SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs78880136 | snp | C/T | 0.214843 | 0.247516 | intron-variant | HACE1 | GRCh38.p7 | 6:104705939 | ATTTATATTAAAGGG[C/T]GGAAGATAATAACTT | 57531 |
rs78882404 | in-del | -/TAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773763 | AGAATAGATAAGGAG[-/TAA]ACTTTTTTAAAAAAA | 57531 |
rs78916577 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104849522 | TTTTTTTTTTTTTTT[C/T]TGTAGAGAAGAGACC | 57531 |
rs78928985 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | HACE1 | GRCh38.p7 | 6:104726459 | ATTTTAGAAACAGTA[G/T]GACAAACAAAACATG | 57531 |
rs78932280 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104808577 | ATTCAAATACAAAGA[A/C]AACAGTTTCAGTAGT | 57531 |
rs78991390 | snp | C/T | 0.0127726 | 0.0788871 | intron-variant | HACE1 | GRCh38.p7 | 6:104777337 | CTCAAAAAATAAGAG[C/T]AAAATATGTTAGCAG | 57531 |
rs79031856 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856439 | CTTCCTTTTATTTAT[G/T]TGTTTTTTTTTTGAG | 57531 |
rs79080215 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104830494 | ATTAAACATAAGACA[A/G]TGTCACCTTTGCCTA | 57531 |
rs79083306 | snp | A/T | 0.0693013 | 0.172766 | intron-variant | HACE1 | GRCh38.p7 | 6:104809135 | CATTCATTCAAAAAC[A/T]TCTACTATGCATCTA | 57531 |
rs79092984 | snp | G/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104843886 | CTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGCC | 57531 |
rs79116406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104745768 | TACAGGGATGTAGAT[A/G]CCCTGTGATTCAAAA | 57531 |
rs79147057 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HACE1 | GRCh38.p7 | 6:104845257 | ATCAACTCAGTAGTA[A/G]GCATAGCCAGGCTCA | 57531 |
rs79160191 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104810342 | AAGGCACATCAGAGA[C/T]CCCAACAAGAAGCTA | 57531 |
rs79171350 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778594 | TTCCTGAGGCTGGTC[C/T]CAAACTCCTGGGCTC | 57531 |
rs79176909 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104686518 | AAAAAAAAAAAAAAA[A/G]GTAACTCAGGCTTGT | 57531 |
rs79177812 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104700144 | GTGGGAGAAAAGACA[A/G]AAAAAAAAAAAGAAA | 57531 |
rs79227838 | snp | G/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104843885 | ACTTTTTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 57531 |
rs79256298 | snp | A/G | 0.0788843 | 0.182262 | intron-variant | HACE1 | GRCh38.p7 | 6:104683741 | GCCTGCACAGATAGT[A/G]GGGATTTGTGGAGTA | 57531 |
rs79351811 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | HACE1 | GRCh38.p7 | 6:104701325 | CCAATAACTACTAAT[G/T]GTTTCAGTCACATCA | 57531 |
rs79372241 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104716898 | ATACAGCGATACCAG[C/T]TGACACCAACTGTAT | 57531 |
rs79373510 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104769054 | TTTTTCTTTTTTAAG[C/T]GATAGGATCTTGCTC | 57531 |
rs79401487 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716239 | AAGATTTTAACACGC[A/C]TCAGTGGTTGAAAGC | 57531 |
rs79411253 | snp | G/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104767216 | AAAAACAGAATTAAT[G/T]ATAATGAGGTTGATG | 57531 |
rs79520232 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104707981 | CTGAATGCTTTCCCC[A/T]TAAGAGCAAGAACGG | 57531 |
rs79597266 | in-del | -/AAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785380 | GGATTAAAAAAAAAA[-/AAA]CAAAACACAACTAGA | 57531 |
rs79615333 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104691142 | AAAATATTCCAACAA[A/T]TCATTAAGAAAATAT | 57531 |
rs79732163 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104700046 | CTTGATGAAAACCAT[A/G]CACAACACTGGTGAG | 57531 |
rs79745800 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104769375 | AAACCTCACCAGATA[C/T]AGTATTCACAGATAA | 57531 |
rs79750043 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104823770 | AATTAAAAAAAAAAA[A/G]AGATGTTTGCTGGCG | 57531 |
rs79771375 | in-del | -/AAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700423 | AGAAAAAAAAAAAAA[-/AAA]GAGAGAAACTAAAAT | 57531 |
rs79797342 | snp | A/G | 0.198014 | 0.244535 | intron-variant | HACE1 | GRCh38.p7 | 6:104813835 | AATGAAACTCAGAAT[A/G]ACAAAGACAGTAAAG | 57531 |
rs79810902 | snp | A/C | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104816073 | AGCAAAACTACAACT[A/C]AAAAAAAAAAAAAGA | 57531 |
rs79818401 | in-del | -/TATATG | 0.489837 | 0.0705577 | intron-variant | HACE1 | GRCh38.p7 | 6:104727131 | ATGGGTATATATATG[-/TATATG]GGTATATAGATACAC | 57531 |
rs79820472 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104798083 | CGAAAAAAAAAAAAA[A/G]GAAAGAAAGAAAGAA | 57531 |
rs79831763 | snp | C/T | 0.0637235 | 0.166737 | intron-variant | HACE1 | GRCh38.p7 | 6:104798245 | GACCTATACTCTTTC[C/T]ACAATAACATTACCT | 57531 |
rs79890500 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | HACE1 | GRCh38.p7 | 6:104751520 | TGTACTCCTAGTTAC[C/T]AGGGGAGGCTGAGGT | 57531 |
rs79900630 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104719327 | TTAAAAAAGATTTCT[C/G]CCATAGGACAAAAAA | 57531 |
rs79900718 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104850098 | GGGATTACAGGCGCA[C/T]GCCATCACGCCGAGC | 57531 |
rs79932330 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689123 | TGAATGAATTCATAA[A/G]GTTGACCAAAGTTAT | 57531 |
rs79936023 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104814806 | CTCACGCTCTTTCTC[C/T]CTCTCTCCTGCCACC | 57531 |
rs79987817 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HACE1 | GRCh38.p7 | 6:104711015 | TTCATTGTTCTTCCC[A/G]GAAGACAAATCTTTT | 57531 |
rs80035411 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104822546 | CAACAGAGTGAAACC[C/T]TGTCTCTAAATAAAA | 57531 |
rs80095095 | snp | G/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104845495 | TTTTTTTTTTTTTTT[G/T]AGACAAGAGTCTCAC | 57531 |
rs80161414 | snp | A/C | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104792654 | GATCAACTCAGTATA[A/C]CACTGGAGGCTATAT | 57531 |
rs80169711 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104837740 | ATCAGGCAAAAGAAA[G/T]AAATAACGGACATTC | 57531 |
rs80186123 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783146 | CATGCTCCAGCCCAC[A/G]TGGTGGCTAGAAAGT | 57531 |
rs80223955 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104704267 | TCAGAAAAGGAGGAA[A/G]TACAACATGTTCTTT | 57531 |
rs80238022 | snp | G/T | 0.234401 | 0.249513 | intron-variant | HACE1 | GRCh38.p7 | 6:104832384 | ATTTTCCTGTTTTTT[G/T]TTGTTGTTGTTGTTG | 57531 |
rs80268864 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | HACE1 | GRCh38.p7 | 6:104723678 | GGAGAACAGAGAAAC[A/T]TGTTTCACATGAAAA | 57531 |
rs80279675 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104719808 | TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTCTTG | 57531 |
rs111064462 | snp | A/G | 0.498908 | 0.0233371 | intron-variant | HACE1 | GRCh38.p7 | 6:104727401 | CATGTATATGTATAC[A/G]AATATATATACACAC | 57531 |
rs111210420 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104727306 | ACGAATATATATACA[C/T]ATGTATGTATACGAA | 57531 |
rs111210421 | snp | A/G | 0.494976 | 0.0498674 | intron-variant | HACE1 | GRCh38.p7 | 6:104727309 | AATATATATACACAT[A/G]TATGTATACGAATAT | 57531 |
rs111210422 | snp | A/G | 0.495407 | 0.0477027 | intron-variant | HACE1 | GRCh38.p7 | 6:104727335 | AATATATATACACAT[A/G]TATGTATACGAATAT | 57531 |
rs111353266 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104832889 | GGGCAACAAAGTGAG[A/G]CCCTGTCTCAAAAAA | 57531 |
rs111385154 | in-del | -/C | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104791203 | AAAGCATGGTGGCTG[-/C]ATATTACATTAAAAA | 57531 |
rs111412865 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HACE1 | GRCh38.p7 | 6:104769287 | CAATCCCCCTGCCTT[A/G]GTCTCCCAAAGCACT | 57531 |
rs111419939 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835557 | GAAAAGAAATGAGAA[A/G]AAGTAGGAAAATTAA | 57531 |
rs111439178 | snp | G/T | 0.021333 | 0.101051 | intron-variant | HACE1 | GRCh38.p7 | 6:104690217 | TAGGCCCTCTCCAAG[G/T]CTTGTCAGTTTTGTG | 57531 |
rs111454775 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104853211 | GGATGACTCTTACTC[A/G]ATGCTGGTGCCACAC | 57531 |
rs111515010 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860547 | CACAGCCTAGTGGGA[A/C]ATCCAAAGGATTTGA | 57531 |
rs111520756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835806 | CACTAAGGACAAAGT[A/C]GATTCTATAAGTTTC | 57531 |
rs111541394 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104856870 | TCCATTACTTAGGGT[A/G]ATACTCAGGTTTTCA | 57531 |
rs111558107 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | HACE1 | GRCh38.p7 | 6:104848553 | AATTCCAATCATTTT[A/G]GTCTGATTTCTCAGA | 57531 |
rs111566392 | in-del | -/A | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104831584 | GCGAGCCTCCGTCTC[-/A]AAAAAAAAAAAGAAA | 57531 |
rs111596303 | snp | C/T | 0.000330721 | 0.012855 | intron-variant | HACE1 | GRCh38.p7 | 6:104744273 | CATATTTCAGAGCAA[C/T]TGTAGACTTCTCAAT | 57531 |
rs111598805 | snp | A/C/T | 3.33923e-05 | 0.00408596 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750411 | CCCTGTAAAAAAGCA[A/C/T]TGATCTGAGGCTGAA | 57531 |
rs111610820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770992 | TTAGGAACCAACTCA[A/G]CACAGCTAGCACAAT | 57531 |
rs111615064 | snp | A/G/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729189 | CAAAATACGTATTTG[A/G/T]GGCTTTATAGACAAT | 57531 |
rs111625990 | in-del | -/CTCT | 0.5 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854014 | ATGTGGTCTCTCTCC[-/CTCT]CTCTCAAAATATTGT | 57531 |
rs111629529 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104796419 | CCAGCCTATTCTAGT[C/T]ATCTTAAGGAGAGAC | 57531 |
rs111633322 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | HACE1 | GRCh38.p7 | 6:104803554 | GGGATGCAAGGCTGG[C/T]TCAACATATGCAAAT | 57531 |
rs111636473 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104746561 | TATGGCTACCATCAG[A/G]TGGCCCCTCCTTGGT | 57531 |
rs111663997 | snp | A/G | 0.252983 | 0.249982 | intron-variant | HACE1 | GRCh38.p7 | 6:104695708 | GGTGCCCACCACCAT[A/G]CCTGGCTAATTTTTG | 57531 |
rs111685928 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104713872 | GAAAATGTGGACCTA[C/G]AGAGGCATGCTCAAC | 57531 |
rs111711027 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104759568 | TGTAGAAGGAAATTT[C/T]TAGCACTAAACGCCC | 57531 |
rs111732820 | in-del | -/A | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104797489 | CTTGTAATACTTTGT[-/A]AAAAAAAAAAAAAAT | 57531 |
rs111774153 | snp | C/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104715920 | ATCTGTACAACAGAC[C/T]CCTATGACATGAGTT | 57531 |
rs111786869 | in-del | -/ACT | 0.0681886 | 0.171594 | intron-variant | HACE1 | GRCh38.p7 | 6:104807881 | AAGACTCACAGAAAC[-/ACT]ACATTATAAAACAGT | 57531 |
rs111802833 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104757136 | ACCTCTAGGGGCAGG[A/C]CGTACCTGAACAAAA | 57531 |
rs111804141 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104839066 | TATCATCTCACCCCT[A/G]TTAAAATGGCTTATA | 57531 |
rs111812600 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104747396 | AGTACACTGGAGCTA[C/T]TCGATACCTTCTCCT | 57531 |
rs111814182 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104783401 | AGTAAGTTTTCTATC[A/T]CCAAAACAACTACCA | 57531 |
rs111815632 | in-del | -/GT | 0.252983 | 0.249982 | intron-variant | HACE1 | GRCh38.p7 | 6:104695495 | TGAATGAGGCACAGA[-/GT]GTGAAGAGAAACAGA | 57531 |
rs111854880 | in-del | -/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104823015 | ATCATAGAAAAAAAA[-/G]CATGATTTACAATAT | 57531 |
rs111897456 | snp | A/G/T | 0.0380029 | 0.132588 | intron-variant | HACE1 | GRCh38.p7 | 6:104696436 | GGATGCTGATCCAAA[A/G/T]CTATACACAGAGTCT | 57531 |
rs111964296 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104832640 | AAGAGATCCACCCAT[C/T]TCAGCCTCCCAAAGT | 57531 |
rs112038948 | snp | A/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104717399 | CTTCTTCGGCCTCCC[A/T]AAGTGCTGGGATTAC | 57531 |
rs112039505 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774099 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTGAGACGG | 57531 |
rs112042686 | snp | A/G | 0.5 | 0 | intron-variant, synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833126 | ACTGACATGCTGCAC[A/G]AGGTCATGGAGTAGT | 57531 |
rs112072588 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104834226 | CCAATCATCAAATAC[C/T]CTGCTTCTCAGATAA | 57531 |
rs112094402 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104785822 | TTAAACAAATGTCTT[C/T]TTTCAATTAAAAAAT | 57531 |
rs112113369 | in-del | -/AC | 0.312104 | 0.242163 | intron-variant | HACE1 | GRCh38.p7 | 6:104732706 | TTATGATATGCATTT[-/AC]ACACACACACACAAA | 57531 |
rs112119485 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852232 | GTGTGTGTGTGTGCG[C/T]GCGTGCGCGTGCACG | 57531 |
rs112142064 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774184 | AAGCTCCGCCTCCCG[A/G]GTTCACGCCATTCTC | 57531 |
rs112213349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104812500 | CTTCTGGATTGAACA[C/T]ATCTGTTCATCTTTT | 57531 |
rs112215701 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104797193 | CTCAATGTTAAGCCA[C/T]GCTTTCACTACGTAG | 57531 |
rs112229978 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794999 | AATAATCATTTCTCA[C/G]TGGCTGCTTATTCCT | 57531 |
rs112245351 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104806439 | TGCACTCCAGCCTGG[A/G]TGGCAGAACAAGACC | 57531 |
rs112255525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722590 | AAATCTAGAGAATAA[A/T]GTAGCAATTCACTTA | 57531 |
rs112259132 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104705866 | TGTAAAAGTTTAAGG[A/G]GGGAAGAAAGTTCAC | 57531 |
rs112264629 | in-del | -/AA | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104837440 | GACATTCATAGGCAG[-/AA]AAAAAAGAGTAAACC | 57531 |
rs112318689 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HACE1 | GRCh38.p7 | 6:104819883 | TACAAAAATTAACTC[A/G]AAATGGATTAAAGAC | 57531 |
rs112319852 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104755567 | CAAAAGAAATGAAAT[A/C]ATAACAAACAGTCTC | 57531 |
rs112323367 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104772510 | GCCAGTGCAGTAAGT[A/G]TTTGCTAGTTTTTGC | 57531 |
rs112410111 | snp | A/C | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104746751 | GTTTCGATATTTGAA[A/C]CATCTGGAGAAATTC | 57531 |
rs112423466 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734549 | TTTGAACTCAAAATA[C/T]AGAGCTCTAATTACA | 57531 |
rs112431776 | in-del | -/A | 0.0704125 | 0.17392 | intron-variant | HACE1 | GRCh38.p7 | 6:104805866 | TAATAATAATAAAAC[-/A]AAAAAAAAACAATTT | 57531 |
rs112457756 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104731870 | AAAGAATTCCCATAG[A/G]AAAAAAAAAAAATCC | 57531 |
rs112476281 | snp | C/G | 0.5 | 0 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683242 | ACCAGCAGAGGGCGC[C/G]AGACCACCAGCGGCG | 57531 |
rs112500733 | in-del | -/TG | 0.5 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852231 | GTGTGTGTGTGTGCG[-/TG]CGCGTGCGCGTGCAC | 57531 |
rs112512899 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840774 | TTCAAGACCAGCCTG[A/G]CCAACATGGAGAAAC | 57531 |
rs112576265 | snp | G/T | 0.0402882 | 0.136092 | intron-variant | HACE1 | GRCh38.p7 | 6:104687260 | ACCAAACACTATATG[G/T]AAGCTGGCTGGGGAG | 57531 |
rs112580715 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104783910 | CAGACCTCTGTACAT[A/C]GTAGGCACTCAGTAC | 57531 |
rs112584345 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | HACE1 | GRCh38.p7 | 6:104727252 | GTATACGAATATATA[C/T]ACATGTATGTATACG | 57531 |
rs112604984 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797496 | ATACTTTGTAAAAAA[A/G]AAAAAAATTAAAAGG | 57531 |
rs112610480 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852246 | GCGCGTGCGCGTGCA[C/G]GGGCATGCAGTACAC | 57531 |
rs112643090 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | HACE1 | GRCh38.p7 | 6:104759814 | GCTAGCAAGACTAAT[A/G]AAGATGAAAAGAGAG | 57531 |
rs112657526 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104701959 | CAGCAATATAAATGC[A/G]TTCATTTCCTGGGAA | 57531 |
rs112681119 | in-del | -/C | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104783379 | AGAATCCTCTTAGAG[-/C]AAGGGAAGTAAGTTT | 57531 |
rs112762719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718687 | CTACACTGATTCTCC[A/G]TTGCTGAACCATCAC | 57531 |
rs112763559 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104803929 | AAGTCAAACTGTCCC[C/T]GTTTGCAGATGACAT | 57531 |
rs112764062 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104820141 | TGGAGTTTGCAGTGA[A/G]CCGAGATTGTGCCAC | 57531 |
rs112770239 | snp | A/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104777524 | TGACTACCTAGAGAA[A/T]TGTATTTTTTTAAAT | 57531 |
rs112772860 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | HACE1 | GRCh38.p7 | 6:104801561 | AGTGGGGGCTAATAT[C/T]TGACATTCTTAAAGA | 57531 |
rs112774848 | snp | C/T | 0.311369 | 0.242351 | intron-variant | HACE1 | GRCh38.p7 | 6:104742872 | gcacacatatgttta[C/T]tgcggcattattcac | 57531 |
rs112776563 | in-del | -/CG | 0.5 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852235 | GTGTGTGTGCGCGCG[-/CG]TGCGCGTGCACGGGC | 57531 |
rs112857354 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699222 | AGACACATAATACTA[C/T]GTTAATGTTCTTGGG | 57531 |
rs112914546 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104732725 | CACACACACAAATGG[C/T]TGAAAATATGCACCA | 57531 |
rs112935756 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852821 | AATTTTAAATATATA[C/T]GGATATTAAATATAT | 57531 |
rs112937216 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | HACE1 | GRCh38.p7 | 6:104825130 | AGAAAATGGCAGAAT[A/G]TATGGATCAAAATGA | 57531 |
rs112957120 | snp | C/T | 0.5 | 0 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727956 | ACAGGCACATGCCAC[C/T]ATGCCCAGCTTATTT | 57531 |
rs112993767 | snp | A/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727721 | AATATATACACACAT[A/T]TATATGTATATGAAT | 57531 |
rs113030068 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104712359 | GGTAGTAAGGTTTGA[C/T]GTTTGTCCCCTCCAA | 57531 |
rs113046238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104708863 | GGGACAAGTGGATAT[C/T]CACATGAAAAGCAAA | 57531 |
rs113063048 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | HACE1 | GRCh38.p7 | 6:104793262 | ATAGAGCGAGACTAC[A/G]TCTCAAAAAAAAAAA | 57531 |
rs113063216 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104823101 | CACTTTTAATATATC[C/T]TACAAAGACATTAAT | 57531 |
rs113076758 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104759704 | TAACTAAGATCAGAG[A/C]AGAATTGAAGGAGAC | 57531 |
rs113079974 | in-del | -/CTAT | 0.289165 | 0.246913 | intron-variant | HACE1 | GRCh38.p7 | 6:104754168 | CTCAGAGCTTGAAGA[-/CTAT]CTGTCCAAAATAAGA | 57531 |
rs113108775 | snp | A/G | 0.000263658 | 0.0114787 | intron-variant | HACE1 | GRCh38.p7 | 6:104796783 | ATCTAAAATTATCCA[A/G]GTTTAAAAACAGTCC | 57531 |
rs113139863 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104798158 | AGCATGAATCCAAAA[A/G]GAACTCTGTAGATGA | 57531 |
rs113148434 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | HACE1 | GRCh38.p7 | 6:104703839 | ATTTATAATGGGCTG[A/G]GCGCGGTGGCTCATG | 57531 |
rs113168563 | in-del | -/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104815371 | ATCTGGTGGAAGAAA[-/T]TTTTTTTTTTTTTTG | 57531 |
rs113185230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104772190 | GCTAAGGTTACATTA[C/T]GTATAAACTTCCAGA | 57531 |
rs113188535 | snp | A/C | 0.0681886 | 0.171594 | intron-variant | HACE1 | GRCh38.p7 | 6:104805466 | ACCCAAATGTCCATC[A/C]GTGATAGACTGGATT | 57531 |
rs113204852 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HACE1 | GRCh38.p7 | 6:104817172 | GTTGAGAAGGGATAA[C/T]TGTATTTTCCAATAC | 57531 |
rs113223055 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HACE1 | GRCh38.p7 | 6:104849852 | AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 57531 |
rs113292040 | snp | G/T | 0.0543475 | 0.155628 | intron-variant | HACE1 | GRCh38.p7 | 6:104832387 | TTCCTGTTTTTTGTT[G/T]TTGTTGTTGTTGTTG | 57531 |
rs113354600 | in-del | -/TTATA | 0.43655 | 0.16643 | intron-variant | HACE1 | GRCh38.p7 | 6:104710234 | TCAAAAGGGCACATC[-/TTATA]TTATATTATTCCACT | 57531 |
rs113382352 | in-del | -/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104823116 | CTACAAAGACATTAA[-/T]TTTTTTTTAAGAGAG | 57531 |
rs113449711 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104820964 | CGATGGTAGACTGGA[C/T]AAAGAAAATGAGGTA | 57531 |
rs113495010 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104821039 | CAATGTCCTTTTCAG[A/G]GACATGAATGGAGCT | 57531 |
rs113495552 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104735686 | AAAAGGAGTACATTC[C/T]CTCATTCTCTACTGA | 57531 |
rs113583558 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | HACE1 | GRCh38.p7 | 6:104720119 | AAGTGCTGGGATTAC[A/G]GGCGTGAAGCCACTG | 57531 |
rs113591574 | snp | A/G | 0.0681886 | 0.171594 | intron-variant | HACE1 | GRCh38.p7 | 6:104803635 | ATTATCTCAATAGAT[A/G]CAGAAAAGGCCTTCG | 57531 |
rs113592836 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104792225 | AGGTTTGTTCTCTAC[A/C/G]TAACGGGCTGCCTTA | 57531 |
rs113596687 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104848094 | TGACCTCAGATGATC[C/T]GCCCGCCTTGGCCTC | 57531 |
rs113610651 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104758081 | ATTTGATTGGTGTGC[C/T]TGAGAGTGACGGGGA | 57531 |
rs113652191 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104753594 | TGATACCTCCAGGTA[A/T]GGGAGAAACCAAGGC | 57531 |
rs113653168 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104824478 | CATGTGTGCCCAAAG[A/G]TTAAAACTTAGATAG | 57531 |
rs113734617 | snp | C/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104690133 | CAGGAGCTGCCTCTC[C/G]CTGTCATAAGGGCAT | 57531 |
rs113737385 | snp | C/T | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104836184 | AGACATTCCAAACAA[C/T]TGTGCAGCAGACCTA | 57531 |
rs113739197 | in-del | -/TAAGT | 0.276267 | 0.248616 | intron-variant | HACE1 | GRCh38.p7 | 6:104711573 | CTAGCCTCTCGTGCA[-/TAAGT]TAATGATCACTGCAT | 57531 |
rs113790415 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104801093 | TTCAATAGCCGATTC[A/G]ATCAAGTGGAAGAAA | 57531 |
rs113821694 | in-del | -/A | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104794899 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAATA | 57531 |
rs113830176 | snp | C/T | 0.5 | 0 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682831 | CCTGAGGATGAGGCG[C/T]TTCTGCCTAACTTCT | 57531 |
rs113857615 | snp | C/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104846360 | CACAACCTAAGAACA[C/T]ACAATAATTTTAAAG | 57531 |
rs113875487 | snp | C/G | 0.00458211 | 0.0476451 | intron-variant | HACE1 | GRCh38.p7 | 6:104744238 | CAGAACCACTAACAA[C/G]AAGAACAAAAAACTT | 57531 |
rs113887672 | snp | A/G | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104782689 | AGTACCTGACCTAAA[A/G]TCAGTAAATGTAAGT | 57531 |
rs113904752 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | HACE1 | GRCh38.p7 | 6:104694188 | ATTCAGCCACACACA[A/C]AAAAAAAGATTCTGT | 57531 |
rs113914131 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104694039 | AGAAAGGAAATCAGT[A/C]TATCGAAGAGATATC | 57531 |
rs113923310 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104701969 | AATGCGTTCATTTCC[C/T]GGGAATCAAACTCAA | 57531 |
rs113945003 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | HACE1 | GRCh38.p7 | 6:104688291 | GAATCCCCACTCCTG[A/G]TAAGACAGAAGAGAG | 57531 |
rs114115380 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | HACE1 | GRCh38.p7 | 6:104746196 | CTGTTTTAATTTCAA[A/G]TAAATATCCATTGAC | 57531 |
rs114133783 | snp | A/C/T | 0.0178198 | 0.0927755 | intron-variant | HACE1 | GRCh38.p7 | 6:104735100 | AACCACAAAGGAAAG[A/C/T]AATGATAATCAATTT | 57531 |
rs114134099 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | HACE1 | GRCh38.p7 | 6:104781734 | CAACCACCGCCAACA[C/T]GGACATCCTCCTTAT | 57531 |
rs114178936 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104847627 | GTTTTAATCTTTATA[C/T]GCAAAAATTTGGCCT | 57531 |
rs114212234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707645 | TTCTGTGTCTGTGAA[A/G]CCCTCCTTGCTGCAT | 57531 |
rs114294940 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | HACE1 | GRCh38.p7 | 6:104786566 | CTGTGATCATGTCAC[A/T]ATACTCCAGCCTGGG | 57531 |
rs114448623 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766610 | TATAAGACTAGCAAT[A/G]AAACCATATTAAAAT | 57531 |
rs114462284 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | HACE1 | GRCh38.p7 | 6:104842356 | CACACCTGTAATCCT[A/T]GCACTTTGGGAGGCC | 57531 |
rs114516566 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HACE1 | GRCh38.p7 | 6:104704316 | TAATAAAAGAAAGTC[A/G]GCATTGGAAAAACAT | 57531 |
rs114520127 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HACE1 | GRCh38.p7 | 6:104683364 | TTATTAAACCTCATG[A/G]CCAGAACACTAACAA | 57531 |
rs114564400 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104841886 | AATAATGACAATTTG[A/G]TTAAAACTTTGGGAT | 57531 |
rs114578831 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | HACE1 | GRCh38.p7 | 6:104693090 | GGGTGGGGGTAGAAC[A/G]CATACATTTTTTCTT | 57531 |
rs114592795 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104834479 | GGACTATGCTATCCA[G/T]TAATTTTTCACATGA | 57531 |
rs114609754 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104731471 | GATTTGAAAACTTAT[A/T]ACAAAGCTGTGGTAA | 57531 |
rs114625591 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | HACE1 | GRCh38.p7 | 6:104703639 | AACACCTCTACTCCT[C/T]TCCCATTCTAACTTC | 57531 |
rs114640264 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104770750 | AATAATCAAGTTATA[C/T]AGTCAAAAAAATATC | 57531 |
rs114642305 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858868 | GAGTTTTACCTGTCC[C/T]GAGGGAACCCTGGCA | 57531 |
rs114705739 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HACE1 | GRCh38.p7 | 6:104757637 | CCAGAACACCTCTTC[A/G]CCTCCAAAGGAACAC | 57531 |
rs114769698 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104795035 | GGGTAGCCAGCCACA[C/T]AGAAAGAAGTGTAGC | 57531 |
rs114792223 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104780673 | TACAAACAAGGGAAT[C/T]TTCCTCTATAACTAG | 57531 |
rs114808547 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104718061 | CTAAGGTTTGTGCTT[C/T]TGGAGTCTTATTTAT | 57531 |
rs114894136 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | HACE1 | GRCh38.p7 | 6:104694271 | ACAGACACAGAGAGA[C/T]GAACTTCACATTTTC | 57531 |
rs114899491 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104723700 | ACATGAAAAAATCTT[A/G]ACTGCTGATACACAC | 57531 |
rs114914086 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | HACE1 | GRCh38.p7 | 6:104768271 | TTCAATAGTTCAAAA[G/T]TATAAAGTCGAACTC | 57531 |
rs114975606 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104752821 | ATTATTTTCCACATG[C/T]ATTTCAGTAACCCAG | 57531 |
rs114983543 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104699642 | ATGTACCCTCAGTAA[C/T]GGGAGAGTTGAATGG | 57531 |
rs115055563 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104704644 | TCTAGCCTCTGGACT[C/T]ACTTTTTACTAGGAT | 57531 |
rs115115128 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104704417 | AAAAGTAGAGGTCAT[A/G]AGTCACATTCCTTAA | 57531 |
rs115118923 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104747662 | TATCACTAACACATG[C/T]TCTATGACCATGAAC | 57531 |
rs115205861 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | HACE1 | GRCh38.p7 | 6:104788112 | GGTAGCAGCCACCAA[C/T]AAAAAGGATTCAAAT | 57531 |
rs115220680 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104756939 | ATGGAGCCTTGCTTG[C/T]TGCCAGCACAGGAGT | 57531 |
rs115235203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709309 | ACTAAGTACATGAAA[A/G]GATGTTCATCCAATG | 57531 |
rs115279741 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104749046 | ATATCATAACCCAAA[A/G]TTTTATAAACTTATT | 57531 |
rs115294815 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104834679 | AGCAAAGAAAGTAGA[C/T]GATGCTTTTTATCTT | 57531 |
rs115546031 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104718135 | AGGTTTTATCTGTAG[A/T]TTTTTTTGTGTGTGT | 57531 |
rs115612892 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104733732 | TGTGTGCACCTGTAA[C/T]TGGAGGCTAAGGAAG | 57531 |
rs115637480 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | HACE1 | GRCh38.p7 | 6:104829059 | CCCCATTTAAAGTTT[A/T]CTATTTTATTCTATA | 57531 |
rs115687188 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104794260 | GTAAACTTAAAAACA[C/T]AGATACATCAAAACA | 57531 |
rs115700886 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104708690 | CAAGGCTACAGTAAT[A/C]AAGACAATACAAGAC | 57531 |
rs115704825 | snp | A/T | 0.030278 | 0.119257 | intron-variant | HACE1 | GRCh38.p7 | 6:104768895 | ATTTATTCAATATTT[A/T]CCATCTTTCTAGATT | 57531 |
rs115839837 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | HACE1 | GRCh38.p7 | 6:104813017 | GAGCAAAGATGAGGA[A/G]CCATCGTGAAAACAA | 57531 |
rs115843056 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104838352 | ATGTTACTGGTATAA[A/G]AACAGACACACAGAC | 57531 |
rs115849592 | snp | A/G | 0.0379877 | 0.132479 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851719 | AATTATACCAGGTAG[A/G]AAATTTAAAACAAAA | 57531 |
rs115889177 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | HACE1 | GRCh38.p7 | 6:104783135 | TTTTCGGTCTACATG[C/T]TCCAGCCCACATGGT | 57531 |
rs115967454 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104823153 | ACTTGATTAAAAAAT[C/T]GGAGGCTGGGCACAA | 57531 |
rs116021472 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104708457 | CCTGTATTTGTGGGT[C/G]TCTAGAAGATTTGTT | 57531 |
rs116046078 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | HACE1 | GRCh38.p7 | 6:104712528 | CTCATAATCCCAGCA[C/T]ATTGGGAGGCTAAGG | 57531 |
rs116092472 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104732761 | GTCTATTTGAAATCA[C/T]TGATATGTATACATC | 57531 |
rs116187646 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | HACE1 | GRCh38.p7 | 6:104857164 | ATATATATTTACATA[C/T]ATATATTTATTTACA | 57531 |
rs116196642 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104816203 | TACATAAGTAACAAG[A/G]AGCTGAATGTTAATA | 57531 |
rs116197011 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104714955 | AATAATTTAGCACTC[A/C]TACCCGTATTATCTG | 57531 |
rs116197167 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | HACE1 | GRCh38.p7 | 6:104756905 | CCCTTCTGTGCCTGG[C/T]TCAGAGGGTCGCATG | 57531 |
rs116219390 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HACE1 | GRCh38.p7 | 6:104839699 | ACATAAACATACACA[C/T]ACACATACAATTAAA | 57531 |
rs116228459 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HACE1 | GRCh38.p7 | 6:104727476 | ATGAATACACACACA[C/T]ATGTATATGAATACA | 57531 |
rs116273598 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104753244 | TTTGGTATCTCACTG[A/G]GACCGAGCTCCGGGG | 57531 |
rs116303180 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104723442 | TTTCTCACCTGTAAA[G/T]TGAAGGGACTAATTA | 57531 |
rs116316537 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | HACE1 | GRCh38.p7 | 6:104693353 | AGGCTTGCTATTTAA[C/T]GAATTTCATATGAAA | 57531 |
rs116418167 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104818171 | AAAACTATATTATAA[C/T]CTATGTAATTCCTCT | 57531 |
rs116505342 | snp | A/T | 0.00406623 | 0.0449064 | intron-variant | HACE1 | GRCh38.p7 | 6:104744140 | AATTATTTCCATATT[A/T]TCATAAAAATACTGC | 57531 |
rs116587914 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104799753 | ACAATTTAGTCTCAA[G/T]ACTCCCATTCCAAGA | 57531 |
rs116616660 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | HACE1 | GRCh38.p7 | 6:104816410 | GCTCCAGCCATGGCT[A/C]AAAGGGGCAAAGGTA | 57531 |
rs116628751 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104734800 | TTCTAGTGTTTTACT[C/G]TATAGGAGCAGCCAC | 57531 |
rs116787520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104771585 | TTTCACATTGTTACA[A/G]TGTAATCTTTCTTTG | 57531 |
rs116791654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696759 | ACTGTGCCATTCTGA[C/T]TAGCTACTAGCCTAA | 57531 |
rs116825765 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104707498 | CTTCTGGATAAAACC[A/G]CTTACCAAACTGGGA | 57531 |
rs116828750 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104766910 | GCTTGAAATTTACAG[A/T]CTGCATGGAGAAAGC | 57531 |
rs116846728 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104751266 | CCAACTTCTAAAAAG[G/T]GGCTGCCACTTTGAA | 57531 |
rs116848899 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104830271 | CACTCAAGATTAGGA[C/T]ATTTCACATCTTTTT | 57531 |
rs116935456 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104789452 | AATAAGAAAGTATTT[A/G]TATATTATATATATC | 57531 |
rs116963011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716863 | AACTTTTTAATAATT[C/G]GGAAAATGAAAATTA | 57531 |
rs116963735 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | HACE1 | GRCh38.p7 | 6:104732280 | ACAGCAGCATTATTC[A/G]CAATAGCCAAATGGT | 57531 |
rs117000026 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104725450 | CCCATATATATTCTA[C/T]TTCACATTAGTCATT | 57531 |
rs117086465 | snp | C/G | 0.0364509 | 0.129988 | intron-variant | HACE1 | GRCh38.p7 | 6:104774024 | AACTAAGCATTTTCA[C/G]ATATCAGCTAACTGA | 57531 |
rs117087313 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104794679 | GAGGCCGAGATGAGC[A/G]GATTGCCAGAGCTCA | 57531 |
rs117184555 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104750838 | ATTTTTGCCCCTGTA[A/C/T]TGATGCTTCTCCACA | 57531 |
rs117242905 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104765450 | ATCAGCTGTAGTCAG[G/T]GTCTTTCTGAGGCAA | 57531 |
rs117270660 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104733733 | GTGTGCACCTGTAAT[A/T]GGAGGCTAAGGAAGG | 57531 |
rs117272607 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | HACE1 | GRCh38.p7 | 6:104689275 | AGGAAAACTAATGAA[A/G]TGCTCAACTTTTTCC | 57531 |
