678 |
| rs768470392 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113477 | GTTGAATACCAATAT[A/T]AACAACTAACATTTT | 9678 |
| rs768494521 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11004330 | AAATATGCTTAAAAC[C/T]TTAGTGTTTGTTCTT | 9678 |
| rs768504846 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993921 | GGCTAAGGCAGGAGA[G/T]TTGCTGGAACCTAGG | 9678 |
| rs768539176 | snp | C/T | | | intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11066371 | CTCAAGCAATCCTCT[C/T]ACCTCAGCCTCCCGA | 9678 |
| rs768539299 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156751 | GTGAGCAGAAGTCGT[A/G]CCATTGCATTCCAGC | 9678 |
| rs768557029 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095508 | ATTTTTTTGAGAGTC[A/G]AGGGCATTTCGTTTA | 9678 |
| rs768580984 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006061 | CCTCCCAAAGTGCTG[A/G]GATTACAGGGAAGTA | 9678 |
| rs768584783 | snp | C/T | 9.04773e-05 | 0.00672536 | intron-variant | PHF14 | GRCh38.p7 | 7:11040653 | AAACAATATATACTA[C/T]ATTTGTTCAAATCAA | 9678 |
| rs768602425 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108937 | AGTAAATATGCAGTA[A/G]TTAGGTAGTAAATTG | 9678 |
| rs768659811 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125314 | AATCCCTTTGCAAAG[A/G]TAGTTTAAGAATATT | 9678 |
| rs768674652 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012078 | TGGTTTCTAAGATAC[C/T]GGCAGCCTCATCAAT | 9678 |
| rs768685850 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153532 | TATAGATGTGAGGGC[C/T]GAAGATATAAATGGG | 9678 |
| rs768780354 | in-del | -/TATATATATACA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122344 | TTTTATATATATATA[-/TATATATATACA]CACACACACACACAC | 9678 |
| rs768811827 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128736 | CTCCCGTTCTCCTTC[C/T]GTCTCTCCCATTCTC | 9678 |
| rs768833963 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986735 | TTGCCCTTTAGTTTT[C/T]TGAGGTAAGTTTTTT | 9678 |
| rs768847345 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032427 | CTCAATGTACAAGAC[C/T]GAAGTTGTGTCTTCT | 9678 |
| rs768864099 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959001 | GTCTTTTTAAAACGC[A/G]TATCAGTCAAAGTAC | 9678 |
| rs768865950 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005994 | AGACGGGGTTTCACC[A/G]TGTTGGCCAGGTTGG | 9678 |
| rs768871120 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002023 | GTTGAGGAAATTACT[C/G]CTTATTTCTGTTTGT | 9678 |
| rs768871407 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977406 | AATTTCTTCTTACCT[G/T]CATCTTGAAATCTGA | 9678 |
| rs768888491 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980282 | TACCTTTTCTTTCAT[C/T]TTCATCTCCTAGCTC | 9678 |
| rs768895445 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128185 | TAATTTAAACCAGAC[C/T]TCATTGCTATCTTTT | 9678 |
| rs768954494 | in-del | -/AGA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002252 | GAGAGACATTGGTTT[-/AGA]AGAAAGTAAAAATGG | 9678 |
| rs768957739 | snp | A/G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11132184 | TAGCCCTCATATTGT[A/G/T]TATTTTATCTCTAGA | 9678 |
| rs768965881 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041797 | TCAGAATATATTTTA[A/G]GTGATTTTTCTTTTT | 9678 |
| rs769007689 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999203 | TCACTTTCTTCTAGC[A/G]CAATCTGCTGGAGCT | 9678 |
| rs769036221 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096389 | AATTTTGTAAAGAAG[A/G]TCATCCTCCACAATT | 9678 |
| rs769041219 | snp | A/G | 1.72722e-05 | 0.00293867 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983109 | AACAGTGCTGATGAT[A/G]AGGAACTGACCAATG | 9678 |
| rs769069271 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147096 | CAAGAGATCTGCCCA[C/T]CTCGGCTTCCCAAAG | 9678 |
| rs769075457 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072049 | TATTAGTCCATTCTT[A/G]CATAGCTGTAAAGAA | 9678 |
| rs769114819 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959904 | GTCCCACATCCAGGA[A/G]GAATGAGGTTATGTG | 9678 |
| rs769122703 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11068183 | GTGAAACCCCGTCTC[C/T]ACTAAAAAATACAAA | 9678 |
| rs769124727 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079298 | CTTTTGCCATGGCAT[A/G]TAAGCTGAGCGGTTA | 9678 |
| rs769131229 | snp | C/G | 0.000117299 | 0.0076574 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036477 | ACTAGCTCGATCTAC[C/G]AGACCCCAGGCCTGG | 9678 |
| rs769137100 | snp | C/T | | | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11107951 | GATTATAGTCCCTTA[C/T]GAGTTTTTTTAAATG | 9678 |
| rs769160852 | snp | A/T | | | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11061816 | GACGAAAACGAAGCT[A/T]CGTTCCTGAGGAAGA | 9678 |
| rs769162502 | snp | C/T | 1.69723e-05 | 0.00291305 | intron-variant | PHF14 | GRCh38.p7 | 7:11013915 | CTGGAAGGTTAATGT[C/T]CTAATTATGTTGGTT | 9678 |
| rs769163358 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11044123 | TCACTTACAGGTGGA[A/C]GCTAAACACTGGATA | 9678 |
| rs769177056 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046757 | GGGACTGAGGTATTA[C/T]TTGTCTGAGAAGAAT | 9678 |
| rs769180118 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11139400 | GTCATTTGCATTATA[C/T]AAGAAGATTAATTTT | 9678 |
| rs769190326 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081632 | GAGGCCGAGGTGGGC[A/G]GATCATGAAGTCAGG | 9678 |
| rs769216276 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078333 | ATAACAGAATATGAA[C/T]CTCACTTGAAAATTC | 9678 |
| rs769240226 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153922 | CATAGAGGCAAGCCT[A/T]TGAAAGTGGTCCCTG | 9678 |
| rs769269964 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089895 | CCTGCCTCAGCCTCC[C/T]GAGTAAACTGGGATT | 9678 |
| rs769270507 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981050 | TAAATGTTAGTGTTT[A/C]TTTTTTATGCAATTT | 9678 |
| rs769295276 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006353 | TTTCTTTTTTTTTCT[A/G]GTGAAAACATACACA | 9678 |
| rs769302777 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027579 | ATCTGAGAGGATTTG[C/T]GGTAATTTCAACAGT | 9678 |
| rs769329326 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147159 | AGCCTATTTTTTATT[C/G]AAAGTGAAAGCTGAG | 9678 |
| rs769346039 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11151982 | GAAGTATACCACAAT[A/G]AATCCTAAATATTTT | 9678 |
| rs769348271 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034169 | GATTTTTTTTTCTTT[A/C]TGTTCTTATATGTCT | 9678 |
| rs769366861 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147897 | GATAACTAAAGATTG[C/G]CTCAAACTTAATGTT | 9678 |
| rs769379981 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133925 | TTATTAAGGTAAGGA[C/G]TAACCTGGACCAGGT | 9678 |
| rs769381833 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11121168 | TAAATATCAGCAACA[C/T]ACCCTTTTTATTATA | 9678 |
| rs769413443 | snp | A/G | 6.68516e-05 | 0.00578112 | intron-variant | PHF14 | GRCh38.p7 | 7:11013725 | AAACCCTATTTAATC[A/G]TAGTGTTTTTGTTTT | 9678 |
| rs769415356 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159077 | CTATTTTATATCTTA[A/G]TGCAAATTATAGTTT | 9678 |
| rs769427762 | snp | A/C | 7.30273e-05 | 0.00604221 | intron-variant | PHF14 | GRCh38.p7 | 7:10974970 | TCCTTCTCTCTTCCC[A/C]TTTCCCAGCTTTCTG | 9678 |
| rs769446513 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138385 | AAGGTGATAATGAAA[A/C]AAAAACACAGTTGAG | 9678 |
| rs769451375 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099108 | CTGCCACTGAATTTT[C/T]CTTATTAAGGTGGTA | 9678 |
