| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs142074592 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254828 | CAGTGTCAGCTTTTT[C/G]AGAGATCTGATATTA | 84333 |
| rs142082682 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173096 | TCTCCTAGGTATTCA[A/G]TGTGAAAACTCTTTG | 84333 |
| rs142119704 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237693 | AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 84333 |
| rs142131091 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251820 | TTATCCTTTATTTCT[C/G]TATTTTTATTTGCAA | 84333 |
| rs142135129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170963 | GAGGAAGCTTAAATG[C/T]ATATTCCTAAGTCAA | 84333 |
| rs142163289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216249 | TTTGGCAGCTTTGAG[A/G]TGCCTGAGAAGGTGA | 84333 |
| rs142174191 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174831 | TAGAATTTGGTGGAT[A/G]GAACGCATGTGTTTA | 84333 |
| rs142185157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205649 | TCCTTGCCCTGCATC[A/G]GACCACATCAGAATC | 84333 |
| rs142219246 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256625 | TGATAAATTCAAAGA[A/G]ATTCATACCTAGGCA | 84333 |
| rs142222160 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171909 | TATCAGTGTCAGTGT[A/C]TGTCTTTAAAACTAT | 84333 |
| rs142269656 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277275 | AGTCTAGCCCTTTTA[A/T]CTATATGAAAGAATA | 84333 |
| rs142309734 | snp | A/G | 0.135825 | 0.222405 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188167 | ATTTCCATCTGAGGT[A/G]CTGGGTTCATCTCAC | 84333 |
| rs142468863 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195244 | ATGCCACCATACACC[A/G]TTGAAAAAAGTGCCT | 84333 |
| rs142481328 | snp | A/C | 0.000214262 | 0.0103482 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240533 | TAGCAATGATTGCCC[A/C]AGGTGTGGCAACCAA | 84333 |
| rs142497201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277939 | ACTAACTGAATGCCT[A/G]TAAGCAGGGTGTGTG | 84333 |
| rs142498816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182983 | GTGGTCCAAGAGACT[A/G]TTTGTTACTATTTCA | 84333 |
| rs142512146 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227534 | TTCTCAAATCTGTCC[C/G]TTTAGTTTCATCCCT | 84333 |
| rs142527674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202770 | AAGGGGTAGTTAGGC[A/G]AAAAGATTGGCCATT | 84333 |
| rs142539040 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186791 | CTAACATTCTTTCCA[C/T]GTATAGGGAGCTGTC | 84333 |
| rs142568452 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190298 | CCCATCACCTTGGGG[G/T]TTAAGATTTCAACAT | 84333 |
| rs142578695 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282691 | TATGGAGTCTTTCTG[A/G]TAGGTCACTAGGTAA | 84333 |
| rs142605295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233493 | GTGAAATTGCAACTC[G/T]TGTAGGCCTTTGAAA | 84333 |
| rs142643165 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183652 | GTTTATGTAGTTCCC[A/G]TATAGTGTCACTGGT | 84333 |
| rs142695368 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274785 | GCCTGAGGCAACACA[C/T]TGCAAAGGCCCTGAG | 84333 |
| rs142716800 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278980 | TGTTAGCCCTCCAGA[C/T]TGAAAATGTATGTGA | 84333 |
| rs142725531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205310 | ACACACACACACACA[C/T]GGCCCAGCTAACATG | 84333 |
| rs142763163 | snp | A/G | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219162 | CATTCTGGCAACCCC[A/G]CCTCCACATTCATCC | 84333 |
| rs142787161 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164131 | ACACGCGCGCGTACT[C/T]GCTATGTACCTCTGA | 84333 |
| rs142826108 | in-del | -/GATAGATAGATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246966 | ATAGATGGATAGATG[-/GATAGATAGATA]GATAGATAGATAGAT | 84333 |
| rs142909174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267468 | CCAGCACCTAGGGCA[G/T]TGCCCAGCATATATA | 84333 |
| rs142919858 | in-del | -/TATCT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174693 | CATTAATTGGGAAAG[-/TATCT]TATCTAATCAGGCAT | 84333 |
| rs142951998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253911 | GCAGCACAGACAATA[A/G]TAAATGAATGGGCTT | 84333 |
| rs142980825 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282476 | GTGACACAGCGAGTC[A/T]CCATCTCCAAAAAAA | 84333 |
| rs143020849 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226405 | TATGCAGAAGAAACT[C/T]GTGTTTTGTGAAATT | 84333 |
| rs143034492 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241755 | TTATCTGTGTGATAT[A/T]TGCCATCATTCTATA | 84333 |
| rs143045780 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164514 | CCTCCTAGTAATTGC[A/G]TCTACCTAACTGGTT | 84333 |
| rs143084989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201999 | CTGGACTTGGGAGCT[A/G]CACTGTCCAGGATTA | 84333 |
| rs143136796 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245915 | TAGTATGATTCCTGG[A/C]AAACTTAAAGGCATG | 84333 |
| rs143186487 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244764 | GATATAGGATATGGG[A/G/T]TAAAGAAAAGAGTTG | 84333 |
| rs143197358 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196324 | AACCATAATCAGACC[A/C]TAATTTCAGTTTACA | 84333 |
| rs143275367 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258290 | TAAGTAGTGATACAA[A/G]CATCATTTCTGGAGA | 84333 |
| rs143289082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198695 | GAATCTCCCTGGCCT[A/G]TTCAGTAGCATTGAA | 84333 |
| rs143333470 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218432 | TCATGTTGTAGCTTC[C/T]GTCATTTGTCCTCTG | 84333 |
| rs143338803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186792 | TAACATTCTTTCCAC[A/G]TATAGGGAGCTGTCC | 84333 |
| rs143433812 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278990 | CCAGATTGAAAATGT[A/G]TGTGACCTCTTGAAC | 84333 |
| rs143439952 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183523 | ACTCTTTCTCCAGCT[C/T]GCCATTCTGTGTCTT | 84333 |
| rs143454791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266783 | TGCCTTTTTCTTTCA[C/T]CCATCCTTTCTTAGC | 84333 |
| rs143467658 | in-del | -/CCT | 0.0189856 | 0.0955633 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253355 | CACCTTCAAGTAGGG[-/CCT]CATGTCTGTTGTTCT | 84333 |
| rs143510557 | in-del | -/CAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249789 | TGTAACAACAACAAC[-/CAA]AAAAAAATGGCAAAG | 84333 |
| rs143547716 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273706 | CTTTGCCATTCTTAA[C/T]AGCAAAAACTGACAG | 84333 |
| rs143609513 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196671 | TTCCGTATTTCAGAG[A/G]GTGACAAATGCTATT | 84333 |
| rs143621499 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216998 | GTTAAAATATTAAAC[A/G]GCATTCTTAGGTACA | 84333 |
| rs143682185 | in-del | -/TG | 0.077417 | 0.180873 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171142 | AGTGAAACTACTCTG[-/TG]ATATAACAGTGCATA | 84333 |
| rs143695853 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204315 | TAATTAAACCTTAAT[C/G]TGAATTAAGGTTTTC | 84333 |
| rs143714612 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221697 | CTTTCATGTTGTGTT[G/T]TCTGAGAGGATACAT | 84333 |
| rs143756695 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272759 | GCCTGGGTGACAGAG[C/G]AAGACTCTGTTTCAG | 84333 |
| rs143789698 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246660 | AGGTGGGACAGATAT[C/T]GAGAGGGAGCTCTGA | 84333 |
| rs143802519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210724 | CCTGCTTTCTGTTGT[C/T]TGGTCTCTCCCTTTC | 84333 |
| rs143839613 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168728 | GGTCAAGAGTTCCAG[A/G]CCAGTCTGGCCAACA | 84333 |
| rs143861496 | in-del | -/GGGGGG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174740 | AGAAAAATTATGGCT[-/GGGGGG]GTTAAAAGAAATTGA | 84333 |
| rs143874139 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194560 | CTGCAGAGCTATAAG[A/G]TAATACATTTGTGTT | 84333 |
| rs143901840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197757 | CTTCCTATTTTCAGT[A/G]CACTTTCATTTTGTT | 84333 |
| rs143953412 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172656 | GTGTTGGTTACCCTT[A/G]AACATAGGTTATTGA | 84333 |
| rs144006190 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166061 | TTGAAATTACTTGGC[A/G]CAGTTCATTCCTTTT | 84333 |
| rs144046980 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248210 | TTTTAAAGCCAGACC[A/G]TATTTCCAAGGCAGG | 84333 |
| rs144052226 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169195 | TGGATAATAATGCCC[A/G]ATTTTAATCTTAAAA | 84333 |
| rs144071656 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178688 | GCCCCTGCACCTGGC[A/C]TGCTGTTTCTCATTT | 84333 |
| rs144097787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216197 | TAAATGTGAGTTGTT[A/C]ATGTATGAATATGGT | 84333 |
| rs144117695 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181010 | TTCAATTTGTGTCAT[C/T]TCTGATTTTTTTAAG | 84333 |
| rs144151432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206886 | CTAACTAAATCCTTC[C/T]CTCACCTCCCTATTT | 84333 |
| rs144261949 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269913 | TGTTATGTGTTACAG[C/T]TATTTTCTTCCAATT | 84333 |
| rs144295612 | in-del | -/TAAAA | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229030 | TAATCATAGAATTGT[-/TAAAA]TAAATGCTAATAAAG | 84333 |
| rs144309280 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241599 | ATCTTTAAGAAACTA[C/G]TCGTCTAGAATCCAG | 84333 |
| rs144312552 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181375 | CTAATTGCCCTGGCC[A/G]GAACTTTGAATACTA | 84333 |
| rs144351361 | snp | G/T | 0.000544721 | 0.0164944 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91271664 | GAACTGCTCAGCTTC[G/T]CAAGTCTGCTCTCAG | 84333 |
| rs144393625 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168677 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 84333 |
| rs144400171 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256959 | AAAAGAAATAGATAA[A/G]TTGTAAATGTAAAAC | 84333 |
| rs144443468 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263300 | CTTTGCTTATGAATT[A/G]ATTTACAAAAAAGAT | 84333 |
| rs144475420 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261791 | CAATTCTTTATAGAC[A/T]TCTTCAGAATGTAAA | 84333 |
| rs144518362 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202626 | CCAGAAGTTGTTACT[A/G]TATTTGACTCCTTAG | 84333 |
| rs144531926 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203185 | ACTAACCCATTCAGC[A/C]GGGCTTTGTATAGCC | 84333 |
| rs144540770 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188439 | AAGCAGAAAATACAA[G/T]TTTATGTATATTAAA | 84333 |
| rs144576272 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267811 | GCCAGGATGTCTGAA[A/G]AGCTCTTATTAGTCT | 84333 |
| rs144581783 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178664 | AAAGTGCTGGGATTA[C/T]AGGTGTGAGCCCCTG | 84333 |
| rs144600725 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191432 | ACACTACTCAGATGG[C/T]ACACAATTTAAAACT | 84333 |
| rs144613662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234248 | AAGGAATTGGGAAGC[A/G]GCAAAACAAAATAGC | 84333 |
| rs144690508 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282356 | AGGTGTGGTGGCACG[C/T]GCCTGTAATCCCAGC | 84333 |
| rs144807100 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283691 | GCTGTGGTCCACGAC[A/G]GGAGCTTGTTGGGGG | 84333 |
| rs144865237 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198043 | CCTCACAGAGCTTAC[A/G]TTCTAATGGGTAGAG | 84333 |
| rs144886924 | snp | G/T | 0.0766824 | 0.180169 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188248 | GCGAGCTGAAGCAGG[G/T]CTAGGCATTGCCTCA | 84333 |
| rs144904822 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263313 | TTAATTTACAAAAAA[A/G]ATAAAAATGAAATTA | 84333 |
| rs144933226 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229255 | GAACAGGCATAGTCT[A/G]TGCCCTCCTAGAACT | 84333 |
| rs144962553 | in-del | -/C | 0.0704125 | 0.17392 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161467 | GACAAACCCACACTA[-/C]CCTAACAGGGCCGGA | 84333 |
| rs144975291 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210418 | ATGCTAACCTGCAAA[G/T]CTAGTAAGATACACA | 84333 |
| rs145116406 | in-del | -/T | 0.0825414 | 0.185628 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209167 | TTTTATCATTAATCC[-/T]TTTTTTCTGACATAA | 84333 |
| rs145142605 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266003 | TTTCTGTAACATTTT[A/G]TAATGTTTTAAATGA | 84333 |
| rs145165809 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271322 | AAGAGGATGTCCCTC[A/G]TGTATGCAAGAAGTG | 84333 |
| rs145165877 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205529 | AACATTATAAATGAT[A/G]AGTTTCTCAGGCCAG | 84333 |
| rs145206415 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228490 | AATCCCTAACCTAAG[A/G]ATAAATTATTTGCAA | 84333 |
| rs145226284 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181387 | GCCGGAACTTTGAAT[A/G]CTATGTTGAATAGGA | 84333 |
| rs145260944 | snp | A/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208038 | TAGACTATCTCTGTC[A/G/T]AGAGACACTGTACAA | 84333 |
| rs145285683 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175367 | AGCCCAAACCTAGGA[G/T]AGGTAATTCAGTCAG | 84333 |
| rs145324237 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189348 | CACTAGACAGTGCAC[C/T]CAGCAAAGGCAGGGA | 84333 |
| rs145361820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277897 | GGAATCCAGGCTGCT[A/G]ATCTGTCTTGTTCGC | 84333 |
| rs145365824 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236540 | TCTTAACCTTAGACT[A/G]GGACCTTTTTAACAT | 84333 |
| rs145534771 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244117 | TAATTTATATGGTAT[C/G]TTAGAAAGTGAAAAT | 84333 |
| rs145554658 | in-del | -/CA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186611 | TGTATATATACACAC[-/CA]ATATATATGTAACAA | 84333 |
| rs145564813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232937 | GGTCATGAATTTAAG[A/G]TGAGAGACCAGTCAG | 84333 |
| rs145588188 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236369 | ATTTGGTTAGTGCTC[A/C]TTAAATATTAGCTAA | 84333 |
| rs145672416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170386 | TCAAATAATAGTCTG[C/T]TATCTAAAATATACA | 84333 |
| rs145675563 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185834 | AGATTCCCTTGACTC[C/T]GTGTGGCTCCCTGGT | 84333 |
| rs145681541 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243142 | CTAGAAAGCAAACTG[A/G]TGATGGTGATAGTTG | 84333 |
| rs145689366 | in-del | -/ACTT | 0.220843 | 0.248294 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203358 | GTGTTCCTTTGTTTA[-/ACTT]ACTTTTTATTAGGAT | 84333 |
| rs145754127 | in-del | -/AAACGAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209799 | AAAAAAAAAAAAGAA[-/AAACGAAG]AAAGGAATTGGAGGA | 84333 |
| rs145780046 | snp | C/T | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 10:91203909 | GATTTCAGTCAGGCC[C/T]ACATTTCTGAAATGA | 84333 |
| rs145801799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190066 | TACAATAGAAATTTA[C/T]TTCTCACTGTTTTTA | 84333 |
| rs145837383 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274160 | TTTTATAGAGATGCC[A/G]GTTCACCCCACAATT | 84333 |
| rs145865790 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271929 | AGGCTATTACTTATG[A/C]ATCAGGAATTTTTAA | 84333 |
| rs145873805 | in-del | -/GAAAGT | 0.234723 | 0.250368 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232773 | GTTTTCAGTAAAATA[-/GAAAGT]GAGGTCCTCAGTGGA | 84333 |
| rs145879253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183062 | ATTTTAAGAGTACAT[C/G]TTTTGTGGCAATGAG | 84333 |
| rs145900081 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176109 | AGGGCAGGCCTGGTG[A/G]TGAAAAAATCTCTCG | 84333 |
| rs145906357 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278050 | AGGCCTTTGAACTTG[A/G]CCTCTGCTGCATATT | 84333 |
| rs145919833 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259185 | TCTGCACATTTTACA[A/G]ATGAGACACATCAGG | 84333 |
| rs145928441 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197182 | GTCAGGAATTTGGAG[G/T]CTGGTCAGCAGCGTA | 84333 |
| rs145992869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233675 | ACGTGTAAGAATAGG[C/T]ATCAAAAGCAGGAAA | 84333 |
| rs145994948 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181028 | TGATTTTTTTAAGCA[C/G]TGGTTTGTTGTTCTC | 84333 |
| rs146008354 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200607 | TTTGTTTTGTTTTTA[A/G]GATATTGAGTCTTGA | 84333 |
| rs146014426 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244980 | AGGTCTGGGCTGGAG[-/A]AAAACATTTGGTAGT | 84333 |
| rs146020112 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183712 | CTGGTAATAGTCCTT[C/T]TTTGCCATATGTAGT | 84333 |
| rs146036498 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186543 | ATATGTGTGTGTGTG[-/TA]TATATATATATATAT | 84333 |
| rs146104676 | snp | C/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280691 | TTTTGGTATATTCAA[C/G]TACAGCTTTCTAAGG | 84333 |
| rs146115638 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198193 | TTTCCGTCTCTCTAA[A/G]TTGAACCCACAGTCC | 84333 |
| rs146237275 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221435 | TTTGCTGAAGGTCAT[A/G]CAGGGGTAAGGGCCA | 84333 |
| rs146262755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227510 | CCTGCTGGTCTCTCT[C/T]TTTAATACTTCTCAA | 84333 |
| rs146265633 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238653 | TTCCCAAATTTCAGA[A/G]ACTTATCTATCATCC | 84333 |
| rs146346593 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228119 | GGAGAGACTCTGGAC[G/T]GGGGACTAGAAATTG | 84333 |
| rs146359255 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169026 | GAAAGGAATGAAGAT[C/T]GAGGGAGGACGTAGG | 84333 |
| rs146384722 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172163 | GGCGCGGTGGCTCAT[A/G]CCTGTAATCCCAGCA | 84333 |
| rs146428084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244650 | TAGAAAGTAATTGCA[A/G]TGACCCTGGTGAGCG | 84333 |
| rs146439628 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248837 | TCCTGCACAAAATTC[A/G]TGCACCCTTTTATTT | 84333 |
| rs146440208 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190960 | TTTGCCTTTCTGCTG[A/G]CAACGAGTCCAGATC | 84333 |
| rs146460099 | snp | C/T | 0.000247621 | 0.0111243 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91271676 | TTCGCAAGTCTGCTC[C/T]CAGGATGGCCCTTTG | 84333 |
| rs146466277 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195982 | CCAAGAATGTGCCTT[A/G]AAATTGGCTACTAGA | 84333 |
| rs146550590 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270008 | TAATGAAATATTATA[C/T]ACTGAAGTGTTTAGC | 84333 |
| rs146564114 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275747 | CGTGAGCCACTGCGC[C/T]CAGCCAGAACTACCT | 84333 |
| rs146566940 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201066 | GGGGAAAGTTTTATA[A/T]AAGTGAGAAGAGCTG | 84333 |
| rs146590122 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216386 | CCTATCTATCTAGCT[A/G]GAGAGTAAAGAGGTA | 84333 |
| rs146609559 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186570 | TATATGTGTGTGTGT[A/G]TATATATATGTGTGT | 84333 |
| rs146672621 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196449 | CAGAGCTTTATGTCC[C/T]TTCTCACCCCAGGGC | 84333 |
| rs146683574 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161159 | GGGTTCCGGCTGTCT[A/C]CTCTCTTTGCCCCTC | 84333 |
| rs146683930 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198772 | CCTTGTCATACCACG[A/G]GGCAGTACCTCTTAA | 84333 |
| rs146710236 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165720 | GAGTTATTTAAAATT[A/G]TATTTTAAACATCTT | 84333 |
| rs146804082 | snp | C/T | 0.144632 | 0.226711 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177541 | GGCCTCCTTGAGCTG[C/T]GGTGGGCTCCACCCA | 84333 |
| rs146804924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222008 | TTAGAACCTGCAGAG[A/G]AGACGGTGGGAGAGG | 84333 |
| rs146829759 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275446 | TAAAACTACATTTTA[A/T]TTTTTTTTTTTTTGA | 84333 |
| rs146830629 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178779 | TAGTAAAAAAAAAAA[A/T]GTAATGATGATGAGT | 84333 |
| rs146896243 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224291 | CTTATTCAATTAGCA[A/G]TTAACTATGTACTAT | 84333 |
| rs146947830 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219319 | ATCACATTTAAGCCC[C/T]CTGGACTCCACTGTT | 84333 |
| rs146979359 | in-del | -/TA | 0.237501 | 0.250947 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274117 | ATCAATCTGTGTATG[-/TA]TATATATATATGTAA | 84333 |
| rs146982591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167504 | GAGACGACTTCAATC[A/G]GCAAAAATGTAGGGA | 84333 |
| rs146991448 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170595 | AATGGCCAAAATTCA[A/G]AACACTGACAACAGC | 84333 |
| rs147054106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245939 | AGGCATGTTTGTGTT[A/G]TAGTTAGGAATTTGA | 84333 |
| rs147085242 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230491 | CCAGGGCGCAAAGCT[A/G]TATTTTCTCAGAATA | 84333 |
| rs147085376 | in-del | -/TTTAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261034 | GACCTTTTTTTCTTT[-/TTTAA]TTAAGCTCATGTTTT | 84333 |
| rs147096185 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182210 | CCCGTAGGAATGGTC[A/G/T]CAGCTCTTCTTTGTA | 84333 |
| rs147115404 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179326 | GCCAATATTTGTTTC[-/T]TTTTTTAAAAAAAAA | 84333 |
| rs147134754 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266849 | AGAATCCAGCTATGT[C/G]TCACTACATCCACTT | 84333 |
| rs147136809 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178555 | TCACCACACCCGGCT[A/C]ATTTTTAAAATTTTT | 84333 |
| rs147158306 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180354 | CTTTAGTTTAATTAG[A/T]TCCCACTTGTCAACT | 84333 |
| rs147230229 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262370 | GAGGCGGAGGTTGCA[G/T]TGACCCGAGATCACG | 84333 |
| rs147240947 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195031 | GTGTGTGAGTTCTCT[A/T]CTGATGACTCAGTTT | 84333 |
| rs147264405 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197850 | TTATTTAAAAACAGA[C/T]GTTCCAAGGAAATAG | 84333 |
| rs147274705 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164193 | CGCCCGGAGGGGCGG[A/G]GAAGACTTAGTGCAA | 84333 |
| rs147337782 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189351 | TAGACAGTGCACTCA[A/G]CAAAGGCAGGGAGGT | 84333 |
| rs147339302 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276936 | AAATGGAGATAATCT[-/G]TGTCTTGCTCCCTCC | 84333 |
| rs147369927 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176882 | TGGAGAAGTTTGATC[A/G]TCTGAAGCCTTCTTC | 84333 |
| rs147375551 | in-del | -/TG | 0.125874 | 0.217008 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240151 | GTTTTTATCTTTTTC[-/TG]TCCTACTTCTTTAAA | 84333 |
| rs147379640 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177798 | AATTTTCCAGGTGCC[A/G]TCTGTCACCCCTTTC | 84333 |
| rs147441863 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207074 | TGAGAACATAGCCTC[A/G]CCCACTGTAGAAGGA | 84333 |
| rs147450855 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241980 | AGATCACTTCGTTTA[A/G]CAAGCTCTCTAGGTG | 84333 |
| rs147483591 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192977 | GGTTAACCTGGATTA[C/T]CTGGGTGGCCCAATC | 84333 |
| rs147546107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234428 | GCATTCAAAGATAGG[C/T]TCTTCCTATTCAGGT | 84333 |
| rs147593970 | in-del | -/ATGCAGGTACCTGG | 0.0379877 | 0.132479 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185915 | CCTTGATTAGTCCCA[-/ATGCAGGTACCTGG]ATGCAGGTACCTGGA | 84333 |
| rs147619762 | snp | A/C | 0.0314385 | 0.121371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250732 | GTATGCCATTGAGAT[A/C]TCTTTAATGGAGTTG | 84333 |
| rs147620788 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170666 | ATTACTAGTGGGAAT[G/T]TCAAACAGTACAGCT | 84333 |
| rs147629506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256448 | CTCAGAGAGCTGTAG[A/G]CACCATCAAGCTTAC | 84333 |
| rs147630859 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174433 | AATCACTTGAACCCA[C/G]GAGGTGGAGATTGTA | 84333 |
| rs147702798 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257844 | ACATGTTCACACAAA[A/C/G]TCTTGTATATGTATA | 84333 |
| rs147724459 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182781 | GAACTTGATTTCTGC[C/G]TTAATTTCATTATTT | 84333 |
| rs147733453 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282551 | TAGAATTTAGCCATA[C/T]AGCCAACTTTGACAA | 84333 |
| rs147734075 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186621 | ACACACATATATATG[C/T]AACAAATTAAAATGT | 84333 |
| rs147743323 | in-del | -/TTTAA | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261033 | TGACCTTTTTTTCTT[-/TTTAA]TTTAAGCTCATGTTT | 84333 |
| rs147805190 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284004 | TATGTATTTTTGTAA[A/G]GGAAAAGCACTTGTA | 84333 |
| rs147829584 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200610 | GTTTTGTTTTTAAGA[C/T]ATTGAGTCTTGAACA | 84333 |
| rs147829933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263322 | AAAAAAGATAAAAAT[A/G]AAATTATCTCCTTTA | 84333 |
| rs147839557 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203237 | ATGTTTAGGAAAATT[A/T]TCCAACATTTGGGAA | 84333 |
| rs147934054 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224877 | GGCTACCCTAGAGTT[A/G]TATTCTACTTCCGTT | 84333 |
| rs147943858 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229431 | TCTATGAAAAGGTTT[A/G]AGGGAAGAGTATTTC | 84333 |
| rs147972947 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279523 | TACAAAATGTCCTGT[A/G]TTTTGCAGTTTTGTT | 84333 |
| rs148015263 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272899 | TACATAACAAACTTA[A/G]CTGGCATACTTACCT | 84333 |
| rs148047422 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196699 | ATTTGTGTATTTCTT[A/G]TTGGTCCCCCTCACA | 84333 |
| rs148052181 | in-del | -/AG | 0.0337553 | 0.125452 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217055 | TTTTTTTTTTGAGAC[-/AG]AGTCTCTCGCTCTGT | 84333 |
| rs148070647 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91161821 | AGAGCTGCAGACACT[C/T]GGAGGCAATATTAGT | 84333 |
| rs148091595 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204754 | CTCTTCTTCAGATTT[A/C]TTCCTCCTTTCACTG | 84333 |
| rs148101936 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171241 | GGAAGAAAGAAGTTA[A/G]ATGAAAACAAAAGGA | 84333 |
| rs148144689 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211513 | AGGTCATTTACTATC[A/G]GACCTGATCTGCATA | 84333 |
| rs148238977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234062 | AGCTCACTCTCTGTG[A/G]TACATAAGAGACCTG | 84333 |
| rs148262261 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167329 | GGCTTAAGAGTCATG[C/T]AGAGCACATAAGACA | 84333 |
| rs148281018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226525 | TATTAGTAGCTCTCT[C/T]TGCTTTGATATGGGT | 84333 |
| rs148301306 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258362 | GAGTCTTCCAGTACA[C/G]GTTGAGTATCCCTTA | 84333 |
| rs148321964 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241640 | AAAAGGGGTCAATTC[C/T]GGAGTTAGCTTTTTA | 84333 |
| rs148324240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201120 | GGAGCTGTCTTAGTT[C/T]GTTTTCTGTTGCTAC | 84333 |
| rs148353938 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266027 | TAAATGATTGTACAT[A/T]CATCAATCACCCTCA | 84333 |
| rs148354935 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177732 | ATAATCTCCTGGTGC[A/G]CCATTTGCTAAGACC | 84333 |
| rs148404482 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262235 | GTTTGAGACCAACCT[G/T]GCCAACATGGTAAAA | 84333 |
| rs148426156 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202750 | GTGCTTCTTAATGTT[A/G]GGGCAAGGGGTAGTT | 84333 |
| rs148448372 | in-del | -/G | 0.0528381 | 0.153711 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226703 | TAGATATAGAAAGAA[-/G]GGCCCAAAAGGTGAG | 84333 |
| rs148457383 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178687 | AGCCCCTGCACCTGG[A/C]CTGCTGTTTCTCATT | 84333 |
| rs148467786 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268117 | GTGTGTGTGTGCATA[C/T]GTGTGTGTGTGTTCC | 84333 |
| rs148499126 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282470 | GCCTGGGTGACACAG[C/T]GAGTCTCCATCTCCA | 84333 |
| rs148583700 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198084 | AACATTTTTACTTTT[A/C]AGGCAATGAGAAATA | 84333 |
| rs148664640 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216233 | TGTATACAGGAGGCT[C/T]TTTGGCAGCTTTGAG | 84333 |
| rs148669111 | in-del | -/GT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254203 | CTTCCCCTCCACCTC[-/GT]GTGTGTGTGTGTGTG | 84333 |
| rs148688975 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176956 | GCTGATGAGGAGCTG[C/T]GTTCCTTTGGAGGAG | 84333 |
| rs148707974 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229141 | TTACCCAACCAAGAA[C/T]CCTTCTAGTTAGGTG | 84333 |
| rs148710899 | snp | C/T | 0.00172975 | 0.0293578 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240500 | CTGTAAGACTTGTAT[C/T]GTTCAGCACTTTGAA | 84333 |
| rs148751751 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188709 | CCTTAGGAATCTTCT[A/G]CCAGAGTCCTCTGTT | 84333 |
| rs148795155 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246904 | GCATCTGTTGGAAAT[A/G]TGGAACTTGAAATCA | 84333 |
| rs148813690 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231772 | TCAGACTACTATGTC[A/G]AAAGCAGACCTGTTA | 84333 |
| rs148814753 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250912 | ATACTTATTTATAAA[-/TT]CGAGTATAATTTATA | 84333 |
| rs148815477 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196505 | TCCTTTATTCTCCCA[G/T]ATCTTTCCATGGCTT | 84333 |
| rs148831879 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186578 | TGTGTGTGTATATAT[A/G]TGTGTGTGTATATAT | 84333 |
| rs148862312 | in-del | -/CTGCACCCACTGAC | 0.145305 | 0.227022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177906 | TTGGTGCACGGTGCA[-/CTGCACCCACTGAC]CTGCACCCACTGTCC | 84333 |
| rs148896474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250219 | CTCTATAAATAAGGA[A/G]AAGAAAACATGTAGA | 84333 |
| rs148939327 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265357 | AATTATCTTCATAAT[A/C]TGAGTGCATAAATAA | 84333 |
| rs148949691 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204028 | GAAGCATGACACCAC[A/G]AAATCATAAAAATGT | 84333 |
| rs148973781 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190291 | TCTTAATCCCATCAC[C/T]TTGGGGGTTAAGATT | 84333 |
| rs148992362 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272501 | TTTTAGGCCAGACAC[A/G]GTGGCTCACCTCTGT | 84333 |
| rs149107243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200124 | GATGCTAACTTCCCT[A/G]CATTTTTGCCTCACT | 84333 |
| rs149159049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257998 | ACTGATACATGCTAC[A/G]AAATAGATGAATCTT | 84333 |
| rs149182929 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237170 | TAGGAATGTAGTAAA[A/G]ATTAGATTATTAAAT | 84333 |
| rs149186622 | in-del | -/GCC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238632 | TTTTTTTTTTTTTTT[-/GCC]TCTTTCCCAAATTTC | 84333 |
| rs149277172 | snp | A/G | 0.242201 | 0.249878 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176691 | CCTTTCTTCCAGTTG[A/G]TCGAATCAGCTACTG | 84333 |
| rs149284993 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241511 | TTCCCAGCTACAGGC[C/T]GTATGTCCTCACCAC | 84333 |
| rs149338195 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197924 | AGAGTTCTCCTGGTT[C/T]TCAAGATGTTTCATT | 84333 |
| rs149355551 | in-del | -/GTGA | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171543 | GGAAGTAGAGATGCT[-/GTGA]GTATCACTGAAACTG | 84333 |
| rs149434965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253547 | ACTTTGGTCCAAACA[C/T]GCAGTTTTAGTTATG | 84333 |
| rs149467686 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226255 | TTCTGGACTCTCTGG[C/T]CAAGTGAAGAAAGAG | 84333 |
| rs149498759 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192949 | ATTATGGTTACAAAT[A/G]TTAAAATATAGAGGT | 84333 |
| rs149552721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168536 | GGGAAGGAAATGGAG[A/G]AAGCAAATGTAAATT | 84333 |
| rs149576954 | in-del | -/T | 0.0655868 | 0.168795 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183994 | TCACTGTCTTTAATA[-/T]TTTTTCTTCGTTTCG | 84333 |
| rs149603960 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172608 | ATGGATGGGTCATCT[C/G]TCTCCTTTAAACACT | 84333 |
| rs149653928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170356 | GACTGGGAGAAAATA[G/T]TTGCAAAAGATATAT | 84333 |
| rs149750422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178641 | CAGTCCTCCCACCTC[A/G]GCCTCCCAAAGTGCT | 84333 |
| rs149781537 | snp | A/T | 0.00358891 | 0.0422285 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184825 | CTTGGATTTTTCAGT[A/T]TCTGGAGGTATCACC | 84333 |
| rs149802136 | snp | A/T | 0.0737376 | 0.17729 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177364 | GGTCAGGGACCCACT[A/T]GAGGAGGCAGTCTGT | 84333 |
| rs149824440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244048 | ATAAAGATCTTTGCC[C/T]TTGTAGATTTAATAT | 84333 |
| rs149833811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189456 | ATGAATATAAGATTT[A/C]TCTGTAAATTATTGA | 84333 |
| rs149960658 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255857 | CCCATGTCCCTTATA[A/T]AAAATGGTGTAGTAT | 84333 |
| rs149961021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215568 | TGCTGAGTTTGCTGT[A/C]TTTGAAAAGAGATGG | 84333 |
| rs149990757 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228340 | GGTTCTTAACCCTTT[C/T]GTGGTCAGAGGCCCC | 84333 |
| rs150107611 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230989 | TCCTGGACTCAAGCA[A/G]TCCTCCCACCTCAGC | 84333 |
| rs150123808 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213033 | TCCTAAGCGCTGCTC[A/G]TCTGTATCTTATTCT | 84333 |
| rs150140069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174912 | GGCAACAGTAGAGAA[A/G]AGGCATCAGCAAATT | 84333 |
| rs150147298 | snp | A/G | 0.157642 | 0.232314 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163300 | GCTGGCGGCGCGCGG[A/G]AAGGGGCTGGAGGCA | 84333 |
| rs150157769 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240298 | GCTTTTTGTTTGTGG[C/T]AGTAGACTTTTATTG | 84333 |
| rs150189406 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253003 | CATTCTTAGTTTATA[A/G]ATGACTTTTACTAAG | 84333 |
| rs150191296 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171815 | GCTGAGCTTGGGGAT[G/T]TTGAGTGACACAGGC | 84333 |
| rs150220551 | in-del | -/AAC | 0.0821764 | 0.185298 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249777 | CTATTTTTTATCTGT[-/AAC]AACAACAACAACAAA | 84333 |
| rs150273943 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179482 | TTAGTTGTTTCTCCT[G/T]ATCCTCTCTCTACTT | 84333 |
| rs150304500 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187703 | CTTCATGTTTTCTTC[A/G]AAGAAGTCTATATAT | 84333 |
| rs150309562 | in-del | -/G | 0.0263992 | 0.111815 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179171 | CTCTCTCATTACTTT[-/G]GTTTCAAGTCATGTA | 84333 |
| rs150345155 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245831 | GATAGAGGAAAGGGA[C/T]TTGGAGAGTTAGGGC | 84333 |
| rs150369530 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192306 | TCAAGGTGTTTTGCT[C/T]GTATACCTGGATAAT | 84333 |
| rs150398877 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201342 | AGCCACTAGTCCTAT[C/G]ATGGTCCCCCCAGTG | 84333 |
| rs150475474 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277891 | TTTAGTGGAATCCAG[A/G]CTGCTGATCTGTCTT | 84333 |
| rs150485672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217622 | GGAAGAGTCTGGGCC[A/G]ATACTCAAATGCAGC | 84333 |
| rs150540209 | in-del | -/G | 0.0818113 | 0.184966 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256860 | TATAGCCTTCCAAAA[-/G]GAAGGAGAAATTAAG | 84333 |
| rs150577718 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279856 | GAATTTCAAAATGAT[G/T]CTTAGAAATAAGATA | 84333 |
| rs150600510 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221169 | GTACCGCTGGGTCCT[C/G]CCGGAGAACGCAGAA | 84333 |
| rs150630195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234119 | GCAACAACAAATGAC[C/T]TTGTACCTTTTGTGT | 84333 |
| rs150651081 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280450 | TTTCCAAGGAAATAT[A/G]TAGGAAGCAATTATG | 84333 |
| rs150653576 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184370 | AATACTTTTTATTCC[A/G]TTATGAAATCCTTGT | 84333 |
| rs150682967 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243149 | GCAAACTGGTGATGG[G/T]GATAGTTGAGCGGAC | 84333 |
| rs150683841 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238609 | TTTCTTTCTTTTTTT[C/T]TTTTTTTTTTTTTTT | 84333 |
| rs150684612 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165177 | TTCATTTTCTGCTCT[C/G]TGATGTTAACCTACA | 84333 |
| rs150723951 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254878 | ATATAGAGCATTTTA[C/T]CAAGAAGATGACTAA | 84333 |
| rs150758131 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266322 | GTTCTTTACAAGAAC[G/T]CCTCCCAAAGTTGCC | 84333 |
| rs150798272 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180914 | AGTTTAATAGAAATA[A/G]CATTGAATCTATAAA | 84333 |
| rs150808844 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275031 | TGAAGAACTGATCTC[A/G]GAGTGGGGATGGCCT | 84333 |
| rs150841393 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189198 | TTGCCTGGCAAAATC[G/T]TCTTTTACAACCCTG | 84333 |
| rs150843779 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168175 | TCCTTATGGAGGGGG[A/T]TGGTGAACCTGTCAG | 84333 |
| rs150872267 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247410 | CAGAAATAATGTAGG[C/T]TTTATTTTCACATTT | 84333 |
| rs150925231 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202943 | TAAAGAAATGTGTTT[G/T]TGAAAATGACTAAAA | 84333 |
| rs150948312 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169530 | AACAATCTCATTTAC[A/G]TTAGCACCTCAGACA | 84333 |
| rs150965948 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230586 | CAAATGATCAATGTT[A/C]TATTTTAGTTTATAT | 84333 |
| rs150989939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208050 | GTCGAGAGACACTGT[A/C]CAACTATGTAAATAT | 84333 |
| rs151042545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179181 | ACTTTGGTTTCAAGT[A/C]ATGTACTCTCTATCC | 84333 |
| rs151125630 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222738 | ATCAACGATCTCATG[A/G]TAAATCTGGATGCTA | 84333 |
| rs151137639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173175 | GATGCAACACACACT[C/G]TGATATTTAAGAGCT | 84333 |
| rs151157481 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239569 | AGCCAATCTATACCA[C/T]GTGAAAATTTCAGGT | 84333 |
| rs151179849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186963 | TAGGCCAGTGATTCT[C/T]ATACTTGAATGTGCA | 84333 |
| rs151198194 | in-del | -/CG | 0.144632 | 0.226711 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164119 | TGCGGGGTACACACA[-/CG]CGCGCGTACTCGCTA | 84333 |
| rs151220719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244839 | GTTGCCATTAACTGA[A/G]TTGGGAAGATTAATA | 84333 |
| rs151283040 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268908 | TGGTCAGACTTAGCT[C/T]GTAAAATTTTTTCAG | 84333 |
| rs151319761 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173820 | GGCTAAGGATCTTCA[A/G]ATTTGTGTCCTTTGG | 84333 |
| rs151323358 | snp | C/T | 5.01224e-05 | 0.00500586 | missense | PCGF5 | GRCh38.p7 | 10:91251316 | CAAAAGCTGACAAAC[C/T]GAAAGTAGATGAAGA | 84333 |
| rs151335676 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277306 | CAAAGTTCTCTATAC[C/T]GTATTTTTATATTCA | 84333 |
| rs151337116 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182112 | CGCTGATGGTTGTTT[A/G]TATTTCTGTGAGGTC | 84333 |
| rs180750680 | snp | A/C | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219843 | TGGCTGCTGGACTAG[A/C]GGTTGTTAAGTTTGT | 84333 |
| rs180760378 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197380 | GGATGGCTGCACAGA[C/T]GTATATCTTTGGAAA | 84333 |
| rs180795307 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191004 | AGGTTTTGTCAAAAT[C/T]CTTACGCTGACAGTT | 84333 |
| rs180813910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271808 | AAAACTGTTACTGGA[A/G]CTACAAAAACTTATC | 84333 |
| rs180820131 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280747 | TACACTGTATTCCCC[A/G]TTAATTATCCCTTAA | 84333 |
| rs180822302 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182172 | TTGTGTTTGTTTGAC[C/T]TTTTCAATTTTTTGG | 84333 |
| rs180826165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247906 | GTTCCCTGAGTTAGC[C/T]GGGTGGTTCATCTGG | 84333 |
| rs180826637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254770 | TAAGTATCTCTGAAA[A/G]TTCACTTTTCCATGA | 84333 |
| rs180835535 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177536 | AGACAGGCCTCCTTG[A/C]GCTGCGGTGGGCTCC | 84333 |
| rs180843750 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211859 | GTTATAGAGCTTATC[C/T]GGAACCAGGCCCCAG | 84333 |
| rs180853894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263861 | ACCTGTGGCATAGTC[A/G]TAACTTTTGTATCAA | 84333 |
| rs180866724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168392 | AGAGGATGGGCTGAG[C/T]TGAAGACTGGGAAAA | 84333 |
| rs180870740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231092 | TACTAGTAAACTCAG[C/T]CGTCTCCCTTGCTTT | 84333 |
| rs180972007 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163616 | GCCGCTGGCTCGGGG[C/T]GCGAGCATCTGCTCC | 84333 |
| rs180977270 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179604 | AACATGTGGCGTTTG[A/G]TATTCTGTTCCTGTG | 84333 |
| rs181069419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193328 | ACCCAGCTCAGCCAA[A/G]TTGTACTTAGACTTC | 84333 |
| rs181083999 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226242 | ATAGAACCTGCCCTT[A/C]TGGACTCTCTGGTCA | 84333 |
| rs181100369 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267424 | TATAATCTGAGGACA[A/G]GGATTTTTGTTTGTT | 84333 |
| rs181106345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251799 | TTTATTCATTCTCTT[A/C]TAATTTTATCCTTTA | 84333 |
| rs181111084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205380 | CACTCTAAATCCTTC[A/G]CAGATAATCTGTGAA | 84333 |
| rs181115033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233624 | CATGGAAGCGAATTA[C/T]AGCTATTCTGGATTT | 84333 |
| rs181116983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215030 | ATATTGTAAAGGAAA[C/T]GGTGATCTATGAATT | 84333 |
| rs181154603 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173658 | AAGTCCAAAATATGC[A/G]CTTTTTTCAAGTGGA | 84333 |
| rs181162307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275927 | GGACTAAACTCAAAT[A/G]TGCAGCAAAAGGAGA | 84333 |
| rs181164126 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259502 | ACCAAAAAAGAGCCC[A/G]CATTGCCAAGTCAAT | 84333 |
| rs181164892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187187 | ATCTGGGACCTATCT[A/G]TAGTGATTCGGATTT | 84333 |
| rs181170944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243981 | AATATTTACTGGATG[C/T]CTGCTGTGTCTGGGC | 84333 |
| rs181181369 | snp | C/G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282206 | AAAGCAACTCTAGGC[C/G/T]GGGCACAGTGGCTCA | 84333 |
| rs181299368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190723 | AAAAGTGAATGAAAG[A/G]TTGTCTTAAATACCA | 84333 |
| rs181309286 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183038 | GTTTTACTTCCGATT[A/G]TATGATCAATTTTAA | 84333 |
| rs181322672 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229871 | ATATAATGTTTTAAG[A/G]TATACTAGAAATGAT | 84333 |
| rs181383797 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279738 | AATATTTGAGAAATA[C/T]GACGAGCACAATCTG | 84333 |
| rs181386376 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177255 | TGTTGCTGCCTGATC[C/G]TTCCTCTGGAAGTTT | 84333 |
| rs181388260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263462 | AACTGAAACTATACT[C/T]ATCTTAAAGTTCAAA | 84333 |
| rs181388365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247452 | GAAGGAAAGATTGAG[A/G]AACAGAATAATAGTT | 84333 |
| rs181391734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198628 | CTTGTCTCTGTCCTT[C/T]GATCTTCTTGGGAGT | 84333 |
| rs181394346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255916 | TATACTTTAAATCAT[C/T]TCTAGATTACTTGTA | 84333 |
| rs181449846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211019 | TTTACCATGCATTAG[A/G]TACCAGGAGGCATTT | 84333 |
| rs181517540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272630 | ATACAAAAATTAGCC[A/G]GGTGTGGTGGCACAC | 84333 |
| rs181530777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239652 | TATTTTATAGTTCAG[G/T]TACTGTAAATATTGT | 84333 |
| rs181575886 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237510 | CACTTTGGGAGGCCG[A/G]AGTGGGCAGATTACT | 84333 |
| rs181579242 | snp | A/G | 0.00517822 | 0.0506191 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284696 | GATGGTTTCTAGCTC[A/G]GCCCCATTGTGATTT | 84333 |
| rs181580696 | snp | A/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268325 | TTCTAGGTTGCTTTA[A/T]GATGTGTATTAGTAC | 84333 |
| rs181581645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243780 | AATGTATTATTAAAG[A/G]TATTTTAATATATAG | 84333 |
| rs181592600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225236 | GATATATATCATATA[C/T]GTATATATGATATAT | 84333 |
| rs181595769 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186221 | GCCCTCAAGTTATTT[C/G]ATCTCACCTGGATTT | 84333 |
| rs181597493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204617 | TTCTCAAGTCTTGGA[A/G]GATGATAAACATGAG | 84333 |
| rs181686887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252463 | TGTGAACAGTAGACA[C/G]TGAAGATGTAAGTAG | 84333 |
| rs181691168 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275645 | TTTTTAGTAGAGGCG[A/G]GGTTTCACCGTGTTG | 84333 |
| rs181709370 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177202 | CCTGGGTATCAGCAG[C/T]AGAGGCTGCAGAACA | 84333 |
| rs181775076 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280882 | TTCTTTAAATAACCT[A/G]TAGGAATCATCTGAA | 84333 |
| rs181801136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272174 | AAAAATGATAGTGAG[A/C]TAATTTAGTAATGCA | 84333 |
| rs181817660 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258674 | AGATAACAGAGAAGA[C/T]AGACGTGTACATTTA | 84333 |
| rs181899521 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179884 | ATGGGATTGCTGGGT[C/T]GAATGGTATTTCTAT | 84333 |
| rs181904392 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193712 | AAGCAATATAATTTG[A/G]TGTAATTTTTTAAAG | 84333 |
| rs181910684 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215955 | ATCCTTTGTAAGGAT[C/G]CCTTCAAGAAGAAAC | 84333 |
| rs181925314 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238925 | GTCTTTTACCCACAT[A/T]TTGTGAGAATTGTCA | 84333 |
| rs181939310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197643 | TGGTGGTAGAGAGTG[C/T]GTGGGAGCCTTGCTT | 84333 |
| rs181980522 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284030 | TTGTAGATATTTAAT[C/T]AGTACAAGATATGTC | 84333 |
| rs181983822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267802 | CAGCAAGATGCCAGG[A/G]TGTCTGAAGAGCTCT | 84333 |
| rs181986611 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252390 | TTCAGATTAAGTTTT[C/T]CTGGCATCTTATAAC | 84333 |
| rs181996447 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233841 | GGAAGAAAAAATATG[C/G]ATCTAAGTTGACAGA | 84333 |
| rs182141068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185181 | TCCCAGGAGGTTCTT[A/C]AATCTCTGTCAGCCA | 84333 |
| rs182146289 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164034 | CGTCATAGTACACCC[A/G]GAACGTGTGGCCGTG | 84333 |
| rs182187445 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224879 | CTACCCTAGAGTTAT[A/T]TTCTACTTCCGTTTC | 84333 |
| rs182197057 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255737 | AATGTCTAGTTTCAA[C/T]AACAACAACAACAAA | 84333 |
| rs182201868 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91161996 | TTGGGGGAGCAGGAA[A/G]ACTGCACAGAGATGG | 84333 |
| rs182215454 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221869 | AAATAAAAGGCAAAT[A/G]TAATAGGAAAGAAGT | 84333 |
| rs182237076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178637 | CAGCCAGTCCTCCCA[A/C]CTCGGCCTCCCAAAG | 84333 |
| rs182247315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192019 | TCAGGTTCCTCCTCT[A/G]TAAAGTTTGGATTTT | 84333 |
| rs182248275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182914 | ATTCAATTTCCATGC[A/C]ATTGTATGGTTTTGA | 84333 |
| rs182251077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240715 | TTCATTTTAAAGCAT[C/T]TTATTTTAAAGTATT | 84333 |
| rs182260362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222684 | TGAAATGATTTTGGA[A/C]ACAGACATGGGAAAG | 84333 |
| rs182270019 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199936 | AGGAAAAAGAAAGCA[A/G]TAAAGGGTATAGTTT | 84333 |
| rs182330110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273045 | CCTTTTGTCAGTGCT[A/G]TGATATGGGAATTCT | 84333 |
| rs182333030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257102 | TATGAAGAACTCTTA[A/T]AAATCAACAATAAAA | 84333 |
| rs182399255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171899 | AATGATTTTGTATCA[A/G]TGTCAGTGTCTGTCT | 84333 |
| rs182405295 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261565 | TAAAAATTTAATTTT[C/T]AGAATGTATTATTCT | 84333 |
| rs182408272 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245763 | TGGAAGTTTGTTTTT[C/G]ATTGCTTTGACATTT | 84333 |
| rs182444535 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242534 | CCATTAGATACCTGA[A/G]GGAATCCAGTCACTG | 84333 |
| rs182462326 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204011 | TTTATTGTTGAGTTT[A/G]TGAAGCATGACACCA | 84333 |
| rs182483549 | snp | C/T | 1.65581e-05 | 0.00287728 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278363 | CCTGCACTATTTGTT[C/T]ACTCGTCAACAGATT | 84333 |
| rs182494340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183726 | TCTTTGCCATATGTA[G/T]TGTGTCCTTCAGGAG | 84333 |
| rs182565932 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164900 | GAGTTCTTTTAGTCT[G/T]ATCTCTTCTTACTGG | 84333 |
| rs182575886 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180489 | TTACATTTAAGCCTT[C/T]AACCCATCTTGAGTT | 84333 |
| rs182577519 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216844 | GCAAACATAGATTTA[A/G]AGTTATAATATTCAT | 84333 |
| rs182578013 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281344 | TTTGCTCAACTACAT[G/T]ACACACTCAAATGTA | 84333 |
| rs182581309 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195595 | CCTCAAGTAATCCTC[C/T]ACCTCATTTTTTAAT | 84333 |
| rs182599560 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249403 | TATATATATATATAT[A/G]TATATATATATATAT | 84333 |
| rs182631981 | snp | C/G | 3.30333e-05 | 0.00406393 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248577 | TAAGTGGCTCTTTAG[C/G]TTCTTGCAGACTTTT | 84333 |
| rs182706305 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169667 | ATATAGTCCATCTTC[A/T]TAGGTAGGAAGACTC | 84333 |
| rs182707254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265397 | AATTAAGATTGGCTA[C/T]AAGGTTGGAGTAGAT | 84333 |
| rs182708660 | snp | A/G | 0.0111196 | 0.0737302 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281107 | TAATCACATCAGTTA[A/G]TAGAGAAATCAAAAT | 84333 |
| rs182748430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170239 | TTTAGATATGACATC[A/G]TAGGCACAGCCATGA | 84333 |
| rs182819130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174972 | GGCAACTGCCTTAGT[A/G]TAACAGAGGAAGTTG | 84333 |
| rs182832220 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269003 | GTGGGAGGAAAAAGG[A/G]AAAAAAAACATGCTT | 84333 |
| rs182845094 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208149 | ACATGGTTATAAAAT[A/G]GTGATTTTATAATTC | 84333 |
| rs182853081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206218 | AGCTCCTGCCGTCAA[A/G]GAGCTGAACAGCAGA | 84333 |
| rs182855640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235855 | TCCCCAGCCATTTGG[A/G]ACTGTAAGTCCAATA | 84333 |
| rs182875989 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266064 | CCTTACAACCAAAAT[C/G]TTCCAGGTACCAGGT | 84333 |
| rs182885806 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232188 | GGTTGAGTAAGATGG[A/G]GTTGAGAATAGATTC | 84333 |
| rs182913829 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260965 | AAAGCATAATAATAA[C/T]AATAATAATAAAAGC | 84333 |
| rs182922173 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245290 | GTACAAGTAAGGTGA[A/G]AACTGAGAATTCATG | 84333 |
| rs182925735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227019 | ATTAACCATGGTTTA[C/T]ATGGCTGTGAGATAA | 84333 |
| rs183049546 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161485 | TAACAGGGCCGGAAG[A/G]CTCTTAGCCTAGGAA | 84333 |
| rs183066441 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212498 | ATTATTTGACCAGAA[C/G]TAGCTGGAAGTTTGG | 84333 |
| rs183122518 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231961 | TATTCAAATGGAGAT[A/G]TCCATTTGGGAGTTG | 84333 |
| rs183130543 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177751 | TTTGCTAAGACCGTC[A/G]GAAAAGTGCAGTATT | 84333 |
| rs183135217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264885 | AATATGATTAATGGT[G/T]GATAAGGGTGTTTAT | 84333 |
| rs183143441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191485 | CTTTCCATTTAATAT[C/T]TTTGGACTGAAGTTG | 84333 |
| rs183144413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227776 | CCCCTACCACCTAAC[A/G]CTCACACATACAAAT | 84333 |
| rs183148697 | snp | A/C | 0.000115675 | 0.00760421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248455 | GACTATTTACATGTC[A/C]GATCTTGGTGTCTTC | 84333 |
| rs183151661 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231427 | GATAGGCCTCATTAA[C/G]AGTGACTTTTGAACA | 84333 |
| rs183152146 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252992 | CCTTGTACCTTCATT[A/C]TTAGTTTATAAATGA | 84333 |
| rs183179991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191706 | CACTCTGATTGCAAG[A/G]TCTTTGGCCATGCTT | 84333 |
| rs183214124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258130 | TAGGGTTGTCAGGGG[A/G]TGGGAGGAGGGAAGG | 84333 |
| rs183281619 | snp | A/C | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174435 | TCACTTGAACCCAGG[A/C]GGTGGAGATTGTAGT | 84333 |
| rs183336236 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180028 | TTTTTTTACTTTTTA[A/G]TAATAGCCATTCTGA | 84333 |
| rs183395469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212866 | GCTTGATGTCTCCTC[C/T]CTTTGTAAAGATCTG | 84333 |
| rs183405939 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216579 | TGGCTGTGCTGTGGA[A/C]GATGCTTTGGCAGAA | 84333 |
| rs183426938 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178500 | GCTCAAGCAATACCC[C/G]CATCACAGCCTCCAA | 84333 |
| rs183444126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274589 | ATGGAACTTACACTA[A/G]TGATGGTAACAGACA | 84333 |
| rs183445557 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278018 | CTAGTCATATATACA[A/G]CCTGTATGATGTCTG | 84333 |
| rs183492618 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271848 | TATATACCCAAGATT[C/T]CCCATTATTTTAGTT | 84333 |
| rs183496234 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237272 | GATAATGCCTGGTAC[A/G]TAAACCCATTAAGTG | 84333 |
| rs183503852 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217412 | TATGCCATTAAAAGT[A/C]AGTTAATTAATGATG | 84333 |
| rs183551010 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196660 | CTGATGTGTTTTTCC[A/G]TATTTCAGAGGGTGA | 84333 |
| rs183554005 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269632 | AAGTAGATTTTCAGC[A/G]GAGTATGCATGTTTT | 84333 |
| rs183570820 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164378 | TTGCGTTCTCGAAAG[A/G]GTTACAAAATTCCAC | 84333 |
| rs183582729 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194701 | TCAAAAGCATAGAGA[C/T]GGTTTAAAGCCACAG | 84333 |
| rs183595213 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253107 | TTGATATATGTAAGT[A/C/G]TGTCCTAATACTTTC | 84333 |
| rs183622826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258482 | TGAGTGTCATGTCAG[C/T]CCTCAGTTTCAGATT | 84333 |
| rs183633801 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242205 | GGGACAGGGATGCTA[C/T]TAAGCATCCTACAAT | 84333 |
| rs183636865 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224367 | AACAGTTAATTAACT[A/G]TCATCGAACAGACAT | 84333 |
| rs183691545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273873 | ACATTTTATATATTT[A/T]ATACATATATACTCT | 84333 |
| rs183708392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274912 | ACTGAGACTGGGTGG[A/G]GAATTCAATTCTACC | 84333 |
| rs183717095 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241444 | CCAATTAGGAAATCT[A/G]GAGAAGTGATATGAC | 84333 |
| rs183741388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202040 | TTGCATTTTATTAGC[A/G]TTGTGACCAGGTGTA | 84333 |
| rs183744417 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170795 | AAACTTGTGGCCACA[C/T]AGAAACCTGCACACT | 84333 |
| rs183817642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167965 | GACAGAAGCTCAGTC[A/G]CTTAAGTTGATGTTG | 84333 |
| rs183826409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182023 | GTTCAGTCTTTGGAG[G/T]GTGTATGTGTCCAGA | 84333 |
| rs183849451 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219500 | TTAGTCTCTGAAATG[A/G]AAGATATGAAGCATA | 84333 |
| rs183856651 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197212 | AGCCTGTCTCCATTC[C/T]GCTTGGCATCAGCAG | 84333 |
| rs183859458 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184089 | TTCTCTGCATTTCCT[G/T]AATTTGAAGGTTGGC | 84333 |
| rs183918874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257540 | AATCCTGTATATACT[A/G]GTTTTTTTAATTTGA | 84333 |
| rs183934027 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223215 | ATTGTAAAATATTCT[A/G]AAAATCATAAGCATA | 84333 |
| rs183937921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238195 | ATGCTTAGTAGCCAC[A/G]TGTGGCTAGTGACTT | 84333 |
| rs184000349 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260396 | CCATTGTGGAAGTCG[A/T]TGTGGCGATTCTTCA | 84333 |
| rs184033189 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226569 | TCAGTCTTCTTTCAG[A/G]TGACTATGCAAGTGC | 84333 |
| rs184053107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188038 | ATGTGCAGGTTAGTT[A/G]CATATGTATACATGT | 84333 |
| rs184063538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165775 | TATAAGTCAGTGATA[C/T]AATGTAAAAAGGATG | 84333 |
| rs184085117 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223674 | CAGCATGATTTCATT[G/T]TTTATTTCAGTGAAA | 84333 |
| rs184092441 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202641 | ATATTTGACTCCTTA[C/G]AAGCCTTGAAAACTT | 84333 |
| rs184146635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184433 | AGTACTCTCTACTGG[C/T]TGTTTTGTCTGTCAG | 84333 |
| rs184153038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241832 | TTAATGCCTGTTTGG[A/G]ATAATTTGTCTACAG | 84333 |
| rs184156504 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276291 | TAAGGAAAAAAGTAC[A/G]TCAAAGGCAGTTTTA | 84333 |
| rs184172104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244858 | GGAAGATTAATAATA[C/G]AGCAAGGAAGGGGTA | 84333 |
| rs184186422 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205648 | TTCCTTGCCCTGCAT[C/T]GGACCACATCAGAAT | 84333 |
| rs184219280 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180846 | AGGCTCTTTTTTGGT[A/T]CCATGTGAATTTTAA | 84333 |
| rs184313387 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281947 | TACATACTTTGAAAA[C/G]AAAGTTCAGATTTTT | 84333 |
| rs184409974 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185065 | TGCTAGGGGTACCCC[C/G]TCTGCCCCCAGTTGG | 84333 |
| rs184412430 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283004 | ACCAGAGACTCAAAC[A/C]CTTTCAAGGCACACA | 84333 |
| rs184438597 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251867 | TGTCAGAGCTAACAT[A/G]TTTTGTGAATAATTT | 84333 |
| rs184506352 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203565 | TTCAGTCTTTCCTGT[A/G]TTACATTGAACCAGA | 84333 |
| rs184526396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171829 | TGTTGAGTGACACAG[A/G]CCAATGGAGGTAGAA | 84333 |
| rs184538029 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246953 | GTCAGGCAGATAGAT[A/G]GATGGATAGATGGAT | 84333 |
| rs184546638 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228997 | CTAGCATCCTTTAAA[A/G]TAGGCAGTTTGTATT | 84333 |
| rs184549185 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267571 | TATATCCTACAGATA[A/C]TTTTTATTTATCTGA | 84333 |
| rs184552970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210854 | CTGGAGATAGTAGTA[A/G]GTAGGAGAGCAAGTT | 84333 |
| rs184555841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176091 | TCCTTCAGGAGCTCT[C/T]GTAGGGCAGGCCTGG | 84333 |
| rs184595722 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177210 | TCAGCAGCAGAGGCT[G/T]CAGAACAGCGAATAT | 84333 |
| rs184604226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189564 | TTCTATTCTAATATA[C/T]CCTTACCAAATATCC | 84333 |
| rs184608338 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279322 | TCAAAAGTCTCAAAA[C/T]AGTTGTAGATTAAAA | 84333 |
| rs184621823 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262927 | TGATTCATTGAGTTA[A/T]CATTTTCTAATTTTT | 84333 |
| rs184677048 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271493 | ATCTTTTTTTCAAAA[A/G]CAACCACCATTTTTT | 84333 |
| rs184696918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188531 | TATAATTTTGCTGCT[A/G]AGAAATTGGAATCTT | 84333 |
| rs184738228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178787 | AAAAAAATGTAATGA[A/T]GATGAGTAGTTTGGA | 84333 |
| rs184742703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192530 | CAAACAGTTGAAAGT[A/G]AAAATAACCCCATGG | 84333 |
| rs184750556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172073 | GATTTGCCCAGGATT[A/G]CAGACGTGTGGCAGA | 84333 |
| rs184769580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232635 | CTGGCATATAGGGCA[A/G]AGGATGGCTTTAGAT | 84333 |
| rs184776286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213666 | CTTTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT | 84333 |
| rs184820353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254400 | TTTTATTTTTTGTGA[C/T]GCTTTTCCCAACCTA | 84333 |
| rs184844609 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255405 | TCAGGAAGGACCTGA[A/G]AAGGCCCTAAGCTCT | 84333 |
| rs184845729 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238715 | GAAGGAATTCAGCTT[C/T]TCTGTCTTCTACTTC | 84333 |
| rs184851487 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281639 | CCATGTTGGAGAGAC[A/G]GTTTTAACAGTTTGG | 84333 |
| rs184855181 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220452 | CCGAGATAATATTTG[G/T]CCAGAGCTACGTGTA | 84333 |
| rs184856445 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266468 | GTGAATAGTTTAAAT[G/T]TTTTGGTTGTTTAAG | 84333 |
| rs184861961 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250179 | GAGTTTGGTTCATAG[A/G]AGGCAACTCCTATCT | 84333 |
| rs184881079 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193096 | AGACTCCACCCACCC[A/G]TGCTGAGAGTGCATG | 84333 |
| rs184934548 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266859 | TATGTCTCACTACAT[A/C]CACTTCACTACTAGT | 84333 |
| rs184966063 | snp | C/G | 0.106633 | 0.204807 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163170 | TTTCCGCGGGGCCGG[C/G]GGGGAGGCCCCGGGA | 84333 |
| rs185048084 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251077 | GCCTAGAAATCTTAA[A/G]CTATGTTAATAAGTT | 84333 |
| rs185071957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214260 | TGAGGCGTGATTGCA[A/C]CACTGCATTCTGGCC | 84333 |
| rs185079581 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179413 | CAGTAAACTTGTGTC[A/G]TGGGGTTTGTTGTAC | 84333 |
| rs185084321 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215293 | TGGTATCAAAGCCTC[A/G]TCTTTTATAATTCAG | 84333 |
| rs185101503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176700 | CAGTTGATCGAATCA[C/G]CTACTGAAGCTTGTG | 84333 |
| rs185107820 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189042 | TTTAAAGTAAGATTA[G/T]CTAGCATGTGGCTGC | 84333 |
| rs185118189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181124 | TTGTGCATGGGAGTT[C/T]ATTTGTGATTTGGCT | 84333 |
| rs185124839 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273403 | CCTTAGAAATGAAGA[C/T]GTCCTTAAACCATGA | 84333 |
| rs185143387 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163662 | CTTCCGTTTTGATTA[G/T]CTCAGGTTATTATAT | 84333 |
| rs185154445 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179679 | ACAAAGGACATGATC[G/T]TGTTCTTTCTTATGG | 84333 |
| rs185161256 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193441 | AAACTAAAAGGGATG[C/G]GGGGGTGGGACATTA | 84333 |
| rs185204885 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218795 | ATGTCACCATGCCCG[A/G]CTGATTTTTGTTTTA | 84333 |
| rs185223211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166083 | ATTCCTTTTTAATCA[A/G]TCCCTTCACTAAAGA | 84333 |
| rs185341582 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196915 | CTGGTGGACGAGATA[C/T]AATCCCCACCTCAAG | 84333 |
| rs185363464 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275959 | TTACTGATAACTCAC[A/C]GTTCATTTCTATAAC | 84333 |
| rs185379520 | snp | G/T | 0.236434 | 0.249632 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259768 | AACTGGCTAGCCATA[G/T]GTAGAAAGCTGAAAC | 84333 |
| rs185412966 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204178 | TTTGCATAAGTTTAT[A/G]TCTACTCTTTACTCC | 84333 |
| rs185474030 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275323 | AAAAAAAAATACTAT[C/T]TTATGCTTATTAAAT | 84333 |
| rs185493891 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242559 | TCACTGTTTAATCAA[A/G]CCCGCTCCCTTGGCT | 84333 |
| rs185500087 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91162485 | GGGCACGCTTCCTCC[A/G]TCTGTGGGGGGAGAA | 84333 |
| rs185529488 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185914 | TTCCTTGATTAGTCC[C/T]AATGCAGGTACCTGG | 84333 |
| rs185608377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258602 | ATGATTCTTTGTAAG[C/T]TGTTTGGGGCAAGAA | 84333 |
| rs185608732 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239677 | TATTGTCTAAGGTTT[G/T]GGGGCAAAACATTGG | 84333 |
| rs185612737 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263660 | AATTAGTGAATTATA[A/G]CCACAGTTCCTGTAG | 84333 |
| rs185615722 | snp | C/T | 0.0130921 | 0.0798413 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279741 | ATTTGAGAAATATGA[C/T]GAGCACAATCTGTGT | 84333 |
| rs185617989 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222308 | TGAAGGGTTAAAAAT[A/G]GAAATGGGGAACATT | 84333 |
| rs185630665 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225039 | AAGGCACAAACTCTC[A/G]CATTTCTATCTATAT | 84333 |
| rs185666585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169708 | GGACTTCCCAACTGT[A/G]TTCATATATTTAATG | 84333 |
| rs185672643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183041 | TTACTTCCGATTATA[C/T]GATCAATTTTAAGAG | 84333 |
| rs185701187 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256458 | TGTAGACACCATCAA[A/G]CTTACCAGCATACAC | 84333 |
| rs185726721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262263 | AAACCCTGTGTGTTC[C/T]AAAAATATAAAAATT | 84333 |
| rs185736707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197415 | AATCTCCACGGGCAG[C/T]GTTATCACAACTGCT | 84333 |
| rs185741176 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228424 | AGAATTCTGTGGTAC[A/G]GAAAAGGAAAGCTTT | 84333 |
| rs185791068 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264169 | AGGTTACATTGCATT[A/T]GTAAATTATGTGTAT | 84333 |
| rs185794583 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182198 | TTTGGAATAGTTCCC[A/G]TAGGAATGGTCGCAG | 84333 |
| rs185801360 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231197 | TAGTATTCCTAACCA[C/T]TGTGTTCTCATTTAT | 84333 |
| rs185808281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172799 | TCCTTAGTTTATTGC[C/T]TTCACAGCTATATTT | 84333 |
| rs185852369 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243896 | TCACATTATATTTCT[A/G]TTGGTCATCACTTAT | 84333 |
| rs185855100 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278769 | GAAATTATTTTGTAT[A/G]GAAGTATATTTAGAA | 84333 |
| rs185856507 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225776 | GTTTTTGCCTCTAAG[C/T]CTCAATATAAATACA | 84333 |
| rs185863328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245981 | TGTGTTTTTATCCAG[C/G]CATGGGTGCCAGTGC | 84333 |
| rs185867320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204635 | TGATAAACATGAGAA[C/T]CCAGAAAATGCAAAG | 84333 |
| rs185879634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191586 | CATGTAGGTAATCTA[C/G]TCAGACACAATTGTG | 84333 |
| rs185884199 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210205 | TCCCCTTATAGCAAA[C/G]AGTCCACCTGCTGCT | 84333 |
| rs185903355 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280755 | ATTCCCCGTTAATTA[C/T]CCCTTAAGTCAGATT | 84333 |
| rs185919525 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265312 | GGACTCATATATGAC[A/G]CTAAGGAATATAGCA | 84333 |
| rs185922531 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248079 | TCCTCCAGCCTTGTT[C/T]TCATGGTAGCAGGAT | 84333 |
| rs185923538 | snp | C/T | 4.95438e-05 | 0.00497689 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248492 | AGTATTTTCTTTCTC[C/T]CCCCTTTCGAAGGTT | 84333 |
| rs185930384 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275733 | GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC | 84333 |
| rs185935861 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231529 | AAGACTCTAAAGCAG[A/G]AGTGTGACTGAGTTG | 84333 |
| rs185946059 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258976 | GTAATATCTTTAAAA[G/T]ATTCTATTGTTGTTT | 84333 |
| rs185956271 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187479 | GAGGTAGAGGTCGCT[A/G]TCAGAGAAGCACACC | 84333 |
| rs186011849 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281013 | CTTTTATCTGCCTTA[C/G]AAATTATAAGTATAA | 84333 |
| rs186037840 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226369 | ATAGCAGATGTGTAT[C/G]AGGATACTGGAGCAG | 84333 |
| rs186155691 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243982 | ATATTTACTGGATGC[C/G]TGCTGTGTCTGGGCA | 84333 |
| rs186163186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267877 | TCAGCTTATTTCCTA[A/T]ACTAATGACCACTAT | 84333 |
| rs186169201 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252404 | TCCTGGCATCTTATA[A/G]CAACATATATGAGCA | 84333 |
| rs186171951 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169064 | TTAATACACTAGGCT[C/G/T]TCCTCAAGCAGGAGA | 84333 |
| rs186175119 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234590 | TCTGTTATTTATGAT[G/T]AGTGCATCAAACTAA | 84333 |
| rs186176201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205404 | CTGTGAATAAAAACA[C/T]ACCCATAGACCTAGA | 84333 |
| rs186184396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216445 | GGGGGTGGGGAGGCT[A/G]TAGAAGTGACAGGGA | 84333 |
| rs186185003 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233643 | TATTCTGGATTTTTT[A/T]AATTAGTGTTAGTTT | 84333 |
| rs186198436 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177264 | CTGATCGTTCCTCTG[A/G]AAGTTTTGTCTCAGA | 84333 |
| rs186223378 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193901 | TGATCAGATTCTAGA[G/T]ATGTGTTAAAGACGA | 84333 |
| rs186252705 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284139 | TCTATGGAATGTTCT[A/G]TACAAAGCTGTATAA | 84333 |
| rs186275469 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247529 | ATGTGAGAAACCTCT[A/C]TGTGTTTGTAGTCTT | 84333 |
| rs186293214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211421 | TGCTATAGAGGTTAT[C/T]GTAAATTTATCCAGC | 84333 |
| rs186342263 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272643 | CCGGGTGTGGTGGCA[A/C]ACCCCTGTAGTCCCA | 84333 |
| rs186393462 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177560 | GGGCTCCACCCAGTT[C/T]GAGCTTCCTGGCCGC | 84333 |
| rs186402116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191260 | TGGGGCCATTAAGTA[A/G]AATAAGGGTTAGTTG | 84333 |
| rs186423585 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211868 | CTTATCTGGAACCAG[A/G]CCCCAGAGGTGTTGC | 84333 |
| rs186438602 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230396 | AAAAAGACAAAAGAT[A/C]ATTTTCATTTGGGTA | 84333 |
| rs186467522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190785 | TGGATTATTGTGCTG[C/G]TTTTCATTCCTGTTA | 84333 |
| rs186488334 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164409 | CTGGCTACATTAACC[C/G]GTTGAGGAGCGCTGG | 84333 |
| rs186500671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194988 | TGGTGAAAGCAGACA[A/G]TATAGGGGGAGTAGA | 84333 |
| rs186561208 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268583 | CTCCTCATATTGGAT[A/G]CCACTCTCTGCCCCG | 84333 |
| rs186581901 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235606 | TCCCCACCCAAATCT[C/G]AAATTGAATTGTAAC | 84333 |
| rs186609810 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232621 | CATGGTGACAGGATC[C/T]GGCATATAGGGCAGA | 84333 |
| rs186612758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257205 | TAAGCACAGGAAAAG[C/T]TGCTAAATATCACTA | 84333 |
| rs186621109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213293 | TCTATTTCTTAGTCT[A/G]TGCAGTCCTTAAAAT | 84333 |
| rs186627167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240862 | TTCAGTATTTTAATA[A/G]TCCATGTTATGTTGA | 84333 |
| rs186651948 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162045 | GCTGAGTCCAACAAA[G/T]TTTGACAGGTGGAGG | 84333 |
| rs186661347 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178650 | CACCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 84333 |
| rs186667334 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192171 | TTCTGATAGTACTTC[C/T]TTAAACAAAAATGGT | 84333 |
| rs186705568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180335 | CTTTTGCTGTACAGA[A/G]GCTCTTTAGTTTAAT | 84333 |
| rs186761917 | snp | C/T | 9.95405e-05 | 0.0070541 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278367 | CACTATTTGTTTACT[C/T]GTCAACAGATTGCAC | 84333 |
| rs186773038 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284777 | AAACCCCAGTCCTTC[A/G]GTGAGATAGGGAAAG | 84333 |
| rs186791282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252491 | TAGTAAGAAAAAACA[C/T]CTTTCACTCAAGGAA | 84333 |
| rs186801519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164996 | AACAGTGCCTGGCAT[A/G]TATGAAACACTTAGT | 84333 |
| rs186807686 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180697 | GTTCTCTATTATGTT[A/C]CATTGGTCTATGTGT | 84333 |
| rs186816288 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196470 | ACCCCAGGGCTTTTG[C/T]ACTTGCTAAGCCTTC | 84333 |
| rs186820394 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216732 | AATTATTGGATTGTG[A/G]GAGAGGGGTGCAGTA | 84333 |
| rs186847814 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255907 | AACCTGCTATATACT[G/T]TAAATCATCTCTAGA | 84333 |
| rs186848858 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235873 | TGTAAGTCCAATAAA[C/T]CTCTTTCTTTTGTGA | 84333 |
| rs186854680 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182931 | TTGTATGGTTTTGAG[A/T]GAATTTCTTAGTCTT | 84333 |
| rs186857200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216961 | ATTACAGAGAGTAGT[G/T]TATATGTTAAAGACA | 84333 |
| rs186865106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222242 | TATACAAGTAGAGCA[A/G]CCGGGCATGGAATAG | 84333 |
| rs186919555 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184506 | GTTATAATGTACTCC[A/T]TTAGCTCAGAAAGTT | 84333 |
| rs186934226 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253048 | CCTTTTTTTCCTGTG[G/T]CATTCCTGCTTTGTC | 84333 |
| rs186971471 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258373 | TACAGGTTGAGTATC[A/C]CTTATCCAAAATGGT | 84333 |
| rs186973250 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241930 | AGGTCTCAGACCACA[C/T]ATCAGACCTGCTAAC | 84333 |
| rs186973701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177958 | CCAGTGAGATGAACC[C/T]GGTACCTCAGTTGGA | 84333 |
| rs186979627 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281332 | AAACGTAATGACTTT[C/G]CTCAACTACATTACA | 84333 |
| rs186982944 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223799 | TTGGAGTAGATGTAG[C/G]GGGAGAGAGAAGGTA | 84333 |
| rs187004411 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203322 | ACCAGCCAAGGATCA[C/T]GTAATTCTCTAGGAA | 84333 |
| rs187016233 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171549 | AGAGATGCTGTGAGT[A/G]TCACTGAAACTGCCA | 84333 |
| rs187032122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272239 | TATCTGATAAAGATA[C/T]ATTTTAAAAATTTGG | 84333 |
| rs187051772 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274728 | TTGATCAAAAGAAAT[C/T]GAGAGACGTTGCTAT | 84333 |
| rs187052555 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239326 | AGAGGAAATGCTGCT[A/G]ATCTCTGTATGTACT | 84333 |