rs117288462 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104832635 | AGCTCAAGAGATCCA[C/T]CCATCTCAGCCTCCC | 57531 |
rs117288598 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | HACE1 | GRCh38.p7 | 6:104763836 | GGGCAGATCACTTGG[A/G]GTCAGGATATCGAGA | 57531 |
rs117327166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697816 | ATGATCTCGGCTCAG[C/T]GCAACCTCCATCTCC | 57531 |
rs117330697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104824133 | TACTGAGCCTTGTTC[A/G]GAAGGTGAGCCCTCC | 57531 |
rs117382733 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104803145 | GGACTAAACCAGGAA[A/G]AAGTTGAATCTCTGA | 57531 |
rs117421060 | snp | A/G/T | 0.00398691 | 0.0444912 | intron-variant | HACE1 | GRCh38.p7 | 6:104793576 | TCCAAAAGTGTGCTG[A/G/T]ATAACACCTTAGTTG | 57531 |
rs117467230 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | HACE1 | GRCh38.p7 | 6:104818494 | TTCCCATTCAAACTA[C/T]TCCAAAAAATTGAGA | 57531 |
rs117529879 | snp | A/G | 0.0584853 | 0.160693 | intron-variant | HACE1 | GRCh38.p7 | 6:104726537 | AAGCTTGCGTTTCCC[A/G]ATACCCAAAAGACTG | 57531 |
rs117547313 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | HACE1 | GRCh38.p7 | 6:104691361 | AAACAAGGGCTCTTA[C/T]ACAGTGTTGTTGGGA | 57531 |
rs117583354 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104846296 | CCCTTTATGAGCTCA[C/T]AATCACCTAAAAAAT | 57531 |
rs117667670 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104764062 | AAACAAACAAACAAA[A/C]AAAAAGTACTGCACA | 57531 |
rs117711728 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | HACE1 | GRCh38.p7 | 6:104750963 | CTCTCTTGCTCAAAA[C/T]CCTATAATGACTTCT | 57531 |
rs117741526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709684 | CCAAATAAACCTCTT[C/T]TCTTTGTAAATTATC | 57531 |
rs117926886 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104791071 | GCAAACCCAGTAAAT[C/G]AAAGTACCTTACTTT | 57531 |
rs117929323 | snp | G/T | 0.0663309 | 0.169604 | intron-variant | HACE1 | GRCh38.p7 | 6:104720664 | CGGAGTTTTGCTTTT[G/T]TTGCCCAAACTGGAG | 57531 |
rs117993096 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104789995 | CTAACTAGAGCTCAA[G/T]GAAGTGGTACGTGAA | 57531 |
rs118024091 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104766912 | TTGAAATTTACAGAC[C/T]GCATGGAGAAAGCTA | 57531 |
rs118026640 | snp | A/G | 0.0165278 | 0.0893908 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861888 | ACAGAACTTTCTGCA[A/G]TGATAGAAATATTCT | 57531 |
rs118061297 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860384 | CGGCTTTATGAGGGC[A/G]GGGACATTTAATCTT | 57531 |
rs118112134 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104825341 | TGAAAGTACCACTGA[C/T]TGGTTGTAAAAAGCA | 57531 |
rs118142482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104705618 | ATGGTGCTGGACTCA[C/T]CATGGGCATGTTTTC | 57531 |
rs137858316 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104818223 | CTATAGCTTTCAAAT[A/G]TAAGAAAAACAAGTA | 57531 |
rs137863013 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104846304 | GAGCTCATAATCACC[G/T]AAAAAATAAAGAAAA | 57531 |
rs137903606 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104734012 | ACAAAATTAGCTGGG[C/T]ATGGTGGTAAGCGCC | 57531 |
rs137915497 | snp | A/C | 0.0221141 | 0.102801 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859992 | GCGCCCAGGCCACGC[A/C]AACGCGGGCGCAGGG | 57531 |
rs137939187 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729608 | ACATTTTCCCAAATT[A/T]CTTCTGCCATTCTGA | 57531 |
rs137941861 | snp | A/C | 4.94548e-05 | 0.00497242 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785184 | CAAATGGAGGAATGG[A/C]AGCAGCATCTTGATC | 57531 |
rs137942840 | snp | C/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104780819 | CCTTTAATTGTCCTG[C/T]CCTGTCTCCTTCACT | 57531 |
rs137973780 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104810862 | AGAGAAAGAAAAGAC[A/G]TGGCTCTGGATCAAG | 57531 |
rs137986300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104692375 | ATGGAGGAAAACTTG[C/T]ATTTTTTTAAATTTT | 57531 |
rs137992468 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104767084 | TAAGGCTGTTTCCAC[A/T]CTAAATAAAGAGAAA | 57531 |
rs138002694 | in-del | -/GTGTGTGTGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693023 | TCTGTCCAAAGAGTG[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 57531 |
rs138016166 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104683563 | CAGGTTTGCTATGAA[A/G]GCTGATAAATAAAAG | 57531 |
rs138016258 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728276 | AGGCAGTGACTTCTA[C/T]AATTAAATTTCAAAA | 57531 |
rs138056014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727160 | AGATACACATACATG[C/T]ATACGAATATATATA | 57531 |
rs138067677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806248 | TGGAGAATCACTTGA[A/G]GCCAGGCGTTGAAGA | 57531 |
rs138099979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104845131 | GCAAAAGTAATGGTG[A/G]TTTTTGCCATTACTT | 57531 |
rs138117738 | in-del | -/AC | 0.366266 | 0.221319 | intron-variant | HACE1 | GRCh38.p7 | 6:104727489 | CATATGTATATGAAT[-/AC]ACACACACATATGTA | 57531 |
rs138131289 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104687630 | AAAGGCTTCTCTCTC[A/G]AAGGCCTTTCCCACA | 57531 |
rs138164464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721599 | ATCGAACAGGAAGTC[A/G]GTGACTTCTCCCCTT | 57531 |
rs138177488 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104831657 | CCAGCATTTTAGGAG[G/T]CCGAGGCAGGCGGAT | 57531 |
rs138217957 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HACE1 | GRCh38.p7 | 6:104799432 | CTCATTACTTACAAA[C/T]TGCTGGGAAGAGCTC | 57531 |
rs138247063 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104781302 | ATTCAAGCTGTCTTC[C/T]GAGTCATGTTAACAT | 57531 |
rs138295108 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104826193 | TCTGACTGTGGAAAA[C/T]TTGTCTTCCATGAAA | 57531 |
rs138330323 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | HACE1 | GRCh38.p7 | 6:104802187 | CTAAATATATATGCA[C/T]TCAACACAGGAGCAC | 57531 |
rs138332428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754085 | AATGGAGCTGAAAAA[C/T]ACAACATGAGAACTT | 57531 |
rs138355319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772935 | AAATAGATAGTGGCC[A/G]ATGGTTGCACAACAC | 57531 |
rs138356364 | snp | C/T | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744213 | TTGAGTAATGTCTTC[C/T]ACAACTTCCCAGAAC | 57531 |
rs138359520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854856 | TATTTTACTGTGAGT[A/G]TATACATGAAAAACA | 57531 |
rs138376240 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104830813 | ATTCACTAGCATGAT[C/T]CCACAAACAGACCAG | 57531 |
rs138407199 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774390 | CCACCGCGCCCGGCC[G/T]CTCTTTTTTTTTTGA | 57531 |
rs138407487 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104752266 | TTATAGAGAGGGAGA[C/T]AGAAATGTGTACCCA | 57531 |
rs138432418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104841918 | TCAACAATCTCTTCA[A/G]CAATATCCCATACCA | 57531 |
rs138435903 | in-del | -/ATCT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754167 | CCTCAGAGCTTGAAG[-/ATCT]ACTGTCCAAAATAAG | 57531 |
rs138476843 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729098 | TCAACTGTTAGTATC[A/C]TCAGTCTAAATTTTA | 57531 |
rs138483788 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104707846 | CATTACAATGGAAAT[G/T]AAGTTTCAACATGAA | 57531 |
rs138506667 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HACE1 | GRCh38.p7 | 6:104807231 | GTTTCACCATGTTGG[C/T]CAGGATGGTCTCAAT | 57531 |
rs138558454 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104734998 | GTTTAAAAATTGGAA[C/T]GTAAAAACAGAAATT | 57531 |
rs138567482 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104818523 | GAAGGGACTATTCCC[G/T]AACTCATTCTATAAA | 57531 |
rs138605212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104812228 | CAATAGGTGGCTTGA[A/G]GCCAGTAGTTTGAGA | 57531 |
rs138630229 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104683339 | ATTATTATTATTGTT[A/C]CCATGTTATTTATTA | 57531 |
rs138652228 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726496 | GGAATCATCTCCTGG[A/G/T]CCTCCAACTTGTGAG | 57531 |
rs138652812 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104696821 | GAAACATATAGGGTC[C/T]GCTTGCCCCTACTTG | 57531 |
rs138656573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805754 | AGAAACACCTAATGT[A/C]AATGACGAGTTGATG | 57531 |
rs138660467 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104691482 | CATCAAAATTAAATA[G/T]CTGTGAAACCTTTAC | 57531 |
rs138666748 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104766539 | TTTGTGCTTGTATGT[A/G]CATTAAATGTGTATG | 57531 |
rs138689202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821336 | CCCCTGAACTCAAAA[C/T]AAAAGTTAAAAAAAA | 57531 |
rs138708989 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104763253 | AACTGTAGACTTACA[C/T]TACCTGTTTTAAAAG | 57531 |
rs138728785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104699864 | ATCAGGCCTCCCTCG[A/G]CTGAGGCAGGCCTGC | 57531 |
rs138745891 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104792875 | CTCCTCCCTGCTCTT[C/T]CTACCCAATAAATAC | 57531 |
rs138791274 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104826533 | CCATGAAGTCCAAAA[A/C]ACCTAACAATTGTGA | 57531 |
rs138904903 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104836190 | TCCAAACAACTGTGC[A/G]GCAGACCTAGGTATC | 57531 |
rs138917853 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791532 | CTTCTTGGAGTTTTA[C/T]TCCCATTGTAGCCCA | 57531 |
rs138945872 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104758109 | GGAGAATGGAACCAA[C/G]TTAGAAAACACTCTT | 57531 |
rs138949698 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697052 | TGTTTGTCTTTTTGA[C/T]AACTTTCAAAGCTGA | 57531 |
rs138975990 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104708524 | AAATTCAATGCAATC[C/T]GTGTCAAATCTCAAC | 57531 |
rs138982130 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104785955 | TGGCATATTTATGTA[C/T]ATACATATACTTACA | 57531 |
rs139057166 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104684972 | GCTTTAGACAAGGAC[A/G]TGAGAGAGGAAGTCC | 57531 |
rs139062351 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104761027 | GGAGAACTACAAACC[A/G]CTGCTTTAAGGAAAT | 57531 |
rs139067630 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104713418 | ATATATTGAGCACTT[A/C]ATATTTTCCATAAAT | 57531 |
rs139071780 | snp | A/G | 0.030278 | 0.119257 | intron-variant | HACE1 | GRCh38.p7 | 6:104760084 | CTAAAAAAAGTCCAG[A/G]ACCAGTGGATTCACA | 57531 |
rs139124821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104743009 | GAGTTCATGTTCTTC[A/G]TAGGGACATGGATGA | 57531 |
rs139130194 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104823231 | CTGAGGTCAGGAGTT[C/T]AAGATCAGCCTGGCC | 57531 |
rs139149946 | snp | C/T | 0.221439 | 0.248363 | intron-variant | HACE1 | GRCh38.p7 | 6:104720893 | ATCCGCCTGCCTCGG[C/T]CTCCCAAAGTGCTGA | 57531 |
rs139211039 | in-del | -/AAAAGAAATGAGAAA | 0.49334 | 0.057322 | intron-variant | HACE1 | GRCh38.p7 | 6:104835543 | CCTAAAAGTACAAAG[-/AAAAGAAATGAGAAA]AAGTAGGAAAATTAA | 57531 |
rs139217182 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723757 | TAACCAAATTTTTAT[A/G]TTTTTTTTATTTTAC | 57531 |
rs139231075 | snp | A/G | 1.65239e-05 | 0.00287431 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776813 | TATCAAACCACTCAC[A/G]CACAACACCTTGACC | 57531 |
rs139234567 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104818884 | AGGTATTGAAGGAAC[A/T]TACCTCAAAATAATA | 57531 |
rs139253264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709274 | AGAAATTTCTCCAAA[A/G]GAAGAGATATAAAAT | 57531 |
rs139315027 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | HACE1 | GRCh38.p7 | 6:104694541 | ACAAAGGATAAATGC[G/T]TGAGGTGATGGATGC | 57531 |
rs139318534 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104855429 | GCCTGGGCAACAGAG[C/G/T]GAGACTCCATCTCGG | 57531 |
rs139368310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858631 | TATCCTACAAACCAC[C/T]CAGCAGCAATTCAAA | 57531 |
rs139390243 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104776249 | ATATCATGATTTCTA[A/G]ACTTGGGTTTTCCTA | 57531 |
rs139401838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104846982 | TTGCTGAATAGCTAT[A/G]TGAATCATGTAATAT | 57531 |
rs139422742 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104764330 | TGATCCACTCACCTC[A/G]GCCTCCCAAAGTGCT | 57531 |
rs139437562 | in-del | -/T | 0.0126979 | 0.078662 | intron-variant | HACE1 | GRCh38.p7 | 6:104781331 | ATAACCCCATCAGTC[-/T]TTGAACACTTCCTTA | 57531 |
rs139466283 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104735883 | AAGAATCAATTAAAG[A/G]AAGTCCCTAAAAATA | 57531 |
rs139481190 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724739 | AAAACAAAATGCTAA[C/G]TAAATAAAGAAGATA | 57531 |
rs139542832 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104832956 | TAATGCTTCATGTTC[C/T]CAAATATGCACAATG | 57531 |
rs139549761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782990 | GGCTCCTAACAGCCT[A/G]GCAAACAAAGAAAAT | 57531 |
rs139586271 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104717805 | CTTTTCATATACTTG[C/T]TAGCTAGTCAGACTT | 57531 |
rs139592577 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104800272 | CCTCCATAGACTCCA[C/T]TTCTGTGGGCAGGGC | 57531 |
rs139624197 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104793448 | AATATATAGAAAGGA[C/T]GATAAAATTTCATTT | 57531 |
rs139666282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747230 | TCATGAAAGTATTCA[C/T]AGGCATCAGCTTACC | 57531 |
rs139682460 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104857774 | CATCCTAGCTAACAC[A/G]GTGAAACCCCGTCTC | 57531 |
rs139705105 | snp | C/T | 6.7981e-05 | 0.00582974 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796727 | CGGGTGATATTGAAT[C/T]AATACTTCACAAGTC | 57531 |
rs139705484 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710469 | TTGTTGTGAGGATAA[C/T]GGACACCAAATTTAC | 57531 |
rs139710697 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104788236 | ATACCATTTGTTACC[C/G]AACAATGAGTTAATT | 57531 |
rs139712518 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837054 | GACTCAATCAACACA[A/G]TAAAGATAACAATTC | 57531 |
rs139749028 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104801121 | AAAGGATATCAGTGA[C/T]TGAAGATCAAATTAA | 57531 |
rs139751098 | in-del | -/CT | 0.367503 | 0.220665 | intron-variant | HACE1 | GRCh38.p7 | 6:104721612 | TCGGTGACTTCTCCC[-/CT]TTTAGCCTCTTGCTT | 57531 |
rs139757180 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104815528 | CACCACACCCAGCTA[A/G]TTTTTTCTGTTTTTA | 57531 |
rs139790020 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | HACE1 | GRCh38.p7 | 6:104759252 | AGAATATAGATTCTT[C/T]TCAGCACCACATCGC | 57531 |
rs139802412 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104731888 | AAAAAAAAAATCCCG[A/G]TTAAAAATGGGCAAA | 57531 |
rs139875915 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104760698 | GAAATTCTGGCCAGG[A/G]CAATCAGGCAAGAGA | 57531 |
rs139963182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851514 | GCTGGTGCTGAAGGT[C/T]TCCTCATCTGCCACT | 57531 |
rs139964321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807905 | TAAAACAGTGCCCAG[A/G]GCCAGGCACGGTGGC | 57531 |
rs139998496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697950 | TGGTCTTGAACTCCT[A/G]ACCTCAGGTGATCCC | 57531 |
rs140003796 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | HACE1 | GRCh38.p7 | 6:104775112 | TTTGGGAGGCCGAGG[A/C]GGGTAGATAACCTGA | 57531 |
rs140022767 | snp | A/C/T | 4.94233e-05 | 0.00497087 | intron-variant, synonymous-codon, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833042 | CATGGCTCAACTTAC[A/C/T]GTCTTGTGACCGTTC | 57531 |
rs140033038 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104685426 | CCAGGCTTTCAGAGC[A/G]AACACAGCTCAGCAT | 57531 |
rs140033079 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104730521 | ATCCAACTCTAGGAC[A/C]ATGACAACACGACAC | 57531 |
rs140044971 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104814845 | AAGATGCTTGCTTCC[C/T]CCTTTGCCTTCCACC | 57531 |
rs140049272 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104822932 | CTTACAATATAAAAA[C/T]AATTTATTCATTAGA | 57531 |
rs140051988 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104750877 | AGAGTGATTTAAAAA[A/T]ATATATATGTGTATA | 57531 |
rs140136491 | snp | A/G | 9.88712e-05 | 0.00703035 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772027 | ACCGAAAATAGTTCA[A/G]GTGATCAGGATTTAC | 57531 |
rs140136704 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104808820 | AGTAAAATTAAAAGT[A/G]TGCCTGCAGAAGAAC | 57531 |
rs140137656 | snp | C/T | 0.26271 | 0.249677 | intron-variant | HACE1 | GRCh38.p7 | 6:104740155 | ccagaatctctggga[C/T]gcattcaaagcagtg | 57531 |
rs140142086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794638 | GCCAGGCGCATTGGC[A/G]CACGCCTGTAATCCC | 57531 |
rs140171026 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104759564 | AATGTGTAGAAGGAA[A/G]TTTTTAGCACTAAAC | 57531 |
rs140176828 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | HACE1 | GRCh38.p7 | 6:104733581 | TAATTGGCCAGGCGC[A/G]GTGGCTCACGCCTGT | 57531 |
rs140188755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104817462 | AACCTTCCACCATGA[C/T]TGTAAGTTTCCTGAG | 57531 |
rs140204194 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104689685 | CTGTGGAGAGCAAGG[C/T]CACGTGCTACCTTAA | 57531 |
rs140217940 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859938 | AACTGTAGTTTCCAG[C/T]TGGCAGAACGGAGCG | 57531 |
rs140258164 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104715014 | GCAATCTTTGATTGA[C/T]GGGATATGAAAGCTA | 57531 |
rs140305854 | in-del | -/TAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756428 | AAAAAAAAAAAAAAA[-/TAT]ATATATATATATATA | 57531 |
rs140324770 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104770156 | GAACATTGTTTCTTA[A/T]AGTTAAATTGATTCT | 57531 |
rs140328377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692662 | TACACTTTTGAACCT[C/T]GAGTTTCTCAACTAT | 57531 |
rs140343186 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104766684 | ACATTCACTGCCTTA[C/G]TAAATGAGAAGCCTA | 57531 |
rs140387014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810630 | GTGTATAATTATACT[A/G]ATAGCTCCTTAGGGA | 57531 |
rs140403427 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104698968 | GCAATTCTCCCACCT[C/T]GGCCTCCCAAAGTAC | 57531 |
rs140417888 | snp | C/T | 6.59402e-05 | 0.00574158 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785173 | TCCTGGAGGTTCAAA[C/T]GGAGGAATGGAAGCA | 57531 |
rs140432320 | snp | A/G | 0.0146672 | 0.084371 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853902 | TTTTCCCTACATGAT[A/G]AAGTTTAATTTATAA | 57531 |
rs140447734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104762640 | CCACCATGGCACGTG[C/T]ATACCTATGTAACAA | 57531 |
rs140458998 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754443 | GATCAACCCCAAGAC[A/C]TATAATCAGATGTGT | 57531 |
rs140467732 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104832594 | TAGAGATGGGGTTTC[A/G]CCATGTTGCCCAGGC | 57531 |
rs140468289 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104687424 | TCATTGACTTTACTC[A/G]CAAATCTCCACAGAG | 57531 |
rs140502708 | in-del | -/AA | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104792564 | ATGTCGGAGCAAAGC[-/AA]AGAGTTGCATGAACT | 57531 |
rs140507751 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | HACE1 | GRCh38.p7 | 6:104828549 | AGTTATATAAAAATA[A/G]AATTATTAAGAAGTT | 57531 |
rs140531049 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104716505 | GACCAGCCTGGCTAA[C/T]ATGGTGAGACCCCGT | 57531 |
rs140546283 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822244 | AAAAATTATCCAGGC[A/G]TGGTGGCAGGAGCCT | 57531 |
rs140552153 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750077 | CTTCAACATCTCCCA[C/T]ATAGAAGAAACAGGA | 57531 |
rs140553470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732693 | TTAAATGATACATTT[C/T]ATGATATGCATTTAC | 57531 |
rs140554620 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104839776 | TTTGGAAGGCCAAGG[C/T]GGGTAGATCACCTGA | 57531 |
rs140577582 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | HACE1 | GRCh38.p7 | 6:104759640 | TCACAATTGAAAGAA[A/C]TAGAGAAGCAAGAGC | 57531 |
rs140630940 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825715 | TAGACCCCAGAAGAT[A/T]CTGTATCCAGAACCT | 57531 |
rs140648577 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104797347 | CACTTCCTAATCCCT[C/T]TCTCCACCTTAACTT | 57531 |
rs140663403 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104710900 | ATTGGATTTTAGCAT[A/G]CTACTATTTCATTCC | 57531 |
rs140674995 | in-del | -/TATAT | 0.029116 | 0.117091 | intron-variant | HACE1 | GRCh38.p7 | 6:104808614 | TTGAATATGATATAA[-/TATAT]TATATCTAGTAATAC | 57531 |
rs140679889 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104820926 | CACAATAGCAAAGAC[A/C]TGGAATCAACCTAAA | 57531 |
rs140770221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104772426 | ACACACGCACATATA[C/T]ACAGTTTCCTAGGCA | 57531 |
rs140848215 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104756537 | TTCAGCTTCCTTGAG[A/G]CAAATTCAGTCATTG | 57531 |
rs140871262 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | HACE1 | GRCh38.p7 | 6:104737063 | CCGAGGCGGGTGGAT[C/T]ACCTGAGGTCAGGAG | 57531 |
rs140874071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766124 | AAGACATGAGTAATG[C/T]ACAAATGCACATCGG | 57531 |
rs140875770 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | HACE1 | GRCh38.p7 | 6:104768143 | TATTTTCATCTATTT[A/G]GTTTCACTTTATAAT | 57531 |
rs140877935 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104725596 | TATTAGTCAGCCCCC[C/T]ACTGATAGACACTGA | 57531 |
rs140885867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851334 | TGATCTGCCTGCCTC[A/G]GCCTCCCGAAGTGCT | 57531 |
rs140966573 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104765048 | ATGCAACAAAGTGTT[A/G]TATTTATTCTTCACT | 57531 |
rs140984762 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | HACE1 | GRCh38.p7 | 6:104844469 | CTGTCTCAGCCTCTC[A/G]AGTAGCTGGGATTAC | 57531 |
rs141019252 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104812065 | ACGCTACTATAAAAT[A/C]TTAAAAATACATATC | 57531 |
rs141043028 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727514 | ATATGTATATGAATA[C/T]ACACACACGTATGTA | 57531 |
rs141053166 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859311 | TCGACAGACGTTGCG[A/G]GACCTTTGTCTCGCT | 57531 |
rs141061092 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728504 | AACTTTCAACTTACA[C/T]GTCTCTCAAACATTA | 57531 |
rs141082184 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | HACE1 | GRCh38.p7 | 6:104700183 | TGGTGTAGCTGGTGG[A/G]CCTCCCCATGATGAC | 57531 |
rs141091408 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104690689 | GAATTTAAGATATGA[A/T]CAAAGTGTCATTTCA | 57531 |
rs141091439 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803666 | ACAAAATTCAACAGC[C/G]CTTCATGCTAGAAAC | 57531 |
rs141092108 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104779692 | ATGGGCTTTGAAGTC[A/G]GATAAACATGGTTTG | 57531 |
rs141092522 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104830321 | TTAAATTTAATAATA[C/T]TGACTCTAAGTAAAA | 57531 |
rs141118216 | in-del | -/C | 0.0240643 | 0.107019 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859151 | TAAAAGCCCGCCTGG[-/C]CCCCCCGATGCAGCT | 57531 |
rs141133900 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104825325 | GAGGCAGATGGGAAA[C/T]TGAAAGTACCACTGA | 57531 |
rs141158561 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104807619 | AACATAAGGATTGAA[C/T]ATAAAACCAATCTAA | 57531 |
rs141233836 | in-del | -/CTT | 0.473634 | 0.111748 | intron-variant | HACE1 | GRCh38.p7 | 6:104764608 | TGTCATCTATAGGCA[-/CTT]CTTCTTCAGTTTTAA | 57531 |
rs141252598 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104707078 | ACCAGACAGCTTCTC[C/T]GAGTGAATTCTACCA | 57531 |
rs141257981 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695467 | AATGGTGCATCAATG[C/T]GAAGAGCCTAATTGA | 57531 |
rs141290524 | snp | C/T | 0.021333 | 0.101051 | intron-variant | HACE1 | GRCh38.p7 | 6:104691566 | AAAAAGGGAAATTAA[C/T]GCAATATTTTTTGGT | 57531 |
rs141330573 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104756714 | GTGGGTGCAGCCCAC[A/G]GAGGGCGAGCCAAAG | 57531 |
rs141335802 | snp | A/C/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104834341 | AATTAACATAGCAAT[A/C/G]CTATATTCCTTACTT | 57531 |
rs141355531 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104830913 | AGAGGTCACCATATT[A/C]ATGCCAAACTTAGTG | 57531 |
rs141400881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104753861 | TCTCCTCCAAATGAC[C/T]GCAACACCTCTCCAG | 57531 |
rs141402302 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104711794 | ATGTATTTATTTTGA[A/G]GCAGGGTCTCGCTCT | 57531 |
rs141442427 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104818784 | TAAAGACAAAAACCA[C/T]ATGATTATCTCAACA | 57531 |
rs141461716 | snp | C/G/T | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104708602 | AATGCAAGGGACCTA[C/G/T]AATAGCCAAAACAAA | 57531 |
rs141474199 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861802 | TCTGCAATATGATGC[C/T]GTCTCCCAATAGCTC | 57531 |
rs141508122 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104721429 | CCCCAGTAGTTTTCA[A/G]CTCCCAGCTCTCCCC | 57531 |
rs141516522 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104848494 | TATAAAATATAAGTT[A/C]TTCAAGTCCTGAATC | 57531 |
rs141516572 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104801558 | GAGAGTGGGGGCTAA[C/T]ATTTGACATTCTTAA | 57531 |
rs141555660 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HACE1 | GRCh38.p7 | 6:104844819 | AGGCGCCCGCCACCA[C/T]GCCCAGCTAATTTTT | 57531 |
rs141567530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701870 | GGAACTCATTCGATT[C/T]CTTTTTTATTTTCCA | 57531 |
rs141575659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813996 | CAATAAATAAAAATT[C/T]AACAGAAGTTTAAAA | 57531 |
rs141628349 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104763286 | TTCAGAGTAGTAAAA[A/C]AACAAATCTCATAGT | 57531 |
rs141629819 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104689438 | ACAGAACTTATTTTT[A/G]TAAATTTTAGTTTTA | 57531 |
rs141634105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763661 | GGGTAGCTACAGCAG[C/T]ACAGAGGCATCACCA | 57531 |
rs141665849 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104760705 | TGGCCAGGGCAATCA[A/G]GCAAGAGAAAGCAAT | 57531 |
rs141677143 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104842049 | GACAAAATGTTAACA[C/G]TAATTTTATCTTTGG | 57531 |
rs141696686 | snp | C/T | 1.65214e-05 | 0.0028741 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771931 | GAGCCATACCAAGAA[C/T]GTGCTTGTAGAAGGA | 57531 |
rs141711114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726497 | GAATCATCTCCTGGG[C/T]CTCCAACTTGTGAGC | 57531 |
rs141719783 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104717569 | AAATATGAAGCATGA[A/G]ATGTTGGGTCATAGG | 57531 |
rs141738619 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | HACE1 | GRCh38.p7 | 6:104760608 | GAATAGGGAAAAAAA[C/T]GGGAAGCATTCTCTT | 57531 |
rs141743825 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104841598 | TGATTGAGTTTATTC[A/T]ATAATAAGCCATTCA | 57531 |
rs141753109 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104723330 | TAACAGAAACCCTAG[C/T]GGACTAAGAATCAGA | 57531 |
rs141822697 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104713285 | CTCCTCTTATTAACA[G/T]TTAGAGGATTGTTTT | 57531 |
rs141847468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835528 | TATTGAGGAAGTCTC[C/T]CTAAAAGTACAAAGA | 57531 |
rs141891518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104774692 | CCCAAGCAGGTATCA[C/T]CATTTTTAAATGAGG | 57531 |
rs141905383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792506 | TGTTGGTTGATGGTG[A/G]TTTTATTTTGAAATC | 57531 |
rs141974218 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104850852 | ATAATGCTGTTCAAA[A/G]CTTACTGATCCTTGC | 57531 |
rs141974722 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826932 | ATAAGAAACTATTGC[A/G]GAGGAACCGCAAAAG | 57531 |
rs142003839 | in-del | -/AGA | 0.137527 | 0.223271 | intron-variant | HACE1 | GRCh38.p7 | 6:104759828 | TAAAGATGAAAAGAG[-/AGA]AGAATAAAATACATG | 57531 |
rs142028357 | snp | C/T | 3.37844e-05 | 0.00410987 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796712 | AGTCTGAAAAAGCCT[C/T]GGGTGATATTGAATT | 57531 |
rs142033214 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104786294 | TGCAGTGAGCTAAGA[C/T]CACACCACTGCACTC | 57531 |
rs142044309 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104696662 | AGTTTGGGGGATACA[A/T]GAGGCCTATTTTATA | 57531 |
rs142045992 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104684346 | CCTGTCATTTGCCTC[A/G]TGGGCTCGTTCAAAT | 57531 |
rs142052305 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104824783 | ACAAACATTTAGAAA[G/T]GCAAAGAAGGCCGGG | 57531 |
rs142071128 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | HACE1 | GRCh38.p7 | 6:104782457 | CAACTATACTCCAGC[A/C]TGAGTGACAGGTAAA | 57531 |
rs142072791 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104831201 | TCTTAATGAGAGAGA[A/C]ATAGCAATTTCAAAA | 57531 |
rs142073690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104838123 | ATACTGTCAAAATGT[C/T]CATACTACTCAAAGC | 57531 |
rs142106181 | snp | A/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859403 | TGGGAGCGTCGGGCC[A/T]GGGGAGTTCGGGGCC | 57531 |
rs142127452 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104714612 | AGAATCTCTCTCTGC[C/T]TATTATTAGGTTGAC | 57531 |
rs142132999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793949 | GCACAGTTTAGCAGA[C/G]TAATTTTTTAAAAAC | 57531 |
rs142150565 | snp | C/T | 0.000839789 | 0.0204741 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791590 | GACCAATTCGAAAGA[C/T]GTGACAAAACATTCT | 57531 |
rs142172304 | snp | A/G | 0.000182444 | 0.00954928 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784472 | CAAATTCAATGAAAC[A/G]AGGTGAAGTCATTCT | 57531 |
rs142199391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853524 | TACAAAGATGAAACC[C/T]TGACAACCCCCACTC | 57531 |
rs142216965 | snp | C/G | 1.64993e-05 | 0.00287218 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776755 | CCATCAGCTGACTGG[C/G]TAAACAATGCATAAT | 57531 |
rs142237732 | snp | A/G | 1.66128e-05 | 0.00288204 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730308 | GTCAACATACCATGT[A/G]CTTGAAGTTGGTAAA | 57531 |
rs142238230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787338 | TTGACAGATTTGGAG[A/T]CCCTGAACTGCTTAA | 57531 |
rs142260380 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810027 | AATATGTGAGATTCT[A/G]TGGTACTTCTAAGTG | 57531 |
rs142323394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723853 | GCCTTGGTTTCCCAA[A/T]ATGCCAGGATTACAG | 57531 |
rs142324894 | snp | A/G | 0.030665 | 0.119967 | intron-variant | HACE1 | GRCh38.p7 | 6:104759956 | AAATCCAGAAGAAAT[A/G]GATAAATTCCTAGAC | 57531 |
rs142325753 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104809801 | GTTTTGGTTGAGTTA[A/G]AAGTTCAGATTCCGA | 57531 |
rs142345089 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104805372 | TATACCCAATGGATT[A/G]TAAATCATGCTACTA | 57531 |
rs142372594 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846447 | GGAAGCAACTATATT[A/C]CTGCTCAGATATTGC | 57531 |
rs142406507 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104694423 | TTCAAAAAAATAGAA[A/G]GAATAAAAAAGATCT | 57531 |
rs142416036 | snp | G/T | 0.0418186 | 0.138422 | intron-variant | HACE1 | GRCh38.p7 | 6:104804436 | AAAAGAACAAAGCTG[G/T]CAGCATCATGCTACC | 57531 |
rs142421281 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822407 | AAAAAAAAAAAATTA[C/G]CCAGGTGTGGTGGTG | 57531 |
rs142422933 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849836 | TTTGTATTTTTAGCA[A/G]AGACGGGGTTTCACC | 57531 |
rs142441673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727165 | CACATACATGTATAC[A/G]AATATATATACACAT | 57531 |
rs142448879 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725245 | GTTTATATATATGTA[-/TG]TGTGTATATACATAC | 57531 |
rs142460198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104686486 | GTGACAGATTCCTCT[A/G]CTCACCAAATCTATT | 57531 |
rs142463116 | in-del | -/GTGC/GTGTGC | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852228 | TGTGTGTGTGTGTGT[-/GTGC/GTGTGC]GCGCGCGTGCGCGTG | 57531 |
rs142489874 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104803194 | CTGAAATTGAGGCAA[C/T]AATTAATAGCCTACC | 57531 |
rs142518152 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104687728 | TTTACTCAAAATGCT[A/G]AAGACCAGAGCTGCA | 57531 |
rs142561367 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710792 | CTCAGCTTCCATTTC[A/C]TCTACAGCTCATGCA | 57531 |
rs142584696 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104833233 | ATATAAAAACAGCAG[A/G]TAAATAATGTTATTT | 57531 |
rs142619769 | in-del | -/A | 0.383824 | 0.211166 | intron-variant | HACE1 | GRCh38.p7 | 6:104771873 | AAACTGAAAAAAAAA[-/A]CAATATAAATAAATG | 57531 |
rs142629060 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842453 | TACTGAAAATACAAA[A/G]GTTTTTTTTTTTTTT | 57531 |
rs142643874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782766 | CAAAAGATCCCTCTA[C/T]ATAGTTATGTATAAT | 57531 |
rs142684621 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104705178 | CTTCTAGTTCTAAAC[A/G]TCTATAGGGAAAAAA | 57531 |
rs142701904 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104773359 | TGGTCTTTGATTTCT[C/T]GGTGCTGACACCAGG | 57531 |
rs142724054 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104696847 | ACTTGCACAAAATGT[A/C]TTTATTTGTCTCTAG | 57531 |
rs142731684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827723 | GTTTACATGGCTGTC[C/T]GTAACTGGATGAAAA | 57531 |
rs142819344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104765802 | CTTCAGTTTTAGCTT[C/T]ATGCAGTGTTATTCT | 57531 |