| rs769452013 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036908 | GGTTTATCAATGTGA[-/T]CATCTTTATAGCTAG | 9678 |
| rs769464546 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048834 | TGTGGCGGTTGTCTT[A/G]AAATAGGAATGGATA | 9678 |
| rs769491798 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001770 | AGGAAATTTTTGGCT[A/G]CTCTTCCAGATTTTC | 9678 |
| rs769495824 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990330 | AAAACACATGTATAG[G/T]ATCAATGATTACTTT | 9678 |
| rs769496262 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062148 | TTTATTTTCTCATCA[C/T]AGAAAAAATGAAAAA | 9678 |
| rs769515447 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980490 | GATTTTTCTTGGTAG[A/G]TTGGGTTTAATTGCT | 9678 |
| rs769541596 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974701 | ACCCCAACCTTCTCC[A/T]GACCCCTTTTGCTGA | 9678 |
| rs769554506 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062180 | CAATTGCAGGATAAG[A/T]CCTTTCTTAAAATAT | 9678 |
| rs769570944 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987471 | TTAGAGCCTGTGGAG[A/T]ACATTGATCAGTATT | 9678 |
| rs769589072 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010705 | AGACGAGATTTTGCT[C/T]TGTTGCCCAGGCTGG | 9678 |
| rs769589869 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11054083 | TATTCTTTTTCTTAA[C/T]TTGTTTTTATCAAAA | 9678 |
| rs769595315 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10963982 | TGTCTTTGCAAATGA[A/G]ATGGGTCTCCTGAAT | 9678 |
| rs769602445 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039886 | AGATTATGTTTTATA[C/G]TTAATATTTAGAGGA | 9678 |
| rs769603156 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125476 | GAGTATAAATACAAT[G/T]CAGTTTACACTCGTT | 9678 |
| rs769621618 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10962519 | TGCATCAATGTTCAT[C/T]GGGGATATTGGCCTG | 9678 |
| rs769643836 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11053957 | AAGAGTCCATGACCA[C/G]TAATTTCAGGAAATG | 9678 |
| rs769644590 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101941 | AAACATATTTCTAAT[A/G]TAGTCTTTTTAAAAG | 9678 |
| rs769657222 | in-del | -/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964971 | GCCATTCATCTAACC[-/T]TTTTTTCTAGGTTTC | 9678 |
| rs769659618 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095234 | TTAATCCTTAAACTC[C/T]ATAAGGTGGTTACTG | 9678 |
| rs769678449 | snp | A/G | 3.33417e-05 | 0.00408286 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982776 | ACTACGACAACCGCT[A/G]CAGAGGAACAAGTCA | 9678 |
| rs769689201 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137225 | GCCACAGAACATGAC[A/T]AATGGCTGTGAGGGG | 9678 |
| rs769692184 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043679 | GATTGCTTTTTTATA[A/G]TGTTCTTTGTATCAG | 9678 |
| rs769700991 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166302 | TCTTTCATTGGGAAA[C/T]AAACAGATGTCTTAT | 9678 |
| rs769725747 | in-del | -/CTCTTGCTCCAG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002911 | AAAGAGATGTGCCAC[-/CTCTTGCTCCAG]CTCTTCTACTGTCTT | 9678 |
| rs769732229 | snp | C/G | 2.54793e-05 | 0.00356918 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111383 | CTGCTACCATTTTGG[C/G]TGTTTGGATCCTCCT | 9678 |
| rs769732803 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11067694 | TTTATTTGGCTCACA[A/G]TTCTCATTGTTGGGA | 9678 |
| rs769734495 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11052800 | CCAGTTTTTCTGTTG[G/T]GGTGTTTACCTTTTT | 9678 |
| rs769735487 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128866 | ATGTCCAGTTTAAAT[C/T]ATAGTTTTCTAGTTG | 9678 |
| rs769738354 | snp | A/C | 1.6596e-05 | 0.00288058 | intron-variant | PHF14 | GRCh38.p7 | 7:11038741 | TTAATGAAGTTTACT[A/C]ATTTGGCTTACTTTG | 9678 |
| rs769751818 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11097678 | AGTTCAGGCTAGTTC[A/G]GTCCTCATCTGAAAG | 9678 |
| rs769766951 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11082838 | GACAAGATTTCTCTT[C/T]AAATAGCCTATTAAT | 9678 |
| rs769767613 | snp | C/T | 2.72246e-05 | 0.00368938 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982705 | TGGCTGCTTCTGCTG[C/T]TGCCACCACACCAGC | 9678 |
| rs769805595 | in-del | -/TTTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122618 | CATAGCATATGTTTC[-/TTTA]TTTGTTTCCCTTCAT | 9678 |
| rs769817622 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956256 | TGGGAAGTGGGGAGC[A/G]CCTCGGCCCAGCTGC | 9678 |
| rs769820672 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022750 | TTGCGAGATTTTAAC[A/G]TTTGATTACAGAATT | 9678 |
| rs769833218 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155074 | AACTGTCGTAAAGTT[A/G]AGCCTAGAAAGAGGA | 9678 |
| rs769876958 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073640 | GCCCTTCCCACAGCT[C/T]CACCAGGTAGTTCCC | 9678 |
| rs769880441 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002907 | TGCTAAAGAGATGTG[C/T]CACCTCTTGCTCCAG | 9678 |
| rs769913708 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11137130 | TCTTAAGATTTAATC[-/T]CTCAGGTTTTCTTGG | 9678 |
| rs769919936 | snp | A/G | 6.29162e-05 | 0.0056084 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983070 | GGGGGTTGCAAGAAG[A/G]AGAAGAGTAAAGTTC | 9678 |
| rs769933887 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11104224 | CATTTTCCATCTTGC[A/G]TTTTCAGTGGTGGTG | 9678 |
| rs769955378 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966855 | TAAGGTAACTCTTCC[C/T]AATATAGATGAAAAC | 9678 |
| rs769956633 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162850 | ACCACCACTGCCCTA[G/T]TTCTTTGCTACGAAA | 9678 |
| rs769959324 | snp | C/T | 0.00014044 | 0.00837855 | stop-gained, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040696 | ATACCGGCAATTTTG[C/T]GAGCACCCAAGGAGA | 9678 |
| rs769965782 | in-del | -/AAACCTCTTTTATAAGTGTGATTTTAAAAATGT | 1.70472e-05 | 0.00291947 | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102539 | CGGAGGCAATCCCGG[lengthTooLong]AAACCTCTTTTATAA | 9678 |
| rs769970195 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11013182 | TTTATTTTTTATGAG[A/G]TGGAATTTTGCTCTT | 9678 |
| rs769990139 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003892 | TACCAGGGGTTTTTT[A/G]ACTTTATTTTATTAT | 9678 |
| rs769992904 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117867 | TGAAGCATATAACTG[A/G]CGCATAAAAAAGAGA | 9678 |
| rs770010906 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134989 | AATGAAACCCACCTT[G/T]TTCTTCACTTGACAG | 9678 |
| rs770050227 | snp | C/G | 3.00071e-05 | 0.00387332 | nc-transcript-variant, missense, intron-variant | PHF14 | GRCh38.p7 | 7:11169432 | AAGATGAAAATGAAG[C/G]TGAAAGAAAAAATAT | 9678 |
| rs770052403 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967941 | TTATTTTCCACTGGT[A/C]ATCAAGATATCATTG | 9678 |
| rs770076731 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072346 | TTCATGAGAAATCTA[C/T]CCCCGTGATCCAGTC | 9678 |
| rs770078455 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129997 | GGATATGCTAAGTTA[C/T]GCAGCAAAAAAAAGA | 9678 |
| rs770084151 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959711 | GTGGTTTATGCTGTG[A/G]GTACCGGCATCTGGA | 9678 |
| rs770136040 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167216 | CGGGAAGTCATACGG[C/T]GGAGAAACTTAGTAG | 9678 |
| rs770148195 | snp | G/T | 3.44442e-05 | 0.00414981 | intron-variant | PHF14 | GRCh38.p7 | 7:11035829 | GTTTTTGTTTTAAGG[G/T]TATGTAAGGATTTTA | 9678 |
| rs770154948 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977270 | ATCTGTCTGATCATA[C/T]CTTCTTTCAAAACAA | 9678 |