| rs187147364 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179899 | CGAATGGTATTTCTA[C/T]CTTTAGGTATTTGAG | 84333 |
| rs187166991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276682 | AGCCATTTTACTTCC[C/T]TCTGTACCTTTATCC | 84333 |
| rs187174622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244891 | TCAGGACTTCAATTG[C/T]GGACATGCTGAGTTA | 84333 |
| rs187192225 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260988 | ATAAAAGCTTAAATA[A/G]TAAAAAATATATATA | 84333 |
| rs187217232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245345 | ATCAACTTTGAAAAG[A/G]GCACTTTCTTTAGAG | 84333 |
| rs187221581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227171 | AGATAAATGTGAAAT[A/G]TATACACTATTGAGC | 84333 |
| rs187227397 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207345 | TCAAAATCTACAGAA[A/C]AGTTGCCAAAATCTT | 84333 |
| rs187231698 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164115 | TTCATGCGGGGTACA[C/T]ACACGCGCGCGTACT | 84333 |
| rs187248065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175235 | AATTAAAGTAAAATA[A/G]AGGTTCTGGATGTAG | 84333 |
| rs187255456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188353 | CAGATGGATGATTCT[A/G]TTGGCTCTAAAATCA | 84333 |
| rs187271379 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226689 | CCTGTAGAAGTAGGT[A/G]GATATAGAAAGAAGG | 84333 |
| rs187278345 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278160 | TTGTAATCACTAGTA[C/T]CAGGAAATACTGTAA | 84333 |
| rs187372106 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260621 | TACACCATGGAATAC[C/T]ATGCAGCCATAAAAA | 84333 |
| rs187396151 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171052 | AAGCAAAACCATAGA[C/G]TAAAAAGATCAGTGG | 84333 |
| rs187399006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184241 | ATCCCATATTTCTTG[A/G]AGGTTTTGTTCATTT | 84333 |
| rs187418818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168693 | CAGCACTTTGGGAGG[C/T]CGAGGTGGGCAGATC | 84333 |
| rs187467486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200512 | GTATGGATGAGATTG[C/T]ATTGAAAGCTGTGCA | 84333 |
| rs187509667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266195 | CTTTGATAGTTTAGC[A/G]GGCATTGCAGTGTGT | 84333 |
| rs187609815 | snp | G/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281782 | CAGTCAAATGCAGGC[G/T]TTTCTTGCAATAATC | 84333 |
| rs187613973 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266509 | ATAAAAGTTCAAAAA[G/T]TGATTCAGTAGCTAT | 84333 |
| rs187629508 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188794 | AGTGTCATTTGGAGC[C/T]TGTTGACCTACCCAA | 84333 |
| rs187685848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249684 | ATTATCATTTTATTC[A/G]TTCAACTTAACTGTG | 84333 |
| rs187706837 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261777 | AGATCCATTATTACC[A/G]ATTCTTTATAGACTT | 84333 |
| rs187712596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223113 | TAATAATTATTTTAA[C/T]TTTGAATTTTCAGAA | 84333 |
| rs187717828 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227918 | ATTTGGGTTAAGTGT[C/G]TCAATAAAATCTTAA | 84333 |
| rs187734296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174542 | TATTTGTTTGATTAT[A/G]ATCTACTGTAATAAA | 84333 |
| rs187743236 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188071 | CATGCTGGTGTGCTG[C/T]ACCCGTTAACTCCCC | 84333 |
| rs187750853 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281411 | GTGTTATATAATATT[A/G]TGAACTGTTTAGCTT | 84333 |
| rs187854247 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270421 | AAATTGCCACTTTCC[A/G]GCTTACTCTTGTTGA | 84333 |
| rs187868684 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253108 | TGATATATGTAAGTA[C/T]GTCCTAATACTTTCT | 84333 |
| rs187870698 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237481 | GGCGCAGTGGCTCAC[A/G]CCTGTAATTCCAGCA | 84333 |
| rs187899738 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176377 | GTTTGGTGAATCTGA[C/T]AATTATGTGTCTTGG | 84333 |
| rs187916841 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210041 | TTTAGATGGATAGCA[G/T]ATCATAGCATTAGAC | 84333 |
| rs187955539 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179870 | GTATATACCCAGTAA[A/T]GGGATTGCTGGGTCG | 84333 |
| rs187962835 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178614 | AGGCTGGTCTCAAAC[C/G]CCTGGGCCAGCCAGT | 84333 |
| rs187965048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248854 | GCACCCTTTTATTTA[C/T]ATTACGAACCTTTTT | 84333 |
| rs187965668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193474 | CTGATAGTGGAGTAA[A/G]AATGTGTTCTAGACA | 84333 |
| rs187978906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213019 | CAATAAGTTATACTT[C/T]CTAAGCGCTGCTCGT | 84333 |
| rs188003532 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245881 | CAGGGGAGTGAGAGG[A/T]TCAGTGCACTTGTGA | 84333 |
| rs188007619 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269508 | ATAATTTGATTAACA[C/G]ACCCCTTTGATGGAC | 84333 |
| rs188011221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251916 | TAAAATTAGATGTTG[C/T]AAAATGCCTCTGAAC | 84333 |
| rs188015433 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275052 | GGGATGGCCTTTCAC[A/G]TTGTACCTAAAAAAA | 84333 |
| rs188023044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233720 | CTTTGAACATGACCA[C/T]AGTTTACTTATAAAC | 84333 |
| rs188031387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215858 | GATATATTGCTCCAT[A/G]ATTGTTTCTTGTGGA | 84333 |
| rs188033341 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258547 | AACCTACACCCTTAT[A/C]TTCTTCTCTGACTTA | 84333 |
| rs188051019 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91163797 | CCACCTGTACGCCCT[A/C]CGCGCCCCCTGCGGG | 84333 |
| rs188198904 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168358 | TAAGGAAGGAGATTT[C/T]GAAGGATCCTGATAG | 84333 |
| rs188233377 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265532 | TGAAAATGTAAATCA[C/T]AAAAAAAAACAAAAT | 84333 |
| rs188235209 | snp | C/T | 0 | 0 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161549 | TTTCATGATTTACTC[C/T]ATTCTCTTTGATCAC | 84333 |
| rs188251203 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270655 | ATTTTATTTAAAAGG[A/C]TACAAATATATTTGT | 84333 |
| rs188251928 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231969 | TGGAGATGTCCATTT[A/G]GGAGTTGGACTTATG | 84333 |
| rs188255361 | snp | A/C | 0.000462657 | 0.0152024 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271728 | GACTGTACATATGAC[A/C]ATCATGACACCATGG | 84333 |
| rs188256273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191732 | TGCTTCTTTGGGATT[A/G]TCCCCTGTCCAGAAC | 84333 |
| rs188258947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254694 | GTTTATACAGAATAT[C/T]TACTGCTTTTATAAT | 84333 |
| rs188267237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238337 | TGCACCTTTGGATGC[C/T]TGAGCCCTACAACTC | 84333 |
| rs188276841 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237641 | CCCAGCTACTAGGGA[A/G]GCTGAGGCAGGAGAA | 84333 |
| rs188278473 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219553 | AGTCATTTGACCTCA[C/T]TTGTTTTCTCTTACT | 84333 |
| rs188287201 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197272 | GAAGGCTCGCGAGCT[C/G]ACTGTCATGTCCTGG | 84333 |
| rs188306403 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182130 | TTTCTGTGAGGTCAG[C/T]GGTAATGTCCCCCTT | 84333 |
| rs188431695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223450 | CTAGATTTAATGAGC[C/T]GGAGACTCTGAGAGT | 84333 |
| rs188464826 | snp | C/G | 0.0310518 | 0.120672 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163563 | CGCTCGGGCCCTTCC[C/G]CCGCCGGCAGCCGCG | 84333 |
| rs188471017 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218960 | CCAGACAAATGTTTG[A/G]GTTTTTAAACTTGTT | 84333 |
| rs188474806 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161128 | TGGCTCCAACTCCTA[C/T]TGGACAAGCCCTCCA | 84333 |
| rs188509995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257793 | AGGAAAGTGAAACTG[C/T]AGATAAGGAGGGACT | 84333 |
| rs188685575 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205926 | ACACGGGAGGCTGAG[G/T]TGGGAGAATTGCTTG | 84333 |
| rs188686920 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275904 | AGTTATAATAGCAAA[A/G]GAAAAAAGGACTAAA | 84333 |
| rs188690802 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259113 | GCTTGGGTGTCCCTT[C/T]TGGATTGGTTCTTAT | 84333 |
| rs188706664 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243906 | TTTCTATTGGTCATC[A/T]CTTATATAGACAATA | 84333 |
| rs188723540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202466 | ATACAAAGTAGTTAA[C/T]AGGATTGTTGTGAGG | 84333 |
| rs188761102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217792 | AAAAAGTTAATCTGT[A/G]TGTTTTTTCTTTAGA | 84333 |
| rs188770719 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180886 | TTCTAGTTCTGTGAA[G/T]AATGTCAATGGTAGT | 84333 |
| rs188786919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274199 | AAGTTAAATGTAATT[A/C]CAAACACACTTTTAC | 84333 |
| rs188803301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241515 | CAGCTACAGGCCGTA[C/T]GTCCTCACCACTAGA | 84333 |
| rs188810328 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166934 | CCATGGGAGCAGCTT[A/C]ATCTCTCAGAAGTTT | 84333 |
| rs188914641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170465 | GACCTTAACAGACAC[C/T]TCACCAGAGAAGATA | 84333 |
| rs188924445 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279551 | GTTAAGTCTTCCATT[C/T]GTTTTAGGATTAGTC | 84333 |
| rs188940281 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263010 | GCATGTATATATTTC[A/G]CTATAAACAAAGATG | 84333 |
| rs188944270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247058 | GAAGCCACAAAAGCA[A/G]ATGAAATCCACAAGG | 84333 |
| rs188954794 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229717 | ATCTGAATTTATGAT[G/T]CTGAATGAATAGCCA | 84333 |
| rs188959774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196683 | GAGGGTGACAAATGC[C/T]ATTTGTGTATTTCTT | 84333 |
| rs188964951 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210942 | TTATCAGACAGGTGA[G/T]CTGCTTCACACAAAA | 84333 |
| rs188973423 | snp | C/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189786 | TAAGAAGCATCTGAG[C/G/T]CAGTATTGAGCACAT | 84333 |
| rs188977056 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203972 | TTATGCAGTTTTCAT[A/T]AGTGATTGTACAACT | 84333 |
| rs189027099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267626 | AAATTTTCAATTTTT[C/G]TTCAACTTCCAATTA | 84333 |
| rs189040968 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165787 | ATATAATGTAAAAAG[A/G]ATGTGTATGTCATAT | 84333 |
| rs189054594 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171878 | ACTATGAGGCCAAAA[C/T]ATCAAAATGATTTTG | 84333 |
| rs189055044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242409 | CTATAATAACTTATT[C/T]TTATTAAAATAAAAA | 84333 |
| rs189193349 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204389 | GATGATTGCACTCAA[C/G]TAACTGTCTTATATA | 84333 |
| rs189193393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250715 | TTTGTATATAATATA[A/C]AGTATGCCATTGAGA | 84333 |
| rs189199762 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233027 | TAGAGAGTTAGATAG[A/G]GTTAGCCAGGATTAG | 84333 |
| rs189203085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183883 | TAAGAATGTTGAATA[C/T]TGGCCCCCAATCTCT | 84333 |
| rs189209557 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213683 | TAGAGATGGGGTTTC[A/T]CCATGTTGGTCAGGC | 84333 |
| rs189225821 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172723 | TAACCTTTGTGGCCG[C/T]AGACACATTGTTATA | 84333 |
| rs189237350 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185994 | TTGAGAGCCACGCAC[C/T]CTAGCTGCTTCTAGT | 84333 |
| rs189273850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230927 | TGTGCCCAGCCTATT[G/T]ATTTTAGAGACGGGA | 84333 |
| rs189345268 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185090 | AGTTGGCTTGGGCTC[G/T]CCAAGCATGAAGCTG | 84333 |
| rs189346280 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271944 | AATCAGGAATTTTTA[A/G]TAATTACTACTTTCA | 84333 |
| rs189351910 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190936 | CCTTAAAATATGCTT[C/T]ACTTCATTTTTGCCT | 84333 |
| rs189352116 | snp | A/G/T | 0.00239393 | 0.0345281 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255506 | TAGTTGAATATTGGT[A/G/T]GTATGCCCCCAAACA | 84333 |
| rs189352780 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224370 | AGTTAATTAACTATC[A/C]TCGAACAGACATTTA | 84333 |
| rs189358150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263730 | TCGAGCAAAACTTAA[C/T]GCTGATAAGTATGCT | 84333 |
| rs189378683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176832 | CTCAAGGTTTTTAAC[C/T]TCTTTGCCATAGGTT | 84333 |
| rs189388770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189501 | TGTTTGAGGTTCAAG[A/G]TGAATTCTACTTAGT | 84333 |
| rs189395525 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283756 | CAACACAACAGAGAT[A/C]ATCAGTTTTAAATAG | 84333 |
| rs189430960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228571 | ATAATATAGTTGACG[C/T]GATAAGAGACTCGGC | 84333 |
| rs189437260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210237 | GAGATCCTTTTTCTG[C/T]CAGAGAGTGCTACAG | 84333 |
| rs189495704 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179563 | GTCCATATGTTCTCA[A/T]CATTTAGCTCCCACT | 84333 |
| rs189529431 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214717 | AAAGGCTAAAGAACT[A/G]CAGATAAAATATGAT | 84333 |
| rs189568730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211731 | ATTCCAGTTAGTAGG[A/G]CTCAGTGTAAGCAGA | 84333 |
| rs189589853 | snp | A/G | 0.00398564 | 0.0444627 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282194 | TTTTCCCCTTAAAAA[A/G]CAACTCTAGGCCGGG | 84333 |
| rs189609495 | snp | A/T | 0.00153565 | 0.0276671 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251266 | CTTTGATTTATAGCT[A/T]ACTTAGTTTTGTTTA | 84333 |
| rs189639049 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280592 | AAGGCATCAGTTGTC[A/G]TTTGGAGAAAGGTAC | 84333 |
| rs189652272 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247868 | TTGATGCTTGAAAAA[G/T]CAAGCATTTATTATT | 84333 |
| rs189764344 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269585 | AGTACCTACTACATA[C/T]ATGCAAGCATATCCA | 84333 |
| rs189767975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253104 | TACTTGATATATGTA[A/T]GTATGTCCTAATACT | 84333 |
| rs189774324 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276010 | AAAATTATGTAGCAC[C/T]GTACCAAATGGTATG | 84333 |
| rs189777609 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193187 | GGGCATCAGTCCTGC[A/T]GCTGCAAGAAACTGA | 84333 |
| rs189780634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236994 | ATATATCGTAGATCT[A/G]TGTAAATAAAGTGTG | 84333 |
| rs189786628 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217250 | GTGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 84333 |
| rs189799753 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233537 | CAATATACGGCACAT[C/T]ATGTAATATATATAC | 84333 |
| rs189878776 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267079 | GTGGCCCCCATACAG[C/G/T]CTTCCCCAGATACTC | 84333 |
| rs189883957 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177240 | TTGGTGAACAGCAAA[C/T]GTTGCTGCCTGATCG | 84333 |
| rs190004605 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272754 | TTCCAGCCTGGGTGA[C/T]AGAGCAAGACTCTGT | 84333 |
| rs190018927 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257011 | TGTGTATCAAAGGAC[A/G]CTTAAAGTGAAAAAA | 84333 |
| rs190019368 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91162502 | CTGTGGGGGGAGAAG[A/G]TGCCCCCTCAGAGGC | 84333 |
| rs190030888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169905 | ATCAAGACAGTGGTA[A/T]TGGCAAAAAATTAAA | 84333 |
| rs190035924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222583 | CTATTCACCTATTCA[A/C]CCAATTGGGAACATG | 84333 |
| rs190041843 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183509 | ATCGATGAATTTTGA[C/G]TCTTTCTCCAGCTTG | 84333 |
| rs190100527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225217 | TTATATATATCATAT[A/G]TTTGATATATATCAT | 84333 |
| rs190119290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181330 | ACTTCCTCTTTTCCT[A/G]TTTGAATGCACTTTA | 84333 |
| rs190139643 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91192647 | TCTTGATCTAATGGA[A/G]TCTGTTTTCTATCAG | 84333 |
| rs190181314 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258652 | TGGGATAGTTGAGAA[C/G]GTGAACAGATAACAG | 84333 |
| rs190194771 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187035 | AGTTAGTCTCAGGTG[C/G]GGTCTGAGATTCTGC | 84333 |
| rs190280637 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178940 | CAGCACTCACTCTAT[C/G]TCAACATCTTTTGGG | 84333 |
| rs190282032 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226123 | TAAGAATGAGTAAAC[A/G]CTAGGTTTTATGGAG | 84333 |
| rs190288421 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204976 | TATTTAAATTGAAAT[A/C]TATCTGTAAACTATC | 84333 |
| rs190298778 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164649 | TGCCATTCATGAATA[C/G]AGAATTTTTCCCAAT | 84333 |
| rs190309113 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180475 | TATATTTTTTTGTTT[A/T]ACATTTAAGCCTTTA | 84333 |
| rs190320709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182727 | AGCAGTGTCCTGGAG[A/G]CTCTGTTACATTGTA | 84333 |
| rs190337519 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246406 | AATTCTTGGGATAAT[C/T]GAATAAGCCAGTTGG | 84333 |
| rs190346954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243175 | CGGACCTCAGAGGCC[C/T]GAGTATACCAGGAGA | 84333 |
| rs190416217 | snp | A/G | 0.00517822 | 0.0506191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278935 | TCTAAGCATCTGTCC[A/G]TGTAGTCTACCAATT | 84333 |
| rs190422800 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281019 | TCTGCCTTAGAAATT[A/G]TAAGTATAAAAGGGT | 84333 |
| rs190427251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275507 | ATGCAGTGGTGCGAT[A/C]TTGGCTCATTGCAGC | 84333 |
| rs190430337 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265377 | TGCATAAATAAATAA[A/G]TATGAATTAAGATTG | 84333 |
| rs190430546 | snp | C/G/T | 0.00479476 | 0.0487406 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248495 | ATTTTCTTTCTCCCC[C/G/T]CTTTCGAAGGTTGGA | 84333 |
| rs190435952 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221512 | GCACGAATACGGTTT[C/T]CCAAGAGGATAGGAT | 84333 |
| rs190441255 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231809 | CATTGCAGTAATCCA[A/G]GCAGGAGATGGTAAT | 84333 |
| rs190451087 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169216 | AATCTTAAAAGAGAG[C/T]CTATTTTTGAATAAT | 84333 |
| rs190457202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182999 | TTTGTTACTATTTCA[A/G]TTCTTTTGCTTTTGC | 84333 |
| rs190515748 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198269 | ACCTCAGTCCCATCT[A/G]CTCATTCTCAACCAC | 84333 |
| rs190563156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168868 | GGGAGGCGGAGGTTG[C/T]AGTGAGCTGAGATTG | 84333 |
| rs190592293 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197561 | GTGAAGCAATGGGGA[A/C]TCACCAAAGTTAAAT | 84333 |
| rs190601215 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174434 | ATCACTTGAACCCAG[C/G]AGGTGGAGATTGTAG | 84333 |
| rs190604361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188102 | CGAACAGGAACAGCT[C/T]CGGTCTACAGCTCCC | 84333 |
| rs190647711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205549 | TCTCAGGCCAGGCCA[C/T]ACAAGTCCTATCTAA | 84333 |
| rs190665700 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268038 | AATGTATTGAATATT[A/G]AATAATCCATATTTA | 84333 |
| rs190667449 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284266 | AATTGCATAATTTAT[C/T]ATTGTTTGTCATCTT | 84333 |
| rs190673600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226894 | CTCTTCCCTTCAGTA[A/G]GCCAGGGACATTTGA | 84333 |
| rs190674847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238896 | TTTTTCTTTTTTTAA[C/G]GTTTTCTGATACTGT | 84333 |
| rs190680483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206009 | CCTGGGTGACGGACC[A/G]CGACTCTGTCAAAAA | 84333 |
| rs190682157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252426 | ATATGAGCACAGTAA[C/T]TCAGTGAATATTTAT | 84333 |
| rs190684960 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262362 | GAACCTGGGAGGCGG[A/G]GGTTGCAGTGACCCG | 84333 |
| rs190690422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235125 | CTTGGCCAATGTTTC[C/T]GAGTCATCTTTTGGC | 84333 |
| rs190697090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174909 | AGAGGCAACAGTAGA[A/G]AAGAGGCATCAGCAA | 84333 |
| rs190733240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244597 | TGTTGAGAACACCGC[A/G]CGTATAACAAGGCAA | 84333 |
| rs190863275 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187552 | AAAAACCCAGCTATC[A/G]CTTGATATAGGAAAG | 84333 |
| rs190888403 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226456 | GCCATCTCAGGCAGA[C/T]AGTAGCCCTTGAGTA | 84333 |
| rs190908807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248328 | TTTTGTTATCAGTCT[A/G]CTACTGGGGAAGGCT | 84333 |
| rs190915060 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231222 | ATTTATATTATAAAT[C/T]ATTACTAAGCACTTT | 84333 |
| rs190923177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212430 | TCAGAGTAATTTGGA[A/G]TGTCTCTTAATAGTC | 84333 |
| rs190941189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177700 | AGGCGTAGGACCCTC[C/T]AAGCCAGGTGCAGGA | 84333 |
| rs190950632 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191393 | GATGATTCACCACAG[A/G]GAGGGACCACATGAG | 84333 |
| rs190972814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260260 | TCAAACCACAATGAG[A/C]TACCATCTCACACCA | 84333 |
| rs191027718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265634 | TTTCCAAAACATATT[C/T]ATATTGAATGTAAAC | 84333 |
| rs191119635 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273517 | ATGGCTCATTAATAG[A/T]CTTCATTAATAGTCC | 84333 |
| rs191186117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252745 | CAATACATGAGTTAG[C/T]TCATACTGAAAGTTA | 84333 |
| rs191205612 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216775 | GGTCAAGGGTGATTG[G/T]AAGTTCTCTTCAATT | 84333 |
| rs191216091 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175513 | CCCATCATTCAACAA[C/T]CCTATAACCTTCCTC | 84333 |
| rs191257053 | snp | C/G | 0.00517822 | 0.0506191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281335 | CGTAATGACTTTGCT[C/G]AACTACATTACACAC | 84333 |
| rs191258758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165454 | AAACAGCCTGAAGTT[A/T]AGCTGCAGTTTGGGA | 84333 |
| rs191270841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180803 | CCTCCAGCTTTGTTC[C/T]TTTTGCTTAGGATTG | 84333 |
| rs191362511 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173502 | CATGTAACTACCACC[C/T]AGCTCAAGAAATAGA | 84333 |
| rs191379350 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196530 | TGGCTTCACAGTCAT[A/G]CAGGTTTCAGCAGAA | 84333 |
| rs191409950 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178147 | CTGACTGCAATGTAG[C/G]CTGGGAAAAAACATT | 84333 |
| rs191431638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235706 | TCACGCTGTTTTCTC[A/G]ATAGTGAATAAGTCT | 84333 |
| rs191433134 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212707 | TTCACACTTTGGGTA[A/G]GTAAGAAAATGGAAG | 84333 |
| rs191436134 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203510 | ATTTCTAAATTAGCA[A/G]TCTTATTTCAGTATT | 84333 |
| rs191437820 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239497 | AAACTTTTAGATAGT[A/G]TTGATCTTGAGGAGA | 84333 |
| rs191492108 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195560 | TGCAGTCACGGCTCA[C/G]TGCAGCCTTGGCCTC | 84333 |
| rs191500797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274736 | AAGAAATTGAGAGAC[A/G]TTGCTATGTGAATAT | 84333 |
| rs191505247 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258471 | TCTGAAATGAATGAG[G/T]GTCATGTCAGCCCTC | 84333 |
| rs191510546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268901 | AAACAGCTGGTCAGA[C/G]TTAGCTCGTAAAATT | 84333 |
| rs191520202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272397 | TGCCTGTAATCCCAG[C/T]GCTTTGGGAGGCTGA | 84333 |
| rs191520745 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242111 | AGGAGTGATTTTGCC[C/T]CCGGGATACATTTAG | 84333 |
| rs191526616 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223890 | CATAGCTAATGAGTG[A/G]TGGACCTATATTCAA | 84333 |
| rs191530148 | snp | G/T | 0.0154538 | 0.0865337 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161668 | CATAGCTAGGTGTGG[G/T]GGGGAGGAGATATAG | 84333 |
| rs191655077 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161230 | CAGGATTGCCTCACC[C/T]TACCCTAGTTGAACG | 84333 |
| rs191670538 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191686 | CTATGTAGCCCTCTG[A/G]GAATCACTCTGATTG | 84333 |
| rs191682409 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181374 | TCTAATTGCCCTGGC[C/T]GGAACTTTGAATACT | 84333 |
| rs191684896 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207725 | TCTTTCATGACATTA[A/T]TATTTTCAAAAAGTG | 84333 |
| rs191692672 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197019 | TAAACAACAACAACA[A/T]AAAAAACATGATGTG | 84333 |
| rs191702700 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222246 | CAAGTAGAGCAGCCG[A/G/T]GCATGGAATAGCAGA | 84333 |
| rs191746944 | snp | C/T | 4.95242e-05 | 0.0049759 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91278310 | ACCAAGAATTGATTT[C/T]GGTTAGACCAAGGGG | 84333 |
| rs191759489 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164338 | TTTTGGGGGGTCAGG[A/G]TCCACACATTCCCCA | 84333 |
| rs191760973 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91261346 | AATGAAGAAATTCAT[C/T]CGATGTTCTACACGT | 84333 |
| rs191767350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245606 | AGTTAATCATGTGGG[A/T]GAGTAGGGAATGCAA | 84333 |
| rs191776252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167049 | AGAAACCAATAAAGA[A/G]ATATACAGTTCTCCT | 84333 |
| rs191778055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194237 | TTGCACATGTGATGG[C/T]TAAGATAACAACTTT | 84333 |
| rs191778547 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227731 | CATTAAAGCTACTTA[A/G]TGGTGACTGGTTTCT | 84333 |
| rs191784108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255911 | TGCTATATACTTTAA[A/G]TCATCTCTAGATTAC | 84333 |
| rs191926023 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171223 | ATACAGATGTGGCAT[C/G]GAGGAAGAAAGAAGT | 84333 |
| rs191972269 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223178 | TGCTTTTATTTGAAT[C/G]TCAGTAGTTGACTCT | 84333 |
| rs192015669 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223646 | AGATTACACATACTC[C/T]TTGTGTTTCTGCCAG | 84333 |
| rs192023365 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183968 | TTTGAAAGTGACCTG[C/G]CCTTTCTTTCTCACT | 84333 |
| rs192026768 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202608 | CTGTAATATAATATA[C/T]AGCCAGAAGTTGTTA | 84333 |
| rs192037337 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280815 | AAAATGTACAGGCAA[C/G]TTTTGTGGTTAGCTT | 84333 |
| rs192037718 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257368 | GTGGGAAGGTGAAAG[A/T]GCAGCTACTGTGGAA | 84333 |
| rs192044873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184432 | CAGTACTCTCTACTG[A/G]CTGTTTTGTCTGTCA | 84333 |
| rs192048471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244907 | GGACATGCTGAGTTA[C/T]TCATTTCAGAGAAGA | 84333 |
| rs192068699 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179957 | CTGAACTAATTTACA[A/C]CCCTACCAATAATAT | 84333 |
| rs192085192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216472 | GGGATTTGAAATGGC[C/G]TTATTAAGTGTTTGG | 84333 |
| rs192129725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276873 | AATGGAAAGGATATT[A/G]GTCGTCTCAGAATCT | 84333 |
| rs192139135 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266809 | TTAGCAAATTCTGTA[A/T]CCTTCACCATCAAAA | 84333 |
| rs192141310 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281883 | CCTCAAAGATGAGAA[A/G]GAGGTAAACACAACA | 84333 |
| rs192154399 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250929 | GAGTATAATTTATAT[A/G]TACACCTATAAATAA | 84333 |
| rs192233022 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245889 | TGAGAGGATCAGTGC[A/T]CTTGTGAGTGTAGTA | 84333 |
| rs192244178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210076 | TATAAAGCTTGGGCA[A/G]TTTCTAACATATAAA | 84333 |
| rs192274220 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176401 | GTCTTGGAGTTGCTC[G/T]TCTCAAGGAGTATCT | 84333 |
| rs192293138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264273 | TAAGTAACATATCCA[A/G]ATTGTTAATGCTTTA | 84333 |
| rs192302350 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189524 | TACTTAGTAATATAT[A/C/G]ACATAAAAATTGTAT | 84333 |
| rs192310677 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201168 | TGGGCAATTTATAAA[A/G]GAAAGAAATGTATTG | 84333 |
| rs192315041 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278697 | CAGTTTTCACATACT[C/T]ACTCTTTTATTCTTG | 84333 |
| rs192363771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170586 | CACAATTGAAATGGC[C/T]AAAATTCAGAACACT | 84333 |
| rs192376273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246577 | GAAGATTGATTATGA[A/G]CATGTCTCTGCTCTG | 84333 |
| rs192381003 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270464 | TTCTCAATGTTATGC[A/G]AAGTCTGATGGACCA | 84333 |
| rs192381040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228871 | ACTGTAGACTTACTG[A/C]ATCAGAATCTCTGGA | 84333 |
| rs192387573 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253333 | CCTGTCTCGCCCCCT[A/G]CCATTCCACCTTCAA | 84333 |
| rs192391180 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210496 | TCTCTAATGTCAAAC[C/T]GGATAACTGGCTTAG | 84333 |
| rs192399252 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240912 | AGGGAGAACTCATAG[A/G]AAGACTAATATTAGG | 84333 |
| rs192439004 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191794 | TTGGGACAAGTACAA[A/G]GCTGGTAGGCAAAGT | 84333 |
| rs192448277 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171725 | GGTTCTGAGGGTAGT[A/G]GTGAAGGGCATGAGG | 84333 |
| rs192486346 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232136 | AAGGCAAAGTAAACA[C/G]ATAGTGTTGAGGAGG | 84333 |
| rs192568813 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266197 | TTGATAGTTTAGCGG[A/G]CATTGCAGTGTGTTT | 84333 |
| rs192574621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250176 | TAGGAGTTTGGTTCA[C/T]AGAAGGCAACTCCTA | 84333 |
| rs192581694 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232623 | TGGTGACAGGATCTG[A/G]CATATAGGGCAGAGG | 84333 |
| rs192583484 | snp | A/G | 0.0119091 | 0.0762411 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162327 | GGGGTGGGGTGGGGG[A/G]ACTTTGCGATTAGAA | 84333 |
| rs192586508 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178709 | TTTCTCATTTTAAAC[A/G]TAGTAGTACACTTTG | 84333 |
| rs192591240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213568 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 84333 |
| rs192594663 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192485 | TCTTGCTCATCGTCA[A/G]TTAAGAATCTTTATT | 84333 |
| rs192650255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228303 | TGTTCCAGCAGCTCA[A/G]ATGTGACCAATACAG | 84333 |
| rs192694102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189018 | TCTACTGAGATAGGT[A/G]ATTATGGATTTAAAG | 84333 |
| rs192712792 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262132 | AGTAGCATCTAGAAA[A/G]TTAAAGACCAGGCCA | 84333 |
| rs192738233 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254075 | GTATTCAAGGCCCTT[C/T]CCTAACAAGCACCTC | 84333 |
| rs192745269 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219057 | GCAGAGGCGAAACCA[C/T]AGAACACTTAACTGC | 84333 |
| rs192747597 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188428 | GAAGACCCTAGAAGC[A/T]GAAAATACAATTTTA | 84333 |
| rs192782803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184664 | TTTTCAGTGTTCTTG[C/T]GTTGATTCTTTCTCA | 84333 |
| rs192790979 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249262 | TATGGGAATTTTCTC[C/T]ATCACCCAGATTTCT | 84333 |
| rs192801209 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213032 | TTCCTAAGCGCTGCT[C/T]GTCTGTATCTTATTC | 84333 |
| rs192856208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274373 | AGTAATTAAAATAAG[G/T]TCTTGCCTTAAACAT | 84333 |
| rs192860419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213822 | CATTAAGTGTTATGT[A/G]CTACATGTTAAACAT | 84333 |
| rs192864449 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241743 | TTCATAACTCTCTTA[C/T]CTGTGTGATATTTGC | 84333 |
| rs192889098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179058 | TAAAAGCTTGCTAGC[C/T]GCTTCTGATAAGGAG | 84333 |
| rs192938580 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271104 | TATAGATCTAATGCT[A/G]TATATATATATAATC | 84333 |
| rs192946889 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238173 | ACTTAAACTAGCCAC[A/G]TTTCAAATGCTTAGT | 84333 |
| rs192950658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175454 | TGACATTTGAGGTCC[A/G]ACAATGAAAAAAATG | 84333 |
| rs192959705 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165806 | TGTATGTCATATTTA[A/G]TAATATCCCTTTAGA | 84333 |
| rs192967885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196783 | CTTGTCTATACTTGT[C/T]GAATACCTGGTTATC | 84333 |
| rs193008585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262768 | TAACTATAAAGCCCA[A/G]TGTACTTGGTAAAAA | 84333 |
| rs193062960 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233341 | CCCAGACCATGCTTA[A/G]ACCCCCAGACTCTTT | 84333 |
| rs193063110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257814 | AGGAGGGACTACTGT[A/T]TAAAAGAATTGAAAA | 84333 |
| rs193088555 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91162697 | CGTGCCCGGCAGGAC[A/G]CTCCGGGAGCTGCGC | 84333 |
| rs193111647 | snp | G/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281556 | ATAGGCTCTTGTAAG[G/T]TAATTTTTTTGGAAG | 84333 |
| rs193112386 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258572 | GACTTAACTGGGGCT[C/T]GTAAAAATGTGCTAA | 84333 |
| rs193128453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192783 | GAAATCAAAAGTGGG[C/T]AGGAAGAAGGGAGCT | 84333 |
| rs193185204 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181045 | GGTTTGTTGTTCTCC[C/T]TGTAGAGATCTTTCA | 84333 |
| rs193194354 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218549 | AAAGTCCCATGTTTT[A/G]ATACTTACAATCTGC | 84333 |
| rs193205144 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279077 | TAAAAGTAATGTGTA[A/G]GTAAGGTTAATCTTC | 84333 |
| rs193287891 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275126 | TAAAATATATTTGCA[A/G]TGTATGATAGAAAAA | 84333 |
| rs199500308 | snp | C/T | 3.30644e-05 | 0.00406585 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271741 | ACCATCATGACACCA[C/T]GGCGGTGAGCACATT | 84333 |
| rs199568971 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228383 | TGATTCTTTCCTCAG[-/A]AAAAAAAAAGGATGT | 84333 |
| rs199729122 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206238 | TGAACAGCAGAACTC[A/G]GAGAAAAAGCAGGTT | 84333 |
| rs199846314 | in-del | -/AGAT | 0.0134861 | 0.0810011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169308 | ATATAAAGAAATAAA[-/AGAT]AGCCTGGTTGGAAAG | 84333 |
| rs199879268 | in-del | -/T | 0.103153 | 0.202327 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213640 | AGGCTTTTTTTTTTC[-/T]TTTTTTTTTTCTTTT | 84333 |
| rs200019800 | in-del | -/ATATATATATAATCTA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271105 | TAGATCTAATGCTAT[-/ATATATATATAATCTA]ATATATATATAATCT | 84333 |
| rs200032804 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182305 | GGTGTATGGGTCCAG[A/G]AATTTATCAATTTCT | 84333 |
| rs200063194 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209476 | AAAAAGAAAAAGGAG[G/T]CCGGGCGCGGTGGCT | 84333 |
| rs200063700 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186580 | TGTGTGTATATATAT[A/G]TGTGTGTATATATAT | 84333 |
| rs200094286 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246973 | GATAGATGGATAGAT[A/G]GATAGATAGATAGAT | 84333 |
| rs200105407 | in-del | -/TCTC | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254174 | TATGTATGTGTTCGT[-/TCTC]TCTCTCTGTCTCTTC | 84333 |
| rs200124179 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183287 | TGGGTATATATATAT[-/AT]TTAGAATAGTTAGAT | 84333 |
| rs200127654 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244645 | ACAGTTAGAAAGTAA[-/T]TGCAATGACCCTGGT | 84333 |
| rs200207751 | in-del | -/TAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275146 | TGATAGAAAAAGGTT[-/TAA]TGTTATTAATACATA | 84333 |
| rs200220048 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197704 | CCTCTGTCAACCGGT[-/A]CTGGACATCATCCTC | 84333 |
| rs200285344 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173595 | TTTTTTTTTTTTTTT[C/T]CCCACAGAAGCCATG | 84333 |
| rs200308190 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264543 | GCTTTTATATTTACC[C/T]ATGTGTTTATTTAGT | 84333 |
| rs200357985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248646 | GACTTTTACTTTTAT[A/T]CTCTTTCTTTTAAAT | 84333 |
| rs200360234 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262281 | AAATATAAAAATTAG[A/C]CGGGTGTGGTGGCAG | 84333 |
| rs200364547 | in-del | -/T/TTA/TTT | 0.233746 | 0.253805 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236099 | AGAAATAATAATAAA[-/T/TTA/TTT]TTAAAAAAATATGAT | 84333 |
| rs200419072 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191450 | ACAATTTAAAACTTA[C/T]GAATTGTTTATTTCT | 84333 |
| rs200474008 | in-del | -/GAG | 0.0146672 | 0.084371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239506 | GATAGTGTTGATCTT[-/GAG]GAGAAAGAAGTAGCT | 84333 |
| rs200475271 | snp | A/G | 0.000685986 | 0.0185074 | missense | PCGF5 | GRCh38.p7 | 10:91261332 | TTCCTTTAGGGTTTA[A/G]TGAAGAAATTCATTC | 84333 |
| rs200495344 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209445 | AGGCTTTGTCTTTAC[-/A]AAAAAAAATTAGATT | 84333 |
| rs200503086 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246957 | GGCAGATAGATAGAT[A/G]GATAGATGGATAGAT | 84333 |
| rs200536765 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209804 | AAAAAAAGAAAAACG[A/G]AGAAAGGAATTGGAG | 84333 |
| rs200541835 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230810 | GTATTTTGTGTAGAG[A/G]CGGGGTTTGGCCATG | 84333 |
| rs200562325 | in-del | -/AGAA | 0.00755907 | 0.0610114 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229356 | CTATGAGTTAAAAAC[-/AGAA]AGGTCTTTCTTGGAA | 84333 |
| rs200571872 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166544 | TTTTTATGCCTCCAG[-/T]TTTTTTTTTAAAGTC | 84333 |
| rs200575636 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268088 | TCACCATGTCTGTGC[A/G]TATGTGTGTATATGT | 84333 |
| rs200599159 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206276 | AGGAGAATGGAAAGG[-/T]AGGTACAGATGTAAC | 84333 |
| rs200646588 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275449 | ACTACATTTTATTTT[-/A]TTTTTTTTTTGAGAT | 84333 |
| rs200707971 | in-del | -/AGAT | 0.0221141 | 0.102801 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246945 | GATATATAGTCAGGC[-/AGAT]AGATAGATGGATAGA | 84333 |
| rs200723061 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213750 | TCGGCCTCCCAAAGT[A/G]CTGGGATTACAGGCG | 84333 |
| rs200756374 | in-del | -/A | 0.081446 | 0.184634 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213464 | TTATTTTATTTCATT[-/A]AAAAAAAATTTTTTT | 84333 |
| rs200792982 | snp | C/G/T | 3.30449e-05 | 0.00406467 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248592 | GTTCTTGCAGACTTT[C/G/T]GTGTTTTATGAAATC | 84333 |
| rs200887569 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183426 | CTGCTTTTTTTTTTT[-/T]CCTCCATCCTTTTAT | 84333 |
| rs200889008 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256706 | TATAAAAGTGACTCA[C/T]GCACAAAGGACCCCC | 84333 |
| rs200984387 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257493 | TGTTCCAAGACCCCC[-/A]GGGGATGTTGCAACC | 84333 |
| rs201038324 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271121 | TATATATATAATCTA[-/AT]ATATATATATAATCA | 84333 |
| rs201041533 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180773 | TAGTATAGTTTGAAG[A/T]TGGGTAGCATGATGC | 84333 |
| rs201051260 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269002 | GTGGGAGGAAAAAGG[-/A]AAAAAAAAACATGCT | 84333 |
| rs201065071 | in-del | -/TATATATATATATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249372 | AAAAGGCTTTTAGTG[-/TATATATATATATA]TATATATATATATAT | 84333 |
| rs201075264 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195481 | GCATGCATATATATA[G/T]ATATAGAGAGAGAGA | 84333 |
| rs201127184 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174742 | GAAAAATTATGGCTG[G/T]TAAAAGAAATTGATA | 84333 |
| rs201280663 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213472 | ATTTCATTAAAAAAA[A/T]TTTTTTTTTAAGATG | 84333 |
| rs201286198 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197705 | CTCTGTCAACCGGTA[A/C]TGGACATCATCCTCT | 84333 |
| rs201328713 | in-del | -/TTGAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180767 | GCCCTGTAGTATAGT[-/TTGAAG]TTGGGTAGCATGATG | 84333 |
| rs201406347 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232776 | TTTCAGTAAAATAGA[C/T]GTCCTCAGTGGAGAG | 84333 |
| rs201495363 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271105 | ATAGATCTAATGCTA[-/T]ATATATATATAATCT | 84333 |
| rs201519533 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205726 | GCTCACCCCTGTAAT[C/T]CCAGCACTTTGGGAG | 84333 |
| rs201522911 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195635 | GAGATGAGGTTCTCA[C/G]TGTGTTACCCAGGCT | 84333 |
| rs201559478 | in-del | -/T | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254523 | GGCACTGATACTATC[-/T]TTTTTTTTATATGTG | 84333 |
| rs201580698 | snp | A/G/T | 2.92907e-05 | 0.00382681 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261468 | ATTTTGATAATTCTG[A/G/T]TTTGAAGTAAAATTC | 84333 |
| rs201651893 | in-del | -/A | 0.0260927 | 0.1112 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197017 | TTAAACAACAACAAC[-/A]AAAAAAAACATGATG | 84333 |
| rs201669512 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182298 | TTCGGAGGGTGTATG[G/T]GTCCAGGAATTTATC | 84333 |
| rs201670497 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209803 | AAAAAAAAGAAAAAC[A/G]AAGAAAGGAATTGGA | 84333 |
| rs201674112 | snp | C/T | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284727 | TGATGCCTGAAGCTT[C/T]GTCTTAATGTTAGTG | 84333 |
| rs201770246 | in-del | -/CTT | 0.133435 | 0.221162 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176891 | TTGATCGTCTGAAGC[-/CTT]CTTCTCTCAACTCAT | 84333 |
| rs201814529 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174204 | TTGCATTAAAAAAAA[-/A]GTCTGTATTTTTAGG | 84333 |
| rs201888183 | in-del | -/AGGA | 0.0170251 | 0.090679 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167995 | GGCAAGGATTGAAAT[-/AGGA]AGGGACACTAGTAAA | 84333 |
| rs201892816 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209475 | TAAAAAGAAAAAGGA[A/G]GCCGGGCGCGGTGGC | 84333 |
| rs201966632 | in-del | -/AG | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193489 | GAATGTGTTCTAGAC[-/AG]AGAGAACAGTGACAG | 84333 |
| rs201971171 | in-del | -/TTG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180767 | GCCCTGTAGTATAGT[-/TTG]AAGTTGGGTAGCATG | 84333 |
| rs201996434 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249791 | TAACAACAACAACAA[-/C]AAAAATGGCAAAGAA | 84333 |
| rs202010725 | snp | C/T | 4.98732e-05 | 0.00499341 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251464 | ACAAGTACTATGGTA[C/T]TTTTATGATCAGTTT | 84333 |
| rs202091272 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186572 | TATGTGTGTGTGTGT[A/G]TATATATGTGTGTGT | 84333 |
| rs202146987 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275459 | ATTTTTTTTTTTTTT[-/T]GAGATGGAATCTTGC | 84333 |
| rs202241348 | snp | G/T | 0.0991586 | 0.199366 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195489 | ATATATATATATAGA[G/T]AGAGAGAGAGAGAGA | 84333 |
| rs207471260 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202990 | AGCAAATTTTCTGAT[A/G]CAGAATACAGGCCAA | 84333 |
| rs207471261 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276710 | TCCCTAGTAGAATTA[A/G]TGGATACTTCCATAT | 84333 |
| rs367590859 | snp | C/T | 0.000165939 | 0.00910726 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240440 | TTAACATTAAATGAG[C/T]GTTCATATGATGCGT | 84333 |
| rs367608907 | snp | C/T | 3.30169e-05 | 0.00406293 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91278307 | TCGACCAAGAATTGA[C/T]TTCGGTTAGACCAAG | 84333 |
| rs367708950 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223789 | TGGGAGCATTTTGGA[G/T]TAGATGTAGGGGGAG | 84333 |
| rs367724730 | snp | G/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220758 | CCAGGCCGCGGCGGG[G/T]GCTGTTTCTGTTTCA | 84333 |
| rs367767720 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250490 | TCCTGTATTTGTCTG[G/T]TTTTTTCTTTTTTTT | 84333 |
| rs367796895 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177625 | CGCCCGTCCCCCAGC[C/T]TCACTGCTGCCTTGC | 84333 |
| rs367823899 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266194 | TCTTTGATAGTTTAG[C/T]GGGCATTGCAGTGTG | 84333 |
| rs367889733 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247724 | TCAGAAGGTAGAACA[A/G]TAAAGTGGTCTAAAT | 84333 |
| rs367901714 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187112 | GAGAAGCTTCAGGCT[A/G]GTAGTTCTCAACCCT | 84333 |
| rs367997859 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190491 | AAAACATGAGATTTG[C/G]TCTAAATTATTACCA | 84333 |
| rs368015202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187685 | ATATACACAACTTCA[A/G]TGCTTCATGTTTTCT | 84333 |
| rs368053128 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170159 | AGACCTGAATGTAAA[A/G]CTGTAAAACTCCTAG | 84333 |
| rs368074326 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273005 | GAAAATGTTTAATTA[A/G]CAGTTTATCTAGAAT | 84333 |
| rs368082487 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252329 | AATTTTTTACTAATA[C/T]GTTTAATGGCATTTT | 84333 |
| rs368101842 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175623 | GACATTGGAAGAAGG[C/G]CTTCAATAAAAAAGG | 84333 |
| rs368113087 | snp | C/T | 4.97434e-05 | 0.00498691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248642 | TCATGACTTTTACTT[C/T]TATACTCTTTCTTTT | 84333 |
| rs368121556 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260331 | GCTGGAGAGGATGTG[A/G]AGAAATAGGAACACT | 84333 |
| rs368126194 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267583 | ATAATTTTTATTTAT[A/C]TGAATCTCAGCTTCC | 84333 |
| rs368134239 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281007 | TTATCTCTTTTATCT[A/G]CCTTAGAAATTATAA | 84333 |
| rs368167985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210504 | GTCAAACTGGATAAC[C/T]GGCTTAGCTTGGTAA | 84333 |
| rs368208012 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259620 | CTGGTACCAAAACAG[A/G]GATATAGACCAATGG | 84333 |
| rs368236296 | snp | C/T | 3.31702e-05 | 0.00407235 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248762 | TCTGACAGCACCTCT[C/T]AAACTGGTCAGCTTT | 84333 |
| rs368386528 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270201 | TTCTTGGGTAGTTCT[C/T]AGTACAGCCCCCTTT | 84333 |
| rs368387825 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250489 | ATCCTGTATTTGTCT[C/G]GTTTTTTCTTTTTTT | 84333 |
| rs368388225 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189203 | TGGCAAAATCTTCTT[G/T]TACAACCCTGATTGA | 84333 |
| rs368440015 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172041 | TTAAAATCCTTTAAA[C/T]ATTTTTAGATATATG | 84333 |
| rs368472677 | multinucleotide-polymorphism | CT/GG | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186689 | CACCAGTTCCATCCC[CT/GG]GCCTCCCTAGATTCA | 84333 |
| rs368473545 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181393 | ACTTTGAATACTATG[-/T]TGAATAGGAGTAGCC | 84333 |
| rs368526989 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249851 | CTTGTTTTACCCACG[C/T]GTACACTGCAATTAA | 84333 |
| rs368597926 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194933 | GTAGGGCAATAAAGA[C/T]GAGATGCAGACCATG | 84333 |
| rs368638959 | snp | C/T | 6.70803e-05 | 0.005791 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222860 | ACTAAAGCCAGTCTT[C/T]ACTAGCCACGAATGG | 84333 |
| rs368780520 | in-del | -/C | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187857 | TTTTCTATACAGTTA[-/C]TTGTCCTAAAAACTA | 84333 |
| rs368824122 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250766 | CATGTTATGTATTAA[C/T]AGCTATATACATGTT | 84333 |
| rs368888264 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184187 | TTCTCCTCATCTCTT[G/T]CAGGTATACCAGTCA | 84333 |
| rs369012074 | snp | C/T | 1.65078e-05 | 0.00287291 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91248551 | AAGCTGGTCCCTGGA[C/T]TACGAGAACGTAAGT | 84333 |
| rs369073230 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280885 | TTTAAATAACCTATA[A/G]GAATCATCTGAATCT | 84333 |
| rs369091613 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179232 | TCTCTTTTAAGTCAG[A/G]GGAATAGGAGGAAAG | 84333 |
| rs369093946 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264060 | AGGAGCTGAGAGGAA[C/G]TGTGAGGTTTCTGCA | 84333 |
| rs369118285 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216535 | AGAGAGCAGCATGAC[C/G]CTCATTTATATAGTT | 84333 |
| rs369150715 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262293 | TAGCCGGGTGTGGTG[G/T]CAGGTGCCTGTATTC | 84333 |
| rs369165531 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205681 | TTGACAGTATATTTA[C/G]AGTTAATAAAACTGA | 84333 |
| rs369166471 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165972 | CTTTCCATAATAGTA[A/G]CTGTGATCACTTGCA | 84333 |
| rs369207455 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278751 | AACTAATAATTATAT[C/G]TTGAAATTATTTTGT | 84333 |
| rs369226871 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175901 | AATTGGAGCATTTAG[C/T]CCATTTACATTTAAG | 84333 |
| rs369241567 | snp | C/T | 0.000155988 | 0.00883005 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261295 | TTTTAACTGGTAGAA[C/T]ATTTTAACTGGTAAT | 84333 |
| rs369260763 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247892 | TATTATTCCTCCTGG[C/T]TCCCTGAGTTAGCTG | 84333 |
| rs369277926 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224745 | CAAATCAGTTAGAAG[C/G]CTATTACTGTAGGAA | 84333 |
| rs369297205 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248872 | TACGAACCTTTTTCT[C/T]TATATGAGATTTTAT | 84333 |
| rs369304048 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236347 | GAGTCCTGAGGCCAA[A/G]CCTGATATTTGGTTA | 84333 |
| rs369380650 | in-del | -/CAGGTACCTGGATG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185932 | GCAGGTACCTGGATG[-/CAGGTACCTGGATG]TTTCAATTGAAAGTG | 84333 |
| rs369459925 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215837 | AACACTTTATTAATA[A/C]ATTTTGATATATTGC | 84333 |
| rs369466241 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246422 | GAATAAGCCAGTTGG[C/T]TAGAGAAGGGAGACA | 84333 |
| rs369480937 | in-del | -/CT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251796 | CCTTTTATTCATTCT[-/CT]TCTAATTTTATCCTT | 84333 |
| rs369517477 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187207 | GATTCGGATTTAATT[A/G]TTCTAGGATGGGGCC | 84333 |
| rs369517487 | in-del | -/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279194 | TTTAATGAGTGCATT[-/T]ATTTCTCTTTTTAAG | 84333 |
| rs369545460 | snp | A/T | 0.000601293 | 0.0173287 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251491 | GTTTATAGTAAACCC[A/T]TGATAATTTGTTGAC | 84333 |
| rs369577544 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193537 | GGTACACCTGCGTGT[C/T]TGAGGGGTGGCGAGG | 84333 |
| rs369730900 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264846 | TATATGGAATGGGAG[A/T]GGGGGAAACTTAAGT | 84333 |
| rs369738642 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208658 | GAACTCTGGTAGGCA[C/T]AGGGGAGAGAGGATG | 84333 |
| rs369751375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167981 | CTTAAGTTGATGTTG[A/G]CAAGGATTGAAATAG | 84333 |
| rs369840094 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210876 | GAGCAAGTTTCACCT[A/G]TTCTCTCATTTAAAT | 84333 |
| rs369899767 | snp | A/G | 0.000153988 | 0.00877328 | missense | PCGF5 | GRCh38.p7 | 10:91251325 | ACAAACCGAAAGTAG[A/G]TGAAGAAGGTGATGA | 84333 |
| rs369901642 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238325 | CTCTTTAATGTATGC[A/G]CCTTTGGATGCTTGA | 84333 |
| rs369990161 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277959 | CAGGGTGTGTGACTT[C/T]CAGTCCTTCCCAGTT | 84333 |
| rs370010935 | in-del | -/TCTCTC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195487 | ctcTCTCTCTCTCTC[-/TCTCTC]TATANtatatatata | 84333 |
| rs370015618 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244397 | GCAAGGAGACCTGGG[C/T]GGCTGGGGAACAGTG | 84333 |
| rs370101427 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169682 | ATAGGTAGGAAGACT[C/T]AATATTGTCAGGACT | 84333 |
| rs370117189 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254740 | AAGAGTGGGATGTCA[A/G]TAAAAAGAGTAGAGT | 84333 |
| rs370118186 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204479 | TGATGACCAGGCCAG[A/G]TCTATTTTATTTACT | 84333 |
| rs370124703 | in-del | -/TCT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267252 | GCTTCTACCTCACCT[-/TCT]CAGTGAGGCCTCTGA | 84333 |
| rs370142979 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251575 | AAATAAAATGCCATT[C/G]TTTGACAATCCTATG | 84333 |
| rs370183711 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209794 | AAAAAAAAAAAAAAA[A/T]AGAAAAACGAAGAAA | 84333 |
| rs370230688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243790 | TAAAGATATTTTAAT[A/G]TATAGCAAAACATTA | 84333 |
| rs370236862 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259664 | CCTCAGAAATAATGC[C/T]GCATATCTACAACTA | 84333 |
| rs370238940 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280644 | GTGATATGGTATTAC[C/T]ACTAGAATCACAGAT | 84333 |
| rs370351436 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179885 | TGGGATTGCTGGGTC[A/G]AATGGTATTTCTATC | 84333 |
| rs370354499 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182057 | TTATCAATTTTTTCT[A/G]GATTTTCTAGTTTAT | 84333 |
| rs370382154 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193210 | GAAACTGAATCCAGC[C/G]AAAGACCCAAAGGAG | 84333 |
| rs370410442 | in-del | -/AAGG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167998 | AAGGATTGAAATAGG[-/AAGG]GACACTAGTAAAGCA | 84333 |
| rs370420209 | snp | C/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209069 | ATTTGTAGTTTGTTA[C/G/T]TGTTACATTCAATTC | 84333 |
| rs370421566 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228868 | TTCACTGTAGACTTA[C/G]TGAATCAGAATCTCT | 84333 |
| rs370425550 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91221846 | AGAATGAACGTAACT[A/G]TAAATCAAAATAAAA | 84333 |
| rs370486467 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212791 | TCTTTAATCTTAAGA[-/T]TTTTTTCTTAGCTGG | 84333 |
| rs370531049 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198225 | TACAGTGGCCCAGAA[C/G]AGCCTGCGAGACCCA | 84333 |
| rs370533943 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260657 | GTGTTCGTGTCCTTT[A/G]TAGGGACATGGATGA | 84333 |
| rs370555635 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243155 | TGGTGATGGTGATAG[A/T]TGAGCGGACCTCAGA | 84333 |
| rs370574662 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188952 | TTTGGGAGAAAGGGA[A/G]AGTAGATAGCACAAG | 84333 |
| rs370611137 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199072 | GGTTTGTATCTGTCT[C/G]TCCCATTTTATTAAA | 84333 |
| rs370620079 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191420 | TGAGATATCATCACA[C/T]TACTCAGATGGCACA | 84333 |
| rs370655804 | snp | C/T | 0.000137819 | 0.00830003 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261463 | TGATCATTTTGATAA[C/T]TCTGATTTGAAGTAA | 84333 |
| rs370686993 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236759 | TTTTACTTTTTCCAG[G/T]TTCACCGAGCTTCAA | 84333 |
| rs370745652 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230650 | TCACTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 84333 |
| rs370749383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170181 | AACTCCTAGAAGATA[A/G]CATAGGAGAAAATCT | 84333 |
| rs370759691 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283249 | AAAATTAAAATGCTC[A/G]AGCACTTCCTTTCAG | 84333 |
| rs370806479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202137 | TATTGTGAGAAATAA[A/G]TAAGTTTTTATATGT | 84333 |
| rs370822277 | snp | A/G | 6.73786e-05 | 0.00580386 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271595 | TTTAAATATGTGTCC[A/G]GTTGTGGATGCCTCT | 84333 |
| rs370832412 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246793 | TTTAGTTTAAAAAAA[A/G]CGAGACAATGACTGG | 84333 |
| rs370867539 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193902 | GATCAGATTCTAGAT[A/T]TGTGTTAAAGACGAA | 84333 |
| rs370948118 | snp | A/C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228492 | TCCCTAACCTAAGAA[A/C/T]AAATTATTTGCAAAA | 84333 |
| rs370985132 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169743 | GTCAATCAAAATCCC[A/G]GCAAGTTATTTTGTA | 84333 |
| rs370986976 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203923 | CCACATTTCTGAAAT[A/G]AGCGTTATGTCAGTG | 84333 |
| rs371026791 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187838 | TTAGAAAAAACTTAG[A/G]GTATTTTCTATACAG | 84333 |
| rs371042281 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234563 | CACATTTCAAGTTCC[A/T]TCGGCATGATATCTG | 84333 |
| rs371047268 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267104 | ATACTCTGTCTCCTC[A/G]TTTATTCTGTCTCCC | 84333 |
| rs371066450 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247592 | GAGATGAGGCAGGAA[A/G]GGGGTGTTGTGGGGG | 84333 |
| rs371107264 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183963 | TTCCCTTTGAAAGTG[A/C]CCTGGCCTTTCTTTC | 84333 |
| rs371108937 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259657 | ACAGAGCCCTCAGAA[A/G]TAATGCCGCATATCT | 84333 |
| rs371154302 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91163687 | TTATATAAGATGTCA[C/G]GGAGAGGAAAGGGGC | 84333 |
| rs371161307 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209797 | AAAAAAAAAAAAAGA[-/TT]AAAACGAAGAAAGGA | 84333 |
| rs371164236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202613 | ATATAATATACAGCC[A/G]GAAGTTGTTACTATA | 84333 |
| rs371164883 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214361 | AATGTCATGCGAAGA[C/T]AGATGCACAGAGAGA | 84333 |
| rs371214434 | in-del | -/AC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205291 | TTTCTAAATGACTGG[-/AC]ACACACACACACACA | 84333 |
| rs371251001 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272713 | AGGAAATGGAGGTTG[C/T]AGTGAACTGAGATTG | 84333 |
| rs371321435 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246981 | GATAGATAGATAGAT[A/G]GATAGATAGATAGAT | 84333 |
| rs371323568 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195804 | AGTAGCAGAGCCTAG[A/G]CAGGGGCTTAGGGGC | 84333 |
| rs371337282 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255854 | GATCCCATGTCCCTT[A/G]TATAAAATGGTGTAG | 84333 |
| rs371340689 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191400 | CACCACAGAGAGGGA[A/C]CACATGAGATATCAT | 84333 |
| rs371342848 | snp | A/G | | | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162285 | GCATCAGGGCGGCAA[A/G]GTCACTTCTGGTGGG | 84333 |
| rs371395223 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245028 | TCTTTCAAACTGTAA[A/G]CAGGATGAGATCACT | 84333 |
| rs371417553 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268752 | CACCATACATACTCT[A/G]TGCCACTGCTCTCCT | 84333 |
| rs371420601 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184306 | TGTCTTATTTCAGAA[A/T]CACAGTCTTTAAGCT | 84333 |
| rs371495747 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175907 | AGCATTTAGCCCATT[G/T]ACATTTAAGGTTAAT | 84333 |
| rs371501310 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91218068 | CTGGGATTACAGGCG[C/T]GAGCCACCGTGCGCA | 84333 |
| rs371532480 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279300 | AACATTAGCTATTTT[A/G]TGGATTTCAAAAGTC | 84333 |
| rs371543858 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234583 | CATGATATCTGTTAT[C/T]TATGATTAGTGCATC | 84333 |
| rs371580963 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226289 | CAAGTTAAGAAATGT[-/A]AAAAAAAAAAAAAAA | 84333 |
| rs371600976 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266360 | CCATTATTTTAATGT[C/T]AAAGTATGAAAGAGC | 84333 |
| rs371607692 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280591 | AAAGGCATCAGTTGT[C/T]GTTTGGAGAAAGGTA | 84333 |
| rs371615550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229804 | TAAAAAACATGTTTT[A/G]GAATAAAAAAGGCCA | 84333 |
| rs371629038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237564 | CCTGGCTAACATGGC[A/G]AAACCCCGTCTCTAC | 84333 |
| rs371629301 | snp | C/T | 1.65844e-05 | 0.00287957 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248653 | ACTTTTATACTCTTT[C/T]TTTTAAATTAGAAGA | 84333 |
| rs371637065 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188654 | TGGATTCTCATTCAC[A/G]TTCATTTCCTCACTG | 84333 |
| rs371655114 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172194 | CTTTGGGAGGAGGAG[A/G]TGGGCAGATCACTTG | 84333 |
| rs371682306 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277129 | GGAGAGCAAGACCTA[C/G]GGCATTTGTATTCCT | 84333 |
| rs371743887 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248448 | CATCTCAGACTATTT[A/G]CATGTCAGATCTTGG | 84333 |
| rs371773697 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262282 | AATATAAAAATTAGC[C/T]GGGTGTGGTGGCAGG | 84333 |
| rs371779774 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268276 | TAAATTTGGATGAAG[C/T]TTAAACATGTTTTAT | 84333 |
| rs371780716 | snp | G/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218372 | AGGCCTTTGTTTACT[G/T]GAGGGTCCCACTGGT | 84333 |
| rs371833280 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277579 | CAGATATATGATACC[G/T]TTTCTACATAGTGAC | 84333 |
| rs371896515 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200046 | TCCTACCCAAAGGAC[A/G]GGGAAATTGGGTTAC | 84333 |
| rs372101494 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91218076 | ACAGGCGTGAGCCAC[C/T]GTGCGCAGCCCTAAT | 84333 |
| rs372276157 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213551 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 84333 |
| rs372282252 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196005 | CTACTAGATAAAATT[A/G]GGGTGGGTGGTATTC | 84333 |
| rs372354206 | in-del | -/ACCTGCACCCACTG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177918 | GCACTGCACCCACTG[-/ACCTGCACCCACTG]TCCAACAATCCCCAG | 84333 |
| rs372409169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210775 | TAAAAATAATCACTG[A/G]AAATCAGAAATGTTT | 84333 |
| rs372484596 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235574 | CCGGGCATGGTGGCC[A/G]ATATGGTTTGGCTGT | 84333 |
| rs372557091 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161432 | AGGGTCAGGGTCTAC[C/T]TCAGTGTGTGATCAG | 84333 |
| rs372558761 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266566 | CCAATAAACAGAAAA[-/A]TTACTACCTTTTACA | 84333 |
| rs372569296 | snp | A/G | 1.64836e-05 | 0.0028708 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91240520 | AGCACTTTGAAGATA[A/G]CAATGATTGCCCAAG | 84333 |
| rs372635304 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171370 | TAAAGTGTAAAGCTG[A/G]AGTGGAGGAGAGTTG | 84333 |
| rs372661166 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184031 | GATAATCTGATGATT[A/T]TGTGTCTTGGGGATG | 84333 |
| rs372672254 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186829 | GTTTCTGGGGGATTG[C/T]TTTACATTTATATAC | 84333 |
| rs372684384 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281321 | CCACATTTTATAAAC[A/G]TAATGACTTTGCTCA | 84333 |
| rs372695479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176050 | GCAGTGGCTGGTACC[A/G]GTTGTTCCTTTCCAT | 84333 |
| rs372696858 | snp | A/G | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222927 | CTTACATTACCTGCT[A/G]TATCTGTAAAGGGTA | 84333 |
| rs372716286 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266766 | ATGTCAGCACTGATT[C/G]CTGCCTTTTTCTTTC | 84333 |
| rs372777415 | snp | A/G | 1.65094e-05 | 0.00287305 | missense | PCGF5 | GRCh38.p7 | 10:91248558 | TCCCTGGACTACGAG[A/G]ACGTAAGTGGCTCTT | 84333 |
| rs372781593 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211378 | GAGTGTTTCTCCATG[A/G]CAGTGTGCTGTGTTA | 84333 |
| rs372855937 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201806 | TCTTAACAAGGCTGA[A/T]TGAAAACCTTTTAAT | 84333 |
| rs372881794 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258448 | ACTTACAGTTGAACC[-/C]TCCCAAATCTGAAAT | 84333 |
| rs372905464 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189391 | AAATCCCAGTTTACA[A/G]CATGGTGCCTGGTAC | 84333 |
| rs372940859 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217322 | TAGGCATGAGCCACC[A/G]CACCCAGCTGAAAAA | 84333 |
| rs372942712 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168632 | TGTCAATGAAGCTTT[C/T]TTAAAAACAAAACCG | 84333 |
| rs372967837 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280746 | ATACACTGTATTCCC[C/T]GTTAATTATCCCTTA | 84333 |
| rs373030793 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283528 | ATGGAGAGATAGTCA[A/G]CAAATTTATTTATCC | 84333 |
| rs373035452 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216754 | GGTGCAGTAAGAGAA[A/G]GACATGGTCAAGGGT | 84333 |
| rs373063285 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247287 | AAACTTAAAAAATAA[C/T]TTTTAAGTTTAAATT | 84333 |
| rs373083726 | snp | C/G | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220513 | GCGAGCAGCGCAGGC[C/G]GCAGGCGCGGCCTCC | 84333 |
| rs373128336 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253042 | ATTCTTCCTTTTTTT[C/T]CTGTGGCATTCCTGC | 84333 |
| rs373134451 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260579 | TGTCCAACAACGATA[A/G]ACTGGATTAAGAAAA | 84333 |
| rs373140970 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200884 | CCTAGAGCTTGCTGT[G/T]TAGGAGGTTGATAAC | 84333 |
| rs373155095 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242277 | AATGTCAGTAGTACT[A/G]CAGTAAGGAAACTGA | 84333 |
| rs373196380 | snp | C/G | 8.31566e-05 | 0.00644759 | missense | PCGF5 | GRCh38.p7 | 10:91251333 | AAAGTAGATGAAGAA[C/G]GTGATGAAAATGAAG | 84333 |
| rs373197080 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266935 | CCTTGTCCCACCTCT[A/G]TCTTCACCTCACACA | 84333 |
| rs373253983 | in-del | -/TTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167163 | TTGTCTAAATTAACT[-/TTT]ATGATAAGTACATTT | 84333 |
| rs373340139 | snp | C/G/T | 8.25479e-05 | 0.00642405 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248500 | CTTTCTCCCCCCTTT[C/G/T]GAAGGTTGGACAATA | 84333 |
| rs373375841 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284370 | ATTGAAATTTATTGA[C/G]TATTTGAGATCATAA | 84333 |
| rs373393846 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200956 | AAGGGGGAGGGTCAG[A/G]TGGGAGAATGGTCAG | 84333 |
| rs373435188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205984 | CTGAGATCACACCAC[C/T]GCACTCCGACCTGGG | 84333 |
| rs373473374 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248880 | TTTTTCTCTATATGA[C/G]ATTTTATATAAATGA | 84333 |
| rs373481605 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234141 | CTTTTGTGTAGACAC[C/T]CTCAAGAACTTGAAA | 84333 |
| rs373529611 | snp | C/T | 0.000387398 | 0.0139122 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264382 | AAATATGCAAAATAC[C/T]TTTGAATTCAACATT | 84333 |
| rs373534645 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249059 | CCACAGCTTGCAACT[A/C]AACAGTGAAGAGTTT | 84333 |
| rs373540014 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268446 | TGCGACTGGCATTGC[A/G]TTATATTTCTAGATT | 84333 |
| rs373541718 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260574 | CCAAATGTCCAACAA[C/T]GATAAACTGGATTAA | 84333 |
| rs373564396 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167187 | AGTACATTTTCATTA[A/T]TTTATATGCTATATG | 84333 |
| rs373568407 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199412 | TGACTTGGGCCAAGA[C/T]GGCCAGGCCTTTATA | 84333 |
| rs373576281 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178816 | GAAAATGATTTACTT[G/T]TGTCCAGAGCCATTC | 84333 |
| rs373576888 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251547 | TGCTTTCAAAGTTTT[A/C]ATTAACATAATTAAA | 84333 |
| rs373595783 | snp | A/C | 0.000134318 | 0.00819397 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264542 | TGCTTTTATATTTAC[A/C]TATGTGTTTATTTAG | 84333 |
| rs373637339 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209932 | CTCAATGAGATTGAC[-/AT]GTGGAAATTGAGATT | 84333 |
| rs373728508 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268861 | GATGCATTTTTGAAA[G/T]ATTTTTATCTTTAGG | 84333 |
| rs373746114 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233858 | TCTAAGTTGACAGAT[A/T]AAACCAACACACCTA | 84333 |
| rs373755980 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225549 | AGTCAGGTACTCCAT[C/T]GCATCTCTGAGGAGA | 84333 |
| rs373818833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244573 | CCGATATGAACATGT[C/T]GATGACTGTGTTGAG | 84333 |
| rs373860075 | snp | G/T | 0.282105 | 0.24793 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259891 | AGGCAATACCATTCA[G/T]GACATAGGCATGGGC | 84333 |
| rs373861292 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91221956 | AGGATAGGTGGCATG[C/G]AGACAGAGGAGAGAA | 84333 |
| rs373876389 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198691 | ATGGGAATCTCCCTG[A/G]CCTATTCAGTAGCAT | 84333 |
| rs373944701 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182748 | TTACATTGTATCTTT[C/G]CTTTCATTAGTTTCA | 84333 |
| rs373948677 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187570 | TGATATAGGAAAGAG[A/G]TTTGAAGTGATAAAT | 84333 |
| rs373987743 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272777 | GACTCTGTTTCAGAC[A/C]AACAAATAAATAATA | 84333 |
| rs374018525 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253602 | TAAGTTCAAAAGCTT[C/T]GCGTCATCTTTGATC | 84333 |
| rs374036974 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187242 | CATGATATATAGATA[C/T]ATAAGATAGATATAT | 84333 |
| rs374070064 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256726 | AAAGGACCCCCAGTA[C/G]GGTTAGTAGCTGATT | 84333 |
| rs374075294 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280533 | CATTTTTATTGAAAT[A/G]CAATGGAATATGTGC | 84333 |
| rs374082031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262941 | AACATTTTCTAATTT[C/T]TAGAAAGCTGTTATT | 84333 |
| rs374098752 | snp | A/C | | | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220669 | CCGCGCCCTGTCGGG[A/C]CTGAGCCGAGTGGCC | 84333 |
| rs374108811 | in-del | -/CTT | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267250 | TTGCTTCTACCTCAC[-/CTT]CTCAGTGAGGCCTCT | 84333 |
| rs374133648 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212790 | TTCTTTAATCTTAAG[A/G]TTTTTTTCTTAGCTG | 84333 |
| rs374137704 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271634 | GAGTTCATCTCCTCC[A/G]CAGTTTCGGTGTCTG | 84333 |
| rs374140554 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169453 | TAAGAGACAAGGCTA[A/G]TATATGAAAGTTCAT | 84333 |
| rs374173276 | in-del | -/AAAAG | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260171 | GAACAGACACTTCTC[-/AAAAG]AAGACATATATGCAG | 84333 |
| rs374179310 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272365 | ATATCCATTGTTGGG[C/T]CAGGCATAGTGGCTC | 84333 |
| rs374274424 | snp | A/G/T | 3.41479e-05 | 0.00413195 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222845 | CTCTTTGCCCAGACT[A/G/T]CTAAAGCCAGTCTTC | 84333 |
| rs374321708 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246989 | GATAGATAGATAGAT[A/G]GATAGATAGATAGAT | 84333 |
| rs374357986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211386 | CTCCATGACAGTGTG[C/T]TGTGTTACTCTTACT | 84333 |
| rs374370353 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190384 | TTTCCTTAGGAGTGA[G/T]GAGACTTGAGTTCTG | 84333 |
| rs374410845 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232025 | TCATTATTTAAACAA[C/T]GAAAGTTTGAAGGGA | 84333 |
| rs374435372 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253807 | TGAGGGCCATGACCA[A/G]TCTCAGGGTCAGATG | 84333 |
| rs374452653 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214546 | TATGAGAAATAGGAG[A/T]CAATTTGTCCAGGCA | 84333 |
| rs374490603 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216328 | CTTAGCAGAGGTGGG[A/G]AAGGGTGAGGGGATA | 84333 |
| rs374519943 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189023 | TGAGATAGGTGATTA[C/T]GGATTTAAAGTAAGA | 84333 |
| rs374524017 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279319 | ATTTCAAAAGTCTCA[A/G]AACAGTTGTAGATTA | 84333 |
| rs374527989 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267562 | TATGCAAAATATATC[C/T]TACAGATAATTTTTA | 84333 |
| rs374611072 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261611 | GTACTCTAATTGAAC[A/G]TATCCTGAATAAACT | 84333 |
| rs374631456 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225255 | TATATGATATATATC[A/G]TATATATGTATATAC | 84333 |
| rs374632015 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185949 | TTCAATTGAAAGTGC[C/T]GTATTTACTCGCCCC | 84333 |
| rs374662818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241361 | GTGTGAGCCACCACA[C/G]CTGGCCTAATCATAT | 84333 |
| rs374663064 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164581 | AAAGAAGACTCCTTA[A/G]GACTAGTTTTTTGAG | 84333 |
| rs374729236 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229354 | TGCTATGAGTTAAAA[A/G]CAGAAAGGTCTTTCT | 84333 |
| rs374748106 | snp | A/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182896 | GTAATTCAGGAGCAG[A/G/T]TTATTCAATTTCCAT | 84333 |
| rs374749297 | in-del | -/GT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195639 | TGAGGTTCTCACTGT[-/GT]TACCCAGGCTAGTCT | 84333 |
| rs374755655 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195700 | CTTTGGCCTCCCAGT[A/G]TTGGGATTACAGGCA | 84333 |
| rs374775203 | in-del | -/GATAGATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246966 | ATAGATGGATAGATG[-/GATAGATA]GATAGATAGATAGAT | 84333 |
| rs374791823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195134 | TGAGAAATAGTCCAT[C/T]GGGAAATTGGGAGAT | 84333 |
| rs374815810 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280960 | TTCTTAAGCAATAAA[C/T]TGAAAGACCTTTACT | 84333 |
| rs374890179 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251455 | GGTGAGTGAACAAGT[A/G]CTATGGTATTTTTAT | 84333 |
| rs374930618 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251222 | TTTGTTTTGATTATC[A/G]ATGTATGATTGCTTA | 84333 |
| rs374956066 | snp | A/G | 1.68267e-05 | 0.00290053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223024 | CCTATCAAAGTTTAT[A/G]TGTACATTTTGTTCT | 84333 |
| rs374991204 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226228 | GTGCAAAACCAGACA[C/T]AGAACCTGCCCTTCT | 84333 |
| rs375016216 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260287 | ACCAGTTAGAATGGC[C/G]ATCATTAAAAAGTCA | 84333 |
| rs375062131 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236839 | TTTTAAAAGCCATGT[A/G]GGAGATGTATCTTCT | 84333 |
| rs375085565 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197409 | AAATAAAATCTCCAC[A/G]GGCAGTGTTATCACA | 84333 |
| rs375129964 | snp | C/G/T | 6.60567e-05 | 0.00574665 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248489 | GTTAGTATTTTCTTT[C/G/T]TCCCCCCTTTCGAAG | 84333 |
| rs375207949 | snp | A/G | 1.65619e-05 | 0.00287762 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248740 | GTGACTTTTTCTTAT[A/G]TCTGTTTCTGACAGC | 84333 |
| rs375250914 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282355 | CAGGTGTGGTGGCAC[A/G]CGCCTGTAATCCCAG | 84333 |
| rs375262186 | in-del | -/CCCCC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229487 | AGAGAGGTTAAGTAA[-/CCCCC]CAGCCAGTAAGTGCT | 84333 |
| rs375287111 | snp | C/T | 1.68878e-05 | 0.00290579 | missense | PCGF5 | GRCh38.p7 | 10:91251298 | ATTATACAGATGATA[C/T]TTCAAAAGCTGACAA | 84333 |
| rs375372675 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165287 | AAGTATGTTACTATG[A/T]AACTTCTGGATGATT | 84333 |
| rs375378177 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215011 | AGAATCAATGGTTAC[A/G]GAAATATTGTAAAGG | 84333 |
| rs375384905 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246907 | TCTGTTGGAAATATG[A/G]AACTTGAAATCAGCA | 84333 |
| rs375431648 | snp | G/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282900 | ATGCAATTATCAATA[G/T]TTTGTAATATATATT | 84333 |
| rs375493108 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264400 | TGAATTCAACATTAT[A/G]TTAATAGATCTATAA | 84333 |
| rs375493332 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212948 | ACAGCATATGTGTTA[C/T]ACTATATGAAGAAAT | 84333 |