rs142842066 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104746078 | AGTACCAGTCTTCCC[A/G]CTGTTTCTGTTTTGT | 57531 |
rs142850005 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104826332 | CCTTCAAGAAGTTTA[C/T]AGTAGAAAGGGAAGA | 57531 |
rs142881949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104713425 | GAGCACTTAATATTT[C/T]CCATAAATCTGGATG | 57531 |
rs142911441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844083 | CTTGTTGCCCAGGCT[A/G]GAGTGCAGTGGCGGA | 57531 |
rs142920004 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708362 | TAAGAATAAACTTAA[A/C]AAAAGAAATGCAACA | 57531 |
rs142929114 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104731048 | CAGGAAGGCTAACAT[A/G]TAATGCATAACACAT | 57531 |
rs142931940 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104762020 | TCTCACACCATTTAG[A/G]ATGGCGATCATTAAA | 57531 |
rs142958163 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104702871 | AAAGAGTAATCAAAT[A/G]AAAGATTTTAAATGA | 57531 |
rs142990878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720311 | CCCCTGATGACAACT[C/G]ATCTGGTTTTTGTTC | 57531 |
rs143056703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104778934 | ACTGGTGGAAATATG[A/G]GTAAGATTTTATGTA | 57531 |
rs143124303 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104845654 | GGCTAATTTTCTGTA[C/T]TTTTAGTAGAGAAGG | 57531 |
rs143143325 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104733215 | TTATACAAATTATAG[C/T]ACAGTATTTCAATAT | 57531 |
rs143145910 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772403 | TATACACATACACAT[-/AC]ACACACACACACGCA | 57531 |
rs143205669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722802 | CAGTCCCTAAACCAC[A/G]GTTAAGTACATGGGA | 57531 |
rs143211805 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104802446 | ATCACACTTATTCTA[A/C]AATTGACCACATAAT | 57531 |
rs143236851 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851485 | ATCCAAAAACCAAAC[A/G]CCTTGACCAATAAGC | 57531 |
rs143247605 | snp | A/G | 0.216349 | 0.247725 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727667 | TGAATACATACACAC[A/G]TATGTATATGAATAC | 57531 |
rs143256597 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104718462 | CTTAAAGAGATCTTA[A/T]TGAGAAGGGCAGTTT | 57531 |
rs143267273 | snp | A/C/G | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104753622 | GGCAACTGGGGTCTG[A/C/G]AGAGGACCCCTGGCA | 57531 |
rs143305770 | snp | C/T | 0.021333 | 0.101051 | intron-variant | HACE1 | GRCh38.p7 | 6:104686614 | CTCCTTTCTTATTTG[C/T]GCTTCCAGAGCTATT | 57531 |
rs143306286 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104781156 | CTGAGACTGTGTAAT[A/C]ATCCTACCCTTCATC | 57531 |
rs143314080 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | HACE1 | GRCh38.p7 | 6:104798346 | TTCATTCTCTTTCAC[A/G]AAACGGCACTGTATG | 57531 |
rs143330104 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104856464 | TTTGAGACTGAGTTT[C/T]GCTCTTGATGTCCAG | 57531 |
rs143344349 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | HACE1 | GRCh38.p7 | 6:104774446 | CTGGAGTGCAGTGGC[A/G]CAACCTCAGCTCACT | 57531 |
rs143353438 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780282 | AAAAGCTCAGATCAA[-/AC]ACACACACACACATA | 57531 |
rs143370136 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744328 | AAAGCACATTTTATT[C/G]TACAAAACTCGTTTA | 57531 |
rs143375877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825483 | AACTGAAGGTAGTTA[G/T]GTGCAAGCAATCGGA | 57531 |
rs143419821 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104734615 | TGAAGCTAGCTCCGT[A/G]TTGTTTCCCCTCAGC | 57531 |
rs143435191 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104769895 | AGGTAAAATTATGTC[A/G]CTTGCTAATAAGTTT | 57531 |
rs143435330 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | HACE1 | GRCh38.p7 | 6:104822983 | TCTCATCAAACTGGT[A/G]AGACAAACTTGAAGC | 57531 |
rs143454206 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104700250 | TCCTTCCAGAAAGCT[A/G]AATAAAAATGGTGTT | 57531 |
rs143477414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820335 | CAAGAGTAAAAATTG[A/G]AAGTTGGGATCTAAT | 57531 |
rs143479866 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104695540 | AATTCATCTTCATTC[A/G]GTTTGTATGTGTCCT | 57531 |
rs143518205 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756433 | AAAAAAAAAATATAT[-/AT]ATATATATATATACA | 57531 |
rs143541179 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104805816 | CTATGTAACAAACCC[A/G]CACGTTGTGCACATG | 57531 |
rs143557622 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104696556 | GAAGGATTTACCCCA[A/G]TGTCAGGAGTTTGGT | 57531 |
rs143598638 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104697989 | TGCTGAGATTACAGG[C/T]GTGATCCACCACACC | 57531 |
rs143606994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775553 | AAAGAGAAGAAATAA[A/G]TCTAAAATATAATGC | 57531 |
rs143685803 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104712924 | CAGACATCAAACTTG[C/T]CAGCTCCTTGATCTT | 57531 |
rs143710257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835403 | CATACTGATTGCATC[C/T]CTGAAATGAGAAAAG | 57531 |
rs143724149 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104802327 | ACAGAAGGCTAACAA[G/T]GATATCCAGGAATTG | 57531 |
rs143733256 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104757452 | ACCTGCAGCTAAGGG[G/T]CCTGTTTGTTAGAAG | 57531 |
rs143761201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799559 | CAGTATTCACCCAAT[G/T]TTTCAGATGAGAAAA | 57531 |
rs143796785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104785452 | ATCTTCCCAAGTTAA[C/T]GTGATAGTAATGCCT | 57531 |
rs143836574 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | HACE1 | GRCh38.p7 | 6:104757804 | AAAACCTTGAAAAAA[C/G]GTTAAACGAATGGCT | 57531 |
rs143843970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104830625 | GGAATTCTCCCTTCT[C/T]CCAACAAGAGATAAG | 57531 |
rs143857542 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104843603 | TTCATGAAATAGTAA[C/T]ATTCATTAGAAATAT | 57531 |
rs143862467 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104767351 | TATAAATTCTATTAT[C/T]CTCAAAAGCTTAAAA | 57531 |
rs143900309 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104715060 | CTTTCACTCTTGGTG[A/G]ACAATTCTGAGATGT | 57531 |
rs143924043 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714035 | AGACCTCAATGTAAA[G/T]AATTCATAACAACAA | 57531 |
rs143957899 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837535 | AACACAGAAACATAA[A/C]ACTTGTAGAAAAAAA | 57531 |
rs143999881 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104801072 | CTTCATAATGCATGC[A/G]CAAGCTTCAATAGCC | 57531 |
rs144080298 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | HACE1 | GRCh38.p7 | 6:104693081 | CGCGCGCTGGGGTGG[C/G]GGTAGAACGCATACA | 57531 |
rs144090261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767477 | TCCTGACTCTAGTAC[C/T]GCCCCATTTCAACCC | 57531 |
rs144090326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821808 | TTTATTTAGTACTAA[C/T]GGCTAATCTGACACA | 57531 |
rs144101640 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104709806 | GATAACATTTCATGC[A/C]CACTAGGATGGCTAT | 57531 |
rs144110724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104786687 | AAAGATTAATAGTTT[A/G]TAAGTGGTACAGTGG | 57531 |
rs144127696 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104816052 | CACTCCAGCCTGGGC[A/G]ACAAGAGCAAAACTA | 57531 |
rs144129360 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104818641 | TCCCTAACAAAAACA[C/G]TGGCAAGCAGAATCC | 57531 |
rs144150431 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | HACE1 | GRCh38.p7 | 6:104832474 | TCTCAGCTCACTGCA[A/C]CCGCTGACTGCTGAG | 57531 |
rs144210342 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104736497 | ATGTTGCCCAGGCTG[G/T]TCCCAAACTCCTGAG | 57531 |
rs144268583 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104781893 | AGGCAACAAACACCT[C/T]CCTCTCTGGGTCAAC | 57531 |
rs144282444 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | HACE1 | GRCh38.p7 | 6:104697755 | ATGTTTATTTTTTCT[C/T]TGAGGCGGAGTTTCA | 57531 |
rs144303355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750815 | CAACATCTGGTGTCC[C/T]TGTTTCCATTTTTGC | 57531 |
rs144324878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694547 | GATAAATGCTTGAGG[C/T]GATGGATGCCCCATT | 57531 |
rs144350782 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861268 | TTAGCCGGGCGTGGT[A/G]GTGTGCCTCTGAAAT | 57531 |
rs144386659 | in-del | -/G | 0.24019 | 0.249807 | intron-variant | HACE1 | GRCh38.p7 | 6:104758544 | CAAGAGCTCCTGAAG[-/G]GAAGCACTAAACATG | 57531 |
rs144406034 | snp | C/T | 6.58935e-05 | 0.00573955 | intron-variant, synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833096 | CTGCCCCATGGCATC[C/T]TCAACATCAACATCA | 57531 |
rs144421604 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754664 | AGAATTTCCAACTGA[C/G]AATTTCATATCTGGA | 57531 |
rs144421707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706226 | GCCACAGTAGGTTCT[C/T]ATTCCCATCTGGCAA | 57531 |
rs144430388 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729198 | TATTTGTGGCTTTAT[A/G]GACAATCTAAATCCA | 57531 |
rs144434713 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104812863 | CAATAGAAGAAACAG[A/G]CTCTCCCCCTAGGAC | 57531 |
rs144478320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754988 | ATTAAAAGACCAAGA[A/G]TGGCAAGCTGGATGA | 57531 |
rs144515541 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104689185 | CATTGACAAATGAGG[C/T]TCCTGCAGAGACAGA | 57531 |
rs144587730 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104826986 | GGCCTTCAAGAGATC[C/G]TTAAGAAGAAATAAC | 57531 |
rs144639270 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104812221 | CATGAGGCAATAGGT[A/G]GCTTGAGGCCAGTAG | 57531 |
rs144644595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104683517 | GGAAAAAATAATAAT[C/T]GTAGCAATGGTGTGT | 57531 |
rs144670690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765132 | TTGAGGGAAAATACA[C/T]GGCAAACACATTATT | 57531 |
rs144672667 | snp | C/T | 0.00112269 | 0.0236661 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796938 | ACACACCTGTACACA[C/T]AAATCCAGAGGAGTT | 57531 |
rs144694757 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791518 | CCTTGAACACCTGGC[A/T]TCTTGGAGTTTTATT | 57531 |
rs144739682 | snp | A/G | 9.89821e-05 | 0.00703429 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777253 | ACTGGCCTGTGCACC[A/G]TATCTGAATCTGGCT | 57531 |
rs144755163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816849 | CCAAGGCCTCAGGAT[A/C]CCAACCCATGCATCA | 57531 |
rs144770301 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844504 | ATGCACCACCACGCC[A/T]GGCTAATTTTTGTGT | 57531 |
rs144774291 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104697236 | GACTGCTTTCTCTTA[C/T]GTGGAACTTGAAATG | 57531 |
rs144777260 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104774663 | TGCTGGGATTACAGG[C/G]ATGAGCCACCGCGCC | 57531 |
rs144799977 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104688269 | AATACAGGCATCCTG[C/T]GAGGAAGAATCCCCA | 57531 |
rs144806716 | snp | A/G | 1.6522e-05 | 0.00287414 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791639 | CTTCATTTGAGCATC[A/G]TAATTGCTAGAGAGG | 57531 |
rs144837898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725926 | GCGAACTGGTCTGGT[A/G]TGGTGACATAATCCC | 57531 |
rs144888351 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104707428 | AATGACAAAGACCTC[A/G]TGATCATTTCAATAG | 57531 |
rs144906964 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104751078 | ACTTCTTTCCATTCT[A/C]CCCCTAGTTCATTCA | 57531 |
rs144925715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766136 | ATGCACAAATGCACA[C/T]CGGCCTTGGCCCCAC | 57531 |
rs144993573 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104699319 | CTTTTTTCAGTGATT[C/T]GGAGGGCACCTTAGG | 57531 |
rs144996544 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104777724 | AAAATAATCTCTTAC[A/C]CCTAATCTTATTTAT | 57531 |
rs145019572 | snp | A/C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104824495 | TAAAACTTAGATAGA[A/C/T]GAAAATGTACTCTGA | 57531 |
rs145037394 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104831049 | TACTGGCACACACCT[G/T]TACATTCTATTACCA | 57531 |
rs145082989 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788344 | AAGAATTATATTCTA[C/G/T]ATATAGTAACAATGA | 57531 |
rs145098704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834438 | CTATAAGTCTACCAC[C/T]CAAAGATAATCAATG | 57531 |
rs145119096 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708434 | GACCTAAATAAATGG[A/G]AAGACATCCTGTATT | 57531 |
rs145170321 | in-del | -/T | 0.25801 | 0.249872 | intron-variant | HACE1 | GRCh38.p7 | 6:104686426 | GGCAAAACATCGATG[-/T]TTATCTAAGAATTTT | 57531 |
rs145186009 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790224 | AAGACTACCATATCT[A/G]TTCTAAGTATTAATC | 57531 |
rs145189361 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104769634 | CTTACATTAAAAATC[A/G]AGTAAGTTCTTCCTC | 57531 |
rs145194415 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852723 | AAAAACCTTTCTGTA[C/G]CTTTAACAATTGAAA | 57531 |
rs145211482 | snp | C/T | 3.31802e-05 | 0.00407296 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104777105 | AGCTACTCCTAAAAA[C/T]AGAATCTAAATATGT | 57531 |
rs145250661 | snp | A/G | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727643 | TGAATACATACACAC[A/G]TATGTATATGAATAC | 57531 |
rs145252565 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104793449 | ATATATAGAAAGGAC[A/G]ATAAAATTTCATTTC | 57531 |
rs145254272 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104743035 | GATGAAATTGGAAAT[C/G]ATCGTTCTCAGTAAA | 57531 |
rs145261358 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | HACE1 | GRCh38.p7 | 6:104840115 | AAAATGTTACCACTG[A/G]AGGAAACTCGGCAAA | 57531 |
rs145305742 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104766703 | ATGAGAAGCCTAGCA[A/G]TTACACTGTCTTATA | 57531 |
rs145313059 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104748714 | AAGGAAACTGAAATG[C/T]TATACAGCAATTAAA | 57531 |
rs145338984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849002 | GAGACAAAAAAAATA[G/T]AGAAAATAAAATATG | 57531 |
rs145369786 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104798064 | CAAGAGCAAAACCCC[A/G]TCTCGAAAAAAAAAA | 57531 |
rs145404016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104809088 | CTATTATAAATGGCA[C/T]TGTTTTTTATAAGAT | 57531 |
rs145408819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725372 | CATCCCACTATACAA[C/T]TCATTCCCAGATATA | 57531 |
rs145455796 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104743629 | TCATCTAGTTTTCTA[A/G]TATCTATTATATTTA | 57531 |
rs145476993 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789789 | CATTACTGATGAGTA[G/T]AAAGTATGAGTCAAA | 57531 |
rs145480370 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104727154 | GTATATAGATACACA[A/T]ACATGTATACGAATA | 57531 |
rs145480420 | snp | A/G | 0.000463292 | 0.0152129 | intron-variant | HACE1 | GRCh38.p7 | 6:104771146 | AACTAGCAAACTATC[A/G]GGGCCAAGTTACAAA | 57531 |
rs145493699 | snp | C/T | 0.219947 | 0.248187 | intron-variant | HACE1 | GRCh38.p7 | 6:104804883 | TAAACTAAAGAGCTT[C/T]TGCACAGCAAAAGAA | 57531 |
rs145528193 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104689764 | TATCCCCTTATTATG[C/T]AGCCTGAAACTTCAT | 57531 |
rs145542919 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | HACE1 | GRCh38.p7 | 6:104849908 | GCCCGCCTCGGCCTC[C/T]CAAAGTGCTAGGATT | 57531 |
rs145555886 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732536 | GTTGTTAGAGGCGGG[G/T]GGGAAAGGAGGAGGG | 57531 |
rs145560712 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104685995 | AAGAATTAGAATCGC[G/T]TTTAAAGCAACATTT | 57531 |
rs145575625 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815088 | AAGGGGCAGAGGTTG[C/G]AACAGTTTGGAGGGC | 57531 |
rs145597465 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728146 | TAACTACTTGCAAAA[A/G]AAACTAATATGACAA | 57531 |
rs145625970 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104695653 | AGTGGTGCAATCTTG[A/G]CTCACTGCAACCTCT | 57531 |
rs145643607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690630 | GGAAGAACAGAACAA[C/T]AGAGCACAACAGGGA | 57531 |
rs145672142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104791333 | AAGCTCACCAACTTG[C/T]TGTTGATTAGACAGA | 57531 |
rs145693685 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104764341 | CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG | 57531 |
rs145748970 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104821199 | CAAAGGGGTGGAGGA[C/T]GGGAGGAGGGAAAGG | 57531 |
rs145764902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765389 | TGCACTAGGACATCC[C/T]TGCACATTTATTCTG | 57531 |
rs145770122 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104801368 | GGAAATACAGAGAAC[A/G]CCACAAAGATGCTCC | 57531 |
rs145770492 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104797724 | CTTCTTGTAGAAGTA[C/G]AATTGTGTAACTATC | 57531 |
rs145792075 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | HACE1 | GRCh38.p7 | 6:104762637 | AAACCACCATGGCAC[A/G]TGTATACCTATGTAA | 57531 |
rs145870247 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104699615 | AGTCCCTACACTCAG[A/G]TGAGGCACGCAATGT | 57531 |
rs145901440 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104696766 | CATTCTGATTAGCTA[C/T]TAGCCTAAGATTTGG | 57531 |
rs145955397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683900 | GGAAAGATCTAATAG[A/G]AAAACCAAATCCAGG | 57531 |
rs145958523 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104760613 | GGGAAAAAAACGGGA[A/G]GCATTCTCTTTGAAA | 57531 |
rs145970519 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104807168 | AGCTGAGACTACAGG[C/T]GTGCGCCACAATGCC | 57531 |
rs146055202 | snp | A/G | 0.221737 | 0.248397 | intron-variant | HACE1 | GRCh38.p7 | 6:104740416 | caaaattgatagacc[A/G]ctagcaagactaaaa | 57531 |
rs146071296 | snp | A/G | 0.000297516 | 0.012193 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784991 | CTTTCTTACCCCGGA[A/G]GCATCTGACAAGAAC | 57531 |
rs146079065 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104703234 | GGCAATTCAGCCAAG[C/T]GGCAGCGCAGTCTCT | 57531 |
rs146093170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826471 | AGCAAATTTCTTGCC[C/G]CTAAAATCCCACAAA | 57531 |
rs146096655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836054 | CACTCTCAGGAAACT[C/T]TCAGGGTTGTGCTCC | 57531 |
rs146105083 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104746638 | TCTTCAGTCCTAGGG[A/C]TGATAAAGGCTTTCC | 57531 |
rs146117584 | snp | A/G | 3.29598e-05 | 0.00405941 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771980 | GACCAGCTGCCTGTG[A/G]TTCAACGCTAATCCC | 57531 |
rs146178585 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104760828 | AAAATCTCCTTAAGC[C/T]GATAAGCAACTTCAG | 57531 |
rs146181017 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104843098 | CCTGAGTGACAGAGC[A/G]AGACTCTGTCTCAAA | 57531 |
rs146201351 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723574 | CTGCTCACATTAAAA[G/T]AGCTTAAAACAAACA | 57531 |
rs146207667 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730319 | ATGTGCTTGAAGTTG[A/G]TAAAAGATTTGGAGT | 57531 |
rs146228039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763560 | ACCAATAAGCAACCA[C/T]TTTCTTACACTTACA | 57531 |
rs146228088 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104719215 | TACCTCACAAAAGAT[A/T]TAAAAATACCTATTC | 57531 |
rs146297656 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104782487 | AACCCTGTGTCAAAA[A/T]AAATAAATAAATAAA | 57531 |
rs146300146 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848999 | TGAGAGACAAAAAAA[-/A]TATAGAAAATAAAAT | 57531 |
rs146338061 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104840553 | GCTGAGAGAGGCCCG[A/T]CGCGGTGGCTCACAC | 57531 |
rs146346704 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104735638 | TCCGTCTCAAAAAAA[A/C]AAAAAGTAAAAATGA | 57531 |
rs146393808 | snp | A/G | 0.000297138 | 0.0121853 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776797 | ATCTCATTGGACAGA[A/G]TATCAAACCACTCAC | 57531 |
rs146397688 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104843712 | CAAAACATTTAAAAC[A/G]TAACACTAAGATGTT | 57531 |
rs146430636 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104801111 | CAAGTGGAAGAAAGG[A/C]TATCAGTGATTGAAG | 57531 |
rs146467524 | snp | C/G | 0.0441095 | 0.141807 | intron-variant | HACE1 | GRCh38.p7 | 6:104720759 | CAGCCTCCCGAGTAG[C/G]TGGGATTACAAGCGC | 57531 |
rs146485248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858966 | CCAGCTAGCCCACTC[A/G]ATACTAGTCTGATGA | 57531 |
rs146498234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854206 | AAAAGTCTCACGACC[A/G]TTAAACACAAAGAAA | 57531 |
rs146509124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736817 | GTGTGAGTCCAACTA[C/T]TTTTCTAACTATACA | 57531 |
rs146509422 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104690656 | AGGGAGTCCTGGAAT[G/T]GACTCAAATACATGC | 57531 |
rs146518477 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104732767 | TTGAAATCACTGATA[C/T]GTATACATCCACAGG | 57531 |
rs146521492 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | HACE1 | GRCh38.p7 | 6:104816666 | GAACCCCATACAGGG[C/T]ACTGTCTAGTAGAGC | 57531 |
rs146531508 | snp | C/T | 0.239902 | 0.249796 | intron-variant | HACE1 | GRCh38.p7 | 6:104803649 | tgcagaaaaggcctt[C/T]gacaaaattcaacag | 57531 |
rs146542459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695261 | TTCTTAATCTTTTGC[A/G]TGCAATAAACAAGAG | 57531 |
rs146554881 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104819750 | ACTCTGACAACTATC[A/T]GATCTTCCACAAACC | 57531 |
rs146603745 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811758 | TAATTATAGCTCATT[-/T]GAATCTAAATAGCCA | 57531 |
rs146603959 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774392 | ACCGCGCCCGGCCTC[C/T]CTTTTTTTTTTGAGA | 57531 |
rs146626431 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104716871 | AATAATTGGGAAAAT[G/T]AAAATTAAAATATAC | 57531 |
rs146627301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711232 | CAAAACCATACCCTG[A/G]AGTCTTGCTAACTCA | 57531 |
rs146627302 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104759435 | GAAACTGAACAACGC[A/G]CTCCTGAATGACTAC | 57531 |
rs146637780 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | HACE1 | GRCh38.p7 | 6:104756623 | TACAGCTCCCAGCGA[C/G]ACTGACACAGAAGAT | 57531 |
rs146640330 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104834243 | TGCTTCTCAGATAAT[A/C]CTGGACTCTATGCAT | 57531 |
rs146648729 | snp | C/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727636 | ATGTATATGAATACA[C/T]ACACACGTATGTATA | 57531 |
rs146669089 | snp | C/T | 0.261608 | 0.24973 | intron-variant | HACE1 | GRCh38.p7 | 6:104740119 | gttctttgaaaccaa[C/T]gagaacaacgacaca | 57531 |
rs146672040 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688725 | AACTTCTAGAGGCTG[G/T]GGGCTTTTCCCGGCT | 57531 |
rs146674316 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104838405 | CAGAAATAAATCCAC[A/C]CATCTACAGTGAACT | 57531 |
rs146736474 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816891 | ATATGAGACACGGAG[A/T]CAACGGAAATTATTT | 57531 |
rs146748092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775625 | TGACTTCACTGAACT[C/T]GTCATTCACAAAGAC | 57531 |
rs146782864 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104732256 | GGACTCAAAGAAGTA[A/T]CTGCGCATACAGCAG | 57531 |
rs146792589 | snp | C/G | 0.0132253 | 0.0802776 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858460 | AATCCCAACACTTTG[C/G]GGGGAGCAGGGTGCG | 57531 |
rs146796380 | in-del | -/CAAAGTAGGGCGGGGCATC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799892 | TTGGACAGTAGGTGC[-/CAAAGTAGGGCGGGGCATC]AGCCCACGGAGGGTG | 57531 |
rs146832393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839748 | TGGTGGCTCACACCT[A/G]TAATCCCAGCATTTT | 57531 |
rs146858910 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104834646 | AAAGATACAGAGGAG[A/G]GAACAGCAAGTTTTG | 57531 |
rs146880057 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716349 | TATATAGAACATTTT[A/C]CTCAAAGAGTGGAGA | 57531 |
rs146894053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773484 | TTAAGGACCTTTGGA[A/G]AATAATTCACTGTCA | 57531 |
rs146925253 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104779869 | TTATGATAATTATAA[G/T]AATCATAATAATAAA | 57531 |
rs146967749 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104784330 | TATTTTGAATAGTAC[A/G]AGAAATAGTATTTTT | 57531 |
rs147030514 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104801667 | AGACATGCAAATGCC[A/G]AGAGATTTTGTCACC | 57531 |
rs147041366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721486 | TCACTGTACTCAACC[C/T]GAGTCCATAAAACCA | 57531 |
rs147070449 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104726269 | GAAATGGCAAACTGG[A/G]GAGGGCATTTAGTTA | 57531 |
rs147125647 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860489 | ACAACCTGAAAAAAT[A/T]TTTTCATTTATTTGG | 57531 |
rs147146663 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | HACE1 | GRCh38.p7 | 6:104692490 | ATTGTCAGCACCACT[A/G]AGCCTTGTTGACACA | 57531 |
rs147159092 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104793493 | CATTATGTGCAAACG[C/T]CTCAGTAAATGTTTA | 57531 |
rs147231366 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | HACE1 | GRCh38.p7 | 6:104754338 | ACATACTTCAGGATA[C/T]CATATAGGAGAACTC | 57531 |
rs147251351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713383 | ACCTTGAAAGAATAA[C/T]AATAATTATGTTAGC | 57531 |
rs147295810 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104818660 | CAAGCAGAATCCAGC[A/T]GCACATCAAAAAGCT | 57531 |
rs147296197 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104764458 | GAATGAGGAGTCATT[C/G]TGCTGGATGGATTTT | 57531 |
rs147301473 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789534 | TAAAAAGGAAAAACA[C/G]ATATCCTTTTCTACT | 57531 |
rs147305984 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104815404 | ACAAAGTCTCACTCT[C/G]TCTCCTAGGCTGGAG | 57531 |
rs147313568 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104696883 | GCTGTCATTTGGTTC[C/T]ACTTCTATCAGGCAA | 57531 |
rs147326105 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104767478 | CCTGACTCTAGTACC[A/G]CCCCATTTCAACCCA | 57531 |
rs147337250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104693680 | GTTGTTTGTATCAGA[C/G]GATGTGGAATCTGAG | 57531 |
rs147402248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787578 | AAACTGCTTGAAACA[A/G]AAAGAAAAAAGAATA | 57531 |
rs147443428 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | HACE1 | GRCh38.p7 | 6:104713469 | AATTTATTAAATGCT[C/T]ATCACAAGCCTATGC | 57531 |
rs147498409 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | HACE1 | GRCh38.p7 | 6:104856494 | GGCTGGAATGCAGTG[C/G]CGCGATCTTGGCTCA | 57531 |
rs147503941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763574 | ATTTTCTTACACTTA[C/T]ACCTAACTACTTAAT | 57531 |
rs147508071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808733 | CCTATATTCCTTTCC[C/T]TTTCATTTATCAGAA | 57531 |
rs147518037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851508 | CAATAAGCTGGTGCT[A/G]AAGGTTTCCTCATCT | 57531 |
rs147526353 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104734642 | CAGCTTCCTTGGCTT[C/T]TACTCTTCACCCACA | 57531 |
rs147547875 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104729983 | AGAAAATACGTTCCT[G/T]TCAGCTTAAAATAAA | 57531 |
rs147561219 | snp | A/C | 1.65378e-05 | 0.00287552 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784427 | CTTACCTATTAACAA[A/C]GCATTTTAAAACTTC | 57531 |
rs147581741 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743176 | GTGGGGTGGGGGGAG[C/G]GGGGAGGGATAGCAT | 57531 |
rs147590645 | snp | A/G | 0.216649 | 0.247765 | intron-variant | HACE1 | GRCh38.p7 | 6:104737693 | ACCCCACGGAGTCTC[A/G]CTGATTGCTAGCACA | 57531 |
rs147591378 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104788577 | CACAACCCACAAGAT[A/G]AGATCTTGAAGTTAA | 57531 |
rs147607852 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777278 | CTGGCTGTCCTGAAT[A/G]CAAATGTTCATAGAA | 57531 |
rs147667421 | snp | A/T | 0.0528381 | 0.153711 | intron-variant | HACE1 | GRCh38.p7 | 6:104805278 | TAAATTAGTTCAATC[A/T]TTGTGGAAGACAGTG | 57531 |
rs147685338 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104686002 | AGAATCGCTTTTAAA[A/G]CAACATTTGTCTGCT | 57531 |
rs147696116 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104759735 | AGGAACATGAAAAAC[C/G]CTTCAAACAAATCAA | 57531 |
rs147696453 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104809245 | TGTAGGGGAGACAGA[C/G]TATAAGAAAGTAAAT | 57531 |
rs147714454 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104689836 | AAGATATCACTAAGA[C/T]CAGTGTCACATGGGA | 57531 |
rs147758732 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | HACE1 | GRCh38.p7 | 6:104825310 | CCCCCACCTCTTTGC[A/G]AGGCAGATGGGAAAT | 57531 |
rs147788835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706480 | TCAGTAGTGCTACAC[A/G]AGATTGGGCAAAGAC | 57531 |
rs147801359 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104779207 | AGCAAGGTGGTGCAA[C/T]ACCATCACAAAAGCT | 57531 |
rs147801724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104830208 | TCCTCTGAGAGCTAT[C/T]GGCTAGACTCATTCT | 57531 |
rs147818525 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | HACE1 | GRCh38.p7 | 6:104710417 | GGTTGCATAACTCCA[A/T]GAATATACTAACAGA | 57531 |
rs147831372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104783438 | GAGCATATATCACAG[C/T]CATTCCTGACAATTT | 57531 |
rs147895757 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104725980 | GGTGGATCACTTGAG[A/G]TCCCTAGGGGTTCAA | 57531 |
rs147905940 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811336 | AGTACAATGGAGTTG[C/T]TCCTGATACATTTGG | 57531 |
rs147907733 | snp | A/G | 0.0444908 | 0.142359 | intron-variant | HACE1 | GRCh38.p7 | 6:104848411 | CAGCGAGCCGAGACT[A/G]TGCCACTGCACTCCA | 57531 |
rs147942742 | in-del | -/ATAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811248 | TTTCTTTATTTATAC[-/ATAT]ATATATATATATATA | 57531 |
rs147968898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104685306 | CTGTAACTGGTAGAG[A/G]TCAGGGAAGGGGTCA | 57531 |
rs147992090 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104813060 | AAACCTCCAGCCTCC[A/G]TGTTCCAACTAGGCT | 57531 |
rs147999416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696613 | CCTCAACTCCCATCA[C/T]TGTTATTAGATTATT | 57531 |
rs148042139 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771845 | ATCTCATCCAAAATA[C/T]TACTGCTTATCTAGT | 57531 |
rs148064339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717430 | AGGCGTGAGCCACCA[C/T]GCCCGGCCAGCAATA | 57531 |
rs148075604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104835482 | TACTATGATAGAGAC[A/G]TGCAAACTCAAAACA | 57531 |
rs148116615 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104712955 | GAGTTCCCTGCCCCT[C/G]TAACTGTGAGAAATA | 57531 |
rs148118608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791334 | AGCTCACCAACTTGC[C/T]GTTGATTAGACAGAG | 57531 |
rs148201992 | snp | C/T | 0.221737 | 0.248397 | intron-variant | HACE1 | GRCh38.p7 | 6:104738569 | AAGAAAGGGTATCAG[C/T]GATGGAAGATGAAAT | 57531 |
rs148203257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767362 | TTATCCTCAAAAGCT[G/T]AAAAGCTATTCCATT | 57531 |
rs148205991 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104850768 | AGAACGGATAGCACA[C/T]CACGCGCTCAAACAG | 57531 |
rs148234720 | snp | C/G | 0.0681886 | 0.171594 | intron-variant | HACE1 | GRCh38.p7 | 6:104802463 | ATTGACCACATAATT[C/G]GAAGTAAAGCACTCC | 57531 |
rs148246399 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104722930 | CTCGATTCACTCACA[C/T]AAGTACTACATATAG | 57531 |
rs148253911 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104733506 | ATATTATGACACTTA[C/G]ATTATACAGTATAAA | 57531 |
rs148257988 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104845658 | AATTTTCTGTATTTT[C/T]AGTAGAGAAGGGGTT | 57531 |
rs148286463 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | HACE1 | GRCh38.p7 | 6:104798697 | AAACAATAGCTAACA[A/G]TGGTTAATGTTTCAT | 57531 |
rs148320151 | in-del | -/GTTTTTTTTTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823786 | GATGTTTGCTGGCGG[-/GTTTTTTTTTT]TTTTCTTTTTGTAAA | 57531 |
rs148328623 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104753673 | CAGTAAAGTGGCCAG[A/T]TTACTAAAAGAAAAA | 57531 |
rs148369523 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104701248 | TCCAAGAACAAATGC[A/G]CTACAGGTTAGTTAT | 57531 |
rs148379395 | snp | C/T | 0.00964182 | 0.0687601 | intron-variant | HACE1 | GRCh38.p7 | 6:104744488 | CAAAACTTAACTTCA[C/T]TCTAAGCTCTAGAGA | 57531 |
rs148393284 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | HACE1 | GRCh38.p7 | 6:104801071 | ACTTCATAATGCATG[C/T]ACAAGCTTCAATAGC | 57531 |
rs148401539 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689265 | AGAGACCCTTAGGAA[A/C]ACTAATGAAGTGCTC | 57531 |
rs148423082 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104755958 | AAGAAGACAGAGACA[A/C]AAAACAACCCTTCAA | 57531 |
rs148476677 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104827316 | AACAAAAAAAGTGTC[C/T]TTACTTTTTTTATTA | 57531 |
rs148508598 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | HACE1 | GRCh38.p7 | 6:104816050 | TGCACTCCAGCCTGG[A/G]CGACAAGAGCAAAAC | 57531 |
rs148517613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704810 | TTTAAGCTGAGTCCA[C/T]CTGCCAAAATGTTGC | 57531 |
rs148528324 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822632 | GAGGCCGAGGCAGTC[A/G]GATCACTAGAGGTCG | 57531 |
rs148570115 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104774673 | ACAGGCATGAGCCAC[C/T]GCGCCCAAGCAGGTA | 57531 |
rs148580892 | snp | C/G/T | 1.6492e-05 | 0.00287154 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795645 | ATCTTTAGGTACTGG[C/G/T]TTTCACTTTGCTGAG | 57531 |
rs148590875 | in-del | -/AGGAGA | 0.493432 | 0.0569306 | intron-variant | HACE1 | GRCh38.p7 | 6:104716596 | TCAGGAAGCTGAGGT[-/AGGAGA]AGGAGAATTGCTTGA | 57531 |