| rs770158571 | snp | A/G | 1.66272e-05 | 0.00288328 | intron-variant | PHF14 | GRCh38.p7 | 7:11042638 | GTAAACTGTTTCACT[A/G]TGATAATTATTATTG | 9678 |
| rs770183354 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086073 | TGTGAGGATTAAATG[A/T]ATAAAAATATGTAGT | 9678 |
| rs770200014 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006720 | CTCCAGAGTCTCAGT[A/G]TCTTGGGCTGCTGGA | 9678 |
| rs770202158 | in-del | -/TCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11047443 | TGAAATTCCATTGGG[-/TCA]TCATTCTGATTATAG | 9678 |
| rs770204870 | snp | G/T | 5.09282e-05 | 0.00504594 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036466 | GCCAAAGCAGAACTA[G/T]CTCGATCTACCAGAC | 9678 |
| rs770253109 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057133 | ATTTAGTGACCTGGT[A/C]ACAAGTGAATATGTG | 9678 |
| rs770265809 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070849 | TACTGATACACTGCC[A/G]TATCTGTATATTTTT | 9678 |
| rs770268426 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988146 | AGGGAAATATTTTAT[C/G]TCTAGTTTTCCCTAT | 9678 |
| rs770293331 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096487 | ATGCTAATACAGACC[A/T]GACAGTTCCACTTAC | 9678 |
| rs770294125 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960197 | CTGCACCCATCAACT[C/T]GTCATTTACATTAGG | 9678 |
| rs770303440 | in-del | -/AGAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11110341 | TAAAGAAAATCTGAC[-/AGAT]TGGTTGAGAAAGTAT | 9678 |
| rs770340979 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069939 | AAAGTGTTCCCTTAT[C/T]CTTTGTTTTTAAAGC | 9678 |
| rs770344409 | in-del | -/TAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990852 | GTCCATGAAGGTAAT[-/TAC]GTTGCTTTCTTTTCT | 9678 |
| rs770390997 | snp | A/G | 6.99912e-05 | 0.0059153 | intron-variant | PHF14 | GRCh38.p7 | 7:11102482 | TTATCACTTTACTGT[A/G]TAGATACCCTTCATG | 9678 |
| rs770395986 | in-del | -/AG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078109 | TTGTTTTCTGACGAA[-/AG]AGAAGAGAAGCTATC | 9678 |
| rs770405187 | in-del | -/TG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131830 | CCTACGTTCTCTCTC[-/TG]TCTCTCTCTCTCATT | 9678 |
| rs770409569 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050268 | TATGAGAATTATAAG[C/G]TACATTCAAAGATAC | 9678 |
| rs770417476 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993082 | GCAGTTACTGGTGAT[A/G]TTACTATTACTTTTT | 9678 |
| rs770429797 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123756 | CTACACTCCAGCCTG[A/G]GTGAATCGCTTGAAC | 9678 |
| rs770435660 | snp | A/G | | | nc-transcript-variant, utr-variant-3-prime, intron-variant | PHF14 | GRCh38.p7 | 7:11169567 | ATTGTAAAATGTTAA[A/G]TTGTAAAATCTAATT | 9678 |
| rs770442727 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986140 | ACTGGCTAATGCTTT[C/T]ATTTTTGATTTTTTT | 9678 |
| rs770450800 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11134103 | AGAATTTGAAATAGG[C/G]CTTGTGGTGGGGCTG | 9678 |
| rs770464656 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103784 | AGTTACAGTGAGGAA[C/T]GCTATGATTGGATGA | 9678 |
| rs770496910 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010187 | ATTGCATAGCACATG[A/G]AGAAAATAGATTGAT | 9678 |
| rs770509329 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11167405 | GCAATCTTAATTTAC[A/G]ATAGTTAAGAACAAT | 9678 |
| rs770518271 | snp | C/G/T | 0.000251864 | 0.0112196 | intron-variant | PHF14 | GRCh38.p7 | 7:11036966 | TACTAAAGTAAAATT[C/G/T]GATATTTCATTTAAA | 9678 |
| rs770519754 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135978 | CATTCCTCGTTAAAG[C/T]TAACTGGTATTAAAA | 9678 |
| rs770539326 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102509 | CATGAGACCCAACTC[A/T]GCCACAGCTCATCCT | 9678 |
| rs770549969 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078176 | CTTATTCTCTAGGTG[A/G]CATGTGTGTCATTAG | 9678 |
| rs770551452 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090050 | TGCTGGGATTACAGG[C/T]GTGAGCCACCTCACT | 9678 |
| rs770562138 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10955958 | ATTGAGAACACTCAA[A/C]TAATGTTTAAGAGTA | 9678 |
| rs770580152 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10996470 | ATGGGTGATGACCCA[C/G]AGAAAACTGTTTCAA | 9678 |
| rs770611496 | snp | C/G | 5.75888e-05 | 0.00536573 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982527 | GCAGAGGAAGAAGTA[C/G]TATCATCAGAAAAAC | 9678 |
| rs770640474 | in-del | -/GTT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11094963 | GGAGTGTTATTTCCA[-/GTT]GTTGTTGTTGTTATT | 9678 |
| rs770698787 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10967091 | GAAAATGATGCTCTG[A/G]GATTTTGAGGCTTGG | 9678 |
| rs770712946 | snp | A/C | 0.000602591 | 0.0173474 | intron-variant | PHF14 | GRCh38.p7 | 7:11013713 | CTTTAACAAAATAAA[A/C]CCTATTTAATCATAG | 9678 |
| rs770726673 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11001922 | CATCCTTGCCTCATA[C/T]CTCATCTTTGTGGGC | 9678 |
| rs770730432 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11113666 | GCTGAAACTTCCGGA[G/T]ACTTAATTGATTCCC | 9678 |
| rs770734377 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11027428 | CAATTCTTTAATTGT[C/T]CATTGTCAGTCTTTC | 9678 |
| rs770749387 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079609 | TTTTCTTCATTAAAA[A/G]GAAACCAAAGTTAGG | 9678 |
| rs770766470 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140294 | ATCCTTACTATGTGC[A/G]ATATACCCTATTTTA | 9678 |
| rs770768518 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126911 | GATTCTCAAGTGAGC[A/T]ATTTTTAACAGACCA | 9678 |
| rs770770547 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11011833 | AATCTATTTAGGAGT[C/G]ATGACTATCATCAGT | 9678 |
| rs770791202 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056710 | ATATTTTTAGGAATT[A/T]TGTATATGTATAATT | 9678 |
| rs770796445 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041237 | TTTTCTCTTGATGCT[C/T]AGTTGCAATCACTTT | 9678 |
| rs770823579 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062426 | TTTATGTCAGAAAAC[A/G]ATAAAGTTACTAAGC | 9678 |
| rs770829137 | snp | C/T | 1.65699e-05 | 0.00287831 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11028805 | GTCTGCTTTCAGAGG[C/T]AGCGGCGGAAGAGGT | 9678 |
| rs770833666 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074839 | CTCTAAGAAGTTCCA[A/T]ATTGTCCCTTGTCTT | 9678 |
| rs770882052 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050259 | AATACTTGCTATGAG[-/A]ATTATAAGCTACATT | 9678 |
| rs770882254 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056190 | GCTCAAGTAATCTTA[C/T]TCAGAACCCTGAGAC | 9678 |
| rs770883650 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11118030 | AAATTCAGTACTCTT[C/G]TAGCGTTTGTGGGAC | 9678 |
| rs770884769 | in-del | -/TT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11127360 | AGTTCCGTTTATCTC[-/TT]TTTTGATTGGCATTA | 9678 |
| rs770888178 | snp | A/G | 2.21791e-05 | 0.00333002 | intron-variant | PHF14 | GRCh38.p7 | 7:11062094 | TTGTCAGGTAAGTTG[A/G]ATGCTAAAACCTTGT | 9678 |
| rs770900859 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145805 | ATTAACATCATAGAT[A/G]CCTAAACCTTTTAAT | 9678 |
| rs770918557 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025883 | TTGGGAGGCCGAGTT[A/G]GGTGGGTCACCTGAG | 9678 |
| rs770921291 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980615 | TCCAAGAAGCTTAAA[A/G]ATCCAAGTGTTTTGT | 9678 |
| rs770930283 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087020 | TCAGTTAAATTAGAT[C/G]TCACTACATCTTAAT | 9678 |