| rs375531319 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171516 | ACTTTCTCCAGCAAT[C/G]CTCAGAAAATTGGAA | 84333 |
| rs375564267 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260354 | GGAACACTTTTACAC[C/T]GTTGGTGGGACTGTA | 84333 |
| rs375567760 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264731 | TGTATTAGATTTAAA[A/G]TGAGATTAAAACCCT | 84333 |
| rs375587789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241242 | ACCACATTAATTTTG[C/T]ATTTTTAGTAGAGAC | 84333 |
| rs375692189 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263786 | AAGAGGATCCTGTAA[A/G]TATTGTGCAAATCAC | 84333 |
| rs375699378 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280594 | GGCATCAGTTGTCGT[C/T]TGGAGAAAGGTACAC | 84333 |
| rs375713292 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209793 | AAAAAAAAAAAAAAA[A/T]AAGAAAAACGAAGAA | 84333 |
| rs375740021 | snp | A/G | 0.000437904 | 0.0147905 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248439 | AAGATTATACATCTC[A/G]GACTATTTACATGTC | 84333 |
| rs375756259 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239151 | GGAGGCAGGTAAAAA[-/A]TACCACTTATCACTA | 84333 |
| rs375770054 | in-del | -/ATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260955 | CCTAAAACTTAAAGC[-/ATA]ATAATAATAATAATA | 84333 |
| rs375772913 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255924 | AAATCATCTCTAGAT[C/T]ACTTGTAATACCTAA | 84333 |
| rs375825781 | snp | C/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219476 | GTGATTTTTCACATA[C/G]TGTTCTGTTTAGTCT | 84333 |
| rs375857728 | snp | C/T | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284517 | AAATCCAAAAGAACG[C/T]TTTGAAAGTAATTAG | 84333 |
| rs375880797 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234113 | AAGATAGCAACAACA[A/G]ATGACCTTGTACCTT | 84333 |
| rs375897178 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219729 | AATGGCAATTTTTAA[A/G]CATGTCAAAGTTTGA | 84333 |
| rs375907350 | in-del | -/T | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284704 | CTAGCTCGGCCCCAT[-/T]GTGATTTTGATGCCT | 84333 |
| rs376002108 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182244 | TTTCAGAACTCGTTA[C/T]TGGTTTGTTCAGGGA | 84333 |
| rs376043720 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264830 | TGTTGGAACATTTAT[A/G]TATATGGAATGGGAG | 84333 |
| rs376056221 | in-del | -/ATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164829 | AGGAGCCACCCCATA[-/ATA]CTATTTTATTTTCTT | 84333 |
| rs376086662 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202118 | TGTACTCACCCCCTA[-/G]GATTATTGTGAGAAA | 84333 |
| rs376098418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278186 | TGTAAATTATAACTC[C/T]GAATTCTTAAAATCT | 84333 |
| rs376123459 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244371 | TGTATCTACGCCTTG[C/T]TGGACGACCAGCAAG | 84333 |
| rs376232038 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201072 | AGTTTTATAAAAGTG[A/G]GAAGAGCTGCCCACT | 84333 |
| rs376233227 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256135 | TCGCTGAGGAAGCCC[A/G]GACATTGTACTTATT | 84333 |
| rs376237880 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240297 | TGCTTTTTGTTTGTG[A/G]CAGTAGACTTTTATT | 84333 |
| rs376238542 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248898 | TTTATATAAATGAGT[A/G]TAAATCTGAAGTCAC | 84333 |
| rs376257372 | in-del | -/ATTTGAAAATTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262629 | GCTGATCCTGAGCTT[-/ATTTGAAAATTT]CTCTCAGATGACTAG | 84333 |
| rs376320858 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271188 | AGAAAATAGATGCCT[C/T]ACAGGTTGAGCGGAG | 84333 |
| rs376420853 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211494 | CATACTTGTCCCTGC[A/C]TTCAGGTCATTTACT | 84333 |
| rs376506102 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240389 | TATTCTACTTGTAGT[A/T]GGTAGTTTTAAGGTC | 84333 |
| rs376545723 | in-del | -/A | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281387 | ACTGATTATTTAAGG[-/A]AAAAAAGTGTGTTAT | 84333 |
| rs376552037 | snp | A/G | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221208 | CCTTGCCCCCGCCCC[A/G]TCATTGCAAGTTCTT | 84333 |
| rs376625259 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205327 | GCCCAGCTAACATGG[A/G]GCAAATTATCTTCCA | 84333 |
| rs376696694 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274257 | AGTCATTCTAAAGCT[C/T]ATAAGGAAATATCAG | 84333 |
| rs376720830 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226164 | AAATATAAAGATTTT[C/T]GTCTTACTATTCAAG | 84333 |
| rs376723741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200019 | AGGAACTAGTCTACA[C/T]GCTTCAGGCTATCCT | 84333 |
| rs376745036 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243161 | TGGTGATAGTTGAGC[A/G]GACCTCAGAGGCCTG | 84333 |
| rs376823345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200549 | TTGTCATTGTTGAGG[G/T]GCTGCTATAAGGGAC | 84333 |
| rs376905858 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268586 | CTCATATTGGATACC[A/G]CTCTCTGCCCCGTGG | 84333 |
| rs376913737 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226289 | TCAAGTTAAGAAATG[A/T]AAAAAAAAAAAAAAA | 84333 |
| rs376945598 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187243 | ATGATATATAGATAT[A/G]TAAGATAGATATATA | 84333 |
| rs376958554 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170664 | TTATTACTAGTGGGA[A/G]TGTCAAACAGTACAG | 84333 |
| rs377003763 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174230 | TGTATTTTTAGGCTG[A/G]GCACAGTGGCTCATG | 84333 |
| rs377017293 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181142 | TTGTGATTTGGCTCT[A/T]GGCCTGACCCTTGTT | 84333 |
| rs377033344 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254204 | CTTCCCCTCCACCTC[A/G]TGTGTGTGTGTGTGT | 84333 |
| rs377093132 | in-del | -/GAGT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171545 | AAGTAGAGATGCTGT[-/GAGT]ATCACTGAAACTGCC | 84333 |
| rs377130868 | snp | G/T | 8.23825e-05 | 0.00641751 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261460 | GCTTGATCATTTTGA[G/T]AATTCTGATTTGAAG | 84333 |
| rs377227564 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198204 | CTAAATTGAACCCAC[A/G]GTCCTTACAGTGGCC | 84333 |
| rs377291299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226165 | AATATAAAGATTTTC[A/G]TCTTACTATTCAAGT | 84333 |
| rs377347222 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274751 | GTTGCTATGTGAATA[A/T]CTGAGGTAGAGCACT | 84333 |
| rs377348422 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249812 | TGGCAAAGAAGCTAA[C/G]CCTGGCCAAAAAAAT | 84333 |
| rs377365036 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194343 | CCCATGGTGGTCAGA[A/G]GCTGAGGTGACTACG | 84333 |
| rs377401619 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259234 | TCCAGTAAAGTACTG[G/T]CACAGCCTATCAGAC | 84333 |
| rs377401878 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165394 | CTATGTTTCCACTTA[C/T]TTGGAATACTAATAT | 84333 |
| rs377405434 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251590 | CTTTGACAATCCTAT[A/G]CTTAGAAATGGTTAC | 84333 |
| rs377542124 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238732 | CTGTCTTCTACTTCA[A/G]CTTGGCATAATAAGG | 84333 |
| rs377547819 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275641 | TGTATTTTTAGTAGA[A/G]GCGGGGTTTCACCGT | 84333 |
| rs377561962 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91271656 | CGGTGTCTGAACTGC[C/T]CAGCTTCGCAAGTCT | 84333 |
| rs377591276 | snp | A/C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181676 | AAATTACACTTACTG[A/C/G]TTTGTGTATGTTGAA | 84333 |
| rs377653920 | snp | C/T | 0.000619792 | 0.0175929 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264553 | TTACCTATGTGTTTA[C/T]TTAGTTATATACCAT | 84333 |
| rs377659613 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275745 | GGCGTGAGCCACTGC[A/G]CCCAGCCAGAACTAC | 84333 |
| rs377720213 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167016 | GATTTCTAAGATCTC[A/G]TCCAGCTCTATGGTT | 84333 |
| rs386746505 | multinucleotide-polymorphism | CCA/TCG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186022 | AGTCAGCCATCTTGG[CCA/TCG]CTCCCTGCTTCAATA | 84333 |
| rs386746506 | multinucleotide-polymorphism | CT/TC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210717 | GACCACACCTGCTTT[CT/TC]GTTGTTTGGTCTCTC | 84333 |
| rs386746507 | multinucleotide-polymorphism | CCTGACCTT/TCTGACCTC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217260 | GGATGGTCTCGATCT[CCTGACCTT/TCTGACCTC]GTGACCACCCGCCTC | 84333 |
| rs386746509 | in-del | AAC/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257156 | CAAAAGGCTTGAATA[AAC/T]ATTCCTCTAAAGAAG | 84333 |
| rs386746510 | multinucleotide-polymorphism | AT/TC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265369 | AATCTGAGTGCATAA[AT/TC]AAATAAATATGAATT | 84333 |
| rs397701854 | in-del | -/A | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242425 | TATTAAAATAAAAAA[-/A]CTGTTAATAAAAACA | 84333 |
| rs397716469 | in-del | -/AC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205310 | CACACACACACACAC[-/AC]GGCCCAGCTAACATG | 84333 |
| rs397744188 | in-del | -/A | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264560 | GTGTTTATTTAGTTA[-/A]TATACCATTATGTTA | 84333 |
| rs397748736 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204342 | TTCATTTAAAAAAAA[-/A]ACCCTTACATTAGTC | 84333 |
| rs397766167 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270392 | TAGAAAAAAAAAAAA[-/A]GAATCACTTAGTGAA | 84333 |
| rs397779543 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178777 | ATAGTAAAAAAAAAA[-/A]ATGTAATGATGATGA | 84333 |
| rs397797156 | in-del | -/T | 0.375 | 0.216506 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265541 | AATTTCTTAATTTTG[-/T]TTTTTTTTATGATTT | 84333 |
| rs397797535 | in-del | -/G | 0.375 | 0.216506 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257497 | CCAAGACCCCCAGGG[-/G]ATGTTGCAACCACAG | 84333 |
| rs397799717 | in-del | -/CA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186612 | GTATATATACACACA[-/CA]TATATATGTAACAAA | 84333 |
| rs397830014 | in-del | -/A | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168958 | AAAAAAAAAAAAAAA[-/A]GAAGGCTTGATAACA | 84333 |
| rs397845872 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224499 | AGGAAAACTAATTTT[-/T]AAAAATGCCATATTA | 84333 |
| rs397846757 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275316 | AGAAATGAAAAAAAA[-/A]TACTATCTTATGCTT | 84333 |
| rs397847845 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237756 | TAAAAAAAAAAAAAA[-/A]TTGCATCAGAAAACC | 84333 |
| rs397937482 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250513 | TTTTTTTTTTTTTTT[-/T]AGCTTGCCTTTATTT | 84333 |
| rs397943001 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181434 | CCTTGTCTTGTGCCA[-/A]GTTTTCAAGGGGAAT | 84333 |
| rs397947293 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213481 | AAAAAATTTTTTTTT[-/T]AAGATGAAGTTTTGC | 84333 |
| rs398014420 | in-del | -/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214323 | TCTGTCTGTCTCTCC[-/T]TTTTTTTTTTTTTTA | 84333 |
| rs398014421 | in-del | -/A/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226314 | TTGCACTTAACAGCA[-/A/T]TTTTTTTTTTTTTTT | 84333 |
| rs398046166 | in-del | -/A | 0.5 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236108 | AATAAATTAAAAAAA[-/A]TATGATATGAATTTT | 84333 |
| rs527256385 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282072 | AAAGGCAGACTTTGG[C/T]AAAAGTGCCAACACA | 84333 |
| rs527288530 | in-del | -/TTATTTGAAAAT | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262627 | CCGCTGATCCTGAGC[-/TTATTTGAAAAT]TTCTCTCAGATGACT | 84333 |
| rs527315490 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183033 | AGAGTGTTTTACTTC[C/T]GATTATATGATCAAT | 84333 |
| rs527383456 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247004 | AGATAGATAGATAGA[C/T]AGATAGATAGATAGA | 84333 |
| rs527397067 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261552 | ATTATTTTTGTGTTA[A/G]AAATTTAATTTTCAG | 84333 |
| rs527434367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263031 | AACAAAGATGGAAGG[A/G]GGAGAGATTCAGTAC | 84333 |
| rs527445134 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272222 | TGTGTCTGAGGAAAG[C/T]TTATCTGATAAAGAT | 84333 |
| rs527450251 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171718 | GGAGGGAGGTTCTGA[A/G]GGTAGTGGTGAAGGG | 84333 |
| rs527477270 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205039 | ATTTTTTAAAATTTT[A/T]TGAGTAAACTAAGTT | 84333 |
| rs527516775 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177740 | CTGGTGCGCCATTTG[A/C]TAAGACCGTCGGAAA | 84333 |
| rs527545585 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213260 | ATCAAAAGTATGACT[A/G]ATATTTGAAGGAACA | 84333 |
| rs527558003 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278448 | ATAAGGCCATTGTCT[A/G]TCTCTAAATTGTCAG | 84333 |
| rs527601646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225578 | GATCTGAGGATTCCG[A/G]TAGCACTAATCTTTA | 84333 |
| rs527614178 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269019 | AAAAAAAACATGCTT[C/T]TTGATCTTTAATGCA | 84333 |
| rs527635395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269485 | ATAACTCCTTTTGTG[G/T]CTGTAGCATAATTTG | 84333 |
| rs527655575 | in-del | -/TA | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213355 | GTATTTGTATATACG[-/TA]TGCATAAGTAACCTC | 84333 |
| rs527657550 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169403 | ACAACAACAAAAAAA[A/C]CTCCTGGAACTAATA | 84333 |
| rs527677374 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215970 | CCCTTCAAGAAGAAA[C/T]CCAAGAAAGAATACA | 84333 |
| rs527677971 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224865 | GAAGAACCAATTGGC[A/T]ACCCTAGAGTTATAT | 84333 |
| rs527678994 | in-del | -/AGTC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213288 | ACACATCTATTTCTT[-/AGTC]TGTGCAGTCCTTAAA | 84333 |
| rs527716250 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210662 | GAAAGCAGAAAGGCT[G/T]TTTCAGTGCCTCTAG | 84333 |
| rs527723834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268589 | ATATTGGATACCACT[C/T]TCTGCCCCGTGGAGT | 84333 |
| rs527736509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232432 | ACTATGTCAAGGAGT[C/T]TTACTGCAAAAGAAA | 84333 |
| rs527763680 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284791 | CGGTGAGATAGGGAA[A/G]GCAGCTTTCCTCTGA | 84333 |
| rs527784406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181158 | GGCCTGACCCTTGTT[A/G]GTATATAGGAATTTG | 84333 |
| rs527802344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244664 | AATGACCCTGGTGAG[C/T]GGTGGTAGCAGTAGA | 84333 |
| rs527844204 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241152 | CGATCTCAGCTCACC[A/G]CAACCTCCACCTCCC | 84333 |
| rs527855679 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198891 | AGTCTTCTTCCTTTT[A/C]TTGCCAGGCCATTCT | 84333 |
| rs527890219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208751 | GCTTATTTTGCATTT[C/T]TCTTGAAATCCTGAA | 84333 |
| rs527905021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262106 | CCCCTTCTTCCCTTT[C/T]GAGTTCTGATAGTAG | 84333 |
| rs527929352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253529 | TCATTATACTTTCAT[C/T]TAACTTTGGTCCAAA | 84333 |
| rs527993713 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180964 | CATTTTCACAATATT[A/G]ATTCTTCCTATCTAT | 84333 |
| rs528027592 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265937 | ACATGTTTGTGGCTC[A/G]TATTTTTAAAGATCT | 84333 |
| rs528034972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251608 | TAGAAATGGTTACTA[G/T]TCCCACAACTGAACT | 84333 |
| rs528061668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173973 | ATTGATGATGATTTT[A/G]GGCAGCAAAGATCTT | 84333 |
| rs528063176 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167045 | TTTCAGAAACCAATA[A/G]AGAAATATACAGTTC | 84333 |
| rs528120877 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282037 | GCTCCTGTATTATTC[A/G]TAATATGAGAAATTT | 84333 |
| rs528132662 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246801 | AAAAAAAGCGAGACA[A/G]TGACTGGGCTACTTA | 84333 |
| rs528146872 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201050 | ACACCAGGGAGGTGA[C/T]GGGGAAAGTTTTATA | 84333 |
| rs528160180 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220163 | CTCCACAACGTTCCC[A/G]TTTGCTTATAGTTGT | 84333 |
| rs528169011 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273113 | TCTTTTAAGTCCTAG[A/C]TTTTCAGCAATCTAG | 84333 |
| rs528188902 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178755 | TTCATGGGTTACTTT[G/T]ATTAAAAATAGTAAA | 84333 |
| rs528205524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228135 | GGGGACTAGAAATTG[A/G]TGGCCCTAGATTAAG | 84333 |
| rs528255563 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251148 | CTGAGTTGGTTGGAA[A/C]ATTTTAAAGATACTA | 84333 |
| rs528294222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205456 | GGGTATATTCCAGCG[C/T]TCATTCATAAACTGA | 84333 |
| rs528301117 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197912 | GCCATTTAGGAAAGA[A/G]TTCTCCTGGTTCTCA | 84333 |
| rs528318216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250554 | CCTGACCACTGTGAG[A/G]GAGAGGATGATAGCT | 84333 |
| rs528379625 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257852 | ACACAAAATCTTGTA[A/T]ATGTATATTCATAAT | 84333 |
| rs528381670 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187007 | AATGGTATTACATTG[A/C]AGATTCTGGTTTAGT | 84333 |
| rs528383155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167505 | AGACGACTTCAATCG[C/G]CAAAAATGTAGGGAC | 84333 |
| rs528459578 | in-del | -/AGCC | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238188 | TTTCAAATGCTTAGT[-/AGCC]AGCCACATGTGGCTA | 84333 |
| rs528471920 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203258 | CATTTGGGAATAAGG[C/G]ACAGGATGATTGCAT | 84333 |
| rs528474412 | snp | C/G | 1.65754e-05 | 0.00287879 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248752 | TATGTCTGTTTCTGA[C/G]AGCACCTCTTAAACT | 84333 |
| rs528491373 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236243 | TGCTGCACAGCTGTG[C/T]AGCTGTGAGCAGCCT | 84333 |
| rs528536243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202557 | TGCATAGTAGTCATC[A/G]TTACTGTTAATTATT | 84333 |
| rs528544064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211260 | CACAGAAATGCATAC[C/T]TTGTTGATGTGATTA | 84333 |
| rs528700280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190845 | GTGGTAAATTTAGAA[A/G]CTATTTCACATCAGT | 84333 |
| rs528719641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235198 | AATCTCCTAGATATT[A/C]TGAATTAATTGGTCT | 84333 |
| rs528730808 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189952 | GTTTACAAATCAATA[A/C]AAGCCAGACAGAAAT | 84333 |
| rs528744003 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197206 | CAGCGTAGCCTGTCT[C/G]CATTCCGCTTGGCAT | 84333 |
| rs528766716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190126 | GCAGATTGGTCTCTG[A/G]TGAGGACCCACTTCC | 84333 |
| rs528806724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249553 | GTGTGTGTGTTCTTA[C/T]AGGGTCACTTGTAAG | 84333 |
| rs528865597 | in-del | -/TT | 0.286564 | 0.247312 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275608 | ACCATGCCCGGCTAA[-/TT]TTTTTTTTTTTTTTT | 84333 |
| rs528878620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245339 | GAGTTCATCAACTTT[A/G]AAAAGAGCACTTTCT | 84333 |
| rs528932481 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275388 | TTATTGATGAGGCTA[C/T]AGAGGAATGGGCATT | 84333 |
| rs528993306 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260245 | TCAGAGAAATGCAAA[G/T]CAAACCACAATGAGA | 84333 |
| rs529003954 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91163324 | GGAGGCACGGCGGGG[C/G]CGGGCGCCGGGCGGG | 84333 |
| rs529023676 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206108 | AATTGGCTTTTTAAT[A/C]TTTTATTTATAAAAT | 84333 |
| rs529043052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182096 | AGGTGTTTATAATAT[G/T]CGCTGATGGTTGTTT | 84333 |
| rs529066551 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277289 | ATCTATATGAAAGAA[A/T]ACAAAGTTCTCTATA | 84333 |
| rs529098975 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181280 | TGGGGTTTTCTAGAT[A/G]TAGGATCCTGTCATC | 84333 |
| rs529106482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185502 | CGTGGAAGTGAGGCC[C/T]GCTGACCATCACTGC | 84333 |
| rs529167016 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187084 | AGATGCAACTGGTCT[G/T]CAGACCACATTAGAG | 84333 |
| rs529190828 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209776 | TCGAAGAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 84333 |
| rs529194507 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284215 | CCAAGTATATTTCAC[C/T]ATGTTAAAATACAGT | 84333 |
| rs529204564 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183543 | TTCTGTGTCTTTTAA[C/T]TGGGGCATTTAGCCC | 84333 |
| rs529207571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179997 | CTTTTTTTCCACAAA[C/T]TCACCAGCACCTATT | 84333 |
| rs529217870 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282954 | GAACATGTCTGCTAG[A/G]TCTGGTTTATGAAAA | 84333 |
| rs529254287 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282242 | GTAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAG | 84333 |
| rs529330554 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237274 | TAATGCCTGGTACGT[A/G]AACCCATTAAGTGTT | 84333 |
| rs529358367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193125 | TGGCAAACGCAAGAA[A/G]GAAGGCATGTAGCCT | 84333 |
| rs529434543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191640 | TTCTTGGTGTGTGTT[A/G]TCATAAGCTTGTCCT | 84333 |
| rs529442907 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268462 | TTATATTTCTAGATT[G/T]ATTTGGCTGGAATTG | 84333 |
| rs529481786 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175664 | AACAAATGAACAACA[A/G]TAAAAAAATCACAGA | 84333 |
| rs529504828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267558 | TGGTTATGCAAAATA[C/T]ATCCTACAGATAATT | 84333 |
| rs529507648 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217146 | TCACGCCATTCTCCT[A/G]CCTCAGCCTCCTGAG | 84333 |
| rs529520436 | in-del | -/GTT | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255964 | AATGCTATGTAAGTA[-/GTT]GTTAATACTATATTA | 84333 |
| rs529522599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275524 | TGGCTCATTGCAGCC[C/T]CCGTCTCCCAGGTTC | 84333 |
| rs529545587 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214473 | AGAAGAAGGGACTAT[A/G]CTTAGCTACCTCTGG | 84333 |
| rs529547568 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250783 | GCTATATACATGTTA[A/G]AAAGCTAATTCATTA | 84333 |
| rs529613019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271540 | ACCATTAATCATGTT[A/G]ACTCTTGTGTTTGAC | 84333 |
| rs529613092 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279488 | TATTATTTTATACAT[A/G]AGTTCATTAAGATCA | 84333 |
| rs529624004 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184132 | GTTGGGTACATTCTC[A/C]TGGATGATATCCTAA | 84333 |
| rs529636515 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229212 | TGTGCCAGTCATCAT[C/T]CTAGCCACTGCAACA | 84333 |
| rs529649056 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278525 | CTACTGAACCATCTG[C/T]ATAAGGTATTTGTGT | 84333 |
| rs529652241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235110 | TACCTCCTACTCTCC[C/G]TTGGCCAATGTTTCC | 84333 |
| rs529671720 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230537 | ATACATATATGAATA[C/T]ATAATGTCAGAACCA | 84333 |
| rs529673453 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226197 | TGAAATGCATAAATG[A/C]AGCTTTATAATTGGT | 84333 |
| rs529721060 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183693 | CAGTGTGTTTCTGTA[G/T]TGGCTGGTAATAGTC | 84333 |
| rs529748350 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274276 | AGGAAATATCAGCAG[A/G]TGCTTCGATCAGTCA | 84333 |
| rs529756240 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252798 | CTTCTCATAAACAAA[C/T]GTAAAGTCCACTTCT | 84333 |
| rs529805354 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189291 | CCTGTGTTCTGTCCC[A/C]ATTTTTCCATGCCAT | 84333 |
| rs529815063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241309 | CCCGACCTCAGGTGA[C/T]CTGCCTGCCTCGGCC | 84333 |
| rs529866816 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256018 | TTGTTTTTAAAAATA[G/T]TTTTGATCTGTGATT | 84333 |
| rs529878745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172357 | CCAGGAGGCGGAGGT[C/T]GTAGTAAGCTGGGAT | 84333 |
| rs529919432 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161380 | GACTGCAAGCAGCGC[A/G]TCGGAGAAAAAAATC | 84333 |
| rs529919924 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272285 | ATAGTAAAGATTATT[G/T]TTGGGTACAGATGTG | 84333 |
| rs529940110 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171830 | GTTGAGTGACACAGG[C/G]CAATGGAGGTAGAAG | 84333 |
| rs530016467 | in-del | -/CTC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268521 | GGCACTATGGGATGT[-/CTC]CTCATCTATTCTACA | 84333 |
| rs530052045 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218379 | TGTTTACTTGAGGGT[C/G]CCACTGGTACTTGAG | 84333 |
| rs530053937 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227463 | TGCTCCATGCTTGAC[A/T]CTTTACCCTCACTAA | 84333 |
| rs530059278 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222578 | ATGTTCTATTCACCT[A/G]TTCACCCAATTGGGA | 84333 |
| rs530071537 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261623 | AACATATCCTGAATA[A/G]ACTATGATACTAATA | 84333 |
| rs530088429 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266236 | GAAATCATCGTGATG[A/G]ATAGACTTGCCTTAA | 84333 |
| rs530088829 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170740 | CTCTTACTGCACAAT[C/G]CAGCAGTTGTGTCCT | 84333 |
| rs530096485 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227602 | CCAAAGCCACTGCAG[C/G]ACATTCTTAACTGTG | 84333 |
| rs530104493 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225355 | TAAAGCCTAAAGGGG[C/T]AAATTAAATGACAGT | 84333 |
| rs530117448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269599 | ATATGCAAGCATATC[C/T]ATTGGCTAGATTCTT | 84333 |
| rs530145867 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191566 | ACTGCACTTTTTCCT[A/G]CTAACATGTAGGTAA | 84333 |
| rs530151369 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170240 | TTAGATATGACATCA[G/T]AGGCACAGCCATGAA | 84333 |
| rs530166834 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224912 | GTTTCACCAAGCATG[A/G]AACCTGGACCCAGTC | 84333 |
| rs530214236 | snp | A/G | 0.00014834 | 0.00861092 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91240535 | GCAATGATTGCCCAA[A/G]GTGTGGCAACCAAGT | 84333 |
| rs530216383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176903 | AGCCTTCTTCTCTCA[A/G]CTCATCAAAGTCTTT | 84333 |
| rs530274280 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195927 | TCATCAACTTGGTCA[C/G]TATTGTGGGCAACTG | 84333 |
| rs530275551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255128 | AAGATTGTCAGTATT[C/T]GACTTGACTTGGAGC | 84333 |
| rs530334972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254336 | CCCTTCCTTTTTGGC[A/G]TGTTCTTTCCTCTTC | 84333 |
| rs530336648 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176009 | TCTTCCTAGCCTCCA[C/T]GGTCTTTACAATTTG | 84333 |
| rs530359688 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175139 | AAAATCTGTAAGGGA[A/G]CTAGATCCTCACTTC | 84333 |
| rs530388381 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177457 | GAGACATTTAAGTCT[A/G]CAGAGGTTTCTGCTG | 84333 |
| rs530394727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258566 | TTCTCTGACTTAACT[A/G]GGGCTTGTAAAAATG | 84333 |
| rs530432078 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198831 | AGCCCTTCTTCAGAT[G/T]GGTTATTTCTACCCC | 84333 |
| rs530433983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213620 | TAGGCATGCACCACC[A/G]CACCAGGCTTTTTTT | 84333 |
| rs530470247 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208922 | TCTCCTAATCAAAAA[G/T]AAAATTCTCATTTTT | 84333 |
| rs530497065 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221892 | AAAGAAGTAAGCATT[A/C]AAAACTAGGGAAAGA | 84333 |
| rs530538610 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205150 | AATATATTTATCTCT[C/G]TCACTAGAGTCACTA | 84333 |
| rs530556061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221224 | TCATTGCAAGTTCTT[G/T]CTTCCCTTAACTGTC | 84333 |
| rs530562351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167554 | GAAGGTAAGGATATA[C/T]GAGCATGTCCAGGAT | 84333 |
| rs530566485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266739 | TTCCAGTTGCTCAGA[C/T]CAAAATCCCTGATGT | 84333 |
| rs530583315 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236638 | TAAGATATTTTTAAA[A/C]TGTGCTGTACTGCTA | 84333 |
| rs530584511 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282433 | AGGTTGCAGTGAGCC[A/G]CAATTACACCACTGC | 84333 |
| rs530610722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266019 | TAATGTTTTAAATGA[C/T]TGTACATACATCAAT | 84333 |
| rs530624386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174066 | AATGAAGATTTTTCA[A/C]TGAATCCTTCATGCC | 84333 |
| rs530693102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198701 | CCCTGGCCTATTCAG[C/T]AGCATTGAATCAATC | 84333 |
| rs530710321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237468 | CACATCAACGCTGGG[C/T]GCAGTGGCTCACGCC | 84333 |
| rs530719411 | snp | A/G | 3.52883e-05 | 0.00420035 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251267 | TTTGATTTATAGCTA[A/G]CTTAGTTTTGTTTAA | 84333 |
| rs530830765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197266 | TCATCTGAAGGCTCG[C/T]GAGCTGACTGTCATG | 84333 |
| rs530892794 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203979 | GTTTTCATAAGTGAT[G/T]GTACAACTATTTGAT | 84333 |
| rs530911253 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242394 | ACCAACTGTTAAAAT[A/C]TATAATAACTTATTT | 84333 |
| rs530914789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257037 | AAAAAGTTACAGAAC[A/G]GGAAAAAATATTTGC | 84333 |
| rs530953021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212148 | TGGAAGAGCTCATTC[C/G]ATTGTTAGTTATTAG | 84333 |
| rs530970941 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249604 | TTTCCCATAAGATCA[C/T]AGGATTGTCAATTAT | 84333 |
| rs531010369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229204 | CTTTTACATGTGCCA[A/G]TCATCATTCTAGCCA | 84333 |
| rs531095665 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273945 | AAATTCAATGTGAAG[C/T]CCTGATGTTTTCCTA | 84333 |
| rs531127968 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193333 | GCTCAGCCAAATTGT[A/T]CTTAGACTTCTAACC | 84333 |
| rs531158605 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187958 | GATTCTTTTTTTTTT[A/T]ATTTTAAACTTTTAA | 84333 |
| rs531159174 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173292 | GACAACTTTTCTCTT[C/G]TTATCCCTGTGATAG | 84333 |
| rs531164192 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178868 | ATTACTTTTGCACCA[A/C]CGTAATACATGAAGC | 84333 |
| rs531164220 | in-del | -/ATATATGCATATATATATATGCATGC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195446 | ATAAATCATATGTAT[-/ATATATGCATATATATATATGCATGC]ATATATATATATATA | 84333 |
| rs531229938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184900 | GTGGGAGTCCCATCC[C/T]AGGGAGTTATGGACC | 84333 |
| rs531256540 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235876 | AAGTCCAATAAACCT[A/C]TTTCTTTTGTGAATT | 84333 |
| rs531282368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194130 | ATCCAGTTAAAGATG[C/T]AGAGTGTGGTAGGCA | 84333 |
| rs531312628 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239801 | TGTGGCCCCAAATCC[A/T]CAAGTCATATTTCCA | 84333 |
| rs531318342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163722 | GAGAGGCGCGTTGGG[A/G]AGGGCGCGGTGGCCT | 84333 |
| rs531345242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200056 | AGGACAGGGAAATTG[A/G]GTTACTTGCCCATCA | 84333 |
| rs531353361 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194712 | GAGATGGTTTAAAGC[C/G]ACAGACTGAATGAGA | 84333 |
| rs531359274 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199405 | GTTGTCTTGACTTGG[A/G]CCAAGATGGCCAGGC | 84333 |
| rs531413230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200751 | ATCACTTTGTGGTCA[C/T]TGGACAGTGGGCAAA | 84333 |
| rs531428512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182892 | CAAAGTAATTCAGGA[A/G]CAGGTTATTCAATTT | 84333 |
| rs531435817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176938 | GTCCAGCTTTGTTCC[A/G]TTGCTGATGAGGAGC | 84333 |
| rs531439570 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245527 | CCAAGAAGGTTCTTT[A/G]TTTTGTTTTGATATA | 84333 |
| rs531470617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222143 | AAGACACTGACATTC[A/G]TTGATAAGAAGACCC | 84333 |
| rs531488571 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233838 | GAAGGAAGAAAAAAT[A/G]TGCATCTAAGTTGAC | 84333 |
| rs531491337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188281 | CGGGAAGCGCAAGGG[G/T]TCAGGGAGTTCCCTT | 84333 |
| rs531506997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270546 | AGCTGAGCCCGCCTT[A/G]CAGCATGTTGATGCA | 84333 |
| rs531516789 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267257 | TACCTCACCTTCTCA[G/T]TGAGGCCTCTGACCT | 84333 |
| rs531522202 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232641 | TATAGGGCAGAGGAT[G/T]GCTTTAGATAGGTAC | 84333 |
| rs531522672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225496 | CAAATGTGGCCTTTA[C/T]CGTCAACAGAGAACA | 84333 |
| rs531559163 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217439 | GATGTATTTATTAGG[C/G]AGGAAAGGAATGTGA | 84333 |
| rs531569487 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175854 | ACTGATGGGTCTTGA[C/T]TCTTTATCCAGTTTG | 84333 |
| rs531576713 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263911 | TGAAAATTCTCATAT[A/G]CCTTTAAGGCCCCAT | 84333 |
| rs531604185 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275553 | TCAAGTGATTCTCCT[A/G]CCTCAGCCTCCTTAG | 84333 |
| rs531654926 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240424 | TCTAATTACACTTAG[C/T]TTAACATTAAATGAG | 84333 |
| rs531671990 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230955 | GGATCTTACCATGTT[G/T]CCCAGGCTGCTCTTG | 84333 |
| rs531699537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181108 | ATTATTTTTATGGCA[A/G]TTGTGCATGGGAGTT | 84333 |
| rs531706435 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283042 | TTCTGGATTTACCTG[A/G]CAAACCTAGTTGAGT | 84333 |
| rs531712415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236986 | CTTTTTCTATATATC[A/G]TAGATCTATGTAAAT | 84333 |
| rs531712471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238082 | TTCAAAATGTAATTA[A/G]TATAAAATTATTGAG | 84333 |
| rs531729148 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231688 | TACTCTGAGAGAAAT[G/T]AAGATCCGTTTCAGG | 84333 |
| rs531735736 | snp | C/T | 0.000217535 | 0.0104269 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222862 | TAAAGCCAGTCTTCA[C/T]TAGCCACGAATGGCT | 84333 |
| rs531751026 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269954 | TCCTAGTTTTGCCTC[A/G]GTTTTTTGATTCTTT | 84333 |
| rs531825580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169202 | TAATGCCCAATTTTA[A/T]TCTTAAAAGAGAGCC | 84333 |
| rs531834932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186349 | CTAGTTGTCTATGGC[A/G]AGAATTCTTAGGTGA | 84333 |
| rs531839642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260340 | GATGTGAAGAAATAG[G/T]AACACTTTTACACCG | 84333 |
| rs531866725 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268506 | TTTTTTATTCTATTT[G/T]GCACTATGGGATGTC | 84333 |
| rs531884571 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168789 | AAAAACTAGCCGAGT[A/G]TGGTGGTGTGTGTCT | 84333 |
| rs531923793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224859 | TTGAAGGAAGAACCA[A/G]TTGGCTACCCTAGAG | 84333 |
| rs531955058 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264054 | AGCCAAAGGAGCTGA[G/T]AGGAACTGTGAGGTT | 84333 |
| rs531979463 | in-del | -/TTAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201114 | TTCATGGGAGCTGTC[-/TTAG]TTTGTTTTCTGTTGC | 84333 |
| rs532017538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215906 | GTGTGATTTTAATTA[A/G]TAATCCAAGAAGGCA | 84333 |
| rs532023872 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280440 | ATTTCACTATTTTCC[A/C]AGGAAATATATAGGA | 84333 |
| rs532080179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215083 | ACTTCCTCATCAGTA[C/G]TTGTAATAAGCATCA | 84333 |
| rs532094635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235136 | TTTCCGAGTCATCTT[C/T]TGGCTGCATCAGTGA | 84333 |
| rs532098221 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172423 | AACTCCCCTTCAGAG[A/T]AAAAAAAAATGCCCT | 84333 |
| rs532156285 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167500 | AATTGAGACGACTTC[A/T]ATCGGCAAAAATGTA | 84333 |
| rs532171489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184685 | TTCTTTCTCATCTTT[A/G]TGGGCTTATCTACCT | 84333 |
| rs532177477 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201996 | GTCCTGGACTTGGGA[C/G]CTACACTGTCCAGGA | 84333 |
| rs532272874 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188529 | AATATAATTTTGCTG[C/T]TAAGAAATTGGAATC | 84333 |
| rs532287272 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260576 | AAATGTCCAACAACG[A/G]TAAACTGGATTAAGA | 84333 |
| rs532299349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249671 | CTGTAAAATGGAGAT[C/T]ATCATTTTATTCGTT | 84333 |
| rs532310670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173060 | CATCTGTAGTGTAGG[A/G]AAAAAATTACATCTG | 84333 |
| rs532363022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257097 | AGGTATATGAAGAAC[C/T]CTTATAAATCAACAA | 84333 |
| rs532411674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212326 | AAGATACATGAAATA[C/T]TGTGTTGCATGAGGC | 84333 |
| rs532433184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209076 | GTTTGTTACTGTTAC[A/G]TTCAATTCATTTATT | 84333 |
| rs532443594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217993 | GATTTCACCATGTTG[C/G]CCAGGCTGGTCTTGA | 84333 |
| rs532476291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211526 | TCGGACCTGATCTGC[A/G]TAAATGTGAAACGTC | 84333 |
| rs532495686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217184 | GACTACAGGCACCTG[C/T]CACCACGCCCTGCTA | 84333 |
| rs532521896 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170081 | CCATATGCAAAAAAA[G/T]AAAAAAGTTAATCTA | 84333 |
| rs532521928 | in-del | -/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91162490 | GCTTCCTCCGTCTGT[-/G]GGGGGGAGAAGGTGC | 84333 |
| rs532549214 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234227 | GCATCAGAGAGGGTA[A/T]ATGCAAAGGAATTGG | 84333 |
| rs532549300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241703 | CTACTCATCTAAAGA[C/T]AGAGCTAGATAGTCT | 84333 |
| rs532634857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271353 | AGATTTTCCCAGGAA[A/G]TAGTATTTGTAAAGG | 84333 |
| rs532636739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262193 | ACTTGGGGAGGCGGA[A/G]GCTAGTGGGGTCACT | 84333 |
| rs532704873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190019 | TTTGTTTGTGCTGCT[A/G]CAACAAAGCACCACA | 84333 |
| rs532815930 | in-del | -/T | 0.00517822 | 0.0506191 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279192 | TATTTAATGAGTGCA[-/T]TTATTTCTCTTTTTA | 84333 |
| rs532828471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205610 | TCCATCAAACACCTA[C/G]AGAGTTTCTACTTTA | 84333 |
| rs532878406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202469 | CAAAGTAGTTAACAG[A/G]ATTGTTGTGAGGATT | 84333 |
| rs532889847 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213717 | TCTCAAACTCCCGAC[C/T]TCAGAGAGGTCCCCA | 84333 |
| rs532890151 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168231 | TAAAAGGCTAGGATA[C/G]AGCCTTGTAAAAGCC | 84333 |
| rs532937256 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238824 | CAAGAAATTTGGGAA[G/T]AAGGCAAAGTATTCA | 84333 |
| rs532939497 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161519 | GCTGTAAAATGACTG[G/T]GTTCATGTCTACTTT | 84333 |
| rs532969855 | snp | C/T | 3.32364e-05 | 0.00407641 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251338 | AGATGAAGAAGGTGA[C/T]GAAAATGAAGATGAT | 84333 |
| rs533008131 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206887 | TAACTAAATCCTTCT[C/G]TCACCTCCCTATTTT | 84333 |
| rs533009833 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214929 | CTTATTACAGAAAGT[C/G]TTTCCTTTTCTAGTA | 84333 |
| rs533009984 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180371 | CCCACTTGTCAACTT[C/T]TGCTTTTGTTGCAGT | 84333 |
| rs533043124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199784 | AGATAGGGAAGTGGA[A/G]TAAATAAACAAAGGA | 84333 |
| rs533080570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244798 | ATGACTTTAAGATTT[C/G]TGACCTGAGCAACTG | 84333 |
| rs533093081 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239915 | TTTGTCCCAACTTGA[C/T]ACCATTATTCATACT | 84333 |
| rs533109715 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187017 | CATTGCAGATTCTGG[A/T]TTAGTTAGTCTCAGG | 84333 |
| rs533151999 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283137 | GTTCAATAGTTTTTA[C/T]TGCAGTGATGTTTTT | 84333 |
| rs533176432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193917 | ATGTGTTAAAGACGA[A/T]GTCCATTTCTTTGTG | 84333 |
| rs533185738 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186384 | CAAGCAAGAGATGAA[A/G]GAATATAAAAGCTGC | 84333 |
| rs533191579 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245303 | GAAAACTGAGAATTC[A/G]TGGTTGGATTTAGCA | 84333 |
| rs533269623 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250436 | TTGGGTTTATTGTCT[C/T]TTTTATATGTGCATG | 84333 |
| rs533308834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192284 | GAGACAAGATTAACT[C/T]AACAACTCAAGGTGT | 84333 |
| rs533320439 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247502 | AGAAAGGTTTTGGGG[-/T]TTTTTTTTAAGATGT | 84333 |
| rs533339994 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236569 | ATCATTCTTGGACCA[A/G]TTGGGTTAACCACTA | 84333 |
| rs533352490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222020 | GAGGAGACGGTGGGA[C/G]AGGAGTGATCCCTTC | 84333 |
| rs533377434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179926 | TGAGGAATCGCCATA[C/G]TGTTTTCCATGGTGG | 84333 |
| rs533405164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243202 | GAGACTAAGGAGGTT[A/G]TGGGGAGGGGAAGAT | 84333 |
| rs533410482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230172 | AAGGACAACAGACGT[A/G]AAAGAGTGAAATCTT | 84333 |
| rs533443106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179356 | ATTAATCTTTTAAAA[A/G]TTTATTTTAACTTTA | 84333 |
| rs533453683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191112 | CCCTATGTATGTTAT[A/G]TTTTGTTCCTGTGTA | 84333 |
| rs533517572 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197278 | TCGCGAGCTGACTGT[C/T]ATGTCCTGGGTCTAG | 84333 |
| rs533524042 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211031 | TAGGTACCAGGAGGC[A/T]TTTGTTAAATAAGTG | 84333 |
| rs533541007 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266784 | GCCTTTTTCTTTCAT[C/T]CATCCTTTCTTAGCA | 84333 |
| rs533567525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176444 | CTGTATTTCCTGAAT[C/T]TGAATGTTGGCCTGC | 84333 |
| rs533624756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181390 | GGAACTTTGAATACT[A/G]TGTTGAATAGGAGTA | 84333 |
| rs533630000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221310 | GCATTTCCTCTTCCA[G/T]AGGACTTTCTCTTAC | 84333 |
| rs533643852 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275136 | TTGCAATGTATGATA[A/G]AAAAAGGTTTAATGT | 84333 |
| rs533653414 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274129 | TATGTATATATATAT[A/G]TAATAGTACATTACA | 84333 |
| rs533671087 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284639 | GCACTTGCCTCAGGA[A/G]TTCATTAGGCCAAAG | 84333 |
| rs533673394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239933 | CATTATTCATACTTC[A/G]TGCTCCATGGAATTA | 84333 |
| rs533685534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237199 | ATTGTATTGAATTAA[A/T]TATATGTTGATTAGG | 84333 |
| rs533719094 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164853 | TATTTTCTTCACTGC[G/T]CTTAATCGCTATCTG | 84333 |
| rs533732032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201315 | TGTCAGCTCAGGTCT[C/G]TCTTCATGTAAAGCC | 84333 |
| rs533741204 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209298 | GAGGGACTTCCTCTT[G/T]AGACATCTGTCAGAA | 84333 |
| rs533778962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171072 | AAGATCAGTGGTTGC[C/T]AAGGGTTAGAATGGA | 84333 |
| rs533831445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232771 | TTTGTTTTCAGTAAA[A/G]TAGAGGTCCTCAGTG | 84333 |
| rs533895445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232055 | AGGACCAAGGACTGA[A/G]CCCTGAGGTACCACT | 84333 |
| rs533902036 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161783 | CCTCTTGATAAAGAC[A/T]CCTGAACTTTTCCAG | 84333 |
| rs533914941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252500 | AAAACATCTTTCACT[C/T]AAGGAACTTGGTTAG | 84333 |
| rs533931837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187197 | TATCTATAGTGATTC[A/G]GATTTAATTGTTCTA | 84333 |
| rs533948777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254782 | AAAATTCACTTTTCC[A/G]TGAAAGTATAAAAAT | 84333 |
| rs533960189 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215153 | TTGTTCAAATCAGGA[A/G]CAACAGTTCTTGACA | 84333 |
| rs533967374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259931 | ATGTCTAAAACACCA[A/C]AAGCAATGGTAACAA | 84333 |
| rs533971906 | in-del | -/T | 0.44651 | 0.154543 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251098 | TTAATAAGTTTCCAA[-/T]TTTTTTTTTTTTTTT | 84333 |
| rs534014319 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253628 | TGATCTGTTACTCTT[G/T]TCTTTCAACCAGTCA | 84333 |
| rs534018495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262256 | CATGGTAAAACCCTG[C/T]GTGTTCTAAAAATAT | 84333 |
| rs534025964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164163 | CCAGGGAGAGTGGCC[C/T]CTCTGCAGTGATGAC | 84333 |
| rs534027610 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237652 | GGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC | 84333 |
| rs534041249 | in-del | -/T | 0.0614824 | 0.164198 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284175 | TGTTGGGCTAGATAC[-/T]TTTTTTTTTTTAATC | 84333 |
| rs534052249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214250 | GAGGCTGCAATGAGG[C/T]GTGATTGCACCACTG | 84333 |
| rs534077632 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261862 | ATTTCCGTGAAATGC[A/C]GAAGTGGTTTTGTTT | 84333 |
| rs534089352 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170409 | AATATACAAGGAACT[A/C]TTAAAACTGAATATG | 84333 |
| rs534104532 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200035 | GCTTCAGGCTATCCT[A/G]CCCAAAGGACAGGGA | 84333 |
| rs534164593 | in-del | -/ATATAT | 0.02016 | 0.0983543 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195472 | TATATATATGCATGC[-/ATATAT]ATATATATAGAGAGA | 84333 |
| rs534200699 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235699 | GTCTTTCTCACGCTG[C/T]TTTCTCAATAGTGAA | 84333 |
| rs534230041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168808 | TGGTGTGTGTCTGTA[A/G]TCTCAGCTACTAGGG | 84333 |
| rs534235391 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245009 | GTCTTCAACATATAG[A/C]AGGTCTTTCAAACTG | 84333 |
| rs534240732 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205863 | GGCACGGTGGTGGAT[G/T]CTTGTAATCCCAGCT | 84333 |
| rs534255019 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215175 | TTCTTGACAAAATTT[C/G]CTTTTTAAAAGCATA | 84333 |
| rs534290396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249249 | ATTTCTGGGTGCTTA[C/T]GGGAATTTTCTCCAT | 84333 |
| rs534290543 | snp | C/T | 0.0737376 | 0.17729 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257158 | AAAGGCTTGAATAAA[C/T]ATTCCTCTAAAGAAG | 84333 |
| rs534295268 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175945 | TGTGTGAATTTGATC[C/T]TGTCATTATGATGTT | 84333 |
| rs534316455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223117 | AATTATTTTAACTTT[A/G]AATTTTCAGAATATT | 84333 |
| rs534325608 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181145 | TGATTTGGCTCTTGG[C/T]CTGACCCTTGTTGGT | 84333 |
| rs534350565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256453 | AGAGCTGTAGACACC[A/G]TCAAGCTTACCAGCA | 84333 |
| rs534357027 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166454 | GAAGAAGTTTTCTGA[C/T]AACAGAATTAGATAT | 84333 |
| rs534399167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264154 | GATTTGGACTAAGAA[A/G]GGTTACATTGCATTT | 84333 |
| rs534413560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194170 | CCTCTAAAGATGTTC[A/T]TCCTAATCCCCAGAA | 84333 |
| rs534452957 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219389 | ATAGGAACATACCAA[G/T]TCTTTTTTATATATT | 84333 |
| rs534520647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253038 | CCTGATTCTTCCTTT[C/T]TTTCCTGTGGCATTC | 84333 |
| rs534525452 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191254 | ATGCTTTGGGGCCAT[G/T]AAGTAAAATAAGGGT | 84333 |
| rs534526463 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207225 | TGGTGAGGGATGTGC[A/T]GCTGGTGGTAGTATT | 84333 |
| rs534530454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199490 | AAGGAGGATCTTTGC[A/G]GCTGAGGACATGCCT | 84333 |
| rs534550610 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214888 | ACAGTTATTTTAAAA[G/T]CAATTTATGCTTATA | 84333 |
| rs534563354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242610 | TTTTAACTTTTTATT[C/T]GGAAATAACTTCAAA | 84333 |
| rs534703441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196049 | TTTCTCGCATCCCCT[A/G]CTGGTCAAGTGTTGC | 84333 |
| rs534872879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272476 | ATAGCAAGACAAAAA[A/C]AAATTATTTTTTTAG | 84333 |
| rs534932969 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166863 | TAATGTGTGTGGTGT[A/T]TAAAAGGCTCTTAAT | 84333 |
| rs534948310 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204335 | TTAAGGTTTTCATTT[A/T]AAAAAAAACCCTTAC | 84333 |
| rs535008421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234368 | GAAAAGCATTGGTCA[A/G]TCTTGGACACACACC | 84333 |
| rs535022965 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283651 | TTTTTTAGAATGGGG[A/G]TGGGGGCCTAAGTGT | 84333 |
| rs535050760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189381 | TGATGTTTTGAAATC[C/T]CAGTTTACAACATGG | 84333 |
| rs535073514 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201954 | CTTTTGAAATTGTTA[G/T]AAGAAGCAGGGTGGC | 84333 |
| rs535098752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193355 | CTTCTAACCTACACA[A/G]CTGTGAGATGCTAAG | 84333 |
| rs535106827 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171816 | CTGAGCTTGGGGATG[G/T]TGAGTGACACAGGCC | 84333 |
| rs535130952 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247503 | AGAAAGGTTTTGGGG[G/T]TTTTTTTAAGATGTG | 84333 |
| rs535159629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192685 | CATACAATAAAACAG[A/G]CATAGTAAACATTTA | 84333 |
| rs535185241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263465 | TGAAACTATACTCAT[A/C]TTAAAGTTCAAAACT | 84333 |
| rs535190661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178546 | AAGTGCAATTCACCA[C/T]ACCCGGCTAATTTTT | 84333 |
| rs535204899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244507 | AAACATTTTATCTTT[C/T]ACTCTGAATGAAATG | 84333 |
| rs535215792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198743 | TAGCAGCAATTGCCA[A/G]GATGACGTTTTGGCC | 84333 |
| rs535218069 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218721 | CACTGCAACTTCCAC[C/G]TCCTAGGTTCAAGCG | 84333 |
| rs535218509 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170342 | AAAGATGAGCCACAG[A/T]CTGGGAGAAAATATT | 84333 |
| rs535252035 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259981 | GGATCTAATTAAACT[A/C]AAGAGCTTCTGCACA | 84333 |
| rs535255570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177899 | CTCACACTTGGTGCA[C/T]GGTGCACTGCACCCA | 84333 |
| rs535266124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224097 | TGTTACATTTATGTT[A/G]CATTTATTTTACCAC | 84333 |
| rs535274344 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277560 | TCTAGTTCTGTATGA[C/T]AGCCAGATATATGAT | 84333 |
| rs535303671 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237461 | AAAAATTCACATCAA[C/T]GCTGGGCGCAGTGGC | 84333 |
| rs535316522 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269452 | GTAAACTTTGAAACA[A/G]TTTTTAATACATTAA | 84333 |
| rs535329634 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278848 | AAAAAAGTTCATTCT[C/T]GAGTGTGCAAGTCCT | 84333 |
| rs535385709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231112 | TCCCTTGCTTTAGTT[A/G]AAAATGTAAGCTTCT | 84333 |
| rs535445507 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244681 | GTGGTAGCAGTAGAG[A/G]GGACAAGAAATGCTC | 84333 |
| rs535464674 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282582 | AATGGGTCACAGAAC[A/C]AGCATGTACATCAAG | 84333 |
| rs535478363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244881 | AAGGGGTAGATCAGG[A/G]CTTCAATTGTGGACA | 84333 |
| rs535487479 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274169 | GATGCCAGTTCACCC[C/T]ACAATTAAATTATAA | 84333 |
| rs535544886 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281537 | TGAATGGTTTCATAT[A/C]TAAATAGGCTCTTGT | 84333 |
| rs535608836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168890 | CTGAGATTGCACCAT[C/T]GGACTCCAGCCTGGG | 84333 |
| rs535648777 | snp | A/T | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161066 | GCCAGGGGGACTCTC[A/T]TCCCCTACTTTGGAA | 84333 |
| rs535668838 | in-del | -/TAA | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230040 | GTCATCTATTATTAG[-/TAA]TAATGTTAAAGTTAT | 84333 |
| rs535745519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205296 | AAATGACTGGACACA[A/C]ACACACACACACACG | 84333 |
| rs535781859 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283293 | TAAAAATAATTATTT[A/T]AAATGCTCATTCAAA | 84333 |
| rs535806145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213403 | GCACAAATTAGTTCT[A/G]TGTCAGATATTATAA | 84333 |
| rs535811369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171219 | CAAAATACAGATGTG[A/G]CATGGAGGAAGAAAG | 84333 |
| rs535851490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270787 | TATTTAATTTTTTCC[A/G]TTTTGAAAAGTATGC | 84333 |
| rs535870586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170558 | ATCAAAACAACCATG[A/T]TATACCACTATACAC | 84333 |
| rs535904119 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171256 | GATGAAAACAAAAGG[A/C]AATTTTGAGTTCTGA | 84333 |
| rs535909586 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229554 | TACATCTACATAATA[C/T]ATGTTATGACATTTT | 84333 |
| rs535909651 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220739 | GACGGGGCGCGGGGA[C/T]CGGCCAGGCCGCGGC | 84333 |
| rs535930855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177084 | TACAGATGGGGTTTT[A/G]GTGTGGATGTCCTTT | 84333 |
| rs535951263 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166326 | CCTCCCATGTGCCTG[A/C]AACATCTAGGGGCTC | 84333 |
| rs535957596 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183007 | TATTTCAGTTCTTTT[G/T]CTTTTGCTGAAGAGT | 84333 |
| rs535960987 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222416 | AGATAGTTAAAATGC[A/G]TTAGTGAAGAGGTAA | 84333 |
| rs535961684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270207 | GGTAGTTCTCAGTAC[A/G]GCCCCCTTTTCCCAG | 84333 |
| rs535969287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236656 | TGCTGTACTGCTAGT[A/G]TGGACTTCAAATTAT | 84333 |
| rs535972694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228597 | TCGGCGATTTTATGT[C/G]GTAATATGTAAGAAG | 84333 |
| rs535982443 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206132 | ATAAAATAGTGCCAC[A/C]AATATTTATCGGAGA | 84333 |
| rs535987775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233617 | GAAGATGCATGGAAG[C/T]GAATTACAGCTATTC | 84333 |
| rs535988264 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275357 | CAAATTAAGAGGTGG[A/G]GAAAGATAGTACTCA | 84333 |
| rs536003756 | snp | G/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218424 | CTACCCCCTCATGTT[G/T]TAGCTTCCGTCATTT | 84333 |
| rs536029712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251493 | TTATAGTAAACCCTT[A/G]ATAATTTGTTGACAA | 84333 |
| rs536045404 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187771 | AATATATGTACCTGA[A/G]AAATGTCTGTGTAGC | 84333 |
| rs536054293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205671 | ATCAGAATCATTGAC[A/G]GTATATTTACAGTTA | 84333 |
| rs536061270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202660 | CCTTGAAAACTTCCT[C/T]CTTGTACTTAATTGG | 84333 |
| rs536083077 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168292 | AGGTAGACAGGATGC[G/T]GAGAAGAAAGAAGCA | 84333 |
| rs536088406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250771 | TATGTATTAATAGCT[A/G]TATACATGTTAAAAA | 84333 |
| rs536088654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258811 | ATTTTATCATCTGTA[A/T]TGTGACCAGGTTGTT | 84333 |
| rs536091409 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215452 | AATTCCCTTGTTTAA[C/T]GTCATAGAAATAAAA | 84333 |
| rs536116114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213770 | GATTACAGGCGTGAG[A/C]CACCATGCCCAGCCA | 84333 |
| rs536123775 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249587 | AGCCTCCCAATCTTG[A/G]TTTTCCCATAAGATC | 84333 |
| rs536126278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266888 | GTCCAACCCACCATC[A/G]CCATTCTCCTAGCAA | 84333 |
| rs536214281 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253557 | AAACATGCAGTTTTA[A/G]TTATGACTGCTGTCT | 84333 |
| rs536216341 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245701 | AGGCAGGCAGACAGC[A/G]AGTACATGGTGCAGA | 84333 |
| rs536240587 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173747 | CTTATTTCTTAAACT[G/T]TGAATTTAGTATTTA | 84333 |
| rs536279136 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253062 | GGCATTCCTGCTTTG[A/T]CTCCACTGCCTCTAC | 84333 |
| rs536300134 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185294 | AAGCAGTCTGGCCAT[A/G]TTTTGGTAGAGCAGC | 84333 |
| rs536315287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226045 | TTGACTTAGGCATAT[A/G]CAAAGAGTATCTTAC | 84333 |
| rs536381389 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206658 | GGCAGCAGTCAGCTT[A/T]GAGTAAAGGGTGAAG | 84333 |
| rs536525821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187340 | GATAGATAAAGATCT[C/T]CATGTGCAGATTTTG | 84333 |
| rs536548813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164939 | CTCCACTATGCTAGG[C/G]ATTTGGGCTGTTTTG | 84333 |
| rs536556841 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246279 | CTGGGAAAACTTTAC[A/G]AATGACCTTGTCTTG | 84333 |
| rs536584249 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209878 | CAATGGGCATTAGGG[A/C]ATGAATGAATGAATG | 84333 |
| rs536596032 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215501 | AGGAGGCTGTCAGGT[C/T]TGATCTAGTTCCCAT | 84333 |
| rs536609637 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197979 | CTAAGTGCCAGACAT[G/T]GGGGAAGTGAATCCA | 84333 |
| rs536611607 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230939 | ATTTATTTTAGAGAC[A/G]GGATCTTACCATGTT | 84333 |
| rs536643187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197428 | AGTGTTATCACAACT[G/T]CTGATGTTTATTGAG | 84333 |
| rs536651444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200269 | GTGACAGTGTCTGCT[A/G]TAGGGGATTGCCTGA | 84333 |
| rs536673428 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184814 | TCCCTAGTGGCCTTG[G/T]ATTTTTCAGTATCTG | 84333 |
| rs536687280 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91162727 | CGGCGGCGGCTCGAG[A/G]AGGCCTGGCGGGCGG | 84333 |
| rs536692694 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228304 | GTTCCAGCAGCTCAA[A/G]TGTGACCAATACAGT | 84333 |
| rs536728089 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215117 | TCCTAACATTTTTGG[A/G]AAGTGAAATATCATT | 84333 |
| rs536741302 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169569 | TACTTAGATATACAT[A/C]TAACAAAATATGTAT | 84333 |
| rs536747418 | in-del | -/CGC | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91162879 | GCCCGCCGCCGCCAG[-/CGC]CGCCGCCGCCGCCGC | 84333 |
| rs536796509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179662 | GCTCCAACCATGTCC[C/T]CACAAAGGACATGAT | 84333 |
| rs536839016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232881 | GACTTGGGGCATTGA[A/G]TATGACAGCCTGGCA | 84333 |
| rs536850602 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278580 | TAAAAATCAGTTAGC[C/T]GTGCCGCCATGATTC | 84333 |
| rs536889968 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236741 | TGGGAAACCAAATCC[A/T]CATTTTACTTTTTCC | 84333 |
| rs536924024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194905 | AAAAGAGTTTCTGGG[A/G]TGTTATCCTCAAGTA | 84333 |
| rs536987416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194198 | GAAAATGTGAATGTG[C/T]CACTTTAGGGAGCCA | 84333 |
| rs537000319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184426 | TGGTTACAGTACTCT[C/T]TACTGGCTGTTTTGT | 84333 |
| rs537001567 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166968 | TTTTTTCAATCGGAG[A/C]ATAGGTGGTCAGGAT | 84333 |
| rs537004486 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223380 | TAGACTAGCAGCACC[A/G]GTGTCATTGCAAGTT | 84333 |
| rs537007717 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191360 | TGGCACAGACAGCAT[A/G]GGTACACTGGACAAA | 84333 |
| rs537026040 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226927 | AATAGATAAAATTTT[A/T]AAATGAGTTAAAATT | 84333 |
| rs537029149 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229746 | CATTTTAATGAAAAA[A/C]AGATATAAATTGAAC | 84333 |
| rs537035704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235260 | ATTCTAATTAGTGAT[C/T]ATGATGCCCATTTAA | 84333 |
| rs537064826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190152 | CTTCCTGGTTTCCAG[A/G]TGGCACCTGATCCCT | 84333 |
| rs537092607 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91218077 | CAGGCGTGAGCCACC[A/G]TGCGCAGCCCTAATC | 84333 |
| rs537188145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196112 | ACATTTGTCAGAATG[A/G]CTCACTGGTTTCCTA | 84333 |
| rs537219332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265407 | GGCTATAAGGTTGGA[A/G]TAGATAACATCTAAG | 84333 |
| rs537256529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185529 | CTGCTGAGCCCCATG[A/G]ATTCAACCTCTTTCC | 84333 |
| rs537320047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185109 | AGCATGAAGCTGGAA[C/T]AGCTAAGTCACCCAG | 84333 |
| rs537357216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236298 | CCTCACTTGCCCAGG[A/G]AGGATAGTAACTGTC | 84333 |
| rs537409275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177944 | CTGTCCAACAATCCC[C/T]AGTGAGATGAACCCG | 84333 |
| rs537481565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231195 | TTTAGTATTCCTAAC[C/T]ATTGTGTTCTCATTT | 84333 |
| rs537489338 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255773 | GGAGATACTAACAAA[-/T]ACAGTGGTCCCTCAG | 84333 |
| rs537494172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234567 | TTTCAAGTTCCATCG[A/G]CATGATATCTGTTAT | 84333 |
| rs537504227 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283650 | ATTTTTTAGAATGGG[C/G]GTGGGGGCCTAAGTG | 84333 |
| rs537604567 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91176512 | GCAGAGTGTTTTCCA[A/G]CTTGGTTCCATTCTC | 84333 |
| rs537607124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166553 | CCTCCAGTTTTTTTT[A/T]AAAGTCTTAAAACTT | 84333 |
| rs537637939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216682 | GTGGCTAAACAGAGG[G/T]ATTTAAGAGACATTT | 84333 |
| rs537651525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273263 | AGGTGTATAGATGTT[C/T]CAGCTGCTTTAGCCT | 84333 |
| rs537658800 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260709 | GCAAACTATCACAAG[C/G]ACAAAAAACCAAACA | 84333 |
| rs537668049 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172687 | GTACTCATAACTTTT[C/G]TGTTTGCCCCCAAGT | 84333 |
| rs537669537 | snp | A/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219847 | TGCTGGACTAGCGGT[A/T]GTTAAGTTTGTTGGT | 84333 |
| rs537726036 | in-del | -/G | 0.0138799 | 0.0821421 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185299 | GTCTGGCCATGTTTT[-/G]GTAGAGCAGCTGTGC | 84333 |
| rs537735582 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163844 | CCGGGGTGGTGGGGT[-/G]GGGGGGGCACGGACG | 84333 |
| rs537758223 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171005 | TGAAAAAGCTTCATA[C/G]TGTGTGATTCCAACT | 84333 |
| rs537771496 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238662 | TTCAGAGACTTATCT[A/G]TCATCCCTGGGAAAA | 84333 |
| rs537774614 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279910 | AAAGTACAGCTAAAT[A/C]TTAATATATTTCACT | 84333 |
| rs537804037 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259014 | TTTAGTATTCTGATA[A/C]CTTTTGAGGTTGTGG | 84333 |
| rs537832464 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251027 | TTTGGCTAAATACAG[C/G]TAGTCCTGAATCTTT | 84333 |
| rs537858780 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266960 | CACACAGCAGCCAGC[A/G]TGATCCTCTTAGGAC | 84333 |
| rs537885730 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205478 | ATAAACTGAGCCAAG[C/T]TCAAAGTACATTTTT | 84333 |
| rs537945177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174541 | TTATTTGTTTGATTA[C/T]AATCTACTGTAATAA | 84333 |
| rs537945567 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238342 | CTTTGGATGCTTGAG[A/C]CCTACAACTCTTTCA | 84333 |
| rs537983403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274354 | AAACATATTTTAAAG[C/G]TGAAGTAATTAAAAT | 84333 |
| rs538007062 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235051 | GAGCCAAATCCTGGA[A/G]TGGGCACCCTAACGA | 84333 |
| rs538008182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170341 | AAAAGATGAGCCACA[C/G]ACTGGGAGAAAATAT | 84333 |
| rs538049187 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269745 | AGAGTGCCCATTTTC[G/T]GACATCCTCCCCAAC | 84333 |
| rs538097368 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265652 | ATTGAATGTAAACAT[G/T]TGTGGAATTATTATA | 84333 |
| rs538101967 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215706 | CTCATTTATCATTCA[G/T]ATGCCATTACCATTC | 84333 |
| rs538122226 | snp | A/C | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227621 | TTCTTAACTGTGTCC[A/C]AGTGGTAATAATTAA | 84333 |
| rs538131421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198791 | AGTACCTCTTAAGGA[C/T]TGGATGTAGTTTTGT | 84333 |
| rs538134779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176383 | TGAATCTGACAATTA[C/T]GTGTCTTGGAGTTGC | 84333 |
| rs538136012 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262676 | GGGTTGAAAATTGTT[A/G]TTATGGTATGGTTCT | 84333 |
| rs538137075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268829 | CCCTGCCCTCTCTAG[A/T]CCCTTGTCTCCATTG | 84333 |
| rs538146014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251661 | TAGTGGCTAATGCCC[A/G]GAATCACACCTCTGT | 84333 |
| rs538181212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205769 | GGATCACTTGTGGTC[A/G]TTTGTTGGTCAGGAG | 84333 |
| rs538214514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165733 | TTATATTTTAAACAT[A/C]TTAAATGGATTCTAA | 84333 |
| rs538231981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214005 | AAGACTCATGTCCTT[A/G]TAAGAAGAGGAAAAG | 84333 |
| rs538237284 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183485 | AGGTAGGTCTCTTGA[A/G]TATAGCACATCGATG | 84333 |
| rs538259218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263386 | AACATTTTGAGGTCC[A/G]TATAAGTCATCATAA | 84333 |
| rs538277507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164981 | AACCCTAGCACCTAG[A/G]ACAGTGCCTGGCATA | 84333 |
| rs538293344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213508 | TTGCTCTTGTTGCCC[A/T]GGCTGGAGTGCAATG | 84333 |
| rs538325579 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180057 | GACTGGTGTGAGATG[A/G]TATCTCATTGTGGTT | 84333 |
| rs538352281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230520 | TATATATGTATTCAT[A/G]TATACATATATGAAT | 84333 |
| rs538361616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197186 | GGAATTTGGAGTCTG[G/T]TCAGCAGCGTAGCCT | 84333 |
| rs538391605 | in-del | -/TT | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213628 | ACCACCACACCAGGC[-/TT]TTTTTTTTTTCTTTT | 84333 |
| rs538403911 | in-del | -/CTC | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198911 | CAGGCCATTCTTGTT[-/CTC]CTCCTCTCTCAGATG | 84333 |
| rs538409919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244931 | GAGAAGAGAGGAAGG[C/T]AAGTGGATATATGTG | 84333 |
| rs538433704 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199369 | ATGGCAGGAGCTCTG[G/T]AACTAGAATGACTCC | 84333 |
| rs538457738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189603 | AAGATCTTTCCATAT[A/G]TACATACATATCTAC | 84333 |
| rs538509635 | in-del | -/ATA | 0.240472 | 0.249818 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260961 | ACTTAAAGCATAATA[-/ATA]ATAATAATAATAAAA | 84333 |
| rs538520521 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259881 | AAGAAAACCTAGGCA[A/G]TACCATTCAGGACAT | 84333 |
| rs538533965 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218827 | TAGAGATGGGGTTTC[A/G]CCATATTGGCCAGGC | 84333 |
| rs538579960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255653 | AGAATACAGACTTTA[C/T]GGAATTAGTTTAGGA | 84333 |
| rs538611918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240157 | ATCTTTTTCTGTCCT[A/G]CTTCTTTAAATGAGA | 84333 |
| rs538628746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210717 | GACCACACCTGCTTT[C/T]TGTTGTTTGGTCTCT | 84333 |
| rs538644975 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262097 | CATTAATTTCCCCTT[C/T]TTCCCTTTCGAGTTC | 84333 |
| rs538689605 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209930 | AACTCAATGAGATTG[A/C]CATGTGGAAATTGAG | 84333 |
| rs538695200 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234976 | TTAATTATTTTTTGT[A/C]CTGTCATAATGGTTT | 84333 |
| rs538746578 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162131 | GACAGACACATTTCA[C/G]GTGTTGTCTGTAAAC | 84333 |
| rs538755449 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217734 | TTCCCTCCCTCTCCT[C/T]ATCCATTCTTCCCTT | 84333 |
| rs538774657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208289 | TTAAATTCAGTGTGT[A/G]TGATCCATTCCTCTT | 84333 |
| rs538788107 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267134 | CTGGCCTCACAGCAC[A/T]CCAGCCACACTGGCC | 84333 |
| rs538811990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271002 | GTTTTAAAGTGTGTT[C/G]ACTCATTGCTTTACT | 84333 |
| rs538863941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241553 | TCATTTCATTGTTCC[C/T]ACCATAGCTCTAAGG | 84333 |
| rs538896712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196194 | CAGTGCAGCTGAAGT[A/G]ACATTCTGTCAGCAA | 84333 |
| rs538969495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233115 | AGAGTGACACTATCA[A/G]GGGTATGTGTGAGGA | 84333 |
| rs539073586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191935 | CTCTCTCCTGTAGTA[A/C]TCTTTATCCAAAGTA | 84333 |
| rs539081561 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181448 | CAGTTTTCAAGGGGA[A/G]TGCTTCCATCTTTTG | 84333 |
| rs539175092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205217 | TCATCCAGCCTTGAG[C/T]GCAATTGTTCCCAAA | 84333 |
| rs539226082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231061 | TGGCCTAACTTACTT[C/T]AATTGTCAAAAAAAT | 84333 |
| rs539235322 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222288 | TGGTTTGACTCGTAA[A/C]TGGATGAAGGGTTAA | 84333 |
| rs539323345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182402 | GTGAGGTCAGTGGTA[G/T]TGCCCTCCTTATCAT | 84333 |
| rs539325145 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188854 | TCCCTAGATAGCAGT[G/T]TATTCATTCCTTAGC | 84333 |
| rs539341518 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282535 | CTTAGTTTATTGTTA[C/T]TAGAATTTAGCCATA | 84333 |
| rs539352215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229861 | GTAGGTGCAAATATA[A/G]TGTTTTAAGATATAC | 84333 |
| rs539383901 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244402 | GAGACCTGGGCGGCT[A/G]GGGAACAGTGAGTGA | 84333 |
| rs539387658 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188169 | TTCCATCTGAGGTAC[G/T]GGGTTCATCTCACTA | 84333 |
| rs539413260 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273414 | AAGATGTCCTTAAAC[C/G]ATGATCCAAAGTATT | 84333 |
| rs539428379 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198710 | ATTCAGTAGCATTGA[A/T]TCAATCCTGAGTTTA | 84333 |
| rs539470663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184980 | TGAGGTCTCACCCAG[C/T]CAGGAGGAACAACAC | 84333 |
| rs539527131 | in-del | -/TTGA | 0.0256215 | 0.110247 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180767 | GCCCTGTAGTATAGT[-/TTGA]AGTTGGGTAGCATGA | 84333 |
| rs539569353 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270768 | GTACCTTATATTTTT[A/T]ATGTATTTAATTTTT | 84333 |
| rs539584476 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275690 | GATCTCTTGACCTCG[C/T]GATCTGCCCGCCTCG | 84333 |
| rs539595032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190251 | TCATGTTCTCATGAT[C/T]CAGTCACCTTCCAAA | 84333 |
| rs539637353 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204589 | AGCCATTCCTTTCCA[G/T]ACAAATGTTTGGTTC | 84333 |
| rs539637474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213324 | ATACTCTACATATGT[A/G]TGGATATATCTGTAT | 84333 |
| rs539668147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180149 | CATGTATGTCTTCTT[C/T]TGAAATTTGTCTGTT | 84333 |
| rs539677948 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167267 | TATATATAAAGCAAT[A/G]TAAGAAGAATACTGG | 84333 |
| rs539688614 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207957 | CAATGGATTGCTCCA[C/T]TGTAGGGGTACCTTT | 84333 |
| rs539721050 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241644 | GGGGTCAATTCCGGA[A/G]TTAGCTTTTTAGTAC | 84333 |
| rs539732072 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179777 | AGTTTGATTCCATGT[C/G]TTTGCTACTGTGAAT | 84333 |
| rs539739667 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173381 | TCTGCCTTTTTATTT[C/T]TCTTTTAACCTTAAA | 84333 |
| rs539759870 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179178 | ATTACTTTGGTTTCA[A/T]GTCATGTACTCTCTA | 84333 |
| rs539762553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220529 | GCAGGCGCGGCCTCC[C/G]GGCGTGGTGGTGGGC | 84333 |
| rs539769642 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192613 | TAGTCTTTGGAATAT[C/T]AATAAACAAAACAAT | 84333 |
| rs539807970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169824 | AATAGCACAATACTG[A/G]AGGAGAAGAACAAAG | 84333 |
| rs539842721 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216356 | ATAAAGACAGGGTGG[G/T]CATTTGGAAGAAGAC | 84333 |
| rs539843928 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229419 | AGGAAGGATCAATCT[A/G]TGAAAAGGTTTAAGG | 84333 |
| rs539879330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236135 | TTTTTGATTTTGATG[C/T]CAGGGACCAAATGTT | 84333 |
| rs539912446 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280033 | TGGTGAAAAAGGTTA[C/T]GGCAATACTTTAACT | 84333 |
| rs539941035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235369 | AATGGTAAAAGTAGG[A/G]AATTCACTTAGTAAA | 84333 |
| rs539975600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214952 | TTCTAGTAGAAATGA[A/G]TGTTCTACTTAAAAT | 84333 |
| rs539983869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267485 | GCCCAGCATATATAC[C/T]CAATCAATACTTGTT | 84333 |
| rs539985543 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282840 | TCAAAAATGAATGAG[C/T]TTGCCATAACTTTAA | 84333 |
| rs539986481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175603 | TTAAATGTAAATGAA[C/T]AGGAGACATTGGAAG | 84333 |
| rs539993268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167697 | TGGGCTAAGGAGACT[C/G]TTTAGTTGGCAGTAG | 84333 |
| rs540013828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258059 | ACACAAAAGGTCACA[G/T]ATTATGTGATTCCAT | 84333 |
| rs540017479 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197851 | TATTTAAAAACAGAC[A/G]TTCCAAGGAAATAGA | 84333 |
| rs540026920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246656 | GAATAGGTGGGACAG[A/G]TATTGAGAGGGAGCT | 84333 |
| rs540044676 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239146 | GAGGGGGAGGCAGGT[-/A]AAAAATACCACTTAT | 84333 |
| rs540075899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257496 | TCCAAGACCCCCAGG[A/G]GATGTTGCAACCACA | 84333 |
| rs540076002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266116 | TTCTTTCTTACCCAA[C/T]ACTGTTGAGGAATGG | 84333 |