rs148603174 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837633 | ATGCAAAAAACTGAT[C/G]AATTTGACTTCAAAG | 57531 |
rs148632431 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104793631 | CAGTTATTTTCTTAA[C/T]GAAAATTTCTATTAA | 57531 |
rs148643328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714501 | AAAACCTTCCCTTTG[A/C]CTTAACCACTTTGGA | 57531 |
rs148684166 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104787334 | ACGGTTGACAGATTT[G/T]GAGTCCCTGAACTGC | 57531 |
rs148740081 | snp | A/G/T | 1.64953e-05 | 0.00287182 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777232 | AGCAGGATATCATTT[A/G/T]CATTCACTGGCCTGT | 57531 |
rs148760960 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104803778 | GAATGGGCAAAAACT[A/G]GAAGCATTCCCTTTG | 57531 |
rs148771269 | snp | C/T | 0.136166 | 0.22258 | intron-variant | HACE1 | GRCh38.p7 | 6:104848191 | CCGGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA | 57531 |
rs148782527 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104818743 | ATACACAAATCAATA[A/T]ATGTAATTCAGCACA | 57531 |
rs148836542 | snp | C/T | 0.000148705 | 0.00862151 | intron-variant | HACE1 | GRCh38.p7 | 6:104744260 | AAAAAACTTAGCTCA[C/T]ATTTCAGAGCAATTG | 57531 |
rs148878147 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104820126 | CTTGAACCCGGGAGG[C/T]GGAGTTTGCAGTGAG | 57531 |
rs148909867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805794 | AACCAACATGGCACA[C/T]GTATACCTATGTAAC | 57531 |
rs148912002 | in-del | -/TTG | 0.360421 | 0.224293 | intron-variant | HACE1 | GRCh38.p7 | 6:104723636 | CCTTAAAAGTGAATT[-/TTG]TTGTCTAAGAACTGT | 57531 |
rs148916982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690438 | CACCAACAGGAATAT[C/T]TAGAATGAAACCAGC | 57531 |
rs148920043 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104765780 | TCTTTAAATACACAA[G/T]TGAGATCTTCAGTTT | 57531 |
rs148951524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757450 | AGACCTGCAGCTAAG[A/G]GGCCTGTTTGTTAGA | 57531 |
rs148953538 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104834839 | AAAGAGGTTGAAAGT[A/T]TATTTAATAAGATTT | 57531 |
rs149004742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104830502 | TAAGACAATGTCACC[C/T]TTGCCTACTATCTTG | 57531 |
rs149013029 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104720219 | ATGTGACCAGTACTA[C/T]GATCCAGATACAGAA | 57531 |
rs149044922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707448 | CATTTCAATAGACAC[A/G]GTAAAAGTATTGTAT | 57531 |
rs149076247 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732984 | ACAGCAAGAGAATAT[A/C]TACAGAAGACCTGGC | 57531 |
rs149086124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778485 | AGAGATACTACTTCT[C/T]TGAATAAGCATTAAA | 57531 |
rs149119727 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104845273 | GCATAGCCAGGCTCA[C/T]AGTAGCTCTCAATAA | 57531 |
rs149154223 | in-del | -/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104794129 | ATCATTTAACTTCAA[-/T]TTTTTTTACATGTAA | 57531 |
rs149159147 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104716732 | AACACATTCTGGGCC[A/G]TGAAACGAAATTCAA | 57531 |
rs149162205 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104798248 | CTATACTCTTTCCAC[A/G]ATAACATTACCTAAA | 57531 |
rs149214879 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104790035 | GAATTACAAGAATGC[A/G]TAACTTCATTCTTCC | 57531 |
rs149237544 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729160 | AAATCATTGCAATAT[A/G]GAATACACTGTGGCA | 57531 |
rs149247645 | snp | C/T | 0.000247609 | 0.011124 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744551 | ATAGCCACTTGTGTA[C/T]TCTGTATTTTTTATC | 57531 |
rs149266940 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | HACE1 | GRCh38.p7 | 6:104688726 | ACTTCTAGAGGCTGT[A/G]GGCTTTTCCCGGCTG | 57531 |
rs149270056 | in-del | -/AAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756412 | CCAGATTCCATCTCA[-/AAA]AAAAAAAAAAAAAAA | 57531 |
rs149270975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800855 | TGGAACAAAGTTGGA[C/T]GGAGAATGACTTTGA | 57531 |
rs149318712 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683420 | ACTTGGAGTCTGAAA[A/T]GCCAGATTCTAGCAT | 57531 |
rs149322842 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104793128 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGCCCAT | 57531 |
rs149352421 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104747369 | TACAATGGATGACTA[C/T]ACCTCCAGTTCAGTA | 57531 |
rs149394738 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104697075 | AAAGCTGATTTTGCC[A/G]GCGATTTCTAAGGTT | 57531 |
rs149417404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712362 | AGTAAGGTTTGACGT[G/T]TGTCCCCTCCAAAAC | 57531 |
rs149447713 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104692445 | GAAAAAATGTTAAGC[A/G]AGGCCTTGAAATATT | 57531 |
rs149450812 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104767268 | TCAGACATTAGGTGG[C/T]CCAATCCACAACAGT | 57531 |
rs149460567 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104818314 | GATCATTGACCTAGA[A/G]GTGGTGTCTGTAAGG | 57531 |
rs149471846 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104837356 | ATATGCCCAACTGAT[G/T]TTTGAAACAGATGCA | 57531 |
rs149502179 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | HACE1 | GRCh38.p7 | 6:104762888 | CCAGCTACTCGGGAG[G/T]CTGAGGCAGGAAAAT | 57531 |
rs149531615 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104722186 | GGAATTTGAATACCA[A/G]TTTATTTTTTCTCTA | 57531 |
rs149608119 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104735367 | GGTGCGGTGGCTCAC[A/G]CCTACATGTAATCCC | 57531 |
rs149622724 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861042 | CTCTGTAATCTTCAC[C/T]TAATCAGATGATACC | 57531 |
rs149672325 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104789281 | GTTAATACTTATTAA[C/T]GTGTTTAAAAACTAG | 57531 |
rs149765076 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104858032 | ATTTTAACTTGTTAG[A/G]GAGGGAAAAAGAAAT | 57531 |
rs149796410 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690180 | ATGGAAGATCAAGTA[C/T]ATAAGGGAGACCATC | 57531 |
rs149806616 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104731893 | AAAAATCCCGATTAA[A/G]AATGGGCAAACAATT | 57531 |
rs149848776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104685142 | ACCTCCAAGTTGGAC[A/G]CGCAGTTTAGACAAA | 57531 |
rs149851628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761085 | CATTCCATGCTTATG[A/G]ATAGGAAGAAGCAAT | 57531 |
rs149872432 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830392 | TCAGATGATAAAAGA[C/T]AAAAAATGCAAATGA | 57531 |
rs149882838 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | HACE1 | GRCh38.p7 | 6:104750879 | AGTGATTTAAAAATA[C/T]ATATATGTGTATATA | 57531 |
rs149933298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104714018 | CCGGGGAGTCTAATA[A/G]GAGACCTCAATGTAA | 57531 |
rs149937663 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104823246 | CAAGATCAGCCTGGC[C/T]AACATGGTGAAACAC | 57531 |
rs149965462 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104698977 | CCACCTCGGCCTCCC[A/G]AAGTACTAGGATTAC | 57531 |
rs149966854 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | HACE1 | GRCh38.p7 | 6:104777406 | AAATGCCTTTTCTAC[A/G]AATAATCATTCTTAG | 57531 |
rs149983249 | snp | A/G | 0.000232242 | 0.0107734 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104777103 | ACAGCTACTCCTAAA[A/G]ATAGAATCTAAATAT | 57531 |
rs150010531 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696164 | GCCCCATGGTGGGGG[-/C]GGGGGGGGGGGTTGT | 57531 |
rs150020878 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852086 | TAAGAAAATCTATCA[C/T]AAAATGTTACAGCTC | 57531 |
rs150051564 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104833472 | TGCCTCAGCCTCCTA[A/C]ATAGCTGAAATTAGG | 57531 |
rs150059419 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104724759 | TAAAGAAGATACTAC[A/G]TGCTATATTCTTTAT | 57531 |
rs150071968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847261 | CTAATCTCTCCTTTC[A/G]TTAACATAGTTGTTG | 57531 |
rs150091297 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104710948 | CTTCTGTTAAATTCC[C/T]GAGTCCATTCAGAAA | 57531 |
rs150103378 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729066 | AAGCTTTCATATATA[A/C]ATTATATGTCATTTC | 57531 |
rs150114951 | snp | A/C | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854785 | GAAATATAAACTGAG[A/C]TATTTATAGGGGAAA | 57531 |
rs150126103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104772745 | AATAAGTTACCAATT[A/G]CTATGAAAATCCAGT | 57531 |
rs150155165 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104726493 | GTAGGAATCATCTCC[C/T]GGGCCTCCAACTTGT | 57531 |
rs150281830 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | HACE1 | GRCh38.p7 | 6:104739168 | GAGCCTGAAGGAAGC[A/G]CTAAACATGGAAAGG | 57531 |
rs150287728 | snp | A/G/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859943 | TAGTTTCCAGCTGGC[A/G/T]GAACGGAGCGCCCTG | 57531 |
rs150291385 | snp | A/C/G | 4.94575e-05 | 0.00497259 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785183 | TCAAATGGAGGAATG[A/C/G]AAGCAGCATCTTGAT | 57531 |
rs150296992 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104740380 | taatgaatccaggag[C/G]tggttttttgaaagg | 57531 |
rs150310585 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104691817 | GTCCCAGCACTTTAG[A/G]AGGCCAAGGCAGGAG | 57531 |
rs150332565 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104707242 | AAACTATAAGCCAAG[A/G]TTCCTTGTAAATATA | 57531 |
rs150333550 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | HACE1 | GRCh38.p7 | 6:104733800 | AGCTGAGATCAACCA[C/T]TGCACTCCAGCCTGG | 57531 |
rs150336238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817639 | TATCCAATGAATCTG[C/T]CTTTGTAGAAGAGAG | 57531 |
rs150375710 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687457 | CTCATCAAACGGTAT[A/G]GGAGCTGCCCCAGAA | 57531 |
rs150419476 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840086 | CTTACTGTAATATTA[C/T]AGTATAGTTTTGCAA | 57531 |
rs150451719 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104826063 | GATTCTCATAGGAGC[A/G]TGAACTCTGTTGTAA | 57531 |
rs150495908 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104781258 | TTATTTTGATGCTCA[A/G]ATTCTTCCAAATTTG | 57531 |
rs150504157 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104724678 | TCCATCTCTAGATAA[C/T]GCACTTTTTTTAATT | 57531 |
rs150516639 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104846955 | CATGAATTCTTTTTA[C/T]TCCTTTTCTTCTTGC | 57531 |
rs150529052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841797 | AACATTTTCTGCCAT[G/T]ATTTCAAAACAACTA | 57531 |
rs150558915 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799635 | ATGGCAGACCAGAAT[C/T]TGAATCTGCATCAGT | 57531 |
rs150601429 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774391 | CACCGCGCCCGGCCT[C/G]TCTTTTTTTTTTGAG | 57531 |
rs150606553 | snp | C/T | 0.000186341 | 0.00965069 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796721 | AAGCCTCGGGTGATA[C/T]TGAATTAATACTTCA | 57531 |
rs150610790 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104792525 | TATTTTGAAATCTCT[A/G]ACATCAGTTATCTTG | 57531 |
rs150629499 | in-del | -/CC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787142 | AAAAACACAACAAAA[-/CC]AACAAAACCACCACT | 57531 |
rs150632580 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104731348 | CTTTCTTAAAAATAT[A/G]ATTTATAACATAAAG | 57531 |
rs150642002 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104774852 | CATCTTAATTTCATT[A/C]GAAAACAAGTTCTTT | 57531 |
rs150650898 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HACE1 | GRCh38.p7 | 6:104857350 | AAAGCAAATGCAAAC[A/G]ATGCCATTTTTGCCT | 57531 |
rs150683979 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104727432 | ACATGTATATGAATA[C/T]ACACACATGTATATG | 57531 |
rs150685825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104807684 | ATAAAAGACTTAAAG[A/G]TGTGTAAAGATGGCA | 57531 |
rs150695375 | snp | A/G | 1.64779e-05 | 0.00287031 | missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104850910 | CTTTAGTCTTACTTT[A/G]CTGCAATGTGAAGCA | 57531 |
rs150737119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802816 | GAACTAGAGAAGCAA[C/G]AGCAAACACATTCAA | 57531 |
rs150819459 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104753941 | AGTCTTCAGAAGGTG[A/G]GTAATAATAAACTTC | 57531 |
rs150840670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694534 | TTGTAATACAAAGGA[C/T]AAATGCTTGAGGTGA | 57531 |
rs150843619 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104769075 | GATCTTGCTCTGTCA[C/T]TCAGGCTAGAGGGCA | 57531 |
rs150853414 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104818829 | TTTTGATAAAATTCA[A/G]CATCGATTTATGTTT | 57531 |
rs150862864 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104708668 | TTCCTGATTTCAAAA[C/T]TTTCCACAAGGCTAC | 57531 |
rs150950000 | in-del | -/GCAGGTCTTTCAACCT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810371 | TAAACAAGAAAAAAA[-/GCAGGTCTTTCAACCT]AAAACCAACTTCCAA | 57531 |
rs150957921 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104710829 | GAATGTAATTTCAGG[A/C]ATTAGGCTTAAATTT | 57531 |
rs150962517 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | HACE1 | GRCh38.p7 | 6:104820705 | CAGATGCTGGCAAGG[C/T]TGCAGAGAAAAAGGA | 57531 |
rs151011925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104782833 | GACAAGTGTCCCTAA[A/G]GACATTAAAAACCAC | 57531 |
rs151022842 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705557 | TGCGTGTCTTTAGTC[A/G/T]TTTCCCAGGATGGCT | 57531 |
rs151043749 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104765893 | TTTCTTCAAGTTATA[A/T]AGTGTGGTCATTCCA | 57531 |
rs151046155 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104849604 | TACCTCAGCCTCCCA[A/G]AGTGCTGGGATTACA | 57531 |
rs151085825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720319 | GACAACTGATCTGGT[C/T]TTTGTTCCAGTAATT | 57531 |
rs151170313 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104750819 | ATCTGGTGTCCCTGT[G/T]TCCATTTTTGCCCCT | 57531 |
rs151212280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104698870 | CAATTAATGGACTTA[C/T]CTAAAGTGTTTTTAT | 57531 |
rs151219790 | snp | A/G | 0.000230825 | 0.0107405 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785040 | GAATGACAGCACTTA[A/G]CCGGTTAGCTGTCAT | 57531 |
rs151227095 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853837 | ACATTCCAAGACCCC[A/G]AGTCAATGCCTAAAA | 57531 |
rs151244450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687295 | CATTTCCTGAGGGCC[A/G]CATGCTGGGAGTCTG | 57531 |
rs151307547 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104804631 | CCTATTTGATAAATG[C/G]TGCTGGGAAAACTGG | 57531 |
rs180682191 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104846221 | TAAGTCAAATCAACC[C/T]AATAAATAAGTAGCT | 57531 |
rs180703814 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104835661 | AAAGAAATCATGAAA[A/G]TAATAATTTATGAAT | 57531 |
rs180706102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104824397 | ACAACGGAGTTTCAA[A/G]ACTCCACATACATTC | 57531 |
rs180711639 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104785690 | CTGTATTAATATGAT[C/G]AATGTCAACCACTTT | 57531 |
rs180717310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770668 | AGGTTGCAGTGAGCC[A/G]AGATCATACCACTGC | 57531 |
rs180721831 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104804005 | TAAGCTGATAAGCAA[C/T]TTCAGCAAAGTCTCA | 57531 |
rs180725674 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854888 | TTTAGTCCTTGGCAA[C/T]ATTCACAAGTTCAGT | 57531 |
rs180730438 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794580 | TTCATGATCACCTCA[C/G]AGATGGCCTAATGGA | 57531 |
rs180732262 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104730804 | ATGCCTGGAGTAGAC[A/G]TTCATTAAATGTTTG | 57531 |
rs180734533 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104759619 | TCTAAAATCAACACC[C/T]TAACATCACAATTGA | 57531 |
rs180737659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104752272 | AGAGGGAGACAGAAA[C/T]GTGTACCCAACAGTC | 57531 |
rs180738253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723836 | CCTTCAGCAATCCTC[C/T]TGCCTTGGTTTCCCA | 57531 |
rs180740342 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104716463 | TTGGGAGGCCGAGGC[C/G]GGCGGATCACAAGGT | 57531 |
rs180743466 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104814121 | CTGCAGAAAATAAGA[A/C]TAAAGAAAAGAAAGG | 57531 |
rs180749532 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743402 | AACATAGAAGAAAAT[A/G]TATTAAATTGTTTAT | 57531 |
rs180760485 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104693340 | ATAAAGTTCTTAAAG[C/G]CTTGCTATTTAACGA | 57531 |
rs180761068 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706680 | ACGGGGAGGTTACAT[C/G]CTGGGAAGACCAAGA | 57531 |
rs180778902 | snp | A/G | | | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682332 | TGATATAGGTAATTT[A/G]CCATCTTTCTTCTGA | 57531 |
rs180935967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789878 | AACAACTTTGTGTGA[C/T]ATGAATGTTTGAAGC | 57531 |
rs180943105 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104762226 | AGGATTATAAATCAC[A/G]CTACTATAAAGACAC | 57531 |
rs180943437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819328 | AGGAATACAACTAAG[C/T]AGGGAGGCGAAAGAT | 57531 |
rs180953045 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104831717 | GCTAACGCAGTGAAA[C/T]CCCATCTCTACTAAA | 57531 |
rs180965091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749234 | GTCAGGTCTAATAAT[A/G]TAATAGCTCAAATAG | 57531 |
rs180971906 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104799249 | ACTTTTGAGTTCCTC[C/T]GTAACAAACTTCAAC | 57531 |
rs180972059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104712501 | GCTGTTGGCTGGGCG[C/T]GGTGGCTCACACTCA | 57531 |
rs180978276 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686281 | AACTTCTTCCTCTGG[C/T]AATGGGAGTGAAATT | 57531 |
rs180993957 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104850123 | CCGAGCTGATTTTTG[A/T]ATTTTTAGTAGAGAT | 57531 |
rs181014155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809909 | ATAACCTAATTATTT[C/G]TAATTTAAACAACTG | 57531 |
rs181020276 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104755966 | AGAGACACAAAACAA[A/C]CCTTCAAAAAATTCA | 57531 |
rs181038867 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776379 | TTAATTTATGAAATA[A/C]AACATTTAATTCAAA | 57531 |
rs181042658 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104719888 | TCACTCTGTTGCCCA[A/G]GCTGGAGTGCAGTGG | 57531 |
rs181045792 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104733820 | CTCCAGCCTGGGCAA[C/T]AGAGCAAGACTTCAT | 57531 |
rs181057928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699162 | GAAATGCCCCTAGTG[A/G]TATTATTTAGACTTA | 57531 |
rs181155384 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104836956 | AAACATGCACAAAAT[C/T]CCCACTGTGCTGTAC | 57531 |
rs181158041 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104815586 | CAGGCTGGTCCTTAA[A/G]TCCTGATCTCAAGTG | 57531 |
rs181166685 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104855777 | CATTAAGTCACCCCA[C/T]AATAAAGTCATAAAA | 57531 |
rs181179474 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739265 | TATATCAACTAACGA[A/G]CAAAATAACCAGCTA | 57531 |
rs181192723 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795498 | TCACTGACAAAAGGT[A/G]TCCCACAGAATAAAC | 57531 |
rs181281003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104731214 | AAAAAAAAAATTCTA[C/T]TGCTTTTAAAATGAG | 57531 |
rs181288658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104739166 | AAGAGCCTGAAGGAA[A/G]CGCTAAACATGGAAA | 57531 |
rs181292671 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104694469 | AACAGGGTGACAATA[C/G]TCAATAATAACTTAA | 57531 |
rs181304572 | snp | A/C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104722801 | ACAGTCCCTAAACCA[A/C/T]GGTTAAGTACATGGG | 57531 |
rs181312145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706162 | ATTTGGAGGTTTCCC[A/G]CGAATATCCAGATTT | 57531 |
rs181339442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752492 | TATATTATATTTTTT[A/G]AGATGCCAGGAAAGA | 57531 |
rs181364114 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104832411 | GTTGTTGTTGTTGTT[G/T]GATACAGGCTCTCAC | 57531 |
rs181371899 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104810304 | CAGGGTTGTTAAATA[G/T]ATGATCTGAATTGGT | 57531 |
rs181382187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850201 | GTGATCTACCCACCT[C/T]AGCCTCCAAAAGTGC | 57531 |
rs181393439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716976 | AGAAAAACCACATCT[C/T]TTAGACACTGCTAGA | 57531 |
rs181494780 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104735124 | TCAATTTGGCAATAC[C/T]GTAATTTAAAACTTT | 57531 |
rs181504258 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104721105 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGAGGCA | 57531 |
rs181520706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700531 | ACCCAGACTGGCTCC[C/T]AAGAGGGCAGTGCCC | 57531 |
rs181527692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776946 | CTAAATATTAAACTT[C/T]ATTCAAAAGGCATTT | 57531 |
rs181635049 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104842374 | ACTTTGGGAGGCCGG[C/T]GGGTGGATCACCTGA | 57531 |
rs181664877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845423 | GAAGTTAAATATCAC[G/T]TAAAATTAGCATTAT | 57531 |
rs181667484 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104756266 | AAACACAAAAAATTA[C/G]CCAGGCATGGTGGTG | 57531 |
rs181684167 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104803500 | ATGCAGCAGCATATC[A/C]AAAAGCTTATCCACC | 57531 |
rs181696977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104824183 | TAATTGGACATACAG[C/T]AGTGTGCAAAATGGA | 57531 |
rs181701497 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758905 | GGGGTTGCAATCCTG[G/T]TCTCTGATAAAACAG | 57531 |
rs181709064 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783651 | GGTAGGGGAAAGGTG[G/T]TCAGGTCAAATAAGT | 57531 |
rs181717720 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104742966 | GCACATAAACACCAT[A/G]GAATACTATGCAGCC | 57531 |
rs181725659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722995 | GGTTTTGCAACATTA[G/T]ATGCACAATATATTT | 57531 |
rs181754640 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685143 | CCTCCAAGTTGGACA[A/C]GCAGTTTAGACAAAT | 57531 |
rs181817839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837657 | TTCAAAGTTAAAAAA[C/T]TTTTGCTCTTCAAAA | 57531 |
rs181843722 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795941 | TATAGTTTTGGAAAT[A/T]TAATTCTAAACCTCT | 57531 |
rs181846859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104753059 | AGTCGAACTGCTTCT[A/G]AAATGTTTCCCTGCC | 57531 |
rs181890498 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104849773 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 57531 |
rs181892107 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104800015 | CTGCCAAAATACGGC[A/G]CTTTTCCCAAGGTCT | 57531 |
rs181899171 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685788 | GTACTGGCATCTTAC[A/G]AATGCAGAAAGTAAT | 57531 |
rs181903885 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104842558 | ACTAGCTATCTAATT[C/T]TACAATGAACATATT | 57531 |
rs181903929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820744 | ACACCGTTGGTGGGA[A/G]TAAATTATTTCAGCC | 57531 |
rs181907730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756565 | TTGAAAATAGTGATC[A/G]AAGAGTCGTTTCCAA | 57531 |
rs181916902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104777720 | CATGAAAATAATCTC[C/T]TACACCTAATCTTAT | 57531 |
rs181917461 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104735290 | AAATAATAAAGATAG[A/G]TAATTCATACCACAC | 57531 |
rs181931845 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104721371 | AGGAGAGGGGAGTGA[C/T]GGTGGGGAGGCTTGA | 57531 |
rs182036150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857649 | TTAAGCCTATTGAAG[A/C]ATACAAAAAAAAAAA | 57531 |
rs182056432 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104816357 | GCTCTGTGCAGCTTC[A/G]GGACTTAGTGCTCTG | 57531 |
rs182101545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809170 | CAAAACACTGTACTA[C/T]ACTTTGGACATAAAG | 57531 |
rs182104522 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839301 | GGTGAACAGTCCAAC[A/C]AATGGTGGTATATCC | 57531 |
rs182109537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816765 | CTGAAAAAGCCACAC[A/G]TACTCAATGTCAGCC | 57531 |
rs182123322 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104731904 | TTAAAAATGGGCAAA[C/T]AATTGAAAAAGACAT | 57531 |
rs182128335 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700906 | TTTAGCCACTTTAAT[C/G]TGCTTTACCTGGGAG | 57531 |
rs182129605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772461 | GGCAATAGGCTGTTC[A/G]CTAGGACAGACATTA | 57531 |
rs182133307 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104753479 | AGCCACCTCTTATAG[A/G]TGCATGCAGGCCAAC | 57531 |
rs182136437 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761918 | CTTCTCAAAAGAAGA[C/G]ATTTATGCACCCAAC | 57531 |
rs182137736 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104706296 | TAATCTCTAAAATCC[C/T]TCCAGAAACAAAATC | 57531 |
rs182141177 | snp | A/G | 0.224412 | 0.248687 | intron-variant | HACE1 | GRCh38.p7 | 6:104727547 | TGAATACACACACAC[A/G]TATGTATATGAATAC | 57531 |
rs182151242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695971 | CCTGACCTCGTGATC[C/T]GACCACCTCAGCCTC | 57531 |
rs182340039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811992 | TGATTGCCATTAATA[C/T]ATACTTAGCCCCCTA | 57531 |
rs182346254 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104792560 | ACAAATGTCGGAGCA[A/T]AGCAAAGAGTTGCAT | 57531 |
rs182346480 | snp | C/T | 0.00043122 | 0.0146773 | intron-variant | HACE1 | GRCh38.p7 | 6:104843319 | AAGAAAAAAGAGTCA[C/T]GGATAACTGGTACTT | 57531 |
rs182359551 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104745931 | TTTCCAACTTATCTG[C/T]ATGAGGTTGAGTTTT | 57531 |
rs182365332 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104787672 | TAACGCAAGAAATGA[A/C]ACAGGCTGATCATGC | 57531 |
rs182373753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821281 | TGTACAACAAAGCCC[C/T]GTGACACAAGTTTAC | 57531 |
rs182373948 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728376 | AATGGTAACTTTTAA[A/G]TAATTCCTAAATTTC | 57531 |
rs182376608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767618 | ATAATTTTCAAAGTA[C/T]TATTTGTGGATGCAA | 57531 |
rs182376798 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104750965 | CTCTTGCTCAAAACC[C/G]TATAATGACTTCTCA | 57531 |
rs182377304 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104789089 | CTCAGTAACTAGCAA[A/C]GATTTTTACTTGAAA | 57531 |
rs182382023 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104714588 | CCCAAATAAACTGAT[C/T]GTCTTTGGAGAATCT | 57531 |
rs182391238 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | HACE1 | GRCh38.p7 | 6:104831312 | GAAAATAGCCAGGCA[C/T]GGTGGCTCACACCTG | 57531 |
rs182399032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748184 | AGAAAATATTCATAA[A/T]ACATATATCTGATAA | 57531 |
rs182408573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690843 | ATACAAAATGAAGCC[A/G]TTAAAATTGCTAAAA | 57531 |
rs182424264 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104711151 | ATTAAAAGCAATGTA[C/G]TCCTGCCTCCTTCAC | 57531 |
rs182494769 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104759973 | ATAAATTCCTAGACA[C/T]ATACACCATCCCAAG | 57531 |
rs182510865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104744338 | TTATTCTACAAAACT[C/T]GTTTACCAAAAATGA | 57531 |
rs182520871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104724334 | CCTTCAAGTAGTAAT[C/T]CTATGACCACAGAGC | 57531 |
rs182528519 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682541 | TTTTCTATTTTCCCA[C/T]AGAAGACTATGAAAC | 57531 |
rs182533858 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104707009 | TCAGTAAATCTGTAA[A/C]AGATAAAAAGCGTAA | 57531 |
rs182586315 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858811 | GTCTGAATTCCTGAC[A/G]CTGCAAACAAAACTG | 57531 |
rs182592105 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104839658 | GGTAACCTACACAAG[C/T]AATAAAAATGAATAG | 57531 |
rs182611714 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797110 | TAATATGAGTCAATG[A/G]AAGAGTATCACTTTT | 57531 |
rs182627898 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104817778 | AAGAACGTTATTACA[G/T]TTCACTACTTGACTG | 57531 |
rs182632344 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104760524 | AACTCTCAGTAAACT[A/G]GGAATTGATGGAATG | 57531 |
rs182634116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104832981 | ACAATGAAAAACTTT[C/T]CATGAAATCAATTTT | 57531 |
rs182636774 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726812 | ACCATGTTTTAAGAA[A/T]TGAGTCATTTTCCTA | 57531 |
rs182645091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800368 | GAGAGCAGTGGTTCT[C/T]CCACCACAGCCTTTG | 57531 |
rs182674465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757039 | GAGGTTCTCTGCTCA[C/T]AGTATAAACAAAGAG | 57531 |
rs182685416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721656 | CGATTTAAGACTTAA[C/T]TCTTTCATTTTTGGC | 57531 |
rs182732270 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737041 | GTAATCCTAGCACTT[C/T]GGGAGGCCGAGGCGG | 57531 |
rs182736322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765013 | ACAATTACAATTCTG[C/T]TCACTGATGCTAGCA | 57531 |
rs182742719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757282 | GGGTCCCTGACTCCC[A/G]TGTAGCCTGACTGGA | 57531 |
rs182745230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721943 | AACAAGACTTGGTGA[C/T]GGGTTGGATACACTA | 57531 |
rs182749234 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791199 | TTCAAAAGCATGGTG[C/G]CTGCATATTACATTA | 57531 |
rs182760822 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104704656 | ACTCACTTTTTACTA[C/G]GATGGCCAGCCATCT | 57531 |
rs182884559 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852240 | GTGTGCGCGCGTGCG[C/T]GTGCACGGGCATGCA | 57531 |
rs182913987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846788 | AAACATCAGCCACTA[C/T]AGGAAGTACTCAAGT | 57531 |
rs182928458 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104825550 | TTTGTAACTTCACTT[C/T]AGCCTCTGATTAGTT | 57531 |
rs182934289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778048 | ACAGGCATGAGCCAC[C/T]GCGCCCGGCCTCTTA | 57531 |
rs182946570 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104847366 | TAATGTACCTAGACC[G/T]GAGATCAATTCAGCA | 57531 |
rs182959138 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104805623 | AAAACTAAACACCGC[A/G]TGTTCTCACTCATAG | 57531 |
rs182964870 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760350 | AAAGCTTATCCACCA[A/C/T]GATCAAGTCGGCTTC | 57531 |
rs182967372 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104804863 | ACAGACAAATGGGAT[C/G]TAATTAAACTAAAGA | 57531 |
rs182967391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732771 | AATCACTGATATGTA[C/T]ACATCCACAGGGAAA | 57531 |
rs182968513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786950 | AACCTTAGAAAATGT[C/T]TGAACTATTCTGCCA | 57531 |
rs182971091 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736466 | ATTTTTGTATTTTTG[A/T]AGAGACGGTTTCGCC | 57531 |
rs182973106 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | HACE1 | GRCh38.p7 | 6:104703716 | CATTACATTCTACTT[A/C]ACTTCACTTTCAGAA | 57531 |
rs182977603 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696128 | GACTCCTCACCTACA[C/G]TAGCTTGAATCTCAC | 57531 |
rs182980036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745290 | AATGAAATTAAGAAT[A/G]GCAAAGTATTTACCT | 57531 |
rs183146825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104717198 | AGGCTGGAGTGCAGT[A/G]GTGTGATCTCGGCTC | 57531 |
rs183154731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694880 | GGGCCCACATTTTCA[C/T]CTTGCCTTGGGCCCA | 57531 |
rs183162876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822619 | CCTAGCACTTTGGGA[A/G]GCCGAGGCAGTCGGA | 57531 |
rs183167776 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104844327 | GGCGTGAGTCACCAC[A/G]GTGGCCCATCATAAA | 57531 |
rs183174743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780874 | TTAATTTTCATAACC[C/T]TGATAGTTTTAAAGA | 57531 |
rs183187157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802481 | AGTAAAGCACTCCTC[A/G]GCAAATGTAAAAGAA | 57531 |
rs183201337 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104825302 | TTTGCAAACCCCCAC[C/G]TCTTTGCGAGGCAGA | 57531 |
rs183227884 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786259 | GGCAGGACGATCACT[G/T]GAACCCAGGAGGCAG | 57531 |
rs183230006 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754374 | GATTATCAGGACAGG[C/G]CAACATTCAAATTCA | 57531 |
rs183234152 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104779441 | TGCTTTCAGTAAGAA[A/G]AGAATAAATGCTACC | 57531 |
rs183243082 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821968 | ACCACAGGGCTTTGG[G/T]AGACCAAAGTGGGAG | 57531 |
rs183259586 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104718143 | TCTGTAGATTTTTTT[C/G]TGTGTGTTCTTTGAA | 57531 |
rs183298509 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104749803 | AGTACAATAAAGGCA[A/C]ATTAAAGTAGCAAAA | 57531 |
rs183308589 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104713407 | TGTTAGCTAATATAT[A/C]TTGAGCACTTAATAT | 57531 |
rs183361896 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104688320 | AGGAAAAGTTTATAC[A/C]AATTGCCCTTTGAAT | 57531 |
rs183365001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713612 | ATTAGCCAACCTGTG[C/T]TCTGATAATGATGTG | 57531 |
rs183441842 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104843961 | TCCCGGGTTCAAGTG[A/G]TTCTCCTGCCTCAGC | 57531 |
rs183457803 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104733685 | GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAT | 57531 |