| rs770932925 | snp | A/G | 3.67249e-05 | 0.00428498 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982691 | AGTATCTGAGAATGT[A/G]GCTGCTTCTGCTGCT | 9678 |
| rs770941960 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046365 | TTGTGTTGCCTTTTC[C/T]AATTGTTTGAAGAAT | 9678 |
| rs770943999 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030928 | CAGAATATTGCATGA[A/T]TCAATATTAATGAAG | 9678 |
| rs770950085 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117295 | GAGCTGTCTTAGCTT[G/T]GAGACTTCTATTTGG | 9678 |
| rs770965311 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981708 | TTTTATTGATACGAA[A/C]AGTATCCTAATAAAC | 9678 |
| rs771000701 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147446 | CTCTCAGTCCCTCTT[G/T]AAGCTATTTTGAACA | 9678 |
| rs771044288 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165608 | TGTAATTTGTATCCA[C/G]GTATTACCTGAGTGA | 9678 |
| rs771058992 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020155 | GTGCAGTGGCACGAT[A/G]TTGGCTCACTGTAAC | 9678 |
| rs771069110 | snp | A/G | 8.51303e-05 | 0.00652364 | intron-variant | PHF14 | GRCh38.p7 | 7:11035810 | TTCATGTCAAAACCC[A/G]TATGTTTTTGTTTTA | 9678 |
| rs771072798 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10984191 | TTTTTCTGCCTACAA[C/G]TTTTACATAGCAGTG | 9678 |
| rs771076933 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092643 | GCATATGCCTTTTTT[A/G]CATATGCCCACATAT | 9678 |
| rs771091879 | snp | A/G | 2.46357e-05 | 0.00350959 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10983059 | CTGCCAGTGAAGGGG[A/G]TTGCAAGAAGAAGAA | 9678 |
| rs771094723 | snp | A/T | 2.66606e-05 | 0.00365097 | nc-transcript-variant, synonymous-codon | PHF14 | GRCh38.p7 | 7:11111437 | AGGCTACGGATGGAT[A/T]TGTCAGGAATGTGAT | 9678 |
| rs771096480 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11003675 | GTGACAAGAACAGCT[A/G]AAATTTACATTTAAC | 9678 |
| rs771099530 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10999206 | CTTTCTTCTAGCACA[A/G]TCTGCTGGAGCTGAA | 9678 |
| rs771101290 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131309 | GAGAGTTGTTGTTCC[A/G]TATCTTTGCCAGCAT | 9678 |
| rs771101671 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140342 | CAGCTTTAAAACAAA[C/T]GTTCACAGCTCAGTA | 9678 |
| rs771118779 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106218 | ACTCTTTAAGTGACT[A/G]TTAAATACAGATTTG | 9678 |
| rs771126857 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077273 | ATGTTAGAAACGTAA[A/G]CATTTGAATTAACCA | 9678 |
| rs771131541 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959826 | TCTTGTTCCTGCCAT[A/C]CATGGCACAGCGAGC | 9678 |
| rs771143332 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11108713 | TTTAATTGTACGAGT[A/C]GTTGAAATCAGCAAC | 9678 |
| rs771180807 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10958780 | ATCTCACTGTGTCCT[C/T]AAACACCTGGGCTCA | 9678 |
| rs771219894 | snp | G/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10961590 | AAATTTAAAGTAGCT[G/T]TTTCCAATTCTGTGA | 9678 |
| rs771226879 | in-del | -/AAA | 5.18229e-05 | 0.00509006 | intron-variant | PHF14 | GRCh38.p7 | 7:11061946 | TATGTTTTATTTTAT[-/AAA]TATCCCTTGTATGGC | 9678 |
| rs771243244 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036137 | ATATACATTAAACCT[A/T]TGGAGACAATAGCAG | 9678 |
| rs771246849 | snp | A/G | 1.74705e-05 | 0.00295549 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051643 | GACCAGGCAGGGAGC[A/G]GTGACATGGAAGCAG | 9678 |
| rs771247880 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016285 | TTTGATTAAAGGTAT[-/A]AAAAGCCAAGAAAAT | 9678 |
| rs771271645 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11155417 | TAGAACCAGAAAAGC[A/G]GAATTCCCAACCTTT | 9678 |
| rs771289035 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968117 | TGTAGAAAAATATTT[C/T]GGTATGTATAAAATC | 9678 |
| rs771299528 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11119064 | AACTAAGCCATTTTC[C/T]AAGTGGCATGTGGCC | 9678 |
| rs771343250 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156740 | CAGAGGTTGCAGTGA[A/G]CAGAAGTCGTGCCAT | 9678 |
| rs771375171 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023698 | CTGGGCGTGGTGGCG[C/T]GTGCCTGTAATCCCA | 9678 |
| rs771379573 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976237 | AATTGATAAGTTTAT[C/T]TTGATTAACTGTTTT | 9678 |
| rs771391532 | snp | A/G | 1.6989e-05 | 0.00291449 | intron-variant | PHF14 | GRCh38.p7 | 7:10974798 | CCCTGTGTTTGGTGT[A/G]ATTATGAATGACAAT | 9678 |
| rs771391734 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099215 | AGACACATGGAATGG[C/T]TAACCTGTCTAACAC | 9678 |
| rs771403504 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142536 | CCGCAAGCTTATAAC[A/C]AAGATAACATCAGCA | 9678 |
| rs771404160 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043889 | TTGCCATGAACTTAT[A/G]TAGAGTTATGCAGTT | 9678 |
| rs771407368 | in-del | -/T | 1.80987e-05 | 0.00300816 | intron-variant | PHF14 | GRCh38.p7 | 7:11036705 | CAGTATAGACACTGG[-/T]TACATGCACATTTTC | 9678 |
| rs771433215 | snp | A/C | 3.31252e-05 | 0.00406958 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11062083 | CAATGAAAATCTTGT[A/C]AGGTAAGTTGGATGC | 9678 |
| rs771433691 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11086182 | TATCCAGTTGTCTTA[C/G]TAAAACATGAATTTG | 9678 |
| rs771445083 | snp | A/G | 1.65822e-05 | 0.00287938 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11035687 | GCAACATGCAGATAG[A/G]TTAGACAGAAAGTGG | 9678 |
| rs771445644 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10997726 | CAGAGACCTCAGTTT[C/T]CTACTGCATGGACCT | 9678 |
| rs771466768 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023277 | TTATTTACAATTAGA[C/T]GGATCAAATATAAGC | 9678 |
| rs771483134 | snp | C/G | 1.67742e-05 | 0.002896 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11013894 | GAATTTTCAAGGAGA[C/G]AGATGCTGGAAGGTT | 9678 |
| rs771487470 | snp | C/G | 1.66178e-05 | 0.00288247 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974293 | AGCCTCTCCCTAAGT[C/G]TTCTCCAAACGACCA | 9678 |
| rs771494864 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087336 | AGCTGGGACTACAGG[C/T]GCACACCACCATGCC | 9678 |
| rs771497038 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10989055 | ATTTGCCAGCCATTT[A/G]TCAGCCCCAGACCTA | 9678 |
| rs771514276 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036259 | GTAACTCAAAAATTA[C/T]ACAGTATACCTTAAG | 9678 |
| rs771525955 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071741 | GGTTTCTCATAGCCC[C/T]GAGACATGTTTCTGA | 9678 |
| rs771534275 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138799 | TACAATTTGAAGACT[-/TC]TGTTATTTTATACTC | 9678 |
| rs771534303 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034579 | TTTGAGACAGACTGT[C/T]GCTCTGTCACCCAGG | 9678 |
| rs771548132 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078482 | ACCTCTCTGCGAGCC[A/G]GTTTTCTCATTCATA | 9678 |
| rs771562102 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111755 | CAAACAGATCACTCT[C/T]TGCTAACTTAACACA | 9678 |
| rs771572123 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146853 | GTTTTTATTTACTTA[C/T]GTATTTATTTAGAGA | 9678 |
| rs771572830 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009403 | TGAGTTGTGTACATT[A/G]CATATATTAGTCAAA | 9678 |
| rs771591656 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11062641 | TTTGTTTCTTTGTTT[C/T]GTTTTGGTACTTTAT | 9678 |
| rs771621773 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11092282 | TCCTTAAACATTAGG[A/G]TGCATTTGAAGCACC | 9678 |