| rs540105462 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200444 | CTTTCTGGGAAGTGC[A/G]CATATATGTTTGAAA | 84333 |
| rs540114132 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265574 | ACCTCACACAAGAAT[A/G]AGAAATAAGAATCCA | 84333 |
| rs540124934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193937 | ATTTCTTTGTGACTT[A/G]GATTTGGGATGTAAG | 84333 |
| rs540149689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245308 | CTGAGAATTCATGGT[C/T]GGATTTAGCAACATG | 84333 |
| rs540153645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163493 | GACGCTCGCGGCTTC[C/T]TGATGGGGACCGGCA | 84333 |
| rs540167745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207589 | TATCTAATGTGCAGA[A/C]CTGTCCCAATGATAT | 84333 |
| rs540185269 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162047 | TGAGTCCAACAAAGT[A/T]TGACAGGTGGAGGCG | 84333 |
| rs540194814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260863 | TACCTAATGCTAAAT[A/G]ACCAGTTAATGGGTG | 84333 |
| rs540245841 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233408 | TTGCTTTGTCTTAGC[-/A]AAAAAATAAAAATAA | 84333 |
| rs540246697 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169036 | AAGATCGAGGGAGGA[C/T]GTAGGAGGGCAATTA | 84333 |
| rs540249680 | in-del | -/AT | 0.0178098 | 0.0926698 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241042 | TTTAGCAGTATAATC[-/AT]ATATATATATATAAT | 84333 |
| rs540265947 | in-del | -/ATATATATAACAT | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225290 | TATATCATATATAAC[-/ATATATATAACAT]ATATATATAACATAT | 84333 |
| rs540304718 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243983 | TATTTACTGGATGCC[G/T]GCTGTGTCTGGGCAC | 84333 |
| rs540315818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268249 | CCCTCCAGTTGTCTA[C/T]TTTCTTTGGGATAAA | 84333 |
| rs540350951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275921 | AAAAAAGGACTAAAC[C/T]CAAATGTGCAGCAAA | 84333 |
| rs540391752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239589 | AAATTTCAGGTTATA[C/T]GGGGTAATAGAATGG | 84333 |
| rs540427903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194459 | AAGGTGGAAATGGCA[A/T]GGAAACAAATTCTCC | 84333 |
| rs540433063 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179360 | ATCTTTTAAAAATTT[A/G]TTTTAACTTTAGGGG | 84333 |
| rs540435475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180428 | TTTGCCCATGCCTAT[G/T]CCCTGAATGATAGGT | 84333 |
| rs540445252 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283745 | CTGCATCTGAGCAAC[A/G]CAACAGAGATCATCA | 84333 |
| rs540494785 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168805 | TGGTGGTGTGTGTCT[C/G]TAATCTCAGCTACTA | 84333 |
| rs540501563 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200924 | GTTCGTGATTACTGT[C/T]GACAGAGGGAAGTGG | 84333 |
| rs540556170 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186513 | TTTTAGACCTCAGGG[A/G]AAAACTTCATATATA | 84333 |
| rs540627082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198864 | GGTCTTTGGCTGAGT[A/G]TGTTTCGTATTAGTC | 84333 |
| rs540638549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241630 | TGAAAAGCACAAAAG[A/G]GGTCAATTCCGGAGT | 84333 |
| rs540687899 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198545 | TATTTCAGCATGACC[A/G]TTGGCAAAGCAGCAT | 84333 |
| rs540723748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255846 | AATCTGTGGATCCCA[C/T]GTCCCTTATATAAAA | 84333 |
| rs540748799 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205407 | TGAATAAAAACACAC[A/C]CATAGACCTAGATAT | 84333 |
| rs540780828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172313 | AATCTCAGCTACACC[A/G]GAGGGTGAAGCAGAA | 84333 |
| rs540780916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178648 | CCCACCTCGGCCTCC[C/G]AAAGTGCTGGGATTA | 84333 |
| rs540838332 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229935 | AGTATTTTGGCAGAA[A/T]CTAGTCATTCATTCA | 84333 |
| rs540859938 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178578 | AAATTTTTGTAGAGA[A/C]AGGGTTTCACCATGT | 84333 |
| rs540870245 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239779 | GGAAATGTGGGCTGT[A/G]TAGGCTTGTGGCCCC | 84333 |
| rs540885440 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279398 | ATAAATGCAGTATAG[A/T]ACTATGCTAACCAAA | 84333 |
| rs540939148 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237700 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCTAG | 84333 |
| rs541009871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225332 | TATGTATGTTCTCAA[C/T]AGCAATTTAAAGCCT | 84333 |
| rs541032569 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213399 | AGTAGCACAAATTAG[C/T]TCTGTGTCAGATATT | 84333 |
| rs541067775 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185211 | AGAAAACACCAGTGG[A/G]GTGGCTGGAGGCCTG | 84333 |
| rs541071291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233192 | AATGGGGCCATCCCA[A/G]TCTTACCACTGAGCT | 84333 |
| rs541094204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195853 | AATAATCCCAAAGAA[C/T]AGCATTTGTGACTGG | 84333 |
| rs541104753 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182345 | TTTAGTTTATAAGCA[C/T]AGAGGTGTTTATAAT | 84333 |
| rs541115132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247918 | AGCTGGGTGGTTCAT[A/C]TGGTCTTGGCTGGGC | 84333 |
| rs541154481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247213 | AAGGAAATTTTCAGG[A/G]AGGCAGGCAGTGTTA | 84333 |
| rs541161153 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268790 | GGGGTAGTTCCACTT[C/T]AGGCTAAGCCTGTTT | 84333 |
| rs541179005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240261 | GAATGCATTTAAGAA[A/G]ACAATAAGCAAAATA | 84333 |
| rs541185522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255101 | GGTTGTTTCCTCGGA[C/G]ACCCCACTTACAAGA | 84333 |
| rs541186934 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243470 | TTCTATGTACTTTTT[C/G]TCAGTAAGCTATTGG | 84333 |
| rs541199835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195071 | AATAGGAAGCAGCTG[A/G]GAGTGAGGATGGGGA | 84333 |
| rs541214769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227890 | CCTCTAAGATGTGCC[C/T]TACCACCTGCAGATT | 84333 |
| rs541231573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262452 | AAAGAAAAGAAAATT[A/G]AAGACCAGGACTAGT | 84333 |
| rs541237096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184498 | TTGCTTGGGTTATAA[C/T]GTACTCCTTTAGCTC | 84333 |
| rs541240923 | in-del | -/ACTG | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222133 | TTGTAAAGAGAAGAC[-/ACTG]ACATTCGTTGATAAG | 84333 |
| rs541260552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210101 | TATAAATGATTTGCA[A/G]CTTCATATGCCCCAC | 84333 |
| rs541276195 | snp | C/T | 0.000422268 | 0.0145243 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227346 | TCTTAGCTGCAGAAT[C/T]CTACTGGATGTCCAC | 84333 |
| rs541287123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171413 | AAACTTTGGGTTTGC[A/G]CAGTGGGGAGCCAAA | 84333 |
| rs541308691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262117 | CTTTCGAGTTCTGAT[A/G]GTAGCATCTAGAAAA | 84333 |
| rs541346028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226324 | AAAAAATGCTGTTAA[A/G]TGCAATGAGGAAGGA | 84333 |
| rs541348100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269030 | GCTTCTTGATCTTTA[A/G]TGCAAATTCAGATCA | 84333 |
| rs541389208 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278215 | CTTTCATATATAAAC[A/T]GTATTGTTTTTATCC | 84333 |
| rs541410335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221812 | TATTGAAGAGTTTTT[A/G]GTCTAACAAAGAAGG | 84333 |
| rs541421438 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249789 | CTGTAACAACAACAA[A/C]AAAAAAATGGCAAAG | 84333 |
| rs541507318 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280237 | TATAAATTTGTCACA[C/T]CTAGGTCAGCGATTA | 84333 |
| rs541509841 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206759 | GCACCTAAGCATGAT[C/T]CTGCCTCCATGCCTT | 84333 |
| rs541535755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229028 | TTTAATCATAGAATT[A/G]TTAAAATAAATGCTA | 84333 |
| rs541555868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187663 | GAGATCATGGGGAAA[A/G]TGTATTATATACACA | 84333 |
| rs541598849 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235010 | AATGGTGATAATAAA[A/G]TGACTTCTGATGATG | 84333 |
| rs541634090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164419 | TAACCGGTTGAGGAG[C/T]GCTGGTTCGCTGCAG | 84333 |
| rs541634580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201834 | AATCTGTTCTTGATG[A/G]CTTTTGATCATAGTG | 84333 |
| rs541670486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208772 | AAATCCTGAACTTTC[A/G]GGGAGCTGGCTTCAG | 84333 |
| rs541696344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170672 | AGTGGGAATGTCAAA[A/C]AGTACAGCTACTTTG | 84333 |
| rs541710896 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280951 | ATCTGTTGTTTCTTA[A/G]GCAATAAACTGAAAG | 84333 |
| rs541719674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205459 | TATATTCCAGCGTTC[A/G]TTCATAAACTGAGCC | 84333 |
| rs541731439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177649 | GCCTTGCAGTTCAAT[C/G]TCAGACTGCTGTGCT | 84333 |
| rs541738258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258538 | GGGATGATCAACCTA[C/T]ACCCTTATATTCTTC | 84333 |
| rs541741187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270463 | ATTCTCAATGTTATG[C/T]AAAGTCTGATGGACC | 84333 |
| rs541746281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168063 | GTCTAATTAATGGAG[A/G]TGATTATTGGTTTGG | 84333 |
| rs541791744 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246911 | TTGGAAATATGGAAC[G/T]TGAAATCAGCAGAGA | 84333 |
| rs541794048 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210399 | CATTACTCATTACTT[C/G]TAAATGCTAACCTGC | 84333 |
| rs541818436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203961 | ATTTAACACTTTTAT[G/T]CAGTTTTCATAAGTG | 84333 |
| rs541830437 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244170 | GTGTTGTGAGGTGAG[A/G]AGGTCAAGAGTGTGA | 84333 |
| rs541857692 | in-del | -/TGTC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180157 | TCTTCTTTTGAAATT[-/TGTC]TGTTCATGTTCTTTG | 84333 |
| rs541868388 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274524 | GCATTGGGCAGTCTT[C/T]TAGGCCTTCGAGGTT | 84333 |
| rs541885113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166872 | TGGTGTATAAAAGGC[C/T]CTTAATAAATGGTAA | 84333 |
| rs541890208 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185694 | CATAGTTCTGTGTGT[C/T]GGACTGAAGGCCCTA | 84333 |
| rs541947253 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218881 | GATCCGCCCACCTCG[G/T]CCTCCAGAAGTGCTA | 84333 |
| rs541954841 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274502 | ACAAATACCTATTGA[A/G]TATTATGCATTGGGC | 84333 |
| rs541970370 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161327 | AGAATACTTTCGCTG[C/G]ATTCACTTGCAGAGT | 84333 |
| rs541981603 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219569 | TTGTTTTCTCTTACT[C/T]ATTGTGATTGCTGCG | 84333 |
| rs541991056 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281320 | GCCACATTTTATAAA[C/T]GTAATGACTTTGCTC | 84333 |
| rs542025379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259246 | CTGGCACAGCCTATC[A/G]GACACTATTCTCCCC | 84333 |
| rs542028621 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236358 | CCAAGCCTGATATTT[G/T]GTTAGTGCTCATTAA | 84333 |
| rs542068010 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214482 | GACTATACTTAGCTA[C/T]CTCTGGGTTAGAGAA | 84333 |
| rs542091578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243057 | AGCTCCTCATGATAG[A/G]TTCTCAGTAAACACT | 84333 |
| rs542102899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267320 | ATTCTTACTCCCTTT[C/T]CATGCCTTATTGTTT | 84333 |
| rs542140203 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264136 | TCTAAGAGACATGAC[-/AG]AGATTTGGACTAAGA | 84333 |
| rs542168176 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167402 | CATAAAGAAAATACT[A/T]TGTGAATTCAGAGGA | 84333 |
| rs542177060 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275346 | TATTAAATTGCCAAA[A/T]TAAGAGGTGGGGAAA | 84333 |
| rs542199722 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249581 | AAGTTCAGCCTCCCA[A/G]TCTTGGTTTTCCCAT | 84333 |
| rs542213208 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265646 | ATTTATATTGAATGT[A/G]AACATTTGTGGAATT | 84333 |
| rs542262373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256994 | TTAAAATGTAAAACT[C/T]TTGTGTATCAAAGGA | 84333 |
| rs542273915 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194651 | AGTAAGCAGTTGGAT[A/T]TGAGTCTGGAGGTGA | 84333 |
| rs542274409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261970 | TGATATTAATCACAG[C/T]ATAGCTTTTCATGTG | 84333 |
| rs542303741 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170021 | AATACAGTGGAGAAA[A/G]GATAGTCTTTTCAGC | 84333 |
| rs542341175 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263809 | CAAATCACTGACCAG[G/T]CAAACCAGAGAAGCC | 84333 |
| rs542380085 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243892 | TGACTCACATTATAT[G/T]TCTATTGGTCATCAC | 84333 |
| rs542445844 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166499 | CTAGAATTAACCTTA[C/G]AACTTTTACAATAAT | 84333 |
| rs542477363 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195135 | GAGAAATAGTCCATC[A/G]GGAAATTGGGAGATT | 84333 |
| rs542500088 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213038 | AGCGCTGCTCGTCTG[C/T]ATCTTATTCTGAATA | 84333 |
| rs542507160 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186787 | GCCTCTAACATTCTT[G/T]CCACGTATAGGGAGC | 84333 |
| rs542536079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250302 | CAGTCATCAAAAAGG[A/G]TCTGGCCAGTCACTT | 84333 |
| rs542538794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194645 | ACACAGAGTAAGCAG[C/T]TGGATATGAGTCTGG | 84333 |
| rs542581958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201533 | TGTGTAAAAAAAATA[C/T]GTAAACAGAGTTATG | 84333 |
| rs542656913 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186321 | TGGGATCACCAGCAG[G/T]TTTCATAGCTCACTA | 84333 |
| rs542686865 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261005 | AAAAAATATATATAT[A/T]TTTATGCTTTTTGTG | 84333 |
| rs542703068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244714 | ATTCTGAATATATTT[C/T]GAAAGTAGATCCAGC | 84333 |
| rs542704077 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172732 | TGGCCGCAGACACAT[C/T]GTTATATCAACTAGA | 84333 |
| rs542705041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252575 | GAATTTATTGGACAG[A/G]GCATGTAATAAAGTG | 84333 |
| rs542740827 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193143 | AGGCATGTAGCCTTG[A/T]AGAGCAAAGAATGGC | 84333 |
| rs542742054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269004 | TGGGAGGAAAAAGGA[A/G]AAAAAAACATGCTTC | 84333 |
| rs542764037 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176550 | CTTTCAGGTACACCA[A/G]TCAGACATAGATTTG | 84333 |
| rs542764212 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169101 | ATAGGGTAACCATAC[A/G]TGCAATTGCCCAGGG | 84333 |
| rs542767883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216403 | AGAGTAAAGAGGTAC[A/G]TTATGGCTGGAGCAC | 84333 |
| rs542768907 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188191 | ATCTCACTAGGGAGT[A/G]CCAGACAGTGGGCGC | 84333 |
| rs542770978 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233358 | CCCCCAGACTCTTTC[C/T]TAACCCTGTTCAAGC | 84333 |
| rs542825607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176190 | AGTTTGGCTGGATAT[A/G]AAATTCTGGGTTGAA | 84333 |
| rs542836354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240338 | GTTATTACAGTGTTA[C/T]AATTGTAAGGTTTTT | 84333 |
| rs542870746 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276001 | CAGCTGTTAAAAATT[A/G]TGTAGCACCGTACCA | 84333 |
| rs542873602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268475 | TTGATTTGGCTGGAA[C/T]TGGCATCTTTGCGGG | 84333 |
| rs542962733 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283758 | ACACAACAGAGATCA[G/T]CAGTTTTAAATAGAG | 84333 |
| rs543044236 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242051 | CTGGTCTGTAATTCT[C/G]AGTAAGCCTTGTTCT | 84333 |
| rs543105522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249356 | ACATTACTGAGCAGA[C/T]AAAAGGCTTTTAGTG | 84333 |
| rs543109317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199601 | TTCCACATTAATGTA[C/T]GTGAAATTCAGCCAC | 84333 |
| rs543140034 | in-del | -/TTATTTTATTA | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218632 | CTTTTGTTATTATTC[-/TTATTTTATTA]TTATTATTGAGACAG | 84333 |
| rs543168494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173752 | TTCTTAAACTGTGAA[G/T]TTAGTATTTAGGACA | 84333 |
| rs543188230 | in-del | -/ACTTATTTAAAAAC | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197819 | CCTTTTCCATTGTGA[-/ACTTATTTAAAAAC]ACTTATTTAAAAACA | 84333 |
| rs543216456 | snp | A/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91220116 | GCAAACAGTAATGCT[A/T]CTTTACCACTCACCC | 84333 |
| rs543228846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224450 | AAGGGCACAAGATAA[C/T]AAAGAAGTCTCTGCT | 84333 |
| rs543230270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173016 | CTATTTGTGATCTTA[C/T]TAATCAATAATAAGT | 84333 |
| rs543261906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268059 | TCCATATTTAACCTT[A/G]TTGTTTTGAGATGTC | 84333 |
| rs543298681 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209256 | ATTGATGGAATCTTC[C/T]TTGTAGAAGAAGAGA | 84333 |
| rs543308136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231624 | GGGTTGGGCATGGCC[A/G]CAGGCACGTGGCGCA | 84333 |
| rs543329371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178667 | GTGCTGGGATTACAG[A/G]TGTGAGCCCCTGCAC | 84333 |
| rs543337402 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244010 | GCACTATTCTAGGTG[C/T]TTGAGGTCCATTCGC | 84333 |
| rs543353868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228008 | AATGCAGTGATAGGT[A/G]ACTTGAAACATGTAG | 84333 |
| rs543360341 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280401 | AAATCTCTTTAAATT[A/T]GGCTGGTTGCCTTGT | 84333 |
| rs543387335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217860 | GGCGCGATCTTGGCT[C/T]ACTGCAACCTCCACC | 84333 |
| rs543392776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184551 | TTCTGAATTCTACTT[C/T]TGTCATTTCAGCCAT | 84333 |
| rs543408554 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184175 | AAATTGGTTCCATTC[A/T]CCTCATCTCTTTCAG | 84333 |
| rs543426244 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188434 | CCTAGAAGCAGAAAA[C/T]ACAATTTTATGTATA | 84333 |
| rs543437006 | snp | G/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235119 | CTCTCCCTTGGCCAA[G/T]GTTTCCGAGTCATCT | 84333 |
| rs543442926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190478 | TTTCCCCATGTATAA[A/G]ACATGAGATTTGGTC | 84333 |
| rs543505252 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197104 | TAAAGCTGAGTGACA[A/C]ACTACTCCAAAACTT | 84333 |
| rs543507212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189904 | CCATGTGGAAACATA[C/T]GGAGATTTTAACTGC | 84333 |
| rs543528999 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183369 | TCTTTTTTAATCTTT[G/T]TTGTTTTAAAGTCTG | 84333 |
| rs543548585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189047 | AGTAAGATTAGCTAG[C/T]ATGTGGCTGCAGGAA | 84333 |
| rs543553953 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233937 | AGCATTACTAATCAA[A/T]GAAGACACTTAAAGA | 84333 |
| rs543569550 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212884 | TTGTAAAGATCTGAA[C/T]AAGTTGTGCTTCAGA | 84333 |
| rs543612536 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222264 | ATGGAATAGCAGAGG[A/T]TATCAACTTGGTTTG | 84333 |
| rs543620931 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220861 | GGGCGGGCTGGGGAG[C/G]TGCAGGGACGCCAGA | 84333 |
| rs543626376 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264916 | TTTTGGTTGTGGTAG[A/T]GGGGACACATAGGGT | 84333 |
| rs543640682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228809 | CATCCACCATCAGCA[A/G]CATCACCTGGGAACT | 84333 |
| rs543655271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203136 | TAAGCATTTTAAGGG[C/T]TAATTTAGGTCTCTA | 84333 |
| rs543661173 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281050 | CAAGGGAACTTAGAT[A/G]TAAAGAATGACTGTG | 84333 |
| rs543680404 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219835 | CACTTGTATGGCTGC[C/T]GGACTAGCGGTTGTT | 84333 |
| rs543720784 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218932 | CGTGCCAGGCCTATT[A/G]TTATTTTTTTAACCA | 84333 |
| rs543758282 | in-del | -/AGGGACTTTCC | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192916 | AAATTACATGGCAAA[-/AGGGACTTTCC]AGACCTAATTATGGT | 84333 |
| rs543779767 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259599 | AGTAACCAAAACAGC[A/G]TGGTACTGGTACCAA | 84333 |
| rs543783454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214682 | CTGGTAGAGGAGCAC[A/G]ACAAACAGATGAACG | 84333 |
| rs543790388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251026 | TTTTGGCTAAATACA[C/G]CTAGTCCTGAATCTT | 84333 |
| rs543794690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171471 | AAGGCCTTAGCCTAG[C/T]GATAGGATGAATCAC | 84333 |
| rs543817707 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257266 | ATGAGATATCATTTT[A/G]TACCTACTAGGATGG | 84333 |
| rs543844820 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219144 | TCTCCCTCATCCCAA[A/G]TCCATTCTGGCAACC | 84333 |
| rs543908623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221903 | CATTAAAAACTAGGG[A/G]AAGATTGCACTGAGA | 84333 |
| rs543934837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182885 | TTTACTCCAAAGTAA[C/T]TCAGGAGCAGGTTAT | 84333 |
| rs543986208 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274625 | TAAACAGGTTAAAAT[G/T]TATAGTGTTAGAAGA | 84333 |
| rs544004941 | in-del | -/ACAGCACATGCACACA | 0.00119737 | 0.0244387 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91161918 | CAGATCAGAGAGGGT[-/ACAGCACATGCACACA]ACTGACCCCCAGGTC | 84333 |
| rs544034882 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174414 | GGGGAGGCTGAGGCA[C/T]GAGAATCACTTGAAC | 84333 |
| rs544042320 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281274 | AGTATATTATTTCTT[A/T]ATACATTAAACATCT | 84333 |
| rs544056077 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202450 | AAAAATGAGGCAAAT[A/T]ATACAAAGTAGTTAA | 84333 |
| rs544058817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165829 | CCTTTAGAGGATAAA[C/T]TTTGATAAAGTTTAT | 84333 |
| rs544108144 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210156 | TCCTAGAGGGATGGG[C/T]CCCCACCTGTCTGCT | 84333 |
| rs544115268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215453 | ATTCCCTTGTTTAAC[A/G]TCATAGAAATAAAAA | 84333 |
| rs544115347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205991 | CACACCACTGCACTC[C/T]GACCTGGGTGACGGA | 84333 |
| rs544117397 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247010 | ATAGATAGATAGATA[-/G]ATAGATAGATAATCT | 84333 |
| rs544119054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165191 | TGTGATGTTAACCTA[C/T]AGCACAACAAGGGTT | 84333 |
| rs544119284 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172351 | TTGAACCCAGGAGGC[A/G]GAGGTTGTAGTAAGC | 84333 |
| rs544120933 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172006 | GGAAGTTGTTCCTTT[A/G]TTTTAAAGATGAGGA | 84333 |
| rs544130567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262875 | CTTTATTTTCTTCAC[G/T]CAAAATACCATGTAT | 84333 |
| rs544138336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199077 | GTATCTGTCTCTCCC[A/G]TTTTATTAAAAGCCT | 84333 |
| rs544155058 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252074 | TTTATAGATTTTCTT[G/T]GGTCTTTAAATGGTG | 84333 |
| rs544182272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168580 | GAAAATCAGAGACTA[A/G]GGATAGGGAGAAGGC | 84333 |
| rs544199484 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254172 | TTTATGTATGTGTTC[A/G]TTCTCTCTCTCTGTC | 84333 |
| rs544250197 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267453 | TTCACTGCTAAATCT[C/G]CAGCACCTAGGGCAG | 84333 |
| rs544259650 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239777 | TAGGAAATGTGGGCT[-/G]TATAGGCTTGTGGCC | 84333 |
| rs544272964 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189268 | CCCTCATGATTCTTG[A/G]TCATCTCCCTGTGTT | 84333 |
| rs544296068 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230814 | TTTGTGTAGAGACGG[G/T]GTTTGGCCATGTTGC | 84333 |
| rs544331120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204696 | ACATAACAAAAGTTC[C/T]CCACTGCCAACTCAT | 84333 |
| rs544349877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274599 | CACTAATGATGGTAA[A/C]AGACAAAAAATAAAC | 84333 |
| rs544356931 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257740 | TTTTCCATTTTGTAT[A/T]TTTGGACAGTGATAT | 84333 |
| rs544393407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199734 | TAGAGTCCAAAGAGG[A/C]CATAAAAATCCTTTA | 84333 |
| rs544409418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252696 | TTTTTGGGAAGTTCT[G/T]TTTCATAGAGTTCAT | 84333 |
| rs544413066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185724 | AGTGGAGTGGTTTCA[C/T]GAAGGGTTCTCCTGA | 84333 |
| rs544472261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260155 | AGTGGGCAAAGGGTA[C/T]GAACAGACACTTCTC | 84333 |
| rs544477541 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192213 | CCCCAGAGGCATTTG[G/T]GGAATTTTTTTAAAA | 84333 |
| rs544484132 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241119 | TACTCTTGTTGCCCA[G/T]GCTGGAGTGCAATGG | 84333 |
| rs544492683 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282146 | GTAAGTGCTTTCTCT[A/G]TATTCAAAATATTTC | 84333 |
| rs544509689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168963 | AAAAAAAAAAAGAAG[A/G]CTTGATAACATTTGT | 84333 |
| rs544546328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250865 | AGAACTTAATTTTAT[C/T]ATTTGAAAAGTATTT | 84333 |
| rs544632608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250387 | AGCTTAGAGGTATCT[C/T]ATCTGGAAATCGTCC | 84333 |
| rs544676192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202281 | TTAAGCCTATAGACT[C/T]TGAAGCAAAATAACC | 84333 |
| rs544692501 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254926 | GAGCTTTGTGGCATT[C/T]TAACTTGCTTTAGTT | 84333 |
| rs544721889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171220 | AAAATACAGATGTGG[C/T]ATGGAGGAAGAAAGA | 84333 |
| rs544841551 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91192507 | ATCTTTATTCTAATT[A/G]GCATTTTCAAACAGT | 84333 |
| rs544844705 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237116 | TCAAATTCTCTACTC[A/T]TTTTTTTATCTATAA | 84333 |
| rs544875971 | in-del | -/A | 0.234401 | 0.249513 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237742 | AGTGAGAATCCATCT[-/A]AAAAAAAAAAAAAAT | 84333 |
| rs544962129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200296 | CTGAAACTGAACCAG[A/G]ACTCTGGTATCCTGA | 84333 |
| rs544985391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195266 | AAAGTGCCTCTGAAC[A/G]TTAGCTATCACCTCC | 84333 |
| rs545011364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195747 | GCCTAAATCATATTT[C/T]TTTTAATGAAATTTA | 84333 |
| rs545026436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239503 | TTAGATAGTGTTGAT[C/T]TTGAGGAGAAAGAAG | 84333 |
| rs545046547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201607 | CCACCCACAGCCCCT[A/G]AGGGAATTCTGAGAA | 84333 |
| rs545086274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254001 | GGACATGGTCATTGT[A/G]CAGGCCAAAAGTTTG | 84333 |
| rs545086650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245770 | TTGTTTTTCATTGCT[C/T]TGACATTTTTCATTG | 84333 |
| rs545137785 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182349 | GTTTATAAGCATAGA[A/G]GTGTTTATAATATTC | 84333 |
| rs545140952 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208618 | CTCATTATCATGGAA[A/G]AGAATGATCTCTTGG | 84333 |
| rs545145668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194255 | AGATAACAACTTTGA[A/G]ATGGAGAGATGATCC | 84333 |
| rs545154720 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163802 | TGTACGCCCTCCGCG[A/C]CCCCTGCGGGCGCTG | 84333 |
| rs545158991 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262045 | ACATAGTAAGGAAAT[A/T]TCATTTCTCACCTGC | 84333 |
| rs545166774 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246429 | CCAGTTGGCTAGAGA[A/G]GGGAGACAGTGAGCA | 84333 |
| rs545188142 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234615 | AACTAATCATAGTCT[A/G]ATATTATTCAGTATT | 84333 |
| rs545197488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270389 | TCAATAGAAAAAAAA[A/G]AAAGAATCACTTAGT | 84333 |
| rs545201425 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278420 | GGAACACAACCAGAT[C/T]TTCAGCATGCAAATA | 84333 |
| rs545280219 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204147 | AAACTTTTAGAATTA[A/T]GAATATAATGTTTAA | 84333 |
| rs545294471 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177163 | TGTTGGAGTTTGCTG[C/G]AGGTCCACTTCAGAC | 84333 |
| rs545312226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241084 | TTATTTATTTATTTA[C/T]TTATTTTGAGGTGGA | 84333 |
| rs545354765 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232295 | ATAATGTCAGCAGTT[A/G]GAAATTTTTTTATTT | 84333 |
| rs545364915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277627 | CCATTCAGTTATTTT[A/G]TGTAATAGTCAAATC | 84333 |
| rs545378033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228956 | AAAGTTTAAGAAGCA[A/C]TGCTTTGGATCAGAC | 84333 |
| rs545400777 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284765 | GGAGGTAGCTAGAAA[A/C]CCCAGTCCTTCGGTG | 84333 |
| rs545429262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187472 | CAGAGATGAGGTAGA[A/G]GTCGCTATCAGAGAA | 84333 |
| rs545430845 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181121 | CAATTGTGCATGGGA[G/T]TTCATTTGTGATTTG | 84333 |
| rs545440342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236319 | AGTAACTGTCCATAC[C/T]ATAATCCATACAGAG | 84333 |
| rs545447623 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204464 | GAATGCAGACTCTAT[-/G]GATGACCAGGCCAGG | 84333 |
| rs545488210 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279879 | ATAAGATATTGTACA[A/G]CTCTAGCAAACATAC | 84333 |
| rs545500039 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281130 | ATCAAAATATGTATG[A/G]CCTTTTCTCTAGATT | 84333 |
| rs545504613 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235791 | GCCTGCTGTCATTCA[C/T]GTAAGATGTGACTTG | 84333 |
| rs545518191 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193914 | GATATGTGTTAAAGA[C/G]GAAGTCCATTTCTTT | 84333 |
| rs545531149 | snp | G/T | 0.00119737 | 0.0244387 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284687 | GAACACTGTGATGGT[G/T]TCTAGCTCGGCCCCA | 84333 |
| rs545587058 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195208 | CACTTAAAGTTTGTG[C/G]TTATGAATTTAAAGG | 84333 |
| rs545588118 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184725 | GAGGTTGCTGTTTTG[-/T]TTTTTTTTTCCTATT | 84333 |
| rs545589431 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224794 | CCTCCAACCAAGGCT[A/G]TAAGATATGAAATGG | 84333 |
| rs545597203 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217072 | AGTCTCTCGCTCTGT[A/C/T]GCCCAGGATGGAGTG | 84333 |
| rs545604081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170112 | GACACAGACTTCACC[C/T]GTGTCCCAAAAATTA | 84333 |
| rs545614411 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282503 | AAAAATTCAACTCTT[C/G]GTCTTGTTTCTCAGC | 84333 |
| rs545658430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216460 | GTAGAAGTGACAGGG[A/G]TTTGAAATGGCCTTA | 84333 |
| rs545667119 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176673 | ATCTTCCATCACTGA[A/T]ACCCTTTCTTCCAGT | 84333 |
| rs545689639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224685 | AGGGAAAATTAAGTA[C/T]AGAGGCCTTGAGATG | 84333 |
| rs545702668 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167501 | ATTGAGACGACTTCA[A/G]TCGGCAAAAATGTAG | 84333 |
| rs545709920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277178 | GAGCTGAATGGTTAC[A/G]GATTCCAACATTGAG | 84333 |
| rs545763004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181969 | TTGTACAATTTCAGA[A/G]CTCATTATTGGTCTG | 84333 |
| rs545766126 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273850 | GTGTATAATATAAAA[C/T]ATTTTATACATTTTA | 84333 |
| rs545772709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211061 | GGTCCAAAGCAAAAA[G/T]GAATGGTAATGGAGT | 84333 |
| rs545808538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273822 | TAGTGTATAATATAG[C/T]GTATATTATATAGTG | 84333 |
| rs545838971 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280499 | TATAGAATTCTTTTA[C/T]TTACTGATAATGCAT | 84333 |
| rs545854629 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247342 | TTCAATATGGAAGTT[A/G]TAGATGATTTTGAGA | 84333 |
| rs545875475 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233767 | TTTTCAAGACAAAAA[C/T]GTATATAAAATGAGC | 84333 |
| rs545894119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242973 | GAAATTACCACAAAG[A/G]AATTTTTTTAAAGAC | 84333 |
| rs545896738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172098 | GGCAGAGCTAGCTCT[C/T]GAAATAACTGGGATC | 84333 |
| rs545918992 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219058 | CAGAGGCGAAACCAC[A/T]GAACACTTAACTGCA | 84333 |
| rs545942198 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263695 | CTTAAAGATTTAGGG[A/G]TTGTTCGGTTCTTGC | 84333 |
| rs545942441 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184049 | TGTCTTGGGGATGTT[C/T]TTCTCATGGAGTATC | 84333 |
| rs545958997 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213550 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 84333 |
| rs545959500 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242168 | CAGATCTGGGTGGGT[C/G]CTCCTGGCATCTAGT | 84333 |
| rs545982125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221150 | GCTGGGACCCCACAG[A/G]GCTGTACCGCTGGGT | 84333 |
| rs546006904 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279230 | CTTAGGTATATGTCA[C/T]TGTGGCATGCAGAGG | 84333 |
| rs546013894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204727 | TATTGCCACGTCCTG[C/T]CCTTTTTCTCTCTCT | 84333 |
| rs546028931 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181442 | TTGTGCCAGTTTTCA[A/G]GGGGAATGCTTCCAT | 84333 |
| rs546067530 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274389 | TCTTGCCTTAAACAT[A/C]GACATATGAATAAAA | 84333 |
| rs546076661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212913 | GACTCATCTTCATGG[C/T]AGAAACTATGAAAAA | 84333 |
| rs546104701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211984 | TCCATTGTCAGGAGC[A/G]GTGTGATACTGGTTG | 84333 |
| rs546139010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255917 | ATACTTTAAATCATC[A/T]CTAGATTACTTGTAA | 84333 |
| rs546151278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240001 | GGCCAGCAAAGTCCA[C/T]TGTGACTCCCAGTTT | 84333 |
| rs546178289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165906 | GCAATATTTTCAGGA[C/T]TCAGTACTTCTGAAG | 84333 |
| rs546182527 | snp | G/T | 0.000399281 | 0.0141238 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91264439 | TTTAAAGTTGGATGT[G/T]CTGTGCAATGGTGAA | 84333 |
| rs546188978 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196439 | AAGCACAAAGCAGAG[C/T]TTTATGTCCCTTCTC | 84333 |
| rs546221265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263768 | AGCTTTGTGCAAAGT[A/G]GGAAGAGGATCCTGT | 84333 |
| rs546243271 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198711 | TTCAGTAGCATTGAA[A/T]CAATCCTGAGTTTAA | 84333 |
| rs546270527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192668 | TTTCTATCAGGAAAC[A/G]ACATACAATAAAACA | 84333 |
| rs546277992 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226335 | TTAAGTGCAATGAGG[A/C]AGGACAGACTATGAT | 84333 |
| rs546283556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91218111 | TTCTTACCAGACCTC[C/T]CTTAAGTTCTGGGAC | 84333 |
| rs546309271 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272135 | ATTAGCCCTTCCCTA[C/G]TACTTTACTTGAGTT | 84333 |
| rs546343718 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272781 | CTGTTTCAGACAAAC[-/AAAT]AAATAATAAAATAAT | 84333 |
| rs546360469 | snp | A/G | 0.000132571 | 0.00814051 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251419 | ACGAAATAATGGGCA[A/G]TCAGGGGACAATGTA | 84333 |
| rs546363809 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231787 | GAAAGCAGACCTGTT[A/C]GAAGGCCATTGCAGT | 84333 |
| rs546458939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275702 | TCGTGATCTGCCCGC[A/C]TCGGGCTCCCAAAGT | 84333 |
| rs546509971 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238833 | TGGGAAGAAGGCAAA[A/G]TATTCAATTGTACAT | 84333 |
| rs546513452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166771 | ACTTAACTTTTTGGA[A/G]CATTCTGTCATCTCT | 84333 |
| rs546519364 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256950 | CAACAAAAGAAAAGA[A/C]ATAGATAAATTGTAA | 84333 |
| rs546540958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176123 | GGTGAAAAAATCTCT[C/T]GGCATTTGCTTGTCT | 84333 |
| rs546616275 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282818 | ATATTGGTTGGTAGT[A/T]GGAACTTCAAAAATG | 84333 |
| rs546637857 | in-del | -/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279193 | TATTTAATGAGTGCA[-/T]TATTTCTCTTTTTAA | 84333 |
| rs546656028 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185002 | GAACAACACAGGGGA[A/C]CTGCTTACAGAAGCA | 84333 |
| rs546722755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168268 | TGTGGACTTGAGGGA[A/G]ATAGGAGGAGGTAGA | 84333 |
| rs546808495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191163 | TAATTTACAAATTAG[A/G]CACAGTAAAAGATTA | 84333 |
| rs546821572 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180870 | ATTTTAAAATAGTTT[C/T]TTCTAGTTCTGTGAA | 84333 |
| rs546887183 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283188 | CTTCCTAGTATAATA[C/T]AGTTTTCATAAATAA | 84333 |
| rs546917165 | in-del | -/A | 0.0770498 | 0.180522 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174203 | AAGCTTCATTGCATT[-/A]AAAAAAAAGTCTGTA | 84333 |
| rs546924574 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213357 | ATTTGTATATACGTA[G/T]GCATAAGTAACCTCT | 84333 |
| rs546985237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229263 | ATAGTCTGTGCCCTC[A/C]TAGAACTTAACATTC | 84333 |
| rs546985955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221380 | GTTAATCCCAACTTA[C/T]AGAGGAGGAAGCCGA | 84333 |
| rs547039515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191616 | GTTTTACCCCATAAG[C/T]TTTTTGGTTTCTTGG | 84333 |
| rs547066280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243264 | TTTAGCCAAAACTAG[G/T]TCACATGACAGCCAC | 84333 |
| rs547109875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236136 | TTTTGATTTTGATGC[C/T]AGGGACCAAATGTTA | 84333 |
| rs547145419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188464 | ATTAAAATTATGCTA[A/T]TTGCAATTTCTTAGG | 84333 |
| rs547156158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213737 | AGAGGTCCCCACCTC[A/G]GCCTCCCAAAGTACT | 84333 |
| rs547171958 | snp | C/G | 0.000181511 | 0.00952483 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240462 | ATGATGCGTTTTAAC[C/G]TAACATCTTCTTTCT | 84333 |
| rs547216980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222039 | AGTGATCCCTTCAGG[C/T]TGAAGAAAGTTGTTG | 84333 |
| rs547240143 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180464 | TCCAGGGTTTTTATA[C/T]TTTTTTGTTTTACAT | 84333 |
| rs547244701 | in-del | -/AGATA | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249910 | CTCTAGTAAAAATAC[-/AGATA]AGATAAGGCTAATTA | 84333 |
| rs547265692 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177747 | GCCATTTGCTAAGAC[C/T]GTCGGAAAAGTGCAG | 84333 |
| rs547271233 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266133 | CTGTTGAGGAATGGA[C/T]ATTATGATATTACAC | 84333 |
| rs547294675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263118 | TCTTTTTCAGTTCCC[C/T]CCTTATTTTGCTGCC | 84333 |
| rs547322331 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218329 | TCCTGCCTTTTTTTT[C/T]CCCCTGGTCCTATAT | 84333 |
| rs547323496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230329 | AGGTATGTTTAAGAG[G/T]CTAGCACAAGGGTTC | 84333 |
| rs547332453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271502 | TCAAAAACAACCACC[A/T]TTTTTTTGGAAAGTG | 84333 |
| rs547334147 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278456 | ATTGTCTATCTCTAA[A/G]TTGTCAGTTGCATTC | 84333 |
| rs547393360 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260439 | TAGAAATACCATTTG[A/G]CCCAGCCATCCCATT | 84333 |
| rs547461154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216493 | AAGTGTTTGGGCATT[A/G]TTCTAGAAATGAGGT | 84333 |
| rs547478577 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210833 | TCTCAAAAATGTGTA[G/T]GTATTCTGGAGATAG | 84333 |
| rs547482674 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265638 | CAAAACATATTTATA[C/T]TGAATGTAAACATTT | 84333 |
| rs547497103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224025 | TAATGTTATACCAGT[A/G]GTTTTAAATGAATGC | 84333 |
| rs547512419 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232816 | AGGAGGATATGTTGG[A/G]GGTTTGAAGAGAGAG | 84333 |
| rs547515125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207839 | GCAGAAACATTACAT[A/G]GGTGATAATGTATCC | 84333 |
| rs547617955 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209817 | CGAAGAAAGGAATTG[G/T]AGGATATCTGCTGAT | 84333 |
| rs547633685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247053 | GTTTTGAAGCCACAA[A/C]AGCAGATGAAATCCA | 84333 |
| rs547682043 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217278 | GACCTTGTGACCACC[C/T]GCCTCGGCCTCCCGA | 84333 |
| rs547688482 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241218 | TAGCTGGGATTACAG[A/G]CATGCGCCACCACAT | 84333 |
| rs547707065 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202359 | AATTTTTGTGAACCT[A/C]ATGATTTCAGTAAAA | 84333 |
| rs547712258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183624 | TGATGTTAGCTGATT[A/G]TTTTGCAGACATGTT | 84333 |
| rs547713570 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256886 | TTAAGATATTCCCAT[G/T]ACCTTGGATTTGGCA | 84333 |
| rs547720564 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91162536 | ACGATTCGAAGTCTC[C/T]GGCCTGAGAAGTTTC | 84333 |
| rs547725637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226612 | TCTCACCTCAAACCA[C/G]ATAGGTTGGTGCTTC | 84333 |
| rs547726951 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272687 | TTGAGGCGGGAGGGT[C/T]GCTTGAGCCCAGGAA | 84333 |
| rs547745822 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234638 | TCAGTATTGTGATGC[C/T]GATTCTCCTTATCAT | 84333 |
| rs547759653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163938 | TTTTCGCTGCCACCT[C/G]TCCTGGGTCTACAGG | 84333 |
| rs547796915 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208053 | GAGAGACACTGTACA[A/G]CTATGTAAATATCCT | 84333 |
| rs547823191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170222 | GGGTTTGGTGATGAC[C/T]TTTTAGATATGACAT | 84333 |
| rs547825833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268608 | GCCCCGTGGAGTCTT[C/T]CATCTCTGACAAGGG | 84333 |
| rs547863628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204351 | AAAAAAAACCCTTAC[A/G]TTAGTCTTTCCTCCT | 84333 |
| rs547889206 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176318 | TTTGTGGGTAACCCA[A/G]CCTTTCTCTCTGACT | 84333 |
| rs547891694 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220225 | GTAACAAGTTTGTCA[A/G]TCATTTTCAGATAAG | 84333 |
| rs547896486 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244785 | AAAAGAGTTGAACAT[A/G]ACTTTAAGATTTCTG | 84333 |
| rs547929476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239948 | GTGCTCCATGGAATT[A/G]TAGTACCTATGAGCA | 84333 |
| rs547951742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175972 | TGTTAGCTGGTTATT[C/T]TGCTCGTTAGTTGAT | 84333 |
| rs547952010 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181217 | ATTTTGTATTCTGAG[G/T]TTTGCTGAAGTTATT | 84333 |
| rs547990707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246075 | AGACAAATCAAGGGT[A/G]CATGTAAGGAAGTGA | 84333 |
| rs547999593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251182 | TCTTCTTCAAAAACT[A/G]TTAGGAAATTTTTTA | 84333 |
| rs548001948 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194755 | TAAGTAGAGATAGAG[A/C]AGAGAAGAGGATCAA | 84333 |
| rs548008649 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232716 | TAGGTGAATAGGTGT[A/G]GTGGTAAAAGTTCTC | 84333 |
| rs548034988 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236701 | AAGTGAGTTTTGTAG[G/T]GATGAGAAGTTTTTT | 84333 |
| rs548060078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250582 | GCTCTAGTTTCAGTA[C/T]TGTTCCCTCAGGCCT | 84333 |
| rs548104013 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243447 | ACACATGTAGCAAAA[A/C]ATTTACCTTCTATGT | 84333 |
| rs548120057 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249792 | TAACAACAACAACAA[A/C]AAAATGGCAAAGAAG | 84333 |
| rs548120176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257958 | AGGAAATGTGATACT[A/G]TTCAGTCATAAACTG | 84333 |
| rs548125057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200139 | GCATTTTTGCCTCAC[G/T]GTGGGAGAGGGCCCA | 84333 |
| rs548186681 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207300 | TTTTGATCTTACACA[-/T]TTTTTTCTACTTTCA | 84333 |
| rs548189877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265983 | TGGTAAATTAACAAC[C/T]TGCCTTTCTGTAACA | 84333 |
| rs548207168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254116 | TTTATCTCCCATTAA[A/G]CCCATTAGTAAATCG | 84333 |
| rs548229567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196058 | TCCCCTACTGGTCAA[C/G]TGTTGCCCCATGGGG | 84333 |
| rs548237022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203284 | TGCATGTCTTTTTAG[C/T]GTTTTCTTGGAGCAC | 84333 |
| rs548244028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241793 | ATTTGCAAATCTTAC[A/T]TTTCAGCCTTTTGTT | 84333 |
| rs548262730 | snp | A/G | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183910 | CTCTTCTGGCTTGTA[A/G]GGTTTCTGCTGAGAG | 84333 |
| rs548281883 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212561 | TGTATACTCAGAGGC[C/T]ACTCTACTGACAGGA | 84333 |
| rs548303623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237038 | ACACATACATTGGTT[A/G]ACAAAATGGATTCAA | 84333 |
| rs548318933 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244116 | GTAATTTATATGGTA[C/T]GTTAGAAAGTGAAAA | 84333 |
| rs548339641 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219398 | TACCAAGTCTTTTTT[A/G]TATATTGTGGTATAT | 84333 |
| rs548340088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232007 | GAATGATCAGCATAT[A/G]CATCATTATTTAAAC | 84333 |
| rs548341107 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177748 | CCATTTGCTAAGACC[A/G]TCGGAAAAGTGCAGT | 84333 |
| rs548390734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270267 | GCAACCTCTGCCAGT[C/G]CAGCACCTAAAGTTA | 84333 |
| rs548393649 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198672 | CCTGATTAGTGGCAG[C/G]ACCATGGGAATCTCC | 84333 |
| rs548415932 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233964 | AAGACATGAGAGAAA[A/C]GATTATTATTGTTTT | 84333 |
| rs548500609 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177988 | AAATGCAGAAATCAT[C/T]CATATTCTGCGTCGC | 84333 |
| rs548563197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184337 | CTGAGATTCCTCTAC[A/G]TGGTCTATTCTGATA | 84333 |
| rs548580381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241499 | CTCAAATGCCACTTC[C/T]CAGCTACAGGCCGTA | 84333 |
| rs548591836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235217 | ATTAATTGGTCTGGG[A/G]TGGAGCCTGTGAGTC | 84333 |
| rs548628821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190143 | GAGGACCCACTTCCT[A/G]GTTTCCAGGTGGCAC | 84333 |
| rs548661307 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260384 | AAACTAGTTCAACCA[-/T]TGTGGAAGTCGATGT | 84333 |
| rs548682999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248384 | AAGAGTATGGTATAG[C/T]AGATGTGCTAAAATT | 84333 |
| rs548683062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255978 | AGTTGTTAATACTAT[A/G]TTATTTTTATTATTG | 84333 |
| rs548686276 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211303 | AGTTGTTAAGTTAAA[G/T]AATATTCTGGAAAGT | 84333 |
| rs548693663 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199319 | GTGGGAAGGCAGCAA[C/G]GGGGGCAGAAAAGGA | 84333 |
| rs548743303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255504 | CTTAGTTGAATATTG[A/G]TGGTATGCCCCCAAA | 84333 |
| rs548792399 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224128 | AATAAAAAATAGAAT[A/C]ATCTGGGAAGCTATT | 84333 |
| rs548794034 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162201 | TGAAAAATGGAGGCC[C/T]AGCTATTGAGGACTC | 84333 |
| rs548807076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178551 | CAATTCACCACACCC[A/G]GCTAATTTTTAAAAT | 84333 |
| rs548829007 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206885 | CCTAACTAAATCCTT[C/G]TCTCACCTCCCTATT | 84333 |
| rs548831089 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187731 | TATTTACTTCTTACT[A/C]TCTGTGTGTATATGT | 84333 |
| rs548852876 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261852 | AAGTAATCACATTTC[C/T]GTGAAATGCAGAAGT | 84333 |
| rs548859014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242304 | CTGAATAAAGCAAAC[A/G]TTTTCTCTCAAGTAA | 84333 |
| rs548931206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232634 | TCTGGCATATAGGGC[A/C]GAGGATGGCTTTAGA | 84333 |
| rs548950333 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274791 | GGCAACACACTGCAA[A/G]GGCCCTGAGAATTGA | 84333 |
| rs548952327 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282997 | TAAATACACCAGAGA[C/T]TCAAACCCTTTCAAG | 84333 |
| rs548984310 | in-del | -/T | 0.00119737 | 0.0244387 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284703 | TCTAGCTCGGCCCCA[-/T]TGTGATTTTGATGCC | 84333 |
| rs549073433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230938 | TATTTATTTTAGAGA[C/T]GGGATCTTACCATGT | 84333 |
| rs549078626 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252816 | AAAGTCCACTTCTCT[G/T]CATGATTTCTCATAT | 84333 |
| rs549183430 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168755 | AACATAGTGAAACCC[A/C]GTCTCTACTAAAAAT | 84333 |
| rs549186854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277295 | ATGAAAGAATACAAA[A/G]TTCTCTATACCGTAT | 84333 |
| rs549245517 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185742 | AGGGTTCTCCTGACC[C/T]GGGAGTTGCAAAGAT | 84333 |
| rs549246672 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168305 | GCTGAGAAGAAAGAA[A/G]CAGGAGGGGGATGAG | 84333 |
| rs549246793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175715 | GAAAATAAAAATATC[A/G]GAGACTAGGATTGCA | 84333 |
| rs549247919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231989 | TTGGACTTATGACTC[C/T]TGGAATGATCAGCAT | 84333 |
| rs549272852 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276797 | CAATAGAATCAGGAA[A/T]CAAACGCAAAACTAG | 84333 |
| rs549308280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174984 | AGTATAACAGAGGAA[G/T]TTGATACCTAAGTGC | 84333 |
| rs549314542 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187827 | TTGCTAATTATTTAG[A/G]AAAAACTTAGAGTAT | 84333 |
| rs549362765 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222172 | CCAACCAAGTGTCAC[A/G]AAATAAAATGTGCCT | 84333 |
| rs549426442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230460 | TTTTTACCAGTATTA[C/T]GTCAAAAATTTAAAG | 84333 |
| rs549448314 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237294 | CATTAAGTGTTAACT[A/C]TGATAATAACAGTAT | 84333 |
| rs549509568 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161586 | CCTTGGCTTAAGGAA[C/T]ATCTCTGTAGAATTC | 84333 |
| rs549520612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177759 | GACCGTCGGAAAAGT[A/G]CAGTATTAGGGTGGG | 84333 |
| rs549527182 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192335 | ATAGTCTAAAAATGA[A/C]GCATTCTTATTTTCA | 84333 |
| rs549529899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206211 | ACAGGGTAGCTCCTG[C/T]CGTCAAGGAGCTGAA | 84333 |
| rs549542931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226736 | CATCAAAAGGAAATA[A/G]GAGGTAGAGATGGTG | 84333 |
| rs549556539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259799 | TGGATCCCTTCCTTA[C/T]ACCTTATACAAAAAT | 84333 |
| rs549583375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166181 | TCATAAAGAGCTTAA[A/G]TGGTTGGAAGTTCCT | 84333 |
| rs549601007 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217235 | AAAAGGAGTTTCACC[A/G]TGTTAGCCAGGATGG | 84333 |
| rs549647085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165705 | AAGAGTACATAAAAG[C/G]AGTTATTTAAAATTA | 84333 |
| rs549688178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203335 | CATGTAATTCTCTAG[A/G]AAAGTGTTCCTTTGT | 84333 |
| rs549700932 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222785 | ACATCCTACTGGGAA[C/T]GACACACCAGCTCCT | 84333 |
| rs549710256 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171848 | ATGGAGGTAGAAGAT[C/T]ATTGGTCTTCGGGAA | 84333 |
| rs549768742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263882 | TTTGTATCAAATTAG[A/G]TATTGGTAATTACTG | 84333 |
| rs549800787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217134 | CACCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 84333 |
| rs549845977 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267690 | CAGTTGAGTGACATG[A/G]ACGAATGCAGCAGTA | 84333 |
| rs549866015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216600 | TTTGGCAGAAAAGAG[C/T]TGTAGGAAGACTACT | 84333 |
| rs549883015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208951 | TTCTTGCTCTACAGG[A/G]GTGTGAGCTTTCTGC | 84333 |
| rs549883592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183008 | ATTTCAGTTCTTTTG[C/T]TTTTGCTGAAGAGTG | 84333 |
| rs549909480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262167 | TGGTGGCTTATGCCT[A/G]TAATCCCAGCACTTG | 84333 |
| rs549913239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241318 | AGGTGATCTGCCTGC[C/T]TCGGCCTCCCAAAGT | 84333 |
| rs549937264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189297 | TTCTGTCCCCATTTT[C/T]CCATGCCATGAAAGG | 84333 |
| rs549976401 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240563 | AGTTCATGAGACAAA[C/T]CCATTAGAAATGTTG | 84333 |
| rs550040648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211487 | CAGGGGCCATACTTG[C/T]CCCTGCCTTCAGGTC | 84333 |
| rs550090716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178279 | GCAGTTTAAACATTT[A/G]AGAATATGCAATTAA | 84333 |
| rs550101437 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219284 | GAATACTGATTAACC[G/T]CACTTGTGATAGGTC | 84333 |
| rs550103585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210575 | GCACAGGGCCAGCAG[A/C]ACCTGTGGTCTGTGG | 84333 |
| rs550114398 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211410 | TCTTACTGTATTGCT[A/G]TAGAGGTTATTGTAA | 84333 |
| rs550134100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201070 | AAAGTTTTATAAAAG[C/T]GAGAAGAGCTGCCCA | 84333 |
| rs550150026 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253595 | AATCAAATAAGTTCA[A/G]AAGCTTCGCGTCATC | 84333 |
| rs550164262 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207461 | ACAATTTTCAATGAA[C/G]CATTTAAGAATAGTT | 84333 |
| rs550211754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261756 | ATTTTTTATCTGAGA[G/T]CTTTGAGATCCATTA | 84333 |
| rs550247391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254341 | CCTTTTTGGCGTGTT[C/T]TTTCCTCTTCCACCA | 84333 |
| rs550248115 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256222 | TGGGCACTATATGAA[A/C]ATACAAGAATGATCT | 84333 |
| rs550264305 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213224 | ATTCTATTTGTGTTT[C/T]AGAAAATGTAAGAGA | 84333 |
| rs550277435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170251 | ATCATAGGCACAGCC[A/G]TGAAAGAATTGATAA | 84333 |
| rs550289678 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198039 | GTGCCCTCACAGAGC[G/T]TACATTCTAATGGGT | 84333 |
| rs550292860 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252004 | GTTTTCCTCTGCCTC[C/T]GCTAATTGAATCTTT | 84333 |
| rs550311957 | snp | A/G/T | 0.00835141 | 0.0640778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202545 | GTGAGTAGTCATTGC[A/G/T]TAGTAGTCATCGTTA | 84333 |
| rs550346915 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205156 | TTTATCTCTCTCACT[A/G]GAGTCACTAAGTTGG | 84333 |
| rs550376438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244775 | TGGGATAAAGAAAAG[A/T]GTTGAACATGACTTT | 84333 |
| rs550395131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237480 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATTCCAGC | 84333 |
| rs550416985 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225053 | CGCATTTCTATCTAT[A/G]TGCTACAAATTTTAT | 84333 |
| rs550459077 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244343 | AGCCAGTGCAGAGTG[A/C]CTAAGTCAGGAGTGT | 84333 |
| rs550473780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230523 | ATATGTATTCATATA[C/T]ACATATATGAATATA | 84333 |
| rs550513687 | in-del | -/A/AA | 0.153665 | 0.230694 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276105 | ATGATTCCAGTTTTG[-/A/AA]AAAAAAAAAAACGAA | 84333 |
| rs550525577 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193409 | CATTAGTGGTAATTT[C/G]TCATGGCAGCAATAG | 84333 |
| rs550651749 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236087 | CTGTCTTAAACAAAG[A/C]AATAATAATAAATTA | 84333 |
| rs550679233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167649 | TGCATGGGGAGGGGA[A/G]ATTAGGACTATATTG | 84333 |
| rs550696514 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174137 | CTGTAATTGGGCTAC[A/C]ACTTGGGCCACTGTA | 84333 |
| rs550730634 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221273 | GCCTTAGGATCTTAG[G/T]ACCACCCCAGGTCGG | 84333 |
| rs550790058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220477 | CGTGTAGCACAGGGA[A/G]CCAGGGCGGCAGCTG | 84333 |
| rs550790781 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185989 | TGTCTTTGAGAGCCA[C/T]GCACCCTAGCTGCTT | 84333 |
| rs550793029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193267 | CTCCAAAAGGAATAC[A/G]TCCCTGCTGTCACTT | 84333 |
| rs550813952 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239123 | CTCTATCTTATTTTT[-/G]GGGGGGCGGAGGGGG | 84333 |
| rs550835056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185417 | CCCAGGAACTGTGTC[A/G]CAGCTCCATGCAACA | 84333 |
| rs550872796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198707 | CCTATTCAGTAGCAT[C/T]GAATCAATCCTGAGT | 84333 |
| rs550901775 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173297 | CTTTTCTCTTGTTAT[C/G]CCTGTGATAGTGTGT | 84333 |
| rs550972459 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169566 | AAATACTTAGATATA[C/T]ATCTAACAAAATATG | 84333 |
| rs551018832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187193 | GACCTATCTATAGTG[A/T]TTCGGATTTAATTGT | 84333 |
| rs551070178 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279968 | TCTGTTCCTTCTATC[-/T]TTTTTTGAGTCAAAA | 84333 |
| rs551070430 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249628 | CAATTATACATGATT[A/C]AGGTGGATGAGATCT | 84333 |
| rs551072321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241844 | TGGGATAATTTGTCT[A/G]CAGGTAAATGTCTAG | 84333 |
| rs551120292 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236544 | AACCTTAGACTAGGA[C/T]CTTTTTAACATCATT | 84333 |
| rs551149260 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194716 | TGGTTTAAAGCCACA[A/G]ACTGAATGAGATCAC | 84333 |
| rs551164965 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179334 | TTTGTTTCTTTTTTA[A/T]AAAAAAATTAATCTT | 84333 |
| rs551184723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229237 | GCAACACAGCAATAA[A/G]TAGAACAGGCATAGT | 84333 |
| rs551208214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274037 | ATTACCTAGATTCAT[C/G]AATTAACATTTTGCC | 84333 |
| rs551245616 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236501 | CTGTTGAGAATGAAG[A/G]CTCTACTTGGTCTGT | 84333 |
| rs551248790 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273270 | TAGATGTTTCAGCTG[A/C]TTTAGCCTCATGGCT | 84333 |
| rs551298571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177289 | CTCAGAGGGGTACCC[G/T]GCTGTGTGAGGCGTC | 84333 |
| rs551341422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277910 | CTGATCTGTCTTGTT[C/T]GCCTCCTAGGGTTAC | 84333 |
| rs551367311 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232717 | AGGTGAATAGGTGTG[G/T]TGGTAAAAGTTCTCT | 84333 |
| rs551391701 | in-del | -/TGCT | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186926 | AACTTGCCCACACAA[-/TGCT]TGCAAGACCAGTGAA | 84333 |
| rs551472849 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194156 | AGGCAGAATAATGGC[C/T]TCTAAAGATGTTCAT | 84333 |
| rs551615105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180061 | GGTGTGAGATGGTAT[C/T]TCATTGTGGTTTTGA | 84333 |
| rs551618437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270595 | GGACTGACTGCTAGA[A/G]AAAAAAATTACTAAA | 84333 |
| rs551643547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260380 | CTGTAAACTAGTTCA[A/G]CCATTGTGGAAGTCG | 84333 |
| rs551645777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253399 | AAAGGACTTTTAAGT[C/T]CTCATTTCCAGCCCT | 84333 |
| rs551655187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269800 | TCTTCTGTGAACTTA[C/T]CTATCATATTCATTC | 84333 |
| rs551663787 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224988 | TTAATTTTTGGATTC[A/C]TCCAGCAAAAACTGT | 84333 |
| rs551694680 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277387 | TGATTCCATAAAAGT[A/G]GCTCCTCAAATTTCA | 84333 |
| rs551709022 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233437 | AAAAAAAAATAAAGT[G/T]TTGTACTCGGTAGAA | 84333 |
| rs551712975 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277246 | AATGGTCATTTTCAG[G/T]ATTGTTAAATCTCAG | 84333 |
| rs551772252 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264080 | AGGTTTCTGCAGGTT[C/G]TTGTTCAGAAAGGGG | 84333 |
| rs551779154 | snp | C/G | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221237 | TTGCTTCCCTTAACT[C/G]TCTTGGTCACAGGGC | 84333 |
| rs551782675 | snp | A/G | 0.000171259 | 0.00925204 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223035 | TTATATGTACATTTT[A/G]TTCTTTTAAAATTGC | 84333 |
| rs551827605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180777 | ATAGTTTGAAGTTGG[A/G]TAGCATGATGCCTCC | 84333 |
| rs551844144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230978 | TGCTCTTGAACTCCT[G/T]GACTCAAGCAATCCT | 84333 |
| rs551847683 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199300 | AGGGAATGCCCTTTG[A/G]AGGGTGGGAAGGCAG | 84333 |
| rs551889743 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283047 | GATTTACCTGACAAA[C/G]CTAGTTGAGTAGCAT | 84333 |
| rs551897424 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172441 | AAAAAAATGCCCTCT[A/C]GGGCAGAAGAAGTAA | 84333 |
| rs551924687 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197195 | AGTCTGGTCAGCAGC[A/G]TAGCCTGTCTCCATT | 84333 |
| rs551926213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200752 | TCACTTTGTGGTCAT[C/T]GGACAGTGGGCAAAT | 84333 |
| rs551940105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272432 | GTAGGATTGCTTGAG[G/T]CCAGGAGTTTGAGAC | 84333 |
| rs551941560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186366 | GAATTCTTAGGTGAT[C/T]AGCAAGCAAGAGATG | 84333 |
| rs551993351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227537 | TCAAATCTGTCCCTT[C/T]AGTTTCATCCCTCTG | 84333 |
| rs552009414 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170604 | AATTCAGAACACTGA[C/T]AACAGCAAATGCTGA | 84333 |
| rs552015637 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229982 | GTTCATTTTGATGAC[-/TT]TTTTTAAATAAGAAA | 84333 |
| rs552026304 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279576 | TTAGTCTGCAAGTCA[A/C]AGAAAGTCTTGTTAC | 84333 |
| rs552046147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207102 | GGAATTAGGAGGTGC[A/G]TTTTCTAAGAAGGGG | 84333 |
| rs552080522 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217632 | GGGCCAATACTCAAA[C/T]GCAGCAGTTATCACT | 84333 |
| rs552081057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197314 | GACTCCTGGGCTCCT[C/T]GGGCACGTCCCTCTC | 84333 |
| rs552082001 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265324 | GACACTAAGGAATAT[A/G]GCAGTAATGCTATCA | 84333 |
| rs552094889 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190526 | CATTTTGAATCATCT[A/G]TGATTCTGGAAAGTT | 84333 |
| rs552098397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256389 | GAATTGAGATTATTC[A/G]GTCTGAGAAACAGAA | 84333 |
| rs552107547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206248 | AACTCGGAGAAAAAG[C/T]AGGTTTGATTAAAGG | 84333 |
| rs552107919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249683 | GATTATCATTTTATT[C/T]GTTCAACTTAACTGT | 84333 |
| rs552109363 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215910 | GATTTTAATTAATAA[A/T]CCAAGAAGGCAGGGA | 84333 |
| rs552166212 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272948 | AGTTGGGACAAATGA[A/T]TGTATGTTAAGCATT | 84333 |
| rs552184900 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211599 | TCCAGCAGTTCTTCT[A/G]TCTTCATAGGAAGAG | 84333 |
| rs552236403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166301 | AATAATGTCTTATTC[A/G]CCTTTGTATCCTCCC | 84333 |
| rs552259036 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189886 | TTGAAAGGTTTTCCT[A/C]AACCATGTGGAAACA | 84333 |
| rs552261001 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205413 | AAAACACACCCATAG[A/G]CCTAGATATTAGTAT | 84333 |
| rs552272884 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264370 | TGAAATTTCAAAAAA[G/T]ATGCAAAATACTTTT | 84333 |
| rs552297750 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236671 | ATGGACTTCAAATTA[C/T]AAACTAAGAATTAGA | 84333 |
| rs552310435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255382 | CATATGTAGAGTTGT[A/G]TGCATGTTCAGGAAG | 84333 |
| rs552358623 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226904 | CAGTAGGCCAGGGAC[A/G]TTTGATAAATAGATA | 84333 |
| rs552390557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241731 | TCTCTGGAACCTTTC[A/G]TAACTCTCTTATCTG | 84333 |
| rs552409302 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238011 | ACACTAAAAAAGAAA[C/T]AAGTAAAATTAATTT | 84333 |
| rs552425022 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181088 | GCTGTATTTTTAGCT[A/G]TTTTATTATTTTTAT | 84333 |
| rs552443650 | in-del | -/TAAT | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258254 | ATAGTATAAAAACTA[-/TAAT]TAATCTGTGAAAGAT | 84333 |
| rs552450253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241366 | AGCCACCACACCTGG[C/T]CTAATCATATATTTT | 84333 |
| rs552457467 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204269 | GGGATTCCAGCATTG[A/G]ATAATAAATTGAACT | 84333 |
| rs552482987 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200416 | GGTATAGAAAGAACA[G/T]GGGATGTAGCCCCTT | 84333 |
| rs552493529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173071 | TAGGAAAAAAATTAC[A/G]TCTGGTCTATCTCCT | 84333 |
| rs552520579 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203506 | TTTTATTTCTAAATT[A/G]GCAATCTTATTTCAG | 84333 |
| rs552526300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195527 | AGGGTCTCTGTCACT[C/T]AGACGGGAGTGCAGT | 84333 |
| rs552549159 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194010 | TAGCTAGAAAAATGG[A/G]GTTGTTATCAACCAA | 84333 |
| rs552563917 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247427 | TTATTTTCACATTTT[G/T]TTCCAGTTAGAAGGA | 84333 |
| rs552614851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196040 | TTTGTCCACTTTCTC[A/G]CATCCCCTACTGGTC | 84333 |
| rs552636015 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235017 | ATAATAAAGTGACTT[A/C]TGATGATGGTTTAGC | 84333 |
| rs552677417 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91192345 | AATGAAGCATTCTTA[-/T]TTTCATAAAAACAAT | 84333 |
| rs552696621 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173944 | TTTAGAAGTAAAACA[A/G]CTAAGACTCCAGTAT | 84333 |
| rs552733594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262234 | AGTTTGAGACCAACC[A/T]GGCCAACATGGTAAA | 84333 |
| rs552804094 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215942 | TATGCCTTAACACAT[C/T]CTTTGTAAGGATCCC | 84333 |
| rs552833728 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243022 | AAAACAAGATATCCT[A/G]TATCTTTGACAGCTG | 84333 |
| rs552846618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230587 | AAATGATCAATGTTA[C/T]ATTTTAGTTTATATT | 84333 |
| rs552874059 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237059 | ATGGATTCAAATATT[C/G]GTTTTAACCACTAAC | 84333 |
| rs552888014 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249615 | ATCATAGGATTGTCA[A/G]TTATACATGATTAAG | 84333 |
| rs552926350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185657 | CTGTGTATGCCTGAG[C/T]GGCTGCTCTGCCAAG | 84333 |
| rs552990710 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221733 | ACAGTTAAAAAAAAA[A/G]AAAAACCTGAGACAG | 84333 |
| rs552999592 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281910 | AACAAATAGCCTTCC[A/T]CTGCATGAAAAGTGA | 84333 |
| rs553016281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243846 | AAGTACTGGTGTTAA[C/T]GTTCCTACTAAAAAT | 84333 |
| rs553077661 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250734 | ATGCCATTGAGATAT[A/C]TTTAATGGAGTTGTA | 84333 |
| rs553095207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172741 | ACACATTGTTATATC[A/G]ACTAGAAGTGAATTA | 84333 |
| rs553129779 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219550 | TGAAGTCATTTGACC[C/T]CACTTGTTTTCTCTT | 84333 |
| rs553135529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205233 | GCAATTGTTCCCAAA[C/T]ATTTTGAAAGGCTAT | 84333 |
| rs553160654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272678 | CTAAGGAGGTTGAGG[C/T]GGGAGGGTCGCTTGA | 84333 |
| rs553198641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204610 | TGTTTGGTTCTCAAG[C/T]CTTGGAAGATGATAA | 84333 |
| rs553199604 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280086 | TTCTTGGAATGGCTC[A/G]CAAGCAGAATTTAAA | 84333 |
| rs553204424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275127 | AAAATATATTTGCAA[C/T]GTATGATAGAAAAAG | 84333 |
| rs553267201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174606 | AATAGATTAAAAATA[G/T]ATTAAAAGTCTTGTG | 84333 |
| rs553271454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180176 | TGTTCATGTTCTTTG[C/T]CCACTTTTTAATGGA | 84333 |
| rs553306429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220606 | CGCCGGTTGGAAGTG[A/G]GTGGAGTTGCCCTTG | 84333 |
| rs553314745 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273419 | GTCCTTAAACCATGA[C/T]CCAAAGTATTAGAGA | 84333 |
| rs553334620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179796 | GCTACTGTGAATAGT[A/G]CTGTGATAAACATAT | 84333 |
| rs553385334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264591 | CTCAAATTTAACAAT[A/G]TTAGAAACTAAAAAA | 84333 |
| rs553419709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176519 | GTTTTCCAACTTGGT[G/T]CCATTCTCCCTATCA | 84333 |
| rs553421767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277420 | TTAAGAGAGAGTATC[C/T]ACAGCTTTAAGAAAA | 84333 |
| rs553428591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166787 | CATTCTGTCATCTCT[A/G]AAGTGGGGATAATGC | 84333 |
| rs553458919 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228403 | AAAAAGGATGTTTAT[A/G]GACATAGAATTCTGT | 84333 |
| rs553473554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270138 | ATTGTCAATATCTCT[A/C]TCCAGCCTTAGCTTT | 84333 |
| rs553476772 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181439 | GTCTTGTGCCAGTTT[G/T]CAAGGGGAATGCTTC | 84333 |
| rs553508891 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256201 | CAAAGAACTAAAACC[A/C]TGGTCTGGGCACTAT | 84333 |
| rs553527796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202100 | CAAATTGAGAAGAAT[A/G]ATTGTACTCACCCCC | 84333 |
| rs553611995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258081 | TGATTCCATTTATAC[A/G]AAATATCCAGACAAG | 84333 |
| rs553714860 | in-del | -/AAG | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200458 | CGCATATATGTTTGA[-/AAG]AAGAAGAGAAGATTT | 84333 |
| rs553735201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169876 | CCTTCAAGGCTTGCT[A/G]TAAACCTATAGTAAT | 84333 |
| rs553746298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265602 | CCAGATATAATGAGG[C/G]TTGCCATGTTACCAT | 84333 |
| rs553757377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270274 | CTGCCAGTCCAGCAC[C/T]TAAAGTTACTACACC | 84333 |
| rs553760743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164164 | CAGGGAGAGTGGCCC[C/T]TCTGCAGTGATGACG | 84333 |
| rs553790540 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263599 | CTAAAATGTTATATT[A/T]TTTGTAGGGATCGAT | 84333 |
| rs553793222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260865 | CCTAATGCTAAATGA[C/T]CAGTTAATGGGTGCA | 84333 |
| rs553793787 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208475 | AGATTCTGCATTCCT[A/G]ACAAGATCCCTGCTG | 84333 |
| rs553816860 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259939 | AACACCAAAAGCAAT[A/G]GTAACAAAAGCCAAA | 84333 |
| rs553879908 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181311 | TAAAAACAGGGATAG[G/T]TTGACTTCCTCTTTT | 84333 |
| rs553881682 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181645 | TTTAGTTTGTGTTTA[C/G]TTCTGTTTATGTGAT | 84333 |
| rs553891366 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161791 | TAAAGACTCCTGAAC[G/T]TTTCCAGTCTCACCA | 84333 |
| rs553893681 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245225 | AAGTGAAGATAGTAT[A/G]TATATCAAAGGAGAC | 84333 |
| rs553901406 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173843 | CCTTTGGATGGAAGT[-/A]AAAAAAAATTGTGAT | 84333 |
| rs553982362 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283749 | ATCTGAGCAACACAA[C/T]AGAGATCATCAGTTT | 84333 |
| rs554017676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267941 | TATTAAACATTTTAA[A/G]CTACCCAAGATTAAT | 84333 |
| rs554061139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187247 | TATATAGATATATAA[A/G]ATAGATATATAAGAT | 84333 |
| rs554122372 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194187 | CCTAATCCCCAGAAA[A/T]TGTGAATGTGTCACT | 84333 |
| rs554148890 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245667 | CAGTGGGAGCATTGA[C/G]AAAAAAAATTGTAGC | 84333 |
| rs554184177 | in-del | -/CTTT | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217747 | CTCATCCATTCTTCC[-/CTTT]CTTTCTTCCTTGTTT | 84333 |
| rs554209922 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235811 | GATGTGACTTGCTCC[A/T]CCTTGCCTTCTACCT | 84333 |
| rs554217187 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161238 | CCTCACCTTACCCTA[C/G]TTGAACGTCCAGTTC | 84333 |
| rs554246487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198870 | TGGCTGAGTGTGTTT[C/T]GTATTAGTCTTCTTC | 84333 |
| rs554256618 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206423 | ATTTCTGATGCCTTT[A/G]AATGAGGATTAAAAG | 84333 |
| rs554270151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255871 | ATAAAATGGTGTAGT[A/G]TTTGCACGTAACGTA | 84333 |
| rs554318175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205889 | CAGCTACTTGGGAGG[A/C]TGAGGTGGGAGAATT | 84333 |
| rs554378453 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280174 | AGAAATTATTTTTCT[A/G]TGGTGTGAAACTGTT | 84333 |
| rs554399311 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237664 | CAGGAGAATCACTTG[A/C]ACCTGGGAGGCAGAG | 84333 |
| rs554421946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231446 | GACTTTTGAACAAAG[A/T]CCAGGTAAAGGAGTT | 84333 |
| rs554425785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238650 | TCTTTCCCAAATTTC[A/G]GAGACTTATCTATCA | 84333 |
| rs554491040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245032 | TCAAACTGTAAGCAG[A/G]ATGAGATCACTTCAG | 84333 |
| rs554494507 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226345 | TGAGGAAGGACAGAC[G/T]ATGATATAATAGCAG | 84333 |
| rs554549232 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235677 | GGTAATTGAATCATG[A/G]GGGCGGGTCTTTCTC | 84333 |
| rs554587239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203629 | ACATATGCTTAATAT[A/G]TATTTGTACAAGACT | 84333 |
| rs554591844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197032 | CAAAAAAAACATGAT[A/G]TGGTTTTTATATTAG | 84333 |
| rs554606497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242008 | GTGATGCTAATATAT[A/G]CTAACATTTGGGAAC | 84333 |
| rs554628290 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166457 | GAAGTTTTCTGACAA[C/G]AGAATTAGATATTGG | 84333 |