rs183469709 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104840304 | AATAGTTTTCGTGTA[C/G]TCAAAAAAATAATAA | 57531 |
rs183474529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104719748 | CCTCTGTATACCTCT[A/G]AAACTTCCAGGCCTT | 57531 |
rs183481893 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104801934 | TAAAGAGTCAAGACC[A/C]ATCAGTGTGCTGTAT | 57531 |
rs183511623 | snp | C/T | 0.0596104 | 0.162024 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727660 | ATGTATATGAATACA[C/T]ACACACGTATGTATA | 57531 |
rs183538210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725508 | CTTAGAAACATTTAC[A/G]TATCAGTATGTATTG | 57531 |
rs183553199 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687664 | CAGTTGCTCAGAAAG[A/C]ACAAATTGCCATAAA | 57531 |
rs183575002 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104682953 | AGTGCCAGAGCTGAG[G/T]GGGGCCAGGGCCACA | 57531 |
rs183642954 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104770810 | AAAGTATGTGGAAAG[C/T]TTAAACACTGGCATT | 57531 |
rs183646379 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104683781 | TTCAGAGAGGCACCA[A/C]ATCCCACTGGGTAAT | 57531 |
rs183652703 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814494 | TTTTATAAGATTTTT[A/T]AAATTATCTTCAATG | 57531 |
rs183655716 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794850 | GTGGAGGTTGCAGTG[A/G]GCCAAGATTGTGCTG | 57531 |
rs183658751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844462 | AATTCTTCTGTCTCA[G/T]CCTCTCGAGTAGCTG | 57531 |
rs183669171 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752316 | CACTAAATTTCTGGA[C/G]TCCAACCCGGGAAAT | 57531 |
rs183780536 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708774 | AACTCATACATCTAT[G/T]GCCAATTGATTTTTC | 57531 |
rs183801575 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104731668 | GGATATTCACTACAA[C/T]GAAAATGAAGTTGGA | 57531 |
rs183803826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811019 | CAAATCAAAAGCTCC[A/T]CATGTAACATAAAAG | 57531 |
rs183809475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851788 | TTACATTCTTCTTCT[C/T]ATATCAAAAAATTCA | 57531 |
rs183841515 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104766043 | CACAGGGGTATCTGC[A/C]GGCCTTTTTGACATT | 57531 |
rs183847043 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727773 | TATGAATATGTACAC[A/G]CATATATGTATATGA | 57531 |
rs183884466 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861670 | GAGTTTGTGGGCAGG[C/G]GTAGGAGCCCCCAGC | 57531 |
rs183889496 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104841972 | TAAACTTATTTTTGC[A/C]AAGAAAGTGGTATGG | 57531 |
rs184002054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832731 | TAACCATACAGAATA[C/T]ATTTATCAGAAGTCC | 57531 |
rs184019835 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104750220 | AAAATGGACATTAAA[C/T]CATTTTGTCTCATTT | 57531 |
rs184020028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792211 | TTGCTATCTGCATTA[A/G]GTTTGTTCTCTACGT | 57531 |
rs184079205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828060 | GGTTTCTAAATCCAC[A/G]TTATTCTGAGAAGAC | 57531 |
rs184084476 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104858091 | TGGTGAAATGACATA[C/T]TTTTTTCTATTTTTC | 57531 |
rs184094800 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760866 | TCAGGATACAAAATC[A/T]ATGTGCAAAAATCAC | 57531 |
rs184105974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787911 | AAGTAATAAACCACA[C/T]TGGACCTTTCTTTAC | 57531 |
rs184111750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746486 | TTAGTCTGGAGGTGA[A/G]GGTACTCTCTGCTCC | 57531 |
rs184134428 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104710472 | TTGTGAGGATAATGG[A/G]CACCAAATTTACTAC | 57531 |
rs184138835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104727196 | ATATATGTATACGAA[C/T]ATATACACATACATG | 57531 |
rs184140457 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104684519 | AAGCCCAGATGAACT[A/G]GGAAAATTTTACTGT | 57531 |
rs184157563 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709152 | ATGATAGAAAATACT[G/T]GCAAATCATGTATCT | 57531 |
rs184236316 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806547 | ACAAAATCTGCACAA[C/T]GCAGTTAGGGGCTCA | 57531 |
rs184239000 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848109 | CGCCCGCCTTGGCCT[C/T]CCAAAAGGCTGGGAT | 57531 |
rs184278644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104698793 | ACGTCCTTGACATCC[A/G]TTTCAAAGTTAGAAA | 57531 |
rs184307237 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853723 | GGTAACATCACCAAA[A/G]ATAATATATGCTCAA | 57531 |
rs184331024 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104793192 | GGATGGCATGAACCC[A/G]GGAGGTGGAGCTCGC | 57531 |
rs184340092 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104833622 | GTTGAGGCAAGAGGA[C/T]TGCTTGAAGCAACGA | 57531 |
rs184340204 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104783300 | CTTAAACTCCTAAAG[A/G]TCCAGGTTATGTTGT | 57531 |
rs184340538 | snp | C/T | 0.105569 | 0.204058 | intron-variant | HACE1 | GRCh38.p7 | 6:104739190 | ATGGAAAGGAACAAC[C/T]GGTACCAGCCACTGC | 57531 |
rs184345662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813049 | AAATTAAGTGAAAAC[C/T]TCCAGCCTCCATGTT | 57531 |
rs184355778 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104722866 | TTCTGCACTAACTAT[A/G]TATCCAGCACCCACT | 57531 |
rs184365825 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706221 | ATCCAGCCACAGTAG[G/T]TTCTCATTCCCATCT | 57531 |
rs184383808 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802903 | ACACAAAAAACCCTT[A/C]AAAAAATCAATGAAT | 57531 |
rs184411429 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810091 | TGGAGGTTCAAAAAA[G/T]GTCTGATCTAAAGAT | 57531 |
rs184412123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718724 | CTGAACTCAAACCTA[A/G]TTCATCATTGTTGGA | 57531 |
rs184418872 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758289 | AAAAAATGTTAAGGG[A/C]AGCCAGAGAGAAAGG | 57531 |
rs184420284 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104733245 | TCAATATGATCAATC[G/T]AATGTCCTCCACACA | 57531 |
rs184423455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722613 | TTCACTTAAGCCAGA[C/T]ACCTGAAGCTGCACT | 57531 |
rs184436672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697832 | GCAACCTCCATCTCC[C/T]GAGTTAAAGCGATTC | 57531 |
rs184500109 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854933 | ACTTTTTCACTATAA[A/C]AGTAAAATACTAATA | 57531 |
rs184506427 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823188 | TCACACCTGCAATCC[C/T]AGCACTCTGGGAGGC | 57531 |
rs184546114 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104782402 | CTGAGCTGGGAGGAT[C/T]GCTTCAGCCCAGGAG | 57531 |
rs184546568 | snp | C/T | 3.3071e-05 | 0.00406625 | intron-variant | HACE1 | GRCh38.p7 | 6:104849122 | ACAACTTAAGCCACT[C/T]AAGAAAACTAAATAG | 57531 |
rs184564850 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104738215 | AAACCACAAAGATGG[G/T]GAAAAAACAGAACAG | 57531 |
rs184565949 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788923 | TGGCCTATAAACCCA[C/T]TCATTCTTAATGGAA | 57531 |
rs184570290 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104830739 | TGTTATTATGGTCAG[A/C]AAGAAAATAAATTAC | 57531 |
rs184578001 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104705292 | GTGGTCAGAGGCGTC[A/G]TTCCTCCTCTGTGAG | 57531 |
rs184579442 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104808669 | TACATTCCATTTAAC[C/T]TTTATCTTAGAGCCC | 57531 |
rs184589775 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104761760 | ATCAGAGTGAACAGG[C/T]AGCCTACAGAATGGG | 57531 |
rs184627754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819451 | CAGTATCAATAAAAC[A/G]GCTACACTAACCAAA | 57531 |
rs184630289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848823 | TTTCAGAAAATACAA[A/T]GTCACTATAATACAA | 57531 |
rs184651451 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757640 | GAACACCTCTTCACC[G/T]CCAAAGGAACACAAC | 57531 |
rs184652395 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | HACE1 | GRCh38.p7 | 6:104807236 | ACCATGTTGGCCAGG[A/T]TGGTCTCAATCTCTT | 57531 |
rs184658615 | snp | C/T | 0.00101077 | 0.022458 | intron-variant | HACE1 | GRCh38.p7 | 6:104730440 | TTATATCTTAATACA[C/T]TGTAATCATGAAAGA | 57531 |
rs184658808 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104692344 | ACAGCTATATATGTA[A/C]ATTTTAGGATCAAGG | 57531 |
rs184666515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737471 | GGTCAGTGGGTGTGC[A/G]CACCGTGCGCGAGCC | 57531 |
rs184671115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776487 | GGGCCAACACTAGTC[C/T]TTGAGACAAGCATTT | 57531 |
rs184684727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733951 | TGAGGTCAGGAGATC[A/G]AGACCAGCCTGGCCA | 57531 |
rs184688675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699235 | TATGTTAATGTTCTT[A/G]GGGGGAATACAAAAT | 57531 |
rs184805005 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799359 | TAGGCAAACACACAC[A/C]TAAGGGTAGTCAGTT | 57531 |
rs184809404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104756141 | CAACCTGCCAGGCAC[A/G]GTGGCTCATGCCTGT | 57531 |
rs184813580 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104829918 | AGTATATTATACTTA[C/T]ACCACCTAATTTTCA | 57531 |
rs184817243 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104719907 | GGAGTGCAGTGGGGC[A/G]ATCTCGGCTCACTGC | 57531 |
rs184836643 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840850 | TGCCTGAAATCCCAG[C/G]TACTCAGGAGGCTGA | 57531 |
rs184841717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104818939 | GCCAGTATCATAATG[A/G]ATGGGCAAAACCTGT | 57531 |
rs184854005 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860082 | TCTCACGCCCTGCTC[C/T]TCCTACCCTCCTCCA | 57531 |
rs184857445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775947 | TTAGGAAAAACAAGC[A/G]ACTGTGCAAAGCATT | 57531 |
rs184868649 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755330 | CCACACAATAATAGT[A/G]AGAGGCTTTAACAGC | 57531 |
rs184876879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798613 | ATAATCAGCTTTACC[A/G]GCATCAAGCAAGAAG | 57531 |
rs184882667 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104685880 | AATTTATGAAATCGT[A/G]ACCTTGAAACTCTTA | 57531 |
rs184888796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711171 | GCCTCCTTCACATAT[A/G]CCTGGGGTCACTTGT | 57531 |
rs184944499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823679 | TAGAATTAGGATAAA[A/C]ATGTATAAAGGAATT | 57531 |
rs184974997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751271 | TTCTAAAAAGTGGCT[A/G]CCACTTTGAAAGTAT | 57531 |
rs185008908 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104715574 | GATGAATTTTCCAGA[C/T]TGAATGACTCAAATC | 57531 |
rs185041678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803233 | AAAGTCCAGGAACAG[A/G]CGGATTCACAGCCGA | 57531 |
rs185049894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844944 | GCTGGGATTACAGGC[A/G]TGAGCCACCACACCC | 57531 |
rs185096630 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769264 | TGTCTCGAACTCCTG[A/G]CCTCAAGCAATCCCC | 57531 |
rs185098646 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728969 | AAATTAAAATGAGGC[A/G]TAAGAAAAACATTGA | 57531 |
rs185113242 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104691898 | AGCACTCCAACCTAG[A/G]TGACAGAACAAGACC | 57531 |
rs185128836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730990 | ATTTGATATTCAGAA[C/T]ATCAAATATATTTTT | 57531 |
rs185133062 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682396 | TATATAAATTGCTCC[A/G]TGACTCATCAGAGTG | 57531 |
rs185138958 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706790 | AATTACTACTGTAAT[G/T]TTGTGTAGACTGACA | 57531 |
rs185141850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716464 | TGGGAGGCCGAGGCG[A/G]GCGGATCACAAGGTC | 57531 |
rs185232453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727457 | TATATGAATACACAC[A/G]TATATGAATACACAC | 57531 |
rs185240875 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104798101 | AAGAAAGAAAGAAAA[C/G]AGAAGAAAAGAAATG | 57531 |
rs185252254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754688 | ATCTGGACAAACTAA[A/G]CTTTATAAGCAAAGG | 57531 |
rs185265102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685594 | ATAATTTCTCAAACT[A/G]TAGCTGCTATTTTTA | 57531 |
rs185265571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858315 | TGGATTCAAAGGTGG[A/G]AGTTGGAAAGAAAAT | 57531 |
rs185329827 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832070 | AAGAAAGAACTGTTA[C/T]TTGTACCATACACAA | 57531 |
rs185341504 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104774966 | AACTAAACCTGAGAA[C/T]GTGAAAATATTTCAG | 57531 |
rs185351186 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104763856 | GGATATCGAGACCAG[C/T]CTGGCCAACATGGTG | 57531 |
rs185353401 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104818022 | AGGAAGGGTGGTTTA[A/C]GGGACTAGCATTCTT | 57531 |
rs185356123 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104810250 | TGGAATCAGAAAGAT[A/C]TGGAAGTCTAGAAAC | 57531 |
rs185359534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104747516 | TCTCAGTGCAGCATA[A/G]CCCTCCCCTATGAAA | 57531 |
rs185366547 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104790750 | ACAGAGTGAGGCTCC[A/G]TTTCAAAAAATAAAT | 57531 |
rs185369989 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | HACE1 | GRCh38.p7 | 6:104710941 | ATTGTTTCTTCTGTT[A/G]AATTCCCGAGTCCAT | 57531 |
rs185376932 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749457 | ACTATGAATGATAAA[A/T]TAAAAATACTGATAC | 57531 |
rs185381319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712530 | CATAATCCCAGCACA[C/T]TGGGAGGCTAAGGCA | 57531 |
rs185389993 | snp | C/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727612 | ATGTATATGAATACA[C/T]ACACACGTATGTATA | 57531 |
rs185404789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687273 | TGGAAGCTGGCTGGG[A/G]AGTCTGCATTTCCTG | 57531 |
rs185437931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854422 | ACAAGATGTTAACCT[C/T]AGGGAAAGGTGAGTG | 57531 |
rs185466981 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770122 | TTTACTAAATCTATA[C/G]TTTAAAAAATGGCTC | 57531 |
rs185474312 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104813519 | CTTTTTTATTTTCAT[C/G]ACCAGGGAAGGGAAA | 57531 |
rs185522301 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | HACE1 | GRCh38.p7 | 6:104705012 | TTTTCAATAGAGAGA[A/T]TTTTATACATTTATT | 57531 |
rs185573216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834615 | AAAGAGTATTTCCTT[A/C]AAAGACTAGATCCAT | 57531 |
rs185591075 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104793933 | CATAAGTGGTGAGAG[A/G]GCACAGTTTAGCAGA | 57531 |
rs185596549 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786541 | TCTCGGAAGTCAAGG[A/C]TACAGTGAGCTGTGA | 57531 |
rs185606176 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815626 | CCTTGGCCTCCTAAA[C/G]TGCTGGGATTACAGG | 57531 |
rs185609732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760175 | TCAATAGAAAAAGAG[A/G]GAATCCTCTCTAACT | 57531 |
rs185609849 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104857166 | ATATATTTACATATA[C/T]ATATTTATTTACATA | 57531 |
rs185611612 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104805279 | AAATTAGTTCAATCA[C/T]TGTGGAAGACAGTGT | 57531 |
rs185615281 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104836964 | ACAAAATCCCCACTG[C/T]GCTGTACAAAATTCT | 57531 |
rs185618783 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751705 | AATGAATTATATACA[C/G]AGAGAGAAAGAGTAT | 57531 |
rs185627491 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104744365 | ATGATTTCATGCAAA[C/G]CTTTCATATGCACTA | 57531 |
rs185657227 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104722168 | CACTGTATATAGAAT[A/C]TTGGAATTTGAATAC | 57531 |
rs185686788 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | HACE1 | GRCh38.p7 | 6:104831465 | TGGCACACACCTGTA[A/T]TCCCAGCTACTTAGG | 57531 |
rs185813767 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849892 | CCTGACCTCAAGATC[C/T]GCCCGCCTCGGCCTC | 57531 |
rs185847098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832448 | ACCCAGGCTGGAGTA[C/T]AGTGGCACAATCTCA | 57531 |
rs185853648 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810699 | ATGCATGACACAGTG[A/T]GCGTTAACTAAACAT | 57531 |
rs185857252 | snp | C/T | 0.00146561 | 0.0270307 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104850936 | AAGCAAGCTTCTTTT[C/T]ACACGTCCGAATGCA | 57531 |
rs185931014 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104846469 | AGATATTGCACCAAT[C/T]ATAGGGAGCTTATGG | 57531 |
rs185990798 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104759818 | GCAAGACTAATAAAG[A/G]TGAAAAGAGAGAAGA | 57531 |
rs185994362 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104723916 | ATTATTAGCTAAGCA[C/T]CTATTCATAAAGACA | 57531 |
rs186100921 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104825151 | ATCAAAATGATCCTG[A/C]ATTTGAGTGGTTTTG | 57531 |
rs186130434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735162 | TAAATTTAAATTACA[C/T]GGAAATCTCTATATT | 57531 |
rs186141115 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104756398 | GCCTGAGTGACAGAG[A/C]CAGATTCCATCTCAA | 57531 |
rs186145399 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104721108 | CCCAGCACTTTGGGA[A/G]GCCAAGGAGGCAGAT | 57531 |
rs186163636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700669 | TATTTGGGAAAGGAA[A/G]TGCAAAAGAGAAAAA | 57531 |
rs186216059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821334 | TACCCCTGAACTCAA[A/C]ATAAAAGTTAAAAAA | 57531 |
rs186224296 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850129 | TGATTTTTGTATTTT[C/T]AGTAGAGATGGGGTT | 57531 |
rs186320876 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104845707 | TGGTCTCGATCTCCT[A/G]ACCTCATAATCTGCC | 57531 |
rs186334420 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803875 | GCCAGGGCAATCAGG[A/C]AAGAGAAAGAAATAA | 57531 |
rs186339871 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104843376 | TTTACTGAAATATTA[C/G]CAACAATCAATAACA | 57531 |
rs186344750 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104784868 | ATGAGTATCTTAAAA[A/C]AAGGAGAAAACTTTA | 57531 |
rs186349129 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104824197 | GTAGTGTGCAAAATG[A/G]AGTCTCATTCTCAAA | 57531 |
rs186354819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104753318 | CTCCCACCTGCTGGC[C/T]TTGGAGAATACAGGC | 57531 |
rs186357857 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | HACE1 | GRCh38.p7 | 6:104717332 | TTAGTAGAGACGGGG[C/T]TTCTCCATGTTGGTC | 57531 |
rs186361561 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104759109 | ATAATGGGAGACTTT[A/G]ACACCTAACTGTCAA | 57531 |
rs186365677 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731769 | ACTATAAAACTCTTA[C/G]AAGAAAATATAAGGG | 57531 |
rs186377822 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104695495 | TGAATGAGGCACAGA[C/G]TGTGAAGAGAAACAG | 57531 |
rs186378381 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104801632 | AGCTTCACAAGTGAA[G/T]GAGAAATAAAATCCT | 57531 |
rs186478065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825379 | AGACGTTTGCATAGG[A/G]GTCTAACTCTGTAAC | 57531 |
rs186514198 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104752822 | TTATTTTCCACATGT[A/G]TTTCAGTAACCCAGT | 57531 |
rs186515097 | snp | A/G/T | 8.47449e-05 | 0.00650893 | synonymous-codon, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795682 | GCTCCAGAACTTGCC[A/G/T]TAACTAAATTTTTTA | 57531 |
rs186522718 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104842674 | CCTTAAAAGTCAGTG[A/G]CAAAGGCTAGGGGAA | 57531 |
rs186532388 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716996 | ACACTGCTAGAGAGT[A/G]TCACCCCTTTGGAAA | 57531 |
rs186536223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800038 | CAAGGTCTTAGTAAA[C/T]GACACACCAGGAGAT | 57531 |
rs186553370 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104820783 | AGACAGTGTGGTGAT[A/T]CCTCAAAGACCTAAA | 57531 |
rs186564927 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104777979 | AGCCAGGCTGGTTTC[A/G]AACTCCTGACCTCAG | 57531 |
rs186570604 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104735563 | GTGAACCCAGGAGGC[A/G]CAGCTTACAGTGAGC | 57531 |
rs186666171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104846981 | CTTGCTGAATAGCTA[C/T]GTGAATCATGTAATA | 57531 |
rs186716533 | snp | A/G | 9.90949e-05 | 0.0070383 | intron-variant | HACE1 | GRCh38.p7 | 6:104771164 | GCCAAGTTACAAACA[A/G]TGGTTAAGGTAAAAA | 57531 |
rs186746602 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104731446 | CAAAGGTGGCAGACT[C/T]ACATATCCTGATTTG | 57531 |
rs186756194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694634 | TATAAATGTATATAC[C/T]TACTATGTATCCACA | 57531 |
rs186758994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765408 | ACATTTATTCTGTCC[A/T]TGGTAGCCTACCACA | 57531 |
rs186765780 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104799605 | ATAATGGAGTTGCTC[A/G]AGATGAACAGTTACA | 57531 |
rs186770388 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104842485 | ACCGTGATTATCTCA[C/G]AGTGCAAGGAATACA | 57531 |
rs186779926 | snp | C/T | 9.85154e-05 | 0.00701769 | intron-variant | HACE1 | GRCh38.p7 | 6:104796801 | TTAAAAACAGTCCCT[C/T]TTAAAGTTCATATTC | 57531 |
rs186787461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839331 | CACTACTGGATGGAA[C/T]ACTATTCAGCATTAT | 57531 |
rs186790476 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104817022 | TCAATGCCTGTACCC[C/G]CACTGTATCTTGGAA | 57531 |
rs186796114 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104753969 | TTCACTGAGATAAAG[A/G]AGCATGTTTTAACCC | 57531 |
rs186801518 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104726877 | ACCATTTTTCTATAC[C/T]ACCTTGCATTCAACA | 57531 |
rs186807477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772866 | GAAAGGGGATATGGG[A/T]GATATTGCTTAACGG | 57531 |
rs186807685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683846 | ACTTAAGTGAGGCCG[A/G]CAACAGAGAAGATTC | 57531 |
rs186808597 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104687747 | ACCAGAGCTGCAGGC[A/G]TTTTGGGACCCAGCC | 57531 |
rs186809379 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104732125 | GTAAAATGATGCAGC[C/T]TCTGTGGAAAACAGT | 57531 |
rs186812952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710035 | AAAAAATGTATATGA[C/G]TGTTCATTGCACCAT | 57531 |
rs186973275 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820228 | AAGTAAAACCCAAAA[C/T]CATAAAACCCTGGAA | 57531 |
rs186982353 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749854 | AGAGGATGGCAAAGA[C/G/T]GATGGACTCCATAGG | 57531 |
rs186989154 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104791387 | AATTTTGAAAGTGAT[A/G]TGGGTATAAACCAAA | 57531 |
rs186991325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852531 | GTATTTCAGAATTTA[C/T]GATAGTGAAGAATCT | 57531 |
rs187008468 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104857874 | AGGCAGGAGAATAGC[A/G]TGAACCCCGGAGGCA | 57531 |
rs187008645 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104792846 | CAATCAAGCAGCTGA[C/T]CAATCATTTGCTCCT | 57531 |
rs187013851 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104777616 | ACATGTAATTGAATA[C/T]ATTTATTCTCAATTC | 57531 |
rs187016005 | snp | A/G | 0.000214142 | 0.0103453 | intron-variant, synonymous-codon, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833054 | TACCGTCTTGTGACC[A/G]TTCTGGCAGGCAACA | 57531 |
rs187018954 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713524 | AAAACCAAGACAATT[A/G]GAGGTTGATTAACTT | 57531 |
rs187041787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104816478 | CCTTGAAGCTTCCAC[A/G]TGGTGTTGGGCCTGC | 57531 |
rs187044862 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728652 | CCGTTAGCATTTCTT[C/T]GTGTATGCATGTTCC | 57531 |
rs187048059 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767653 | TTTCAGAATTTGGCC[A/C]CTTTCTCCCTTCCCC | 57531 |
rs187052126 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104751115 | CAATTCTAGTTTCAC[C/T]GGCTTTCTGGCTATT | 57531 |
rs187055354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104714821 | AAGAATCAAACCCCA[A/G]AAGACATCAAGTAGT | 57531 |
rs187086884 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104772383 | AATAATACAGCAGAG[A/G]ATCATATACACATAC | 57531 |
rs187117454 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743075 | GAACAAAAAACCAAA[C/T]ACCGCGTATTCTCAT | 57531 |
rs187121817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104706393 | TAGACTTCCCAAGCA[C/T]GAAACTTAGAATACG | 57531 |
rs187167997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707661 | CCCTCCTTGCTGCAT[C/G]CTGACATGGCAGAAG | 57531 |
rs187174172 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724469 | AATCTAAATGTTAAT[G/T]TTAGAGACATGGTCA | 57531 |
rs187242064 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796402 | GGCGTGAGATACCAC[A/G]CCCAGCCTATTCTAG | 57531 |
rs187246654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858920 | CCTCAGGGACCATGC[C/T]TTATTCCTCTTTGCA | 57531 |
rs187248346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840125 | CACTGGAGGAAACTC[A/G]GCAAAAAGTGCAGGG | 57531 |
rs187251793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838039 | AAGAAAACTATAGAA[A/G]AAGATGCAAGAAACT | 57531 |
rs187284493 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104723146 | CCACACTAGCTTGTT[C/G]TGGCACAGTGAGAGA | 57531 |
rs187350933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780216 | TAAAAACAAATGGAA[C/G]CTTTTCAAGTAATTC | 57531 |
rs187357154 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104757326 | CGGGTGCCCCTCTGG[A/G]ACGAAGCTTCCAGAA | 57531 |
rs187362820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802118 | ATCAAAACAGACAAG[A/G]AAGGACATTACATAA | 57531 |
rs187367955 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104737050 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 57531 |
rs187377558 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789112 | ACTTGAAATCACCCC[C/T]ACAATGAACAGGAGA | 57531 |
rs187396987 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722120 | AAGTTTGAGATTCCT[A/T]AAAAAACATCCAAGT | 57531 |
rs187399556 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748202 | ATATATCTGATAAAA[G/T]ACTCTTATAAAAGAA | 57531 |
rs187401189 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704874 | TTTCAAAAGCATCTC[A/G]TAGTCACTTACTGGT | 57531 |
rs187405904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104721437 | GTTTTCAACTCCCAG[A/C]TCTCCCCCTTCACCC | 57531 |
rs187457911 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853919 | AGTTTAATTTATAAA[A/T]TGGGCACAGTAAGAG | 57531 |
rs187463364 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833836 | CTAAAATACAAAAAA[G/T]TAGCTGGACGTGGTG | 57531 |
rs187557930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826403 | TAGATGGTGATCAGT[A/G]CTATCCAGAAAAATA | 57531 |
rs187561298 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775067 | AAATGTTTGGCCAGA[C/T]GTAGTAGCTTACACC | 57531 |
rs187563098 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104807061 | TGGAGTCTCACTCTG[C/T]TGCCCAGGCTGGAGT | 57531 |
rs187569306 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104848184 | GTTTAGGCCGGGTGC[A/G]GTGGCTCACGCCTGT | 57531 |
rs187583868 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104847678 | TTTTTAGCTCCATAT[A/C]CATCTTATTAGGCAG | 57531 |
rs187586147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733641 | GTGGATCACTTGAGA[C/T]CAGTAGGGACCAGAC | 57531 |
rs187594449 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104760574 | CTATTTATGACAAAC[C/G]CACAGCCAATATCAT | 57531 |
rs187602151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755297 | AGTGCTTAGAGAACT[A/G]CAAAGAGACTGAGAC | 57531 |
rs187604837 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104718798 | GTAAGTCTAATAAGC[A/C]TGTAGTTTTTAAAAA | 57531 |
rs187614823 | snp | A/G/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104805679 | TGGACACAGGGCAGC[A/G/T]AACATCACACACCAG | 57531 |
rs187645881 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104761965 | GCTCATCATCACTGG[C/T]CATTAGAGAAATGCA | 57531 |
rs187652915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809355 | GATTGGTCAGGAACT[A/G]CCTTCCTAAAAAGTT | 57531 |
rs187657485 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104701382 | AAATTACGCATCTTC[C/T]CCTAAGAAAATCCTA | 57531 |
rs187838890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822804 | GGAGGTTGCAGTGAG[C/T]GGAGATCGCGCCACT | 57531 |
rs187839599 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104828917 | GTGCTTAGCTAGTTG[C/T]TCAAAATGTTTTCAT | 57531 |
rs187843020 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778368 | TGTGACTAACACAGA[A/G]TAACACAATATATAT | 57531 |
rs187850711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844343 | GTGGCCCATCATAAA[C/T]ATTTTTTTTTTTTTT | 57531 |
rs187857654 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787674 | ACGCAAGAAATGACA[C/T]AGGCTGATCATGCAG | 57531 |
rs187859018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746064 | CAAAACTGTTAAACA[A/G]TACCAGTCTTCCCAC | 57531 |
rs187867928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802627 | CTATTGGGTAAATAA[C/T]GAAATGAAGGCAGAA | 57531 |
rs187878234 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104781635 | CAACCTGCAACCCCA[C/T]TCCCTTGGTATGTAA | 57531 |
rs187880431 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104736665 | GTAATAATTCCTCGT[C/T]TTAGTTATCTCTAAG | 57531 |
rs187893587 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104704130 | AAAAAGATATTTATA[A/C]TGGGTAAATGAATAA | 57531 |
rs187902000 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104717930 | TGTATGTTAACCCCT[C/T]ATTGGACTTAGACAT | 57531 |
rs188002966 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812802 | AGGTACCTTGGAATA[C/T]AGGAATGGTTATGTA | 57531 |
rs188045417 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104713905 | CAAAGTCAGTTTTCA[C/T]TCTAATGATATGCAC | 57531 |
rs188052646 | snp | C/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728059 | CCCACCTCAGCCTCT[C/T]GAAATGCTGAGATTA | 57531 |
rs188054897 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104689017 | TTCAGTTTACTACAC[C/T]GGCTCTCACATGCCA | 57531 |
rs188099761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840926 | CAAGACAGCACCATT[A/G]CACTCCAGCCTGGGC | 57531 |
rs188101869 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861162 | ACTTTGTGAGGCCAA[A/G]GCAGGCGGATCACTT | 57531 |
rs188105855 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104776089 | CAAATTACGACTCTA[C/T]AGGGCACAAGCACCA | 57531 |
rs188110005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748431 | AAAGATGGAAAATTA[C/T]CAAATGCTAGTGAGA | 57531 |
rs188110367 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754438 | AAAAAGATCAACCCC[A/C]AGACATATAATCAGA | 57531 |
rs188118295 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755710 | AAATTATGGGAGAAA[A/T]CAAGAATTTATCTGA | 57531 |
rs188120349 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798954 | TAGGCTTGTTCCATA[G/T]CACCAAGCATGGCAG | 57531 |
rs188120486 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104718295 | AGTTCCAACAGTCTG[C/T]TCATTCCACATATTT | 57531 |
rs188122088 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104712402 | AAACTTAATCACCTA[A/T]GCAACAGTGTTGGGG | 57531 |
rs188130545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104686089 | AAATTCCTCACCCCA[A/G]TCAGTCTGGTTTTGT | 57531 |
rs188146214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757080 | TTGAACTGGGCGGTG[A/G]CCACTGGAGCTCAGC | 57531 |
rs188157240 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104721681 | TTTGGCTTGTTTTAA[C/T]TGGCTACTCCAACAC | 57531 |
rs188161409 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104691751 | AAAAAATAAGACCCC[A/T]TGTCTACAAAATATT | 57531 |
rs188321427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848963 | CACTATAAAGAAGAA[C/T]AATATCATCAATAAT | 57531 |
rs188330372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836270 | AGACATAATCAAGCA[C/T]ATGAAAGGTACTGAA | 57531 |
rs188331890 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104844212 | CCAGCTAATTTTGTA[C/T]TTTTAGTAGAAACGG | 57531 |
rs188334092 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104814790 | GTGTGGCACATCCCC[A/C]CTCACGCTCTTTCTC | 57531 |
rs188338379 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855057 | TGAAGTAGGTACTAT[A/C/T]ATCCTCATTTTACAA | 57531 |
rs188348638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813304 | ACCAGCCTAGGCAAT[C/T]TAGAGAGATCCCATT | 57531 |
rs188354109 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104770821 | AAAGCTTAAACACTG[C/G]CATTTCTTTTCTCTA | 57531 |
rs188362670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752324 | TTCTGGAGTCCAACC[C/T]GGGAAATAACATATA | 57531 |
rs188366369 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769464 | CTTCATTACCCTTAA[C/T]TGAGGGTAGGCCTCC | 57531 |
rs188371240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104795070 | GGAAAACACTTCATA[C/T]ATAAATTCAAGTAAT | 57531 |
rs188373659 | snp | A/G | 0.29175 | 0.246489 | intron-variant | HACE1 | GRCh38.p7 | 6:104774159 | CAGTGGCGGGATCTC[A/G]GCTCACTGCAAGCTC | 57531 |
rs188378499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817820 | ATACCTTCTTAACTA[C/T]ATATAACCAATACTG | 57531 |
rs188379415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731014 | TATTTTTCAAACATC[A/G]TCTAACATAATGAGG | 57531 |
rs188408682 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733034 | AAATAAAATTCAACA[G/T]TAGTTAATTTATAGA | 57531 |
rs188417376 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104696850 | TGCACAAAATGTCTT[C/T]ATTTGTCTCTAGACC | 57531 |
rs188552045 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705502 | GGTATTCTATCTCTA[G/T]CTCCAAAACAAATAG | 57531 |