| rs771631129 | snp | A/C | 3.97543e-05 | 0.0044582 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982507 | AAGAACAACTTAAAA[A/C]TTCTGCAGAGGAAGA | 9678 |
| rs771641719 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11125121 | TTATGTAGACACAGC[A/G]GAAACTAATCTATTG | 9678 |
| rs771649157 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11098223 | ACTTTAGCCATGTAT[A/G]TAATTTGAAAGCTGA | 9678 |
| rs771710638 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11038135 | AAAATATATGGAGGC[C/T]GAGCGCAGTGGCTCA | 9678 |
| rs771713423 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11162191 | CCTCCCAGGTTCAAG[C/T]GATTCTTGTGCCTCA | 9678 |
| rs771717512 | snp | A/G | 2.15775e-05 | 0.00328455 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022933 | ATATTGACAAATTAC[A/G]ACCAGTAACACTAAC | 9678 |
| rs771723022 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11156690 | ATCCCAGCTACTCGG[A/G]AAGCTGAGGCAGGAG | 9678 |
| rs771755359 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020002 | TTCTGAAATGAAATA[C/T]GGCTTTGAACTAAAT | 9678 |
| rs771770887 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10998844 | TTTCTCTGCTTCATT[A/G]TAATGCTGAGTACCA | 9678 |
| rs771805157 | snp | A/G | 0.000153175 | 0.00875007 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11040681 | CAATAGAAGTTGAAT[A/G]TACCGGCAATTTTGC | 9678 |
| rs771826720 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072014 | TAAGTATGAGGATTT[A/G]TAACCATTCTGCTGA | 9678 |
| rs771852726 | snp | C/T | 4.08147e-05 | 0.00451726 | intron-variant | PHF14 | GRCh38.p7 | 7:11040807 | ATAATGATAGAATAA[C/T]GTTGTGTATTTTTTT | 9678 |
| rs771853843 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11116058 | CTATGTAAAAATATC[C/G]TATTCCTCATCAAAC | 9678 |
| rs771857277 | in-del | -/TC | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990073 | AGATTATTTTCTGTA[-/TC]TCTGTGTATTCATAT | 9678 |
| rs771867440 | snp | A/C | 1.92829e-05 | 0.00310501 | intron-variant | PHF14 | GRCh38.p7 | 7:11036729 | CATTTTCACTGAGAA[A/C]AATTTGTTAATGAAA | 9678 |
| rs771873201 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993112 | TTTCTCATTTTTATT[G/T]CATAAGCCTACCAAT | 9678 |
| rs771884875 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11072455 | TATCAAGGTTTTAAA[A/C]CTTCTTTTGTTATTT | 9678 |
| rs771884997 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11065093 | AGGAGACAAAAGGAA[A/G]TTTGTCATTACATGT | 9678 |
| rs771925856 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993837 | AAAATGGTGAAACGA[C/T]GTCTCTGCTAAAAGT | 9678 |
| rs771934901 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028609 | AATATTTAGTGGACA[C/G]TTTGTATGAGAATGC | 9678 |
| rs771938790 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11160669 | ATTTCGCTGACAATT[A/G]GCGATGTTGAGCATT | 9678 |
| rs771946569 | snp | A/G | | | | | GRCh38.p7 | 7:10970049 | TTTGCTTAATTAGAC[A/G]GAATTGTGGACATTA | 9678 |
| rs771948469 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103925 | AGTAGACTTTTGTTT[A/G]AAAGAATAAGATAGG | 9678 |
| rs771956818 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120068 | TTTCCCAAAAAATTG[C/T]CATTAAATTGGCGGA | 9678 |
| rs771958609 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11075886 | CCTGTAATCCCAGCA[C/G]TTTGGGAGGCTGAGG | 9678 |
| rs771993523 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11152254 | TTCTAACTGTACATA[C/T]GGTATATTGAAAAGG | 9678 |
| rs771995347 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959760 | GCCCCAAAACTTGGA[A/G]ATGCCAGCAATGGCA | 9678 |
| rs771997597 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11033486 | TGGGCATTTCATACA[A/G]CTTATTGGCCAGAAC | 9678 |
| rs772005183 | snp | A/G | 3.58641e-05 | 0.00423448 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982409 | AAGTGAAGATGCTTC[A/G]AAGGACAGTGGAGAA | 9678 |
| rs772009228 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11030977 | CATTCTGTCTTGTCT[A/G]TTTCTAGATGGTTGT | 9678 |
| rs772014436 | in-del | -/GT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122443 | CGTATATATATATAC[-/GT]ATATATATATATTGT | 9678 |
| rs772048717 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078269 | ACCAGGATGATTATC[C/T]TGCCTCTTTTCTGGG | 9678 |
| rs772052969 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966742 | GTGGACAATATCTAG[C/T]CCAATTTTATGCTTT | 9678 |
| rs772055252 | snp | G/T | 1.77178e-05 | 0.00297634 | intron-variant | PHF14 | GRCh38.p7 | 7:11028647 | AGTCTGGAAATAAGT[G/T]TGCTTTGAGAATTTT | 9678 |
| rs772057756 | snp | A/G | | | | | GRCh38.p7 | 7:10971196 | GCATTCACAAAAGGG[A/G]GGGAAAAGTTCAAGC | 9678 |
| rs772081177 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11164850 | GTAGTCCAGGATTCC[A/T]CACTGCATTCAGTCA | 9678 |
| rs772092749 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11020815 | GAACAACCTCCTACT[C/T]AACAGAAGCTTTTAG | 9678 |
| rs772107741 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10975180 | CTTTTTCCAAAGATG[C/T]AAAAGGATTTCTCTG | 9678 |
| rs772116380 | snp | A/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063994 | TCGTTTTGCCTTATT[A/G]AGAAGATAATATCGT | 9678 |
| rs772139654 | snp | C/G | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11149496 | GCTCTCAAATCTTAT[C/G]GCCCTTTAAAGAAAA | 9678 |
| rs772140600 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025077 | AGAAGTTGATTGCAG[C/G]CTTCATGGATAACTT | 9678 |
| rs772180763 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11032345 | ACATCAATTTTACTA[C/T]TAAGATACCAGTAAA | 9678 |
| rs772187277 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11010935 | ATTGGGATTGCAGGC[A/G]TGAACTACACGCCTT | 9678 |
| rs772205139 | snp | A/G | 0.000169611 | 0.00920744 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11051621 | ATGTAGGCAGTGCTC[A/G]GAATGTGACCAGGCA | 9678 |
| rs772210006 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10985544 | TAGCAGGGCCCTTTT[A/G]TAATTACTGCTCTTA | 9678 |
| rs772236303 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11093789 | GCCCTTTTTCCTATG[A/G]CAGCTTTATTCTGGC | 9678 |
| rs772259029 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045360 | TGACTGTGCCTTAGT[C/G]TGCAGCTTGAACTTC | 9678 |
| rs772270311 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11120997 | AAACTGTAAACTTGA[A/G]ACTGAAATGAAAATA | 9678 |
| rs772274356 | in-del | -/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129548 | TTGTGTGTATGTTTC[-/T]TTTTTTTTTTTTTTT | 9678 |
| rs772276387 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106458 | GGTAATTTGCACTAA[A/C]ATTGTTGTAAATTAC | 9678 |
| rs772285050 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138702 | GTTCTTTAAAGAGAA[A/G]AGAGATCGTGAGAGA | 9678 |
| rs772287162 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11021637 | GCGACATTTAATACA[A/T]CAGTGGAGCATGAAA | 9678 |
| rs772289647 | snp | C/T | | | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10968357 | CTGCTGTTACAGCTA[C/T]ACGAACATGGCCTCT | 9678 |
| rs772293555 | in-del | -/T | 0.000101719 | 0.00713086 | intron-variant | PHF14 | GRCh38.p7 | 7:11023020 | CTTGAAAGAGAAAGG[-/T]TTTACTTGTTAGTTT | 9678 |
| rs772300540 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095457 | TCTGTAATTAACTCA[A/G]TTTCCTCTGTGAACT | 9678 |
| rs772301763 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11130107 | GCTCATTATAGTCAC[G/T]TGGGGACCCGAGCTG | 9678 |
| rs772337847 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11005861 | GCAAAGGTGAGATCT[C/T]GGCTCACTGCAACCT | 9678 |