| rs554653723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196387 | GCAAGAAACCTGTGC[A/G]TGCACATTGAAACAC | 84333 |
| rs554656994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183277 | TGAATCTGGGTGTTC[C/T]TGTGTTGGGTATATA | 84333 |
| rs554716991 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202944 | AAAGAAATGTGTTTG[G/T]GAAAATGACTAAAAA | 84333 |
| rs554737578 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191522 | GGTAACTGAAACCAC[A/G]GAAAGCAAACCCCAG | 84333 |
| rs554738538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185086 | CCCCAGTTGGCTTGG[G/T]CTCTCCAAGCATGAA | 84333 |
| rs554746989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240763 | AAATAAGGTTTTACA[C/T]CTTAAATATTTAAGA | 84333 |
| rs554747703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172630 | TTAAACACTTCCTCA[A/G]TGGCAAAAAGGTGTT | 84333 |
| rs554755707 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228683 | TTGAACAAATATCAT[A/C]AATATACAAGTACTT | 84333 |
| rs554756577 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235358 | CAAATCTAACAAATG[C/G]TAAAAGTAGGGAATT | 84333 |
| rs554767218 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236235 | ACCATCTTTGCTGCA[C/G]AGCTGTGCAGCTGTG | 84333 |
| rs554792186 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203496 | TAGTAACTAGTTTTA[G/T]TTCTAAATTAGCAAT | 84333 |
| rs554817054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185648 | CCTGGGTTTCTGTGT[A/G]TGCCTGAGTGGCTGC | 84333 |
| rs554827061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210783 | ATCACTGAAAATCAG[A/T]AATGTTTCCAGTTCT | 84333 |
| rs554828491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242684 | TCTGTTCACCCAGAT[A/T]AGCTTCTTAGTAACG | 84333 |
| rs554831958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226902 | TTCAGTAGGCCAGGG[A/G]CATTTGATAAATAGA | 84333 |
| rs554833898 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215607 | AATCTCACCACCCAG[C/G]CCTTCAGGGCCTCTT | 84333 |
| rs554846959 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174562 | ACTGTAATAAATCCT[A/G]TCATGCTTTAAGACT | 84333 |
| rs554849515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263478 | ATCTTAAAGTTCAAA[A/C]CTGTAGTCTCTGTCT | 84333 |
| rs554885021 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262807 | AGTAACAATGTATGG[A/C]TACAACTACAGTGAA | 84333 |
| rs554897650 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222479 | TCATTAGTATAGAGG[C/T]GGTAGTTGAGGTTCC | 84333 |
| rs554897893 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167730 | AAGTATCAGAAATAT[A/T]TTAAATGGGGGAATG | 84333 |
| rs554903699 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234401 | ACCCTACCCCAGTAA[A/C]AGAAGTGTACTGCAT | 84333 |
| rs554926531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190315 | TAAGATTTCAACATA[C/T]GAATTTTGGGGGAAT | 84333 |
| rs554999639 | snp | G/T | 1.72442e-05 | 0.00293629 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278234 | TTGTTTTTATCCAAA[G/T]ACAGTCTTATTTATT | 84333 |
| rs555066060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186524 | AGGGAAAAACTTCAT[A/G]TATATATGTGTGTGT | 84333 |
| rs555067619 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192742 | GAGCAGTGGTGGAAA[A/C]ATTTTAAAATAGAGC | 84333 |
| rs555082231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238289 | GTGCTGCTTTGACTT[C/T]AAGCAATTAGCATAA | 84333 |
| rs555108273 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216229 | TGTGTGTATACAGGA[C/G]GCTCTTTGGCAGCTT | 84333 |
| rs555144597 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247527 | AGATGTGAGAAACCT[C/G]TATGTGTTTGTAGTC | 84333 |
| rs555207945 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171963 | CTGAGCATTTATTCC[A/G]TAGAGATGGAAAGTA | 84333 |
| rs555235183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223271 | AACTATTTCAGGTTT[C/T]TTTATTTTAAAAATT | 84333 |
| rs555269542 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171432 | TGGGGAGCCAAAGGT[G/T]ATGAGGGCTTGACAA | 84333 |
| rs555360698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230811 | TATTTTGTGTAGAGA[C/T]GGGGTTTGGCCATGT | 84333 |
| rs555377859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275355 | GCCAAATTAAGAGGT[A/G]GGGAAAGATAGTACT | 84333 |
| rs555379704 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283478 | TGGAATAAGAAACTA[A/G]TCTAGTGCAAATGAA | 84333 |
| rs555399939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186093 | TGACATCTTGAATTT[A/C]CTGTGCAGTAATTTT | 84333 |
| rs555407393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173685 | TGGAGCAAGATCAAA[A/C]GTATAATATTAGTGT | 84333 |
| rs555409017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180939 | TATAAATTGCTTTGG[A/G]CAGTATGGCCATTTT | 84333 |
| rs555412909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267399 | TTTATTGTTTGTCCT[C/T]CAAGTAAAATATAAT | 84333 |
| rs555416292 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237576 | GGCGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 84333 |
| rs555416443 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208735 | CTGGCCTCACACTCA[G/T]GCTTATTTTGCATTT | 84333 |
| rs555457484 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242709 | GTAACGTTTTATCTC[A/G]TTTGCTTTATCATGT | 84333 |
| rs555460602 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254074 | AGTATTCAAGGCCCT[G/T]CCCTAACAAGCACCT | 84333 |
| rs555465843 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282591 | CAGAACAAGCATGTA[C/T]ATCAAGAGGAAGTTC | 84333 |
| rs555466035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257595 | TGGACAGGTGGCCTA[C/T]ACAGCATGAATATGC | 84333 |
| rs555480715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167422 | AATTCAGAGGAGGAA[A/G]AGACTATTTCTAGCC | 84333 |
| rs555505221 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212834 | TTCATCTATTGGGAC[A/G]TTTGGATTTTTATTA | 84333 |
| rs555525992 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260047 | TACAGAATGGGAGAA[A/C]ATTTTTGCAACCTAC | 84333 |
| rs555528861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192160 | GTCTCACTCATTTCT[A/G]ATAGTACTTCCTTAA | 84333 |
| rs555538727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239386 | AGTTCTTCCATGACC[A/G]TTGTTGCTTTGGTCA | 84333 |
| rs555538795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244560 | TTGGAGGATTGATCC[A/G]ATATGAACATGTTGA | 84333 |
| rs555541841 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276961 | CCCTCCCAGGTAATC[G/T]GATTCAGGGGGAACT | 84333 |
| rs555552246 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265654 | TGAATGTAAACATTT[A/G]TGGAATTATTATAAA | 84333 |
| rs555590153 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198314 | TGGGGGAACCTTGGA[A/C]ATCAGCATCGTTCCT | 84333 |
| rs555605963 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168920 | GCGACAGTGTGAGAC[G/T]CCGTCTCAGAAAAAA | 84333 |
| rs555671709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176010 | CTTCCTAGCCTCCAC[A/G]GTCTTTACAATTTGG | 84333 |
| rs555680325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167804 | GAGCCACAGGTAGTC[C/T]ATTTAAGCTGTTGAA | 84333 |
| rs555698183 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213473 | TTTCATTAAAAAAAA[A/T]TTTTTTTTAAGATGA | 84333 |
| rs555721347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205700 | TAATAAAACTGAGGC[G/T]GGGCGTGGTGGCTCA | 84333 |
| rs555746248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164300 | GTGCAAAAGGGCAGC[A/G]GGGTCCCCTCTTCCA | 84333 |
| rs555749571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258828 | GTGACCAGGTTGTTA[C/T]TTGTTAATTTATTTC | 84333 |
| rs555790932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270800 | CCATTTTGAAAAGTA[C/T]GCAATGTTGAATTCA | 84333 |
| rs555804566 | in-del | -/AAC | 0.00119832 | 0.0244484 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191180 | CAGTAAAAGATTAAC[-/AAC]AACAACAACAACTAA | 84333 |
| rs555811651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170571 | TGATATACCACTATA[C/T]ACAATTGAAATGGCC | 84333 |
| rs555834909 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277081 | TACTCCAGCCCTTAG[A/G]CAGCTGTAGTAGCAT | 84333 |
| rs555851626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209917 | ATATGCACGTGTCAA[C/T]TCAATGAGATTGACA | 84333 |
| rs555857939 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179117 | ATTAAACATCTTTGC[G/T]TGCTTCCTAAACATC | 84333 |
| rs555880881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278082 | CTGAAAACTTGACTG[A/G]TTCTAGAAAAATAAT | 84333 |
| rs555885825 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220792 | TCCTTCACTCTGAGG[C/G]CGGCGCGCTGGCGGG | 84333 |
| rs555900335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262297 | CGGGTGTGGTGGCAG[A/G]TGCCTGTATTCTCAG | 84333 |
| rs555910640 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239137 | TTGGGGGGCGGAGGG[A/G]GAGGCAGGTAAAAAT | 84333 |
| rs555927810 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161224 | TAATCTCAGGATTGC[C/T]TCACCTTACCCTAGT | 84333 |
| rs555985416 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195697 | CTGCTTTGGCCTCCC[A/G]GTGTTGGGATTACAG | 84333 |
| rs556000042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251533 | TGCTTCAAAATGTTT[G/T]CTTTCAAAGTTTTAA | 84333 |
| rs556004747 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261925 | ATAAATGTAATTTAC[C/T]AGTTTATTTACAGAA | 84333 |
| rs556018904 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177091 | GGGGTTTTGGTGTGG[A/G]TGTCCTTTCTGTTTG | 84333 |
| rs556039919 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283967 | ACCAGGTCATTGTTA[A/G]TGACTTAGTCTATTA | 84333 |
| rs556061475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250801 | AGCTAATTCATTATA[C/T]TCGTTTTTTTTCACT | 84333 |
| rs556121136 | in-del | -/ATAATAATA | 0.00324374 | 0.0401416 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260955 | CCTAAAACTTAAAGC[-/ATAATAATA]ATAATAATAATAAAA | 84333 |
| rs556141955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245722 | ATGGTGCAGATGCTA[C/T]AGGTAGGTATGGTGG | 84333 |
| rs556152992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208568 | GGAAAGAGCCAAAAC[A/G]CATTGCTCTCCCTGT | 84333 |
| rs556192916 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202225 | ATGGTCGATGTATCT[A/G]TTTTTATGGTTCTTC | 84333 |
| rs556197946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261999 | TGTTCCATGTTTAGA[A/G]AATGTTTTTAATCCT | 84333 |
| rs556216546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226126 | GAATGAGTAAACGCT[A/G]GGTTTTATGGAGACT | 84333 |
| rs556224739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217595 | GTTATTAAGAGCCAT[C/T]TGTGGTTCTCTGGAA | 84333 |
| rs556247656 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216599 | CTTTGGCAGAAAAGA[A/G]CTGTAGGAAGACTAC | 84333 |
| rs556264908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252608 | TCTATCTTTAGAGAA[A/G]TGACCACTGTACCTA | 84333 |
| rs556297081 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216097 | ATGCATAGCCAAGCA[A/G]TGGATCCACTGGGCT | 84333 |
| rs556306828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196138 | TCCTACAGATATTTC[A/G]CATGGTGGCAGAGAA | 84333 |
| rs556313966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277537 | TATCCCAAAGAAGCT[A/G]TTTCCTCTCTAGTTC | 84333 |
| rs556350499 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184617 | AGGTGATACAGTCAT[A/T]TGGAGGAAAGAGGGC | 84333 |
| rs556362522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163115 | GACCCAGGCGGCTTC[C/G]CCGCCCGACGCGGCC | 84333 |
| rs556384989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207354 | ACAGAAAAGTTGCCA[A/G]AATCTTTCAATGAAC | 84333 |
| rs556400734 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241646 | GGTCAATTCCGGAGT[C/T]AGCTTTTTAGTACTT | 84333 |
| rs556407590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260523 | CACATATGTTTATTG[C/T]GGCACTATTCACAAT | 84333 |
| rs556409187 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255520 | TGGTATGCCCCCAAA[C/T]ACATACCCAGATTCT | 84333 |
| rs556416260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248429 | TAACATGTATAAGAT[C/T]ATACATCTCAGACTA | 84333 |
| rs556436259 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181499 | CTGTGGGTTTGTCAT[A/G]TATCACTTTTATTAT | 84333 |
| rs556478072 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182285 | TCCTGGTTCAGTCTT[C/T]GGAGGGTGTATGGGT | 84333 |
| rs556478452 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206685 | GAAGTCTCAGTAACA[A/G]CCTGTGGGGGACTGC | 84333 |
| rs556479204 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246321 | AGCATTGGTTTGGTC[A/G/T]GAGAGTACAGAGAGT | 84333 |
| rs556483664 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247596 | TGAGGCAGGAAGGGG[G/T]TGTTGTGGGGGCAAG | 84333 |
| rs556499499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236302 | ACTTGCCCAGGGAGG[A/G]TAGTAACTGTCCATA | 84333 |
| rs556560903 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242914 | CCAGTTTTCTTAATT[C/T]AATGATGTCCTTTAT | 84333 |
| rs556581797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194231 | GGGACATTGCACATG[C/T]GATGGTTAAGATAAC | 84333 |
| rs556660406 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91161972 | GCCAGCCACAAGGGG[G/T]GATTCTGCTTGGGGG | 84333 |
| rs556736622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169609 | GTGAGGAAAACTATC[A/G]AATTTTGATAAAAGA | 84333 |
| rs556757433 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91162422 | AGCCTGGACTTGACC[A/G]TCGCCAGGGAGGCAT | 84333 |
| rs556758061 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249033 | CTAAAGGAAGCTGAA[A/G]TAAGAAATAGCCACA | 84333 |
| rs556777076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181707 | CCAACCTTGCATCCC[A/G]GGGATGAAGACCACT | 84333 |
| rs556796687 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278648 | TTCTAATGTTTAATT[A/G]CACTAGTAAAATGGC | 84333 |
| rs556815714 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208090 | AGCAATTTTTTCTTA[A/G]TAGTTTTAGGATCCC | 84333 |
| rs556815877 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284747 | TAATGTTAGTGAAAC[A/G]TTGGAGGTAGCTAGA | 84333 |
| rs556826800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249360 | TACTGAGCAGATAAA[A/G]GGCTTTTAGTGTATA | 84333 |
| rs556835406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236892 | ATAAGCTACTGAAAA[A/G]GGCTCTATACAGTTT | 84333 |
| rs556854694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239387 | GTTCTTCCATGACCA[C/T]TGTTGCTTTGGTCAG | 84333 |
| rs556858942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188161 | TTCTGCATTTCCATC[C/T]GAGGTACTGGGTTCA | 84333 |
| rs556890927 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218985 | CTTGTTTTTATTTTG[C/T]GTATGTGTGCATTTT | 84333 |
| rs556918483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194908 | AGAGTTTCTGGGGTG[C/T]TATCCTCAAGTAGGG | 84333 |
| rs556961453 | in-del | -/TAG | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245006 | GTAGTCTTCAACATA[-/TAG]AAGGTCTTTCAAACT | 84333 |
| rs556962963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197429 | GTGTTATCACAACTG[C/T]TGATGTTTATTGAGG | 84333 |
| rs556979448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191381 | ACTGGACAAAGGGAT[C/G]ATTCACCACAGAGAG | 84333 |
| rs557006254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250094 | TTCCTATTGTTTCTC[A/C]CATTTTAAAGTATTT | 84333 |
| rs557016466 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188129 | TCCCAGTGTGAGTGA[C/T]GCAGAAGACGGGTGA | 84333 |
| rs557056125 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184009 | TTTTTTCTTCGTTTC[A/G]ACCTTGGATAATCTG | 84333 |
| rs557067962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257414 | CCTCAAAGAGTTGAC[A/G]TGGTAATTCCACTTC | 84333 |
| rs557090456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221627 | TTACCAATGAGTTAA[C/T]AGCTAAGATGGGGGA | 84333 |
| rs557094047 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227002 | AGATGAACTAAATCC[G/T]CATTAACCATGGTTT | 84333 |
| rs557113289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179672 | TGTCCCCACAAAGGA[C/T]ATGATCTTGTTCTTT | 84333 |
| rs557137275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184008 | ATTTTTTCTTCGTTT[C/T]GACCTTGGATAATCT | 84333 |
| rs557139326 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279031 | TTCCCAACCATTCAA[A/G]ATGTTGGCAGCTGAT | 84333 |
| rs557153433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234571 | AAGTTCCATCGGCAT[A/G]ATATCTGTTATTTAT | 84333 |
| rs557161810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275527 | CTCATTGCAGCCTCC[A/G]TCTCCCAGGTTCAAG | 84333 |
| rs557223795 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219447 | ATGCATATTTTAAAC[A/G]CACTAGAAGTAGTGT | 84333 |
| rs557250979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185550 | ACCTCTTTCCTAGGG[G/T]TATGTATGGAGGTCT | 84333 |
| rs557256670 | in-del | -/GTGACCCTGGTGAAAA | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228174 | TGTCTCTTTCACCAG[-/GTGACCCTGGTGAAAA]GAGAAACTTTAAAGC | 84333 |
| rs557282482 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256728 | AGGACCCCCAGTAGG[C/G]TTAGTAGCTGATTTC | 84333 |
| rs557413997 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223451 | TAGATTTAATGAGCC[A/G]GAGACTCTGAGAGTG | 84333 |
| rs557447625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276930 | TTAGTAAAATGGAGA[C/T]AATCTGTGTCTTGCT | 84333 |
| rs557501116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232034 | AAACAATGAAAGTTT[A/G]AAGGGAGGACCAAGG | 84333 |
| rs557510819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208292 | AATTCAGTGTGTATG[A/G]TCCATTCCTCTTGCT | 84333 |
| rs557530474 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241538 | CCACTAGACCCATTT[G/T]CATTTCATTGTTCCC | 84333 |
| rs557535941 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284515 | TCAAATCCAAAAGAA[C/T]GTTTTGAAAGTAATT | 84333 |
| rs557636845 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216277 | TGACCTTTGAAATCA[C/G]CTAATACGTGAAAGG | 84333 |
| rs557640292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264319 | CCTATTTAAAATAAT[A/G]GATAATACTTTTGTT | 84333 |
| rs557718356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172052 | TAAACATTTTTAGAT[A/G]TATGTGATTTGCCCA | 84333 |
| rs557720818 | in-del | -/AAC | 0.00159712 | 0.0282137 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191178 | GCACAGTAAAAGATT[-/AAC]AACAACAACAACTAA | 84333 |
| rs557782237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266996 | AGAACATGCCCACTC[C/T]GTTCTCTGATTCCTC | 84333 |
| rs557795689 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186620 | TACACACATATATAT[A/G]TAACAAATTAAAATG | 84333 |
| rs557802860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275839 | ACTAGCAGTTCCGCT[A/T]TTAGGAATCTATCCT | 84333 |
| rs557804435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167919 | CAGAACTTGTTGGCA[A/G]TTGGATGTAGGAGTT | 84333 |
| rs557894904 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202681 | ACTTAATTGGTTTCA[A/G]TAAATAGAGGTTATT | 84333 |
| rs557914095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200381 | AAATTGTTCAACTAA[C/T]CTAGTTAAGAGAGAG | 84333 |
| rs557914689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186193 | TGGGCTAAATCAGCT[A/G]TACCCTCAGGTTGCC | 84333 |
| rs557920378 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209182 | CTTTTTTCTGACATA[A/G]TTTCATTTACTCATC | 84333 |
| rs557954944 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276107 | TGATTCCAGTTTTGA[A/C]AAAAAAAAACGAATG | 84333 |
| rs557992201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261835 | ATCACAAGGAATTTC[A/G]TAAGTAATCACATTT | 84333 |
| rs557993888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163268 | CCTCGGTGCGGGCCG[A/G]TGGGCGGCGCGGCCG | 84333 |
| rs558031020 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172722 | CTAACCTTTGTGGCC[A/G]CAGACACATTGTTAT | 84333 |
| rs558055647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260819 | CTGTTGTGGGGTGGG[C/G]GAGGGGGGAGGGATA | 84333 |
| rs558112367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199415 | CTTGGGCCAAGATGG[C/T]CAGGCCTTTATACTC | 84333 |
| rs558125472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268890 | GGAATCAAAACAAAC[A/G]GCTGGTCAGACTTAG | 84333 |
| rs558155659 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253142 | TATCTATTTTAGGAG[A/G]TCTTCTCCATTTTCT | 84333 |
| rs558185246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263456 | ACAATTAACTGAAAC[C/T]ATACTCATCTTAAAG | 84333 |
| rs558212898 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272497 | ATTTTTTTAGGCCAG[A/G]CACGGTGGCTCACCT | 84333 |
| rs558213349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214142 | TCTTGTCACTACAAA[A/G]AATACAAAAATTATC | 84333 |
| rs558245812 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283774 | CAGTTTTAAATAGAG[C/T]AGCCCTCACAATCAA | 84333 |
| rs558272745 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239249 | TGGCCCCTGCATCCC[C/G]AACTCCTAATATAAT | 84333 |
| rs558274552 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283182 | AATTCTCTTCCTAGT[A/G]TAATACAGTTTTCAT | 84333 |
| rs558299636 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174313 | GGAGTTGGAGACCAG[C/T]CTGGCCAACATGGTG | 84333 |
| rs558305357 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244386 | TTGGACGACCAGCAA[A/G]GAGACCTGGGCGGCT | 84333 |
| rs558323971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184087 | GGTTCTCTGCATTTC[C/T]TGAATTTGAAGGTTG | 84333 |
| rs558338714 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194292 | ATCTGGTGGGCCCAA[C/T]CTAGTCACAGAAGTC | 84333 |
| rs558343803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238387 | TAGTATAGCTTCTGG[A/G]AAGATAGGGTCCTAC | 84333 |
| rs558377808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268087 | GTCACCATGTCTGTG[C/T]GTATGTGTGTATATG | 84333 |
| rs558408955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244977 | GAGAGGTCTGGGCTG[A/G]AGAAAAACATTTGGT | 84333 |
| rs558434177 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198815 | GTTTTGTGCAATGAA[A/G]AGCCCTTCTTCAGAT | 84333 |
| rs558475885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244598 | GTTGAGAACACCGCG[C/T]GTATAACAAGGCAAG | 84333 |
| rs558485192 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240695 | TTAATATAGGACTTA[G/T]GATTTTCATTTTAAA | 84333 |
| rs558485279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233151 | TTATTTTGATTGATC[A/G]TGGAATTTATATTGG | 84333 |
| rs558517921 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188016 | AGTTTTAGGGTACAT[A/G]TGCACAATGTGCAGG | 84333 |
| rs558528842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189760 | TGCCTGGTGGGAAAC[A/G]GTTAAAATCCTAAGA | 84333 |
| rs558548295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240178 | TTAAATGAGAAGAAC[C/T]TATTTTATGTAAATA | 84333 |
| rs558590825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255079 | ATGGTCATTATTTGA[C/T]TTGTCTGGTTGTTTC | 84333 |
| rs558613591 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255358 | CCTTGAAATCTAGAG[G/T]GCCACGTGCATATGT | 84333 |
| rs558617058 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195279 | ACATTAGCTATCACC[G/T]CCTTCAAAAAAAAAA | 84333 |
| rs558626414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202305 | AATAACCTGGATTTG[A/G]ATCCACCACCGTTGT | 84333 |
| rs558632069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210718 | ACCACACCTGCTTTC[C/T]GTTGTTTGGTCTCTC | 84333 |
| rs558707278 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271012 | GTGTTCACTCATTGC[G/T]TTACTCATAAAACAT | 84333 |
| rs558710551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190267 | CAGTCACCTTCCAAA[A/G]GTCTGACCTCTTAAT | 84333 |
| rs558736835 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241953 | CTGCTAACTCAGAAA[C/G]TTTGGGATTGGAGAT | 84333 |
| rs558799783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249041 | AGCTGAAGTAAGAAA[G/T]AGCCACAGCTTGCAA | 84333 |
| rs558808059 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234682 | AGTGATCTAATTTAT[C/G]GTAAAGCTCACATTT | 84333 |
| rs558815403 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231831 | GATGGTAATGGCTTG[C/T]ATCAAGGTGGTGGTA | 84333 |
| rs558818758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233661 | TTAGTGTTAGTTTCA[C/T]GTGTAAGAATAGGTA | 84333 |
| rs558845262 | snp | C/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218835 | GGGTTTCGCCATATT[C/G]GCCAGGCTGGTCTCA | 84333 |
| rs558854677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217746 | CCTCATCCATTCTTC[C/T]CTTTCTTTCTTCCTT | 84333 |
| rs558869567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188138 | GAGTGACGCAGAAGA[C/T]GGGTGATTTCTGCAT | 84333 |
| rs558882489 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177597 | TACCTACTCAAGCCT[C/G]AGCAATGGTGGGCGC | 84333 |
| rs558935014 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215235 | TGGATTTTTCTTCAG[G/T]TTTCTTAATTTAATA | 84333 |
| rs558984231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188223 | GGACAGTGGGTGCAG[C/T]GCACCATGCGCGAGC | 84333 |
| rs559002218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228126 | CTCTGGACTGGGGAC[C/T]AGAAATTGATGGCCC | 84333 |
| rs559063912 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235815 | TGACTTGCTCCTCCT[C/T]GCCTTCTACCTTGAT | 84333 |
| rs559079056 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173085 | CATCTGGTCTATCTC[C/G]TAGGTATTCAATGTG | 84333 |
| rs559101680 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91220103 | TGTTTTGAACGTTGC[A/T]AACAGTAATGCTTCT | 84333 |
| rs559113338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258455 | AGTTGAACCTCCCAA[A/G]TCTGAAATGAATGAG | 84333 |
| rs559170263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177182 | TCCACTTCAGACCCT[A/G]TTTGCCTGGGTATCA | 84333 |
| rs559193735 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273937 | GTTTGATAAAATTCA[A/G]TGTGAAGTCCTGATG | 84333 |
| rs559202894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225270 | GTATATATGTATATA[C/T]GATATATATCATATA | 84333 |
| rs559207981 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280503 | GAATTCTTTTATTTA[C/T]TGATAATGCATTAAC | 84333 |
| rs559211137 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277631 | TCAGTTATTTTATGT[A/G]ATAGTCAAATCCAAA | 84333 |
| rs559262378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221077 | GCTCGCTCTCCCCGG[C/G]CTGAGCAGCGCGCCC | 84333 |
| rs559265383 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213093 | TAGAGAGTGTTCTTA[C/T]GTGCAGTTTAAGTGT | 84333 |
| rs559283506 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167987 | TTGATGTTGGCAAGG[A/G]TTGAAATAGGAAGGG | 84333 |
| rs559286841 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282027 | CTTAGATTTAGCTCC[C/T]GTATTATTCATAATA | 84333 |
| rs559297076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273840 | ATATTATATAGTGTA[C/T]AATATAAAATATTTT | 84333 |
| rs559312596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188898 | CAGGAAAGAAATATT[A/G]GAGGCTTGAAGAGAA | 84333 |
| rs559320829 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182479 | TCTATATATTTTATT[A/C]TTTTTTTCAAAAGCA | 84333 |
| rs559358288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266484 | TTTTGGTTGTTTAAG[A/G]CATATTTTAATAAAA | 84333 |
| rs559378812 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179202 | CTCTCTATCCTCAGA[A/T]CTGAACTAGTGTGGT | 84333 |
| rs559418992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210356 | TATATGTTATAGAAG[A/G]GTGTTTAACGTAGCC | 84333 |
| rs559427749 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281133 | AAAATATGTATGGCC[C/T]TTTCTCTAGATTAGC | 84333 |
| rs559437191 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91227001 | TAGATGAACTAAATC[C/T]GCATTAACCATGGTT | 84333 |
| rs559442135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185234 | GAGGCCTGGGTTGGG[A/G]GGTCCCACCCAGTGA | 84333 |
| rs559447320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177999 | TCATCCATATTCTGC[A/G]TCGCTCACACTGGGA | 84333 |
| rs559505359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184755 | TTTTAAAATCTGGCT[A/G]CTTTTCTGTAGTGCT | 84333 |
| rs559552841 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165482 | GGAAGGTTCATAATA[A/T]ATACCACTTAGTATG | 84333 |
| rs559611508 | in-del | -/G | 0.495927 | 0.0449436 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209763 | GCGAGACTCCGTCTC[-/G]AAGAAAAAAAAAGAA | 84333 |
| rs559616822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171638 | TGGGAGAATAGCAGG[A/G]AATATGAGATTAGAG | 84333 |
| rs559624771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173951 | GTAAAACAGCTAAGA[C/G]TCCAGTATTGATGAT | 84333 |
| rs559699043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165927 | ACTTCTGAAGTTAGT[A/G]CTGAAGAAGAATGGG | 84333 |
| rs559733710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190094 | TTAAGGTTGGAAAAC[C/G]CAACATCAAGGCATG | 84333 |
| rs559753037 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172776 | ACTGAGAAAGGTTTG[C/T]GCATAGGTCCTTAGT | 84333 |
| rs559761252 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172153 | TCTAGGGCCAGGCGC[A/G]GTGGCTCATGCCTGT | 84333 |
| rs559776785 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255927 | TCATCTCTAGATTAC[G/T]TGTAATACCTAATAC | 84333 |
| rs559794657 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219084 | CTGCAAACTATTGCT[C/G]CCTCTCCAGACACAA | 84333 |
| rs559804582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206080 | GGCAAATTTTGGCAA[C/T]AGCCTAACAATAAAT | 84333 |
| rs559826531 | snp | A/G | 3.31351e-05 | 0.00407019 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91248666 | TTCTTTTAAATTAGA[A/G]GAACTTGAGCGTGAA | 84333 |
| rs559856120 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263782 | TGGGAAGAGGATCCT[G/T]TAAGTATTGTGCAAA | 84333 |
| rs559875389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190812 | GTTATAGGTATTCAA[A/C]AAGCAGAAGGTTGTG | 84333 |
| rs559895347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262949 | CTAATTTTTAGAAAG[C/T]TGTTATTACTAAGAG | 84333 |
| rs559902051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242176 | GGTGGGTGCTCCTGG[C/T]ATCTAGTAGGCAGGG | 84333 |
| rs559965306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249533 | ATTTAAAGTTATTCA[A/G]GAATGTGTGTGTGTT | 84333 |
| rs560012496 | in-del | -/CTA | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240155 | TTATCTTTTTCTGTC[-/CTA]CTTCTTTAAATGAGA | 84333 |
| rs560027663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193977 | AGTTTAGGATGATTC[C/T]TTGGGTTCAGGCCTG | 84333 |
| rs560041685 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251550 | TTTCAAAGTTTTAAT[G/T]AACATAATTAAATAA | 84333 |
| rs560047959 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180871 | TTTTAAAATAGTTTC[C/T]TCTAGTTCTGTGAAG | 84333 |
| rs560145173 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257555 | GGTTTTTTTAATTTG[A/G]TAACTGAGATAGCTA | 84333 |
| rs560145550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217097 | GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC | 84333 |
| rs560159569 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161540 | TGTCTACTTTTTCAT[G/T]ATTTACTCTATTCTC | 84333 |
| rs560195579 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219258 | CCCGCCTTCAAGCTC[A/G]TTTCCTTCAGGAATA | 84333 |
| rs560205121 | in-del | -/A | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282484 | CGAGTCTCCATCTCC[-/A]AAAAAAAATTCAACT | 84333 |
| rs560210022 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281421 | ATATTGTGAACTGTT[G/T]AGCTTTACTGAAATA | 84333 |
| rs560242196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260229 | TCATCGTCACTGGCC[A/G]TCAGAGAAATGCAAA | 84333 |
| rs560273097 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269041 | TTTAATGCAAATTCA[A/G]ATCATCTCAGGATCT | 84333 |
| rs560279945 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257823 | TACTGTATAAAAGAA[C/T]TGAAAACATGTTCAC | 84333 |
| rs560302979 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259714 | GACAAAAACAAGAAA[C/T]GGGGAAAGGATTTCC | 84333 |
| rs560334651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195027 | GAGTGTGTGTGAGTT[C/T]TCTTCTGATGACTCA | 84333 |
| rs560358770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238866 | TAGCTCTAGGCCAAG[C/T]TTTTATATCTAAGCT | 84333 |
| rs560437381 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282721 | AAACTCCTTGGATAG[A/G]GTGAAAATGGATGCA | 84333 |
| rs560447159 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200975 | GAGAATGGTCAGAGC[G/T]TGGGCAAGCACAAGA | 84333 |
| rs560523522 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225498 | AATGTGGCCTTTATC[A/G]TCAACAGAGAACACA | 84333 |
| rs560527578 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259624 | TACCAAAACAGGGAT[A/G]TAGACCAATGGAACA | 84333 |
| rs560572639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192304 | ACTCAAGGTGTTTTG[C/T]TCGTATACCTGGATA | 84333 |
| rs560604057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244005 | TCTGGGCACTATTCT[A/G]GGTGCTTGAGGTCCA | 84333 |
| rs560618189 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257456 | TCATATCCAGTAGTC[C/G]CCCCCTTATCTGTGG | 84333 |
| rs560621435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223569 | GTGGAGCTCCTAGCA[A/G]ATTTCATTCTCAACT | 84333 |
| rs560649673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177900 | TCACACTTGGTGCAC[A/G]GTGCACTGCACCCAC | 84333 |
| rs560682583 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222725 | AAAAGGAGTGATGAT[C/T]AACGATCTCATGATA | 84333 |
| rs560687977 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204307 | TTAGGTTTTAATTAA[A/G]CCTTAATCTGAATTA | 84333 |
| rs560743878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230920 | CAGCCACTGTGCCCA[A/G]CCTATTTATTTTAGA | 84333 |
| rs560769636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189253 | GACATCCTCTCTTGA[A/C]CCTCATGATTCTTGG | 84333 |
| rs560773151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275512 | GTGGTGCGATCTTGG[C/T]TCATTGCAGCCTCCG | 84333 |
| rs560851444 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279471 | TGGGGAAATGAGAAG[A/T]TTATTATTTTATACA | 84333 |
| rs560894998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263840 | AGACAGCCCTAAGAG[A/G]CACAGACCTGTGGCA | 84333 |
| rs560924625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189857 | ACTGAAGTTATGAGT[A/G]TAAAAATGTAGTTTT | 84333 |
| rs560959800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225348 | AGCAATTTAAAGCCT[A/G]AAGGGGTAAATTAAA | 84333 |
| rs560977357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195898 | GAACAAAGGAAACCC[A/G]ATCCAAGGTTTGTTC | 84333 |
| rs561016357 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219611 | TGATCCCAGCTTGGA[C/T]ATTGGCATGTATGAT | 84333 |
| rs561023561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233318 | GCTGGCTTGCTCAGT[C/T]TAAGATCCCCAGACC | 84333 |
| rs561023585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224890 | TTATATTCTACTTCC[A/G]TTTCCCGTTTCACCA | 84333 |
| rs561080475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217123 | ACTGCAAGTTCCACC[A/T]CCTGGGTTCACGCCA | 84333 |
| rs561084456 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219171 | AACCCCACCTCCACA[G/T]TCATCCTCAGGTACT | 84333 |
| rs561135338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255117 | ACCCCACTTACAAGA[C/T]TGTCAGTATTCGACT | 84333 |
| rs561148335 | snp | C/G | 0.000140756 | 0.00838797 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227397 | TGAAACTCAGCATAT[C/G]TACGAATGATCAAAT | 84333 |
| rs561148714 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217344 | GCTGAAAAATTCACC[G/T]TATTTAATATTTCAG | 84333 |
| rs561196578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254273 | CTGTATCTAGATTAT[A/G]TAAAAGCTTGTGTTA | 84333 |
| rs561209940 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226652 | TCAGAGAGAAATTCT[G/T]GATCCAGCACTGCTG | 84333 |
| rs561240933 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182083 | TTTATAAGCATAAAG[A/G/T]TGTTTATAATATTCG | 84333 |
| rs561257990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184107 | TTTGAAGGTTGGCCT[A/G]TCTAGCTAGGTTGGG | 84333 |
| rs561274162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235103 | TTGTGACTACCTCCT[A/C]CTCTCCCTTGGCCAA | 84333 |
| rs561284852 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229162 | TAGTTAGGTGGTATT[A/G]TTTAAGCATCAACAG | 84333 |
| rs561301246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277715 | ACAATCAGCTACTTT[A/T]TCAATATTTTTAAAG | 84333 |
| rs561371250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269558 | TTTTTGACATTACAA[A/G]CAAGGTGTTCCAGTA | 84333 |
| rs561439338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195444 | ATATAAATCATATGT[A/G]TATATATGCATATAT | 84333 |
| rs561441173 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202367 | TGAACCTAATGATTT[C/T]AGTAAAACCCACCAT | 84333 |
| rs561501436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201895 | ATGTGGTGATTTCCA[A/G]CCTCAGAGTTTCTGA | 84333 |
| rs561515625 | in-del | -/AA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168930 | GAGACTCCGTCTCAG[-/AA]AAAAAAAAAAAAAAA | 84333 |
| rs561556143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91210106 | ATGATTTGCAACTTC[A/G]TATGCCCCACTGCTC | 84333 |
| rs561595746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170696 | TACTTTGGAAGACAG[C/G]TTGGTGGTTTCTTAC | 84333 |
| rs561600591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262659 | TCAGATGACTAGTCT[A/G]TGGGTTGAAAATTGT | 84333 |
| rs561608465 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230026 | GTCTTAATCTTGGTG[G/T]CATCTATTATTAGTA | 84333 |
| rs561651306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185695 | ATAGTTCTGTGTGTC[A/G]GACTGAAGGCCCTAG | 84333 |
| rs561662824 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167543 | TGCTAAGACTTGAAG[A/G]TAAGGATATATGAGC | 84333 |
| rs561663248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174801 | TTTTGAGATTTAGTT[C/T]ATGGGACTTCAGATT | 84333 |
| rs561684227 | in-del | -/A | 0.00636936 | 0.0560724 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262428 | GTGAGACTCCATCTC[-/A]AAAAAAGAAAAGAAA | 84333 |
| rs561700074 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266733 | CCATTTTTCCAGTTG[C/T]TCAGACCAAAATCCC | 84333 |
| rs561723462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173989 | GGCAGCAAAGATCTT[C/T]TTGGAAAATGCTTGA | 84333 |
| rs561762700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205947 | GAATTGCTTGAACCC[A/G]GGAGGCACAGGTTTC | 84333 |
| rs561808658 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204995 | CTGTAAACTATCTAG[C/G/T]AAATTTGTAATTTTT | 84333 |
| rs561809525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259394 | GAAATTATTTAAAAG[A/C]TGTGATACCATGTTT | 84333 |
| rs561811182 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244323 | CTATTCCAGGTAAAG[A/G]GAGCAGCCAGTGCAG | 84333 |
| rs561836277 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264181 | ATTTGTAAATTATGT[A/G]TATGAACTTGAGATA | 84333 |
| rs561837227 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192465 | AATTCTTTGGTATTT[A/G]TCCATCTTGCTCATC | 84333 |
| rs561844906 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179282 | AGGTGAGTTAGATTA[C/T]CCATGAATAATCAGA | 84333 |
| rs561875211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172830 | AGTGGATCTCTCCTT[C/T]CTCACTGGGAATGTC | 84333 |
| rs561932683 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234066 | CACTCTCTGTGATAC[A/G]TAAGAGACCTGGGTG | 84333 |
| rs561934989 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168529 | CTGGCTTGGGAAGGA[A/T]ATGGAGAAAGCAAAT | 84333 |
| rs561937191 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177575 | GAGCTTCCTGGCCGC[-/T]TTTGTTTACCTACTC | 84333 |
| rs561992177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191478 | TCTGGAACTTTCCAT[C/T]TAATATTTTTGGACT | 84333 |
| rs561996868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168079 | TGATTATTGGTTTGG[A/G]TTTGGATGTGTTAAC | 84333 |
| rs562007510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205523 | GTTGTAAACATTATA[A/C]ATGATGAGTTTCTCA | 84333 |
| rs562052876 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249595 | AATCTTGGTTTTCCC[A/C]TAAGATCATAGGATT | 84333 |
| rs562132440 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272604 | ATGGTGAAACCCTAT[C/G]TCTACAAAAAATACA | 84333 |
| rs562179989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166920 | ACAGATTTGTGTGAC[C/T]ATGGGAGCAGCTTAA | 84333 |
| rs562193745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184853 | ACCAGTGAAGGCTAC[A/C]AAGCAACAAAGATGG | 84333 |
| rs562201443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256003 | TTATTGTTATTTTTA[C/T]TGTTTTTAAAAATAT | 84333 |
| rs562202417 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212118 | TATAAAATGCTTAGC[A/T]AAATACTGTGTACTT | 84333 |
| rs562203760 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259488 | AAAGTTCATATGGAA[-/C]CAAAAAAGAGCCCGC | 84333 |
| rs562271923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242380 | AATGAAAGATTATTA[C/T]CAACTGTTAAAATCT | 84333 |
| rs562273896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170041 | GTCTTTTCAGCAAAT[G/T]GGTGAGGCTGAAACA | 84333 |
| rs562295196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185340 | GATCCCTTCTGCCCC[C/T]GTGGGTTTGGACTCT | 84333 |
| rs562369152 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227808 | CTTGGTTCAACTGTT[C/T]GCTCTCCTTGAAATG | 84333 |
| rs562377292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200716 | CCTTTCTAGTGGGCA[A/G]TCTAGTTTATCCTAT | 84333 |
| rs562391258 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251100 | AATAAGTTTCCAATT[A/T]TTTTTTTTTTTTTTT | 84333 |
| rs562393653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250309 | CAAAAAGGATCTGGC[C/G]AGTCACTTTGCAGGG | 84333 |
| rs562404425 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201362 | TCCCCCCAGTGACAT[G/T]ACTAATCTTAATTAC | 84333 |
| rs562430126 | in-del | -/T | 0.237882 | 0.249706 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275446 | TAAAACTACATTTTA[-/T]TTTTTTTTTTTTTGA | 84333 |
| rs562436602 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207807 | CCAAATGATTATAGT[C/G]AGGATAGACATTTTG | 84333 |
| rs562452013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187742 | TACTATCTGTGTGTA[C/T]ATGTTTACCTATAAA | 84333 |
| rs562479678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245897 | TCAGTGCACTTGTGA[A/G]TGTAGTATGATTCCT | 84333 |
| rs562492311 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233768 | TTTCAAGACAAAAAT[G/T]TATATAAAATGAGCA | 84333 |
| rs562515101 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253872 | CTGTTGCAATTTACT[C/T]AACTTATTCATTATA | 84333 |
| rs562526557 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182887 | TACTCCAAAGTAATT[C/G]AGGAGCAGGTTATTC | 84333 |
| rs562564124 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236112 | AAATTAAAAAAATAT[G/T]ATATGAATTTTTGAT | 84333 |
| rs562607439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245158 | AGGAAACTGAGAAGG[C/T]ACAACCAGTGAGGTA | 84333 |
| rs562609115 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272470 | GCAATATAGCAAGAC[-/A]AAAAAAAAATTATTT | 84333 |
| rs562638971 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252848 | AAAGTATAAAAGATT[A/G]AATTTTAGAAATTTA | 84333 |
| rs562653417 | in-del | -/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187948 | GCAGATGGATGATTC[-/T]TTTTTTTTTTATTTT | 84333 |
| rs562661680 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233949 | CAATGAAGACACTTA[A/C]AGACATGAGAGAAAA | 84333 |
| rs562719355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91269015 | AGGAAAAAAAAACAT[A/G]CTTCTTGATCTTTAA | 84333 |
| rs562742235 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238693 | GAGCAAATACCAGCA[A/G]TGTTCTGAAGGAATT | 84333 |
| rs562756748 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240413 | TAAGGTCTGTTTCTA[A/C]TTACACTTAGTTTAA | 84333 |
| rs562806820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277161 | CCCTCTAGTTCCATC[C/G]TGAGCTGAATGGTTA | 84333 |
| rs562826493 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174523 | AAACAAAAAACTGTA[C/T]TTTTATTTGTTTGAT | 84333 |
| rs562829656 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222819 | ATCAGACTTTCATCT[A/G]CTTAGGACCCCTCTT | 84333 |
| rs562852868 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190193 | ATAGTGGAAGGGACT[C/T]GCTGGCTTTCTGACA | 84333 |
| rs562866586 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175729 | CAGAGACTAGGATTG[C/T]AACCCCTGCCTTTTT | 84333 |
| rs562918524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193668 | TGTTCCAAGTGAGCT[A/G]GGGAGTCATTGCAGC | 84333 |
| rs562922287 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230948 | AGAGACGGGATCTTA[C/G]CATGTTGCCCAGGCT | 84333 |
| rs562946151 | in-del | -/GT | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191631 | CTTTTTGGTTTCTTG[-/GT]GTGTGTTATCATAAG | 84333 |
| rs562985462 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238073 | TATTTTCATTTCAAA[A/G]TGTAATTAATATAAA | 84333 |
| rs562997603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176210 | TCTGGGTTGAAAATT[C/G]TTTTCTTTAAGAATG | 84333 |
| rs563027856 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216406 | GTAAAGAGGTACATT[A/T]TGGCTGGAGCACAGA | 84333 |
| rs563062840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203896 | TTGTGAACCTAATGA[C/T]TTCAGTCAGGCCCAC | 84333 |
| rs563078736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231637 | CCGCAGGCACGTGGC[A/G]CAGTTCTTGTAGAGC | 84333 |
| rs563090880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224552 | ACAAAGCACAATTGT[A/C]GATAGGAGACATGGA | 84333 |
| rs563091420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241691 | AAAAAAAAGAAGCTA[C/T]TCATCTAAAGATAGA | 84333 |
| rs563091845 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176616 | TGTTCATTTCTTTTC[A/G]TTCTTTTTTCTCTAA | 84333 |
| rs563094041 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260264 | ACCACAATGAGATAC[C/G]ATCTCACACCAGTTA | 84333 |
| rs563121521 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265847 | GAGACTGAACGCTTT[C/T]GCTAGCAGCAGGAAG | 84333 |
| rs563122881 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178380 | TTGCTGTTTCTCTTT[C/T]TTTTCTTTTCTTTTC | 84333 |
| rs563179547 | in-del | -/AATTC | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259815 | CCTTATACAAAAATT[-/AATTC]AAGATGGATTAAAGA | 84333 |
| rs563247687 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272805 | ATAAAATAATAAAAT[C/T]CACCGTTCTTTTATT | 84333 |
| rs563252510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228071 | AACTGTCTCCTAGGA[C/T]CTACATAGGCATCTT | 84333 |
| rs563274121 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186721 | ACTAGGGATGTACTA[A/G]TAACTGTTTCACTTC | 84333 |
| rs563286013 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280432 | CATATGTAATTTCAC[C/T]ATTTTCCAAGGAAAT | 84333 |
| rs563289722 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244077 | ATTTTTGTAGTGAGA[A/G]ACAGTCAATAAACCA | 84333 |
| rs563317104 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190559 | GAAACACAGCCTGTA[A/G]CCATGGTGAGGAAAG | 84333 |
| rs563318929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235733 | GTCTCACGAGATCTG[A/G]TGGTTTTAAAAAGAG | 84333 |
| rs563319298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184198 | TCTTTCAGGTATACC[A/T]GTCAGTGGTAGATTC | 84333 |
| rs563332705 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257089 | TAATGTACAGGTATA[G/T]GAAGAACTCTTATAA | 84333 |
| rs563336707 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173772 | TATTTAGGACAAGTG[A/C]TAGGTTTTCAGCCTT | 84333 |
| rs563354491 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168859 | CATGAATCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 84333 |
| rs563371325 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220895 | CTCACCCAAGTTTGC[A/G]CCTCAGGCGAGAGCG | 84333 |
| rs563374816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217910 | TCCTGCCTCAGCCTC[C/T]CTAGTAGCTGGGATT | 84333 |
| rs563380547 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190007 | TTAATATCTTAGTTT[G/T]TTTGTGCTGCTACAA | 84333 |
| rs563436692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217169 | CTCCTGAGTAGCTGG[A/G]ACTACAGGCACCTGC | 84333 |
| rs563474517 | snp | C/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207233 | GATGTGCAGCTGGTG[C/G/T]TAGTATTCTTCTACT | 84333 |
| rs563482264 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164245 | TCCACAATAACTTGT[-/G]GGGGGGGTCAGGGAC | 84333 |
| rs563511572 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262885 | TTCACGCAAAATACC[A/T]TGTATGGTTTTATTT | 84333 |
| rs563559202 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209259 | GATGGAATCTTCCTT[A/G]TAGAAGAAGAGAACT | 84333 |
| rs563559299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173022 | GTGATCTTACTAATC[A/G]ATAATAAGTGCCTAA | 84333 |
| rs563709781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206008 | ACCTGGGTGACGGAC[C/T]GCGACTCTGTCAAAA | 84333 |
| rs563772785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214903 | TCAATTTATGCTTAT[A/G]AGTTCAGGTTCTTAT | 84333 |
| rs563774738 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270543 | CCGAGCTGAGCCCGC[C/G/T]TTACAGCATGTTGAT | 84333 |
| rs563785563 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230809 | TGTATTTTGTGTAGA[A/G]ACGGGGTTTGGCCAT | 84333 |
| rs563823218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183451 | TTTTATTTTGAGTCT[A/G]TGTGTGTCTCTCCAT | 84333 |
| rs563834310 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269371 | CATTTTTTGAAACAT[A/T]AATGGAATCATATGT | 84333 |
| rs563860232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180385 | TTTGCTTTTGTTGCA[A/G]TTATTTTGGTGTCTT | 84333 |
| rs563860837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255240 | TTACAACTGCCTGAG[A/G]TATAGATAACATTTG | 84333 |
| rs563923836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168614 | GACTTGAGGCAAGAA[A/C]AGTGTCAATGAAGCT | 84333 |
| rs563937714 | snp | G/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281368 | AAATGTAATCTAAAT[G/T]TAAACTGATTATTTA | 84333 |
| rs563976540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277447 | AAAAGGAAAACCACT[A/G]ATGTTTTGGTTCTAT | 84333 |
| rs563985057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175391 | CAGTCAGGACTGGAG[A/G]ACTCTTCTCTGGGTA | 84333 |
| rs564031987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275452 | TACATTTTATTTTTT[G/T]TTTTTTTGAGATGGA | 84333 |
| rs564131555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168221 | GTGAGCAGAATAAAA[A/G]GCTAGGATAGAGCCT | 84333 |
| rs564167674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199771 | CCTCTTGTTTGACAG[A/T]TAGGGAAGTGGAGTA | 84333 |
| rs564195381 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252706 | GTTCTTTTTCATAGA[C/G]TTCATGGTCATCCTT | 84333 |
| rs564200754 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182673 | TAACTTTTTGATATG[A/G]GCATTTAGTGCTATA | 84333 |
| rs564234498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174865 | TCAGTCTCTCCTGCA[A/G]CACCATTACAGGCAT | 84333 |
| rs564267813 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236570 | TCATTCTTGGACCAA[C/T]TGGGTTAACCACTAC | 84333 |
| rs564291238 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222604 | TGGGAACATGTAACA[C/T]TTGCTGTTAATAGAA | 84333 |
| rs564304370 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198524 | CTGGAGGTCACCCCA[A/T]ACCACTATTTCAGCA | 84333 |
| rs564329432 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205129 | ACAGTTATTTTAAAT[A/G]CATAAAATATATTTA | 84333 |
| rs564339623 | in-del | -/ATA | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164826 | CCCAGGAGCCACCCC[-/ATA]ATACTATTTTATTTT | 84333 |
| rs564343025 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216656 | TAGAGATGATAGTGG[A/T]TCTGAACAGGGTGGC | 84333 |
| rs564377442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244793 | TGAACATGACTTTAA[A/G]ATTTCTGACCTGAGC | 84333 |
| rs564387098 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249856 | TTTACCCACGTGTAC[A/G]CTGCAATTAAACAAT | 84333 |
| rs564392552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185734 | TTTCATGAAGGGTTC[C/T]CCTGACCCGGGAGTT | 84333 |
| rs564405601 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260156 | GTGGGCAAAGGGTAT[A/G]AACAGACACTTCTCA | 84333 |
| rs564409547 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161496 | GAAGGCTCTTAGCCT[A/G]GGAATTAGCTGTAAA | 84333 |
| rs564410047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199087 | CTCCCATTTTATTAA[A/G]AGCCTAGTTTTTTCT | 84333 |
| rs564456064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185430 | TCACAGCTCCATGCA[A/G]CACTGTTGTCCGTGC | 84333 |
| rs564478655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243180 | CTCAGAGGCCTGAGT[A/G]TACCAGGAGACTAAG | 84333 |
| rs564517324 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282672 | TTAAAGGTAAAACTC[A/G]TCTTATGGAGTCTTT | 84333 |
| rs564542421 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248333 | TTATCAGTCTACTAC[A/T]GGGGAAGGCTGTAAA | 84333 |
| rs564546367 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197772 | ACACTTTCATTTTGT[G/T]ATATTAAATTTCAAT | 84333 |
| rs564562231 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213414 | TTCTGTGTCAGATAT[C/T]ATAAGTATGTTTCTG | 84333 |
| rs564576568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250390 | TTAGAGGTATCTCAT[C/T]TGGAAATCGTCCCTG | 84333 |
| rs564637859 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257780 | GTAACTGAAATCAAG[G/T]AAAGTGAAACTGCAG | 84333 |
| rs564641853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192225 | TTGTGGAATTTTTTT[A/G]AAAAAGCATTTATGA | 84333 |
| rs564653249 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247495 | ATGAGTTGAGAAAGG[-/T]TTTGGGGTTTTTTTT | 84333 |
| rs564676666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164406 | CACCTGGCTACATTA[A/G]CCGGTTGAGGAGCGC | 84333 |
| rs564721390 | in-del | -/AA | 0.311452 | 0.24233 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221724 | ACATATTTTACAGTT[-/AA]AAAAAAAAAAAAACC | 84333 |
| rs564727045 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230090 | CTTTTGAAACTATGT[A/G]TTAGATAGCAAGGAA | 84333 |
| rs564734847 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282171 | TATTTCATAAGGACC[C/T]GTGGTTTTTTTCCCC | 84333 |
| rs564740237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275093 | TATTAATATTAAAAG[C/T]ACATGGCAAAAATAT | 84333 |
| rs564747256 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172151 | CCTCTAGGGCCAGGC[A/G]CGGTGGCTCATGCCT | 84333 |
| rs564795190 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246993 | GATAGATAGATAGAT[A/G]GATAGATAGATAGAT | 84333 |
| rs564853852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182917 | CAATTTCCATGCAAT[C/T]GTATGGTTTTGAGTG | 84333 |
| rs564867949 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188806 | AGCCTGTTGACCTAC[C/T]CAACCTTTTTTCCAC | 84333 |
| rs564869854 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165089 | GTTGAAATTCAGTGC[-/T]TTTTTTTTGTGGGAA | 84333 |
| rs564876925 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195751 | AAATCATATTTTTTT[A/T]AATGAAATTTAAATG | 84333 |
| rs564892251 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218197 | TGTCTTGGCTCTACC[A/G]GAATCAGCTCTGTAA | 84333 |
| rs564962560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232381 | AGAAAAGGTGAAAAA[A/G]GAATGGGAAGAGAGG | 84333 |
| rs564964252 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278434 | TTTTCAGCATGCAAA[C/T]AAGGCCATTGTCTAT | 84333 |
| rs565018188 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258866 | CTTTGCCAGGAAATA[C/T]GTTTTGCTAGGAAAA | 84333 |
| rs565020537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239559 | GGAGTAGGAGAGCCA[A/G]TCTATACCATGTGAA | 84333 |
| rs565024547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231755 | ATGTTTAAAGGAATC[A/C]CTCAGACTACTATGT | 84333 |
| rs565055020 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262386 | TGACCCGAGATCACG[A/C]CACTGCACTCCAGCC | 84333 |
| rs565083178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238809 | AAACCCTTTTGGGGA[C/G]AAGAAATTTGGGAAG | 84333 |
| rs565130437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262079 | AATGATGATCTTTCA[A/G]CTCATTAATTTCCCC | 84333 |
| rs565138424 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163812 | CCGCGCCCCCTGCGG[G/T]CGCTGCCCGCGCGCG | 84333 |
| rs565162094 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234059 | GGAAGCTCACTCTCT[C/G]TGATACATAAGAGAC | 84333 |
| rs565202472 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189191 | CTCTTCTTTGCCTGG[A/C]AAAATCTTCTTTTAC | 84333 |
| rs565225094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241138 | GGAGTGCAATGGTGC[A/G]ATCTCAGCTCACCGC | 84333 |
| rs565271398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176293 | CAGCTGTTAGTCTGA[C/T]GGGCTTCCCTTTGTG | 84333 |
| rs565297759 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168956 | AAAAAAAAAAAAAAA[A/G]AAGAAGGCTTGATAA | 84333 |
| rs565397650 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284042 | AATCAGTACAAGATA[C/T]GTCTTTTGCAGAAAT | 84333 |
| rs565415110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198403 | CCAACTTCCTTACCT[A/G]TTTTGTGGTCTTTAC | 84333 |
| rs565468436 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253460 | TCTATTTTTAAATAG[A/G]CCAGTTGAGAGTTTC | 84333 |
| rs565477590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227554 | GTTTCATCCCTCTGT[C/T]ACTGTTCTCATTCAG | 84333 |
| rs565491032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212441 | TGGAGTGTCTCTTAA[C/T]AGTCACAGAGAACTC | 84333 |
| rs565510739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217073 | GTCTCTCGCTCTGTC[A/G]CCCAGGATGGAGTGC | 84333 |
| rs565513852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207903 | TCAGATTATCCCATT[A/G]TTAGTGCTGTTAGAT | 84333 |
| rs565523806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248287 | TCAAGAGTCTGGATA[C/T]AGAGAGAGCTGGGGA | 84333 |
| rs565611790 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277869 | GTGGGCTCTCACCAG[C/T]CTAAGCTTTAGTGGA | 84333 |
| rs565620698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221277 | TAGGATCTTAGTACC[A/T]CCCCAGGTCGGGACC | 84333 |
| rs565630548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203528 | TTATTTCAGTATTCT[A/G]TATTTCATTGACTGT | 84333 |
| rs565660829 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166436 | ATATCTCCTTTCCAC[A/G]TTGAAGAAGTTTTCT | 84333 |
| rs565683003 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211618 | TCATAGGAAGAGAGA[G/T]TCCTATGAGGTAGAA | 84333 |
| rs565705029 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270378 | TACCAAAGAGATCAA[A/T]AGAAAAAAAAAAAAG | 84333 |
| rs565714509 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267298 | TACAACCCCCTCTCC[C/T]GATGGCATTCTTACT | 84333 |
| rs565745937 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219385 | CAAAATAGGAACATA[C/G]CAAGTCTTTTTTATA | 84333 |
| rs565762391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202556 | TTGCATAGTAGTCAT[C/T]GTTACTGTTAATTAT | 84333 |
| rs565790324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272450 | AGGAGTTTGAGACCA[C/G]TCTGGGCAATATAGC | 84333 |
| rs565823653 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202023 | AGGATTATATCCAAG[A/C]CTTGCATTTTATTAG | 84333 |
| rs565841526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191183 | GTAAAAGATTAACAA[C/T]AACAACAACTAATAA | 84333 |
| rs565850730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249092 | TGTTTTATTTTGTAT[A/G]TTTGCCTCTAAAGGA | 84333 |
| rs565900551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188911 | TTGGAGGCTTGAAGA[A/G]AAAGGTAAAGAGGCA | 84333 |
| rs565918805 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197351 | TGACTGCTCCGTGAT[A/G]TATTATTTTCTGAGG | 84333 |
| rs565934568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226890 | ATACCTCTTCCCTTC[A/C]GTAGGCCAGGGACAT | 84333 |
| rs565938399 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235189 | CCTGGTGCGAATCTC[C/G]TAGATATTCTGAATT | 84333 |
| rs565978043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197012 | CTCTTTTTAAACAAC[A/G]ACAACAAAAAAAACA | 84333 |
| rs566005838 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256940 | AAAGCACAAGCAACA[A/G]AAGAAAAGAAATAGA | 84333 |
| rs566027649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196046 | CACTTTCTCGCATCC[C/G]CTACTGGTCAAGTGT | 84333 |
| rs566035308 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261163 | AATAATTAGGAATAT[A/T]TTTACTCGCAAATAC | 84333 |
| rs566041395 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215473 | AGAAATAAAAACATA[C/T]GTCCTTCTCCTTAGG | 84333 |
| rs566064315 | in-del | -/TG | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283353 | TCTATAATTCCAAAC[-/TG]AGACTGATTTTTCAG | 84333 |
| rs566083753 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169882 | AGGCTTGCTATAAAC[C/G]TATAGTAATCAAGAC | 84333 |
| rs566167361 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199289 | GGATGTTTATTAGGG[A/T]ATGCCCTTTGAAGGG | 84333 |
| rs566190303 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278846 | GAAAAAAAGTTCATT[A/C]TTGAGTGTGCAAGTC | 84333 |
| rs566252573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184297 | TTCTCTGCCTGTCTT[A/G]TTTCAGAAACACAGT | 84333 |
| rs566256458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189769 | GGAAACAGTTAAAAT[C/T]CTAAGAAGCATCTGA | 84333 |
| rs566256463 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177864 | CTTCCTGGGTGAGGC[A/G]ATGCCTCTCCCTGCT | 84333 |
| rs566276322 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226606 | ACTCTTTCTCACCTC[A/C]AACCAGATAGGTTGG | 84333 |
| rs566283397 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166579 | AACTTGTAAGTGTGC[A/G]TGTTTGCTTACTTGG | 84333 |
| rs566313224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222648 | TTATGAGGAATTTGA[C/T]GCTTTTTTCTCTCAT | 84333 |
| rs566315879 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183747 | CCTTCAGGAGTCTTG[A/T]AAGGCAGGTCTGGTG | 84333 |
| rs566335944 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187936 | CCATGCTAATGGCAG[-/A]ATGGATGATTCTTTT | 84333 |
| rs566393922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241432 | ATCCCTTTATTCCCA[A/G]TTAGGAAATCTAGAG | 84333 |
| rs566396634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91231093 | ACTAGTAAACTCAGT[C/T]GTCTCCCTTGCTTTA | 84333 |
| rs566422102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214624 | AGAACCCAGTTGACC[A/G]GGATAGCATGTTTTT | 84333 |
| rs566452997 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237553 | TTGGAGACCAGCCTG[A/C/G]CTAACATGGCGAAAC | 84333 |
| rs566497192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192681 | ACGACATACAATAAA[A/G]CAGGCATAGTAAACA | 84333 |
| rs566514958 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244463 | AGATCATGAGATTCC[A/C]GATTATGAAGGGCCA | 84333 |
| rs566521026 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173946 | TAGAAGTAAAACAGC[C/T]AAGACTCCAGTATTG | 84333 |
| rs566565006 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235351 | CCTGGTTCAAATCTA[A/G]CAAATGGTAAAAGTA | 84333 |
| rs566575200 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281484 | TTTCTGTTTTAAATT[C/T]ACTGCATAAAGTTTG | 84333 |
| rs566647969 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268036 | ACAATGTATTGAATA[G/T]TGAATAATCCATATT | 84333 |
| rs566654495 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175978 | CTGGTTATTTTGCTC[A/G]TTAGTTGATGCAGTT | 84333 |
| rs566656526 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181221 | TGTATTCTGAGGTTT[C/G]CTGAAGTTATTTGTC | 84333 |
| rs566660513 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276680 | AAAGCCATTTTACTT[A/C]CCTCTGTACCTTTAT | 84333 |
| rs566679601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238197 | GCTTAGTAGCCACAT[A/G]TGGCTAGTGACTTCT | 84333 |
| rs566683241 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178150 | ACTGCAATGTAGGCT[A/G]GGAAAAAACATTGGC | 84333 |
| rs566684283 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275705 | TGATCTGCCCGCCTC[A/G]GGCTCCCAAAGTGCT | 84333 |
| rs566701558 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212664 | GCCTAACTTCTATAA[C/T]GCATGCCCACTAATT | 84333 |
| rs566715643 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253259 | GTGTCACAGGTTTGG[C/T]GTAAGGTTATTTTGT | 84333 |
| rs566739125 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205264 | TATGGAACGATTTTT[C/T]TTTTTTCTGGGTTTC | 84333 |
| rs566787512 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283265 | AGCACTTCCTTTCAG[A/G]AAGTTATAAAATTAA | 84333 |
| rs566827165 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231210 | CATTGTGTTCTCATT[C/T]ATATTATAAATCATT | 84333 |
| rs566839902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174415 | GGGAGGCTGAGGCAC[A/G]AGAATCACTTGAACC | 84333 |
| rs566853238 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191629 | AGCTTTTTGGTTTCT[C/T]GGTGTGTGTTATCAT | 84333 |
| rs566899757 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283415 | GAATCAAGTGAAACA[A/G]ATATGTTAAATACTG | 84333 |
| rs566905053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177502 | ATGCCTTGCCCCCGG[A/G]GGTGGAGTCTACAGA | 84333 |
| rs566939955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236628 | ATGAAATCTTTAAGA[C/T]ATTTTTAAAATGTGC | 84333 |
| rs566967066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185062 | CTGTGCTAGGGGTAC[C/T]CCCTCTGCCCCCAGT | 84333 |
| rs566967517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213767 | TGGGATTACAGGCGT[A/G]AGCCACCATGCCCAG | 84333 |
| rs566968228 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177072 | ATGATGGTGACGTAC[A/G]GATGGGGTTTTGGTG | 84333 |
| rs567028481 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218384 | ACTTGAGGGTCCCAC[C/T]GGTACTTGAGATTTG | 84333 |
| rs567029096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222055 | TGAAGAAAGTTGTTG[A/G]AGGGTATATTAAGGT | 84333 |
| rs567075719 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274760 | TGAATATCTGAGGTA[C/G]AGCACTGAAGCCTGA | 84333 |
| rs567131111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213368 | CGTATGCATAAGTAA[A/C]CTCTATTTGGCTACA | 84333 |
| rs567140671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270766 | TTGTACCTTATATTT[C/T]TTATGTATTTAATTT | 84333 |
| rs567178259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266176 | TGAATGTAACTTCAG[A/C]TTTCTTTGATAGTTT | 84333 |
| rs567262433 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182201 | GGAATAGTTCCCGTA[A/G]GAATGGTCGCAGCTC | 84333 |
| rs567334884 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225199 | AAAGGGATATATATA[G/T]TTTTATATATATCAT | 84333 |
| rs567384364 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260464 | CCCATTACTGGGTAT[A/G]TACCCAAAGGATTAT | 84333 |
| rs567405139 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164937 | AGCTCCACTATGCTA[C/G]GGATTTGGGCTGTTT | 84333 |
| rs567448770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165602 | AAGTGATCCAATATG[A/G]AGTATTAATTTAATC | 84333 |
| rs567515850 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263147 | CCTAGTATGCAGGGG[G/T]ATTATTTAATGAAAT | 84333 |
| rs567549979 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180998 | CATGGAATGTTTTTC[A/C]ATTTGTGTCATCTCT | 84333 |
| rs567568113 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207291 | ATTGCATTACTTTTG[A/G]TCTTACACATTTTTT | 84333 |
| rs567633499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253550 | TTGGTCCAAACATGC[A/C]GTTTTAGTTATGACT | 84333 |
| rs567634077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216130 | CACTCTAGTGGGAGA[C/T]CCAGATGAGTAAATC | 84333 |
| rs567654103 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261436 | TGAGGTAAGTTAAAT[A/G]ATATCTAAGCTTGAT | 84333 |
| rs567654640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268664 | ATCTTGCTCTGCTTC[C/T]AGCCTCTTAGGAAGA | 84333 |
| rs567656100 | in-del | -/TTACCCATCC | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227851 | GTGCCCAGCTAGCAG[-/TTACCCATCC]TTTAAAACTCATCCC | 84333 |
| rs567715947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249996 | GTCATCAGAAGTTAC[A/G]TGGTAGGTTTACTCT | 84333 |
| rs567749159 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239957 | GGAATTATAGTACCT[A/G]TGAGCAGAAACTCAT | 84333 |
| rs567762001 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201575 | GGAGTGGAGAACTAT[C/T]TTCTCCCCTCCTCCC | 84333 |
| rs567768921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168889 | GCTGAGATTGCACCA[C/T]TGGACTCCAGCCTGG | 84333 |
| rs567782362 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176331 | CAACCTTTCTCTCTG[A/G]CTGCCCTTAACATTT | 84333 |
| rs567870204 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281571 | TTAATTTTTTTGGAA[A/G]ATTTTCATAAGAATA | 84333 |
| rs567894268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194891 | GATATAAGGGAAAGA[A/G]AAGAGTTTCTGGGGT | 84333 |
| rs567903516 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173481 | GAATTTTAAAAAGTG[A/G]ACATCCATGTAACTA | 84333 |
| rs567957230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200961 | GGAGGGTCAGGTGGG[A/G]GAATGGTCAGAGCTT | 84333 |
| rs567961629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257978 | GTCATAAACTGCAAT[A/G]AAGTACTGATACATG | 84333 |
| rs567979150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163940 | TTCGCTGCCACCTCT[C/T]CTGGGTCTACAGGTT | 84333 |
| rs567988734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243761 | CAATAAATAAAAATT[A/G]CTAAATGTATTATTA | 84333 |
| rs568048901 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250598 | TGTTCCCTCAGGCCT[G/T]GTATGATGTGTATCC | 84333 |
| rs568051046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242786 | TAAGTTACATGTGTC[A/G]TGGCCCCTTACTCTT | 84333 |
| rs568065886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91204379 | CCTTTTGTTAGATGA[C/T]TGCACTCAAGTAACT | 84333 |
| rs568083925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190151 | ACTTCCTGGTTTCCA[A/G]GTGGCACCTGATCCC | 84333 |
| rs568105731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91211798 | AGTGAGAAGCCTGGT[C/T]GAGTTGTTAAAGTAG | 84333 |
| rs568119500 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167053 | ACCAATAAAGAAATA[C/T]ACAGTTCTCCTGCAA | 84333 |
| rs568211243 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196103 | TGGGACTGCACATTT[G/T]TCAGAATGGCTCACT | 84333 |
| rs568216109 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185503 | GTGGAAGTGAGGCCC[A/G]CTGACCATCACTGCT | 84333 |
| rs568219219 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205640 | ATGCCAGATTCCTTG[C/T]CCTGCATCGGACCAC | 84333 |
| rs568318537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228283 | AACTAAGGACAAAGG[A/G]GCTATGTTCCAGCAG | 84333 |
| rs568320456 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219404 | GTCTTTTTTATATAT[C/T]GTGGTATATATACAG | 84333 |
| rs568337451 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268807 | GGCTAAGCCTGTTTT[C/G]TATGGTCCCTGCCCT | 84333 |
| rs568356308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191308 | GCTGCAACAGTCAAT[A/C]TGATAACTGAGATGG | 84333 |
| rs568397726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227620 | ATTCTTAACTGTGTC[C/T]AAGTGGTAATAATTA | 84333 |
| rs568441160 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239004 | GTATGGGATTCAGGT[-/A]CATTCATCCAACAAA | 84333 |
| rs568451778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241818 | TTTGTTTTTCAAGTT[C/T]AATGCCTGTTTGGGA | 84333 |
| rs568484554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187165 | AGGACTTGTAAAAAA[C/T]ACTGGTATCTGGGAC | 84333 |
| rs568545206 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91194117 | ATGTCTGTTAAACAT[A/C]CAGTTAAAGATGCAG | 84333 |
| rs568545453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186539 | ATATATATGTGTGTG[C/T]GTGTATATATATATA | 84333 |
| rs568597933 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178677 | TACAGGTGTGAGCCC[C/T]TGCACCTGGCCTGCT | 84333 |
| rs568604690 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248397 | AGTAGATGTGCTAAA[A/T]TTGTGTATGTATTTT | 84333 |
| rs568650764 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91176423 | GGAGTATCTTTGTGG[A/C]ATTCTCTGTATTTCC | 84333 |
| rs568667424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216679 | AGGGTGGCTAAACAG[A/G]GGGATTTAAGAGACA | 84333 |
| rs568697252 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280635 | TGGTCCTAAGTGATA[C/T]GGTATTACTACTAGA | 84333 |
| rs568771607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238911 | GGTTTTCTGATACTG[G/T]CTTTTACCCACATTT | 84333 |
| rs568783139 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235224 | GGTCTGGGATGGAGC[C/T]TGTGAGTCAATTCTT | 84333 |
| rs568792634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224220 | GGGCATGCATATTTT[A/G]GAAGAGCTCCCCAAG | 84333 |
| rs568797515 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203562 | CACTTCAGTCTTTCC[G/T]GTATTACATTGAACC | 84333 |
| rs568853554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184099 | TTCCTGAATTTGAAG[A/G]TTGGCCTGTCTAGCT | 84333 |
| rs568874163 | in-del | -/GATAGATAGATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247010 | ATAGATAGATAGATA[-/GATAGATAGATA]ATCTGCCTATATGTT | 84333 |
| rs568877137 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283607 | TGTAATGGGATCAGC[C/T]TAGCATTGTTTGGTG | 84333 |
| rs568898761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175013 | GCCTTTAACTGAGGT[G/T]GAGAGGAGATGCTGG | 84333 |
| rs568927620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200020 | GGAACTAGTCTACAC[A/G]CTTCAGGCTATCCTA | 84333 |
| rs568947024 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245455 | GACAACTCTTTCAAG[G/T]AGTTTTGCTACAAAT | 84333 |
| rs568990999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207364 | TGCCAAAATCTTTCA[A/G]TGAACATCCGTATAT | 84333 |
| rs569005444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176379 | TTGGTGAATCTGACA[A/G]TTATGTGTCTTGGAG | 84333 |
| rs569014669 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269934 | TCTTCCAATTGTGTC[C/T]TGCTTCCTAGTTTTG | 84333 |
| rs569022102 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91227239 | TTTAGATGTATGTTC[-/T]TTTTTTTTTCCTGTG | 84333 |
| rs569025222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274304 | TCATGTTTTTACAAA[G/T]AGTAATGAGAGGGAA | 84333 |
| rs569028911 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282365 | GGCACGCGCCTGTAA[G/T]CCCAGCTACATGGGA | 84333 |
| rs569056761 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169621 | ATCAAATTTTGATAA[A/C/G]AGAAATCAAAGAAGA | 84333 |
| rs569102708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268813 | GCCTGTTTTCTATGG[C/T]CCCTGCCCTCTCTAG | 84333 |
| rs569169609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168783 | AATACAAAAAACTAG[A/C]CGAGTGTGGTGGTGT | 84333 |
| rs569192700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276802 | GAATCAGGAATCAAA[C/T]GCAAAACTAGAGCAG | 84333 |
| rs569212996 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205425 | TAGACCTAGATATTA[C/G]TATTTTAAGTGACAA | 84333 |
| rs569235253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230482 | AATTTAAAGCCAGGG[C/T]GCAAAGCTATATTTT | 84333 |
| rs569253158 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235034 | GATGATGGTTTAGCA[A/G]AGAGCCAAATCCTGG | 84333 |
| rs569294820 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222213 | TATAAGATGGACTGC[A/G]GGTGGAGAGGTGATA | 84333 |
| rs569300077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237308 | TATGATAATAACAGT[A/G]TATCATCCAAACGAA | 84333 |
| rs569301721 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272313 | GTGATTGATGATCAG[A/C]CTTAACCCTGTGAAT | 84333 |
| rs569379605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91229720 | TGAATTTATGATTCT[G/T]AATGAATAGCCATTT | 84333 |
| rs569382312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206213 | AGGGTAGCTCCTGCC[A/G]TCAAGGAGCTGAACA | 84333 |
| rs569385986 | in-del | -/ACAG | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242438 | AAACTGTTAATAAAA[-/ACAG]ACAGTTAATAATTAT | 84333 |
| rs569409737 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259859 | CCTAAAACCATAAAA[A/T]CCCTAGAAGAAAACC | 84333 |
| rs569432372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270862 | GTTTTGTAGTCCAAT[C/T]ACAATTAAAATTACA | 84333 |
| rs569454186 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91267586 | ATTTTTATTTATCTG[A/T]ATCTCAGCTTCCTTT | 84333 |
| rs569527512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205745 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 84333 |
| rs569555822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258960 | ATACATACAAATAGG[A/G]GTAATATCTTTAAAA | 84333 |
| rs569558951 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167366 | TAAAGGCTGTTTTAC[A/T]TGGGAGAACTGTTAG | 84333 |