rs188575480 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861854 | GCAGTACTACTATCA[A/G]CTTATCACCTCCTGT | 57531 |
rs188600086 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859988 | GGGGGCGCCCAGGCC[A/G]CGCCAACGCGGGCGC | 57531 |
rs188616752 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793326 | TCATTGTAAAATCCT[C/T]GCCTTTGGTTTATAT | 57531 |
rs188618478 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104818255 | TTCAGTCACTATTTT[A/G]TAAGAGAAGGACTAC | 57531 |
rs188618867 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104822264 | GGCAGGAGCCTCTAG[C/T]CCCAGCTACTCAGGA | 57531 |
rs188661815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745534 | CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT | 57531 |
rs188666082 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708930 | TTAACTCAAAGTGAA[C/T]TATAGGCCTAGATGT | 57531 |
rs188751662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808339 | CCTATCAACTACTAA[A/G]TGTTGAATACTCTGC | 57531 |
rs188762033 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788216 | TTAAATAAGAAACAC[A/C]ATACATACCATTTGT | 57531 |
rs188773126 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104830077 | TTCTAATCTGAATCC[A/C]AGTATTTTCCTATCC | 57531 |
rs188779281 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761276 | ACAAAGCTGGAGGCA[C/T]CATGCTACCAGACTT | 57531 |
rs188787675 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104699237 | TGTTAATGTTCTTGG[A/G]GGGAATACAAAATTT | 57531 |
rs188795667 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746767 | CATCTGGAGAAATTC[C/T]GTTCCCTGACAGGAC | 57531 |
rs188799949 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104710907 | TTTAGCATACTACTA[A/T]TTCATTCCCCTTGAT | 57531 |
rs188808142 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104727345 | CACATGTATGTATAC[A/G]AATATATATACACAT | 57531 |
rs188855784 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104840462 | CAACAGGTGATACCT[A/G]AAACCAAAAAACCAG | 57531 |
rs188894201 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104758129 | AAAACACTCTTCAGG[A/G]TATTATCCAGGAGAA | 57531 |
rs188898702 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104832870 | CACCACTGCACTCCA[C/G]CCTGGGCAACAAAGT | 57531 |
rs188904058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798382 | TAATTTAAAACCAAT[C/T]GGAATTAAAGTTTTT | 57531 |
rs188917177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792236 | CTACGTAACGGGCTG[C/T]CTTATGACTATACAC | 57531 |
rs188919275 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750802 | ATCTGGATTACTGCA[A/C]CATCTGGTGTCCCTG | 57531 |
rs188925172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760351 | AAGCTTATCCACCAC[C/G]ATCAAGTCGGCTTCA | 57531 |
rs188931262 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104726612 | GATTTCCTTCTATTA[C/T]ATTTTGTTTTGGGGT | 57531 |
rs188963873 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683206 | TGAGGAAACCAAGCA[A/G]CGAGAAAGCCAGGCA | 57531 |
rs189002817 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104803235 | AGTCCAGGAACAGAC[A/G]GATTCACAGCCGAAT | 57531 |
rs189022497 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104824158 | CCCTCCCAAGTCTCT[C/T]ACTACTCCTTAATTG | 57531 |
rs189039742 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104740152 | ATACCAGAATCTCTG[G/T]GATGCATTCAAAGCA | 57531 |
rs189051362 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104706262 | GACTGGTACTGAGTG[A/G]CTGCTGCTTAATCCT | 57531 |
rs189055128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722900 | GACCACTTTCCTCCA[C/T]TTCAGTCAAACAGAC | 57531 |
rs189077200 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104850076 | TGCCTCAGCCTCCCA[A/C]GTAGCTGGGATTACA | 57531 |
rs189112837 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104761969 | ATCATCACTGGTCAT[C/T]AGAGAAATGCAAATC | 57531 |
rs189114924 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104809523 | GTGGTTCAAGTACAG[A/T]GAGCTAAACAGGAGT | 57531 |
rs189155401 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104733712 | AAATTAGCCAGGCGA[A/C]GTGATGTGTGCACCT | 57531 |
rs189159266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811142 | CTCTTAAAAGACAGC[A/G]TATTTGTGGGAAAAC | 57531 |
rs189166628 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104699151 | TTGAATATCAGGAAA[A/T]GCCCCTAGTGGTATT | 57531 |
rs189174650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852104 | AATGTTACAGCTCAT[A/G]TAGATCTTGGAAAAT | 57531 |
rs189188733 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104737618 | ATACTGCGCTTTTCC[A/G]ATGGGCTTAAAAAAC | 57531 |
rs189196694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705060 | GTCATCTCCCAGGCT[A/G]AATGCTCAAGATTTT | 57531 |
rs189205405 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766157 | TTGGCCCCACGTGGG[A/G]CACAGTGGGGAACCT | 57531 |
rs189216076 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104698148 | TACAAATAATGTCTG[A/G]AAAAAGTTTGTCTCC | 57531 |
rs189245243 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104849316 | TGTAGTTCAATTAAA[A/G]AACAAAATATTCTAT | 57531 |
rs189287054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104830940 | AGTGTGGACATCCAA[A/G]CAGCATAGTGCACTA | 57531 |
rs189292990 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104808679 | TTAACCTTTATCTTA[A/G]AGCCCTATAATTTGT | 57531 |
rs189363199 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104831635 | ACGGTGGCTCACGCC[C/T]GTAATCCCAGCATTT | 57531 |
rs189377521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104823228 | CACCTGAGGTCAGGA[A/G]TTCAAGATCAGCCTG | 57531 |
rs189383516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789119 | ATCACCCCCACAATG[A/T]ACAGGAGATCTGATT | 57531 |
rs189405546 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770539 | TCCTGGCCAACATGG[C/T]GAAACCCCGTCTCTA | 57531 |
rs189416192 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104782633 | GTAGCCATCTTATAC[A/T]ATGGTTAAGAAAATA | 57531 |
rs189418344 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104716628 | TTGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC | 57531 |
rs189431845 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104751743 | TATACACATATAAAC[C/T]ATTAGGTTATCATTT | 57531 |
rs189439653 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104715990 | AAATAAAAGTTTAAA[A/T]ATATATATATATTTA | 57531 |
rs189445559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730610 | GCTTCCATGGAGACA[C/T]CCCTCCACATTTCCA | 57531 |
rs189449472 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104719878 | TGACGGAGTCTCACT[C/G]TGTTGCCCAGGCTGG | 57531 |
rs189458039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693167 | TTCAATGAATTCAAC[C/T]CCTCCCTCTATACTG | 57531 |
rs189500910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846022 | CAAAATAAATCATTA[G/T]GTAGGAATGAGCCAG | 57531 |
rs189518190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803977 | ACCACATCGTCTCAG[C/T]CCAAAATCTCCTTAA | 57531 |
rs189528559 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104824298 | GACAATACACACATA[C/T]GATATTGAGATATCA | 57531 |
rs189656875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104842286 | TACACTGCAGCCTGG[A/G]TGACAGTGAGACCCT | 57531 |
rs189665424 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803040 | AGGGGGTATCACCAC[C/G]AATCCTACAGAAATA | 57531 |
rs189667321 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104844567 | ACAGGCTGGTCTTGA[A/G]CTCCTGACATCAGGT | 57531 |
rs189677201 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104756262 | CTAAAAACACAAAAA[A/C]TTAGCCAGGCATGGT | 57531 |
rs189694729 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104719968 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 57531 |
rs189695310 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758445 | TTTCATATCCAGCCA[A/C]ACTAAGCTTCATAAG | 57531 |
rs189700069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104722651 | GAGTTTACATCAAGC[C/T]GCCGCGCCAATGTTT | 57531 |
rs189733002 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842760 | GTAAGCCATAACTTA[C/T]CTTAATATAGCTTAA | 57531 |
rs189741130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684837 | TTTAAGCTCAACATA[A/G]CTTTATTTTGGATCT | 57531 |
rs189747967 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104800074 | CCCGTGCCTGGCTCA[A/G]CGGGTCCCATGCCCA | 57531 |
rs189758082 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104777987 | TGGTTTCGAACTCCT[C/G]ACCTCAGGTGATCCA | 57531 |
rs189769974 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104821005 | ACGGAATACTATGCA[A/G]CCATAAAAAAGAACG | 57531 |
rs189894826 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104819811 | CCTATTCAATAAATG[A/G]TGTTGTAATAACTGG | 57531 |
rs189911843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104744306 | CAGAGAAATATGCAA[C/T]ATTCATAAAGCACAT | 57531 |
rs189931460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845164 | AATGGCAGAGTATAT[A/G]CTATACATGAATATA | 57531 |
rs189932319 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724156 | TTTCCTCCCCTGTTC[C/T]TGGGTAGGAGACTGG | 57531 |
rs189940266 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682431 | TCCTAATTATTAATA[A/C]CAACTTCTAGACGGT | 57531 |
rs189941732 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104706804 | TTTTGTGTAGACTGA[C/T]AAAGAAAAAGACTCA | 57531 |
rs189955522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734929 | GATGGTGTTGAAGTA[C/T]AAACCATTTAGAAAA | 57531 |
rs189974047 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858810 | TGTCTGAATTCCTGA[C/G]GCTGCAAACAAAACT | 57531 |
rs189984739 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729476 | TATATTTTCTAATTG[C/T]ATCACAAACAGAGAA | 57531 |
rs189991171 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104692018 | GAGCAGGAGTGGAAG[A/G]AAGGGAGGAAGGGAG | 57531 |
rs190013195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104839364 | AGGAACAAACTATTG[A/G]TAAGTATAACCTAGA | 57531 |
rs190021092 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817555 | CATAAATTACCCAGC[C/T]TCAGGTAGTTCTTTA | 57531 |
rs190036003 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104772897 | GTACAGAATTTCTGC[C/T]TGGGGTGATGAAAAA | 57531 |
rs190131236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832086 | TTGTACCATACACAA[C/T]GCAAGTAGAAAAATA | 57531 |
rs190151164 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850134 | TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC | 57531 |
rs190159215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764706 | TCAATGAATGAGCAA[C/T]TGGAGCCTTATAACC | 57531 |
rs190167252 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104721687 | TTGTTTTAATTGGCT[A/G]CTCCAACACCTAACA | 57531 |
rs190167478 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104810302 | TACAGGGTTGTTAAA[G/T]AGATGATCTGAATTG | 57531 |
rs190177234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104790934 | AACTCCCTTGGTTTT[C/T]ACATGAATCTTCCAA | 57531 |
rs190179665 | snp | C/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727634 | GTATGTATATGAATA[C/T]ATACACACGTATGTA | 57531 |
rs190183079 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104820375 | GAGTTTCTGCATAGC[A/G]AAAAAAACTATCATC | 57531 |
rs190188221 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104704564 | GGCAAAAGAGAATGA[C/T]AATTATTATTTTTCT | 57531 |
rs190188339 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104749548 | GGGTAAAACTAATTT[G/T]CTGAGACAGAATAAA | 57531 |
rs190195185 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789008 | ATGGAAATTAGGGAT[C/T]AATTGCTACCTCAGA | 57531 |
rs190211978 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747613 | ACTGGCAACAGTGAT[C/G]GTATCTGGGGTCAGG | 57531 |
rs190218242 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104751640 | GTCTCTTAAAGAAAA[A/T]AATAATAATAATAAC | 57531 |
rs190246885 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104715602 | ATCAGATTGACAAAT[C/T]CTAAATTGCTAAAGA | 57531 |
rs190248627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711011 | ACCTTTCATTGTTCT[G/T]CCCAGAAGACAAATC | 57531 |
rs190386257 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104825406 | TAACTTCACTTCAGC[C/T]TCGGATTGGTTGCAC | 57531 |
rs190396263 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847073 | GATCAAAACTATTTC[G/T]TTTCTCTGTGCCACT | 57531 |
rs190415539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760348 | AAAAAGCTTATCCAC[C/T]ACGATCAAGTCGGCT | 57531 |
rs190415718 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104857627 | ATCCTATGAAATTCT[C/G]AAGTCATTAAGCCTA | 57531 |
rs190417957 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805440 | TTCACAATAGCAAAG[A/C]CTTGCAACCAACCCA | 57531 |
rs190424610 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104786922 | TGGAAGGAGATTATA[C/T]AACCATATTTGGAAC | 57531 |
rs190430474 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745103 | ATATAAAAATAGTTA[C/G/T]GATTTTTAAAAAAGA | 57531 |
rs190442982 | snp | C/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104708242 | GACTTGAGATGAATA[C/T]ACAAAAATTGGTTGT | 57531 |
rs190447643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834941 | CAAGAGGCTTGAAAA[C/T]AGTCTCTAGATAAGA | 57531 |
rs190468816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759594 | CGCCCACAAGAGAAA[A/G]CAGGAGAGATCTAAA | 57531 |
rs190469748 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104761845 | AAGAACTTAAACAAA[C/T]TTACAAGAAAAAAAC | 57531 |
rs190478424 | snp | A/G | 0.107694 | 0.205546 | intron-variant | HACE1 | GRCh38.p7 | 6:104727499 | TGAATACACACACAC[A/G]TATGTATATGAATAC | 57531 |
rs190483593 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794327 | ATGACAAATATTTAA[C/G]AAGAAAAAATAAGTT | 57531 |
rs190504914 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104685761 | CGGGAAATACAAATT[G/T]TTTTAATAGCAGTAC | 57531 |
rs190641558 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852178 | AAATAACTTGCCCCA[A/G]AACATCTATGTCCAA | 57531 |
rs190661640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851490 | AAAACCAAACGCCTT[A/G]ACCAATAAGCTGGTG | 57531 |
rs190664011 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104811523 | GGAACTGAGTGGGCA[C/T]GTGACAATTACTATG | 57531 |
rs190667499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832686 | GTGAGCCACGGCTCC[C/G]AGCCCAAAAGCACTA | 57531 |
rs190706297 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854669 | ACAAACTGTATATGG[A/G]CTTGGTATTTTATTT | 57531 |
rs190727104 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104736377 | GCAATCTCCACCTCC[A/C]AGGCTCAAGTGATCC | 57531 |
rs190728493 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813671 | ACATTGGTGTACAGT[C/G]AAACCAAGTAGTCAA | 57531 |
rs190734671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743391 | TATGCAGAAAAAACA[C/T]AGAAGAAAATATATT | 57531 |
rs190735275 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104701395 | TCCCCTAAGAAAATC[C/T]TAAATGCAATATATT | 57531 |
rs190818912 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104799616 | GCTCGAGATGAACAG[C/T]TACATGGCAGACCAG | 57531 |
rs190851564 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777687 | GAAAAATTACGTTGC[A/G]TGTTCCATTTAATTT | 57531 |
rs190851752 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735247 | ACAACACTTAAAACT[G/T]AATTTTTAAAAATGA | 57531 |
rs190859537 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104756404 | GTGACAGAGCCAGAT[G/T]CCATCTCAAAAAAAA | 57531 |
rs190869536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721201 | AATGAAAAATTAGCC[A/G]AGTGTGGTGGCACGC | 57531 |
rs190878220 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700742 | GCATATTCGCTGAGG[C/G]TCCCTCTGGATCAGT | 57531 |
rs190904663 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104847783 | ACAACGCATTTGTAT[A/G]CCGTGTCCATAGAGA | 57531 |
rs190930381 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832979 | GCACAATGAAAAACT[A/T]TTCATGAAATCAATT | 57531 |
rs190939385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825282 | TAACAAAAGGACCAG[C/T]GACCTTTGCAAACCC | 57531 |
rs190948892 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792429 | CCTTTCCACAGAAAA[A/T]CTGTACGAGTTAGGC | 57531 |
rs190955554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754314 | AGGAGAATGGAACCA[A/C]GTTGGAAAACATACT | 57531 |
rs190955718 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786218 | TGGTGGCACACACCT[A/G]TAATTCCAGCTACTC | 57531 |
rs190963341 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104756973 | AGATTGACCTGGGTC[A/G/T]CTGGACCTTGGCGGG | 57531 |
rs190990049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721642 | TTATCCCATCACAGC[A/G]ATTTAAGACTTAACT | 57531 |
rs191070918 | snp | A/C | 0.000542763 | 0.0164647 | intron-variant | HACE1 | GRCh38.p7 | 6:104796629 | AAAGCTTCTTCATTT[A/C]CAAGCTACTATCACA | 57531 |
rs191098148 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731887 | AAAAAAAAAAATCCC[A/G]ATTAAAAATGGGCAA | 57531 |
rs191102440 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104772415 | CATACACACACACAC[A/G]CGCACATATACACAG | 57531 |
rs191106487 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753366 | GTCCCCTTCAACACA[A/G]CACATGTGCTCTACC | 57531 |
rs191110502 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717391 | TGATCCACCTTCTTC[A/G]GCCTCCCAAAGTGCT | 57531 |
rs191130471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695694 | TAGCTGGGATTACAG[A/G]TGCCCACCACCATGC | 57531 |
rs191136859 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822957 | ATTAGACTAACATAC[G/T]CCTCTACTGTTCTCA | 57531 |
rs191154857 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844460 | GCAATTCTTCTGTCT[C/T]AGCCTCTCGAGTAGC | 57531 |
rs191172689 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104802649 | AAGGCAGAAATAAAG[A/G]TGTTCTTTGAAACCA | 57531 |
rs191177750 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846625 | GAGAAATATAGCAGC[A/C]ATCTGATGACAGCTG | 57531 |
rs191182620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843792 | TACTCACTGGAGGGT[A/G]AGGAGGGGGATGTAG | 57531 |
rs191217569 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104732532 | GGTGGTTGTTAGAGG[C/T]GGGTGGGAAAGGAGG | 57531 |
rs191221596 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804480 | TACTACAAGGCTACA[C/G]TAACCAAAACAGCAT | 57531 |
rs191232899 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104801764 | CAAAAACATGCCAAA[C/T]TGTGAAGACCATCAA | 57531 |
rs191239660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759919 | GAGAATACTATAAAC[A/G]TCTCTATGCAAATAA | 57531 |
rs191243159 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104757200 | CTGCCTGACAGCTCT[A/G]AAGAGAGCAGTGGTT | 57531 |
rs191295340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687422 | GTTCATTGACTTTAC[C/T]CGCAAATCTCCACAG | 57531 |
rs191347451 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750837 | CATTTTTGCCCCTGT[A/G]CTGATGCTTCTCCAC | 57531 |
rs191349569 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104767227 | TAATGATAATGAGGT[C/T]GATGAAGAGTATGAT | 57531 |
rs191358291 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104714334 | TTGCTATATGTGTCA[C/T]AAGGACAGAGAGCAG | 57531 |
rs191363136 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728149 | CTACTTGCAAAAAAA[A/C]CTAATATGACAAAGC | 57531 |
rs191366914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689763 | TTATCCCCTTATTAT[A/G]TAGCCTGAAACTTCA | 57531 |
rs191401741 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861634 | TAAATTACCTCCAAC[A/G]TCCTGTGAGGACCAA | 57531 |
rs191401934 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104841046 | GAATCACTTGAACCC[A/G]GGAGGTGGAAGTTGC | 57531 |
rs191452953 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104778844 | AAGATCTCTGCAAGA[C/T]AGAACTTATGAATAG | 57531 |
rs191463621 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104821561 | ATATGTACCCAGACA[C/G]TGTGCTAATAAGCAT | 57531 |
rs191471956 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736755 | AGTAACAAACTGCAA[C/G]AGAAGTACCTTGCCC | 57531 |
rs191491142 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815704 | AAAGCATTCAAGATG[G/T]GACCTGGCTTATTCT | 57531 |
rs191512631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713169 | ATTAGATAAGGAAAC[A/G]AAGACAGCAAATGGG | 57531 |
rs191528878 | snp | A/G | 0.000135364 | 0.00822579 | intron-variant | HACE1 | GRCh38.p7 | 6:104772110 | TAATATATTATTAAG[A/G]ATCTATATGCAGAAG | 57531 |
rs191535385 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731548 | GAACAGAATAGAGGC[A/C]AGAAATAACCCCTCA | 57531 |
rs191543531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694689 | GTTCTACATCCCTTC[C/T]CCCTTGAATCTGACT | 57531 |
rs191575516 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104760598 | ATATCATACTGAATA[C/G]GGAAAAAAACGGGAA | 57531 |
rs191589314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746366 | CATTGACCACCCCCA[A/G]ATACATTCTCTAGCT | 57531 |
rs191599242 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104710282 | ATAAGCAAATCTATG[A/G]AGGCAGAAAGTAGAT | 57531 |
rs191600292 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726994 | TCTCTTTATATTAAC[C/T]ACACTCTTATTTTAA | 57531 |
rs191608546 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104684463 | ACTAAATTTCAGTTT[G/T]CAGTCTTATATGGAT | 57531 |
rs191757831 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104837507 | TCAAAAGAGATCATA[C/G]ACTTAAATGTAAAAC | 57531 |
rs191770494 | snp | G/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853479 | TCAATTCAATGTATT[G/T]TGGAGGTTTATGTTT | 57531 |
rs191775452 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749909 | ATATATATGGCAATA[A/T]AAGAAACTGGAGAAG | 57531 |
rs191776801 | snp | C/T | 0.00023873 | 0.0109228 | intron-variant | HACE1 | GRCh38.p7 | 6:104795720 | AAAAATGTGATTACA[C/T]AGTAATCCATTAAAT | 57531 |
rs191781437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752925 | AAATGTGGATGGCAG[C/T]TGAACTAAATTATTT | 57531 |
rs191789248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793064 | ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT | 57531 |
rs191792911 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104717088 | AGAAAAACTCTGGCA[C/T]GTATATAGATGTAAA | 57531 |
rs191797371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833555 | TTCAAAATCAAGAAC[C/T]CAGTGGGGCTCCAAG | 57531 |
rs191799891 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682896 | CCTCCCCTGGTGTGT[C/T]CTGGAGAAGAATATT | 57531 |
rs191802348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104812801 | CAGGTACCTTGGAAT[A/G]TAGGAATGGTTATGT | 57531 |
rs191806529 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713588 | CAAGTTTCCGTCCTA[G/T]GCAAACTGATTAGCC | 57531 |
rs191819129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104767817 | TCCTTACTCCTACTC[A/G]ACCACTTAATGCTTC | 57531 |
rs191823971 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104751250 | TTTACCAGGATATAT[A/G]CCAACTTCTAAAAAG | 57531 |
rs191990711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849077 | GAGGAATCATCAAAC[A/G]AAGGCAAAGTGCCTT | 57531 |
rs191996211 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104839105 | ACAAGCAATAAGAAA[A/T]GCTGGCAAGGATGTC | 57531 |
rs192006844 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718460 | ATCTTAAAGAGATCT[C/T]AATGAGAAGGGCAGT | 57531 |
rs192008197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104808527 | ACTAGGTTCTTTCCC[C/T]TGTATCTTAATACCA | 57531 |
rs192015679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697215 | TAAAAGGACTTGAAA[C/T]ACCTTGACTGCTTTC | 57531 |
rs192016451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788571 | AAATGCCACAACCCA[C/T]AAGATAAGATCTTGA | 57531 |
rs192021247 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104830253 | TGCCTTAAAAACCTG[A/G]GTCACTCAAGATTAG | 57531 |
rs192037214 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104761334 | CAAAACAGAATGGTA[C/T]TGGTACCAAAACGAT | 57531 |
rs192038824 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104723436 | TCCAATTTTCTCACC[C/T]GTAAAGTGAAGGGAC | 57531 |
rs192041169 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104810827 | AGACTGACTCAAGAT[G/T]TTTTTTTGGTTATAG | 57531 |
rs192054656 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104746911 | ATGCTTTCATTATTC[A/G]TAATTATGAATAAAA | 57531 |
rs192062265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765411 | TTTATTCTGTCCTTG[A/G]TAGCCTACCACAGGG | 57531 |
rs192104872 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104688213 | AATCACCAGTCCTCC[A/G]TGGCTTCTTCAGTTT | 57531 |
rs192221785 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782157 | TTTCACCTATTATCT[C/G]ATTTGCCCCAGAACA | 57531 |
rs192230576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822506 | TACAGTGAGCTATGA[C/T]CACACCACTACGCTC | 57531 |
rs192233422 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737772 | GCCCGCCATTTTCCA[A/C/G]GCTTGATTAGGTAAA | 57531 |
rs192234690 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104705151 | ACACATCCAGTTGTG[C/T]CAGCTCTAAGGCTTC | 57531 |
rs192251615 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104780804 | ATGATTCATGAACTG[A/C]CTTTAATTGTCCTGT | 57531 |
rs192263218 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104757481 | AGGAAAACTAACACA[C/T]AGAAAGGAAGAGCAT | 57531 |
rs192264975 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854044 | TTGTGCTGTGCCTCC[C/T]GCAACTGAAACCTCG | 57531 |
rs192265312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802136 | GGACATTACATAATG[C/G]TAAAGGAATCAATGC | 57531 |
rs192277007 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104692304 | AGTATTCTACCATTT[C/G]TGTATGTATTAGATG | 57531 |
rs192278548 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104737147 | AAATACAAAAATTAG[C/T]TGGACGTGGTGGCAG | 57531 |
rs192290529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704916 | ACAGCTCAATTGCTA[C/T]TCATTAAGAGAGAAA | 57531 |
rs192298395 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104722167 | CCACTGTATATAGAA[A/T]CTTGGAATTTGAATA | 57531 |
rs192304412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104858088 | GGATGGTGAAATGAC[A/G]TATTTTTTTCTATTT | 57531 |
rs192403395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706477 | GAGTCAGTAGTGCTA[C/T]ACGAGATTGGGCAAA | 57531 |
rs192464809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829417 | CTGAAACAGGCAGTA[G/T]TAGCACAACTATGAA | 57531 |
rs192478288 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104818261 | CACTATTTTATAAGA[A/C/G]AAGGACTACGTGGGC | 57531 |
rs192486431 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787780 | TCAGTGGTGCAGAAA[G/T]AACACCAAAGAAAAA | 57531 |
rs192495580 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104775068 | AATGTTTGGCCAGAC[A/G]TAGTAGCTTACACCT | 57531 |
rs192498147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827945 | TATTCTGATAAAAGT[A/G]AAATTTATTTTTAAA | 57531 |
rs192516783 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798450 | TGCCAGAAAACTCTG[A/C]AACGTTATTATAGGT | 57531 |
rs192523442 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104733678 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57531 |
rs192531072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104718099 | CCCACTCTCAGGCCA[C/T]AATTCCTTTAAGTAG | 57531 |
rs192535117 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104755312 | GCAAAGAGACTGAGA[C/G]TCCCACACAATAATA | 57531 |
rs192546488 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104719320 | AAATGTTTTAAAAAA[G/T]ATTTCTGCCATAGGA | 57531 |
rs192560653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698753 | GATGATGACATCAAG[A/G]ACCGTGTTGAAGAAG | 57531 |
rs192626587 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758205 | ACAGAGAACACCACA[A/T]AGATACTCCTCGAGA | 57531 |
rs192637383 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104722592 | ATCTAGAGAATAATG[C/T]AGCAATTCACTTAAG | 57531 |
rs192693164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803080 | ATCAGAGAATACTAT[A/G]AACACCTCTATGCAA | 57531 |
rs192700196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844821 | GCGCCCGCCACCATG[C/T]CCAGCTAATTTTTCG | 57531 |
rs192719475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758551 | GCTCCTGAAGGAAGC[A/G]CTAAACATGGAAAGT | 57531 |
rs192730561 | snp | A/G | 0.00279162 | 0.0372561 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728825 | AAAAGCAAATTTAAG[A/G]AGCAAAAAAATTAAC | 57531 |
rs192740019 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104691752 | AAAAATAAGACCCCA[G/T]GTCTACAAAATATTT | 57531 |
rs192779538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807213 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 57531 |
rs192786614 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104848400 | GATAGAGGTTGCAGC[A/G]AGCCGAGACTGTGCC | 57531 |
rs192817582 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104696051 | TGCATTTCTAACCTC[G/T]GATAGAGTTTGCAGG | 57531 |
rs192838402 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858983 | TACTAGTCTGATGAA[C/T]AAATGAAGAATGAAG | 57531 |
rs192846076 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104774740 | AGTTAAGTTTACTGG[C/T]CCCAAGATTGTATCA | 57531 |
rs192848158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817947 | ATTTGGAAATACATA[C/T]TAAAGGAAAAGTTTA | 57531 |
rs192855372 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104710919 | CTATTTCATTCCCCT[C/T]GATGCTATTGTTTCT | 57531 |
rs192865693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733050 | TAGTTAATTTATAGA[C/T]TTAACTTTTGCCTAA | 57531 |
rs192910964 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104823398 | AAGATCATGCCACTG[C/T]TCCAGACTGGGCAAC | 57531 |
rs192921984 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104782937 | TTTTCTAAAACTTTG[C/T]CAGAATTATGCCATT | 57531 |
rs192942527 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104715337 | AAAATCATTTTCATT[G/T]AAAATTTAAAGGGTG | 57531 |
rs192956294 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | HACE1 | GRCh38.p7 | 6:104834588 | TTCCCTAAACCCCAC[A/G]GAAATGAGAGTAAAG | 57531 |
rs192965680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793588 | CTGGATAACACCTTA[A/G]TTGTCACTAATTAAC | 57531 |
rs192994041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104715673 | AGATATGGAAATAAA[C/T]ATAAATGTACAATAA | 57531 |
rs193040338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840146 | AAGTGCAGGGCAACT[C/G]TCTCTCTCTATTATT | 57531 |
rs193049234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797332 | TTTTTTTCTTACATT[C/T]ACTTCCTAATCCCTC | 57531 |
rs193054826 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104727427 | CACACACATGTATAT[A/G]AATACACACACATGT | 57531 |
rs193090262 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840764 | AGGTCAGGAGTTCAA[C/G]ACCAGCCTGACCAAC | 57531 |
rs193100101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806118 | AAGCTGGAGTAATTT[C/T]TAAAACCACACAGAA | 57531 |
rs193110520 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104760370 | AAGTCGGCTTCATCC[C/T]TGGGATGCAAGGCTG | 57531 |
rs193112786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726684 | ATCTCCTCAAACTAT[C/T]TGGATAACTTAATCT | 57531 |
rs193119908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104683706 | CTTATCACGTACTTC[A/G]GAAAGATACTTATGT | 57531 |
rs193187153 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104844235 | AGAAACGGGGTTTCA[A/C]CATGTTGGCCAGGAT | 57531 |
rs193188520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769700 | TAGACTTGAAATTAG[A/G]AGGCTTGGGTTTTGG | 57531 |
rs193191036 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104813503 | TGGGAACATGAGGCA[A/T]CTTTTTTATTTTCAT | 57531 |
rs193196925 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729579 | TGGGTTGCATTTAGG[C/T]TGCTTTTTTGTTGAC | 57531 |
rs193253312 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860061 | CCTAAGCTTCTGGAA[A/G]GGCATTCTCACGCCC | 57531 |
rs193263189 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104745729 | TACAGGCGTGAACCA[A/C]CGTGCCCGGCCAGGA | 57531 |
rs193271325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104709056 | TAACAGAAAAAGATA[C/T]AGATAAATTGGACTA | 57531 |
rs199502645 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797969 | GCTACTTGGGAGGCT[A/G]AGGCAGGAGAATCAC | 57531 |
rs199507541 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816005 | TTGAACCCAGGAGGC[A/G]GAGATTGCAGTGAGC | 57531 |
rs199554586 | snp | C/T | 0.000280087 | 0.0118307 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771988 | GCCTGTGGTTCAACG[C/T]TAATCCCAAGATCTG | 57531 |
rs199569457 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852385 | ATCTGAGTAAAAAAA[A/C]ACAAAGAGTTCATTT | 57531 |
rs199596685 | in-del | -/C | 0.0123036 | 0.0774623 | intron-variant | HACE1 | GRCh38.p7 | 6:104777801 | GTCTCACTCTGTTGT[-/C]CAGGCTGGAGTGCAG | 57531 |
rs199605189 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807205 | ATTTTTGTATTTTTA[C/G]TAGAGACGGGGTTTC | 57531 |
rs199641990 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773783 | TTTAAAAAAAAAAAA[-/A]GGAAACATATAGGGA | 57531 |
rs199646328 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820151 | AGTGAGCCGAGATTG[A/T]GCCACTGCACTCCAG | 57531 |
rs199673448 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756627 | GCTCCCAGCGAGACT[A/G]ACACAGAAGATGGGT | 57531 |
rs199678020 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734163 | AAAAAAAAAAAAAAA[C/T]AAATCATCAAGTCTG | 57531 |
rs199691207 | in-del | -/GT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725242 | TGTTTATATATATGT[-/GT]ATGTGTATATACATA | 57531 |
rs199701111 | snp | C/T | 0.00013887 | 0.0083316 | intron-variant | HACE1 | GRCh38.p7 | 6:104791687 | AATATGAGATTAGAG[C/T]AAAACAAATTACATA | 57531 |
rs199713569 | in-del | -/TTTA | 0.0267878 | 0.112589 | intron-variant | HACE1 | GRCh38.p7 | 6:104847088 | TTTTCTCTGTGCCAC[-/TTTA]TTTGTTTCTAAAAAA | 57531 |
rs199754509 | in-del | -/CT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756607 | AGGAACAGCTCTGGT[-/CT]ACAGCTCCCAGCGAG | 57531 |