| rs772343208 | snp | C/G | | | nc-transcript-variant | LOC107986767 | GRCh38.p7 | 7:10958954 | AGGTTAACTCTGCAA[C/G]GTAAGAAGGAATTCC | 9678 |
| rs772347046 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11059308 | CATACTTGAAAAATT[C/G]AAAACTACATGATAC | 9678 |
| rs772352687 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090295 | AGGCACTCCCTGTAA[C/T]TGCCCAGTGAATCAG | 9678 |
| rs772365882 | snp | A/C | 1.65935e-05 | 0.00288036 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10982815 | AAAAAATGGAACCTT[A/C]GACGAAACCGACCAC | 9678 |
| rs772382552 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144248 | AAAGGAAAGGGAAAT[C/G]TTGTATACTGTTGGT | 9678 |
| rs772409732 | in-del | -/CAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11016687 | AATGTGAAATAAGCA[-/CAT]CATGGAGAATGGGGT | 9678 |
| rs772423675 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10977212 | TCCCAGCCCTACTTA[C/T]GAATAGGAGATTAAA | 9678 |
| rs772457110 | in-del | -/TA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138438 | ACCCACTTTATCCCT[-/TA]TATTATTACATAGTA | 9678 |
| rs772459923 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11145265 | CAGTACTATTATAGG[A/T]GTATGTCCTCACTTG | 9678 |
| rs772474885 | snp | A/G | 1.66194e-05 | 0.00288261 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974290 | TGCAGCCTCTCCCTA[A/G]GTCTTCTCCAAACGA | 9678 |
| rs772475365 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11107511 | AATTGGGATTCCTTT[A/T]TGCTCTATAGTGTTA | 9678 |
| rs772476043 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976540 | TATTATGTGACAATA[A/C]ATCTTGACTTTATGG | 9678 |
| rs772501611 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11060266 | ATTTTATTAAAACAA[A/G]TTAATTGAGTCTTTA | 9678 |
| rs772531750 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133306 | ACTTTAAAACTTACT[A/G]TAAAGCTACAGTAAT | 9678 |
| rs772546819 | snp | C/T | 5.99287e-05 | 0.00547364 | intron-variant | PHF14 | GRCh38.p7 | 7:10990870 | TGCTTTCTTTTCTCT[C/T]TTTTTAGAAATGGCT | 9678 |
| rs772581763 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11077471 | CCGGGTGTGGTGGCA[C/T]GCGCCTGTAGTCCCA | 9678 |
| rs772600790 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979025 | TTTATAGTACTAACA[C/G]TGTTGTACCAGATCA | 9678 |
| rs772603643 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11031979 | ACAATATAAAACCGG[G/T]TGTGGTGGCACACGC | 9678 |
| rs772609193 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11087305 | CAAGCGATTTTTCTG[C/T]CCCAGCCTCCCGAGT | 9678 |
| rs772614668 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11163900 | GTTTTTCTTTCTACA[C/G]TTGTTCCGTAGCTAC | 9678 |
| rs772622977 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046406 | ACATTATTTAACAGA[G/T]AATTGAGTAATATAT | 9678 |
| rs772623959 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11147254 | AGGTTTCATTAAATA[C/T]AGGACATATAAAATA | 9678 |
| rs772634701 | snp | A/G | 1.81992e-05 | 0.0030165 | intron-variant | PHF14 | GRCh38.p7 | 7:11037115 | GCTACAAAATATGCA[A/G]CATAATGTGATAGAT | 9678 |
| rs772643438 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11102930 | GTTACTGAAGCCTGT[C/G]GGACTTAATAAATAC | 9678 |
| rs772678474 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11126359 | CATATTTTTAGGATA[C/G]ATTATTTACTCTTTT | 9678 |
| rs772730015 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11009404 | GAGTTGTGTACATTG[C/T]ATATATTAGTCAAAG | 9678 |
| rs772731848 | in-del | -/ATATG | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096167 | TTTCGGTGTCTGAGT[-/ATATG]ATATGCATGCATGGA | 9678 |
| rs772733161 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11034295 | CTGTTCCTTTTTGGG[A/G]CAGACATAAAGAATG | 9678 |
| rs772748418 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11078537 | TTAAAAATCCCTTTT[A/G]ATTTTCAAATTTCAT | 9678 |
| rs772761694 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046941 | GGAGGAGAAAAAAGT[A/C]AATCATGAATTATTT | 9678 |
| rs772779326 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165274 | TGTAGAGGGTTTATC[C/T]GATGTTTTCTCAGAT | 9678 |
| rs772784438 | snp | A/G | 2.20044e-05 | 0.00331688 | splice-donor-variant | PHF14 | GRCh38.p7 | 7:11062086 | TGAAAATCTTGTCAG[A/G]TAAGTTGGATGCTAA | 9678 |
| rs772784931 | in-del | -/CTGT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11099220 | CATGGAATGGCTAAC[-/CTGT]CTAACACATTTAGTA | 9678 |
| rs772786098 | snp | C/T | 3.45495e-05 | 0.00415615 | synonymous-codon, intron-variant | PHF14 | GRCh38.p7 | 7:10983126 | GGAACTGACCAATGA[C/T]AGCCTGACCCTATCT | 9678 |
| rs772816950 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979855 | TGATCCCTGTAGTTG[C/G]AGTCTGACTAATGTA | 9678 |
| rs772825524 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006760 | ACATGCGGATCTTCT[C/T]TTTTGGTGGCTGTGG | 9678 |
| rs772828425 | snp | C/T | 3.54258e-05 | 0.00420852 | intron-variant | PHF14 | GRCh38.p7 | 7:11028648 | GTCTGGAAATAAGTT[C/T]GCTTTGAGAATTTTT | 9678 |
| rs772842465 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11112674 | TACTTGGGAGGCTGA[C/G]GCAGGAGAATCACTT | 9678 |
| rs772884184 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10991605 | GTAAGCCACCGCACC[A/T]GGTCCCCCAGTCATC | 9678 |
| rs772905330 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166179 | TGTCTACTTTCCAGT[A/G]GCCTCAAAGGATACA | 9678 |
| rs772912533 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006087 | AAGTAAAATTTCTTA[A/G]TCAAAAGATAAGTGT | 9678 |
| rs772922799 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987567 | TGATTTATTCATATA[C/G]TGTCATTTATTCTTC | 9678 |
| rs772937051 | snp | A/G | 1.79043e-05 | 0.00299196 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982410 | AGTGAAGATGCTTCA[A/G]AGGACAGTGGAGAAG | 9678 |
| rs772961015 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11006368 | GGTGAAAACATACAC[A/G]TATATTTAGAATTAG | 9678 |
| rs772967428 | snp | A/C | | | | | GRCh38.p7 | 7:10969497 | CCCCCTACATCTTGG[A/C]TTTGGTTACCGTAAT | 9678 |
| rs772984138 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964928 | CATTAGGTCATTTAA[C/G]CTCTTCTCTACACTG | 9678 |
| rs772985426 | in-del | -/CA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11165899 | TCTGTTAGAATAACT[-/CA]GTCTCATATTGCCAC | 9678 |
| rs772988904 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083163 | ACAGGGGCAGGATTT[G/T]CGTCAGGGATAAAAA | 9678 |
| rs772999455 | snp | A/T | 5.25114e-05 | 0.00512376 | intron-variant | PHF14 | GRCh38.p7 | 7:11061944 | TGTTATGTTTTATTT[A/T]ATTATCCCTTGTATG | 9678 |
| rs773007094 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11089959 | TATTTTTAGTAAAGA[C/T]GGGGTTTCTCCATGT | 9678 |
| rs773041559 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11138493 | AAGCCAGTTTTGTGC[C/T]CTGCGCACAATTACC | 9678 |
| rs773059947 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11081781 | GAATCACTTGAGCCC[C/T]GGAGGCAGAGGTTGC | 9678 |
| rs773060211 | snp | A/G | 1.94369e-05 | 0.00311738 | intron-variant | PHF14 | GRCh38.p7 | 7:11036731 | TTTTCACTGAGAACA[A/G]TTTGTTAATGAAAAT | 9678 |
| rs773068709 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11025409 | GAAGTTCTACCATGG[C/G]TAAAATGCTGTCAAA | 9678 |
| rs773070633 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11000624 | GATTACAGGCGTGAG[C/T]CACCACACCCACCCT | 9678 |
| rs773076357 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11073957 | CAGCCAGGATTCTGG[G/T]AGCAGTGTCCTGAGG | 9678 |
| rs773088374 | snp | A/C | | | upstream-variant-2KB | PHF14 | GRCh38.p7 | 7:10973712 | GCGGGGATCTCTGCT[A/C]CGCCTTGGCACTACT | 9678 |