| rs569566983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215074 | TTCTAATTAACTTCC[C/T]CATCAGTACTTGTAA | 84333 |
| rs569575966 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166212 | GAATTAGCCAGAGCT[C/G]CTATAGGTGGAGAAG | 84333 |
| rs569619500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263985 | AACTAATAAGAAGAT[A/G]GTAACCCCTTCAAAT | 84333 |
| rs569628323 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219285 | AATACTGATTAACCG[C/T]ACTTGTGATAGGTCA | 84333 |
| rs569662037 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91275362 | TAAGAGGTGGGGAAA[G/T]ATAGTACTCATTATT | 84333 |
| rs569662389 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242048 | ACTCTGGTCTGTAAT[C/T]CTGAGTAAGCCTTGT | 84333 |
| rs569667116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177555 | GCGGTGGGCTCCACC[C/T]AGTTCGAGCTTCCTG | 84333 |
| rs569667693 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274631 | GGTTAAAATTTATAG[A/T]GTTAGAAGAAAAAGT | 84333 |
| rs569680198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177796 | CCAATTTTCCAGGTG[A/C]CGTCTGTCACCCCTT | 84333 |
| rs569699084 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273066 | TGGGAATTCTCGTGC[C/T]TTCATTAAAATGTGT | 84333 |
| rs569699348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226136 | ACGCTAGGTTTTATG[G/T]AGACTCATAAGAAAA | 84333 |
| rs569748409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208976 | TTCTGCCATTGGTAG[G/T]TTTCAGTGGCTTTTG | 84333 |
| rs569766625 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165597 | GGCTCAAGTGATCCA[A/G]TATGAAGTATTAATT | 84333 |
| rs569776226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183716 | TAATAGTCCTTCTTT[A/G]CCATATGTAGTGTGT | 84333 |
| rs569781971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234156 | CCTCAAGAACTTGAA[A/G]ATAGGAAATAGGATA | 84333 |
| rs569800077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196909 | AATTCACTGGTGGAC[A/G]AGATATAATCCCCAC | 84333 |
| rs569809166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248432 | CATGTATAAGATTAT[A/G]CATCTCAGACTATTT | 84333 |
| rs569843539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202760 | ATGTTGGGGCAAGGG[A/G]TAGTTAGGCGAAAAG | 84333 |
| rs569865747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203355 | TGTTCCTTTGTTTAA[C/T]TTACTTTTTATTAGG | 84333 |
| rs569874157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172422 | AAACTCCCCTTCAGA[C/G]AAAAAAAAAATGCCC | 84333 |
| rs569890091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256142 | GGAAGCCCAGACATT[A/G]TACTTATTAGGCATA | 84333 |
| rs569922434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241321 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 84333 |
| rs569980178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201075 | TTTATAAAAGTGAGA[A/C]GAGCTGCCCACTTAG | 84333 |
| rs569984451 | snp | A/T | 6.62548e-05 | 0.00575526 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240606 | TATATTTTACAGTTC[A/T]TCTAATTTACATAAA | 84333 |
| rs570002016 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201992 | GAGGGTCCTGGACTT[C/G]GGAGCTACACTGTCC | 84333 |
| rs570004388 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180711 | TCCATTGGTCTATGT[A/G]TCTGTTCTTATACCA | 84333 |
| rs570045233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247331 | TTTTAAACCTATTCA[A/G]TATGGAAGTTATAGA | 84333 |
| rs570046798 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240152 | TTTTTATCTTTTTCT[G/T]TCCTACTTCTTTAAA | 84333 |
| rs570105168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243792 | AAGATATTTTAATAT[A/G]TAGCAAAACATTAAA | 84333 |
| rs570108852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278096 | GATTCTAGAAAAATA[A/G]TGGCAATCAAAAGAA | 84333 |
| rs570124165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164079 | GAATGAATCATCGCC[C/T]CGCGGACCGGGCCCC | 84333 |
| rs570129198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183031 | GAAGAGTGTTTTACT[C/T]CCGATTATATGATCA | 84333 |
| rs570155421 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236727 | TTTTTAAGCATCTAT[A/G]GGAAACCAAATCCTC | 84333 |
| rs570188418 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170333 | AGAGAATAAAAAGAT[C/G]AGCCACAGACTGGGA | 84333 |
| rs570188509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91163133 | GCCCGACGCGGCCCA[A/G]GGAAGTTTCTGGCGT | 84333 |
| rs570207476 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186314 | TTGCAACTGGGATCA[-/C]CAGCAGTTTTCATAG | 84333 |
| rs570210476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205167 | CACTAGAGTCACTAA[A/G]TTGGGCAAAATCTTC | 84333 |
| rs570211528 | in-del | -/TAAAT | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167153 | TCTTAAGAGTTTGTC[-/TAAAT]TAACTTTTATGATAA | 84333 |
| rs570293197 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211703 | GAAGAGGAAGAGGAG[A/G]AGGAGGGAGAGCATT | 84333 |
| rs570299526 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266399 | AGACATTTTTAGTAA[C/G]AGACTATGATTTAAA | 84333 |
| rs570318466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198708 | CTATTCAGTAGCATT[G/T]AATCAATCCTGAGTT | 84333 |
| rs570321738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238091 | TAATTAATATAAAAT[C/T]ATTGAGATTACCTGT | 84333 |
| rs570347532 | snp | A/G | 6.67768e-05 | 0.00577789 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251317 | AAAAGCTGACAAACC[A/G]AAAGTAGATGAAGAA | 84333 |
| rs570349375 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271231 | CCCAGAGCTCTGATT[A/T]CCTTGAACAGTATTA | 84333 |
| rs570391584 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191836 | TGAGCATTCATGTTG[G/T]ATCCAGCCCTTTGAA | 84333 |
| rs570492432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184936 | CCAGCCTGAATGCAG[C/T]GGTAGGAGGTAGCTG | 84333 |
| rs570510419 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283058 | CAAACCTAGTTGAGT[A/G]GCATTTTGACAGAAA | 84333 |
| rs570545760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258039 | TGCTAAGTGCAAGAA[A/G]CCAGACACAAAAGGT | 84333 |
| rs570555413 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191070 | CAAGGCCCCTAGTGG[C/G/T]TGCCTGATACCATGG | 84333 |
| rs570582865 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266646 | GACAAACCTGTTTTT[C/T]AGTTGCTTTCCTTCT | 84333 |
| rs570589824 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238585 | CCTCCACTCTCATTT[A/C]TTTCTTTCTTTCTTT | 84333 |
| rs570615401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190194 | TAGTGGAAGGGACTC[A/G]CTGGCTTTCTGACAT | 84333 |
| rs570636609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230536 | TATACATATATGAAT[A/G]TATAATGTCAGAACC | 84333 |
| rs570641767 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186373 | TAGGTGATTAGCAAG[C/G]AAGAGATGAAGGAAT | 84333 |
| rs570641792 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180131 | TCATTACATTATTGG[C/T]GGCATGTATGTCTTC | 84333 |
| rs570661567 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184369 | TAATACTTTTTATTC[C/T]GTTATGAAATCCTTG | 84333 |
| rs570680401 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180470 | GTTTTTATATTTTTT[G/T]GTTTTACATTTAAGC | 84333 |
| rs570697635 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207897 | ATAATGTCAGATTAT[A/C]CCATTATTAGTGCTG | 84333 |
| rs570718297 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179160 | CCCATCCTGTCCTCT[C/G]TCATTACTTTGGTTT | 84333 |
| rs570762716 | in-del | -/TTT | 0.01739 | 0.091611 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167162 | TTTGTCTAAATTAAC[-/TTT]TATGATAAGTACATT | 84333 |
| rs570799160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91201766 | CTTGGATGAAATTTT[A/G]TTTAAGTGTGTTACT | 84333 |
| rs570865391 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236118 | AAAAAATATGATATG[A/C]ATTTTTGATTTTGAT | 84333 |
| rs570886011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182143 | AGCGGTAATGTCCCC[C/T]TTATCATTTCTGATT | 84333 |
| rs570906877 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211028 | CATTAGGTACCAGGA[A/G]GCATTTGTTAAATAA | 84333 |
| rs570928272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242456 | GACAGTTAATAATTA[C/T]TACCCTCTCTGTTCT | 84333 |
| rs570928649 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235341 | TGTCCAACAACCTGG[G/T]TCAAATCTAACAAAT | 84333 |
| rs570936951 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181700 | TGTTGAACCAACCTT[A/G]CATCCCGGGGATGAA | 84333 |
| rs570947845 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174151 | CAACTTGGGCCACTG[A/T]AGGTTGGATATGAAG | 84333 |
| rs570991835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241862 | GGTAAATGTCTAGCC[C/T]TGTGGTTTTCAAAGT | 84333 |
| rs571010754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187196 | CTATCTATAGTGATT[C/T]GGATTTAATTGTTCT | 84333 |
| rs571011162 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179342 | TTTTTTAAAAAAAAA[A/T]TAATCTTTTAAAAAT | 84333 |
| rs571047154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167232 | AACTTGAATATTTCA[A/G]CCTCTCATCCAGCTT | 84333 |
| rs571069041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237723 | CACTCTAGCCTAGGC[A/G]ACAGAGTGAGAATCC | 84333 |
| rs571088891 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274046 | ATTCATCAATTAACA[A/T]TTTGCCACATTTTTT | 84333 |
| rs571112054 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220487 | AGGGAGCCAGGGCGG[A/C]AGCTGCACCTGCGAG | 84333 |
| rs571122944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208415 | TTTTTAGTCCATTCA[C/T]AGTGCCACTTCAATT | 84333 |
| rs571266157 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232720 | TGAATAGGTGTGGTG[A/G]TAAAAGTTCTCTTTG | 84333 |
| rs571286445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259908 | ACATAGGCATGGGCA[A/G]GGACTTCATGTCTAA | 84333 |
| rs571293369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215086 | TCCTCATCAGTACTT[A/G]TAATAAGCATCACCC | 84333 |
| rs571307281 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284524 | AAAGAACGTTTTGAA[A/G]GTAATTAGGAATCAA | 84333 |
| rs571329709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91232041 | GAAAGTTTGAAGGGA[G/T]GACCAAGGACTGAGC | 84333 |
| rs571331568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239932 | CCATTATTCATACTT[C/T]GTGCTCCATGGAATT | 84333 |
| rs571396361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239091 | ATTTAAAATAGCTGC[C/T]GGCTCCCAGCACCCT | 84333 |
| rs571427749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216757 | GCAGTAAGAGAAAGA[C/T]ATGGTCAAGGGTGAT | 84333 |
| rs571453604 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270647 | TTCCTTAAATTTTAT[G/T]TAAAAGGCTACAAAT | 84333 |
| rs571458938 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164153 | TACCTCTGACCCAGG[A/G]AGAGTGGCCCCTCTG | 84333 |
| rs571470502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176952 | CGTTGCTGATGAGGA[A/G]CTGTGTTCCTTTGGA | 84333 |
| rs571491016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225008 | GCAAAAACTGTCAAC[C/T]CTGGATGATGAGAAG | 84333 |
| rs571504737 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225577 | AGATCTGAGGATTCC[G/T]GTAGCACTAATCTTT | 84333 |
| rs571560075 | in-del | -/AACCATATAAT | 0.00557542 | 0.0525036 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244088 | GAGAGACAGTCAATA[-/AACCATATAAT]AAGTAATTTATATGG | 84333 |
| rs571624661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260394 | AACCATTGTGGAAGT[C/T]GATGTGGCGATTCTT | 84333 |
| rs571630935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206346 | GATGTTATAAATAAG[A/G]CTCTTCAACATGTCA | 84333 |
| rs571692451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215091 | ATCAGTACTTGTAAT[A/G]AGCATCACCCTCCTA | 84333 |
| rs571861201 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280125 | TTTCATTAACTATAA[A/G]TGGCTGAAAAAACTG | 84333 |
| rs571891685 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173190 | GTGATATTTAAGAGC[C/T]TAATTTTTAAAGTGT | 84333 |
| rs571898745 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199451 | TCCCTCAGTCCTTGC[A/G]TCCTTGGGAAAGTGA | 84333 |
| rs571905991 | in-del | -/T | 0.00924738 | 0.067366 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213640 | GGCTTTTTTTTTTCT[-/T]TTTTTTTTTTCTTTT | 84333 |
| rs571913643 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202116 | ATTGTACTCACCCCC[-/T]AGGATTATTGTGAGA | 84333 |
| rs571932449 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170716 | TGGTTTCTTACAAAA[C/T]GAAACATACTCTTAC | 84333 |
| rs571932546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193331 | CAGCTCAGCCAAATT[A/G]TACTTAGACTTCTAA | 84333 |
| rs571935805 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169259 | CCTAATCATGATGCA[A/C]ATAAAGAAGTTACTT | 84333 |
| rs571968524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196229 | TAGAATGTCAGTGCC[A/T]AGAGAAGTGATGTGA | 84333 |
| rs571968843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195798 | CTTTAAAGTAGCAGA[A/G]CCTAGACAGGGGCTT | 84333 |
| rs572018254 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191074 | GCCCCTAGTGGGTGC[A/C]TGATACCATGGATAA | 84333 |
| rs572094604 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202834 | ACTCAACTTTTAGAT[C/G]TATTTATGTTGAAGG | 84333 |
| rs572096023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233162 | GATCATGGAATTTAT[A/G]TTGGTAAGACGGGGA | 84333 |
| rs572121523 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91184471 | AATGTTTTAGCGTGA[G/T]TTTTAGCTTCCTTGC | 84333 |
| rs572146386 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273309 | AATGCTGAATTGTAA[C/T]GATAACACTGCCTGT | 84333 |
| rs572197281 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241975 | ATTGGAGATCACTTC[A/G]TTTAGCAAGCTCTCT | 84333 |
| rs572208132 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245321 | GTTGGATTTAGCAAC[A/G]TGGAGTTCATCAACT | 84333 |
| rs572242571 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271561 | TGTGTTTGACGTTAA[A/C]CTATTTTAAATAATC | 84333 |
| rs572262272 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227233 | CATGTATTTAGATGT[A/G]TGTTCTTTTTTTTTT | 84333 |
| rs572264218 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239410 | TTGGTCAGTATATGT[G/T]ATATGTCACATTTTC | 84333 |
| rs572267689 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262384 | AGTGACCCGAGATCA[C/T]GCCACTGCACTCCAG | 84333 |
| rs572321034 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91234749 | GTAAACTTTACATAT[A/G]TTATCTCCTTTAAGC | 84333 |
| rs572324019 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277642 | ATGTAATAGTCAAAT[C/G]CAAATGTTTATTAGT | 84333 |
| rs572343279 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219525 | AGCATAAAGAGTAAT[C/T]CTACTGCCATGAAGT | 84333 |
| rs572435930 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247076 | GAAATCCACAAGGAA[A/G]ACAGAAAAGGTCAAA | 84333 |
| rs572437777 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182552 | CGATCTCCTTTAGTT[A/C]AGCTCTGATTTTTGT | 84333 |
| rs572439460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188226 | CAGTGGGTGCAGCGC[A/C]CCATGCGCGAGCTGA | 84333 |
| rs572501695 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195039 | GTTCTCTTCTGATGA[A/C]TCAGTTTTCTCAGTG | 84333 |
| rs572522122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276999 | GTTTAAAATAAAAAC[A/G]AGTAAAACCAGAACA | 84333 |
| rs572579345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171321 | TGAAATGGGTTGGTT[C/T]TTTTATATTGATTTG | 84333 |
| rs572602680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217756 | TCTTCCCTTTCTTTC[C/T]TCCTTGTTTAACAAC | 84333 |
| rs572614547 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217080 | GCTCTGTCGCCCAGG[A/C]TGGAGTGCAGTGGCA | 84333 |
| rs572676187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225309 | ATATAACATATATAT[A/G]TAACATATATGTATG | 84333 |
| rs572751560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274511 | TATTGAGTATTATGC[A/G]TTGGGCAGTCTTCTA | 84333 |
| rs572769314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222328 | TGGGGAACATTTTGA[C/T]AGGGAGGATAATTAC | 84333 |
| rs572770979 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218676 | CTTGCTCTGTCTCCC[A/G]GGCTAGAATGCAGTG | 84333 |
| rs572787902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185692 | CACATAGTTCTGTGT[A/G]TCGGACTGAAGGCCC | 84333 |
| rs572802958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237029 | AAATGTATCACACAT[A/G]CATTGGTTAACAAAA | 84333 |
| rs572829774 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282560 | GCCATACAGCCAACT[C/T]TGACAAAATGGGTCA | 84333 |
| rs572830381 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221734 | CAGTTAAAAAAAAAA[A/C]AAAACCTGAGACAGG | 84333 |
| rs572830691 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230645 | GGGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC | 84333 |
| rs572850351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91179821 | ACATATGCATGCATG[C/T]GTCTTTTTTGTAGAA | 84333 |
| rs572866399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243889 | ATTTGACTCACATTA[C/T]ATTTCTATTGGTCAT | 84333 |
| rs572894086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185280 | GGATTCACTTAAAGA[A/C]GCAGTCTGGCCATGT | 84333 |
| rs572897082 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171554 | TGCTGTGAGTATCAC[A/T]GAAACTGCCAACTCC | 84333 |
| rs572913767 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281912 | CAAATAGCCTTCCTC[C/T]GCATGAAAAGTGAGA | 84333 |
| rs572936280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168482 | GGCAGTGGGGATTAG[A/T]GGGGACAAGTCCGCT | 84333 |
| rs573038240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168057 | ATATTTGTCTAATTA[A/G]TGGAGGTGATTATTG | 84333 |
| rs573043423 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186098 | TCTTGAATTTCCTGT[A/G]CAGTAATTTTAGAGC | 84333 |
| rs573120282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175195 | TGAAGTCTTTAACAG[A/G]GACTGGACATGTTTT | 84333 |
| rs573159764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220714 | CGCTCCCGCCTGCAG[G/T]GGGAGAGCAGACGGG | 84333 |
| rs573172919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166808 | GGGATAATGCCATCT[A/G]CCTTGAAGGATTGTG | 84333 |
| rs573181349 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168460 | CTTTGAGGAACAGAG[G/T]CAGTTGGGCAGTGGG | 84333 |
| rs573181680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174691 | AACATTAATTGGGAA[A/G]GTATCTTATCTAATC | 84333 |
| rs573195110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212034 | CATGGTTTCCTCATT[C/T]ATAAGATGAGGACAA | 84333 |
| rs573215583 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264838 | CATTTATGTATATGG[A/C]ATGGGAGTGGGGGAA | 84333 |
| rs573243136 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203936 | ATGAGCGTTATGTCA[G/T]TGTAAGCTAATTTAA | 84333 |
| rs573256539 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219554 | GTCATTTGACCTCAC[G/T]TGTTTTCTCTTACTC | 84333 |
| rs573258759 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199975 | TTACTGCTGTGGGCA[A/C]CTGGAGCTCAATCCG | 84333 |
| rs573271589 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91278162 | GTAATCACTAGTACC[A/G]GGAAATACTGTAAAT | 84333 |
| rs573346637 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191418 | CATGAGATATCATCA[A/C]ACTACTCAGATGGCA | 84333 |
| rs573405411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227814 | TCAACTGTTTGCTCT[A/C]CTTGAAATGAATGCC | 84333 |
| rs573408710 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176531 | GGTTCCATTCTCCCT[A/G]TCACTTTCAGGTACA | 84333 |
| rs573452092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250758 | AGTTGTAACATGTTA[C/T]GTATTAATAGCTATA | 84333 |
| rs573475788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167332 | TTAAGAGTCATGTAG[A/G]GCACATAAGACAGAT | 84333 |
| rs573497904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212796 | AATCTTAAGATTTTT[C/T]TCTTAGCTGGAAGTA | 84333 |
| rs573526908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249296 | CTGGGTCCCAAAAGA[C/T]TCAGCAATTAGTAAT | 84333 |
| rs573562064 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171188 | TTTGTCCAAATCCCT[A/G]GAATGTAGAAGAATA | 84333 |
| rs573566536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261899 | AGATATAACCAACAT[A/G]TTATAGCTGCATAAA | 84333 |
| rs573608598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91270157 | AGCCTTAGCTTTCAT[C/T]GTGTACTCACGTTCT | 84333 |
| rs573613558 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246501 | TAAACACATGAAGTC[A/G]GGTAGTAGAGAGAAA | 84333 |
| rs573664619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91253332 | TCCTGTCTCGCCCCC[A/T]ACCATTCCACCTTCA | 84333 |
| rs573669163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268968 | TATACTCAAGCTTGG[C/T]ATTAATCTTTTTCTT | 84333 |
| rs573713923 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91188263 | GCTAGGCATTGCCTC[A/C]CTCGGGAAGCGCAAG | 84333 |
| rs573743793 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167302 | TTAGACATAGATACT[C/T]TTTCTTTAAGAGGCT | 84333 |
| rs573753035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240307 | TTGTGGCAGTAGACT[A/T]TTATTGCAGTTGGGT | 84333 |
| rs573759303 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252533 | CTTATACATACAAAT[A/T]GTTAAGGTAATTGAT | 84333 |
| rs573810289 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224396 | ATTTATTGAGTACTT[C/T]GTGTGTCAGGCACTG | 84333 |
| rs573820359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251888 | TGAATAATTTAATCA[A/G]TTAGTTTTGAAGTAA | 84333 |
| rs573820406 | snp | C/T | 0.218151 | 0.247963 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259941 | CACCAAAAGCAATGG[C/T]AACAAAAGCCAAAAT | 84333 |
| rs573847988 | in-del | -/GT | 0.0256215 | 0.110247 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180772 | GTAGTATAGTTTGAA[-/GT]TGGGTAGCATGATGC | 84333 |
| rs573848734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277016 | GTAAAACCAGAACAG[C/T]TTTAGAAGTTTTAAA | 84333 |
| rs573871129 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176179 | TTAGGAAGCTTAGTT[G/T]GGCTGGATATGAAAT | 84333 |
| rs573921196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208511 | GGCTGATCTGTGGAC[C/T]CTGGCTGAAGTAACA | 84333 |
| rs573944789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246704 | AGTAAATGTGTAAAT[A/G]AAGGGAAAGAGAGAA | 84333 |
| rs573950486 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245846 | TTTGGAGAGTTAGGG[C/T]GAGAAAAAAGCGTGT | 84333 |
| rs574036084 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161795 | GACTCCTGAACTTTT[C/T]CAGTCTCACCAGAGC | 84333 |
| rs574040712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193562 | GCGAGGGGTAGTTGG[A/G]GGGGAGAGAGCAGGG | 84333 |
| rs574058259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206508 | TGAAACTAGCAGATA[A/G]GGAAAGCCTGCATGG | 84333 |
| rs574103989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199503 | GCAGCTGAGGACATG[A/C]CTGCAAGAGGCCAAC | 84333 |
| rs574104104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91193118 | GAGTGCATGGCAAAC[A/G]CAAGAAGGAAGGCAT | 84333 |
| rs574111524 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223845 | ATTTTATGGATGTGG[A/G]AACTAATGGATAAGT | 84333 |
| rs574119708 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203643 | TATATTTGTACAAGA[C/T]TCATGTTTTTAATTT | 84333 |
| rs574129479 | in-del | -/T | 0.351578 | 0.228433 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167164 | TGTCTAAATTAACTT[-/T]TATGATAAGTACATT | 84333 |
| rs574151592 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181675 | TAAATTACACTTACT[G/T]ATTTGTGTATGTTGA | 84333 |
| rs574155937 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249317 | AATTAGTAATTTTTA[A/T]TAATAATTTCAGCAA | 84333 |
| rs574183733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91181064 | AGAGATCTTTCACCT[C/G]CCTAGTTAGCTGTAT | 84333 |
| rs574197203 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255883 | AGTATTTGCACGTAA[C/T]GTATGCACAACCTGC | 84333 |
| rs574209495 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284078 | GCTGCTTAGAGATTC[A/T]CCTTAAATATTTTTT | 84333 |
| rs574214042 | snp | G/T | 1.65089e-05 | 0.00287301 | missense | PCGF5 | GRCh38.p7 | 10:91248535 | AGAGGAAATTATATT[G/T]AAGCTGGTCCCTGGA | 84333 |
| rs574249057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273631 | TCTCTAATTTTCAAG[G/T]AATATATCATTCCTA | 84333 |
| rs574265304 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172954 | TAAAATGTTAAAGGA[A/G]CCCTTAATTAGATGT | 84333 |
| rs574285470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238658 | AAATTTCAGAGACTT[A/G]TCTATCATCCCTGGG | 84333 |
| rs574292964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223639 | TATGCCAAGATTACA[C/T]ATACTCTTTGTGTTT | 84333 |
| rs574370009 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280382 | TAAATGAATTTTATC[C/T]ACAAAATCTCTTTAA | 84333 |
| rs574390157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277500 | CAAACACAGAGGTAG[C/T]GTGGCATATGCCATA | 84333 |
| rs574406912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241641 | AAAGGGGTCAATTCC[A/G]GAGTTAGCTTTTTAG | 84333 |
| rs574429606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203833 | ACAACAAAAACAAGT[A/G]TATATATTTAAAAGT | 84333 |
| rs574442838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91190327 | ATATGAATTTTGGGG[A/G]AATTCAAACATTCAG | 84333 |
| rs574469904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256497 | AGTTCCAGAAGGAGA[A/G]GAAATGGAGAAAAAA | 84333 |
| rs574501007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91226351 | AGGACAGACTATGAT[A/G]TAATAGCAGATGTGT | 84333 |
| rs574503689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197049 | GGTTTTTATATTAGA[C/T]GTGGACAAGTGAGCC | 84333 |
| rs574541211 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275344 | CTTATTAAATTGCCA[A/G]ATTAAGAGGTGGGGA | 84333 |
| rs574676640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91255900 | TATGCACAACCTGCT[A/G]TATACTTTAAATCAT | 84333 |
| rs574691610 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219823 | TGGATCTTTGAACAC[C/T]TGTATGGCTGCTGGA | 84333 |
| rs574713068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235684 | GAATCATGGGGGCGG[G/T]TCTTTCTCACGCTGT | 84333 |
| rs574738538 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266562 | TAAACCAATAAACAG[-/A]AAAATTACTACCTTT | 84333 |
| rs574747400 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218227 | ATTATGAATTCACCA[C/T]GTCTCAGGATCTTAG | 84333 |
| rs574753880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227987 | ATTTTTCCTTTCAAA[C/G]ATTCAAATGCAGTGA | 84333 |
| rs574764329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91235411 | AGTTTAATGATGTTT[G/T]TGATGAGGTAAGTAT | 84333 |
| rs574771433 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244595 | TGTGTTGAGAACACC[A/G]CGCGTATAACAAGGC | 84333 |
| rs574832272 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272679 | TAAGGAGGTTGAGGC[A/G]GGAGGGTCGCTTGAG | 84333 |
| rs574833083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182806 | TTATTTGAGATTCTG[A/G]TACATTGTATCTTTG | 84333 |
| rs574846433 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233868 | CAGATAAAACCAACA[A/C]ACCTAAAAGATTTTA | 84333 |
| rs574931836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203132 | GTACTAAGCATTTTA[A/C]GGGCTAATTTAGGTC | 84333 |
| rs574962270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165813 | CATATTTAATAATAT[C/T]CCTTTAGAGGATAAA | 84333 |
| rs575005416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263527 | TTAAAACTCATTCTT[C/T]TTCCCCTCCCACACT | 84333 |
| rs575072990 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174372 | ATTAGACAGGTGTGG[C/T]GGTGCATGCCTGTAA | 84333 |
| rs575109309 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91175301 | ATCGACTGAAAAAGG[A/C]ATTTAATGAAATTCG | 84333 |
| rs575159439 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172287 | AGCTGGGCGTGGTGG[C/T]ATGTGCCTGTAATCT | 84333 |
| rs575176800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215416 | AAAAGCTAGAAAAGG[A/T]GAATACCCATCAGCA | 84333 |
| rs575192071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223341 | TGCAGACTCTTAATT[C/T]GCTGGTTCTCAAAGT | 84333 |
| rs575194367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91197729 | ATCCTCTCCCACCAT[A/G]TTCCCCTTTTTCCTT | 84333 |
| rs575221004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91167805 | AGCCACAGGTAGTCC[A/G]TTTAAGCTGTTGAAA | 84333 |
| rs575223271 | snp | A/T | 0.0944967 | 0.195752 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177918 | GCACTGCACCCACTG[A/T]CCTGCACCCACTGTC | 84333 |
| rs575223385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91171454 | GCTTGACAAGTTGCT[A/G]GAAGGCCTTAGCCTA | 84333 |
| rs575224126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230812 | ATTTTGTGTAGAGAC[A/G]GGGTTTGGCCATGTT | 84333 |
| rs575232339 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282611 | AGAGGAAGTTCCATA[A/T]CCCCCTTGTACCATT | 84333 |
| rs575275892 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237636 | GTAATCCCAGCTACT[A/G]GGGAGGCTGAGGCAG | 84333 |
| rs575300031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91199675 | CAAGGCTAGTTTTAG[C/T]TTAATACTGAAATTT | 84333 |
| rs575328804 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91252658 | CAGTTGTTTCTTATG[G/T]TCTTTCCCAAAAGTC | 84333 |
| rs575333417 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91230028 | CTTAATCTTGGTGTC[A/G]TCTATTATTAGTAAT | 84333 |
| rs575370705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91206741 | CTTTCTCTGTTGCTA[C/T]CTGCACCTAAGCATG | 84333 |
| rs575393196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91260064 | TTTTTGCAACCTACT[C/T]ATCTGACAAAGGGCT | 84333 |
| rs575398889 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185721 | CCTAGTGGAGTGGTT[G/T]CATGAAGGGTTCTCC | 84333 |
| rs575401029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91192761 | TTAAAATAGAGCACA[C/G]AAAGGAGAAATCAAA | 84333 |
| rs575428133 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164328 | CCACACTAACTTTTG[G/T]GGGGTCAGGGTCCAC | 84333 |
| rs575460900 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194327 | GAAGTAGAGTATCTT[C/T]CCCATGGTGGTCAGA | 84333 |
| rs575496457 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91161978 | CACAAGGGGGGATTC[C/T]GCTTGGGGGAGCAGG | 84333 |
| rs575500885 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259501 | AACCAAAAAAGAGCC[C/T]GCATTGCCAAGTCAA | 84333 |
| rs575506800 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | PCGF5 | GRCh38.p7 | 10:91205311 | CACACACACACACAC[A/G]GCCCAGCTAACATGG | 84333 |
| rs575579894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266204 | TTTAGCGGGCATTGC[A/G]GTGTGTTTTAGTGAC | 84333 |
| rs575628671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268063 | TATTTAACCTTATTG[C/T]TTTGAGATGTCACCA | 84333 |
| rs575651582 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238241 | AGATCTAGAATATAG[A/G]TTAGTATTCCCCATC | 84333 |
| rs575683190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91164306 | AAGGGCAGCGGGGTC[C/T]CCTCTTCCACACTAA | 84333 |
| rs575690218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250357 | ATGTTTAGCTGGCTG[A/G]TTTTTTCAAGTGTTA | 84333 |
| rs575709620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265702 | ATTGTCTTATGGGTA[A/G]GATATTTGGCTCTTT | 84333 |
| rs575728350 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213487 | ATTTTTTTTTAAGAT[G/T]AAGTTTTGCTCTTGT | 84333 |
| rs575728905 | in-del | -/AAC | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217766 | CTTTCTTCCTTGTTT[-/AAC]AACAACAAAAAAAGT | 84333 |
| rs575737595 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198642 | TCGATCTTCTTGGGA[A/G]TTTTCTGTAAAGGCC | 84333 |
| rs575772977 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178395 | TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTGAG | 84333 |
| rs575774323 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229066 | AATGAAATATTAGCT[A/G]TTGTTTTATTGAATG | 84333 |
| rs575783300 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232476 | TAATAAGGGAAGTAG[A/G]GTCAACAGAAGTGGT | 84333 |
| rs575789979 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91237114 | GCTCAAATTCTCTAC[C/T]CATTTTTTTATCTAT | 84333 |
| rs575793070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91212853 | GGATTTTTATTAAGC[C/T]TGATGTCTCCTCTCT | 84333 |
| rs575794984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91183472 | GTCTCTCCATGTGAG[G/T]TAGGTCTCTTGAATA | 84333 |
| rs575811398 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177219 | GAGGCTGCAGAACAG[C/G]GAATATTGGTGAACA | 84333 |
| rs575852510 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220807 | CCGGCGCGCTGGCGG[C/G]CGAGGAGCGGCGGCG | 84333 |
| rs575858267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91189169 | CTCCATCTGAAACAC[A/G]TTCCTTCTCTTCTTT | 84333 |
| rs575946356 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91202259 | CTTTTTTGATGTAGT[A/G]TGGTGGTTAAGCCTA | 84333 |
| rs575965004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91243899 | CATTATATTTCTATT[A/G]GTCATCACTTATATA | 84333 |
| rs575973092 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91254921 | AGGGTGAGCTTTGTG[G/T]CATTTTAACTTGCTT | 84333 |
| rs575982150 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276812 | TCAAACGCAAAACTA[A/G]AGCAGTTAGTATAGT | 84333 |
| rs576019219 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91262356 | TTAGGTGAACCTGGG[A/G]GGCGGAGGTTGCAGT | 84333 |
| rs576024084 | snp | C/T | 0 | 0 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239407 | GCTTTGGTCAGTATA[C/T]GTGATATGTCACATT | 84333 |
| rs576027996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250812 | TATACTCGTTTTTTT[C/T]CACTGGCTGATTTTA | 84333 |
| rs576086888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91246809 | CGAGACAATGACTGG[A/G]CTACTTAGTATTTTA | 84333 |
| rs576129792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91209928 | TCAACTCAATGAGAT[A/T]GACATGTGGAAATTG | 84333 |
| rs576130502 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278413 | GACTAGAGGAACACA[A/G]CCAGATTTTCAGCAT | 84333 |
| rs576137969 | in-del | -/AA | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91239310 | AATGAATAAACAAAC[-/AA]GAGGAAATGCTGCTA | 84333 |
| rs576147090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91233972 | AGAGAAAAGATTATT[A/G]TTGTTTTATCATCAG | 84333 |
| rs576149385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245170 | AGGCACAACCAGTGA[A/G]GTAGAGGAAAATCCA | 84333 |
| rs576177384 | in-del | -/AAT | 0.00119737 | 0.0244387 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207621 | CTTTATAACCGTAAC[-/AAT]AATGAAGTCCCAATT | 84333 |
| rs576187518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91196140 | CTACAGATATTTCAC[A/G]TGGTGGCAGAGAAGG | 84333 |
| rs576190982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91208587 | TGCTCTCCCTGTATT[A/C]GTATGAAAAATTCAC | 84333 |
| rs576205559 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | PCGF5 | GRCh38.p7 | 10:91170078 | CATCCATATGCAAAA[A/G]AAGAAAAAAGTTAAT | 84333 |
| rs576222896 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236116 | TAAAAAAATATGATA[C/T]GAATTTTTGATTTTG | 84333 |
| rs576251693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91217062 | TTTGAGACAGAGTCT[A/C]TCGCTCTGTCGCCCA | 84333 |
| rs576253003 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267805 | CAAGATGCCAGGATG[C/T]CTGAAGAGCTCTTAT | 84333 |
| rs576255715 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267540 | TTATCTTTTACAAGG[C/T]AATGGTTATGCAAAA | 84333 |
| rs576275634 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91195727 | GGCATGAGCCACCAT[A/G]CCTGGCCTAAATCAT | 84333 |
| rs576289720 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225721 | AAATAAATACAAATA[C/T]ATATTTATACAAATA | 84333 |
| rs576299339 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241544 | GACCCATTTTCATTT[C/G]ATTGTTCCCACCATA | 84333 |
| rs576312895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91277163 | CTCTAGTTCCATCCT[A/G]AGCTGAATGGTTACA | 84333 |
| rs576358817 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91241054 | AATCATATATATATA[A/T]AATATATATTTTATT | 84333 |
| rs576422345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91247627 | AGAATGGGATTGAAG[A/G]CAAAAGGCCATGAAA | 84333 |
| rs576473942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91187399 | TTTTATGATGTGAAT[A/G]CACCTGCTTTGTGGA | 84333 |
| rs576483546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91242924 | TAATTTAATGATGTC[C/G]TTTATAGAGATCTTT | 84333 |
| rs576554526 | snp | C/T | 0.00260713 | 0.0360106 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248470 | AGATCTTGGTGTCTT[C/T]ATTGTTAGTATTTTC | 84333 |
| rs576556673 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177159 | GGTCTGTTGGAGTTT[G/T]CTGGAGGTCCACTTC | 84333 |
| rs576575094 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257071 | TCATGTCTGATAAGC[C/G]TTTAATGTACAGGTA | 84333 |
| rs576589347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91266364 | TATTTTAATGTCAAA[A/G]TATGAAAGAGCTAAT | 84333 |
| rs576590362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | PCGF5 | GRCh38.p7 | 10:91225244 | TCATATATGTATATA[C/T]GATATATATCGTATA | 84333 |
| rs576594854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91274388 | GTCTTGCCTTAAACA[G/T]AGACATATGAATAAA | 84333 |
| rs576598936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91176648 | CTTCTCGCTTCATTT[A/C]ATTCATTTGATCTTC | 84333 |
| rs576619029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91182380 | TCTGATGGTTGTTTG[C/T]ATTTCTGTGAGGTCA | 84333 |
| rs576633468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224641 | GGACTGAAGGACTCT[A/G]TGGATATATGGGAAA | 84333 |
| rs576654556 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272080 | CAAATTAGGTGAAGC[A/T]AAATAACAGCAACAG | 84333 |
| rs576673416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91265848 | AGACTGAACGCTTTC[G/T]CTAGCAGCAGGAAGA | 84333 |
| rs576678743 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181622 | TTGAGTTAATTGTGG[C/T]TTTTGTCTTTAGTTT | 84333 |
| rs576746489 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281111 | CACATCAGTTAATAG[A/G]GAAATCAAAATATGT | 84333 |
| rs576755423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91236965 | TAAAATAAGGAGTAA[A/G]ACATTCTTTTTCTAT | 84333 |
| rs576790876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91191386 | ACAAAGGGATGATTC[A/G]CCACAGAGAGGGACC | 84333 |
| rs576798852 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233532 | CGTGCCAATATACGG[C/T]ACATTATGTAATATA | 84333 |
| rs576870827 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185163 | CTCCTTCTGGGAACT[C/G]TCTCCCAGGAGGTTC | 84333 |
| rs576883536 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91250108 | CCCATTTTAAAGTAT[A/T]TCTGGTATTTGGTCT | 84333 |
| rs576885942 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263609 | ATATTATTTGTAGGG[A/T]TCGATGATAAACATT | 84333 |
| rs576926192 | in-del | -/A | 0.409645 | 0.192389 | intron-variant | PCGF5 | GRCh38.p7 | 10:91221725 | CATATTTTACAGTTA[-/A]AAAAAAAAAAAAACC | 84333 |
| rs576942612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91174566 | TAATAAATCCTATCA[C/T]GCTTTAAGACTAAGT | 84333 |
| rs577012215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91173923 | GATTTCCTTCCTTTG[C/T]CTGTCTTTAGAAGTA | 84333 |
| rs577032731 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220927 | CACCTCCAGACACCT[G/T]CCCTGGCCGGCCCAG | 84333 |
| rs577049723 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281814 | GAACACACTTCCTTT[C/T]AAATATGTTCATTGT | 84333 |
| rs577053271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91273783 | AGTAGATGATAAATA[A/G]TACACTAATATAGTG | 84333 |
| rs577060235 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215695 | CTTCTGGCCTTCTCA[G/T]TTATCATTCATATGC | 84333 |
| rs577095241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91228925 | ACAAGCCCTGCAGGT[A/G]ATTCTCTGGTACACT | 84333 |
| rs577145668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91178625 | AAACCCCTGGGCCAG[C/T]CAGTCCTCCCACCTC | 84333 |
| rs577178179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227754 | TGGTTTCTGCCTACC[A/G]CTTCCTCCCCTACCA | 84333 |
| rs577207032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177959 | CAGTGAGATGAACCC[A/G]GTACCTCAGTTGGAA | 84333 |
| rs577211564 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91185569 | GTATGGAGGTCTAAC[A/C]TCCCTCTTTGCCTGA | 84333 |
| rs577212177 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280018 | TTGTTGTTCCAACTT[C/T]GGTGAAAAAGGTTAT | 84333 |
| rs577266157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91177709 | ACCCTCCAAGCCAGG[G/T]GCAGGATATAATCTC | 84333 |
| rs577269317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91263731 | CGAGCAAAACTTAAC[A/G]CTGATAAGTATGCTT | 84333 |
| rs577345854 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188550 | AATTGGAATCTTCTC[C/T]CTTATGTACCTACTA | 84333 |
| rs577346298 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | PCGF5 | GRCh38.p7 | 10:91249410 | ATATATATATATATA[C/T]ATATATATATGTATA | 84333 |
| rs577346972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91257471 | CCCCCCTTATCTGTG[A/G]AGCATATGTTCCAAG | 84333 |
| rs577357372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91272066 | GAAATATAAAATGCC[A/G]AATTAGGTGAAGCTA | 84333 |
| rs577391338 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91203907 | ATGATTTCAGTCAGG[A/C]CCACATTTCTGAAAT | 84333 |
| rs577408232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91256832 | CTAGTTAAGTCTATA[G/T]TCATCAAAAATCTAT | 84333 |
| rs577439304 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200421 | AGAAAGAACAGGGGA[G/T]GTAGCCCCTTTCTGG | 84333 |
| rs577481372 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91172698 | TTTTGTGTTTGCCCC[C/G]AAGTTAAACTAACCT | 84333 |
| rs577492153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91207566 | GAAATATGGCATTGT[C/T]ATAATAGTATCTAAT | 84333 |
| rs577547762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91169027 | AAAGGAATGAAGATC[A/G]AGGGAGGACGTAGGA | 84333 |
| rs577565575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91166678 | CATCCAATAGAAAAG[A/C]CTAGACTTTGCAGCC | 84333 |
| rs577566419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91215566 | TTTGCTGAGTTTGCT[A/G]TCTTTGAAAAGAGAT | 84333 |
| rs577569901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91224306 | ATTAACTATGTACTA[C/T]CTTGTATTACTAGTT | 84333 |
| rs577614817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91276938 | ATGGAGATAATCTGT[A/G]TCTTGCTCCCTCCCA | 84333 |
| rs577627558 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91165892 | GCCCCAGTCTTGTAG[A/C]AATATTTTCAGGACT | 84333 |
| rs577632018 | snp | A/G | 0.000267845 | 0.0115694 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264407 | AACATTATGTTAATA[A/G]ATCTATAATGATTCT | 84333 |
| rs577657212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91259018 | GTATTCTGATAACTT[C/T]TGAGGTTGTGGAATG | 84333 |
| rs577674086 | snp | C/T | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220166 | CACAACGTTCCCGTT[C/T]GCTTATAGTTGTCAA | 84333 |
| rs577719041 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91258387 | CCCTTATCCAAAATG[G/T]TTGGGACCAGAAGTT | 84333 |
| rs577752576 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246106 | TTTAATGACTGACCA[C/T]AGAACAGATTAGTCC | 84333 |
| rs577760923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91268222 | CTGGCCACATAACAC[C/G]CCTATCTAAAACCCT | 84333 |
| rs577780438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91180426 | TCTTTGCCCATGCCT[A/G]TGCCCTGAATGATAG | 84333 |
| rs577844307 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | PCGF5 | GRCh38.p7 | 10:91186194 | GGGCTAAATCAGCTG[G/T]ACCCTCAGGTTGCCC | 84333 |
| rs577905924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91216326 | GACTTAGCAGAGGTG[A/G]GGAAGGGTGAGGGGA | 84333 |
| rs577909360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91198824 | AATGAAGAGCCCTTC[G/T]TCAGATGGGTTATTT | 84333 |
| rs577937902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251812 | TTCTAATTTTATCCT[C/T]TATTTCTCTATTTTT | 84333 |
| rs577948058 | snp | C/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219090 | ACTATTGCTGCCTCT[C/G]CAGACACAAAGCACA | 84333 |
| rs578009367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91168414 | CTGGGAAAAGGACAT[C/T]AGATTTGTCAGTGAG | 84333 |
| rs578061416 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250551 | TACCCTGACCACTGT[A/G]AGAGAGAGGATGATA | 84333 |
| rs578134022 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | PCGF5 | GRCh38.p7 | 10:91214242 | GGGAGGTTGAGGCTG[C/T]AATGAGGCGTGATTG | 84333 |
| rs578164322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91245006 | GTAGTCTTCAACATA[C/T]AGAAGGTCTTTCAAA | 84333 |
| rs578171682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91213531 | GTGCAATGGCGTGAT[C/T]TTGGCTCACTGCAAC | 84333 |
| rs578200358 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91244599 | TTGAGAACACCGCGC[A/G]TATAACAAGGCAAGG | 84333 |
| rs578212824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | PCGF5 | GRCh38.p7 | 10:91238434 | GATCCAGGTGAGGAC[C/T]TGTTCTGGGCATGTC | 84333 |
| rs578249821 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | PCGF5 | GRCh38.p7 | 10:91200176 | TCCCAGAGCCAGAAT[-/A]AAAGCCACAGGTGTT | 84333 |
| rs745326187 | snp | C/G | 1.65671e-05 | 0.00287807 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248615 | ATGAAATCAACACTT[C/G]TATTAAAGATTTCAT | 84333 |
| rs745400883 | in-del | -/AAAAAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209770 | TCCGTCTCGAAGAAA[-/AAAAAAG]AAAAAAAAAAAAAAA | 84333 |
| rs745415363 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236488 | CTGTGTGGAGTAGCT[G/T]TTGAGAATGAAGACT | 84333 |
| rs745443741 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272588 | GACCAGCCTTGACAA[A/C]ATGGTGAAACCCTAT | 84333 |
| rs745446251 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172285 | TTAGCTGGGCGTGGT[G/T]GCATGTGCCTGTAAT | 84333 |
| rs745498889 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252181 | TTAGATTTTTGTCAC[G/T]TTATCCTAGCAAATG | 84333 |
| rs745518131 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266025 | TTTAAATGATTGTAC[A/G]TACATCAATCACCCT | 84333 |
| rs745518838 | in-del | -/C | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218735 | CCTCCTAGGTTCAAG[-/C]GATTCTCCTGCCTCT | 84333 |
| rs745537952 | snp | C/T | 1.72293e-05 | 0.00293503 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222839 | GGACCCCTCTTTGCC[C/T]AGACTACTAAAGCCA | 84333 |
| rs745589416 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202463 | ATAATACAAAGTAGT[A/T]AACAGGATTGTTGTG | 84333 |
| rs745627210 | snp | A/T | 1.65195e-05 | 0.00287393 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271709 | TCAGGTAAGAGGCAC[A/T]CACGACTGTACATAT | 84333 |
| rs745694623 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226122 | TTAAGAATGAGTAAA[C/T]GCTAGGTTTTATGGA | 84333 |
| rs745704849 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214094 | ATTGCTTGAGCCCAG[A/G]AGTTCAAGACCAGCC | 84333 |
| rs745747068 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195553 | GCAGTGGTGCAGTCA[C/T]GGCTCACTGCAGCCT | 84333 |
| rs745753598 | in-del | -/AAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232364 | TAATCTTAATAAAGT[-/AAAG]AAAAGGTGAAAAAAG | 84333 |
| rs745761076 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207764 | TTGTTTTGTAAAATG[A/G]CCCTCAATGTGGACT | 84333 |
| rs745787223 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241401 | ACTGGAAGTGGTCTA[C/T]GAGATTCTAATCCAA | 84333 |
| rs745811011 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267478 | GGGCAGTGCCCAGCA[-/T]ATATACTCAATCAAT | 84333 |
| rs745829247 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184598 | TTCTGAACACTTGCT[A/G]GAGAGGTGATACAGT | 84333 |
| rs745836969 | snp | C/G | 1.65756e-05 | 0.00287881 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248754 | TGTCTGTTTCTGACA[C/G]CACCTCTTAAACTGG | 84333 |
| rs745862096 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196921 | GACGAGATATAATCC[C/T]CACCTCAAGTCTCAC | 84333 |
| rs745872444 | in-del | -/CTGA | 8.33345e-05 | 0.00645448 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261465 | ATCATTTTGATAATT[-/CTGA]TTTGAAGTAAAATTC | 84333 |
| rs745875670 | snp | A/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170214 | ATGACCTTGGGTTTG[A/G/T]TGATGACTTTTTAGA | 84333 |
| rs745890344 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271186 | ACAGAAAATAGATGC[A/C]TTACAGGTTGAGCGG | 84333 |
| rs745890676 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212595 | AGATAGAGAATTGAA[C/T]CTGAATAAATCAAAG | 84333 |
| rs745897006 | snp | A/G | 1.64844e-05 | 0.00287087 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240515 | TGTTCAGCACTTTGA[A/G]GATAGCAATGATTGC | 84333 |
| rs745931251 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178869 | TTACTTTTGCACCAA[C/T]GTAATACATGAAGCA | 84333 |
| rs745954452 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206873 | TGCTAAATGTCACCT[A/G]ACTAAATCCTTCTCT | 84333 |
| rs745954698 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215515 | TCTGATCTAGTTCCC[A/G]TAGCTGCAATATTCT | 84333 |
| rs745955649 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205705 | AAACTGAGGCTGGGC[A/G]TGGTGGCTCACCCCT | 84333 |
| rs745985658 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239595 | CAGGTTATACGGGGT[A/G]ATAGAATGGAGGAGG | 84333 |
| rs746061798 | snp | C/T | 0.000140915 | 0.0083927 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227324 | TATTTTTGGCTTACG[C/T]TTTTCTTCTTAGCTG | 84333 |
| rs746109684 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270167 | TTCATCGTGTACTCA[C/T]GTTCTTCCTGCTCAC | 84333 |
| rs746145165 | in-del | -/AAC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249778 | CTATTTTTTATCTGT[-/AAC]AACAACAACAAAAAA | 84333 |
| rs746162237 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245858 | GGGCGAGAAAAAAGC[A/G]TGTTGTCCAGGGGAG | 84333 |
| rs746163825 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188662 | CATTCACGTTCATTT[C/T]CTCACTGACCCTCAC | 84333 |
| rs746181404 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259110 | TCAGCTTGGGTGTCC[C/G]TTCTGGATTGGTTCT | 84333 |
| rs746241393 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233616 | AGAAGATGCATGGAA[A/G]CGAATTACAGCTATT | 84333 |
| rs746263230 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231912 | ATGAATTGTATGTGG[G/T]TCATGAAAAGAAAAC | 84333 |
| rs746275181 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246856 | GAGACAATCTTGACA[C/T]AGATTAATAAAAGGA | 84333 |
| rs746305684 | snp | G/T | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284412 | GGATTCTTCAGCTGT[G/T]TATTTTAAAATGGCA | 84333 |
| rs746306101 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167912 | AATAAAACAGAACTT[G/T]TTGGCAATTGGATGT | 84333 |
| rs746347453 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234872 | ATCTAGGCAGTCTGC[C/G]TCAACATTATCTGGA | 84333 |
| rs746349214 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201961 | AATTGTTAGAAGAAG[C/G]AGGGTGGCATCAAGG | 84333 |
| rs746372818 | snp | C/T | 1.65798e-05 | 0.00287917 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251431 | GCAATCAGGGGACAA[C/T]GTAGTAAAGGTGAGT | 84333 |
| rs746374860 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258967 | CAAATAGGAGTAATA[A/T]CTTTAAAAGATTCTA | 84333 |
| rs746433506 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212647 | CCTAGAAGAATTGTA[C/T]AGCCTAACTTCTATA | 84333 |
| rs746439466 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199052 | AACTGCATCACATAC[A/G]TGCTGGTTTGTATCT | 84333 |
| rs746441600 | snp | C/T | 1.65679e-05 | 0.00287814 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251386 | TGACCCACAAATTGC[C/T]ATCTGTCTAGATTGT | 84333 |
| rs746481383 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263701 | GATTTAGGGGTTGTT[C/T]GGTTCTTGCAACTTC | 84333 |
| rs746523020 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201443 | AGTTATCAGCACATG[A/G]AATTTGGGGAACTCA | 84333 |
| rs746551011 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201697 | ACACCTCATTTGTTC[C/T]GTATTGAGTTCATTT | 84333 |
| rs746571679 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248184 | TGCCACATTCTGCTG[A/G]CCTCAACAAGTTTTA | 84333 |
| rs746581823 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273686 | GAAAAGGTGGAATCC[A/T]TCCACTTTGCCATTC | 84333 |
| rs746609389 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228689 | AAATATCATAAATAT[A/G]CAAGTACTTAAGGTA | 84333 |
| rs746629478 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212818 | CTGGAAGTAAGTTTA[A/T]TTCATCTATTGGGAC | 84333 |
| rs746632970 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198382 | TCCTTTTGATAACTA[-/T]TAAGACCAACTTCCT | 84333 |
| rs746638556 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177611 | TCAGCAATGGTGGGC[A/G]CCCGTCCCCCAGCCT | 84333 |
| rs746639925 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275504 | GGAATGCAGTGGTGC[A/G]ATCTTGGCTCATTGC | 84333 |
| rs746693050 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171187 | ATTTGTCCAAATCCC[A/T]AGAATGTAGAAGAAT | 84333 |
| rs746727671 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248569 | CGAGAACGTAAGTGG[A/C]TCTTTAGGTTCTTGC | 84333 |
| rs746757176 | in-del | -/CT | 1.65814e-05 | 0.00287931 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248647 | ACTTTTACTTTTATA[-/CT]CTTTCTTTTAAATTA | 84333 |
| rs746766255 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275892 | GGGTTAAGATTAAGT[C/T]ATAATAGCAAAGGAA | 84333 |
| rs746794746 | in-del | -/CTG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233301 | TAGACCTTTCAAGGT[-/CTG]CTGGCTTGCTCAGTC | 84333 |
| rs746813802 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241107 | GAGGTGGAGTTTTAC[C/T]CTTGTTGCCCAGGCT | 84333 |
| rs746816433 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183384 | GTTGTTTTAAAGTCT[A/G]TTTTGGCAGAAATTG | 84333 |
| rs746839790 | in-del | -/A | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218581 | TACACATCACACAGG[-/A]AAGTTGCCATTTCAC | 84333 |
| rs746841262 | snp | C/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227423 | CAAATGGGATGCCAG[C/T]ACTCAGTTATCCAAG | 84333 |
| rs746878902 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178183 | AACTGTACAGTATTA[C/T]GAGATGGAAAAAAAT | 84333 |
| rs746925309 | in-del | -/ATAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265365 | TCATAATCTGAGTGC[-/ATAA]ATAAATAAATATGAA | 84333 |
| rs747006633 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194456 | TAGAAGGTGGAAATG[A/G]CAAGGAAACAAATTC | 84333 |
| rs747025050 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238830 | ATTTGGGAAGAAGGC[A/G]AAGTATTCAATTGTA | 84333 |
| rs747025647 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91162425 | CTGGACTTGACCATC[A/G]CCAGGGAGGCATACT | 84333 |
| rs747047309 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268046 | GAATATTGAATAATC[C/T]ATATTTAACCTTATT | 84333 |
| rs747050684 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188547 | AGAAATTGGAATCTT[C/T]TCCCTTATGTACCTA | 84333 |
| rs747072069 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260200 | ATGCAGCCAACAGAC[-/AT]GTGAAAAAATGCTCA | 84333 |
| rs747089788 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217862 | CGCGATCTTGGCTCA[C/T]TGCAACCTCCACCTC | 84333 |
| rs747180279 | in-del | -/CTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175156 | TAGATCCTCACTTCA[-/CTT]CTTCTATGCCATACC | 84333 |
| rs747207999 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198914 | GCCATTCTTGTTCTC[C/T]TCCTCTCTCAGATGT | 84333 |
| rs747215047 | snp | A/C/G | 0.000115588 | 0.00760143 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248494 | TATTTTCTTTCTCCC[A/C/G]CCTTTCGAAGGTTGG | 84333 |
| rs747219721 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245747 | TGGTGGCCGGGGCCT[A/G]TGGAAGTTTGTTTTT | 84333 |
| rs747225516 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231892 | AGGTAAATTCATATT[C/T]GCTAATGAATTGTAT | 84333 |
| rs747299885 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187563 | TATCGCTTGATATAG[A/G]AAAGAGGTTTGAAGT | 84333 |
| rs747322100 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185393 | GGAAAGATGGCAGCC[A/C]CCCCTTCCCCCAGGA | 84333 |
| rs747349101 | in-del | -/AC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205114 | ATTAGATATGTAAAT[-/AC]AGTTATTTTAAATGC | 84333 |
| rs747380495 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211769 | GGTTGGCATTCACAC[G/T]GTGTTCAAGGGATAG | 84333 |
| rs747388876 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186678 | TTTGTACCTTTCACC[A/G]GTTCCATCCCGGGCC | 84333 |
| rs747417700 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256545 | GAAGAAATAATGGCC[A/C]CTAAAAACCAACCAA | 84333 |
| rs747459481 | snp | A/T | 1.65094e-05 | 0.00287305 | missense | PCGF5 | GRCh38.p7 | 10:91264447 | TGGATGTGCTGTGCA[A/T]TGGTGAAATTATGGG | 84333 |
| rs747459734 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229716 | GATCTGAATTTATGA[C/T]TCTGAATGAATAGCC | 84333 |
| rs747477354 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193314 | AGACTAAGTAGAGGA[C/T]CCAGCTCAGCCAAAT | 84333 |
| rs747505821 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180278 | AGGTTGCAAAAATTT[C/T]CTCCCATTCTGTAGG | 84333 |
| rs747558851 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256585 | AAAATATTAAACATT[G/T]GAGAAGCTTAACAAT | 84333 |
| rs747576497 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210365 | TAGAAGGGTGTTTAA[C/T]GTAGCCACACTGTGA | 84333 |
| rs747593585 | snp | A/G | 2.03287e-05 | 0.00318809 | missense | PCGF5 | GRCh38.p7 | 10:91261420 | AACTTCCAAGTTCTT[A/G]TGAGGTAAGTTAAAT | 84333 |
| rs747644578 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276839 | TAGTGAAGGGCAAGC[C/T]GTGGGTTGGGTGAGG | 84333 |
| rs747682982 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184210 | ACCAGTCAGTGGTAG[A/C]TTCAGTCTCTACATA | 84333 |
| rs747694922 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195692 | TCCTCCTGCTTTGGC[C/T]TCCCAGTGTTGGGAT | 84333 |
| rs747701270 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212665 | CCTAACTTCTATAAC[G/T]CATGCCCACTAATTC | 84333 |
| rs747725799 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229281 | GAACTTAACATTCTA[A/G]TAGGACAGACAGACA | 84333 |
| rs747739155 | snp | C/T | 1.75653e-05 | 0.0029635 | missense | PCGF5 | GRCh38.p7 | 10:91261333 | TCCTTTAGGGTTTAA[C/T]GAAGAAATTCATTCG | 84333 |
| rs747750160 | in-del | -/CATTCATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216806 | CTCTGTTCCCCCTAC[-/CATTCATA]CATCATTGATTTTAG | 84333 |
| rs747751957 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194344 | CCATGGTGGTCAGAG[G/T]CTGAGGTGACTACGG | 84333 |
| rs747771594 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239240 | TTGTTTTGTTGGCCC[C/G]TGCATCCCCAACTCC | 84333 |
| rs747796567 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183244 | AGTTTCTATTAGGGT[C/T]TCTAAGAACTTGCTT | 84333 |
| rs747850897 | in-del | -/ATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91260957 | AAAACTTAAAGCATA[-/ATA]ATAATAATAATAATA | 84333 |
| rs747866196 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175404 | AGGACTCTTCTCTGG[A/G]TAAAATGAGCAGCCT | 84333 |
| rs747871281 | snp | A/G | 1.6569e-05 | 0.00287824 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251407 | TCTAGATTGTTTACG[A/G]AATAATGGGCAATCA | 84333 |
| rs747885056 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226705 | GATATAGAAAGAAGG[-/G]CCCAAAAGGTGAGCT | 84333 |
| rs747889941 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273570 | CTAATAGGATGCACC[A/G]TTAACTTCCTGAAAG | 84333 |
| rs747965862 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237775 | CATCAGAAAACCTGA[A/G]TTTATGTCTTTTTGC | 84333 |
| rs747984111 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248880 | TTTTTCTCTATATGA[-/G]ATTTTATATAAATGA | 84333 |
| rs748039589 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174775 | GATTCATCTTTGGTG[G/T]CAATCTCTGGTTTTG | 84333 |
| rs748087479 | snp | A/C | 1.64887e-05 | 0.00287125 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240566 | TCATGAGACAAATCC[A/C]TTAGAAATGTTGAGG | 84333 |
| rs748152883 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203814 | TAATATAGGAAATTT[C/G]TCAACAACAAAAACA | 84333 |
| rs748170501 | snp | C/T | 3.31923e-05 | 0.0040737 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91264520 | ACTAAGAGGCGAAAA[C/T]GTAAATTGCTTTTAT | 84333 |
| rs748172368 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244288 | AGAGGTTAACCATGG[A/G]TAGGTCTAGGAAAGC | 84333 |
| rs748181411 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166339 | TGCAACATCTAGGGG[C/T]TCAACAAATGCTTAT | 84333 |
| rs748204745 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230543 | ATATGAATATATAAT[A/G]TCAGAACCACTGACA | 84333 |
| rs748282032 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267459 | GCTAAATCTCCAGCA[C/T]CTAGGGCAGTGCCCA | 84333 |
| rs748283681 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235923 | GTCTTTATCAGCAGC[A/G]TGAAAACAGACTAAT | 84333 |
| rs748285851 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281935 | AAGTGAGAGAAATAC[A/G]TACTTTGAAAAGAAA | 84333 |
| rs748295805 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197096 | TGGTTGTCTAAAGCT[G/T]AGTGACAAACTACTC | 84333 |
| rs748316843 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166904 | TGCTATAGTTATGAC[C/T]ACAGATTTGTGTGAC | 84333 |
| rs748367883 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237914 | CCTCTTGATAGGAGG[G/T]ATTCTGTCTCCATCT | 84333 |
| rs748368607 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257497 | CCAAGACCCCCAGGG[G/T]ATGTTGCAACCACAG | 84333 |
| rs748376258 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210191 | GATTTGGATGCCCTT[C/T]CCCTTATAGCAAACA | 84333 |
| rs748384650 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243192 | AGTATACCAGGAGAC[C/T]AAGGAGGTTGTGGGG | 84333 |
| rs748459764 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236361 | AGCCTGATATTTGGT[C/T]AGTGCTCATTAAATA | 84333 |
| rs748468471 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197789 | TATTAAATTTCAATT[A/G]TATTTTACCTGTGCC | 84333 |
| rs748485726 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211972 | TCCACTCCTGCCTCC[A/G]TTGTCAGGAGCGGTG | 84333 |
| rs748637952 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190230 | TTATAAGGGCACTAA[C/T]CCCAATCATGTTCTC | 84333 |
| rs748639114 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191752 | CTGTCCAGAACACTC[C/T]ACCCAAAATGAGACA | 84333 |
| rs748657784 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235724 | AGTGAATAAGTCTCA[C/T]GAGATCTGGTGGTTT | 84333 |
| rs748687822 | snp | C/G | 1.65121e-05 | 0.00287329 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91271663 | TGAACTGCTCAGCTT[C/G]GCAAGTCTGCTCTCA | 84333 |
| rs748688366 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223695 | TTCAGTGAAAGTAAT[C/T]CCAGTAAGTTATAGT | 84333 |
| rs748728429 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237644 | AGCTACTAGGGAGGC[C/T]GAGGCAGGAGAATCA | 84333 |
| rs748749732 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252398 | AAGTTTTCCTGGCAT[-/C]TTATAACAACATATA | 84333 |
| rs748770289 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274435 | CAGACCCTAGTATGT[A/G]TGAGTCTGTAAAGAG | 84333 |
| rs748774783 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282432 | GAGGTTGCAGTGAGC[C/T]GCAATTACACCACTG | 84333 |
| rs748781869 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181702 | TTGAACCAACCTTGC[A/G]TCCCGGGGATGAAGA | 84333 |
| rs748808214 | in-del | -/T | 1.72199e-05 | 0.00293422 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264553 | TTACCTATGTGTTTA[-/T]TTAGTTATATACCAT | 84333 |
| rs748835853 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223572 | GAGCTCCTAGCAGAT[G/T]TCATTCTCAACTGTC | 84333 |
| rs748836019 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253769 | GCTAGGGCCACTTGC[C/T]TGAGTGTGTGTAAGG | 84333 |
| rs748928048 | in-del | -/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227943 | TCTTAAATGAATAAA[-/T]GCATGGCTAATAAGT | 84333 |
| rs748935387 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193341 | AAATTGTACTTAGAC[A/T]TCTAACCTACACAAC | 84333 |
| rs749008776 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279030 | ATTCCCAACCATTCA[A/G]AATGTTGGCAGCTGA | 84333 |
| rs749029196 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268116 | TGTGTGTGTGTGCAT[A/G]TGTGTGTGTGTGTTC | 84333 |
| rs749060917 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266094 | TACAGATTGCACAGG[C/T]AGTAAATTCTTTCTT | 84333 |
| rs749097095 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174547 | GTTTGATTATAATCT[A/G]CTGTAATAAATCCTA | 84333 |
| rs749104442 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216944 | TATAGGAAGACCTTT[A/G]TATTACAGAGAGTAG | 84333 |
| rs749119992 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250369 | CTGATTTTTTCAAGT[A/G]TTAGCTTAGAGGTAT | 84333 |
| rs749125347 | in-del | -/TCC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164498 | CAGACTCTGAAGGAA[-/TCC]TCCTAGTAATTGCGT | 84333 |
| rs749208440 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230261 | TGGGTTGAGAAAAAG[C/T]GTGTAACCTAAACTA | 84333 |
| rs749235192 | snp | A/G | 3.30639e-05 | 0.00406581 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248609 | TGTTTTATGAAATCA[A/G]CACTTCTATTAAAGA | 84333 |
| rs749268745 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256121 | GTCAATAGAAACTGT[C/T]GCTGAGGAAGCCCAG | 84333 |
| rs749300099 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231445 | TGACTTTTGAACAAA[A/G]ACCAGGTAAAGGAGT | 84333 |
| rs749307804 | snp | G/T | 1.66507e-05 | 0.00288532 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278258 | ATTTATTATCTGTCT[G/T]TATTTTGTAGTCATA | 84333 |
| rs749323890 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166594 | ATGTTTGCTTACTTG[A/G]TATAATTATTTACTG | 84333 |
| rs749329605 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241727 | ATAGTCTCTGGAACC[C/T]TTCATAACTCTCTTA | 84333 |
| rs749384902 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196997 | TGGAACCATTCAAAT[A/C]TCTTTTTAAACAACA | 84333 |
| rs749390131 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278723 | TCTTGTTTAAATAGC[A/G]TACTCTACAAGAAAC | 84333 |
| rs749491247 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207204 | TATTTAAGTTTAAGA[A/C]CACTTTGGTGAGGGA | 84333 |
| rs749506310 | snp | A/G | | | intron-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91221374 | AAGGCAGTTAATCCC[A/G]ACTTATAGAGGAGGA | 84333 |
| rs749520368 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254902 | TGACTAACTATCAGT[A/G]TAAAGGGTGAGCTTT | 84333 |
| rs749560031 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234809 | TTGTTATCTTCCTTG[C/T]ACACAGAAACACAAA | 84333 |
| rs749572565 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179799 | ACTGTGAATAGTGCT[A/G]TGATAAACATATGCA | 84333 |
| rs749575549 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165225 | GCATCATATCCTAAG[A/C]CACTTAGTATGAAAA | 84333 |
| rs749589874 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166063 | GAAATTACTTGGCGC[A/T]GTTCATTCCTTTTTA | 84333 |
| rs749610667 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235564 | TAAAAATTAGCCGGG[C/T]ATGGTGGCCGATATG | 84333 |
| rs749649751 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219351 | TTCTTTTAAAACATA[C/T]TTAAAATAGTTTCAG | 84333 |
| rs749687820 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205281 | TTTTTCTGGGTTTCT[A/G]AATGACTGGACACAC | 84333 |
| rs749697416 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235682 | TTGAATCATGGGGGC[A/G]GGTCTTTCTCACGCT | 84333 |
| rs749740232 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170476 | ACACCTCACCAGAGA[A/G]GATACACAGATGGCA | 84333 |
| rs749763782 | in-del | -/TATATATATATATATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249376 | GGCTTTTAGTGTATA[-/TATATATATATATATA]TATATATATATATAT | 84333 |
| rs749821646 | snp | C/T | 1.69109e-05 | 0.00290778 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223027 | ATCAAAGTTTATATG[C/T]ACATTTTGTTCTTTT | 84333 |
| rs749824799 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201206 | ATCTGGAGGCTGGGA[A/C]ATCCAAGGGTGAGGT | 84333 |
| rs749851744 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186533 | CTTCATATATATATG[-/TG]TGTGTGTGTATATAT | 84333 |
| rs749876325 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188978 | ACAAGGGAAATGAAG[C/T]GTGATTGCTGGGCAG | 84333 |
| rs749879480 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267186 | CTTGCCCTCACCTCC[C/T]CTGGTATCCACCTAC | 84333 |
| rs749964939 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268534 | GTCTCCTCATCTATT[C/T]TACACACTGTGAGTA | 84333 |
| rs750009595 | snp | A/G | 3.31433e-05 | 0.0040707 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240449 | AATGAGCGTTCATAT[A/G]ATGCGTTTTAACCTA | 84333 |
| rs750014509 | snp | A/G | 1.64879e-05 | 0.00287118 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222967 | GCCAACAACAGTGAC[A/G]GAATGCCTCCATACA | 84333 |
| rs750027811 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198428 | CTTTACCCAGATGCC[A/G]TCTTCTCACTAATGC | 84333 |
| rs750050751 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210420 | GCTAACCTGCAAATC[C/T]AGTAAGATACACAAG | 84333 |
| rs750067476 | snp | A/C | 1.72877e-05 | 0.00293999 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278232 | TATTGTTTTTATCCA[A/C]ATACAGTCTTATTTA | 84333 |
| rs750152724 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183893 | GAATATTGGCCCCCA[A/G]TCTCTTCTGGCTTGT | 84333 |
| rs750168633 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232340 | TTGTACTATGAATAC[A/G]TAAGTATTTAATCTT | 84333 |
| rs750174631 | snp | A/G | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284740 | TTTGTCTTAATGTTA[A/G]TGAAACGTTGGAGGT | 84333 |
| rs750174808 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242816 | TAAATGCTTTAGTGT[A/G]TATTTCCTAAGAATA | 84333 |
| rs750212820 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270534 | AAAAGAGAGCCGAGC[-/T]GAGCCCGCCTTACAG | 84333 |
| rs750264362 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244179 | GGTGAGGAGGTCAAG[A/G]GTGTGAAGTGGGGGC | 84333 |
| rs750270217 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279650 | ACAGTTTTCAAAAAC[C/T]TTACTTGGAAATTGC | 84333 |
| rs750288642 | snp | A/T | 2.02513e-05 | 0.00318202 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261283 | CAAGATAGAACATTT[A/T]AACTGGTAGAACATT | 84333 |
| rs750292386 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228178 | TCTTTCACCAGGTGA[C/T]CCTGGTGAAAAGAGA | 84333 |
| rs750308222 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179709 | GCTGCATAGTATTCC[A/G]TGGTGTGTATGTACC | 84333 |
| rs750312453 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273060 | ATGATATGGGAATTC[C/T]CGTGCCTTCATTAAA | 84333 |
| rs750314944 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222402 | TAGAGCAGTCAAGCA[C/G]ATAGTTAAAATGCAT | 84333 |
| rs750339445 | snp | G/T | 0.000149617 | 0.0086479 | missense | PCGF5 | GRCh38.p7 | 10:91251336 | GTAGATGAAGAAGGT[G/T]ATGAAAATGAAGATG | 84333 |
| rs750359163 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255884 | GTATTTGCACGTAAC[A/G]TATGCACAACCTGCT | 84333 |
| rs750398142 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166512 | TAGAACTTTTACAAT[A/G]ATGAAACTACTGTTT | 84333 |
| rs750404908 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209048 | ATTGTTGTTGGCACT[C/T]TGGCCATTTGTAGTT | 84333 |
| rs750430549 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230433 | AGACTTCTGGTGTTT[C/T]ATATGTACTGATTTT | 84333 |
| rs750517837 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190991 | TATAAATACTTACAG[C/G]TTTTGTCAAAATCCT | 84333 |
| rs750554132 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272077 | TGCCAAATTAGGTGA[A/C]GCTAAATAACAGCAA | 84333 |
| rs750573785 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214504 | GTTAGAGAATTTAAG[A/G]GAACTGATCAAATTC | 84333 |
| rs750586227 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247815 | AGATTTTGAGAATGG[A/G]CATATCAGCTGTTGC | 84333 |
| rs750586537 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171869 | TCTTCGGGAACTATG[A/T]GGCCAAAATATCAAA | 84333 |
| rs750634710 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201024 | AAATAGTGTGAAGTG[C/G]AACTCCTGAGACACC | 84333 |
| rs750639975 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217321 | ATAGGCATGAGCCAC[C/T]GCACCCAGCTGAAAA | 84333 |
| rs750670864 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235339 | TTTGTCCAACAACCT[C/G]GTTCAAATCTAACAA | 84333 |
| rs750721214 | snp | A/G | | | missense | PCGF5 | GRCh38.p7 | 10:91248513 | TTCGAAGGTTGGACA[A/G]TACATTAGAGGAAAT | 84333 |
| rs750783420 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263204 | GCATTGCTAACTGGG[A/G]CAAGATAGTTTAGTT | 84333 |
| rs750784184 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185286 | ACTTAAAGAAGCAGT[C/G]TGGCCATGTTTTGGT | 84333 |
| rs750815595 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213366 | TACGTATGCATAAGT[A/G]ACCTCTATTTGGCTA | 84333 |
| rs750848950 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262872 | GCACTTTATTTTCTT[C/T]ACGCAAAATACCATG | 84333 |
| rs750875279 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91227104 | TTATTATTTAAACTA[A/G]GTAATTACATATCAG | 84333 |
| rs750917779 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266144 | TGGATATTATGATAT[C/T]ACACATAATATTGTG | 84333 |
| rs750922735 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193830 | GGAAGTGATAGCAGG[A/T]ATCCTAATATGAGAG | 84333 |
| rs750959009 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276722 | TTAATGGATACTTCC[A/G]TATATGATTAATGCA | 84333 |
| rs750977977 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184017 | TCGTTTCGACCTTGG[A/G]TAATCTGATGATTAT | 84333 |
| rs750986573 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196141 | TACAGATATTTCACA[C/T]GGTGGCAGAGAAGGC | 84333 |
| rs751008963 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228334 | TGTATTGGTTCTTAA[C/T]CCTTTTGTGGTCAGA | 84333 |
| rs751024678 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279601 | TGTTACCTTAAATTA[C/T]ATGAAAACTGTCATT | 84333 |
| rs751053353 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234306 | TGTAAACATATGTTT[A/C]TTTTTAACATAAATT | 84333 |
| rs751072964 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255420 | GAAGGCCCTAAGCTC[-/T]CACCTCTGCCTCACC | 84333 |
| rs751072995 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214784 | GGGTCTGAGGAAGAC[A/G]AGGAAGGAAATGGAT | 84333 |
| rs751107130 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186037 | TCGCTCCCTGCTTCA[A/G]TATTTATTTCTTTAT | 84333 |
| rs751111638 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281070 | GAATGACTGTGGTTT[A/T]TAAACATTACTTTAA | 84333 |
| rs751179223 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169148 | AGTTTATTTACGGTA[-/T]TAATATCTGGATACA | 84333 |
| rs751237516 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243894 | ACTCACATTATATTT[C/T]TATTGGTCATCACTT | 84333 |
| rs751278549 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179537 | CCAGTGTGTGTTGTT[A/T]CCCTCTGTGTGTCCA | 84333 |
| rs751281989 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229721 | GAATTTATGATTCTG[A/G]ATGAATAGCCATTTT | 84333 |
| rs751307723 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197376 | CTGAGGATGGCTGCA[C/G]AGACGTATATCTTTG | 84333 |
| rs751327491 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207551 | AGTTACTATATTCAG[A/G]AAATATGGCATTGTT | 84333 |
| rs751339515 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281997 | TTCATGGAGGCAGTG[C/T]TAACTAAAATTAAGC | 84333 |
| rs751346129 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254673 | GGGGCAGTAGTTGCA[C/T]GTATAGTTTATACAG | 84333 |
| rs751412465 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166452 | TTGAAGAAGTTTTCT[C/G]ACAACAGAATTAGAT | 84333 |
| rs751415449 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183466 | ATGTGTGTCTCTCCA[G/T]GTGAGGTAGGTCTCT | 84333 |
| rs751432263 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255748 | TCAACAACAACAACA[A/G]CAAAATATGGGAGAT | 84333 |
| rs751445131 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195483 | TGCATATATATATAT[-/AG]ATAGAGAGAGAGAGA | 84333 |
| rs751476584 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190698 | TTTTTCCCCTTAATG[C/T]TAAGTGCTCAAAAGT | 84333 |
| rs751490466 | snp | G/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219014 | TTTTTAAATTGGGGT[G/T]GGAGAGATGGAATGG | 84333 |
| rs751538564 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271171 | AGAACCTACTATAAA[A/T]CAGAAAATAGATGCC | 84333 |
| rs751543665 | snp | A/G | 1.93e-05 | 0.00310638 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261306 | AGAACATTTTAACTG[A/G]TAATCTTTATTTCCT | 84333 |
| rs751563354 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225150 | AAAAAGGAAAACAAA[A/T]GATTATAGAAGTATA | 84333 |