rs199755638 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769035 | TATACCTCATACACA[-/T]TTTTTTTTCTTTTTT | 57531 |
rs199778440 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784585 | GACTGGCTTCTAAAC[A/C]AAAAAAAAAAGAATT | 57531 |
rs199789272 | in-del | -/AT | 0.0640965 | 0.167152 | intron-variant | HACE1 | GRCh38.p7 | 6:104727457 | TATATGAATACACAC[-/AT]ATATGAATACACACA | 57531 |
rs199789320 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857653 | GCCTATTGAAGAATA[A/C]AAAAAAAAAAAAACA | 57531 |
rs199823595 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851731 | TAGGAAATTTAAAAC[A/C]AAAAAAAAAATTTTT | 57531 |
rs199831752 | in-del | -/CT | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104685493 | GACAAGTTCCTTAAA[-/CT]CTCTCAATCTCAGTT | 57531 |
rs199874906 | in-del | -/TATA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842008 | TGGCCAATACTACTT[-/TATA]TAAAATATAAGTCTA | 57531 |
rs199882159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750316 | GTTGTTGTGTTACAA[C/T]ATAAGAACTGATGTT | 57531 |
rs199888034 | snp | A/G | 1.70586e-05 | 0.00292045 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796731 | TGATATTGAATTAAT[A/G]CTTCACAAGTCTCTC | 57531 |
rs199891691 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745495 | TCTGTCACCCAGGCT[A/G]GAGTGCAGTGGCGCG | 57531 |
rs199898723 | snp | A/G | 0.000132177 | 0.0081284 | intron-variant | HACE1 | GRCh38.p7 | 6:104811403 | CACTGTCTGAGGGGG[A/G]AAAAATAATTAAAAG | 57531 |
rs199929128 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | HACE1 | GRCh38.p7 | 6:104823512 | CTTTTCTATTTTTTT[A/T]AAAAAAACAGCCCGA | 57531 |
rs199946047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752131 | TTTAACACAAGGAAA[A/G]CTACCATCTCTGCTA | 57531 |
rs199947750 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843426 | CTTTATCTGTAATAT[G/T]AAGCCATATCTGCAA | 57531 |
rs199961533 | in-del | -/TACTT | 0.122064 | 0.214785 | intron-variant | HACE1 | GRCh38.p7 | 6:104741808 | AGAACTGGAAAAAAC[-/TACTT]TAAAGTTCATATGGA | 57531 |
rs199972875 | in-del | -/CG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727546 | ATGAATACACACACA[-/CG]TATGTATATGAATAC | 57531 |
rs200029689 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739893 | CACACTACACCTATT[A/C]CAAAATTGACCACAT | 57531 |
rs200033506 | snp | A/C | 0.00220375 | 0.0331213 | intron-variant | HACE1 | GRCh38.p7 | 6:104744134 | ACATTAAATTATTTC[A/C]ATATTATCATAAAAA | 57531 |
rs200046496 | snp | A/G | 3.33145e-05 | 0.00408119 | intron-variant | HACE1 | GRCh38.p7 | 6:104784492 | GAAGTCATTCTGTGG[A/G]GGGAAAACATCAATC | 57531 |
rs200049872 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797174 | TCATAATCACAAAAA[A/G]TTTCTCAATGTTAAG | 57531 |
rs200072594 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836225 | AATCCAGCCAAGAGA[C/G]CACAGAAGTCTCCGT | 57531 |
rs200088019 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721609 | AAGTCGGTGACTTCT[-/C]CCCTTTTAGCCTCTT | 57531 |
rs200100402 | snp | C/T | 0.00199805 | 0.0315442 | splice-acceptor-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852373 | AGCAGTTTCATTATC[C/T]GAGTAAAAAAAAACA | 57531 |
rs200107961 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720645 | CCCTCCCCCCCCCCC[A/C]AGACGGAGTTTTGCT | 57531 |
rs200117589 | snp | A/T | 0.0448719 | 0.142907 | intron-variant | HACE1 | GRCh38.p7 | 6:104740678 | AATCAATAGCTTACC[A/T]ACCAAAAAGAGTCCA | 57531 |
rs200139639 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753733 | ACAAAAAGACCCCAC[A/C]AAAACCTCAGTCAAA | 57531 |
rs200147032 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853053 | TTGCTATTATGGCAG[G/T]GTGAAGAGGTGAGGC | 57531 |
rs200149049 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703759 | AGAATTCATGGTAAA[A/C]AAGCCATACTAGCTT | 57531 |
rs200152512 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715539 | GAAATTTTGAGGAAA[C/G]AATATTCAAAGAAGT | 57531 |
rs200152839 | in-del | -/AAATATTA | 0.311859 | 0.242226 | intron-variant | HACE1 | GRCh38.p7 | 6:104743823 | AAACCAGCAATATAC[-/AAATATTA]AAATATTAAAATAAT | 57531 |
rs200157115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772515 | TGCAGTAAGTATTTG[C/T]TAGTTTTTGCTGCTT | 57531 |
rs200196243 | in-del | -/A | 0.0185938 | 0.0946107 | intron-variant | HACE1 | GRCh38.p7 | 6:104801166 | AAGACAAGATTAGAG[-/A]AAAAAAGAGCAAAAA | 57531 |
rs200218780 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756428 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 57531 |
rs200223428 | in-del | -/AC | 0.00914312 | 0.0669923 | intron-variant | HACE1 | GRCh38.p7 | 6:104834331 | GTTAAAAAGTAATTA[-/AC]ATAGCAATGCTATAT | 57531 |
rs200229134 | snp | A/T | 0.000181481 | 0.00952404 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785004 | GAGGCATCTGACAAG[A/T]ACAGCACATGTAAAA | 57531 |
rs200232203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813556 | TTGGCAGCTAGTGGG[C/T]AGAGGTCAGGGATGC | 57531 |
rs200252264 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790482 | AGTTGGCTGGGTGCA[A/G]TGGCTCACGCCTGCA | 57531 |
rs200257833 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823797 | GGCGGTTTTCTTTTT[A/C]TAAAAGCTCTAAAAT | 57531 |
rs200260080 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805191 | AATGGCGATCATTAA[G/T]AAGTCAAGAAACAAC | 57531 |
rs200290493 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784580 | ACTGGACTGGCTTCT[-/A]AAACCAAAAAAAAAA | 57531 |
rs200294864 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773770 | ATAAGGAGACTTTTT[-/A]TAAAAAAAAAAAAGG | 57531 |
rs200305580 | in-del | -/AGGAAGGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831981 | AAGAGAAGAGAAGAG[-/AGGAAGGA]AGGAAGGAAGGAAGG | 57531 |
rs200312384 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737033 | TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC | 57531 |
rs200377221 | snp | A/C/T | 1.65436e-05 | 0.00287602 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777304 | TAGAACCATTCACAG[A/C/T]GATCTTTAAAAGGCT | 57531 |
rs200379570 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783382 | AATCCTCTTAGAGAA[-/G]GGAAGTAAGTTTTCT | 57531 |
rs200387164 | snp | C/T | 0.00115666 | 0.0240207 | intron-variant | HACE1 | GRCh38.p7 | 6:104785360 | AACATCATTCTTAAA[C/T]TACAGGATTAAAAAA | 57531 |
rs200415312 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104848380 | AGAATCACTTGAACT[C/T]GGGAGATAGAGGTTG | 57531 |
rs200424650 | snp | A/C | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682705 | CTGTTGGACTTGGTC[A/C]CAGTCCATGAAGACC | 57531 |
rs200439172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771888 | GAAAAAAAAACAATA[C/T]AAATAAATGTCTGCA | 57531 |
rs200439270 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742639 | ACCAGTTAGAATGGC[A/G]ATCATTAAAAAGTCA | 57531 |
rs200454697 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104741016 | TCAATATACGCAAAT[A/C]AATAAATGTAATCCA | 57531 |
rs200457736 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804328 | CCATCCCCATCAAGC[A/T]ACCAATGACTTTCTT | 57531 |
rs200458623 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807019 | TTAAGTGTAAGAATT[C/T]TTTTTTTTTTTTTTT | 57531 |
rs200467769 | snp | A/C | 1.64781e-05 | 0.00287033 | missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104850925 | GCTGCAATGTGAAGC[A/C]AGCTTCTTTTCACAC | 57531 |
rs200478891 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849504 | CACCACAATTGGGTA[A/T]TTTTTTTTTTTTTTT | 57531 |
rs200519518 | in-del | -/TC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719806 | TTTTCTTTTTCTTTT[-/TC]TTTTTTTTTTTTTCT | 57531 |
rs200534595 | snp | C/T | 3.31961e-05 | 0.00407394 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771340 | CCATTGCAAATTTTT[C/T]GCATATTCTGGATCA | 57531 |
rs200547628 | snp | A/G/T | 3.29757e-05 | 0.00406041 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796978 | TTATCTGGCAGATAT[A/G/T]TGGCTCCTCGTAATA | 57531 |
rs200577612 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852387 | CTGAGTAAAAAAAAA[C/G]AAAGAGTTCATTTAT | 57531 |
rs200577723 | snp | A/G | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727695 | TACATACACACATAT[A/G]TATGTATATGAATAT | 57531 |
rs200648077 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831982 | AGAGAAGAGAAGAGA[A/G]GAAGGAAGGAAGGAA | 57531 |
rs200655847 | snp | C/T | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772025 | AAACCGAAAATAGTT[C/T]AAGTGATCAGGATTT | 57531 |
rs200663284 | in-del | -/CATATGTATATGAATACACACACACG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727498 | ATGAATACACACACA[-/CATATGTATATGAATACACACACACG]TATGTATATGAATAC | 57531 |
rs200694549 | in-del | -/GA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848087 | AAACTCCTGACCTCA[-/GA]TGATCCGCCCGCCTT | 57531 |
rs200714643 | snp | A/G | 0.00029141 | 0.0120673 | intron-variant | HACE1 | GRCh38.p7 | 6:104784213 | ATGGACAGGAAGAAT[A/G]AGTAGCATTAAGTGA | 57531 |
rs200715236 | in-del | -/TG | 0.360421 | 0.224293 | intron-variant | HACE1 | GRCh38.p7 | 6:104725241 | GGATGTTTATATATA[-/TG]TGTATGTGTATATAC | 57531 |
rs200716492 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794812 | TGGGAGGCTGAGGCA[A/G]GAGAATTGCTTGAAC | 57531 |
rs200738594 | in-del | -/AC | 0.0138799 | 0.0821421 | intron-variant | HACE1 | GRCh38.p7 | 6:104812563 | AAATAATAAAACTAA[-/AC]ACCCAAAGGAAGAAC | 57531 |
rs200769758 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690473 | CTAAGATTAATATGG[-/A]AAAAATGAACTCTAA | 57531 |
rs200868370 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840658 | ACCTGGTAAAACCCC[A/G]TCTCTATTAAAAATA | 57531 |
rs200884670 | snp | C/T | 0.000798403 | 0.0199641 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795681 | TGCTCCAGAACTTGC[C/T]GTAACTAAATTTTTT | 57531 |
rs200904828 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | HACE1 | GRCh38.p7 | 6:104734599 | TCTTCAATCCAAGGG[-/T]TGAAGCTAGCTCCGT | 57531 |
rs200906945 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719802 | TTTTCTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT | 57531 |
rs200934556 | snp | A/G | 3.33356e-05 | 0.00408248 | intron-variant | HACE1 | GRCh38.p7 | 6:104744494 | TTAACTTCATTCTAA[A/G]CTCTAGAGAAATTTT | 57531 |
rs200956031 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715542 | ATTTTGAGGAAACAA[G/T]ATTCAAAGAAGTAAT | 57531 |
rs200956978 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104741245 | TTCCCTTTGAAAACT[A/G]GCACAAGACAGGGAC | 57531 |
rs200959045 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787146 | ACACAACAAAACCAA[G/T]AAAACCACCACTACT | 57531 |
rs200973354 | snp | A/C/T | 0.00431017 | 0.0462279 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849237 | AACCAAGCATTCCAC[A/C/T]GATCCACAACTAAAA | 57531 |
rs200982399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730433 | TAAGAGTTTATATCT[C/T]AATACATTGTAATCA | 57531 |
rs201000263 | in-del | -/AT | 0.310386 | 0.242597 | intron-variant | HACE1 | GRCh38.p7 | 6:104727375 | TGTATATGTATACGA[-/AT]ATATATACACATGTA | 57531 |
rs201000549 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751891 | AGCCCTCTTCCTTTA[-/T]TTTTTCTTTTTTTGG | 57531 |
rs201006594 | in-del | -/TC | 0.0596104 | 0.162024 | intron-variant | HACE1 | GRCh38.p7 | 6:104685181 | AATAAGTCTTTGCTA[-/TC]TCAAGCCACTGAGAT | 57531 |
rs201006649 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853055 | GCTATTATGGCAGTG[G/T]GAAGAGGTGAGGCTT | 57531 |
rs201008846 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811617 | ATTATCAGTGTAATA[C/G]AAACTGTGTTAATCT | 57531 |
rs201034094 | snp | C/T | 1.87142e-05 | 0.00305888 | intron-variant | HACE1 | GRCh38.p7 | 6:104796780 | AAGATCTAAAATTAT[C/T]CAGGTTTAAAAACAG | 57531 |
rs201055674 | in-del | -/TGTG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697031 | ATATTCACAGGGTTT[-/TGTG]TGTGTTTGTCTTTTT | 57531 |
rs201057012 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751431 | ATTTTATTTTAAAAT[-/A]ACGTGATAATCATAG | 57531 |
rs201061477 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104748084 | AAAGCTTCTTCCATC[-/A]AAAAAAAACAAAACA | 57531 |
rs201068682 | in-del | -/ACT | 0.0138799 | 0.0821421 | intron-variant | HACE1 | GRCh38.p7 | 6:104808331 | AGTGAGCACCTATCA[-/ACT]ACTAAGTGTTGAATA | 57531 |
rs201106572 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749349 | CAGCTTAAAAACAAT[C/G]AAAAAAACCTCAAAA | 57531 |
rs201177284 | snp | A/T | 3.33517e-05 | 0.00408347 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784132 | ATCAACTCAGGACAT[A/T]CAAGGAGAAAGTGAA | 57531 |
rs201199511 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696166 | CCATGGTGGGGGCGG[-/C]GGGGGGGGGTTGTAT | 57531 |
rs201219137 | in-del | -/AAACAATATTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715536 | AAGGAAATTTTGAGG[-/AAACAATATTC]AAAGAAGTAATGGAT | 57531 |
rs201330390 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | HACE1 | GRCh38.p7 | 6:104771187 | GGTAAAAACTGAAAT[A/G]CTCACTTTATTATTT | 57531 |
rs201334598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744486 | GGCAAAACTTAACTT[A/C]ATTCTAAGCTCTAGA | 57531 |
rs201341372 | in-del | -/AAAAGAAAG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832044 | AGGAGAAAGAAAAGA[-/AAAAGAAAG]AAAAGAAAGAACTGT | 57531 |
rs201359950 | in-del | -/AGAAAAGAAATG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835541 | TCCCTAAAAGTACAA[-/AGAAAAGAAATG]AGAAAAAGTAGGAAA | 57531 |
rs201404500 | snp | A/C | 0.00199792 | 0.0315431 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791510 | TTTTCTCACCTTGAA[A/C]ACCTGGCTTCTTGGA | 57531 |
rs201407414 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737623 | GCGCTTTTCCGATGG[A/G]CTTAAAAAACGGCGC | 57531 |
rs201413555 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785329 | CAGAGGCTGAGAGAA[A/G]CAAAAGTGTTTTTTA | 57531 |
rs201416716 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807039 | TTTTTTTTTTTTTTT[C/T]TTGAGATGGAGTCTC | 57531 |
rs201456423 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851730 | GTAGGAAATTTAAAA[A/C]AAAAAAAAAAATTTT | 57531 |
rs201465673 | snp | C/T | 5.0114e-05 | 0.00500545 | intron-variant | HACE1 | GRCh38.p7 | 6:104777125 | TCTAAATATGTAGCA[C/T]TGGTTAATTTTACAT | 57531 |
rs201515642 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693056 | GTGTGTGTGTGTGTG[C/T]GCACGCGCGCGCGCG | 57531 |
rs201516687 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756430 | AAAAAAAAAAAAATA[A/T]ATATATATATATATA | 57531 |
rs201527620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839938 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 57531 |
rs201578414 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710016 | AAAACAAACTTCTAC[-/A]AAAAAAAAATGTATA | 57531 |
rs201617244 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832408 | GTTGTTGTTGTTGTT[G/T]TTTGATACAGGCTCT | 57531 |
rs201619324 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790069 | AAGAAAAAAAAAAAA[-/A]GAAAACAAAAATACA | 57531 |
rs201639649 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739853 | CTCCACCCCAAATCA[A/G]CAGAATATACATTTT | 57531 |
rs201640865 | in-del | -/G | 0.000719942 | 0.0189592 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858459 | TAATCCCAACACTTT[-/G]GGGGGAGCAGGGTGC | 57531 |
rs201644409 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693635 | GTTATATCAGTTTTT[-/G]TTTTCTTTCCCAAAT | 57531 |
rs201654094 | in-del | -/AGGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831981 | AAGAGAAGAGAAGAG[-/AGGA]AGGAAGGAAGGAAGG | 57531 |
rs201693206 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754814 | AAAGAAAAAATTGTT[A/C]CCAGCCACTACAAAA | 57531 |
rs201723229 | in-del | -/AGAG | 0.24019 | 0.249807 | intron-variant | HACE1 | GRCh38.p7 | 6:104758294 | ATGTTAAGGGCAGCC[-/AGAG]AGAAAGGTCGGGTTA | 57531 |
rs201776642 | in-del | -/TG/TGTGTG | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852195 | CATCTATGTCCAAAC[-/TG/TGTGTG]TGTCTGTGTGTGTGT | 57531 |
rs201777448 | in-del | -/AAATATAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756425 | TCAAAAAAAAAAAAA[-/AAATATAT]ATATATATATATATA | 57531 |
rs201781305 | in-del | -/A/GAAGAG/GAAGAGG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831984 | GAAGAGAAGAGAGGA[-/A/GAAGAG/GAAGAGG]AGGAAGGAAGGAAGG | 57531 |
rs201793472 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant, synonymous-codon, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833060 | CTTGTGACCGTTCTG[A/G]CAGGCAACATGCAGT | 57531 |
rs201799198 | in-del | -/ATATA | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104808608 | TGACCCTTGAATATG[-/ATATA]ATATATTATATCTAG | 57531 |
rs201812032 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830758 | AAAATAAATTACATT[C/T]TTTTTTTTTTTTTTT | 57531 |
rs201815593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791703 | AAAACAAATTACATA[C/T]TAAAATACTTATTTT | 57531 |
rs201821541 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853067 | GTGTGAAGAGGTGAG[C/G]CTTTGGGGAGGCAAT | 57531 |
rs201842752 | snp | C/T | 1.86444e-05 | 0.00305317 | intron-variant | HACE1 | GRCh38.p7 | 6:104796779 | CAAGATCTAAAATTA[C/T]CCAGGTTTAAAAACA | 57531 |
rs201849427 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758904 | AGGGGTTGCAATCCT[A/G]GTCTCTGATAAAACA | 57531 |
rs201851229 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764609 | GTCATCTATAGGCAC[C/T]TCTTCTTCAGTTTTA | 57531 |
rs201878783 | in-del | -/A | 0.0267878 | 0.112589 | intron-variant | HACE1 | GRCh38.p7 | 6:104807705 | AAAGATGGCAGGGGG[-/A]AAAAAAAATCAATGT | 57531 |
rs201882498 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727499 | TGAATACACACACAC[-/AT]ATGTATATGAATACA | 57531 |
rs201907057 | in-del | -/AT/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778376 | ATATATATATATATA[-/AT/TA]ATATCAATTTCTCAA | 57531 |
rs201908636 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727498 | ATGAATACACACACA[C/T]ATATGTATATGAATA | 57531 |
rs201937921 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104741129 | tcatgctaaaaactc[C/T]caataaattaggtat | 57531 |
rs201961664 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682263 | TTTGCATTTCTAATG[G/T]GTTCCCAGATGATGA | 57531 |
rs201964810 | in-del | -/A | 0.0166325 | 0.0896639 | intron-variant | HACE1 | GRCh38.p7 | 6:104764058 | CTCAAACAAACAAAC[-/A]AAAAAAAAAGTACTG | 57531 |
rs202043047 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | HACE1 | GRCh38.p7 | 6:104685084 | TGTACCATATGTTGG[-/A]GGCTCCAACAGCCTG | 57531 |
rs202049586 | snp | C/T | 0.000142136 | 0.00842899 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858531 | ATAGTGAGACCTCAT[C/T]TCTATAAAAGAAAGG | 57531 |
rs202063572 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807359 | GGCTACTTTGATTTT[A/C]AATACTCTAACTGAA | 57531 |
rs202093360 | in-del | -/AAC | 0.0633504 | 0.166319 | intron-variant | HACE1 | GRCh38.p7 | 6:104733309 | AGATCCTCTAGTTTT[-/AAC]ATCTTAATTAAAATT | 57531 |
rs202095975 | in-del | -/AT | 0.0325976 | 0.123435 | intron-variant | HACE1 | GRCh38.p7 | 6:104701224 | TTTCAATTATTCCAC[-/AT]GTTTGGTTCCAAGAA | 57531 |
rs202100727 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850094 | AGCTGGGATTACAGG[C/T]GCACGCCATCACGCC | 57531 |
rs202105471 | in-del | -/TTATCT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807526 | CTAATAGAATAAAAG[-/TTATCT]ACAAACAGAAAATAC | 57531 |
rs202110306 | snp | A/G | 6.72902e-05 | 0.00580005 | intron-variant | HACE1 | GRCh38.p7 | 6:104785322 | GCAATTCCAGAGGCT[A/G]AGAGAAACAAAAGTG | 57531 |
rs202110988 | snp | A/G | 0.472335 | 0.114312 | intron-variant | HACE1 | GRCh38.p7 | 6:104741484 | atacaaaatcaatgt[A/G]caaaaatcacaagca | 57531 |
rs202113530 | snp | A/G/T | 3.53927e-05 | 0.00420658 | intron-variant | HACE1 | GRCh38.p7 | 6:104750317 | TTGTTGTGTTACAAC[A/G/T]TAAGAACTGATGTTT | 57531 |
rs202115117 | snp | C/T | 0.00154848 | 0.0277821 | intron-variant | HACE1 | GRCh38.p7 | 6:104784527 | TACACAGGCAAAAGT[C/T]TGTGATATAATATAG | 57531 |
rs202157348 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742008 | CAGAAATAACGCCAC[A/G]TATCTACAACTATCT | 57531 |
rs202157488 | in-del | -/GGAGGGAGGAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692137 | AAAGGAAGGAAGGGG[-/GGAGGGAGGAAA]GGAGGGAGGAAGGAG | 57531 |
rs202166703 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799404 | CTTTGCTTCCATATT[-/C]AGCCTACAAAAGCTC | 57531 |
rs202183668 | snp | C/T | 0.365439 | 0.221752 | intron-variant | HACE1 | GRCh38.p7 | 6:104740714 | agatggattcacagc[C/T]aaattctaccagagg | 57531 |
rs202193787 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812954 | AAGTTTATTCTCTGC[-/A]CAAAGTGAACAGGGA | 57531 |
rs202226828 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693057 | TGTGTGTGTGTGTGT[A/G]CACGCGCGCGCGCGC | 57531 |
rs367563544 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805389 | AAATCATGCTACTAT[A/G]AAGACACATGGATAC | 57531 |
rs367595179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758677 | TAGCATCATAATGAC[A/G]GCATCAAATTCACAC | 57531 |
rs367608439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104785480 | CCTAAAGGTAAGTAA[C/T]AAAATTATACAAATG | 57531 |
rs367613433 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797173 | TTCATAATCACAAAA[A/C]CTTTCTCAATGTTAA | 57531 |
rs367636983 | snp | C/G | 1.65979e-05 | 0.00288074 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104777107 | CTACTCCTAAAAATA[C/G]AATCTAAATATGTAG | 57531 |
rs367642673 | snp | A/C/T | 5.68223e-05 | 0.00532996 | intron-variant | HACE1 | GRCh38.p7 | 6:104750518 | TTCAAAAACCTTTTA[A/C/T]ATACTTAATGTTAAT | 57531 |
rs367650414 | snp | C/T | 1.648e-05 | 0.0028705 | missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849224 | TCTTTAACAGCAAAA[C/T]CAAGCATTCCACCGA | 57531 |
rs367659650 | in-del | -/AATT | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104715653 | CAAATAAAGAACATA[-/AATT]AAGATATGGAAATAA | 57531 |
rs367702117 | in-del | -/AGGAAGGAAGGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831981 | AAGAGAAGAGAAGAG[-/AGGAAGGAAGGA]AGGAAGGAAGGAAGG | 57531 |
rs367709134 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792639 | AAGGGTGAAGGTCAT[C/G]ATCAACTCAGTATAC | 57531 |
rs367814736 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736984 | TTAAAATAAAAAACA[C/G/T]AGTTTTTAAAAATTA | 57531 |
rs367818943 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702189 | AAATATTTATAATGG[A/G]ACTTAGGGGCAGGAG | 57531 |
rs367844392 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688662 | GGTATTGGCAGAGTT[C/T]GTTCTTTCTGAAAGT | 57531 |
rs367876489 | snp | C/T | 1.64738e-05 | 0.00286995 | intron-variant | HACE1 | GRCh38.p7 | 6:104791467 | AATTCATCTCTTTTA[C/T]GTCTATCTTCCTAAC | 57531 |
rs367906617 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693646 | TTTTTTTTTCTTTCC[-/C]AAATACTTTCCATCA | 57531 |
rs367929125 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759420 | CTGCTCAACTAAATG[A/G]AAACTGAACAACGCG | 57531 |
rs367929560 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838236 | TGGAATCACAAAAGA[C/T]CTAGAATAGCAAAAG | 57531 |
rs367940106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698060 | TAGAAAAGTAATTTA[A/G]CTTCTCTTAGGGGTA | 57531 |
rs367957278 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732985 | CAGCAAGAGAATATA[C/T]ACAGAAGACCTGGCT | 57531 |
rs367961144 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802125 | CAGACAAGGAAGGAC[A/G]TTACATAATGGTAAA | 57531 |
rs367962402 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775278 | CCATACCAGCTACTC[A/G]GGAGGCTGAGGTGGA | 57531 |
rs367980351 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748862 | TGATTTTAGAAGTCA[A/G]GAGAATGGTTACCCT | 57531 |
rs367982932 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799825 | ACTGACACAGAAGAC[A/G]GGTGATTTCTGCATT | 57531 |
rs367990585 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739812 | CAGCTCTGCACCAAG[C/T]GGACCTAATAGACAT | 57531 |
rs368041101 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763492 | AGCCACCCGTGTAGA[C/T]ACAATCTGTGGTTGT | 57531 |
rs368055165 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816917 | TATTTTAGAGCTTTA[A/G]GATTTAATGACAGCC | 57531 |
rs368117555 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794765 | AAAAAATTAGCCGGG[C/T]GTGGTGGTGTGTGCC | 57531 |
rs368123234 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820615 | ACTGATCATTAGAGA[A/C]ATGCAAATCAAAACC | 57531 |
rs368132344 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807792 | AGTTATAATGTCCTG[G/T]CCAGAGTATCCAGAG | 57531 |
rs368147307 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836691 | GCACTGTAGCCTGGG[C/T]GACAGAGTGAGACTC | 57531 |
rs368150461 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686256 | TGAGCCTTACCCAAC[A/G]TGGCTACATAACTTC | 57531 |
rs368152930 | snp | C/T | 1.7947e-05 | 0.00299553 | intron-variant | HACE1 | GRCh38.p7 | 6:104776874 | CAGAAATATGTTATA[C/T]TGGGAAATTTTTTTC | 57531 |
rs368164803 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763024 | AAAGAATCAGTCAAA[A/T]AAGAAATAAACAAAT | 57531 |
rs368169987 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824940 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 57531 |
rs368174009 | in-del | CCCC/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720634 | CTTCCCCGCCCCCCT[CCCC/T]CCCCCCCCAGACGGA | 57531 |
rs368186719 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808209 | AAAAAAAAAAAAGTG[C/T]TTAGAATTAGACAAG | 57531 |
rs368191331 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783538 | AAGGATATTAGGAAA[C/T]GTGCCCAAAGTTCAC | 57531 |
rs368193740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802296 | CCCCACTGTCAATAA[C/T]AGACAGATCAACATG | 57531 |
rs368240868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706936 | ATAACTTAGATGAAA[C/T]GGAAAAACTCCTAGA | 57531 |
rs368283419 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832637 | CTCAAGAGATCCACC[C/T]ATCTCAGCCTCCCAA | 57531 |
rs368339145 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687391 | GATGTGAGCTTTTGG[C/T]GTGCAAACATACACA | 57531 |
rs368370041 | snp | A/C | 0.000153988 | 0.00877327 | intron-variant | HACE1 | GRCh38.p7 | 6:104796885 | TTACCATTCCAGTTT[A/C]TATTATAAAGATAAG | 57531 |
rs368371915 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812324 | AGCACATCATAGTAG[C/T]AGGCCTAGCTACTCA | 57531 |
rs368384864 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821927 | CTTGTGTATGGTTTT[A/C]AAGTAATGCTATTTT | 57531 |
rs368399234 | snp | C/G | 1.64936e-05 | 0.00287168 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785225 | TCCAGAGGCTGAGA[C/G] | 57531 |
rs368418229 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853022 | TCTACCAAAAGTTCA[C/T]GTGTTGGAAATTTGG | 57531 |
rs368481849 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104700335 | CACTACTGAACTGTC[A/G]CAGTTGGTAATCTTC | 57531 |
rs368484301 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709141 | ACAACCACAGAATGA[A/T]AGAAAATACTTGCAA | 57531 |
rs368488221 | snp | G/T | 1.64776e-05 | 0.00287028 | intron-variant | HACE1 | GRCh38.p7 | 6:104850892 | GAGTTTAACTCAAAA[G/T]ATCTTTAGTCTTACT | 57531 |
rs368528740 | snp | G/T | 1.68493e-05 | 0.00290248 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750374 | AAGCTGTATGAGGGA[G/T]GGTGGAATGAACATA | 57531 |
rs368541941 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684945 | GTGAAGTTGGGCAGG[G/T]CCAAGTGAAATGCTT | 57531 |
rs368563913 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725734 | TTTTGTGTCAAAGAC[C/T]ATGCGTACATTGAAA | 57531 |
rs368626388 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742856 | TGCTATAAAGACACA[C/T]GCACACATATGTTTA | 57531 |
rs368628596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739429 | GGAAACCCATCTCAC[A/G]TGCAGAGACACACAT | 57531 |
rs368633921 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739592 | TACATAATGATAAAG[A/G]GATCAATTCAACAAG | 57531 |
rs368711954 | snp | A/C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717962 | ATGGATATCTTTCCC[A/C/G]ATCTGCCATCTTCTG | 57531 |
rs368714945 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730567 | ACTCCAATTCATTAC[G/T]GTAAGTTGCTTTGTG | 57531 |
rs368768811 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757714 | ATGAACTGACAGAAG[C/T]AGGCTTCAGAAGGTT | 57531 |
rs368789880 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791435 | AGCTTTCTGATTAAT[G/T]AATGCATGCTTTGTC | 57531 |
rs368829052 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104792725 | CAAACTGAAAAACTG[A/C]ATCTGCCACCCAGAA | 57531 |
rs368841448 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803709 | AGGTATTGATGGAAC[A/G]TATCTCAAAATAATA | 57531 |
rs368897380 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104722643 | TGGACACAGAGTTTA[A/C]ATCAAGCCGCCGCGC | 57531 |
rs368906462 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736334 | CTGTCACCCCAGCTA[A/G]AGTGCAGTGGTGCAA | 57531 |
rs368907273 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819308 | ACAAAAAGAATTAAA[A/T]ACCTAGGAATACAAC | 57531 |
rs368925340 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838840 | GCAAACTATCCATCT[A/G]ACAAGGGATTAATAA | 57531 |
rs368926767 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852361 | TAATGTATAAACAGC[A/G]GTTTCATTATCTGAG | 57531 |
rs368939425 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776670 | CTGTGGAAATCAAAA[A/G]TAAAATGTACTGAAA | 57531 |
rs368945347 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104841983 | TTGCAAAGAAAGTGG[C/T]ATGGCAAAATGGCCA | 57531 |
rs368957960 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854097 | GTGGACTACTGTTCT[C/T]GCCAAAAATGCATAA | 57531 |
rs368987958 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104767540 | TCTTTTTGTTTTCTT[A/T]ACTGAAATTTGATCA | 57531 |
rs368996338 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104757146 | GCAGGACGTACCTGA[A/T]CAAAAGGCAGCAGAC | 57531 |
rs369028006 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711043 | TTTCTATCCAGATTC[C/T]ACTGGTGGTCAATGT | 57531 |
rs369036934 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823099 | ATCACTTTTAATATA[A/T]CCTACAAAGACATTA | 57531 |
rs369044972 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742296 | CAATGGCAACAAAAG[A/C]CAAAATTGACAAATG | 57531 |
rs369051307 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808697 | CCCTATAATTTGTCC[C/T]GGGGTTAACTTGTTC | 57531 |
rs369060931 | snp | A/G | | | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682196 | AAACTGTAGATTGCC[A/G]GGCCCACCTCCAGAG | 57531 |
rs369123797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833854 | GCTGGACGTGGTGGT[A/G]CGTGCCTGTAATCCC | 57531 |
rs369170537 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829645 | TTTACCTGTATATGA[C/T]CATTGCAGGTAACTA | 57531 |
rs369174734 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762866 | ATGATGGTGGACACC[C/T]GTAGTCCCAGCTACT | 57531 |
rs369206450 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104773449 | ACCTAAATAAGTCAT[A/G]TGAGTCTCATCATTC | 57531 |
rs369253995 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701359 | TAAAATTAAGGTAGA[C/T]GTCTGTGAAATTACG | 57531 |
rs369271638 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104703355 | ATTGCTCTGTCCCCT[C/G]TTTTTTAACATAGGG | 57531 |
rs369322816 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821239 | AATAACTAATGTATA[C/G]TAGGCTACCTATGTG | 57531 |
rs369330231 | snp | A/G | 8.32882e-05 | 0.00645269 | intron-variant | HACE1 | GRCh38.p7 | 6:104796918 | GCTCAGAATATAAAT[A/G]AAAAACACACCTGTA | 57531 |
rs369364377 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767910 | TTATCTTCTTTTTTT[G/T]CTCCAAGCCTGGATG | 57531 |
rs369372008 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795969 | TCTAAAACGAAAGAG[A/G]AATTTAAATTCCGCA | 57531 |
rs369387964 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794654 | CACGCCTGTAATCCC[A/G]GCACTTTGGGAGGCC | 57531 |
rs369415559 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758272 | CAAGGTTGAAATGAA[C/G]GAAAAAATGTTAAGG | 57531 |
rs369423045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104750212 | AATCTCTAAAAATGG[A/G]CATTAAACCATTTTG | 57531 |
rs369448011 | in-del | -/AG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831985 | GAAGAGAAGAGAGGA[-/AG]GAAGGAAGGAAGGAA | 57531 |
rs369449799 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815771 | TTTGAAATTGGAATA[C/T]GTTTAAAAGGGAAAC | 57531 |
rs369450749 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830653 | AAGACTCAGAAAGTT[C/T]GTAACCAAAAAAATA | 57531 |
rs369454820 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739914 | TTGACCACATACTTG[A/G]AAGTAAAGCTCTCCT | 57531 |
rs369455865 | in-del | -/C | 0.0288905 | 0.116664 | intron-variant | HACE1 | GRCh38.p7 | 6:104785383 | TTAAAAAAAAAAAAA[-/C]AAAACACAACTAGAC | 57531 |
rs369472412 | in-del | -/GT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820215 | AAAAAAAAAAAAAAA[-/GT]AAAACCCAAAACCAT | 57531 |
rs369474825 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793135 | AGCCGGGCGTGGTGG[C/T]AGGCCCATGTAGTCC | 57531 |
rs369482362 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736260 | ACCTGTTAATAGTTA[C/T]GTCTTATTTATTTAT | 57531 |
rs369490874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695686 | CTCTCAAGTAGCTGG[A/G]ATTACAGGTGCCCAC | 57531 |
rs369522503 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762989 | GTAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 57531 |
rs369551711 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832378 | AGCACTATTTTCCTG[C/G/T]TTTTTGTTGTTGTTG | 57531 |
rs369559226 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809168 | TGCAAAACACTGTAC[C/T]ACACTTTGGACATAA | 57531 |
rs369563408 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846652 | GCTGAGGGAACAAAA[C/T]AAAAAGCTGGCCCCA | 57531 |
rs369564339 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772273 | GATGATAATCATTTA[C/T]TCATACATATTTGTC | 57531 |
rs369593374 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835867 | AAAGAATCAAGAATC[C/T]AAATAGCACTAAACT | 57531 |
rs369635015 | snp | A/T | 1.65132e-05 | 0.00287339 | intron-variant | HACE1 | GRCh38.p7 | 6:104849127 | TTAAGCCACTTAAGA[A/T]AACTAAATAGTTACC | 57531 |