| rs773094234 | snp | G/T | 1.65556e-05 | 0.00287707 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022945 | TACGACCAGTAACAC[G/T]AACGGAAATGAACTA | 9678 |
| rs773111976 | snp | A/G | 1.65927e-05 | 0.00288029 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982816 | AAAAATGGAACCTTC[A/G]ACGAAACCGACCACT | 9678 |
| rs773154008 | snp | A/C | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965012 | GCGATGGGTTAGAAC[A/C]TGCTCCTTTAGCTCG | 9678 |
| rs773154317 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144297 | AGCCATTATGGAAAA[C/T]AGTATGGATGTTTCT | 9678 |
| rs773165346 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11026914 | GCAAAATCAGATACA[A/G]TGTTGTAAATCATGA | 9678 |
| rs773178211 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10974976 | TCTCTTCCCCTTTCC[C/G]AGCTTTCTGGAGTTA | 9678 |
| rs773179481 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11135016 | ACAGACCCTTCTAAG[A/G]TCTCTAACTTCCTCT | 9678 |
| rs773189678 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002933 | TCCAGCTCTTCTACT[C/G]TCTTCAGGGTGATTT | 9678 |
| rs773211043 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993301 | CTTACCTGCTTTTCT[A/G]GTATTACAGCCCTTG | 9678 |
| rs773239421 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159997 | GCTGAGTTTTGGGGT[A/G]TGATTCATCCCATCA | 9678 |
| rs773253354 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11039944 | TATTTGCCAAGCTAG[C/T]ATTATCTTTTGGCTT | 9678 |
| rs773260946 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11158330 | ACAAGTTGGGTTTGC[G/T]TAATATTTTCTCATG | 9678 |
| rs773267440 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10990369 | GTGGATTCATTTTTC[A/G]TTTTTCCTAGTTTAA | 9678 |
| rs773276196 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11043715 | TTTGAGATATTCATA[C/G]TGGCCTGTTCTTTTG | 9678 |
| rs773284508 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11161077 | CTGTAACACAACTTG[A/G]GTTAATTTTTGCATA | 9678 |
| rs773320866 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11117897 | ACTTTTAAATATTTT[A/T]ACTATTCATTTGACC | 9678 |
| rs773329461 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10956280 | CAGCTGCTGGCTGCC[A/G]TGCAACCCTCTAGGT | 9678 |
| rs773355707 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11045199 | TGTTAGACATTTACT[A/G]GCATATCACTGACTG | 9678 |
| rs773359088 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10979037 | ACACTGTTGTACCAG[A/G]TCAATGAACAGAATT | 9678 |
| rs773360248 | snp | C/G | 4.37369e-05 | 0.00467617 | missense, intron-variant | PHF14 | GRCh38.p7 | 7:10982720 | CTGCCACCACACCAG[C/G]CACAAGTCCTCCTGC | 9678 |
| rs773370053 | snp | A/G | 0.00012033 | 0.00775567 | intron-variant | PHF14 | GRCh38.p7 | 7:11111319 | TTATATTATTTAGAT[A/G]CACCTACCTATAAAT | 9678 |
| rs773373967 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11106116 | GTGTATTTTTATATG[A/T]ATTGTTTTGTCTCAT | 9678 |
| rs773376145 | in-del | -/TTAT | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056400 | TCATTAGACCCATAG[-/TTAT]TTATTTCAGTTTATA | 9678 |
| rs773391037 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11129080 | GAACCTGGATGTTGC[A/G]TATTTTTTCTAAGAT | 9678 |
| rs773407739 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10993949 | AGGAGGTGGAGGCTG[C/T]AGTGAGCCAAGATTG | 9678 |
| rs773501389 | snp | A/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11064341 | TTTTATTACATTGCA[A/T]CTTAAATACTATCTT | 9678 |
| rs773529765 | snp | C/G | 3.31642e-05 | 0.00407198 | intron-variant | PHF14 | GRCh38.p7 | 7:11028843 | TTTAAACCCATAGTT[C/G]GTGAACATGTTCACA | 9678 |
| rs773535094 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10959716 | TTATGCTGTGGGTAC[C/T]GGCATCTGGATGAGG | 9678 |
| rs773564764 | snp | C/G/T | 8.41264e-05 | 0.00648517 | utr-variant-5-prime, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:10974292 | CAGCCTCTCCCTAAG[C/G/T]CTTCTCCAAACGACC | 9678 |
| rs773566575 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10986817 | AAACTAAAGTTTTGC[A/G]TGAGAATTAATCCAT | 9678 |
| rs773570079 | in-del | -/ACA | | | cds-indel, intron-variant | PHF14 | GRCh38.p7 | 7:10982500 | TAAAAGAAGAACAAC[-/ACA]TTAAAAATTCTGCAG | 9678 |
| rs773570650 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992252 | AGAGATGGGGTTTCA[C/G]CATGTTGGCCAGGCT | 9678 |
| rs773575015 | in-del | -/TACA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11055732 | AGAGCCTACTTTTAT[-/TACA]TTTATGTTTTAACTA | 9678 |
| rs773576768 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11095949 | GTATATAGAAGGTCA[G/T]CTTTGGGGCTATACT | 9678 |
| rs773584564 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988158 | TATCTCTAGTTTTCC[C/G]TATTTCCCTCTTTGC | 9678 |
| rs773594981 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11096530 | ACTGGATGCCATTTT[C/T]CAGTTCATTTACGGG | 9678 |
| rs773601347 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11069955 | CTTTGTTTTTAAAGC[A/G]TTTGTTTAAGATACT | 9678 |
| rs773604341 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11076000 | AAAAATTAGCCGGGC[A/G]TGGTGGCGGGCGCCT | 9678 |
| rs773612627 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10966864 | TCTTCCTAATATAGA[C/T]GAAAACACTGTCTCC | 9678 |
| rs773650773 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11057824 | GACAGATTACGAGCA[A/G]GGTGATTTAAGCAGC | 9678 |
| rs773650948 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11042111 | TCAATTGATGTGTGC[A/G]TTTTTAATTTTTTTA | 9678 |
| rs773653790 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11140880 | GAAGCGTCTTTGATA[C/T]ATGGTCAGTTTCTTC | 9678 |
| rs773655053 | snp | C/T | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10960204 | CATCAACTCGTCATT[C/T]ACATTAGGTATTTCT | 9678 |
| rs773664675 | snp | A/G | | | downstream-variant-500B, intron-variant | PHF14 | GRCh38.p7 | 7:11108176 | CTTGTGTCCAGTAAG[A/G]TGTTTCTGTGATTAG | 9678 |
| rs773666336 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11122581 | CCAGTAGAGGGAACC[A/G]TTAATGATATACTTC | 9678 |
| rs773666344 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11007871 | TAGTATGCCAAATTT[C/T]GCTTATTGAATTTAT | 9678 |
| rs773681940 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11084333 | TTTAAAGGACCAAGT[G/T]TTATTTTCTTCTTAC | 9678 |
| rs773687119 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079604 | TTTCTTTTTCTTCAT[C/T]AAAAAGAAACCAAAG | 9678 |
| rs773712937 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11035048 | TAAAAAAATACAGCC[A/G]GCCCTCCGTGTCTGT | 9678 |
| rs773713007 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11022228 | AAATATTTATATTTG[C/G]GGCATATAAATTTTA | 9678 |
| rs773718736 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10976826 | TTTCTGTTCCCTCTT[A/G]TAATATAATATCTAG | 9678 |
| rs773736137 | snp | C/T | 3.31609e-05 | 0.00407177 | intron-variant | PHF14 | GRCh38.p7 | 7:11028841 | TATTTAAACCCATAG[C/T]TGGTGAACATGTTCA | 9678 |
| rs773745425 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11153722 | TCTTTAACAGAAAAC[C/T]CACCTACTTTTAATA | 9678 |
| rs773765343 | snp | A/T | 3.40762e-05 | 0.00412758 | intron-variant | PHF14 | GRCh38.p7 | 7:11042835 | TAAAATAGAGGAGAT[A/T]TAGATGTTTGAATTG | 9678 |
| rs773832149 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11012294 | TAGAAACTTTAAATA[C/T]ACAGTCACCCCTCAG | 9678 |
| rs773847299 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11050271 | GAGAATTATAAGCTA[C/T]ATTCAAAGATACTGA | 9678 |