| rs751593076 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262842 | AGACAATAAATTGTT[A/C]TTATGATTTGGTTTG | 84333 |
| rs751635861 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171792 | TAATGACAAAAATTC[A/G]AAGTGTGGCTGAGCT | 84333 |
| rs751660594 | in-del | -/GATAGATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246970 | ATGGATAGATGGATA[-/GATAGATA]GATAGATAGATAGAT | 84333 |
| rs751662139 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247706 | ACATTTAAAGTTTTC[A/G]TTTCAGAAGGTAGAA | 84333 |
| rs751668507 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234425 | ACTGCATTCAAAGAT[A/G]GGCTCTTCCTATTCA | 84333 |
| rs751680005 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200883 | ACCTAGAGCTTGCTG[C/T]GTAGGAGGTTGATAA | 84333 |
| rs751685584 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228080 | CTAGGATCTACATAG[A/G]CATCTTTGGGGTCTT | 84333 |
| rs751707957 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275092 | CTATTAATATTAAAA[A/G]CACATGGCAAAAATA | 84333 |
| rs751718456 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261922 | TGCATAAATGTAATT[C/T]ACCAGTTTATTTACA | 84333 |
| rs751759232 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169772 | TAGATATTGGCAAAC[A/T]GACTCTAAAGTTTAT | 84333 |
| rs751771566 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199840 | AGAAACAGACCCCAA[G/T]ACAAGAATTTGAGAG | 84333 |
| rs751871481 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213203 | AATAGTTATTAATTA[A/G]TATTAATTCTATTTG | 84333 |
| rs751887657 | snp | C/T | 8.26248e-05 | 0.00642694 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91271641 | TCTCCTCCGCAGTTT[C/T]GGTGTCTGAACTGCT | 84333 |
| rs751896246 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215245 | TTCAGTTTTCTTAAT[A/T]TAATAAATTAAAATG | 84333 |
| rs751907691 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275279 | ATAAACATATAAAAA[C/T]GATTAACTTTCTTAG | 84333 |
| rs751911244 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276649 | GGAAACTGAGAAAAT[C/T]CCAAGCATTGCCAGT | 84333 |
| rs751919540 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195089 | GTGAGGATGGGGAAG[A/G]TGGTTTGAGGGTTTA | 84333 |
| rs751977789 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226891 | TACCTCTTCCCTTCA[G/T]TAGGCCAGGGACATT | 84333 |
| rs751982035 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217182 | GGGACTACAGGCACC[C/T]GCCACCACGCCCTGC | 84333 |
| rs751988533 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237526 | AGTGGGCAGATTACT[C/T]GAGGCCAGGAGTTGG | 84333 |
| rs752038571 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252831 | GCATGATTTCTCATA[G/T]GAAAGTATAAAAGAT | 84333 |
| rs752069926 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188410 | TTTTATTATTATTAC[A/G]ATGAAGACCCTAGAA | 84333 |
| rs752084912 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255483 | CTAAGGCAGAGTTGT[C/G]AACACCTTAGTTGAA | 84333 |
| rs752133035 | snp | A/T | 1.65408e-05 | 0.00287578 | missense | PCGF5 | GRCh38.p7 | 10:91248686 | TTGAGCGTGAATCTG[A/T]ATTTTGGAAGAAAAA | 84333 |
| rs752172867 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242473 | ACCCTCTCTGTTCTT[A/G]AAGGGCCACATCATA | 84333 |
| rs752183492 | snp | A/C/G/T | 6.73839e-05 | 0.00580418 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264385 | TATGCAAAATACTTT[A/C/G/T]GAATTCAACATTATG | 84333 |
| rs752189475 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240379 | TAAATAATGATATTC[A/T]ACTTGTAGTAGGTAG | 84333 |
| rs752239518 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196275 | TGCAGAAATGTGCTA[A/G]TTACAAAAGTATCTC | 84333 |
| rs752261001 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171318 | TTTGAAATGGGTTGG[-/T]TTTTTTTATATTGAT | 84333 |
| rs752284243 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178692 | CTGCACCTGGCCTGC[G/T]GTTTCTCATTTTAAA | 84333 |
| rs752375162 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269085 | ATTCTGACTCAGTAG[C/G]TCTGGGAATAAGACT | 84333 |
| rs752433893 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207477 | CATTTAAGAATAGTT[G/T]CAGACATGACCCTTT | 84333 |
| rs752463383 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233635 | ATTACAGCTATTCTG[C/G]ATTTTTTAAATTAGT | 84333 |
| rs752488535 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189482 | ATTGAGAATCTACAC[G/T]TGCTGTTTGAGGTTC | 84333 |
| rs752488578 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178000 | CATCCATATTCTGCG[C/T]CGCTCACACTGGGAG | 84333 |
| rs752611203 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246465 | TACCAGTTATGGTTT[A/G]TAGGTTGGACTCAAG | 84333 |
| rs752628550 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200724 | GTGGGCAATCTAGTT[C/T]ATCCTATATTCATCA | 84333 |
| rs752632464 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234241 | ATATGCAAAGGAATT[A/G]GGAAGCGGCAAAACA | 84333 |
| rs752636206 | in-del | -/ATAGAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195484 | TGCATATATATATAT[-/ATAGAG]AGAGAGAGAGAGAGA | 84333 |
| rs752637259 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199766 | GCAACCCTCTTGTTT[C/G]ACAGATAGGGAAGTG | 84333 |
| rs752645413 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232987 | TCCACAAAGTTCCAC[G/T]GTAATCTTGTAGAGG | 84333 |
| rs752677081 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283787 | AGTAGCCCTCACAAT[C/G]AAAATATCATAGAAT | 84333 |
| rs752786797 | snp | A/G | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227864 | AGTTACCCATCCTTT[A/G]AAACTCATCCCCTCT | 84333 |
| rs752791328 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168657 | AAACCGGCAGGGCAT[A/G]GTGGCTCACACCTGT | 84333 |
| rs752800081 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193948 | ACTTAGATTTGGGAT[A/G]TAAGAGAGAGAGGAG | 84333 |
| rs752809367 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261614 | CTCTAATTGAACATA[C/T]CCTGAATAAACTATG | 84333 |
| rs752809432 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245646 | CTAAGAGGAGACACT[G/T]GTTTTCAGTGGGAGC | 84333 |
| rs752833574 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212499 | TTATTTGACCAGAAG[C/T]AGCTGGAAGTTTGGT | 84333 |
| rs752879230 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169558 | ACAAAACAAAATACT[C/T]AGATATACATCTAAC | 84333 |
| rs752901029 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181232 | GTTTGCTGAAGTTAT[C/T]TGTCAGCTTGAGAAG | 84333 |
| rs752928919 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211539 | GCATAAATGTGAAAC[A/G]TCAGTACTGACCCAA | 84333 |
| rs752940789 | snp | A/G | 1.656e-05 | 0.00287745 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248738 | AGGTGACTTTTTCTT[A/G]TGTCTGTTTCTGACA | 84333 |
| rs752942939 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224897 | CTACTTCCGTTTCCC[A/G]TTTCACCAAGCATGG | 84333 |
| rs752958947 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270038 | CAGAGTGTCTGACAT[A/G]AATGTTATTAATAAC | 84333 |
| rs752967309 | in-del | -/GA | 1.65145e-05 | 0.00287349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248491 | AGTATTTTCTTTCTC[-/GA]CCCCCTTTCGAAGGT | 84333 |
| rs753037661 | snp | A/G | 1.66322e-05 | 0.00288371 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222999 | GTAAGTATTCTTTTA[A/G]GTTATTATACCTATC | 84333 |
| rs753047063 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241195 | TTCTCCTGCCTCAGC[C/T]TCCTGAGTAGCTGGG | 84333 |
| rs753050430 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204283 | GGATAATAAATTGAA[C/G]TTATTGGATTAGGTT | 84333 |
| rs753122176 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270084 | TTTATTATGACTATA[A/T]TTCTCTCCTCCTTCA | 84333 |
| rs753132706 | in-del | -/GATAAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244763 | GGATATAGGATATGG[-/GATAAA]GAAAAGAGTTGAACA | 84333 |
| rs753152661 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216632 | AAGAGTTCATTGAGT[G/T]ATAGAGAGTAGAGAT | 84333 |
| rs753187304 | snp | C/G | 1.70746e-05 | 0.00292182 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278240 | TTATCCAAATACAGT[C/G]TTATTTATTATCTGT | 84333 |
| rs753240594 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203114 | CTACCAGCAAACCCC[G/T]TGGTACTAAGCATTT | 84333 |
| rs753350213 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164636 | AAGGAACCTCGGTTG[C/G]CATTCATGAATACAG | 84333 |
| rs753364016 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254079 | TCAAGGCCCTTCCCT[A/C]ACAAGCACCTCTTTT | 84333 |
| rs753371531 | snp | A/T | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161781 | AGCCTCTTGATAAAG[A/T]CTCCTGAACTTTTCC | 84333 |
| rs753419195 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188158 | GATTTCTGCATTTCC[A/G]TCTGAGGTACTGGGT | 84333 |
| rs753449789 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186242 | ACCTGGATTTTGCCC[C/T]GACTCTCACAGCTGT | 84333 |
| rs753469298 | snp | C/T | 1.74114e-05 | 0.00295049 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222821 | CAGACTTTCATCTAC[C/T]TAGGACCCCTCTTTG | 84333 |
| rs753507593 | snp | A/G | 1.65732e-05 | 0.00287859 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248751 | TTATGTCTGTTTCTG[A/G]CAGCACCTCTTAAAC | 84333 |
| rs753511890 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268909 | GGTCAGACTTAGCTC[A/G]TAAAATTTTTTCAGT | 84333 |
| rs753514542 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234093 | GGTGGACCACACATA[C/G]ATCTAAGATAGCAAC | 84333 |
| rs753520635 | snp | A/G | 1.66001e-05 | 0.00288094 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271619 | TGCCTCTTATCTGAT[A/G]AGTTCATCTCCTCCG | 84333 |
| rs753525609 | snp | A/C | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281594 | TAAGAATATAGATAT[A/C]ACCAAAGACATTTTA | 84333 |
| rs753528865 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255750 | AACAACAACAACAAC[A/G]AAATATGGGAGATAC | 84333 |
| rs753552716 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177869 | TGGGTGAGGCGATGC[C/G]TCTCCCTGCTTCAGC | 84333 |
| rs753560934 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187262 | GATAGATATATAAGA[C/T]TTGACACTAATGTGC | 84333 |
| rs753612248 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267465 | TCTCCAGCACCTAGG[G/T]CAGTGCCCAGCATAT | 84333 |
| rs753615916 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199602 | TCCACATTAATGTAC[A/G]TGAAATTCAGCCACG | 84333 |
| rs753620866 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257869 | TGTATATTCATAATA[A/G]CATTATTTGTAATAG | 84333 |
| rs753704129 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282921 | AATATATATTCCTAC[A/T]GTTTGGGTAGAAATA | 84333 |
| rs753711778 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230873 | AGTGATCAATCTGCC[C/T]TGACCTCCCAAAGTG | 84333 |
| rs753723085 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211217 | TGTTTATGCACATGT[A/G]TACAATACTGACTTG | 84333 |
| rs753782170 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245468 | AGGAGTTTTGCTACA[A/T]ATGGGAGCAAAGAAA | 84333 |
| rs753782445 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177282 | GTTTTGTCTCAGAGG[A/G]GTACCCGGCTGTGTG | 84333 |
| rs753787448 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173579 | CTAGAGGGAGTTGGC[-/TT]TTTTTTTTTTTTTTT | 84333 |
| rs753789084 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244249 | GTGGGAAAGTGAGAC[G/T]TAAGCGAAGACTTGG | 84333 |
| rs753811064 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198554 | ATGACCATTGGCAAA[A/G]CAGCATCACTGGCTT | 84333 |
| rs753844947 | snp | A/G | 0.00014835 | 0.0086112 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222958 | TCTGATCAAGCCAAC[A/G]ACAGTGACGGAATGC | 84333 |
| rs753856005 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273401 | TTCCTTAGAAATGAA[G/T]ATGTCCTTAAACCAT | 84333 |
| rs753937677 | snp | A/G | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221313 | TTTCCTCTTCCAGAG[A/G]ACTTTCTCTTACTTT | 84333 |
| rs753948277 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275075 | TAAAAAAATTGAATT[A/G]ACTATTAATATTAAA | 84333 |
| rs753952902 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224754 | TAGAAGCCTATTACT[A/G]TAGGAAAGCTAAAAG | 84333 |
| rs753963469 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203071 | AGCCTTGATGGAGGT[A/G]GGGGCAGGGGAAGTG | 84333 |
| rs753971850 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183415 | GATTGCAACCTCTGC[-/T]TTTTTTTTTTTCCTC | 84333 |
| rs753979271 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257459 | TATCCAGTAGTCCCC[C/T]CCTTATCTGTGGAGC | 84333 |
| rs754000160 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247578 | TGAGCAGGATGAAGG[-/A]GATGAGGCAGGAAGG | 84333 |
| rs754040766 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213344 | ATATCTGTATGTATT[-/TA]TGTATATACGTATGC | 84333 |
| rs754049485 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191299 | CACTGTGATGCTGCA[A/G]CAGTCAATCTGATAA | 84333 |
| rs754062315 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222701 | CAGACATGGGAAAGC[A/G]GAACCACCAAAAGGA | 84333 |
| rs754138103 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240668 | ATAATATTTCATGTT[A/G]TCTTGACTCAGTTAA | 84333 |
| rs754183477 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237071 | ATTGGTTTTAACCAC[C/T]AACTAGCTTCATAAT | 84333 |
| rs754183664 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247991 | TGTGCTGATCTTGGG[A/G]GATGGGCTGTCTGTG | 84333 |
| rs754214519 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216279 | ACCTTTGAAATCAGC[G/T]AATACGTGAAAGGAT | 84333 |
| rs754243577 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202091 | CTTCTTTCCCAAATT[A/G]AGAAGAATAATTGTA | 84333 |
| rs754318606 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240479 | AACATCTTCTTTCTT[C/T]TTAGTCTGTAAGACT | 84333 |
| rs754318820 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229673 | AAACCTGTTTTCATG[A/G]CTATGTAACTGTTGT | 84333 |
| rs754406607 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214696 | CGACAAACAGATGAA[C/T]GGCCAAAAGGCTAAA | 84333 |
| rs754438057 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211258 | GACACAGAAATGCAT[A/T]CTTTGTTGATGTGAT | 84333 |
| rs754469738 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206134 | AAAATAGTGCCACAA[A/G]TATTTATCGGAGAAC | 84333 |
| rs754485906 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248617 | GAAATCAACACTTCT[A/C]TTAAAGATTTCATGA | 84333 |
| rs754533370 | snp | C/T | 1.65652e-05 | 0.0028779 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91251392 | ACAAATTGCTATCTG[C/T]CTAGATTGTTTACGA | 84333 |
| rs754537405 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195320 | TTAAAAGAAAATTTA[A/G]GGTGGAATTAGACAG | 84333 |
| rs754558175 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91227134 | GGCACTTTGCTAGCC[A/T]CTGGGGGTAGAGTGG | 84333 |
| rs754567298 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177883 | CCTCTCCCTGCTTCA[G/T]CTCACACTTGGTGCA | 84333 |
| rs754634226 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253315 | AATAGGTAGTTTTTC[A/T]ATCCTGTCTCGCCCC | 84333 |
| rs754657240 | snp | A/G | | | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91161807 | TTTCCAGTCTCACCA[A/G]AGCTGCAGACACTCG | 84333 |
| rs754661722 | snp | A/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218683 | TGTCTCCCAGGCTAG[A/T]ATGCAGTGGTGCGAT | 84333 |
| rs754766541 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232731 | GGTGGTAAAAGTTCT[C/G]TTTGTTTCAGTTATT | 84333 |
| rs754776587 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267475 | CTAGGGCAGTGCCCA[A/G]CATATATACTCAATC | 84333 |
| rs754782380 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217042 | TGAAAATTTCACCTT[C/T]TTTTTTTGAGACAGA | 84333 |
| rs754796740 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283222 | TTACTTGCTTTCTTT[A/G]TATTTTCAAATAAAA | 84333 |
| rs754832578 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252279 | CTCTAATTTTCTTTT[A/G]CTTCCTCTGTGTACA | 84333 |
| rs754834188 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273373 | TTTACTCTTGGTGTT[G/T]ATGCCTATGTATTTC | 84333 |
| rs754857835 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217661 | CTTTGGGATTATGCT[G/T]CTTTGATAGGGAATC | 84333 |
| rs754888281 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231504 | TCAGGTAGAGGGAAT[A/G]GCAAGATTAAAGACT | 84333 |
| rs754917268 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168495 | AGTGGGGACAAGTCC[A/G]CTAGTTACCTGAAGA | 84333 |
| rs754939528 | in-del | -/TGT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247557 | CTTGTAGAAGAGTAA[-/TGT]TGTTGAGCAGGATGA | 84333 |
| rs754955329 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245487 | GGAGCAAAGAAATGG[G/T]GTGGGGGGGTGCTGT | 84333 |
| rs754991354 | in-del | -/AA | 1.70271e-05 | 0.00291775 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222848 | TTTGCCCAGACTACT[-/AA]AGCCAGTCTTCACTA | 84333 |
| rs755017221 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257493 | TGTTCCAAGACCCCC[A/G]GGGGATGTTGCAACC | 84333 |
| rs755063023 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91192491 | TCATCGTCAATTAAG[A/T]ATCTTTATTCTAATT | 84333 |
| rs755065657 | in-del | -/AAAT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268296 | CATGTTTTATAAGGC[-/AAAT]AAATAGTTGGGCCTT | 84333 |
| rs755066917 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244255 | AAGTGAGACTTAAGC[A/G]AAGACTTGGAGACTG | 84333 |
| rs755099790 | in-del | -/AGTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178200 | AGATGGAAAAAAATA[-/AGTT]AGTGTACAATAGGAC | 84333 |
| rs755120461 | snp | C/T | 1.6519e-05 | 0.00287388 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248580 | GTGGCTCTTTAGGTT[C/T]TTGCAGACTTTTGTG | 84333 |
| rs755125715 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272258 | TTAAAAATTTGGGAA[A/C]CAGACAAGGGTATAG | 84333 |
| rs755230440 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202264 | TTGATGTAGTATGGT[A/G]GTTAAGCCTATAGAC | 84333 |
| rs755259056 | snp | A/C/T | 8.56444e-05 | 0.00654341 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222843 | CCCTCTTTGCCCAGA[A/C/T]TACTAAAGCCAGTCT | 84333 |
| rs755302908 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169058 | GGGCAATTAATACAC[C/T]AGGCTCTCCTCAAGC | 84333 |
| rs755312959 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166701 | TTGCAGCCAGTCAGA[C/T]TTGGGGCTAAAACAC | 84333 |
| rs755316155 | snp | A/G | 1.65231e-05 | 0.00287424 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91271642 | CTCCTCCGCAGTTTC[A/G]GTGTCTGAACTGCTC | 84333 |
| rs755342096 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237565 | CTGGCTAACATGGCG[-/A]AACCCCGTCTCTACT | 84333 |
| rs755349545 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235694 | GGCGGGTCTTTCTCA[C/T]GCTGTTTTCTCAATA | 84333 |
| rs755359469 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240798 | CATTTCCAAACTAAA[A/G]GTACAACTTTCTCTT | 84333 |
| rs755384238 | in-del | -/AA | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283265 | AGCACTTCCTTTCAG[-/AA]AGTTATAAAATTAAA | 84333 |
| rs755388795 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203103 | TCAGCCACAATCTAC[C/G]AGCAAACCCCTTGGT | 84333 |
| rs755431754 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207311 | ACACATTTTTTCTAC[C/T]TTCAGCTTCTTGAGA | 84333 |
| rs755460848 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214709 | AACGGCCAAAAGGCT[A/G]AAGAACTGCAGATAA | 84333 |
| rs755491152 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172090 | AGACGTGTGGCAGAG[A/C]TAGCTCTCGAAATAA | 84333 |
| rs755497094 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201235 | GTATCTGGTGAGGGC[C/T]TTCTTGCCGGTGGAG | 84333 |
| rs755588346 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217279 | ACCTTGTGACCACCC[A/G]CCTCGGCCTCCCGAA | 84333 |
| rs755589151 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252144 | CTTTTATTTTTATTA[A/C]AAATCTTCACTACTT | 84333 |
| rs755646414 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193327 | GACCCAGCTCAGCCA[A/G]ATTGTACTTAGACTT | 84333 |
| rs755651665 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281345 | TTGCTCAACTACATT[A/G]CACACTCAAATGTAA | 84333 |
| rs755677094 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252855 | AAAAGATTGAATTTT[A/G]GAAATTTATTTGAAA | 84333 |
| rs755783377 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267204 | GGTATCCACCTACCT[C/T]GTTTCCTTTACCCCC | 84333 |
| rs755805087 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174375 | AGACAGGTGTGGCGG[C/T]GCATGCCTGTAATCC | 84333 |
| rs755840260 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253748 | ATTTTTCTTTTGTTA[C/T]CCAGGGCTAGGGCCA | 84333 |
| rs755894580 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198464 | CTGACACCTTGTTTT[A/G]AATTTCAGTCACCCT | 84333 |
| rs755895974 | snp | C/T | 1.73513e-05 | 0.0029454 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91261343 | TTTAATGAAGAAATT[C/T]ATTCGATGTTCTACA | 84333 |
| rs755903426 | snp | G/T | 1.65236e-05 | 0.00287429 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248598 | GCAGACTTTTGTGTT[G/T]TATGAAATCAACACT | 84333 |
| rs755924539 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230062 | GTTAAAGTTATGTGT[A/G]TAGTTCGTTTAGCTT | 84333 |
| rs755927624 | snp | A/C | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279711 | TAGGAAAAAATCTTG[A/C]AAGTTAGGAAAAATA | 84333 |
| rs755930607 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255599 | TGTTCCATTATTAGC[C/T]GACCTCTAGGCAGAA | 84333 |
| rs755932375 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244193 | GAGTGTGAAGTGGGG[A/G]CAGATTGCAATTTTA | 84333 |
| rs755950668 | in-del | -/ATTTGGT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173237 | AAGATGACTATTGAA[-/ATTTGGT]GGGGGATTGGTTTAG | 84333 |
| rs755968186 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186261 | TCTCACAGCTGTGGT[A/G]TACCAGGCGTTCATT | 84333 |
| rs756016148 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231251 | TTGTCTTCCAGATAC[A/G]ATTCTGGGCACTTGA | 84333 |
| rs756040226 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263866 | TGGCATAGTCGTAAC[-/TT]TTGTATCAAATTAGA | 84333 |
| rs756043708 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209057 | GGCACTCTGGCCATT[C/T]GTAGTTTGTTACTGT | 84333 |
| rs756094273 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236266 | AGCAGCCTAGTCAGG[C/G]TCTCCAGCACTACAT | 84333 |
| rs756122867 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272147 | CTAGTACTTTACTTG[A/G]GTTACCTCTTTAAAA | 84333 |
| rs756133850 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242835 | TTCCTAAGAATAAGG[A/T]TATTATATTACATAA | 84333 |
| rs756144640 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167409 | AAAATACTTTGTGAA[G/T]TCAGAGGAGGAAAAG | 84333 |
| rs756185464 | in-del | -/TGTG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186531 | AACTTCATATATATA[-/TGTG]TGTGTGTGTATATAT | 84333 |
| rs756298498 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188676 | TCCTCACTGACCCTC[A/G]CTACCTCCCCTCTTG | 84333 |
| rs756353262 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202019 | GTCCAGGATTATATC[C/G]AAGCCTTGCATTTTA | 84333 |
| rs756367624 | snp | A/C | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91220865 | GGGCTGGGGAGCTGC[A/C]GGGACGCCAGACTCC | 84333 |
| rs756374847 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189803 | AGTATTGAGCACATT[A/C]ATATTTTCATATTGA | 84333 |
| rs756400788 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246903 | AGCATCTGTTGGAAA[C/T]ATGGAACTTGAAATC | 84333 |
| rs756425803 | snp | A/C/T | 3.30078e-05 | 0.00406239 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240463 | TGATGCGTTTTAACC[A/C/T]AACATCTTCTTTCTT | 84333 |
| rs756447727 | snp | A/G | 1.67061e-05 | 0.00289011 | intron-variant | PCGF5 | GRCh38.p7 | 10:91223008 | CTTTTAGGTTATTAT[A/G]CCTATCAAAGTTTAT | 84333 |
| rs756500154 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240150 | GTTTTTATCTTTTTC[-/TG]TGTCCTACTTCTTTA | 84333 |
| rs756502024 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161553 | ATGATTTACTCTATT[C/T]TCTTTGATCACCGCC | 84333 |
| rs756515880 | in-del | -/TATATATATATATATATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249374 | AAGGCTTTTAGTGTA[-/TATATATATATATATATA]TATATATATATATAT | 84333 |
| rs756516160 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262929 | ATTCATTGAGTTAAC[A/G]TTTTCTAATTTTTAG | 84333 |
| rs756520007 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237186 | ATTAGATTATTAAAT[-/TG]TATTGAATTAAATAT | 84333 |
| rs756555683 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247827 | TGGGCATATCAGCTG[C/T]TGCTGCATAACAGAC | 84333 |
| rs756571185 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201171 | GCAATTTATAAAGGA[A/T]AGAAATGTATTGCTT | 84333 |
| rs756605300 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228384 | TGATTCTTTCCTCAG[A/G]AAAAAAAAGGATGTT | 84333 |
| rs756615773 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237462 | AAAATTCACATCAAC[A/G]CTGGGCGCAGTGGCT | 84333 |
| rs756618337 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276729 | ATACTTCCATATATG[A/C]TTAATGCATTCTAAA | 84333 |
| rs756672877 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170144 | TTCAAAATGGATCAC[A/C]GACCTGAATGTAAAA | 84333 |
| rs756676950 | snp | A/G | 1.6981e-05 | 0.00291379 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278243 | TCCAAATACAGTCTT[A/G]TTTATTATCTGTCTT | 84333 |
| rs756702528 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231403 | AATTTTAAGTAAACT[-/TG]TGTTGAGGATAGGCC | 84333 |
| rs756708200 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277830 | TTCCTAGCAGAGGGG[G/T]TCTCTTTGTTGATTT | 84333 |
| rs756710283 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262127 | CTGATAGTAGCATCT[A/G]GAAAATTAAAGACCA | 84333 |
| rs756750923 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230881 | ATCTGCCTTGACCTC[C/G]CAAAGTGCTGGGATT | 84333 |
| rs756769248 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265898 | CAGCCACCAAATAGT[A/G]TGTGGCCTTGAAGAA | 84333 |
| rs756781193 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272481 | AGACAAAAAAAAATT[-/A]ATTTTTTTAGGCCAG | 84333 |
| rs756805390 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237020 | GTGTGAAGAAAATGT[A/G]TCACACATACATTGG | 84333 |
| rs756845994 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278441 | CATGCAAATAAGGCC[A/T]TTGTCTATCTCTAAA | 84333 |
| rs756861247 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249986 | CTGAGGGATTGTCAT[C/T]AGAAGTTACGTGGTA | 84333 |
| rs756872418 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229749 | TTTAATGAAAAAAAG[A/G]TATAAATTGAACTTT | 84333 |
| rs756936142 | snp | A/C | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279623 | ACTGTCATTTTAAAT[A/C]TTTTAATATTTACAG | 84333 |
| rs756964181 | snp | G/T | 0.000149861 | 0.00865495 | missense | PCGF5 | GRCh38.p7 | 10:91251326 | CAAACCGAAAGTAGA[G/T]GAAGAAGGTGATGAA | 84333 |
| rs757014121 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207559 | TATTCAGGAAATATG[A/G]CATTGTTATAATAGT | 84333 |
| rs757024844 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172170 | TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG | 84333 |
| rs757028996 | snp | C/G | 1.65488e-05 | 0.00287647 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271630 | TGATGAGTTCATCTC[C/G]TCCGCAGTTTCGGTG | 84333 |
| rs757056634 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166458 | AAGTTTTCTGACAAC[A/T]GAATTAGATATTGGC | 84333 |
| rs757080584 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271174 | ACCTACTATAAAACA[A/G]AAAATAGATGCCTTA | 84333 |
| rs757088154 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255768 | ATATGGGAGATACTA[A/G]CAAATACAGTGGTCC | 84333 |
| rs757102601 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196708 | TTTCTTGTTGGTCCC[C/T]CTCACAGACTCTATG | 84333 |
| rs757113008 | in-del | -/TT | 1.65488e-05 | 0.00287647 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248730 | AATGGACAAGGTGAC[-/TT]TTTCTTATGTCTGTT | 84333 |
| rs757175351 | snp | C/T | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221142 | GCGGCTGTGCTGGGA[C/T]CCCACAGGGCTGTAC | 84333 |
| rs757176030 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242770 | CTGAACTATTTGAGG[G/T]TAAGTTACATGTGTC | 84333 |
| rs757252738 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164998 | CAGTGCCTGGCATAT[A/G]TGAAACACTTAGTAT | 84333 |
| rs757279311 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234520 | TAGGGTAGAAATGGC[A/G]GCAGGGAATTAATAC | 84333 |
| rs757284079 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254749 | ATGTCAATAAAAAGA[C/G]TAGAGTAAGTATCTC | 84333 |
| rs757305773 | snp | G/T | 1.6593e-05 | 0.00288031 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278263 | TTATCTGTCTTTATT[G/T]TGTAGTCATACCCTA | 84333 |
| rs757307134 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188625 | TTGTCTACTTCATGG[C/T]CACCGCCTTCATTTG | 84333 |
| rs757313905 | in-del | -/TC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254174 | TATGTATGTGTTCGT[-/TC]TCTCTCTCTGTCTCT | 84333 |
| rs757314692 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189619 | TACATACATATCTAC[A/C]TGAAAATGGAAGAAA | 84333 |
| rs757330858 | in-del | -/GAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209763 | GCGAGACTCCGTCTC[-/GAAG]AAAAAAAAAGAAAAA | 84333 |
| rs757355189 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200899 | GTAGGAGGTTGATAA[C/T]ATTAGCTGTGTTCGT | 84333 |
| rs757366765 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219050 | GAAGAAGGCAGAGGC[A/G]AAACCACAGAACACT | 84333 |
| rs757368826 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235311 | GATGATGCAGTGGCC[A/G]TTTTTCTATTAATTT | 84333 |
| rs757450352 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169931 | TTAAACAAATGGATC[A/G]TGGGACAGAATAGAG | 84333 |
| rs757515605 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246735 | GTTAAGATCATTCTC[A/G]TATTTTGAGCTGATT | 84333 |
| rs757540384 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258833 | CAGGTTGTTATTTGT[A/T]AATTTATTTCTGTTG | 84333 |
| rs757552121 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199905 | ATCAACAGGAAAGTA[C/G]AGAAGTGGGACAGGG | 84333 |
| rs757552129 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213214 | ATTAGTATTAATTCT[A/G]TTTGTGTTTTAGAAA | 84333 |
| rs757553932 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215267 | ATTAAAATGGTGATA[-/T]TGAAATGATCTGGTA | 84333 |
| rs757624979 | snp | A/G | 1.65198e-05 | 0.00287395 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248474 | CTTGGTGTCTTCATT[A/G]TTAGTATTTTCTTTC | 84333 |
| rs757631991 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245804 | AGAAAGTGTTTGTCA[A/G]TCAAAATTAAGGATA | 84333 |
| rs757707788 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238802 | CATTTAGAAACCCTT[C/T]TGGGGACAAGAAATT | 84333 |
| rs757773996 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231761 | AAAGGAATCACTCAG[A/C]CTACTATGTCGAAAG | 84333 |
| rs757791178 | snp | C/T | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161644 | TGCCCATTATGAGTA[C/T]GGAGGGCACATAGCT | 84333 |
| rs757817303 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182416 | AGTGCCCTCCTTATC[A/C]TTTCTGATTGTGTTT | 84333 |
| rs757872235 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247456 | GAAAGATTGAGAAAC[-/AG]AATAATAGTTTGAAA | 84333 |
| rs757902604 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277948 | ATGCCTATAAGCAGG[G/T]TGTGTGACTTTCAGT | 84333 |
| rs757939812 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213713 | CTGGTCTCAAACTCC[C/T]GACCTCAGAGAGGTC | 84333 |
| rs757941568 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229676 | CCTGTTTTCATGACT[A/G]TGTAACTGTTGTGTA | 84333 |
| rs757962489 | in-del | -/GTG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243293 | ACTAGGTAAAGGGAT[-/GTG]GTGGGTTTTGAAATG | 84333 |
| rs757986135 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231294 | AACCTAGTAGGCAAT[A/G]AACAAATGATAGTGT | 84333 |
| rs757989700 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233899 | ACAAAGGAAGTCAGC[C/G]TTTGGTCAGTTTTAA | 84333 |
| rs758004118 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240447 | TAAATGAGCGTTCAT[A/C]TGATGCGTTTTAACC | 84333 |
| rs758032451 | in-del | -/AAACGAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209798 | AAAAAAAAAAAAGAA[-/AAACGAAG]AAACGAAGAAAGGAA | 84333 |
| rs758121069 | snp | C/T | 1.66081e-05 | 0.00288163 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222994 | TACATGTAAGTATTC[C/T]TTTAGGTTATTATAC | 84333 |
| rs758128348 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201039 | GAACTCCTGAGACAC[C/T]AGGGAGGTGATGGGG | 84333 |
| rs758172129 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218918 | CAGGCATGAGCCACC[A/G]TGCCAGGCCTATTAT | 84333 |
| rs758192907 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253407 | TTTAAGTCCTCATTT[C/G]CAGCCCTGCTTTGTT | 84333 |
| rs758196408 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254472 | TGTCAATTAGGGATT[A/C]GTTTGTTATCTATTA | 84333 |
| rs758197185 | snp | C/T | 2.02562e-05 | 0.00318241 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261287 | ATAGAACATTTTAAC[C/T]GGTAGAACATTTTAA | 84333 |
| rs758226626 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177542 | GCCTCCTTGAGCTGC[A/G]GTGGGCTCCACCCAG | 84333 |
| rs758246878 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271030 | ACTCATAAAACATCT[A/G]ATGGCTGATATATGC | 84333 |
| rs758278093 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217847 | ACTAGAGTGCAATGG[C/T]GCGATCTTGGCTCAC | 84333 |
| rs758284604 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239265 | AACTCCTAATATAAT[A/G]TCTAGCATTCAGTAA | 84333 |
| rs758290690 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183419 | TGCAACCTCTGCTTT[C/T]TTTTTTTCCTCCATC | 84333 |
| rs758312545 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206557 | AGAGTACACTTGGCT[G/T]CATTTCCCCACAGTG | 84333 |
| rs758343086 | snp | G/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283956 | GTGAAAGAATTACCA[G/T]GTCATTGTTAATGAC | 84333 |
| rs758348708 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251482 | TTATGATCAGTTTAT[A/G]GTAAACCCTTGATAA | 84333 |
| rs758368353 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234255 | TGGGAAGCGGCAAAA[C/T]AAAATAGCTTCTAGA | 84333 |
| rs758431178 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269157 | GCATCTGATCTTTGG[A/G]CCATCCTTTGAGTAA | 84333 |
| rs758434454 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198781 | ACCACGGGGCAGTAC[A/C]TCTTAAGGATTGGAT | 84333 |
| rs758464955 | snp | C/G | 1.65145e-05 | 0.00287349 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248491 | TAGTATTTTCTTTCT[C/G]CCCCCTTTCGAAGGT | 84333 |
| rs758492080 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187416 | ACCTGCTTTGTGGAT[A/G]CAGTCCATAGAGAAG | 84333 |
| rs758493669 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178927 | CTACAACTGATTTCA[-/G]CACTCACTCTATCTC | 84333 |
| rs758524022 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167708 | GACTGTTTAGTTGGC[A/G]GTAGATAAGTATCAG | 84333 |
| rs758532963 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246516 | AGGTAGTAGAGAGAA[A/G]TTAGTCCTTGAGCAG | 84333 |
| rs758579972 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275111 | ATGGCAAAAATATCA[G/T]AAAATATATTTGCAA | 84333 |
| rs758617840 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173657 | CAAGTCCAAAATATG[C/T]GCTTTTTTCAAGTGG | 84333 |
| rs758621114 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182338 | TAGATTTTTTAGTTT[A/G]TAAGCATAGAGGTGT | 84333 |
| rs758628759 | in-del | -/TTT | 1.65151e-05 | 0.00287355 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248572 | GAACGTAAGTGGCTC[-/TTT]AGGTTCTTGCAGACT | 84333 |
| rs758633001 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211688 | CAACTGAATAGTGAA[A/G]AAGAGGAAGAGGAGG | 84333 |
| rs758644673 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258573 | ACTTAACTGGGGCTT[G/T]TAAAAATGTGCTAAT | 84333 |
| rs758709032 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168661 | CGGCAGGGCATGGTG[C/G]CTCACACCTGTAATC | 84333 |
| rs758717268 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181322 | ATAGTTTGACTTCCT[C/G]TTTTCCTATTTGAAT | 84333 |
| rs758751526 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212109 | CAATAATGATATAAA[A/G]TGCTTAGCAAAATAC | 84333 |
| rs758795897 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194000 | CAGGCCTGAATAGCT[A/G]GAAAAATGGAGTTGT | 84333 |
| rs758806524 | snp | A/C | 1.67223e-05 | 0.00289151 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264410 | ATTATGTTAATAGAT[A/C]TATAATGATTCTTTT | 84333 |
| rs758842395 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251946 | CTTTTAAACTCCTTG[A/G]AGGCCCTCAGTTATT | 84333 |
| rs758871910 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224919 | CAAGCATGGAACCTG[A/G]ACCCAGTCCACAGTG | 84333 |
| rs758904187 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203216 | AAGGTTTTGTTGCAT[A/G]TTAAAATGTTTAGGA | 84333 |
| rs758923161 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246543 | GCAGGGAACTAACAC[A/G]ATCAGATTAGCACTT | 84333 |
| rs758928038 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271469 | TTTACCAGTTACTAA[A/G]TTATTAAAATCTTTT | 84333 |
| rs759029596 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255295 | AGCTTAAATGGAAAA[G/T]CTGGAGAGTGAGATG | 84333 |
| rs759043714 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254117 | TTATCTCCCATTAAA[C/T]CCATTAGTAAATCGT | 84333 |
| rs759046467 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219689 | GCTGTTTCAGAAAAT[A/G]TATTGCTCCTGCTGT | 84333 |
| rs759080108 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262849 | AAATTGTTCTTATGA[-/T]TTGGTTTGCACTTTA | 84333 |
| rs759081445 | in-del | -/CT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191693 | GCCCTCTGAGAATCA[-/CT]CTGATTGCAAGATCT | 84333 |
| rs759138734 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207335 | CTTGAGAAATTCAAA[A/G]TCTACAGAAAAGTTG | 84333 |
| rs759163409 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189373 | CAGGGAGGTGATGTT[C/T]TGAAATCCCAGTTTA | 84333 |
| rs759182214 | snp | C/T | 1.65089e-05 | 0.00287301 | missense | PCGF5 | GRCh38.p7 | 10:91248516 | GAAGGTTGGACAATA[C/T]ATTAGAGGAAATTAT | 84333 |
| rs759194152 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212938 | GAAAAATTGTACAGC[A/G]TATGTGTTATACTAT | 84333 |
| rs759211401 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235064 | GAATGGGCACCCTAA[C/T]GATGGTACTAGTCAG | 84333 |
| rs759238321 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270608 | GAGAAAAAAATTACT[A/G]AAGTATTTCGGGAAA | 84333 |
| rs759248421 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190417 | TGTGATGTGTCGCTA[A/G]AGGTCTGTGGTGTCA | 84333 |
| rs759265654 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199676 | AAGGCTAGTTTTAGT[C/T]TAATACTGAAATTTG | 84333 |
| rs759285802 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234103 | ACATACATCTAAGAT[A/G]GCAACAACAAATGAC | 84333 |
| rs759288734 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230629 | TATTTATTTAGAGAC[-/AG]GGTCTCACTCTGTCG | 84333 |
| rs759290416 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262672 | CTATGGGTTGAAAAT[C/T]GTTATTATGGTATGG | 84333 |
| rs759291949 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183999 | GTCTTTAATATTTTT[-/T]CTTCGTTTCGACCTT | 84333 |
| rs759301879 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264631 | GCTTGGGAAGGAGAA[A/G]AAACTGGTTTTTCTT | 84333 |
| rs759355632 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200456 | TGCGCATATATGTTT[A/G]AAAGAAGAAGAGAAG | 84333 |
| rs759357835 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164001 | TTTGTTTAATATTAA[A/G]AAAGCTGCGTGTGCG | 84333 |
| rs759385841 | snp | C/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227604 | AAAGCCACTGCAGCA[C/T]ATTCTTAACTGTGTC | 84333 |
| rs759387161 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171371 | AAAGTGTAAAGCTGA[A/G]GTGGAGGAGAGTTGA | 84333 |
| rs759426524 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247433 | TCACATTTTTTTCCA[A/G]TTAGAAGGAAAGATT | 84333 |
| rs759454256 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233518 | TTGAAAGAAAGAAAC[A/G]TGCCAATATACGGCA | 84333 |
| rs759513936 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212265 | AGTTGAAAATGAGGT[A/G]TTAGAGGTGTCACCA | 84333 |
| rs759571483 | snp | C/T | 1.68707e-05 | 0.00290432 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264381 | AAAATATGCAAAATA[C/T]TTTTGAATTCAACAT | 84333 |
| rs759578518 | in-del | -/ATATATGCATATATATATATGCATGC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195445 | ATAAATCATATGTAT[-/ATATATGCATATATATATATGCATGC]ATATATGCATATATA | 84333 |
| rs759580395 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275085 | GAATTGACTATTAAT[A/G]TTAAAAGCACATGGC | 84333 |
| rs759584981 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169533 | AATCTCATTTACATT[A/G]GCACCTCAGACAAAA | 84333 |
| rs759618961 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201724 | ATTTTCCAGAAAACC[-/T]TTTTTTTTTTTTTTT | 84333 |
| rs759629901 | in-del | -/TTTAT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245523 | CAGCCAAGAAGGTTC[-/TTTAT]TTTATTTTGTTTTGA | 84333 |
| rs759634010 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183267 | ACTTGCTTTATGAAT[A/C]TGGGTGTTCCTGTGT | 84333 |
| rs759642465 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238299 | GACTTTAAGCAATTA[G/T]CATAACTTTACTCTT | 84333 |
| rs759643528 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203983 | TCATAAGTGATTGTA[C/T]AACTATTTGATGTTT | 84333 |
| rs759646412 | snp | A/G | 1.65375e-05 | 0.0028755 | missense | PCGF5 | GRCh38.p7 | 10:91248701 | AATTTTGGAAGAAAA[A/G]TAAGCCTCAAGAAAA | 84333 |
| rs759655056 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275609 | CCATGCCCGGCTAAT[-/TT]TTTTTTTTTTTTTTT | 84333 |
| rs759672929 | in-del | -/AAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246791 | AATTTAGTTTAAAAA[-/AAG]CGAGACAATGACTGG | 84333 |
| rs759697629 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182098 | GTGTTTATAATATTC[A/G]CTGATGGTTGTTTGT | 84333 |
| rs759730944 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193907 | GATTCTAGATATGTG[C/T]TAAAGACGAAGTCCA | 84333 |
| rs759836035 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229998 | TTTTTTAAATAAGAA[-/AG]AATAATTATAGGTCT | 84333 |
| rs759838829 | snp | A/C | 4.96931e-05 | 0.00498439 | missense, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222879 | AGCCACGAATGGCTA[A/C]CCAAAGGAAACACTT | 84333 |
| rs759845421 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237140 | TCTATAAGAGGCCAA[A/G]TGCTATCTAATTAAT | 84333 |
| rs759863072 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205467 | AGCGTTCATTCATAA[A/G]CTGAGCCAAGCTCAA | 84333 |
| rs759888954 | in-del | -/ACTA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237069 | ATATTGGTTTTAACC[-/ACTA]ACTAGCTTCATAATT | 84333 |
| rs759894800 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279565 | TCGTTTTAGGATTAG[C/T]CTGCAAGTCAAAGAA | 84333 |
| rs759913957 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217190 | AGGCACCTGCCACCA[C/T]GCCCTGCTAATCTTT | 84333 |
| rs759923785 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199450 | ATCCCTCAGTCCTTG[C/G]ATCCTTGGGAAAGTG | 84333 |
| rs760039651 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251676 | AGAATCACACCTCTG[G/T]TTCTCCTTTTATACC | 84333 |
| rs760059225 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91176602 | TTTCTTGGAGGCCTT[A/G]TTCATTTCTTTTCAT | 84333 |
| rs760084014 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244938 | GAGGAAGGTAAGTGG[A/G]TATATGTGTCTAGAA | 84333 |
| rs760096244 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244458 | CAGAGAGATCATGAG[A/T]TTCCAGATTATGAAG | 84333 |
| rs760100741 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198129 | AAACCCAGAGAAGGG[A/G]AAGAGAAGTGTCAGA | 84333 |
| rs760110661 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280818 | ATGTACAGGCAACTT[C/T]TGTGGTTAGCTTTAT | 84333 |
| rs760144539 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268706 | ATTGATTTTGCCTCA[A/G]TTTCTCAAGAATAGT | 84333 |
| rs760190752 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186936 | ACACAATGCAAGACC[A/G]GTGAAAATCGCTAGG | 84333 |
| rs760204949 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172216 | GATCACTTGAGGTCA[A/G]GAGTTTGAAACCAGC | 84333 |
| rs760221354 | snp | C/T | 1.66732e-05 | 0.00288727 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271611 | GTTGTGGATGCCTCT[C/T]ATCTGATGAGTTCAT | 84333 |
| rs760237234 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177857 | CCTTGTGCTTCCTGG[A/G]TGAGGCGATGCCTCT | 84333 |
| rs760292894 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175553 | CCTACCCCTGTGAAC[A/G]TGGAACTTGCAGTCA | 84333 |
| rs760337510 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169250 | ATTGATTACCCTAAT[C/G]ATGATGCAAATAAAG | 84333 |
| rs760342714 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258251 | CGAATAGTATAAAAA[C/T]TATAATTAATCTGTG | 84333 |
| rs760393095 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232518 | CTTTTTGAGCTGGGG[A/G]AATATGTTTAAATGT | 84333 |
| rs760394412 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282797 | GCTAAGCTTTATACT[A/G]ATAAGATATTGGTTG | 84333 |
| rs760403951 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168304 | TGCTGAGAAGAAAGA[A/C]GCAGGAGGGGGATGA | 84333 |
| rs760406538 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211202 | ATGTCAGTCCCTGGC[A/T]GTTTATGCACATGTA | 84333 |
| rs760433295 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188139 | AGTGACGCAGAAGAC[A/G]GGTGATTTCTGCATT | 84333 |
| rs760482135 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212112 | TAATGATATAAAATG[C/T]TTAGCAAAATACTGT | 84333 |
| rs760496255 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187426 | TGGATACAGTCCATA[A/G]AGAAGGGATTCCTCT | 84333 |
| rs760528738 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238136 | AAGTCTAGTGTGTAT[G/T]TTATACTTACATTAC | 84333 |
| rs760536634 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230786 | ACCATGCCCAGCTAG[-/T]TTTTTTTTGTATTTT | 84333 |
| rs760564158 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259225 | GTTTGTTCTTCCAGT[A/G]AAGTACTGGCACAGC | 84333 |
| rs760593161 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245298 | AAGGTGAAAACTGAG[A/C]ATTCATGGTTGGATT | 84333 |
| rs760624545 | snp | A/G | 1.6604e-05 | 0.00288127 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251448 | TAGTAAAGGTGAGTG[A/G]ACAAGTACTATGGTA | 84333 |
| rs760664855 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193526 | TCCTAAGGGGAGGTA[C/T]ACCTGCGTGTTTGAG | 84333 |
| rs760668960 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181008 | TTTTCAATTTGTGTC[A/G]TCTCTGATTTTTTTA | 84333 |
| rs760746475 | snp | A/G | 1.6525e-05 | 0.00287441 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271732 | GTACATATGACCATC[A/G]TGACACCATGGCGGT | 84333 |
| rs760756292 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186726 | GGATGTACTAGTAAC[A/T]GTTTCACTTCAAGCC | 84333 |
| rs760779417 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205829 | ACCCTATCTCTGCTA[A/C]AAATACAAAAAGTAG | 84333 |
| rs760785402 | snp | A/T | | | missense | PCGF5 | GRCh38.p7 | 10:91251310 | ATACTTCAAAAGCTG[A/T]CAAACCGAAAGTAGA | 84333 |
| rs760799357 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216094 | GATATGCATAGCCAA[A/G]CAGTGGATCCACTGG | 84333 |
| rs760803142 | snp | A/C | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280869 | ATGATAAAATGAATT[A/C]TTTAAATAACCTATA | 84333 |
| rs760807569 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248859 | CTTTTATTTACATTA[C/T]GAACCTTTTTCTCTA | 84333 |
| rs760871746 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273130 | TTTCAGCAATCTAGT[A/T]AGTAAATTTAACATC | 84333 |
| rs760918130 | in-del | -/G | 1.65416e-05 | 0.00287586 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271750 | ACACCATGGCGGTGA[-/G]CACATTCATCCCAAA | 84333 |
| rs760982885 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254605 | CTGTATTGCTTTATA[A/G]CCTTCTCAGCCATCT | 84333 |
| rs760984694 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229511 | AAGTGCTAGAGCTGA[A/G]TTCTGAATCCTGGAT | 84333 |
| rs761002324 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280694 | TGGTATATTCAACTA[C/T]AGCTTTCTAAGGATA | 84333 |
| rs761055114 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196146 | ATATTTCACATGGTG[A/G]CAGAGAAGGCCCAGA | 84333 |
| rs761067324 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279520 | AAATACAAAATGTCC[C/T]GTATTTTGCAGTTTT | 84333 |
| rs761074598 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230688 | TCGGCTCACTGCAAC[C/T]TCCCTACCCCACTTC | 84333 |
| rs761108161 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185937 | GTACCTGGATGTTTC[A/C]ATTGAAAGTGCTGTA | 84333 |
| rs761178575 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265006 | TAAGGGTAAGTGAGT[C/T]TGCAGTGCTTTCTGA | 84333 |
| rs761200895 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252435 | AGTAATTCAGTGAAT[-/A]ATTTATCCACTATGT | 84333 |
| rs761232685 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196692 | AAATGCTATTTGTGT[A/G]TTTCTTGTTGGTCCC | 84333 |
| rs761237358 | snp | C/T | 6.61846e-05 | 0.00575221 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271744 | ATCATGACACCATGG[C/T]GGTGAGCACATTCAT | 84333 |
| rs761259082 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268932 | TTTTCAGTTCGTATC[A/G]GTATTGCCACCTCAA | 84333 |
| rs761290977 | in-del | -/GATAGATG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246950 | ATAGTCAGGCAGATA[-/GATAGATG]GATAGATGGATAGAT | 84333 |
| rs761293525 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281279 | ATTATTTCTTTATAC[A/G]TTAAACATCTATCCC | 84333 |
| rs761314809 | in-del | -/AAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247164 | AAAATGCTTAGTAAT[-/AAAG]AAAGAACAGACTTGA | 84333 |
| rs761342788 | snp | G/T | 3.31115e-05 | 0.00406874 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278360 | AATCCTGCACTATTT[G/T]TTTACTCGTCAACAG | 84333 |
| rs761358364 | snp | A/G | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222965 | AAGCCAACAACAGTG[A/G]CGGAATGCCTCCATA | 84333 |
| rs761383467 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282498 | CCAAAAAAAATTCAA[C/T]TCTTGGTCTTGTTTC | 84333 |
| rs761413519 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167095 | GGTAATTCATATATC[A/C]TTGATCCAACAAAAA | 84333 |
| rs761433552 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211907 | AGAGCAAAGTGGTCT[A/G]GAAGGTGGTTGAGCA | 84333 |
| rs761478683 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181849 | GTTGTATTTCTGCTG[G/T]GTTTTGGTAGCAGAA | 84333 |
| rs761484647 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272774 | CAAGACTCTGTTTCA[C/G]ACAAACAAATAAATA | 84333 |
| rs761495756 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168110 | TTGTATGTGGCTATG[G/T]ACCATCTAGATGGAT | 84333 |
| rs761500260 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210788 | TGAAAATCAGAAATG[G/T]TTCCAGTTCTAACTC | 84333 |
| rs761525646 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180602 | ATGCTATTTATGAAT[A/G]GGGAATCCTTTCCCC | 84333 |
| rs761536576 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236745 | AAACCAAATCCTCAT[C/T]TTACTTTTTCCAGTT | 84333 |
| rs761536664 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242861 | CATAACCACAGTATG[A/G]TTGCATTGGTATAAT | 84333 |
| rs761560739 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258140 | AGGGGATGGGAGGAG[A/G]GAAGGTTGCGGAGTG | 84333 |
| rs761586026 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198303 | GGCCCCCTTGCTGGG[A/G]GAACCTTGGACATCA | 84333 |
| rs761592039 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195477 | TATGCATGCATATAT[-/AT]ATATATATAGAGAGA | 84333 |
| rs761595213 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251098 | TTAATAAGTTTCCAA[-/TT]TTTTTTTTTTTTTTT | 84333 |
| rs761622367 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223982 | GTAAGCCTCGTTTTT[C/T]AGCTATTCTTGCTCT | 84333 |
| rs761723242 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274561 | GTAAAAATGAGCACA[A/T]ATCTTTTCTTTCATG | 84333 |
| rs761733041 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236143 | TTTGATGCCAGGGAC[A/C]AAATGTTACTAATTC | 84333 |
| rs761755074 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284277 | TTATTATTGTTTGTC[A/T]TCTTTAATATTAGTC | 84333 |
| rs761760780 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257163 | CTTGAATAAACATTC[C/T]TCTAAAGAAGTTATA | 84333 |
| rs761777151 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188954 | TGGGAGAAAGGGAGA[-/G]TAGATAGCACAAGGG | 84333 |
| rs761790422 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190850 | AAATTTAGAAACTAT[C/T]TCACATCAGTTCCTG | 84333 |
| rs761909224 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264714 | TCTGTGGTAAATGTG[A/T]TTGTATTAGATTTAA | 84333 |
| rs761930595 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214393 | GACGGCCATGGGACT[C/G]CTGGAGCAGCAGCAC | 84333 |
| rs761944574 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277166 | TAGTTCCATCCTGAG[C/T]TGAATGGTTACAGAT | 84333 |
| rs761952751 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262853 | TGTTCTTATGATTTG[A/G]TTTGCACTTTATTTT | 84333 |
| rs761959964 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248888 | TATATGAGATTTTAT[A/G]TAAATGAGTGTAAAT | 84333 |
| rs762009795 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171858 | AAGATCATTGGTCTT[C/T]GGGAACTATGAGGCC | 84333 |
| rs762032493 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250138 | TTTAGCTTGGGTGGA[G/T]AATTCAGATTTTTTG | 84333 |
| rs762137212 | snp | G/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279289 | TTAGAGCACATAACA[G/T]TAGCTATTTTATGGA | 84333 |
| rs762143941 | snp | C/T | 1.66618e-05 | 0.00288628 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251481 | TTTATGATCAGTTTA[C/T]AGTAAACCCTTGATA | 84333 |
| rs762179449 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178573 | TTTTAAAATTTTTGT[A/G]GAGACAGGGTTTCAC | 84333 |
| rs762185828 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167871 | AGGGTGGAGGCAGAT[-/G]AGTTGGGCAAGATAC | 84333 |
| rs762195430 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196066 | TGGTCAAGTGTTGCC[C/G]CATGGGGTGTTAAGT | 84333 |
| rs762235678 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254138 | GTAAATCGTCCTTTC[-/A]AAAACAAGTGATTAT | 84333 |
| rs762260437 | in-del | -/CTGCACCCACTGAC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177905 | TTGGTGCACGGTGCA[-/CTGCACCCACTGAC]CTGCACCCACTGACC | 84333 |
| rs762331460 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277501 | AAACACAGAGGTAGC[A/G]TGGCATATGCCATAT | 84333 |
| rs762365182 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195173 | GAGGGTCACATAGAT[A/T]GCCTGCAGCATTAAA | 84333 |
| rs762371922 | snp | A/G | 9.93986e-05 | 0.00704907 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240452 | GAGCGTTCATATGAT[A/G]CGTTTTAACCTAACA | 84333 |
| rs762398400 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190259 | TCATGATCCAGTCAC[C/T]TTCCAAAGGTCTGAC | 84333 |
| rs762402419 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210554 | GGTTCAGTGGTTGCT[A/G]TAGAAGCACAGGGCC | 84333 |
| rs762420682 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243665 | GTTGCTAGTGCAACT[A/G]AGGAATGGGATTTCT | 84333 |
| rs762424921 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261894 | GCAGTAGATATAACC[A/T]ACATATTATAGCTGC | 84333 |
| rs762472826 | snp | C/T | 1.6534e-05 | 0.00287519 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240595 | GGTAAGGATGTTATA[C/T]TTTACAGTTCATCTA | 84333 |
| rs762488977 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242553 | ATCCAGTCACTGTTT[A/G]ATCAAACCCGCTCCC | 84333 |
| rs762568037 | snp | A/G | 1.65932e-05 | 0.00288034 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278368 | ACTATTTGTTTACTC[A/G]TCAACAGATTGCACA | 84333 |
| rs762586369 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197321 | GGGCTCCTCGGGCAC[A/G]TCCCTCTCTCTATGT | 84333 |
| rs762596824 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265285 | GGCAAATTTGAGGTA[C/T]TAGGGATTGTAGGAC | 84333 |
| rs762629780 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166260 | GTTGATTGTCTGCCT[C/T]TTGCTTGTGAACTCT | 84333 |
| rs762633596 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180452 | GATAGGTTGTCTTCC[A/C]GGGTTTTTATATTTT | 84333 |
| rs762663586 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190623 | TCCTTCTGTGTAACA[C/T]TGATGCTCTCCCATT | 84333 |
| rs762690870 | snp | G/T | 2.91049e-05 | 0.00381465 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261467 | CATTTTGATAATTCT[G/T]ATTTGAAGTAAAATT | 84333 |
| rs762776956 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235901 | TGAATTGCACAGTCT[C/T]AGGTATGTCTTTATC | 84333 |
| rs762860321 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201832 | TTAATCTGTTCTTGA[A/T]GACTTTTGATCATAG | 84333 |
| rs762892737 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228157 | TAGATTAAGGGATGT[A/T]CTGTCTCTTTCACCA | 84333 |
| rs762908518 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171616 | TGACACTAGAGTGTC[A/G]ATGGGCTGGGAGAAT | 84333 |
| rs762952919 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214251 | AGGCTGCAATGAGGC[A/G]TGATTGCACCACTGC | 84333 |
| rs763048560 | snp | C/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164322 | CCTCTTCCACACTAA[C/G/T]TTTTGGGGGGTCAGG | 84333 |
| rs763060587 | snp | C/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227791 | ACTCACACATACAAA[C/T]ACTTGGTTCAACTGT | 84333 |
| rs763061977 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277445 | AGAAAAGGAAAACCA[C/T]TGATGTTTTGGTTCT | 84333 |
| rs763079785 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262742 | TTGTATTAGGAAAAA[A/G]TTATGGAAGTTAACT | 84333 |
| rs763081525 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239727 | TTAGGTGAAAGATGA[C/G]AGAGATTTATAGCCA | 84333 |
| rs763106437 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184829 | GATTTTTCAGTATCT[A/G]GAGGTATCACCAGTG | 84333 |
| rs763107887 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276607 | ACAAATGGCTACTTG[C/G]AGGAGAAAACAAAAT | 84333 |
| rs763149138 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183797 | TTTGCTTGTCTGAAA[G/T]AATCTATTTCTCCTT | 84333 |
| rs763175599 | snp | C/T | 5.35165e-05 | 0.00517256 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251254 | CTTTAAAATCAACTT[C/T]GATTTATAGCTAACT | 84333 |
| rs763209129 | snp | C/T | 1.67379e-05 | 0.00289287 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264537 | TAAATTGCTTTTATA[C/T]TTACCTATGTGTTTA | 84333 |
| rs763248926 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91176721 | GAAGCTTGTGCATTC[A/G]TCACGTAGTTCTTGT | 84333 |
| rs763249161 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204285 | ATAATAAATTGAACT[C/T]ATTGGATTAGGTTTT | 84333 |
| rs763253667 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226745 | GAAATAGGAGGTAGA[A/G]ATGGTGGGGCAGCCC | 84333 |
| rs763275049 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253733 | TTTTCTGTACCCTTA[A/C]TTTTTCTTTTGTTAT | 84333 |
| rs763361462 | in-del | -/GGTGATTATT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168062 | TGTCTAATTAATGGA[-/GGTGATTATT]GGTTTGGATTTGGAT | 84333 |
| rs763406967 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178942 | CACTCACTCTATCTC[-/A]AACATCTTTTGGGGG | 84333 |
| rs763423268 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91248559 | CCCTGGACTACGAGA[A/G]CGTAAGTGGCTCTTT | 84333 |
| rs763424782 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238661 | TTTCAGAGACTTATC[C/T]ATCATCCCTGGGAAA | 84333 |
| rs763503876 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175327 | ATTCGGCTCACAAAA[C/T]AGTGAGACTCCATAC | 84333 |
| rs763514550 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233806 | GAAATGTGTATGAAG[A/C]TTGTGAACTGCTTAA | 84333 |
| rs763554197 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182306 | GTGTATGGGTCCAGG[-/A]ATTTATCAATTTCTT | 84333 |
| rs763566592 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167420 | TGAATTCAGAGGAGG[-/A]AAAGACTATTTCTAG | 84333 |
| rs763612885 | in-del | -/AAAT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187506 | CACCTAAGGAAAAAC[-/AAAT]AGTCTTTTCATTAAA | 84333 |
| rs763625341 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191007 | TTTGTCAAAATCCTT[-/A]ACGCTGACAGTTACA | 84333 |
| rs763652768 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197346 | CTATGTGACTGCTCC[A/G]TGATGTATTATTTTC | 84333 |
| rs763661437 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208602 | AGTATGAAAAATTCA[C/T]CTCATTATCATGGAA | 84333 |
| rs763674255 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279586 | AGTCAAAGAAAGTCT[C/T]GTTACCTTAAATTAT | 84333 |
| rs763696050 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242658 | AAAAGTAGTACAAGA[G/T]CCACTTGCATTCTGT | 84333 |
| rs763738596 | snp | C/T | 4.99704e-05 | 0.00499827 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271613 | TGTGGATGCCTCTTA[C/T]CTGATGAGTTCATCT | 84333 |
| rs763743578 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234121 | AACAACAAATGACCT[G/T]GTACCTTTTGTGTAG | 84333 |
| rs763854037 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222209 | AGAATATAAGATGGA[C/T]TGCAGGTGGAGAGGT | 84333 |
| rs763854529 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235902 | GAATTGCACAGTCTC[A/T]GGTATGTCTTTATCA | 84333 |
| rs763912378 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190672 | TGCCTAAATAAACCA[A/G]TTTCTTGATTTTTTT | 84333 |
| rs763962822 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247603 | GGAAGGGGGTGTTGT[C/G]GGGGCAAGAGAATGG | 84333 |
| rs764004488 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207543 | GGACATACAGTTACT[A/G]TATTCAGGAAATATG | 84333 |
| rs764056225 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230379 | ATTAGTCTAACTTTG[C/T]AAAAAAGACAAAAGA | 84333 |
| rs764060027 | snp | A/G | 1.64822e-05 | 0.00287068 | missense, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222950 | AAAGGGTATCTGATC[A/G]AGCCAACAACAGTGA | 84333 |
| rs764078752 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262804 | GATAGTAACAATGTA[C/T]GGATACAACTACAGT | 84333 |
| rs764101478 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171633 | TGGGCTGGGAGAATA[A/G]CAGGGAATATGAGAT | 84333 |
| rs764110467 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201866 | TGAACATTTAGTTAA[C/G]GTTCTGTGCTTTAAT | 84333 |
| rs764129927 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253604 | AGTTCAAAAGCTTCG[C/T]GTCATCTTTGATCTG | 84333 |
| rs764157391 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246518 | GTAGTAGAGAGAAAT[C/T]AGTCCTTGAGCAGGG | 84333 |
| rs764212345 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201916 | AGTTTCTGAAGTGTT[-/A]AGGACTGTTTACTGG | 84333 |
| rs764248207 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213097 | GAGTGTTCTTATGTG[C/G]AGTTTAAGTGTTTTC | 84333 |
| rs764309868 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239867 | TTATCCCTGTCAGTT[C/T]TTCAGTCATTCTTCC | 84333 |
| rs764353153 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238753 | CATAATAAGGCAGTC[C/G]TCTCTTCCCAAAGAT | 84333 |
| rs764362969 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183838 | TTAGTTTGGCTGGAT[A/G]TGAAATTCTGGGTTG | 84333 |
| rs764414044 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274822 | TTATGTCTGGTTATT[A/T]GAGAATTGCAAGGAG | 84333 |
| rs764427493 | snp | C/T | 1.6522e-05 | 0.00287414 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248464 | CATGTCAGATCTTGG[C/T]GTCTTCATTGTTAGT | 84333 |
| rs764444339 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212507 | CCAGAAGTAGCTGGA[A/G]GTTTGGTTTGCTTTT | 84333 |
| rs764448191 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244991 | GGAGAAAAACATTTG[A/G]TAGTCTTCAACATAT | 84333 |
| rs764493366 | snp | A/C | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161601 | CATCTCTGTAGAATT[A/C]AATTTTATTCCTCAA | 84333 |
| rs764509729 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91240635 | AATTGAATAGGCTCT[A/T]AATTTTTATTGTATG | 84333 |
| rs764516881 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218359 | TCCAGTTGCTTCCAG[A/G]CCTTTGTTTACTTGA | 84333 |
| rs764538049 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268526 | TATGGGATGTCTCCT[C/T]ATCTATTCTACACAC | 84333 |
| rs764549751 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252799 | TTCTCATAAACAAAC[A/G]TAAAGTCCACTTCTC | 84333 |
| rs764588218 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164725 | AGTAAGACTGAATAA[A/G]GTTTTCTCATCATTT | 84333 |
| rs764628257 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217164 | TCAGCCTCCTGAGTA[C/G]CTGGGACTACAGGCA | 84333 |
| rs764658187 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179263 | CAAGGGAGAGACATG[A/G]GAGAGGTGAGTTAGA | 84333 |
| rs764716181 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219333 | CCCTGGACTCCACTG[C/T]TATTCTTTTAAAACA | 84333 |
| rs764736985 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235067 | TGGGCACCCTAACGA[C/T]GGTACTAGTCAGTAA | 84333 |
| rs764745374 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270704 | AAATCTTTCAAAGTA[C/T]ATCTTTTAAAAACCT | 84333 |
| rs764835103 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254128 | TAAACCCATTAGTAA[A/G]TCGTCCTTTCAAAAC | 84333 |
| rs764871600 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222966 | AGCCAACAACAGTGA[C/T]GGAATGCCTCCATAC | 84333 |
| rs764904104 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208482 | GCATTCCTAACAAGA[A/T]CCCTGCTGATGCTGG | 84333 |
| rs764906058 | in-del | -/CAAAG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199793 | AGTGGAGTAAATAAA[-/CAAAG]GAGAATAAATTTTAG | 84333 |
| rs765012443 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219821 | AATGGATCTTTGAAC[A/G]CTTGTATGGCTGCTG | 84333 |
| rs765030335 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200513 | TATGGATGAGATTGC[A/T]TTGAAAGCTGTGCAT | 84333 |
| rs765039988 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245557 | AGGAGAAATAATGGC[A/G]TATTTGAAGGGAATG | 84333 |
| rs765057978 | in-del | -/GA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195482 | ATGCATATATATATA[-/GA]TATAGAGAGAGAGAG | 84333 |
| rs765085338 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199749 | CCATAAAAATCCTTT[A/G]TGCAACCCTCTTGTT | 84333 |
| rs765257694 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169536 | CTCATTTACATTAGC[A/T]CCTCAGACAAAACAA | 84333 |
| rs765261577 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246350 | GTATTTGAGCCAGGA[G/T]GTAAAACATGAGGGA | 84333 |
| rs765307596 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258397 | AAATGGTTGGGACCA[A/G]AAGTTTTTTGGGTTT | 84333 |
| rs765321327 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283432 | TATGTTAAATACTGA[A/G]TCTAGTTTTCTTCCA | 84333 |
| rs765420054 | in-del | -/GTTAAACTAAGTGTAA | 1.65853e-05 | 0.00287964 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240612 | TACAGTTCATCTAAT[-/GTTAAACTAAGTGTAA]TTACATAAATTGAAT | 84333 |
| rs765450122 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175233 | TAAATTAAAGTAAAA[C/T]AGAGGTTCTGGATGT | 84333 |
| rs765466939 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161239 | CTCACCTTACCCTAG[C/T]TGAACGTCCAGTTCT | 84333 |
| rs765501353 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237142 | TATAAGAGGCCAAAT[A/G]CTATCTAATTAATAG | 84333 |
| rs765552152 | snp | A/G | 1.65091e-05 | 0.00287303 | missense | PCGF5 | GRCh38.p7 | 10:91248555 | TGGTCCCTGGACTAC[A/G]AGAACGTAAGTGGCT | 84333 |
| rs765561256 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203113 | TCTACCAGCAAACCC[C/G]TTGGTACTAAGCATT | 84333 |
| rs765563187 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217245 | TCACCGTGTTAGCCA[G/T]GATGGTCTCGATCTC | 84333 |
| rs765589475 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238307 | GCAATTAGCATAACT[G/T]TACTCTTTAATGTAT | 84333 |
| rs765607365 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91269708 | TATTATTTGAAATTT[A/G]TAATCATACCAATAA | 84333 |
| rs765695994 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281069 | AGAATGACTGTGGTT[C/T]ATAAACATTACTTTA | 84333 |
| rs765713898 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266997 | GAACATGCCCACTCC[A/G]TTCTCTGATTCCTCC | 84333 |
| rs765717582 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230854 | TCTTGAACTCCTGGG[C/T]TCAAGTGATCAATCT | 84333 |
| rs765719586 | snp | C/T | 9.90917e-05 | 0.00703818 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248485 | CATTGTTAGTATTTT[C/T]TTTCTCCCCCCTTTC | 84333 |
| rs765736215 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265505 | GTAAACTAGATTTAT[C/T]ATATTTTCTCATGAA | 84333 |
| rs765758633 | snp | A/C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173964 | GACTCCAGTATTGAT[A/C/G]ATGATTTTGGGCAGC | 84333 |
| rs765761903 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216590 | TGGAAGATGCTTTGG[C/T]AGAAAAGAGCTGTAG | 84333 |
| rs765863020 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210684 | TGCCTCTAGTGCTAG[A/G]CACCTGGTACCAATT | 84333 |
| rs765870898 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189302 | TCCCCATTTTTCCAT[A/G]CCATGAAAGGTGTCT | 84333 |
| rs765877540 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246281 | GGGAAAACTTTACGA[A/G]TGACCTTGTCTTGAA | 84333 |
| rs765903820 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244113 | TAAGTAATTTATATG[A/G]TATGTTAGAAAGTGA | 84333 |
| rs765906082 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282890 | AAAACTTGAAATGCA[A/G]TTATCAATATTTTGT | 84333 |
| rs765959024 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188140 | GTGACGCAGAAGACG[A/G]GTGATTTCTGCATTT | 84333 |
| rs765983697 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206010 | CTGGGTGACGGACCG[C/T]GACTCTGTCAAAAAA | 84333 |
| rs765993533 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268809 | CTAAGCCTGTTTTCT[A/G]TGGTCCCTGCCCTCT | 84333 |
| rs766006649 | snp | A/G | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284783 | CAGTCCTTCGGTGAG[A/G]TAGGGAAAGCAGCTT | 84333 |
| rs766029937 | in-del | -/AA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262440 | TCAAAAAAAGAAAAG[-/AA]AAAAGAAAATTAAAG | 84333 |
| rs766044224 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186169 | TTCTTTACTTTTAAC[A/G]TTACCTCTTGGGCTA | 84333 |
| rs766124891 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193004 | AATCTAATCAATAAG[-/C]CCTTGAAAGTCAAGA | 84333 |
| rs766132214 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187521 | AATAGTCTTTTCATT[-/A]AAAAAAAACAAAAAC | 84333 |
| rs766136363 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212196 | AGCTGATACTCAGAA[A/G]TAGGTTAATTGAAGC | 84333 |
| rs766146013 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200155 | GTGGGAGAGGGCCCA[-/G]CCTGCTCCCAGAGCC | 84333 |
| rs766163329 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217292 | CCGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAT | 84333 |
| rs766167399 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224690 | AAATTAAGTACAGAG[A/G]CCTTGAGATGGAAAT | 84333 |
| rs766178080 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257360 | CGTTGCTAGTGGGAA[A/G]GTGAAAGTGCAGCTA | 84333 |
| rs766205757 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281517 | TTATCTGTACCTGTC[A/T]CTTATGAATGGTTTC | 84333 |
| rs766214751 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167423 | ATTCAGAGGAGGAAA[A/C]GACTATTTCTAGCCA | 84333 |
| rs766227950 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197704 | CTCTGTCAACCGGTA[-/C]CTGGACATCATCCTC | 84333 |
| rs766228774 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199521 | GCAAGAGGCCAACAA[C/T]ATCCCCATCAAGTGC | 84333 |
| rs766249120 | snp | A/G | 2.00552e-05 | 0.00316657 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261294 | ATTTTAACTGGTAGA[A/G]CATTTTAACTGGTAA | 84333 |
| rs766274718 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257829 | ATAAAAGAATTGAAA[A/G]CATGTTCACACAAAA | 84333 |
| rs766349013 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274119 | CAATCTGTGTATGTA[-/TA]TATATATATGTAATA | 84333 |
| rs766369105 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226340 | TGCAATGAGGAAGGA[C/T]AGACTATGATATAAT | 84333 |
| rs766377229 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258285 | GATTGTAAGTAGTGA[G/T]ACAAACATCATTTCT | 84333 |
| rs766445441 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281036 | AAGTATAAAAGGGTC[A/G]AGGGAACTTAGATAT | 84333 |
| rs766454640 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233011 | GTAGAGGCAGAGTAC[A/G]TAGAGAGTTAGATAG | 84333 |
| rs766455140 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222542 | ATAGCAGATTTGCAA[A/G]TTAATGATACAATGA | 84333 |
| rs766472202 | snp | C/T | 1.65168e-05 | 0.00287369 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248573 | AACGTAAGTGGCTCT[C/T]TAGGTTCTTGCAGAC | 84333 |
| rs766516826 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193117 | AGAGTGCATGGCAAA[C/T]GCAAGAAGGAAGGCA | 84333 |
| rs766520509 | in-del | -/TTAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224357 | ATTTAACTTGAACAG[-/TTAA]TTAACTATCATCGAA | 84333 |
| rs766533856 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253357 | CCTTCAAGTAGGGCC[C/T]CATGTCTGTTGTTCT | 84333 |
| rs766545372 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179380 | AACTTTAGGGGTACA[A/G]GTGCAAGTTTGTTAC | 84333 |
| rs766616440 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175043 | GGAAGAAACAGTCAC[C/T]GTATCCCTAAGAATT | 84333 |
| rs766618235 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214681 | ACTGGTAGAGGAGCA[C/T]GACAAACAGATGAAC | 84333 |
| rs766628689 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202951 | TGTGTTTGTGAAAAT[A/G]ACTAAAAACAATACA | 84333 |
| rs766647894 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248918 | TCTGAAGTCACTTTA[A/G]TGAGGGTAATTGGAA | 84333 |
| rs766649541 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266895 | CCACCATCGCCATTC[A/T]CCTAGCAAGGCTCTG | 84333 |
| rs766651376 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236270 | GCCTAGTCAGGCTCT[C/T]CAGCACTACATTCCT | 84333 |
| rs766655364 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224821 | ATGGAGGTGGAGAAG[A/G]GTGGTTGTATTGTGG | 84333 |
| rs766697056 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230756 | TTTCTGAGTAGCTGT[A/G]TTACAGGTGTGCACC | 84333 |
| rs766710112 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202081 | GCCTCAATTTCTTCT[C/T]TCCCAAATTGAGAAG | 84333 |
| rs766732374 | snp | A/G | 9.92884e-05 | 0.00704517 | missense | PCGF5 | GRCh38.p7 | 10:91248677 | TAGAAGAACTTGAGC[A/G]TGAATCTGAATTTTG | 84333 |
| rs766748999 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268954 | CCACCTCAAGTTTCT[A/G]TACTCAAGCTTGGCA | 84333 |
| rs766751742 | snp | A/T | | | missense | PCGF5 | GRCh38.p7 | 10:91251359 | TGAAGATGATAAAGA[A/T]TATCACAGAAGTGAC | 84333 |
| rs766804192 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276718 | AGAATTAATGGATAC[-/T]TCCATATATGATTAA | 84333 |
| rs766844008 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279536 | GTATTTTGCAGTTTT[C/G]TTAAGTCTTCCATTC | 84333 |
| rs766844896 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265307 | TTGTAGGACTCATAT[A/G]TGACACTAAGGAATA | 84333 |
| rs766889534 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229548 | CTCAGGTACATCTAC[A/G]TAATATATGTTATGA | 84333 |
| rs766906312 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168785 | TACAAAAAACTAGCC[A/G]AGTGTGGTGGTGTGT | 84333 |
| rs767022259 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267184 | CACTTGCCCTCACCT[C/T]CCCTGGTATCCACCT | 84333 |
| rs767023498 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232251 | TTTTCAAGAGCAGTT[C/T]CAATGAAGTGGTAGG | 84333 |
| rs767039553 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268926 | AAAATTTTTTCAGTT[C/T]GTATCAGTATTGCCA | 84333 |
| rs767091903 | snp | A/G | 1.65094e-05 | 0.00287305 | missense | PCGF5 | GRCh38.p7 | 10:91248530 | ACATTAGAGGAAATT[A/G]TATTTAAGCTGGTCC | 84333 |
| rs767096518 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187180 | TACTGGTATCTGGGA[C/T]CTATCTATAGTGATT | 84333 |
| rs767099491 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230957 | ATCTTACCATGTTGC[C/T]CAGGCTGCTCTTGAA | 84333 |
| rs767103235 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188103 | GAACAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 84333 |
| rs767127316 | in-del | -/CTAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206871 | TGTGCTAAATGTCAC[-/CTAA]CTAAATCCTTCTCTC | 84333 |
| rs767175652 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209901 | AATGAATGTGGAACC[A/C]ATATGCACGTGTCAA | 84333 |
| rs767199381 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183728 | TTTGCCATATGTAGT[A/G]TGTCCTTCAGGAGTC | 84333 |
| rs767220939 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258243 | CAACTTTGCGAATAG[C/T]ATAAAAACTATAATT | 84333 |
| rs767305164 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180774 | AGTATAGTTTGAAGT[A/T]GGGTAGCATGATGCC | 84333 |
| rs767320353 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272045 | GTGAATCATTCAACC[A/C]CAAGTGAAATATAAA | 84333 |
| rs767325926 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209035 | AATTTATAGGCAGAT[A/T]GTTGTTGGCACTCTG | 84333 |
| rs767369955 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211021 | TACCATGCATTAGGT[A/C]CCAGGAGGCATTTGT | 84333 |
| rs767387393 | in-del | -/AA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212202 | ACTCAGAAATAGGTT[-/AA]AATTGAAGCTTGAGA | 84333 |
| rs767413417 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257199 | GACCAATAAGCACAG[A/G]AAAAGTTGCTAAATA | 84333 |
| rs767413924 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197397 | TATATCTTTGGAAAA[C/T]AAAATCTCCACGGGC | 84333 |
| rs767431873 | snp | A/G | 5.1e-05 | 0.0050495 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264562 | TGTTTATTTAGTTAT[A/G]TACCATTATGTTACT | 84333 |
| rs767475837 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91222326 | AATGGGGAACATTTT[A/G]ATAGGGAGGATAATT | 84333 |
| rs767519082 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172881 | GACAGGGACTACTAG[C/T]TTTGAGATCCTGTTT | 84333 |
| rs767575792 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247716 | TTTTCATTTCAGAAG[A/G]TAGAACAATAAAGTG | 84333 |
| rs767580143 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275098 | ATATTAAAAGCACAT[A/G]GCAAAAATATCATAA | 84333 |
| rs767580549 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235335 | TTAATTTGTCCAACA[A/G]CCTGGTTCAAATCTA | 84333 |
| rs767599645 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177035 | TCCCCATCTTTGTGG[-/T]TTTATCTACCTTTGG | 84333 |
| rs767658433 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201986 | TCAAGGGAGGGTCCT[A/G]GACTTGGGAGCTACA | 84333 |
| rs767691267 | snp | A/G | 1.75499e-05 | 0.0029622 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251271 | ATTTATAGCTAACTT[A/G]GTTTTGTTTAAATTA | 84333 |
| rs767715199 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171859 | AGATCATTGGTCTTC[A/G]GGAACTATGAGGCCA | 84333 |
| rs767724921 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196068 | GTCAAGTGTTGCCCC[A/G]TGGGGTGTTAAGTCT | 84333 |
| rs767728581 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262871 | TGCACTTTATTTTCT[A/T]CACGCAAAATACCAT | 84333 |
| rs767742242 | snp | A/C | 1.65564e-05 | 0.00287714 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248735 | ACAAGGTGACTTTTT[A/C]TTATGTCTGTTTCTG | 84333 |
| rs767746438 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190857 | GAAACTATTTCACAT[C/T]AGTTCCTGCTGTCTT | 84333 |
| rs767770880 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202889 | GGTTGACATGATTAA[C/T]GTTCAGATGAGGGGA | 84333 |
| rs767818566 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247717 | TTTCATTTCAGAAGG[C/T]AGAACAATAAAGTGG | 84333 |
| rs767822648 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250417 | CCTGCTTCACTCCCA[A/G]AGTTTGGGTTTATTG | 84333 |
| rs767831660 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213354 | TGTATTTGTATATAC[A/G]TATGCATAAGTAACC | 84333 |
| rs767848315 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91224318 | CTATCTTGTATTACT[A/G]GTTTGCTGTTGCCCT | 84333 |
| rs767913315 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207255 | TCTTCTACTAGAGAG[C/T]TGTGAGATGAGCCAT | 84333 |
| rs767914226 | snp | A/T | 5.13237e-05 | 0.00506549 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278239 | TTTATCCAAATACAG[A/T]CTTATTTATTATCTG | 84333 |
| rs767914797 | in-del | -/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219576 | TCTTACTCATTGTGA[-/T]TTGCTGCGACTTATG | 84333 |
| rs767986779 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229433 | TATGAAAAGGTTTAA[A/G]GGAAGAGTATTTCAG | 84333 |
| rs767996262 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277588 | GATACCTTTTCTACA[C/T]AGTGACATGAAAAAC | 84333 |
| rs768003520 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225741 | TTATACAAATAAAAG[A/T]ATACTTTGCAAGTGG | 84333 |
| rs768030236 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254071 | ATTAGTATTCAAGGC[A/C]CTTCCCTAACAAGCA | 84333 |
| rs768073079 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183098 | TGTATATTCTGTGAT[A/C]CAGTGTTGTGTATAT | 84333 |
| rs768074145 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191981 | GCTGTGAGATTAGAC[A/C]AGTTATTTACCCTCT | 84333 |
| rs768091404 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91265214 | TACAGTAGTAACTTA[-/G]GTTCTACTAAGTTCT | 84333 |
| rs768095484 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211810 | GGTCGAGTTGTTAAA[A/G]TAGAGGCTTTGTCTT | 84333 |
| rs768097696 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181711 | CCTTGCATCCCGGGG[A/G]TGAAGACCACTTGAT | 84333 |
| rs768119918 | in-del | -/GT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254205 | TCCCCTCCACCTCGT[-/GT]GTGTGTGTGTGTGTG | 84333 |
| rs768137457 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164615 | TTTTAAAAAGCCAGA[C/T]CCTAAAAGGAACCTC | 84333 |
| rs768164318 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210561 | TGGTTGCTATAGAAG[C/G]ACAGGGCCAGCAGAA | 84333 |
| rs768165971 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165329 | CTGTGCTAGTTGAAG[A/T]AAAGGTGCAGGATAT | 84333 |
| rs768192705 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276712 | CCTAGTAGAATTAAT[A/G]GATACTTCCATATAT | 84333 |
| rs768262987 | snp | C/T | 9.97208e-05 | 0.00706048 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248774 | TCTTAAACTGGTCAG[C/T]TTTTCATAGTTTAGG | 84333 |
| rs768297550 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202794 | GGCCATTTATGCTAT[A/G]TAATATGCTTACTAT | 84333 |
| rs768308563 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237663 | GCAGGAGAATCACTT[A/G]AACCTGGGAGGCAGA | 84333 |
| rs768327053 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268468 | TTCTAGATTGATTTG[G/T]CTGGAATTGGCATCT | 84333 |
| rs768360849 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223703 | AAGTAATTCCAGTAA[A/G]TTATAGTTTAATGCC | 84333 |
| rs768370575 | in-del | -/TG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186581 | GTGTGTATATATATG[-/TG]TGTGTATATATATGT | 84333 |
| rs768414963 | in-del | -/GGAAGA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244842 | CCATTAACTGAGTTG[-/GGAAGA]GGAAGATTAATAATA | 84333 |
| rs768440040 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195528 | GGGTCTCTGTCACTC[A/G]GACGGGAGTGCAGTG | 84333 |
| rs768446194 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171172 | TACATGGTATTATAC[A/T]TTTGTCCAAATCCCT | 84333 |
| rs768466429 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274450 | ATGAGTCTGTAAAGA[A/G]GGTATTTCAAATTAA | 84333 |
| rs768471111 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239553 | GAAAGGGGAGTAGGA[A/G]AGCCAATCTATACCA | 84333 |
| rs768504907 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236618 | AGAGTTTGGCATGAA[A/C]TCTTTAAGATATTTT | 84333 |
| rs768505604 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266108 | GTAGTAAATTCTTTC[C/T]TACCCAATACTGTTG | 84333 |
| rs768505993 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233897 | TAACAAAGGAAGTCA[-/G]CCTTTGGTCAGTTTT | 84333 |
| rs768541378 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240536 | CAATGATTGCCCAAG[A/G]TGTGGCAACCAAGTT | 84333 |
| rs768579079 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264609 | AGAAACTAAAAAAGA[C/T]AAACTAGCTTGGGAA | 84333 |
| rs768596251 | snp | A/T | 2.23043e-05 | 0.00333941 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261435 | ATGAGGTAAGTTAAA[A/T]AATATCTAAGCTTGA | 84333 |
| rs768649579 | snp | G/T | 1.65455e-05 | 0.00287619 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278357 | ATGAATCCTGCACTA[G/T]TTGTTTACTCGTCAA | 84333 |
| rs768731813 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215377 | TTCACAGATTCTTCT[C/T]AATATGCATATAATA | 84333 |
| rs768772981 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185697 | AGTTCTGTGTGTCGG[A/T]CTGAAGGCCCTAGTG | 84333 |
| rs768773499 | snp | A/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278964 | TTGCACAAGGAAGGC[A/T]TGTTAGCCCTCCAGA | 84333 |
| rs768835618 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167474 | TAGGGAATTTTGAGC[-/A]AGGCTTAAAAAATTG | 84333 |
| rs768852714 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195799 | TTTAAAGTAGCAGAG[C/T]CTAGACAGGGGCTTA | 84333 |
| rs768859235 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232357 | AAGTATTTAATCTTA[A/C]TAAAGTAAAGAAAAG | 84333 |
| rs768923913 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214351 | AGACAAGGAGAATGT[C/T]ATGCGAAGATAGATG | 84333 |
| rs768970486 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165550 | TTGCCCAAGCTGGAG[G/T]GCAGTGGCGCAATCA | 84333 |
| rs768991735 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271271 | GAAGTTGAAGAAGAG[A/C]TCTAGGAGACAGTGA | 84333 |
| rs769075213 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178518 | TCACAGCCTCCAAAG[C/T]AGCTGGAACCACAAG | 84333 |
| rs769139560 | snp | A/C | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279628 | CATTTTAAATCTTTT[A/C]ATATTTACAGTTTTC | 84333 |
| rs769156206 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236521 | ACTTGGTCTGTATAC[A/G]TAGTCTTAACCTTAG | 84333 |
| rs769182613 | in-del | -/ATAG | 1.67725e-05 | 0.00289585 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264404 | TTCAACATTATGTTA[-/ATAG]ATCTATAATGATTCT | 84333 |
| rs769187998 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270315 | TCCTTTGCTTTATTT[G/T]CATTAGTAGGCAATT | 84333 |
| rs769254347 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218748 | AGCGATTCTCCTGCC[C/T]CTGCCTCCTGAGTAG | 84333 |
| rs769276285 | snp | C/T | 1.65567e-05 | 0.00287716 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91264514 | ATGGCGACTAAGAGG[C/T]GAAAACGTAAATTGC | 84333 |
| rs769314425 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180296 | CCCATTCTGTAGGTT[C/G]TCTGTTTATTCTGCT | 84333 |
| rs769325305 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91221922 | ATTGCACTGAGAATA[C/G]CATTGGAGAAGGGCT | 84333 |
| rs769344110 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189834 | ACACGTCTATATTTT[C/G]AAGTTGCACTGAAGT | 84333 |
| rs769369944 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248335 | ATCAGTCTACTACTG[A/G]GGAAGGCTGTAAATA | 84333 |
| rs769427248 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190550 | GAAAGTTATGAAACA[C/T]AGCCTGTAACCATGG | 84333 |
| rs769428213 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214153 | CAAAAAATACAAAAA[C/T]TATCTGAGCATGGTG | 84333 |
| rs769459991 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250095 | TCCTATTGTTTCTCC[C/G]ATTTTAAAGTATTTC | 84333 |
| rs769509576 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235831 | GCCTTCTACCTTGAT[G/T]GTGAGGCCTCCCCAG | 84333 |
| rs769520121 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201598 | CTCCTCCCTCCACCC[A/T]CAGCCCCTGAGGGAA | 84333 |
| rs769532471 | in-del | -/TATATATATATATATATATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249372 | AAAAGGCTTTTAGTG[-/TATATATATATATATATATA]TATATATATATATAT | 84333 |
| rs769616501 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196937 | CACCTCAAGTCTCAC[A/C]GTCTGTCAAGGAGCC | 84333 |
| rs769651772 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171493 | ATGAATCACTCCTGT[A/G]TTTCATGACTTTCTC | 84333 |
| rs769672732 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215193 | TTTTAAAAGCATAAA[C/T]GAATACATGTAATTA | 84333 |
| rs769730591 | snp | C/G/T | 3.30252e-05 | 0.00406346 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248496 | TTTTCTTTCTCCCCC[C/G/T]TTTCGAAGGTTGGAC | 84333 |
| rs769767025 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262684 | AATTGTTATTATGGT[A/G]TGGTTCTACAAATAT | 84333 |
| rs769785822 | snp | C/T | 3.29924e-05 | 0.00406142 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240576 | AATCCATTAGAAATG[C/T]TGAGGTAAGGATGTT | 84333 |
| rs769854005 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270223 | GCCCCCTTTTCCCAG[C/G]TCATCCTGATTTAGT | 84333 |
| rs769859431 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229089 | ATTGAATGTTTGTTA[A/T]ATGAGGCATCATGAG | 84333 |
| rs769874363 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215674 | GTTGACAGCTAACAC[A/G]CTTTTCTTCTGGCCT | 84333 |
| rs769887615 | snp | A/G | 1.66377e-05 | 0.00288419 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264525 | GAGGCGAAAACGTAA[A/G]TTGCTTTTATATTTA | 84333 |
| rs769896721 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254870 | ATAGATGCATATAGA[A/G]CATTTTATCAAGAAG | 84333 |
| rs769940298 | snp | A/T | 8.20894e-05 | 0.00640609 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261461 | CTTGATCATTTTGAT[A/T]ATTCTGATTTGAAGT | 84333 |
| rs769942568 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253706 | CTACATTTTTTAAGT[A/C]GTTATTAAGTGTTTT | 84333 |
| rs769951256 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185707 | GTCGGACTGAAGGCC[C/G]TAGTGGAGTGGTTTC | 84333 |
| rs769973709 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239634 | GATGAGGAATTGAAT[C/T]AATATTTTATAGTTC | 84333 |
| rs770056674 | snp | C/G | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227617 | CACATTCTTAACTGT[C/G]TCCAAGTGGTAATAA | 84333 |
| rs770064948 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241512 | TCCCAGCTACAGGCC[A/G]TATGTCCTCACCACT | 84333 |
| rs770108362 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231928 | TCATGAAAAGAAAAC[A/G]GAATGTAAGTTATAA | 84333 |
| rs770125041 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234676 | TCATCCAGTGATCTA[A/G]TTTATGGTAAAGCTC | 84333 |
| rs770133389 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245030 | TTTCAAACTGTAAGC[A/G]GGATGAGATCACTTC | 84333 |
| rs770142790 | snp | C/T | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284605 | ATAGCTAAGCTTTGT[C/T]TATTAATACTTTCCA | 84333 |
| rs770144172 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261280 | AAGCAAGATAGAACA[-/T]TTTAACTGGTAGAAC | 84333 |
| rs770176763 | snp | C/T | 1.65814e-05 | 0.00287931 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248650 | TTTACTTTTATACTC[C/T]TTCTTTTAAATTAGA | 84333 |
| rs770212432 | snp | C/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218207 | CTACCAGAATCAGCT[C/G]TGTAATTATGAATTC | 84333 |
| rs770217960 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200078 | TGCCCATCAACTATC[C/T]ATCCTCCTTGACTGA | 84333 |
| rs770305030 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201710 | TCTGTATTGAGTTCA[C/T]TTTCCAGAAAACCTT | 84333 |
| rs770306061 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188781 | TCCAGATCTACAGAG[C/T]GTCATTTGGAGCCTG | 84333 |
| rs770329486 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248209 | GTTTTAAAGCCAGAC[C/T]GTATTTCCAAGGCAG | 84333 |
| rs770336589 | in-del | -/TTTTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173580 | AGAGGGAGTTGGCTT[-/TTTTT]TTTTTTTTTTTTTTT | 84333 |
| rs770356386 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245870 | AGCGTGTTGTCCAGG[A/G]GAGTGAGAGGATCAG | 84333 |
| rs770384122 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201449 | CAGCACATGAAATTT[A/G]GGGAACTCATTCAAA | 84333 |
| rs770388889 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177614 | GCAATGGTGGGCGCC[C/T]GTCCCCCAGCCTCAC | 84333 |
| rs770412267 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199145 | TACAGCATTCAAGGG[A/G]TCATCCCTGCTTCCA | 84333 |
| rs770426193 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91176111 | GCAGGCCTGGTGGTG[-/A]AAAAAATCTCTCGGC | 84333 |
| rs770530673 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235008 | TTAATGGTGATAATA[A/C]AGTGACTTCTGATGA | 84333 |
| rs770544789 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216898 | GCCTTATAGGATATT[-/TA]TGTTCAATTGTAATA | 84333 |
| rs770561165 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262406 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 84333 |
| rs770582531 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213864 | ATTCTAAATGCCTGC[C/T]ATGGGTTGAATTGAG | 84333 |
| rs770607409 | snp | G/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227488 | CACTAACAAAACTGG[G/T]CAAAGTCCTGCTGGT | 84333 |
| rs770620642 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235725 | GTGAATAAGTCTCAC[A/G]AGATCTGGTGGTTTT | 84333 |
| rs770620741 | snp | A/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219650 | ATGGTTCTTTAAAGG[A/T]CTATACGAATGTGGT | 84333 |
| rs770640930 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249185 | AATGAAGTTTTTATA[A/G]GTAGAGCTCAGGTGA | 84333 |
| rs770651116 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247262 | CTGCAGAGCAATATA[A/G]AAGAAATATAAACTT | 84333 |
| rs770656748 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169452 | GTAAGAGACAAGGCT[A/G]GTATATGAAAGTTCA | 84333 |
| rs770691395 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166897 | GGTAACTGCTATAGT[-/TA]TATGACTACAGATTT | 84333 |
| rs770774985 | in-del | -/TTTC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207702 | TAATCTTTCTCAATT[-/TTTC]TTTGTCTTTCATGAC | 84333 |
| rs770783921 | snp | C/G | | | upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91162308 | CTGGTGGGGTGGCGG[C/G]GGTGGGGTGGGGTGG | 84333 |
| rs770829675 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164046 | CCCGGAACGTGTGGC[C/T]GTGAGCTCCAGGGCG | 84333 |
| rs770838566 | snp | A/C | 1.65345e-05 | 0.00287524 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248610 | GTTTTATGAAATCAA[A/C]ACTTCTATTAAAGAT | 84333 |
| rs770948118 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91218051 | CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC | 84333 |
| rs771008495 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242108 | CCAGGAGTGATTTTG[-/C]CCCCCGGGATACATT | 84333 |
| rs771026224 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161181 | TTGCCCCTCCAGCCT[C/T]AGGGGAGAAGGCACG | 84333 |
| rs771027398 | snp | C/T | 0.000116342 | 0.0076261 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264422 | GATCTATAATGATTC[C/T]TTTTAAAGTTGGATG | 84333 |
| rs771057354 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187686 | TATACACAACTTCAA[C/T]GCTTCATGTTTTCTT | 84333 |
| rs771080119 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205363 | CCCCAGGTCAGACGT[A/G]GCACTCTAAATCCTT | 84333 |
| rs771103167 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208430 | CAGTGCCACTTCAAT[A/T]TTAATTGTGTATGAA | 84333 |
| rs771114816 | snp | A/G | 1.65105e-05 | 0.00287315 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91271678 | CGCAAGTCTGCTCTC[A/G]GGATGGCCCTTTGTA | 84333 |
| rs771121569 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270035 | TAGCAGAGTGTCTGA[A/C]ATAAATGTTATTAAT | 84333 |
| rs771123715 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252559 | TTGATTTTGTTAAGG[G/T]GAATTTATTGGACAG | 84333 |
| rs771131122 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283975 | ATTGTTAATGACTTA[C/G]TCTATTAAGAATATA | 84333 |
| rs771175434 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254664 | AAATGTGGTGGGGCA[G/T]TAGTTGCATGTATAG | 84333 |
| rs771179601 | snp | G/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227449 | CCAAGCAAGAAATAT[G/T]CTCCATGCTTGACTC | 84333 |
| rs771281017 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185427 | GTGTCACAGCTCCAT[C/G]CAACACTGTTGTCCG | 84333 |
| rs771288177 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256936 | ACCAAAAGCACAAGC[A/G]ACAAAAGAAAAGAAA | 84333 |
| rs771300447 | in-del | -/TATATATATATATATATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249372 | AAAAGGCTTTTAGTG[-/TATATATATATATATATA]TATATATATATATAT | 84333 |
| rs771347135 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270663 | TAAAAGGCTACAAAT[-/A]TATTTGTTTTAATCA | 84333 |
| rs771354205 | snp | A/T | 1.78229e-05 | 0.00298515 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251258 | AAAATCAACTTTGAT[A/T]TATAGCTAACTTAGT | 84333 |
| rs771395699 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181408 | TTGAATAGGAGTAGC[C/T]AGACAGGGCATCCTT | 84333 |
| rs771455305 | in-del | -/TGTATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186541 | ATATATGTGTGTGTG[-/TGTATA]TATATATATATATGT | 84333 |
| rs771461366 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243580 | AGCAGGCCTGGGGAA[C/T]AAGCAGTCTGTATTT | 84333 |
| rs771474896 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198948 | TCTCTTTCATCACCC[G/T]CTGTGATTGCCTCAT | 84333 |
| rs771501110 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257824 | ACTGTATAAAAGAAT[A/T]GAAAACATGTTCACA | 84333 |
| rs771510112 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274062 | TTTGCCACATTTTTT[C/G]CCTCCTCTTCCCCTC | 84333 |
| rs771521121 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200155 | GTGGGAGAGGGCCCA[C/G]CCTGCTCCCAGAGCC | 84333 |
| rs771525781 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167755 | GGAATGATGTGATCA[A/C]GACTATGCTTTAAGA | 84333 |
| rs771539229 | snp | A/G | 3.31565e-05 | 0.0040715 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248756 | TCTGTTTCTGACAGC[A/G]CCTCTTAAACTGGTC | 84333 |
| rs771541797 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233808 | AATGTGTATGAAGAT[C/T]GTGAACTGCTTAAGG | 84333 |
| rs771554197 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169100 | GATAGGGTAACCATA[A/C]ATGCAATTGCCCAGG | 84333 |
| rs771594188 | snp | A/G | 1.65712e-05 | 0.00287843 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248622 | CAACACTTCTATTAA[A/G]GATTTCATGACTTTT | 84333 |
| rs771679689 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195848 | TGAGGAATAATCCCA[A/C]AGAACAGCATTTGTG | 84333 |
| rs771714551 | snp | C/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227392 | CCACCTGAAACTCAG[C/T]ATATCTACGAATGAT | 84333 |
| rs771719255 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91218044 | TGCCCGCCTTGGCCT[-/C]CCAAAGTGCTGGGAT | 84333 |
| rs771728921 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211986 | CATTGTCAGGAGCGG[C/T]GTGATACTGGTTGTT | 84333 |
| rs771729601 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237855 | TTACCAGCAAAAGTG[G/T]AATAAGATACTGCAT | 84333 |
| rs771739761 | snp | A/C | 4.9652e-05 | 0.00498232 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222880 | GCCACGAATGGCTAC[A/C]CAAAGGAAACACTTG | 84333 |
| rs771745356 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243606 | TATTTGTACTCTCCA[A/G]TATGGTAGCAATTAG | 84333 |
| rs771752812 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183248 | TCTATTAGGGTCTCT[A/G]AGAACTTGCTTTATG | 84333 |
| rs771771767 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247050 | TTAGTTTTGAAGCCA[C/T]AAAAGCAGATGAAAT | 84333 |
| rs771773515 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171578 | CAACTCCATATGGGC[A/C]CTTGGTTGAGTAGGA | 84333 |
| rs771787505 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259177 | AGTACTGCTCTGCAC[A/G]TTTTACAAATGAGAC | 84333 |
| rs771792899 | snp | C/T | 1.65269e-05 | 0.00287457 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271727 | CGACTGTACATATGA[C/T]CATCATGACACCATG | 84333 |
| rs771863423 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175453 | CTGACATTTGAGGTC[C/T]GACAATGAAAAAAAT | 84333 |
| rs771951355 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193440 | AAAACTAAAAGGGAT[G/T]GGGGGGTGGGACATT | 84333 |
| rs771964594 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161014 | TTCTCCTGCTTTCCA[A/C]CACTGGGTGGGCTTG | 84333 |
| rs771975187 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250974 | TATATATTCTGTCCA[C/G]TTTCTAACATAGTCT | 84333 |
| rs772039534 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194396 | AGGTTGCTGGATTTG[A/G]AGATGGAGGAAGGGG | 84333 |
| rs772066050 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267824 | AAGAGCTCTTATTAG[G/T]CTACCTATTGGCTAA | 84333 |
| rs772165684 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231811 | TTGCAGTAATCCAGG[C/G]AGGAGATGGTAATGG | 84333 |
| rs772191727 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230578 | ATTAATAGCAAATGA[A/T]CAATGTTATATTTTA | 84333 |
| rs772231569 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250278 | GGTATACCTGTAGTG[-/C]TTTTACTACAGTCAT | 84333 |
| rs772257669 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217082 | TCTGTCGCCCAGGAT[A/G]GAGTGCAGTGGCACG | 84333 |
| rs772257756 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235974 | TCCAAACTACTCAGG[A/T]GGCTGAGGCAGGAGG | 84333 |
| rs772265950 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266284 | TGGTCATCCACTGCA[C/T]GACCTCTACAAGTGG | 84333 |
| rs772270664 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185835 | GATTCCCTTGACTCC[A/G]TGTGGCTCCCTGGTG | 84333 |
| rs772275327 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181150 | TGGCTCTTGGCCTGA[C/G]CCTTGTTGGTATATA | 84333 |
| rs772321764 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280265 | TTAAAATAGTGTTTT[A/G]CAAATGGAATTTTAA | 84333 |
| rs772363114 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210233 | GCTTGAGATCCTTTT[C/T]CTGCCAGAGAGTGCT | 84333 |
| rs772401063 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256401 | TTCAGTCTGAGAAAC[A/G]GAAAAATAGAATGAA | 84333 |
| rs772401388 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271429 | ACAAAACTCATCTAG[A/G]TGCTAAAATTACTTC | 84333 |
| rs772408536 | snp | C/T | 0.000281611 | 0.0118628 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227340 | TTTTCTTCTTAGCTG[C/T]AGAATCCTACTGGAT | 84333 |
| rs772415227 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282553 | GAATTTAGCCATACA[C/G]CCAACTTTGACAAAA | 84333 |
| rs772430899 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91259442 | TTTCAGAAGTTATAC[-/T]TTTATAATCTTCACA | 84333 |
| rs772461478 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280451 | TTCCAAGGAAATATA[C/T]AGGAAGCAATTATGA | 84333 |
| rs772488457 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243234 | TTTACCAAAGTTTCC[C/T]ACAGCAGGCTTCTTT | 84333 |
| rs772565399 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254457 | GTACTTATATTTATC[C/T]GTCAATTAGGGATTA | 84333 |
| rs772585684 | snp | C/T | 1.97252e-05 | 0.00314042 | synonymous-codon | PCGF5 | GRCh38.p7 | 10:91261415 | ACTAAAACTTCCAAG[C/T]TCTTATGAGGTAAGT | 84333 |
| rs772593042 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188107 | AGGAACAGCTCCGGT[C/T]TACAGCTCCCAGTGT | 84333 |
| rs772596645 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255108 | TCCTCGGAGACCCCA[C/T]TTACAAGATTGTCAG | 84333 |
| rs772598065 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166913 | TATGACTACAGATTT[A/G]TGTGACCATGGGAGC | 84333 |
| rs772638785 | snp | A/T | 1.65908e-05 | 0.00288012 | missense | PCGF5 | GRCh38.p7 | 10:91251439 | GGGACAATGTAGTAA[A/T]GGTGAGTGAACAAGT | 84333 |
| rs772748382 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91169130 | GGCAGTGCTAGTTCA[C/T]ACCAGTTTATTTACG | 84333 |
| rs772849224 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247177 | ATAAAGAAAGAACAG[A/G]CTTGAACATTAAAAA | 84333 |
| rs772865500 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233983 | TATTATTGTTTTATC[A/G]TCAGTGATAGCAGAA | 84333 |
| rs772897422 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212733 | GGAAGGCAGCTCTCT[A/G]TAAAAACAAGAGTTC | 84333 |
| rs772903596 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275867 | CCTGGGGCAAAAGAA[A/G]TAGATCAGTGGGTTA | 84333 |
| rs772940342 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183271 | GCTTTATGAATCTGG[C/G]TGTTCCTGTGTTGGG | 84333 |
| rs772980571 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245099 | GATTGAGCCCTGGAG[A/G]ACTCCAGCATTAAGT | 84333 |
| rs772989708 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275011 | GATCAAGAAGAAAAT[A/G]TAGTTGAAGAACTGA | 84333 |
| rs773000629 | snp | A/C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226216 | TTTATAATTGGTGTG[A/C/T]AAAACCAGACATAGA | 84333 |
| rs773026947 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271104 | ATAGATCTAATGCTA[-/TA]TATATATATATAATC | 84333 |
| rs773030717 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181930 | TTTTGGAATATTTCC[A/G]GTAGGAATGGTAGCA | 84333 |
| rs773036053 | snp | G/T | 1.65124e-05 | 0.00287331 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240586 | AAATGTTGAGGTAAG[G/T]ATGTTATATTTTACA | 84333 |
| rs773054226 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246268 | TATTAAATAGTCTGG[A/G]AAAACTTTACGAATG | 84333 |
| rs773081796 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258250 | GCGAATAGTATAAAA[A/C]CTATAATTAATCTGT | 84333 |
| rs773149616 | snp | G/T | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161092 | TGGAAGATGTCTGCC[G/T]CAGTAGTTGCACTAA | 84333 |
| rs773157543 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252522 | CTTGGTTAGGTCTTA[C/T]ACATACAAATAGTTA | 84333 |
| rs773175486 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91251053 | TCTTTCATTTGGATG[C/T]CCCAATGAGCCTAGA | 84333 |
| rs773245494 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237963 | AGAGATAAAATGTGA[C/G]CCATGTGTATAATTT | 84333 |
| rs773252285 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199902 | AATATCAACAGGAAA[-/G]TAGAGAAGTGGGACA | 84333 |
| rs773303864 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193464 | GGACATTAAGCTGAT[A/G]GTGGAGTAAGAATGT | 84333 |
| rs773343351 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231867 | TGATCAGAATCTTGA[C/T]AGGTTTTGAAGGTAA | 84333 |
| rs773351103 | snp | C/T | 1.64912e-05 | 0.00287147 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261322 | TAATCTTTATTTCCT[C/T]TAGGGTTTAATGAAG | 84333 |
| rs773389313 | snp | C/T | 1.66663e-05 | 0.00288667 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264529 | CGAAAACGTAAATTG[C/T]TTTTATATTTACCTA | 84333 |
| rs773398316 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166915 | TGACTACAGATTTGT[A/G]TGACCATGGGAGCAG | 84333 |
| rs773412093 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202927 | AAAGGAAGAAAAACA[A/G]TAAAGAAATGTGTTT | 84333 |
| rs773421619 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197950 | TCATTCATTCAATAA[A/C]TATTGATTATCTACT | 84333 |
| rs773429972 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230680 | GCAAGATCTCGGCTC[A/G]CTGCAACCTCCCTAC | 84333 |
| rs773466042 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229475 | AGAGGTAAGACTGAG[A/G]GAGGTTAAGTAACAG | 84333 |
| rs773481583 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223667 | TTTCTGCCAGCATGA[-/T]TTCATTTTTTATTTC | 84333 |
| rs773507735 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270433 | TCCAGCTTACTCTTG[-/T]TGACCCTGTTTAGAA | 84333 |
| rs773511458 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186714 | AGATTCAACTAGGGA[C/T]GTACTAGTAACTGTT | 84333 |
| rs773521588 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215991 | AAAGAATACATAGGA[A/T]CAGTTCTTAGAATGT | 84333 |
| rs773543354 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280557 | TATGTGCCAAAACAC[A/G]TGAAAAGCTTACATA | 84333 |
| rs773545391 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264985 | TTGAAAATATAAACT[C/T]GGACTTAAGGGTAAG | 84333 |
| rs773583558 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243417 | CTCCTTCATTAGAAG[C/G]CTAAATTGCCTGTGA | 84333 |
| rs773583615 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254466 | TTTATCTGTCAATTA[A/G]GGATTAGTTTGTTAT | 84333 |
| rs773635052 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266285 | GGTCATCCACTGCAC[A/G]ACCTCTACAAGTGGC | 84333 |
| rs773733615 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198232 | GCCCAGAAGAGCCTG[C/T]GAGACCCATCCTGTC | 84333 |
| rs773741639 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279385 | TGCATAAAATAGAAT[A/G]AATGCAGTATAGAAC | 84333 |
| rs773776961 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165970 | CCCTTTCCATAATAG[C/T]AGCTGTGATCACTTG | 84333 |
| rs773777706 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256465 | ACCATCAAGCTTACC[A/G]GCATACACATAATGG | 84333 |
| rs773830795 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168051 | CAATAAATATTTGTC[C/T]AATTAATGGAGGTGA | 84333 |
| rs773907034 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196363 | ATGTTTATATATTAG[A/G]CTTTCTAAGCAAGAA | 84333 |
| rs773907436 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181834 | CTGAATTCCTTTTCT[A/G]TTGTATTTCTGCTGG | 84333 |
| rs773924368 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245064 | GAGTGAGTACAGAGA[A/G]GCACGAGTAAAGGAC | 84333 |
| rs773945682 | in-del | -/ATAC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233557 | AATATATATACACAT[-/ATAC]ATACATAAGAGAATA | 84333 |
| rs773953700 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223937 | CTTTAATATACCATG[A/G]TACTTTTTTTTTAAT | 84333 |
| rs773961616 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268598 | ACCACTCTCTGCCCC[A/G]TGGAGTCTTTCATCT | 84333 |
| rs773995869 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167026 | ATCTCGTCCAGCTCT[A/G]TGGTTTCAGAAACCA | 84333 |
| rs774019677 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91209251 | TGTTAATTGATGGAA[A/T]CTTCCTTGTAGAAGA | 84333 |
| rs774023504 | snp | C/G | 0.000117395 | 0.00766055 | intron-variant | PCGF5 | GRCh38.p7 | 10:91240630 | ACATAAATTGAATAG[C/G]CTCTTAATTTTTATT | 84333 |
| rs774024637 | in-del | -/TGTCCAGT | 1.6908e-05 | 0.00290753 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271590 | TCAATTTTAAATATG[-/TGTCCAGT]TGTGGATGCCTCTTA | 84333 |
| rs774042831 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226120 | AGTTAAGAATGAGTA[A/G]ACGCTAGGTTTTATG | 84333 |
| rs774044909 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239733 | GAAAGATGAGAGAGA[C/T]TTATAGCCAGAGAGA | 84333 |
| rs774212869 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258115 | AAAGACAAAGTAGAT[G/T]AGGGTTGTCAGGGGA | 84333 |
| rs774266135 | snp | A/G | 1.68088e-05 | 0.00289899 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264544 | CTTTTATATTTACCT[A/G]TGTGTTTATTTAGTT | 84333 |
| rs774285390 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230522 | TATATGTATTCATAT[A/C]TACATATATGAATAT | 84333 |
| rs774310954 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266120 | TTCTTACCCAATACT[A/G]TTGAGGAATGGATAT | 84333 |
| rs774312018 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232665 | TAGGTACATGAAGTT[C/T]TGGAAATAGGCAAGA | 84333 |
| rs774314294 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264611 | AAACTAAAAAAGACA[A/G]ACTAGCTTGGGAAGG | 84333 |
| rs774319513 | in-del | -/A | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91284207 | GACTTAGCCAAGTAT[-/A]ATTTCACCATGTTAA | 84333 |
| rs774364915 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201873 | TTAGTTAAGGTTCTG[G/T]GCTTTAATGTGGTGA | 84333 |
| rs774366904 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215774 | CTTGTCCACCCATAG[C/T]GCTGCTGCTTTCAAC | 84333 |
| rs774384197 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185770 | GATTGGTGGGGCAAG[G/T]GTGGTTTCCTTGGGT | 84333 |
| rs774409098 | in-del | -/CCA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208419 | AGTCCATTCACAGTG[-/CCA]CCACTTCAATTTTAA | 84333 |
| rs774449150 | snp | C/T | 1.65119e-05 | 0.00287327 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91271682 | AGTCTGCTCTCAGGA[C/T]GGCCCTTTGTATCAG | 84333 |
| rs774454568 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202799 | TTTATGCTATATAAT[A/G]TGCTTACTATCAAAC | 84333 |
| rs774500076 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196063 | TACTGGTCAAGTGTT[C/G]CCCCATGGGGTGTTA | 84333 |
| rs774501864 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279254 | GCAGAGGGTTATGAC[A/G]ATTTTAAATATTAGG | 84333 |
| rs774512657 | snp | C/T | 1.66624e-05 | 0.00288633 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222867 | CCAGTCTTCACTAGC[C/T]ACGAATGGCTACCCA | 84333 |
| rs774530990 | in-del | -/CAAAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272915 | TGGCATACTTACCTC[-/CAAAA]CAGTGTTACAGTTTT | 84333 |
| rs774563333 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214380 | TGCACAGAGAGAAGA[C/T]GGCCATGGGACTGCT | 84333 |
| rs774564194 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207971 | ATTGTAGGGGTACCT[C/T]TTCCCCTTTGTAATT | 84333 |
| rs774576871 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207224 | TTGGTGAGGGATGTG[C/T]AGCTGGTGGTAGTAT | 84333 |
| rs774587932 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184909 | CCATCCCAGGGAGTT[A/T]TGGACCTGTTGCCAG | 84333 |
| rs774590561 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241890 | AGTGTGGTTCCCAAA[A/C]CATTAGTATCATGTT | 84333 |
| rs774596772 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235840 | CTTGATTGTGAGGCC[G/T]CCCCAGCCATTTGGA | 84333 |
| rs774623242 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277464 | TGTTTTGGTTCTATA[A/C]GATATGGTACAGGGT | 84333 |
| rs774643542 | in-del | -/TGTG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186579 | GTGTGTGTATATATA[-/TGTG]TGTGTATATATATGT | 84333 |
| rs774676758 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229167 | AGGTGGTATTATTTA[A/C]GCATCAACAGATGTT | 84333 |
| rs774686586 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205454 | AAGGGTATATTCCAG[C/T]GTTCATTCATAAACT | 84333 |
| rs774710868 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255066 | TCATTGCCAAAGAAT[A/G]GTCATTATTTGACTT | 84333 |
| rs774814785 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270337 | TAGGCAATTGTAAGA[A/C]AAGCAAGTATATACA | 84333 |
| rs774835111 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164430 | GGAGCGCTGGTTCGC[A/T]GCAGGGCTGGGTCCT | 84333 |
| rs774862454 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189177 | GAAACACATTCCTTC[C/T]CTTCTTTGCCTGGCA | 84333 |
| rs774871237 | in-del | -/TAAA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272157 | CTTGAGTTACCTCTT[-/TAAA]TAAAAATGATAGTGA | 84333 |
| rs774904974 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91253853 | TCTGTAGGCCATATG[C/G]TCTCTGTTGCAATTT | 84333 |
| rs774910464 | snp | A/G | 1.65787e-05 | 0.00287907 | missense | PCGF5 | GRCh38.p7 | 10:91251430 | GGCAATCAGGGGACA[A/G]TGTAGTAAAGGTGAG | 84333 |
| rs774913327 | in-del | -/TTTA | 1.71522e-05 | 0.00292845 | intron-variant | PCGF5 | GRCh38.p7 | 10:91264549 | ATATTTACCTATGTG[-/TTTA]TTTAGTTATATACCA | 84333 |
| rs774951067 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202767 | GGCAAGGGGTAGTTA[C/G]GCGAAAAGATTGGCC | 84333 |
| rs774963549 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234969 | AAATTCTTTAATTAT[A/T]TTTTGTCCTGTCATA | 84333 |
| rs775031291 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178572 | TTTTTAAAATTTTTG[A/T]AGAGACAGGGTTTCA | 84333 |
| rs775043100 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91221983 | AGAAAGGGCGTGTTG[C/G]ATAGAGTGCTTAGAA | 84333 |
| rs775052773 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223582 | CAGATTTCATTCTCA[A/G]CTGTCCCATTGGAAG | 84333 |
| rs775069030 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91218887 | CCCACCTCGGCCTCC[A/G]GAAGTGCTAGGATTA | 84333 |
| rs775069401 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91264874 | AGTTCTCCCCTAATA[C/T]GATTAATGGTTGATA | 84333 |
| rs775070323 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190580 | GTGAGGAAAGTTGAT[G/T]GGTGGCTCCAGAAAT | 84333 |
| rs775084751 | snp | C/T | 1.65762e-05 | 0.00287886 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248636 | AAGATTTCATGACTT[C/T]TACTTTTATACTCTT | 84333 |
| rs775085532 | in-del | -/GTAT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186542 | TATATGTGTGTGTGT[-/GTAT]ATATATATATATATG | 84333 |
| rs775091666 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256954 | AAAAGAAAAGAAATA[A/G]ATAAATTGTAAATGT | 84333 |
| rs775123343 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91208509 | CTGGCTGATCTGTGG[A/G]CCCTGGCTGAAGTAA | 84333 |
| rs775156569 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91192222 | CATTTGTGGAATTTT[C/T]TTAAAAAAGCATTTA | 84333 |
| rs775353636 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201685 | AACACTACTGTAACA[C/T]CTCATTTGTTCTGTA | 84333 |
| rs775383978 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262685 | ATTGTTATTATGGTA[C/T]GGTTCTACAAATATT | 84333 |
| rs775415140 | snp | A/G | 1.65015e-05 | 0.00287237 | missense, nc-transcript-variant, utr-variant-5-prime | PCGF5 | GRCh38.p7 | 10:91222899 | AGGAAACACTTGGTG[A/G]AAGATTTTAATCCTT | 84333 |
| rs775444332 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257210 | ACAGGAAAAGTTGCT[A/G]AATATCACTAGTCAC | 84333 |
| rs775485529 | snp | A/G/T | 8.25833e-05 | 0.00642542 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278325 | CGGTTAGACCAAGGG[A/G/T]CCCAGACCTCACTGA | 84333 |
| rs775528465 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91229105 | ATGAGGCATCATGAG[C/T]TTTACATTCATTGTT | 84333 |
| rs775530160 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230170 | CAAAGGACAACAGAC[A/G]TAAAAGAGTGAAATC | 84333 |
| rs775582583 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276491 | TTTTATTTCAGAAAA[C/T]CAAAACACAAATAGA | 84333 |
| rs775605214 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183731 | GCCATATGTAGTGTG[C/T]CCTTCAGGAGTCTTG | 84333 |
| rs775654552 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268498 | TTTGCGGGTTTTTTA[A/T]TCTATTTGGCACTAT | 84333 |
| rs775712704 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91206990 | ATTTGTTTATTGCCT[A/G]TTTCCTTCTAGGATG | 84333 |
| rs775714647 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241598 | GATCTTTAAGAAACT[A/G]CTCGTCTAGAATCCA | 84333 |
| rs775735311 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200043 | CTATCCTACCCAAAG[A/G]ACAGGGAAATTGGGT | 84333 |
| rs775740415 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252766 | CTGAAAGTTAAATCA[A/G]TGGAAAGGCTGAATA | 84333 |
| rs775778009 | snp | C/T | 1.70837e-05 | 0.00292259 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251289 | TTTGTTTAAATTATA[C/T]AGATGATACTTCAAA | 84333 |
| rs775805528 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194922 | GTTATCCTCAAGTAG[A/G]GCAATAAAGATGAGA | 84333 |
| rs775822212 | snp | C/T | 1.99722e-05 | 0.00316002 | missense | PCGF5 | GRCh38.p7 | 10:91261417 | TAAAACTTCCAAGTT[C/T]TTATGAGGTAAGTTA | 84333 |
| rs775823411 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202175 | TTAGAACCATGCCTT[C/T]GTATAAAATGTGCTG | 84333 |
| rs775834889 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91225928 | AGGATAGATACAGTT[-/AG]GTTCTGTGATTTGGG | 84333 |
| rs775911867 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91176693 | TTTCTTCCAGTTGAT[C/T]GAATCAGCTACTGAA | 84333 |
| rs775936588 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270491 | ACCAGAGCTTGGGGA[A/C]TCTTTGGAGAGAAAG | 84333 |
| rs775948318 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270242 | TCCTGATTTAGTTTT[A/G]TCTCTTCCAGCAACC | 84333 |
| rs775972175 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177750 | ATTTGCTAAGACCGT[C/T]GGAAAAGTGCAGTAT | 84333 |
| rs775975524 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178601 | CACCATGTTGTCCAG[A/G]CTGGTCTCAAACCCC | 84333 |
| rs775975913 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188844 | ACTTGTCATTTCCCT[A/G]GATAGCAGTTTATTC | 84333 |
| rs776003229 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179111 | AGGTAGATTAAACAT[C/T]TTTGCTTGCTTCCTA | 84333 |
| rs776014922 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274580 | TTTTCTTTCATGGAA[C/T]TTACACTAATGATGG | 84333 |
| rs776016047 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232070 | GCCCTGAGGTACCAC[C/T]AAAAGGAGAAATCAG | 84333 |
| rs776017648 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217249 | CGTGTTAGCCAGGAT[A/G]GTCTCGATCTCCTGA | 84333 |
| rs776063818 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178428 | AGGGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 84333 |
| rs776075350 | snp | A/G | 1.65957e-05 | 0.00288055 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251443 | CAATGTAGTAAAGGT[A/G]AGTGAACAAGTACTA | 84333 |
| rs776084889 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91190314 | TTAAGATTTCAACAT[A/G]TGAATTTTGGGGGAA | 84333 |
| rs776098597 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91245949 | GTGTTGTAGTTAGGA[A/G]TTTGAAGGAGTATGG | 84333 |
| rs776106669 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247384 | TAAAAGAAGCAAAAC[-/AG]AGTATGTGACAGAAA | 84333 |
| rs776120712 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247382 | AGTAAAAGAAGCAAA[A/G]CAGAGTATGTGACAG | 84333 |
| rs776193103 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249765 | AGGTAACAAGAGACT[A/G]TTTTTTATCTGTAAC | 84333 |
| rs776216200 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235802 | TTCACGTAAGATGTG[A/G]CTTGCTCCTCCTTGC | 84333 |
| rs776222090 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246481 | TAGGTTGGACTCAAG[G/T]TATATAAACACATGA | 84333 |
| rs776289478 | snp | A/G | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219657 | TTTAAAGGACTATAC[A/G]AATGTGGTCATTTAA | 84333 |
| rs776314900 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187938 | CATGCTAATGGCAGA[C/T]GGATGATTCTTTTTT | 84333 |
| rs776347631 | snp | A/G | 4.95995e-05 | 0.00497969 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271742 | CCATCATGACACCAT[A/G]GCGGTGAGCACATTC | 84333 |
| rs776352744 | snp | A/G | 1.7871e-05 | 0.00298918 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251250 | TTAACTTTAAAATCA[A/G]CTTTGATTTATAGCT | 84333 |
| rs776371348 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194690 | AGGTCTCGAATTCAA[A/G]AGCATAGAGATGGTT | 84333 |
| rs776423544 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91261478 | TTCTGATTTGAAGTA[A/C]AATTCTAACAAAAGT | 84333 |
| rs776436350 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262626 | GCCGCTGATCCTGAG[C/T]TTATTTGAAAATTTC | 84333 |
| rs776484696 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91163775 | AGGAGGCAGGACCCG[C/G]CGGGACCCACCTGTA | 84333 |
| rs776490037 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235031 | TCTGATGATGGTTTA[A/G]CAGAGAGCCAAATCC | 84333 |
| rs776541620 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184546 | CCATATTCTGAATTC[C/T]ACTTCTGTCATTTCA | 84333 |
| rs776574723 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166671 | GTCACAGCATCCAAT[A/G]GAAAAGCCTAGACTT | 84333 |
| rs776619150 | snp | A/G | 3.29728e-05 | 0.00406021 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91240557 | CAACCAAGTTCATGA[A/G]ACAAATCCATTAGAA | 84333 |
| rs776640136 | snp | A/C | | | upstream-variant-2KB, nc-transcript-variant | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161210 | CGTCCAGCAGTTGCT[A/C]ATCTCAGGATTGCCT | 84333 |
| rs776670608 | snp | A/G | 0.000140756 | 0.00838797 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227401 | ACTCAGCATATCTAC[A/G]AATGATCAAATGGGA | 84333 |
| rs776687680 | snp | C/T | 4.9899e-05 | 0.0049947 | intron-variant | PCGF5 | GRCh38.p7 | 10:91251468 | GTACTATGGTATTTT[C/T]ATGATCAGTTTATAG | 84333 |
| rs776709298 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281212 | GAGGTAATACTCAGT[C/G]TGGAGTACAGGTAAC | 84333 |
| rs776727126 | snp | C/T | 1.65509e-05 | 0.00287666 | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278359 | GAATCCTGCACTATT[C/T]GTTTACTCGTCAACA | 84333 |
| rs776805935 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254666 | ATGTGGTGGGGCAGT[A/G]GTTGCATGTATAGTT | 84333 |
| rs776830127 | snp | G/T | 2.39192e-05 | 0.00345818 | intron-variant | PCGF5 | GRCh38.p7 | 10:91261445 | TTAAATAATATCTAA[G/T]CTTGATCATTTTGAT | 84333 |
| rs776838258 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183120 | TGTGTATATATTTGA[G/T]CCAGTGCTGAGTTCA | 84333 |
| rs776842371 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212527 | GGTTTGCTTTTTTTT[A/C]TTGATTAATATTTTA | 84333 |
| rs776866788 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238257 | TTAGTATTCCCCATC[A/T]CTGTTCTTGGGTACT | 84333 |
| rs776886204 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91218067 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCGC | 84333 |
| rs776891684 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268131 | ATGTGTGTGTGTGTT[A/C]CTAGACATTGTTTTG | 84333 |
| rs776892731 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266906 | ATTCTCCTAGCAAGG[A/C]TCTGTGCCACCACCC | 84333 |
| rs776898385 | snp | C/T | | | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227516 | GGTCTCTCTCTTTAA[C/T]ACTTCTCAAATCTGT | 84333 |
| rs776933977 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185452 | TGTCCGTGCCTGGCT[A/G]GAATTCCAAGCCAGT | 84333 |
| rs776992307 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231932 | GAAAAGAAAACGGAA[C/T]GTAAGTTATAACATA | 84333 |
| rs777064550 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244918 | GTTATTCATTTCAGA[C/G]AAGAGAGGAAGGTAA | 84333 |
| rs777064899 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252576 | AATTTATTGGACAGG[C/G]CATGTAATAAAGTGC | 84333 |
| rs777087746 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282230 | TGGCTCATGCCTGTA[A/G]TCCCAGCACTTTGGG | 84333 |
| rs777114681 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187814 | ATTTATTTTTCCTTT[G/T]CTAATTATTTAGAAA | 84333 |
| rs777146071 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231582 | TGTGGCTGGACAGCA[A/G]TGAGTGAAGGAGTGT | 84333 |
| rs777164487 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263385 | AAACATTTTGAGGTC[C/T]GTATAAGTCATCATA | 84333 |
| rs777185083 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172147 | TTGCCCTCTAGGGCC[A/G]GGCGCGGTGGCTCAT | 84333 |
| rs777214083 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210516 | AACTGGCTTAGCTTG[A/G]TAAGAGATCATTGGC | 84333 |
| rs777234046 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201299 | GGTGAGGGGCTGAGT[A/G]TGTCAGCTCAGGTCT | 84333 |
| rs777259021 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271878 | TCTCCTGAATTATCT[A/T]TTTAATTTTACTGAA | 84333 |
| rs777349023 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273929 | GAAAAGGTGTTTGAT[A/G]AAATTCAATGTGAAG | 84333 |
| rs777360459 | snp | C/G/T | 0.000140756 | 0.00838797 | intron-variant, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91227400 | AACTCAGCATATCTA[C/G/T]GAATGATCAAATGGG | 84333 |
| rs777437820 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91239302 | ATTGAATCAATGAAT[A/G]AACAAACAAGAGGAA | 84333 |
| rs777447783 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228603 | ATTTTATGTGGTAAT[A/C]TGTAAGAAGGAATAA | 84333 |
| rs777536660 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262283 | ATATAAAAATTAGCC[A/G]GGTGTGGTGGCAGGT | 84333 |
| rs777542815 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275500 | GGCTGGAATGCAGTG[A/G]TGCGATCTTGGCTCA | 84333 |
| rs777569591 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196551 | TTCAGCAGAAATGTT[A/G]TATCTTCAGAGAAAG | 84333 |
| rs777571971 | snp | A/C/T | 3.45849e-05 | 0.0041583 | synonymous-codon, stop-gained | PCGF5 | GRCh38.p7 | 10:91261347 | ATGAAGAAATTCATT[A/C/T]GATGTTCTACACGTG | 84333 |
| rs777613706 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189481 | TATTGAGAATCTACA[C/G]TTGCTGTTTGAGGTT | 84333 |
| rs777618431 | snp | A/G | 1.65663e-05 | 0.002878 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248744 | CTTTTTCTTATGTCT[A/G]TTTCTGACAGCACCT | 84333 |
| rs777697057 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178172 | AACATTGGCATAACT[A/G]TACAGTATTATGAGA | 84333 |
| rs777719172 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254580 | TCCCTTAGTGGCAGA[C/G]ACACAATGTCTGTAT | 84333 |
| rs777784190 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205218 | CATCCAGCCTTGAGC[A/G]CAATTGTTCCCAAAT | 84333 |
| rs777801248 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170165 | GAATGTAAAACTGTA[A/C]AACTCCTAGAAGATA | 84333 |
| rs777815584 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233295 | CCTTCCTAGACCTTT[C/G]AAGGTCTGCTGGCTT | 84333 |
| rs777822353 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258599 | CTAATGATTCTTTGT[A/C]AGCTGTTTGGGGCAA | 84333 |
| rs777840755 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168727 | AGGTCAAGAGTTCCA[A/G]ACCAGTCTGGCCAAC | 84333 |
| rs777885872 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198841 | CAGATGGGTTATTTC[C/T]ACCCCATGGTCTTTG | 84333 |
| rs777886510 | snp | C/G | 1.65102e-05 | 0.00287312 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91271675 | CTTCGCAAGTCTGCT[C/G]TCAGGATGGCCCTTT | 84333 |
| rs777889206 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199803 | ATAAACAAAGGAGAA[A/T]AAATTTTAGTGTGGT | 84333 |
| rs777909668 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270437 | GCTTACTCTTGTTGA[C/T]CCTGTTTAGAATTCT | 84333 |
| rs777934684 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244596 | GTGTTGAGAACACCG[C/T]GCGTATAACAAGGCA | 84333 |
| rs778007074 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238581 | AATCCCTCCACTCTC[-/A]TTTCTTTCTTTCTTT | 84333 |
| rs778010936 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267974 | ATTTATACAAAAACA[A/C]AAGGTTAAGATTCTA | 84333 |
| rs778022591 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91283987 | TTAGTCTATTAAGAA[C/T]ATATGTATTTTTGTA | 84333 |
| rs778052856 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91168370 | TTTCGAAGGATCCTG[A/T]TAGGGTAGAGGATGG | 84333 |
| rs778095056 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236374 | GTTAGTGCTCATTAA[A/G]TATTAGCTAAGTTGT | 84333 |
| rs778121753 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272556 | GGCGGGCAGATCTCT[G/T]GAGTCCAGGAGTTTG | 84333 |
| rs778157519 | in-del | -/ACTTTT | 1.65778e-05 | 0.002879 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248632 | ATTAAAGATTTCATG[-/ACTTTT]ACTTTTATACTCTTT | 84333 |
| rs778179822 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91212129 | TAGCAAAATACTGTG[C/T]ACTTGGAAGAGCTCA | 84333 |
| rs778216423 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91257564 | AATTTGATAACTGAG[A/G]TAGCTAAGTCACTAA | 84333 |
| rs778236587 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167717 | GTTGGCAGTAGATAA[C/G]TATCAGAAATATTTT | 84333 |
| rs778244102 | in-del | -/AAA | | | cds-indel | PCGF5 | GRCh38.p7 | 10:91283890 | CATCTTAATACAAAT[-/AAA]AACCTTTTTGTGGTT | 84333 |
| rs778253911 | snp | A/G | 1.68749e-05 | 0.00290468 | intron-variant | PCGF5 | GRCh38.p7 | 10:91278247 | AATACAGTCTTATTT[A/G]TTATCTGTCTTTATT | 84333 |
| rs778256180 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222847 | CTTTGCCCAGACTAC[C/T]AAAGCCAGTCTTCAC | 84333 |
| rs778262012 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91193313 | GAGACTAAGTAGAGG[A/G]CCCAGCTCAGCCAAA | 84333 |
| rs778277927 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91210253 | CAGAGAGTGCTACAG[C/T]TCTTGTGCTTCCTGG | 84333 |
| rs778291332 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91255926 | ATCATCTCTAGATTA[C/T]TTGTAATACCTAATA | 84333 |
| rs778295649 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91276745 | TTAATGCATTCTAAA[A/G]TGAGTGGCTTATGTA | 84333 |
| rs778356534 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91184126 | AGCTAGGTTGGGTAC[A/C]TTCTCATGGATGATA | 84333 |
| rs778385703 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91237306 | ACTATGATAATAACA[A/G]TATATCATCCAAACG | 84333 |
| rs778465399 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91183199 | CAGTGGGGTGTTAAA[G/T]TCTCCCACTATTATT | 84333 |
| rs778472042 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91223342 | GCAGACTCTTAATTC[G/T]CTGGTTCTCAAAGTG | 84333 |
| rs778574211 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226482 | GAGTAGTGGTGCAGA[A/G]GACTACTTATGGGTG | 84333 |
| rs778649953 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204815 | TGGGTATTGTTTTGA[A/T]TCTGTGTAGGTCACC | 84333 |
| rs778748249 | snp | C/T | | | | | GRCh38.p7 | 10:91230878 | TCAATCTGCCTTGAC[C/T]TCCCAAAGTGCTGGG | 84333 |
| rs778752124 | snp | A/G | | | | | GRCh38.p7 | 10:91198559 | CATTGGCAAAGCAGC[A/G]TCACTGGCTTTCTCT | 84333 |
| rs778761301 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91232811 | GATGGAGGAGGATAT[C/G]TTGGGGGTTTGAAGA | 84333 |
| rs778767694 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215816 | TCACTTGATCATGTT[-/C]CATTTAACACTTTAT | 84333 |
| rs778773783 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267521 | AATAAATTGAATGAA[A/G]ATGTTATCTTTTACA | 84333 |
| rs778775143 | snp | A/C | 1.65743e-05 | 0.00287869 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248753 | ATGTCTGTTTCTGAC[A/C]GCACCTCTTAAACTG | 84333 |
| rs778783260 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275479 | TGGAATCTTGCTCTG[A/T]TGCCAGGCTGGAATG | 84333 |
| rs778811033 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91177998 | ATCATCCATATTCTG[C/T]GTCGCTCACACTGGG | 84333 |
| rs778824322 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187343 | AGATAAAGATCTTCA[C/T]GTGCAGATTTTGTAG | 84333 |
| rs778824329 | snp | A/G | 1.65353e-05 | 0.00287531 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248611 | TTTTATGAAATCAAC[A/G]CTTCTATTAAAGATT | 84333 |
| rs778844332 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91217676 | TCTTTGATAGGGAAT[A/C]ACCAGTGGCCACTTC | 84333 |
| rs778847879 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231692 | CTGAGAGAAATGAAG[A/T]TCCGTTTCAGGCAGG | 84333 |
| rs778901682 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91175000 | TGATACCTAAGTGCC[-/TT]TTTAACTGAGGTTGA | 84333 |
| rs778932709 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91197754 | TTCCTTCCTATTTTC[A/T]GTACACTTTCATTTT | 84333 |
| rs778933285 | snp | A/C/T | 5.21602e-05 | 0.00510664 | utr-variant-5-prime, nc-transcript-variant | PCGF5 | GRCh38.p7 | 10:91222829 | CATCTACTTAGGACC[A/C/T]CTCTTTGCCCAGACT | 84333 |
| rs778961006 | snp | A/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91281819 | CACTTCCTTTCAAAT[A/G]TGTTCATTGTTTTTC | 84333 |
| rs778961490 | snp | A/G | 1.64871e-05 | 0.00287111 | missense, intron-variant | PCGF5 | GRCh38.p7 | 10:91240501 | TGTAAGACTTGTATT[A/G]TTCAGCACTTTGAAG | 84333 |
| rs778968801 | in-del | -/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91171402 | AAAGGTTTGGTAAAC[-/TT]TGGGTTTGCGCAGTG | 84333 |
| rs779010470 | snp | A/C | 0.000140915 | 0.0083927 | intron-variant | PCGF5 | GRCh38.p7 | 10:91227306 | TGAGGCCTCTCAAAT[A/C]TTTATTTTTGGCTTA | 84333 |
| rs779015493 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211502 | TCCCTGCCTTCAGGT[C/T]ATTTACTATCGGACC | 84333 |
| rs779020859 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91181137 | TTCATTTGTGATTTG[G/T]CTCTTGGCCTGACCC | 84333 |
| rs779049917 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91243171 | TGAGCGGACCTCAGA[A/G]GCCTGAGTATACCAG | 84333 |
| rs779063491 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91256181 | ATTATCTATTTAAAT[A/G]TGCACAAAGAACTAA | 84333 |
| rs779065501 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273569 | GCTAATAGGATGCAC[C/T]GTTAACTTCCTGAAA | 84333 |
| rs779099732 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167602 | AAACTGGAGGTTGAG[A/G]AGCCTGGAGGCAGTA | 84333 |
| rs779153097 | snp | C/G | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280356 | GCCCCCCAGCCAAAA[C/G]TTAATGGTCATAAAT | 84333 |
| rs779153610 | snp | C/T | 4.96586e-05 | 0.00498265 | missense | PCGF5 | GRCh38.p7 | 10:91278269 | GTCTTTATTTTGTAG[C/T]CATACCCTATGGTAC | 84333 |
| rs779229891 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91201345 | CACTAGTCCTATCAT[C/G]GTCCCCCCAGTGACA | 84333 |
| rs779262384 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272328 | CCTTAACCCTGTGAA[A/T]TAATCATACCATTTC | 84333 |
| rs779295806 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166741 | CCTAATAAGTAGAGC[A/T]TTCCACAGCAAGTTA | 84333 |
| rs779334051 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91214710 | ACGGCCAAAAGGCTA[A/C]AGAACTGCAGATAAA | 84333 |
| rs779375052 | in-del | -/AAC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249780 | TTTTTTATCTGTAAC[-/AAC]AACAACAACAAAAAA | 84333 |
| rs779419477 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91241062 | ATATATATAATATAT[A/G]TTTTATTTATTTATT | 84333 |
| rs779420174 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211892 | GTGTTGCAGTGCTGC[A/C]GAGCAAAGTGGTCTG | 84333 |
| rs779425067 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202283 | AAGCCTATAGACTCT[A/G]AAGCAAAATAACCTG | 84333 |
| rs779434769 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91282282 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCTGGTTA | 84333 |
| rs779498176 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194259 | AACAACTTTGAGATG[C/G]AGAGATGATCCTAGA | 84333 |
| rs779525904 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91248082 | TCCAGCCTTGTTCTC[A/G]TGGTAGCAGGATTCT | 84333 |
| rs779539576 | snp | A/C | 1.66012e-05 | 0.00288103 | missense | PCGF5 | GRCh38.p7 | 10:91251352 | ATGAAAATGAAGATG[A/C]TAAAGATTATCACAG | 84333 |
| rs779592841 | snp | C/T | 3.3162e-05 | 0.00407184 | intron-variant | PCGF5 | GRCh38.p7 | 10:91248760 | TTTCTGACAGCACCT[C/T]TTAAACTGGTCAGCT | 84333 |
| rs779615647 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249606 | TCCCATAAGATCATA[A/G]GATTGTCAATTATAC | 84333 |
| rs779643334 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91250162 | TTTTTTGTTGGAGCT[A/G]GGAGTTTGGTTCATA | 84333 |
| rs779728502 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91252162 | ATCTTCACTACTTCA[A/G]CTGTTAGATTTTTGT | 84333 |
| rs779737119 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274271 | TCATAAGGAAATATC[A/G]GCAGGTGCTTCGATC | 84333 |
| rs779752402 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91174393 | ATGCCTGTAATCCCA[A/G]CCACTGGGGAGGCTG | 84333 |
| rs779798393 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216892 | ATGTGGGCCTTATAG[C/G]ATATTTATGTTCAAT | 84333 |
| rs779801490 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91198298 | ACACTGGCCCCCTTG[C/T]TGGGGGAACCTTGGA | 84333 |
| rs779805069 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91236587 | GGGTTAACCACTACA[A/G]CAGTTGAGCAGTTAG | 84333 |
| rs779813419 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271147 | AATCAGCAATATAAA[A/G]CAACATAAAGAACCT | 84333 |
| rs779840557 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266043 | CATCAATCACCCTCA[G/T]TTAATCCTTACAACC | 84333 |
| rs779893367 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244209 | CAGATTGCAATTTTA[A/T]ATAAGATGGTGATGA | 84333 |
| rs779901364 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242389 | TTATTACCAACTGTT[A/T]AAATCTATAATAACT | 84333 |
| rs779926053 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91279894 | ACTCTAGCAAACATA[C/T]AAAGTACAGCTAAAT | 84333 |
| rs779966189 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187224 | TCTAGGATGGGGCCT[C/T]AGCATGATATATAGA | 84333 |
| rs779988761 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91170788 | GAGTTGAAAACTTGT[A/G]GCCACACAGAAACCT | 84333 |
| rs779990917 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91242910 | TATTCCAGTTTTCTT[A/G]ATTTAATGATGTCCT | 84333 |
| rs779994298 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91231292 | ACAACCTAGTAGGCA[A/G]TAAACAAATGATAGT | 84333 |
| rs779994350 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228441 | AAAAGGAAAGCTTTC[C/T]TTCCTCTTTCTGCTC | 84333 |
| rs780023639 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278585 | ATCAGTTAGCTGTGC[C/T]GCCATGATTCACCCT | 84333 |
| rs780077422 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207817 | ATAGTCAGGATAGAC[A/G]TTTTGGGCAGAAACA | 84333 |
| rs780105104 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271210 | TGAGCGGAGTTCCAC[A/G]TCCCTCCCAGAGCTC | 84333 |
| rs780167474 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196989 | GCATGATGTGGAACC[A/C]TTCAAATCTCTTTTT | 84333 |
| rs780172589 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91192452 | ATATTAAGAAAGCAA[G/T]TCTTTGGTATTTATC | 84333 |
| rs780191231 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230169 | CCAAAGGACAACAGA[C/T]GTAAAAGAGTGAAAT | 84333 |
| rs780197871 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254879 | TATAGAGCATTTTAT[C/G]AAGAAGATGACTAAC | 84333 |
| rs780225683 | in-del | -/TAAA | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91280872 | ATAAAATGAATTCTT[-/TAAA]TAACCTATAGGAATC | 84333 |
| rs780234280 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91179774 | TTTAGTTTGATTCCA[C/T]GTCTTTGCTACTGTG | 84333 |
| rs780257534 | snp | C/T | | | upstream-variant-2KB, intron-variant | PCGF5 | GRCh38.p7 | 10:91219347 | GTTATTCTTTTAAAA[C/T]ATATTTAAAATAGTT | 84333 |
| rs780277805 | snp | C/G | 1.65436e-05 | 0.00287602 | intron-variant | PCGF5 | GRCh38.p7 | 10:91271632 | ATGAGTTCATCTCCT[C/G]CGCAGTTTCGGTGTC | 84333 |
| rs780309126 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91272176 | AAATGATAGTGAGCT[A/G]ATTTAGTAATGCACT | 84333 |
| rs780398897 | in-del | -/CACA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91204516 | TTCCAGGCACATTTT[-/CACA]AACAGCCTGTTTGGA | 84333 |
| rs780420103 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267663 | ATTATAATATTAATA[-/G]ATGAATTCTGACAGT | 84333 |
| rs780426413 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191166 | TTTACAAATTAGGCA[C/G]AGTAAAAGATTAACA | 84333 |
| rs780442814 | snp | A/G | | | upstream-variant-2KB, downstream-variant-500B | PCGF5, LOC105378429 | GRCh38.p7 | 10:91161593 | TTAAGGAACATCTCT[A/G]TAGAATTCAATTTTA | 84333 |
| rs780455748 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234706 | CACATTTATTGAATA[C/T]TTACAAGTTACCAGA | 84333 |
| rs780472559 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91266947 | TCTATCTTCACCTCA[C/T]ACAGCAGCCAGCGTG | 84333 |
| rs780534425 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166009 | TAATCTCAAGAGTAA[G/T]CTCAGAGACAATAGA | 84333 |
| rs780559119 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247852 | ACAGACAACCCCTAA[A/T]TTGATGCTTGAAAAA | 84333 |
| rs780572178 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249995 | TGTCATCAGAAGTTA[C/T]GTGGTAGGTTTACTC | 84333 |
| rs780631552 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91213514 | TTGTTGCCCAGGCTG[A/G]AGTGCAATGGCGTGA | 84333 |
| rs780652644 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91202387 | AAACCCACCATTGTG[A/G]CCTTGAGAGAGTTAA | 84333 |
| rs780666085 | snp | A/G | 1.65655e-05 | 0.00287793 | missense | PCGF5 | GRCh38.p7 | 10:91251396 | ATTGCTATCTGTCTA[A/G]ATTGTTTACGAAATA | 84333 |
| rs780740787 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203223 | TGTTGCATATTAAAA[C/T]GTTTAGGAAAATTAT | 84333 |
| rs780755159 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246946 | ATATATAGTCAGGCA[A/G]ATAGATAGATGGATA | 84333 |
| rs780782322 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91166510 | CTTAGAACTTTTACA[A/G]TAATGAAACTACTGT | 84333 |
| rs780829725 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91196825 | TCTTTGTTTACTCTT[G/T]CCCTGTCATCTGGTT | 84333 |
| rs780835647 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91228754 | GAAAATCTTACACTA[C/T]ATACACATGCTACTC | 84333 |
| rs780932290 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180103 | CTAATGATCAGTGAT[G/T]TTGAGCTTTTTTTCA | 84333 |
| rs780964655 | in-del | -/AG | 1.65715e-05 | 0.00287845 | frameshift-variant | PCGF5 | GRCh38.p7 | 10:91251422 | AAATAATGGGCAATC[-/AG]GGGACAATGTAGTAA | 84333 |
| rs780989742 | snp | C/T | | | utr-variant-3-prime | PCGF5 | GRCh38.p7 | 10:91278484 | TTCATGTTGTTTCTA[C/T]TAGGAGCAAACCAAG | 84333 |
| rs781000941 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91172240 | AACCAGCCTGGCCAA[C/G]GTGATGAAACCCTAT | 84333 |
| rs781025937 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91207578 | TGTTATAATAGTATC[C/T]AATGTGCAGACCTGT | 84333 |
| rs781049460 | snp | A/G | | | intron-variant, upstream-variant-2KB | PCGF5 | GRCh38.p7 | 10:91221172 | CCGCTGGGTCCTGCC[A/G]GAGAACGCAGAAAAG | 84333 |
| rs781052268 | in-del | -/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91267476 | TAGGGCAGTGCCCAG[-/C]ATATATACTCAATCA | 84333 |
| rs781082798 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178307 | TAAATGTCAGAAGAA[A/G]TTGCTAAAATTTTAA | 84333 |
| rs781094071 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91165043 | ATGAATAAACTCTTT[G/T]CCAGATTTCTTGGTA | 84333 |
| rs781137096 | in-del | -/GT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91195014 | GTAGATGTGGTGAGA[-/GT]GTGTGTGAGTTCTCT | 84333 |
| rs781152553 | in-del | -/A | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91268946 | CAGTATTGCCACCTC[-/A]AGTTTCTATACTCAA | 84333 |
| rs781197397 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185553 | TCTTTCCTAGGGGTA[C/T]GTATGGAGGTCTAAC | 84333 |
| rs781222263 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246795 | TAGTTTAAAAAAAGC[A/G]AGACAATGACTGGGC | 84333 |
| rs781250904 | snp | A/G | | | downstream-variant-500B | PCGF5 | GRCh38.p7 | 10:91284355 | CCTGTAGCAAATTTT[A/G]TTGAAATTTATTGAG | 84333 |
| rs781265943 | in-del | -/TTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275608 | ACCATGCCCGGCTAA[-/TTT]TTTTTTTTTTTTTTT | 84333 |
| rs781277716 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188695 | CCTCCCCTCTTGCCC[C/G]TTAGGAATCTTCTGC | 84333 |
| rs781286161 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91189646 | GAAAGTTAAAAAGAC[C/T]AAAGAATATACATAA | 84333 |
| rs781289701 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91164077 | GTGAATGAATCATCG[C/T]CCCGCGGACCGGGCC | 84333 |
| rs781339683 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91270155 | CCAGCCTTAGCTTTC[A/T]TCGTGTACTCACGTT | 84333 |
| rs781341691 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173580 | TAGAGGGAGTTGGCT[-/T]TTTTTTTTTTTTTTT | 84333 |
| rs781348847 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271182 | TAAAACAGAAAATAG[A/G]TGCCTTACAGGTTGA | 84333 |
| rs781351336 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91233530 | AACGTGCCAATATAC[A/G]GCACATTATGTAATA | 84333 |
| rs781371186 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91178795 | GTAATGATGATGAGT[A/G]GTTTGGAAAATGATT | 84333 |
| rs781404660 | snp | C/T | 6.64551e-05 | 0.00576395 | intron-variant | PCGF5 | GRCh38.p7 | 10:91222996 | CATGTAAGTATTCTT[C/T]TAGGTTATTATACCT | 84333 |
| rs781413012 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91262046 | CATAGTAAGGAAATA[C/T]CATTTCTCACCTGCC | 84333 |
| rs781443042 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234621 | TCATAGTCTGATATT[A/G]TTCAGTATTGTGATG | 84333 |
| rs781461035 | in-del | -/GATA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91246974 | ATAGATGGATAGATA[-/GATA]GATAGATAGATAGAT | 84333 |
| rs781558423 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | PCGF5 | GRCh38.p7 | 10:91264515 | TGGCGACTAAGAGGC[A/G]AAAACGTAAATTGCT | 84333 |
| rs781670160 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91188630 | TACTTCATGGCCACC[A/G]CCTTCATTTGGATTC | 84333 |
| rs781672759 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182810 | TTGAGATTCTGGTAC[A/G]TTGTATCTTTGCTGT | 84333 |
| rs781681103 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238828 | AAATTTGGGAAGAAG[A/G]CAAAGTATTCAATTG | 84333 |
| rs781690557 | snp | C/T | 1.65154e-05 | 0.00287358 | synonymous-codon, intron-variant | PCGF5 | GRCh38.p7 | 10:91271647 | CCGCAGTTTCGGTGT[C/T]TGAACTGCTCAGCTT | 84333 |
| rs781690897 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91234593 | GTTATTTATGATTAG[C/T]GCATCAAACTAATCA | 84333 |
| rs781723060 | in-del | -/CTAT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91216372 | CATTTGGAAGAAGAC[-/CTAT]CTATCTAGCTAGAGA | 84333 |
| rs781729575 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199990 | ACTGGAGCTCAATCC[A/G]TTTAAGGAACTCTAG | 84333 |
| rs781734154 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91226922 | TGATAAATAGATAAA[A/C]TTTTTAAATGAGTTA | 84333 |
| rs781752779 | snp | G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91258840 | TTATTTGTTAATTTA[G/T]TTCTGTTGGTCTTTG | 84333 |
| rs781770465 | snp | A/G/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91211796 | ATAGTGAGAAGCCTG[A/G/T]TCGAGTTGTTAAAGT | 84333 |
| rs796103822 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91167165 | GTCTAAATTAACTTT[-/T]ATGATAAGTACATTT | 84333 |
| rs796105943 | in-del | -/AGAGA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91194751 | AGCATAAGTAGAGAT[-/AGAGA]AGAGAAGAGGATCAA | 84333 |
| rs796113349 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91230267 | GAGAAAAAGTGTGTA[A/G]CCTAAACTACAAAAA | 84333 |
| rs796128674 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275654 | GAGGCGGGGTTTCAC[C/T]GTGTTGGCCAGGATG | 84333 |
| rs796149669 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91273857 | ATATAAAATATTTTA[C/T]ACATTTTATATATTT | 84333 |
| rs796187678 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238610 | TTCTTTCTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 84333 |
| rs796208421 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91247009 | GATAGATAGATAGAT[A/G]GATAGATAGATAATC | 84333 |
| rs796226359 | in-del | -/GT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91254204 | CTTCCCCTCCACCTC[-/GT]GTGTGTGTGTGTGTG | 84333 |
| rs796283676 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186121 | TTTAGAGCTCAAGTT[C/G]AAGTAAATTTTAACT | 84333 |
| rs796325209 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238613 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 84333 |
| rs796342766 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91187283 | ACTAATGTGCAAATC[A/G]GTTTGGGAACCACTG | 84333 |
| rs796352242 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91235148 | CTTTTGGCTGCATCA[C/G]TGAGAGGGTTTTGTA | 84333 |
| rs796355885 | multinucleotide-polymorphism | AA/GG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274671 | AATAGAATAGTTTTA[AA/GG]AAGATAGCCAAGAGA | 84333 |
| rs796363785 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238904 | TTTTTAAGGTTTTCT[C/G]ATACTGTCTTTTACC | 84333 |
| rs796368112 | in-del | -/ACTT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91203354 | GTGTTCCTTTGTTTA[-/ACTT]ACTTTTTATTAGGAT | 84333 |
| rs796397116 | in-del | A/TT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91275450 | CTACATTTTATTTTT[A/TT]TTTTTTTGAGATGGA | 84333 |
| rs796432346 | in-del | -/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91173595 | TTTTTTTTTTTTTTT[-/T]CCCACAGAAGCCATG | 84333 |
| rs796433851 | in-del | -/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91263381 | TGAAAAACATTTTGA[-/G]GTCCGTATAAGTCAT | 84333 |
| rs796462573 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91238606 | TTCTTTCTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 84333 |
| rs796468126 | multinucleotide-polymorphism | AGA/GGG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277412 | TTTCATTTTAAGAGA[AGA/GGG]TATCTACAGCTTTAA | 84333 |
| rs796597560 | snp | C/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91199457 | AGTCCTTGCATCCTT[C/G]GGAAAGTGACCTTGG | 84333 |
| rs796615504 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91180080 | TTGTGGTTTTGATTT[A/G]CATTTCTCTAATGAT | 84333 |
| rs796617716 | in-del | -/AT | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91186558 | TATATATATATATAT[-/AT]GTGTGTGTGTGTATA | 84333 |
| rs796627829 | in-del | -/TA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91274118 | ATCAATCTGTGTATG[-/TA]TATATATATGTAATA | 84333 |
| rs796671576 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91249849 | GGCTTGTTTTACCCA[C/T]GTGTACACTGCAATT | 84333 |
| rs796674623 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91191967 | CACATCACTGGTGAG[C/T]TGTGAGATTAGACAA | 84333 |
| rs796707685 | snp | A/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91244040 | CAGACAAAATAAAGA[A/T]CTTTGCCCTTGTAGA | 84333 |
| rs796732228 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91182465 | AGTTTAGCTAGTTGT[C/T]TATATATTTTATTAT | 84333 |
| rs796780267 | snp | C/T | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91185191 | TTCTTAAATCTCTGT[C/T]AGCCAGAAAACACCA | 84333 |
| rs796791264 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91277629 | ATTCAGTTATTTTAT[A/G]TAATAGTCAAATCCA | 84333 |
| rs796885625 | in-del | -/AG | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91200395 | ATCTAGTTAAGAGAG[-/AG]TGAGGGTATAGAAAG | 84333 |
| rs796902764 | snp | A/C | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205913 | GAGAATTGCTTGAAC[A/C]CGGGAGGCTGAGGTG | 84333 |
| rs796912092 | in-del | -/AC | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91205291 | TTTCTAAATGACTGG[-/AC]ACACACACACACACA | 84333 |
| rs796919823 | in-del | -/ATATATATATATAATCTA | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91271103 | TATAGATCTAATGCT[-/ATATATATATATAATCTA]ATATATATATATAAT | 84333 |
| rs796953019 | snp | A/G | | | intron-variant | PCGF5 | GRCh38.p7 | 10:91215497 | CCTTAGGAGGCTGTC[A/G]GGTCTGATCTAGTTC | 84333 |