| rs773855852 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11142523 | TAAATCATTTCAGCC[A/G]CAAGCTTATAACCAA | 9678 |
| rs773879789 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11166501 | GATTTTTATTAATCT[G/T]GAACTGCGTATAAAT | 9678 |
| rs773889490 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11131951 | CTACTGGAATTTTTT[A/C]TTGTTGGGTTTTTTT | 9678 |
| rs773896246 | snp | A/G | 1.9726e-05 | 0.00314048 | intron-variant | PHF14 | GRCh38.p7 | 7:10982368 | TTTCTCATATTTTCA[A/G]CAGATTCTGAAGGGA | 9678 |
| rs773897054 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11070059 | TTTGATAATAAATTC[A/C]GTTTTTAGAATAAAT | 9678 |
| rs773909204 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11023214 | ATAATTGGTACTACT[A/G]CCATTTCCCTGGCAG | 9678 |
| rs773912583 | in-del | -/A | | | intron-variant | PHF14 | GRCh38.p7 | 7:11046938 | TGTGGAGGAGAAAAA[-/A]GTAAATCATGAATTA | 9678 |
| rs773920118 | snp | A/G | | | nc-transcript-variant, utr-variant-3-prime, intron-variant, downstream-variant-500B | PHF14 | GRCh38.p7 | 7:11169623 | TCAAAATGAAATAGG[A/G]GCTTGTATTTGGAAT | 9678 |
| rs773936002 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11154116 | AATGGATTTAACCAG[A/G]TTATTTATATGGAAT | 9678 |
| rs773958495 | snp | A/G | 8.14697e-05 | 0.00638187 | splice-acceptor-variant | PHF14 | GRCh38.p7 | 7:11040670 | TTTGTTCAAATCAAT[A/G]GAAGTTGAATATACC | 9678 |
| rs773978510 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11079633 | AGTTAGGATAGAAGT[A/G]TAGGGGAAGAGTGAC | 9678 |
| rs773978865 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11101466 | TTAGAGACTGAAGCA[C/T]TGAAAAAAGTTAGCA | 9678 |
| rs773997157 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11071066 | GATAATCTTTATTTT[C/T]GTGATAGTTGTTTAC | 9678 |
| rs774008098 | in-del | -/T | 0.0301243 | 0.118974 | intron-variant | PHF14 | GRCh38.p7 | 7:10982345 | TATACATATGTGTGG[-/T]TTTTTTTTTTCTCAT | 9678 |
| rs774019313 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11036236 | ACTAGGGGCAGATAT[A/G]GTTTATTGTAACTCA | 9678 |
| rs774032075 | in-del | -/TTCA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11111073 | GATTATACATATACG[-/TTCA]TTCATATGCTCTTAA | 9678 |
| rs774038401 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11123795 | CGGAGGCTGGAATGA[A/G]CAGAGATCGTGCCAC | 9678 |
| rs774049330 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10981123 | TGTGGGGTTCACTAG[A/G]TACCAGATACTAATT | 9678 |
| rs774069740 | snp | A/G | 1.70778e-05 | 0.00292209 | intron-variant | PHF14 | GRCh38.p7 | 7:11013924 | TAATGTCCTAATTAT[A/G]TTGGTTCATATGTTT | 9678 |
| rs774072166 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11090051 | GCTGGGATTACAGGC[A/G]TGAGCCACCTCACTT | 9678 |
| rs774073222 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11083940 | GAAGATGGGATGCCC[A/G]TCTGGGGCAATAGGT | 9678 |
| rs774084603 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10987985 | CCCACCATTGCACTC[C/T]AGCCTGGGCAACAAG | 9678 |
| rs774087875 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11056874 | TTTTTGAATAGCTGC[C/T]AGAAAGCTACTGGCA | 9678 |
| rs774100351 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11074201 | GAAAATGCCTTTCCT[G/T]TTTTTTCTTTTTTTC | 9678 |
| rs774112740 | snp | A/C | 4.98608e-05 | 0.00499279 | synonymous-codon, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11036498 | CCAGGCCTGGGTTCC[A/C]AGGGAAAAATTGCCC | 9678 |
| rs774116143 | in-del | -/AAC | | | intron-variant | PHF14 | GRCh38.p7 | 7:10992878 | TCACCTTTAATGTAG[-/AAC]AACAGTCCTTGAGTT | 9678 |
| rs774123296 | snp | A/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11146647 | GGGCAACATATATGT[A/T]CATTTTTACAAAAGC | 9678 |
| rs774152517 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114810 | AACATACCTTCTCGC[A/G]TAGGCTATGCTTCAA | 9678 |
| rs774177638 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11128095 | TCACTGTATTGGTTT[A/C]TCTCAACTGTTTCTT | 9678 |
| rs774194458 | snp | A/G | | | | | GRCh38.p7 | 7:10971059 | ATAAGACTAAGTGGA[A/G]GACTGAAAGTTTTCT | 9678 |
| rs774204720 | snp | A/G | 1.67449e-05 | 0.00289347 | intron-variant | PHF14 | GRCh38.p7 | 7:11036385 | ATGTTTCATTTTATT[A/G]TCTTTTAAAATTTGA | 9678 |
| rs774206944 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11144727 | AGGATTTTGAATGTT[C/T]GTAACACAAATGATA | 9678 |
| rs774216743 | snp | C/T | | | intron-variant, utr-variant-3-prime | PHF14 | GRCh38.p7 | 7:11063856 | CTTTAGTTTCTGTTA[C/T]GAAATTTTTATTTCT | 9678 |
| rs774222050 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10964971 | AGCCATTCATCTAAC[C/G]TTTTTTCTAGGTTTC | 9678 |
| rs774231668 | snp | A/G | 2.22794e-05 | 0.00333755 | intron-variant | PHF14 | GRCh38.p7 | 7:11038874 | AGTTTCTTTCCAATT[A/G]CTGTCTCCTTCAGTT | 9678 |
| rs774244161 | in-del | -/ATG | | | intron-variant | PHF14 | GRCh38.p7 | 7:10988202 | TAAGAGCCTCAAGTC[-/ATG]AGGATCAGAGGGCCA | 9678 |
| rs774246355 | in-del | -/AGTA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11028413 | TAGTGACTGGCACAT[-/AGTA]AGTCCTCAAATAATT | 9678 |
| rs774248915 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11048236 | AAAGAAGCCAGGTAT[A/G]TATTTGACTTTAGGA | 9678 |
| rs774258385 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11114422 | AGGGCAAAAATTTCT[A/G]TCTTTACCCCTGTCT | 9678 |
| rs774263844 | snp | A/G | 1.65872e-05 | 0.00287981 | splice-acceptor-variant | PHF14 | GRCh38.p7 | 7:10974833 | TTTTTTTCTCTTCAC[A/G]GTGGATCGCAGCTCC | 9678 |
| rs774265467 | snp | A/G | 2.10201e-05 | 0.00324185 | missense, nc-transcript-variant | PHF14 | GRCh38.p7 | 7:11022926 | TTTGGAGATATTGAC[A/G]AATTACGACCAGTAA | 9678 |
| rs774289026 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11159519 | TATGAAATGATTTTC[C/T]TAATTTTCAAAGAAA | 9678 |
| rs774293313 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:11041424 | AAGATGCTGGTGTTT[G/T]TGTGTGTGTGTGTGT | 9678 |
| rs774299239 | in-del | -/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11018302 | TGTCATTGGTATTTT[-/G]ATAGGGATTGCATTG | 9678 |
| rs774311397 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11133449 | AATTCAGTAAAGAAA[A/G]TATAGTCTTTTCAGT | 9678 |
| rs774322243 | snp | A/G | 0.000107452 | 0.00732901 | intron-variant | PHF14 | GRCh38.p7 | 7:11042824 | TTATTGGTGAGTAAA[A/G]TAGAGGAGATTTAGA | 9678 |
| rs774322383 | snp | C/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994266 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 9678 |
| rs774333486 | snp | C/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:11002767 | AGACTTCTTAATCCT[C/G]TTAATAATGGTTAGG | 9678 |
| rs774362173 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | PHF14 | GRCh38.p7 | 7:11103085 | TGTAAAACAACTATA[A/G]ACTCATATTAAATGT | 9678 |
| rs774385552 | snp | C/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10968191 | TTTCAGTTTCAAGAT[C/G]ATATAACTGTAGCTA | 9678 |
| rs774397477 | snp | A/C | | | intron-variant | PHF14 | GRCh38.p7 | 7:11148067 | AATTCCAAAGCATAT[A/C]ATACTTCTTTCCGTT | 9678 |
| rs774410510 | snp | A/G | | | intron-variant | LOC107986767 | GRCh38.p7 | 7:10965135 | CTGTGTTCCTTTGGA[A/G]GAGAAGAGGTGTTCT | 9678 |
| rs774417228 | in-del | -/TAATAA | | | intron-variant | PHF14 | GRCh38.p7 | 7:11102248 | TTTGACAACCAAAAG[-/TAATAA]TAATAATACAAGAGG | 9678 |
| rs774421987 | snp | G/T | | | intron-variant | PHF14 | GRCh38.p7 | 7:10980636 | AGTGTTTTGTAAGGT[G/T]CACACAAACTTACTT | 9678 |
| rs774429494 | snp | A/G | | | intron-variant | PHF14 | GRCh38.p7 | 7:10994966 | CCCTTCTCTGGCCCC[A/G]CCCACATCCTGCTGA | 9678 |