rs369651693 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800014 | CCTGCCAAAATACGG[C/T]GCTTTTCCCAAGGTC | 57531 |
rs369657379 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717098 | TGGCACGTATATAGA[C/T]GTAAAAGAATATTCA | 57531 |
rs369660108 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849375 | ACAGTCTTGCTCTGT[C/G]GCCCATGCTGGAGTG | 57531 |
rs369670868 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104829423 | CAGGCAGTATTAGCA[C/T]AACTATGAACACAGA | 57531 |
rs369681617 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781206 | TAACTTTTTTCAGTA[C/T]AGACTCATAGATTCC | 57531 |
rs369683790 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754124 | AATCACAAGTATCAA[C/T]AGCAGAATAGACCAA | 57531 |
rs369706409 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709367 | AATCTCGTGTTGAAA[C/T]GTGATCCCCAGTGTT | 57531 |
rs369711059 | snp | A/C/G | 3.31775e-05 | 0.00407282 | missense, stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795670 | GCTGAGACAAATGCT[A/C/G]CAGAACTTGCCGTAA | 57531 |
rs369737109 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850287 | TATAATTTGATTTAA[C/T]TTCTGACACAAATAG | 57531 |
rs369767388 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786621 | AAAAAAAAAAAAAAA[-/C]AAACAAACAAACAAA | 57531 |
rs369767987 | in-del | -/CTCT | 0.320335 | 0.239902 | intron-variant | HACE1 | GRCh38.p7 | 6:104774389 | GCCACCGCGCCCGGC[-/CTCT]CTTTTTTTTTTGAGA | 57531 |
rs369787683 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858384 | TGAATTCTAAATAGA[A/G]ACTAGAGACCATTTT | 57531 |
rs369793779 | snp | A/C/T | 9.93499e-05 | 0.00704742 | intron-variant | HACE1 | GRCh38.p7 | 6:104771922 | ATAATAATAGAGCCA[A/C/T]ACCAAGAATGTGCTT | 57531 |
rs369796621 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104699975 | TTGTGTGGAAAAAAA[A/C]AACAACAAAAAAAAC | 57531 |
rs369840051 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104743056 | TCTCAGTAAACTATC[A/G]CAAGAACAAAAAACC | 57531 |
rs369844412 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822811 | GCAGTGAGCGGAGAT[C/T]GCGCCACTGCACTCC | 57531 |
rs369865705 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710349 | GTGACTACTAATGGA[G/T]ACCTGGGTTTCTTCT | 57531 |
rs369868125 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761331 | AACCAAAACAGAATG[A/G]TACTGGTACCAAAAC | 57531 |
rs369881070 | in-del | -/A | 0.0505692 | 0.150756 | intron-variant | HACE1 | GRCh38.p7 | 6:104847764 | TCTTCAAGAGTAATT[-/A]AAAAAAAAGACACAA | 57531 |
rs369883647 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739843 | CTACAGAACTCTCCA[A/C]CCCAAATCAACAGAA | 57531 |
rs369889800 | snp | A/G | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683155 | ATGGCACATTCTGCT[A/G]AAAGATGTTGCGCCA | 57531 |
rs369894070 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707415 | TATAAACAGAATAAA[A/T]GACAAAGACCTCGTG | 57531 |
rs369896667 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721906 | TTGGCTAATTTAAAA[C/T]ATATACTAGACAGGT | 57531 |
rs369903989 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688353 | ACTTTTCCTTTGTAA[-/AC]ACACACACACACACA | 57531 |
rs369924901 | in-del | -/CTTA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743794 | GATAAACTGAATTGC[-/CTTA]CTATTAAACCAAACC | 57531 |
rs369954617 | multinucleotide-polymorphism | AA/CC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760938 | ATCATGAGTGAACTT[AA/CC]ATTCACAATTACTAT | 57531 |
rs369968280 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690401 | AATTAAACATGTCCA[G/T]TCAAAGCTATCTCAA | 57531 |
rs370044160 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822916 | TATTTATACTGTAGC[A/G]CTTACAATATAAAAA | 57531 |
rs370049285 | in-del | -/TTTTTTT/TTTTTTTTTTT/TTTTTTTTTTTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745455 | AATATCAGGATTTCC[lengthTooLong]TTTTTTTTTGAGACC | 57531 |
rs370062370 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752247 | AGTCACATACAGGTA[C/T]TTATTATAGAGAGGG | 57531 |
rs370071955 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850451 | AAATTAATTTCAACA[C/T]ATCTACCTAAATCCT | 57531 |
rs370087457 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733913 | ATCCCAGCACTTTGG[A/G]AAGCCAAGGCAGGTG | 57531 |
rs370117402 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713350 | AGGGCAATGAAAGAG[G/T]AGATTGGCTCAAAGG | 57531 |
rs370140321 | snp | A/G | 3.35813e-05 | 0.0040975 | intron-variant | HACE1 | GRCh38.p7 | 6:104776990 | CATACAGTGATTTCT[A/G]CATCATCTTCTTTTA | 57531 |
rs370146577 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104816191 | GCTGCAGAAGTGTAC[A/C]TAAGTAACAAGGAGC | 57531 |
rs370180344 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714564 | ACATTTGCAAATCCC[C/T]TGTACATTCCCAAAT | 57531 |
rs370201904 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788343 | GAAGAATTATATTCT[A/G]CATATAGTAACAATG | 57531 |
rs370219491 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780313 | ACAAACACCTACACA[A/G]CCAAATGGTACATTT | 57531 |
rs370219684 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791210 | GGTGGCTGCATATTA[C/T]ATTAAAAACCTATAA | 57531 |
rs370222237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840598 | CTTTGGGTAGCCAAG[C/G]CGGGTGGATCACCTG | 57531 |
rs370227549 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843751 | ATACTCAGAATATCA[A/G]TAAAATGCATGTCTA | 57531 |
rs370256132 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835545 | TAAAAGTACAAAGAA[A/G]AGAAATGAGAAAAAG | 57531 |
rs370296382 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104820371 | TAAAGAGTTTCTGCA[C/T]AGCGAAAAAAACTAT | 57531 |
rs370322522 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858534 | GTGAGACCTCATCTC[C/T]ATAAAAGAAAGGAAA | 57531 |
rs370323438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104717811 | ATATACTTGTTAGCT[A/G]GTCAGACTTACCTTT | 57531 |
rs370340461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696537 | TCTGCAGAAGAGGAA[A/G]GGGGAAGGATTTACC | 57531 |
rs370342948 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831045 | AGACTACTGGCACAC[A/T]CCTGTACATTCTATT | 57531 |
rs370376160 | in-del | -/AGAGA | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104691921 | ACAAGACCCTGTCTT[-/AGAGA]AGAGAAGAGAAGAGA | 57531 |
rs370382836 | snp | C/G | 3.31181e-05 | 0.00406914 | intron-variant | HACE1 | GRCh38.p7 | 6:104843211 | ACATCAGATGAAATT[C/G]ATAGCACTTACTGCT | 57531 |
rs370383954 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731275 | AAATGACAAAGGAAC[A/G]TTTAATGTATAGGTT | 57531 |
rs370410605 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817301 | GGGGAGGTGACTGGA[C/T]CATAGGGGCAAATTT | 57531 |
rs370426751 | snp | C/T | 3.31192e-05 | 0.00406921 | intron-variant | HACE1 | GRCh38.p7 | 6:104744141 | ATTATTTCCATATTA[C/T]CATAAAAATACTGCT | 57531 |
rs370448772 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696731 | TGTGCCCCATAAGGC[C/T]TCCCATCAGAGGACT | 57531 |
rs370463961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104726945 | TAAATTAGAAAGATG[C/T]TACCTCTAAATAGTA | 57531 |
rs370468439 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716410 | AAATTGAACACATTC[A/G]GCCAGGTGCAGTGGC | 57531 |
rs370480086 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763027 | GAATCAGTCAAATAA[A/G]AAATAAACAAATTTC | 57531 |
rs370520811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832636 | GCTCAAGAGATCCAC[C/T]CATCTCAGCCTCCCA | 57531 |
rs370522796 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822057 | CTACAAAAGAAAGTC[A/G]TAATTTTTTTTTTAA | 57531 |
rs370552053 | in-del | -/A | 0.0178098 | 0.0926698 | intron-variant | HACE1 | GRCh38.p7 | 6:104707204 | TGTGATACCAGAACC[-/A]GGCAAAAGCATCACA | 57531 |
rs370568117 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104718015 | GTGAGAAAAAAAAAA[A/C]CCCTTAATTTTGTAG | 57531 |
rs370569847 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104740013 | TCAGGATTAAGAAAC[A/T]CACTCAAAACCACTC | 57531 |
rs370600820 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782185 | ACAGTATCATACAGT[A/G]TAGGTTAAGAAATTG | 57531 |
rs370604300 | snp | A/C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795961 | TCTAAACCTCTAAAA[A/C/T]GAAAGAGAAATTTAA | 57531 |
rs370658990 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765985 | TGACTTTCTGTGCTA[C/T]GGATAAAGACAAATG | 57531 |
rs370659720 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720713 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA | 57531 |
rs370695894 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745491 | TGGCTCTGTCACCCA[C/G]GCTGGAGTGCAGTGG | 57531 |
rs370727119 | snp | C/T | 1.651e-05 | 0.0028731 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744549 | TCATAGCCACTTGTG[C/T]ATTCTGTATTTTTTA | 57531 |
rs370741068 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827020 | TTTCAACAGACTTCA[C/T]AACCTTTCAAGTGAC | 57531 |
rs370756545 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798301 | AAAACACTACACAGA[C/T]TTCTCAGAAACTTAA | 57531 |
rs370765018 | snp | A/C | 1.65244e-05 | 0.00287436 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777052 | TACAGCAATCCCTTG[A/C]TTTAGCTTTGCACAA | 57531 |
rs370775829 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824921 | TACTAAAAAAAAAAA[A/T]AAATACAAAAAATTA | 57531 |
rs370815931 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785108 | CTCCCTGCAAGAGCA[G/T]CTGGTTTAGATTCCC | 57531 |
rs370889456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104693708 | GAGGATATAGAACCC[A/G]CAGATACAGAAGACG | 57531 |
rs370890740 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698028 | GAGTGAGCTTTACAG[A/C]AAGATAGATGTAGTA | 57531 |
rs370929585 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831979 | GAAGAGAAGAGAAGA[-/G]GAGGAAGGAAGGAAG | 57531 |
rs370975078 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800798 | ATTCTAAAAACCAGA[A/G]CACCTCTTCTCCTCC | 57531 |
rs370976098 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807562 | CTGAAAACCATTATA[C/T]ATCCCAACCTTTATT | 57531 |
rs370984553 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703755 | AGTTAGAATTCATGG[C/T]AAACAAGCCATACTA | 57531 |
rs370986058 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745466 | TTTCCTTTTTTTTTG[A/T]GACCGAGTCTGGCTC | 57531 |
rs371023213 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742777 | CAGGGATCTAGAACT[A/G]GAAATACCATTTGAC | 57531 |
rs371026841 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773766 | AATAGATAAGGAGAC[-/T]TTTTTAAAAAAAAAA | 57531 |
rs371040321 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713736 | TATTACAACCTAGTC[C/T]GATTGACCCTTCCAC | 57531 |
rs371046311 | in-del | -/ATA | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104855878 | TGAGCGTTAGTGAGC[-/ATA]ATAAGGTTCACAATG | 57531 |
rs371062730 | in-del | -/T | 0.0539704 | 0.155153 | intron-variant | HACE1 | GRCh38.p7 | 6:104822060 | AAAAGAAAGTCATAA[-/T]TTTTTTTTTTAAATT | 57531 |
rs371064303 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816032 | GAGCCGAGATCACTG[C/T]ATTGCACTCCAGCCT | 57531 |
rs371122105 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802179 | TAACTATCCTAAATA[C/T]ATATGCACTCAACAC | 57531 |
rs371140317 | snp | C/T | 1.64917e-05 | 0.00287151 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796968 | TACTCCATTTTTATC[C/T]GGCAGATATTTGGCT | 57531 |
rs371183617 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792655 | TCAACTCAGTATACC[-/C]ACTGGAGGCTATATG | 57531 |
rs371184478 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770910 | TCATTTAAGCTTATA[C/T]TTCTAATCAAATTTC | 57531 |
rs371196435 | snp | A/C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778800 | AGTGACAAACTGAGA[A/C/T]CTTATCTCTACAAAA | 57531 |
rs371208450 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819618 | AAGTTGGAGGCATCA[C/T]GCTACCCAACTTAAA | 57531 |
rs371325069 | snp | C/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861524 | GCCTCTTATGCTATT[C/G]AAAAAGTCAGGATTC | 57531 |
rs371369417 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806282 | GCTTGGATGACATAC[C/T]TTGACTTTATTAAAA | 57531 |
rs371403698 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769730 | GCCCCAGTTTTGCCA[C/T]TAACTCTTTAGGATT | 57531 |
rs371420571 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845627 | GGACTACAGGCACCC[A/G]CCACCATGCCTGGCT | 57531 |
rs371444076 | in-del | -/TATGTATATGAATACATACACACATATA | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727668 | GAATACATACACACG[-/TATGTATATGAATACATACACACATATA]TATGTATATGAATAT | 57531 |
rs371450175 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807019 | TAAGTGTAAGAATTC[-/T]TTTTTTTTTTTTTTT | 57531 |
rs371472283 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739813 | AGCTCTGCACCAAGC[A/G]GACCTAATAGACATC | 57531 |
rs371491310 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799322 | TGAATCAGACAGCCA[A/G]TTCTTCACACCATGA | 57531 |
rs371493017 | snp | A/G | 0.000164728 | 0.00907398 | intron-variant | HACE1 | GRCh38.p7 | 6:104791468 | ATTCATCTCTTTTAC[A/G]TCTATCTTCCTAACA | 57531 |
rs371498952 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834145 | GAATGACAACCTATT[G/T]CCAAAAAAAAAAAAA | 57531 |
rs371585625 | in-del | -/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727335 | ATATATATACACATG[-/TA]TATGTATACGAATAT | 57531 |
rs371669286 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691580 | ATGCAATATTTTTTG[-/G]TAATAGAAAATAATG | 57531 |
rs371673092 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841655 | ACCTCATTCCCCAAT[G/T]TTTAATCATAAAGGC | 57531 |
rs371686569 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742836 | CAAAGGACTATAAAT[C/T]ATGCTGCTATAAAGA | 57531 |
rs371698801 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834726 | TGACTTGTCAGAATG[A/C]TACACCAGTATTAGA | 57531 |
rs371753942 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769334 | TAGATCTTTCCACTT[C/T]GTCATATATATCTGA | 57531 |
rs371757562 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720461 | GGTATCTGTGGGGGA[C/T]TGGTTCTAGGACCCC | 57531 |
rs371794502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104847644 | CAAAAATTTGGCCTC[A/G]GATTGATGTAATGGA | 57531 |
rs371819932 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847775 | AAAAAGACACAACGC[A/G]TTTGTATACCGTGTC | 57531 |
rs371841472 | in-del | -/AC | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104727467 | CACACATATATGAAT[-/AC]ACACACATATGTATA | 57531 |
rs371849825 | snp | C/T | 8.24926e-05 | 0.0064218 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777258 | CCTGTGCACCATATC[C/T]GAATCTGGCTGTCCT | 57531 |
rs371868133 | in-del | -/ATTTAACAT | 0.241627 | 0.24986 | intron-variant | HACE1 | GRCh38.p7 | 6:104790900 | CTTCATAAAATTATA[-/ATTTAACAT]ATTTAACATGAGTAG | 57531 |
rs371868575 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822301 | GGCAGGAGAATGGCA[C/T]GAACCCAGGAGGCAG | 57531 |
rs371879052 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104737409 | TTCTGCATTTCCATC[C/T]GAGGTACCGGGTTCA | 57531 |
rs371903327 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759263 | TCTTCTCAGCACCAC[A/G/T]TCGCACTTATTCTAA | 57531 |
rs371920456 | snp | A/G | 1.79777e-05 | 0.00299809 | intron-variant | HACE1 | GRCh38.p7 | 6:104776876 | GAAATATGTTATATT[A/G]GGAAATTTTTTTCTA | 57531 |
rs371931826 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806254 | ATCACTTGAGGCCAG[A/G]CGTTGAAGACCCGCT | 57531 |
rs371955460 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795564 | ATTGATTTCCTCTTA[C/T]TGCGAAACACTTACC | 57531 |
rs371996106 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104723517 | GGCAGGTTACAATAA[C/T]TCAGTACCTAAGACT | 57531 |
rs372012924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705311 | CTCCTCTGTGAGACA[C/T]AGTTTCCTCAGGAAG | 57531 |
rs372042076 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820187 | GCAACAGAGTGAGAC[C/T]CCGTCTCAAAAAAAA | 57531 |
rs372058934 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104742880 | ATGTTTATTGCGGCA[C/T]TATTCACAATAGCAA | 57531 |
rs372063105 | in-del | -/GGAGAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716603 | GCTGAGGTAGGAGAA[-/GGAGAA]TTGCTTGAACCCGGG | 57531 |
rs372070155 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793051 | AGGCAGGCAGATCAC[A/G]AGGTCAGGAGATCGA | 57531 |
rs372118926 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104831682 | GCGGATCATGAGGTC[A/G]GGAGATTGAGACCAT | 57531 |
rs372144707 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104737601 | GGGTCACTCCCACCC[A/G]AATACTGCGCTTTTC | 57531 |
rs372153669 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | HACE1 | GRCh38.p7 | 6:104849256 | CCACAACTAAAACAA[C/T]ATTAAAAGACAGTTC | 57531 |
rs372168972 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845025 | AGTGAGTAAACAGTA[A/G]TACATACAATACAGT | 57531 |
rs372177857 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852279 | TTAGAACAATGTATG[C/T]TTCTTAAAAAGCAAA | 57531 |
rs372182189 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104712751 | CACTCTAGCCTGGGC[A/G]ACAGAGCAAGACTCG | 57531 |
rs372202673 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722675 | AATGTTTCTGTAGCT[A/G]GTTTTTTACACCTAA | 57531 |
rs372205019 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104795158 | AATAAAGAACTTAAC[A/T]GAGGGGGACAGGTCA | 57531 |
rs372224444 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819287 | GAACTCCCATTCACA[A/C]CTGCCACAAAAAGAA | 57531 |
rs372241535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687797 | ACCAGGCTGAGAAGC[C/T]TCTGGTAAGAAATAA | 57531 |
rs372272709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725892 | ATAGAGTAGTGAAGC[A/C]TGCTGGGCTAAGAAA | 57531 |
rs372307319 | snp | A/G | 0.000132347 | 0.00813364 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851006 | ACAGACCTATGCCAA[A/G]ATAAAAATGAGGAAT | 57531 |
rs372314912 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692118 | AGCTAGGAAGGGAGG[A/G]AGAAAAGGAAGGAAG | 57531 |
rs372344455 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838461 | ACACATTGGAGGTAG[A/G]GACCATCTCTTCAAT | 57531 |
rs372354003 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777974 | ATGTTAGCCAGGCTG[C/G]TTTCGAACTCCTGAC | 57531 |
rs372362036 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793094 | TACACAGTGAAACCC[C/T]GTCTCTACTAAAAAT | 57531 |
rs372441194 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739707 | ACTTAGACTCCCACA[C/T]ATTAATAATGGGAGA | 57531 |
rs372441551 | snp | G/T | 1.68618e-05 | 0.00290356 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796699 | TCATTTGAATAATAG[G/T]CTGAAAAAGCCTCGG | 57531 |
rs372456611 | snp | C/T | 3.31625e-05 | 0.00407188 | intron-variant | HACE1 | GRCh38.p7 | 6:104795567 | GATTTCCTCTTATTG[C/T]GAAACACTTACCTAA | 57531 |
rs372491538 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104721173 | AACATGGTGACACCT[A/G]GTCTCTACTAAAAAT | 57531 |
rs372515246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104740050 | ATGGAAACTGAACAA[C/G]CTGCTCCTGAATGAC | 57531 |
rs372528688 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715016 | AATCTTTGATTGATG[A/G]GATATGAAAGCTAAT | 57531 |
rs372549469 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860994 | CCAGCTAGTGACCAT[C/T]TGTGCCAGTGGTGCC | 57531 |
rs372572198 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826061 | TTGATTCTCATAGGA[A/G]CATGAACTCTGTTGT | 57531 |
rs372575126 | in-del | -/AC | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727609 | CGTATGTATATGAAT[-/AC]ACACACACGTATGTA | 57531 |
rs372586879 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840945 | TCCAGCCTGGGCAAC[-/AA]GAGTGAAACTCTGTC | 57531 |
rs372603419 | in-del | -/TTAGT | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852909 | TTATTACAAAAGAAA[-/TTAGT]TTAGAAGCTTTTATG | 57531 |
rs372610808 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835546 | AAAAGTACAAAGAAA[A/T]GAAATGAGAAAAAGT | 57531 |
rs372611030 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831991 | AAGAGAGGAAGGAAG[A/G]AAGGAAGGAAGGAAG | 57531 |
rs372637035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104790023 | GAAAAGCCACATGAA[C/T]TACAAGAATGCATAA | 57531 |
rs372641172 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815507 | GCTGGGATTATAGGC[A/G]TGCGCCACCACACCC | 57531 |
rs372664303 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725251 | TATATATGTATGTGT[A/G]TATACATACACACAC | 57531 |
rs372671802 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104808078 | GTAATGCCAGCTACT[C/T]GGGAGGCAGAGGCAG | 57531 |
rs372734651 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856835 | GTTAGGCCTGCCTAG[A/G]AGGACTCAACTACCT | 57531 |
rs372734811 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770587 | ATCTGGGCATGGTGG[C/T]GCACCCCTGTAATCC | 57531 |
rs372745184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838665 | TCTTGAGTAATACCC[C/G]TTGAGCAAATTTCTT | 57531 |
rs372745267 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711722 | TATGCTTGATTCTCC[C/T]AGATGAAAATAAAGG | 57531 |
rs372747982 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763012 | AAAAAAAAAAAAAAA[-/G]AATCAGTCAAATAAG | 57531 |
rs372758596 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104782013 | TTGGTGCAAAAGTAA[C/T]TGCGGTTTTTGCTAT | 57531 |
rs372766264 | snp | A/G | 5.11539e-05 | 0.00505711 | intron-variant | HACE1 | GRCh38.p7 | 6:104791680 | AAATTAAAATATGAG[A/G]TTAGAGTAAAACAAA | 57531 |
rs372769358 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840856 | AAATCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 57531 |
rs372787927 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759860 | GCAATAAAATTATAA[A/C]GGGGATATCACCACT | 57531 |
rs372798301 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832380 | CACTATTTTCCTGTT[G/T]TTTGTTGTTGTTGTT | 57531 |
rs372808549 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701048 | AAAAGGTCACACAGC[G/T]GACATCAGACAGGGC | 57531 |
rs372832826 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852643 | ATTCTTCAGAAGGTT[C/T]TGTCCCATTATCCAC | 57531 |
rs372927685 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847284 | AGTTGTTGAAACAGA[G/T]TACTATGATATTTTT | 57531 |
rs372928901 | in-del | -/AT/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790118 | GTGCACACACACACA[-/AT/CA]TACATATATGGCTAA | 57531 |
rs372940172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723231 | TTCTCAACAGGCTTG[C/T]CATACATGACTATTA | 57531 |
rs372956151 | snp | C/T | 3.29794e-05 | 0.00406061 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785055 | GCCGGTTAGCTGTCA[C/T]AGAAATAACATCCTG | 57531 |
rs372962609 | snp | C/T | 6.68863e-05 | 0.00578262 | intron-variant | HACE1 | GRCh38.p7 | 6:104776996 | GTGATTTCTACATCA[C/T]CTTCTTTTATACCCA | 57531 |
rs372985928 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704354 | CCTCCTTTACCCTGT[A/G]AGCAGACCTTACTTA | 57531 |
rs373012483 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720075 | GTCTCAATCTCCTGA[C/T]ATCGTGATCCACCTG | 57531 |
rs373030270 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721822 | ATAGCGCTATATTGC[C/G]CTCTTTTGTGTTAGA | 57531 |
rs373098151 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737408 | TTTCTGCATTTCCAT[C/G]TGAGGTACCGGGTTC | 57531 |
rs373101462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749719 | CAAATTACCAAAACT[A/G]AAGAGAAAAAGAAAA | 57531 |
rs373105035 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772457 | GTATGGCAATAGGCT[A/G]TTCGCTAGGACAGAC | 57531 |
rs373109069 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104737963 | GCAGTGGTTCTCCCA[G/T]CACGCAGCTGGAGAT | 57531 |
rs373115736 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802333 | GGCTAACAAGGATAT[-/C]CAGGAATTGAACTCA | 57531 |
rs373116941 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800203 | AGTAGGTAAACAAAG[C/T]GACAGGGAAGCTCAA | 57531 |
rs373127404 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713061 | TAGGGAACAAGTAAG[A/G]GGATAGAGTGGGATA | 57531 |
rs373129511 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825169 | TTGAGTGGTTTTGAG[A/G]CAGGAGAATAGGGTC | 57531 |
rs373150515 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739932 | GTAAAGCTCTCCTCA[C/G]CAAATGTAAAAGAAC | 57531 |
rs373159245 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104845623 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCT | 57531 |
rs373199425 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715122 | CCCCACTTGCCCATA[C/G]TGGACAATATCTAAG | 57531 |
rs373199513 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718865 | CTCATAAAATGAGTC[A/G]CCACTTTTCCACATC | 57531 |
rs373209103 | snp | A/G | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727595 | TGAATACACACACAC[A/G]TATGTATATGAATAC | 57531 |
rs373209170 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781913 | TCTGGGTCAACAAAG[A/T]GGATACCTAATACAG | 57531 |
rs373216287 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819173 | AAGCTTCTTAAGCCA[A/G]TTAACAACCTCAACA | 57531 |
rs373233905 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707107 | CACTCATTGAAACAA[C/T]ACCAATTCTTTGCAG | 57531 |
rs373323053 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836751 | GTCTCTACGTGCAGA[C/T]AACATGACTGTCTAT | 57531 |
rs373338837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691133 | GCAATATATAAAATA[A/T]TCCAACAAATCATTA | 57531 |
rs373368264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720691 | GGAGTGTAATGGCGA[C/G]ATCTCAGCTCACTGC | 57531 |
rs373370965 | snp | A/G | 8.65673e-05 | 0.00657846 | intron-variant | HACE1 | GRCh38.p7 | 6:104729769 | GCATGTTGATGCTTT[A/G]AAAGAAAAATATACC | 57531 |
rs373394500 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813345 | AATTTTAAAATTAGC[-/C]ATGCATGGTGCTGCA | 57531 |
rs373398995 | in-del | -/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790107 | TACACACTCAACGTG[-/CA]CACACACACATACAT | 57531 |
rs373403916 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702065 | AACATATACAGTGAG[C/T]GTTTCAATCTATTAA | 57531 |
rs373430471 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781209 | CTTTTTTCAGTACAG[A/G]CTCATAGATTCCTGT | 57531 |
rs373475269 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844412 | GCAGTGATGCGATCT[C/T]GGCTCACTGCAACCT | 57531 |
rs373506580 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717390 | GTGATCCACCTTCTT[C/T]GGCCTCCCAAAGTGC | 57531 |
rs373525558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104747104 | AAAATGTACATATTA[A/G]GAAAAATATTTTAAG | 57531 |
rs373556285 | snp | C/T | 0.000132201 | 0.00812914 | intron-variant | HACE1 | GRCh38.p7 | 6:104744155 | ATCATAAAAATACTG[C/T]TTACCTGCCCGTAAC | 57531 |
rs373624755 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836431 | GAAGAAAGAAATAAA[A/G]GCCTGGCGCGGTGGC | 57531 |
rs373665355 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104761553 | AAAATCAACTCAAGA[C/T]GGATGAAAGACTTAA | 57531 |
rs373682370 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732449 | TAAAGCAATCACAAA[-/A]GGACAAATATTGTAT | 57531 |
rs373684850 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697357 | CTGAAACTAGCTCAC[C/T]AAAAAAGGGAATCAA | 57531 |
rs373690678 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708880 | ACATGAAAAGCAAAA[A/G]AAGTTGTACTCCTTC | 57531 |
rs373701453 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700409 | GAGGGAGTTAAAAAA[-/G]AAAAAAAAAAAAAAA | 57531 |
rs373724640 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711339 | TTCTTCCACCCAAAG[G/T]GTTTAAATTTGACTA | 57531 |
rs373731009 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756426 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 57531 |
rs373749548 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804269 | AGGAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 57531 |
rs373750379 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735544 | GCTGAGGCAGGAGAA[C/T]GGCGTGAACCCAGGA | 57531 |
rs373757320 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739387 | AAATTGGATAAAGAG[G/T]CAAGACCCATCAGTG | 57531 |
rs373759358 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104794910 | GTCTCAAAAAAAAAA[A/T]AATAATTGTATATAT | 57531 |
rs373762304 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720758 | TCAGCCTCCCGAGTA[C/G]CTGGGATTACAAGCG | 57531 |
rs373814649 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797502 | TGTAAAAAAAAAAAA[-/AA]TTAAAAGGAAGGAAG | 57531 |
rs373829458 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845531 | CGCCCAGGCTGGAGT[A/G]CAGTGGCACGATCTC | 57531 |
rs373862529 | snp | A/G | 1.67638e-05 | 0.0028951 | intron-variant | HACE1 | GRCh38.p7 | 6:104784969 | AAAAAAAAATAATAA[A/G]CCAAAACTTTCTTAC | 57531 |
rs373865147 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778343 | AAACTGTTTAATAGA[A/G]TTAAAGAGATGTGAC | 57531 |
rs373867660 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775998 | TCACTTGGAATATGT[C/T]TTTATTAAGTTAGAG | 57531 |
rs373926678 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808072 | ATGCCTGTAATGCCA[A/G]CTACTCGGGAGGCAG | 57531 |
rs373950019 | snp | A/G | 1.6916e-05 | 0.00290822 | intron-variant | HACE1 | GRCh38.p7 | 6:104744472 | TTACAAAATTAAACG[A/G]CAAAACTTAACTTCA | 57531 |
rs373981165 | snp | C/T | 3.33011e-05 | 0.00408038 | intron-variant | HACE1 | GRCh38.p7 | 6:104777344 | AATAAGAGTAAAATA[C/T]GTTAGCAGTGTATCA | 57531 |
rs373984621 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104840176 | TTCTTAGCACTGCAT[A/G]TGAATCTACAATTAT | 57531 |
rs373992020 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749024 | ATGTGTGTCCTTTTC[G/T]GCATGTATATCATAA | 57531 |
rs374003368 | in-del | -/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779166 | GCTTAGCAAATGATA[-/CA]GACGGCAAGAAAAGT | 57531 |
rs374009851 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724686 | TAGATAACGCACTTT[A/T]TTTAATTAAAAAAGT | 57531 |
rs374010234 | snp | C/G | 1.6793e-05 | 0.00289763 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771358 | ATATTCTGGATCAAT[C/G]GATGCCACATCTTGG | 57531 |
rs374011105 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845757 | GCTGGGATTACAGGC[G/T]TAAGCCACCACACCC | 57531 |
rs374031353 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739899 | ACACCTATTCCAAAA[C/T]TGACCACATACTTGG | 57531 |
rs374033174 | in-del | -/TTT | 0.220246 | 0.248223 | intron-variant | HACE1 | GRCh38.p7 | 6:104844345 | GGCCCATCATAAACA[-/TTT]TTTTTTTTTTTTGAG | 57531 |
rs374062637 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104708922 | CACAAAAATTAACTC[A/G]AAGTGAATTATAGGC | 57531 |
rs374083793 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763380 | TTAGATTTTGGAATA[C/T]CTGTATATACAAAAT | 57531 |
rs374093103 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684734 | CTGGAGTAGTCATGT[C/T]TTTTCTGGTCCTTAG | 57531 |
rs374137804 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684649 | TGCCTTTTTAGAGAA[G/T]GAAAACATGTCACCT | 57531 |
rs374151605 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699905 | CCTCAGCTTGCATGG[C/G]CCTGTTTCCTTGGAA | 57531 |
rs374160571 | in-del | -/CAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744238 | CAGAACCACTAACAA[-/CAA]GAACAAAAAACTTAG | 57531 |
rs374184576 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857486 | CTTAGAAATGTATTG[C/T]AGATATTCTTCTTGT | 57531 |
rs374211128 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104739563 | CAAAGATCAAAAGAG[A/C]CAAAGAAGGCCATTA | 57531 |
rs374218039 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104832625 | TGAACTCCTGAGCTC[A/C]AGAGATCCACCCATC | 57531 |
rs374261821 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723392 | CAAGTATCCCAGAAA[C/T]CTTGCACAAGTCACC | 57531 |
rs374264026 | snp | A/C/T | 0.000162609 | 0.00901568 | intron-variant | HACE1 | GRCh38.p7 | 6:104785363 | ATCATTCTTAAACTA[A/C/T]AGGATTAAAAAAAAA | 57531 |
rs374276564 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837313 | GATCAGTGGAATGAA[C/T]ATAAAGTCCACAAGT | 57531 |
rs374279384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822040 | TAGTGAGACCACCAT[C/T]TCTACAAAAGAAAGT | 57531 |
rs374320111 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732620 | GATGGATGGTGGTGA[C/T]AGTCACACATTAATG | 57531 |
rs374320258 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104690053 | TAGGCACAAAGCCCA[C/T]GCTATTTTGCCACCC | 57531 |
rs374331795 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758463 | TAAGCTTCATAAGTG[A/C]AAGAGAAATAAAATC | 57531 |
rs374342644 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686295 | GCAATGGGAGTGAAA[C/T]TGATTGAATCTTTTC | 57531 |
rs374359450 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816866 | CAACCCATGCATCAG[C/T]GTGCCCTGGATATGA | 57531 |
rs374373530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838245 | AAAAGATCTAGAATA[A/G]CAAAAGCCATCCTGA | 57531 |
rs374386813 | snp | A/T | 0.000437904 | 0.0147905 | intron-variant | HACE1 | GRCh38.p7 | 6:104784360 | TTCTGTTTAGATGAA[A/T]CTGTAAGTAAAGAGA | 57531 |
rs374403482 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714148 | GAAATGCACTCAGAT[A/G]TGTGAAAGTTGTCAA | 57531 |
rs374414943 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792167 | AATTATTCACATATA[G/T]AACATTCACAAATTG | 57531 |
rs374437092 | in-del | -/T | 0.35894 | 0.225016 | intron-variant | HACE1 | GRCh38.p7 | 6:104725041 | GCAAGAGAGCATTCC[-/T]TTTTTTTTTTTTTTA | 57531 |
rs374450007 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785705 | CAATGTCAACCACTT[C/T]CAATTAAACAAATAA | 57531 |
rs374459499 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728841 | AGCAAAAAAATTAAC[A/G]TATTTAAATTATAAT | 57531 |
rs374474667 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743598 | TTTCAGAAATACAAG[C/G]TAAAAGATGGTTAAA | 57531 |
rs374474818 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751041 | CCTAAATGATCTGGC[C/T]TCTGCCTTGCTCTCT | 57531 |
rs374543678 | snp | G/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859393 | CCTGCCGGGGTGGGA[G/T]CGTCGGGCCAGGGGA | 57531 |
rs374585149 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824090 | TTAACACTTATCCAA[C/T]CCATCCCATTACTAG | 57531 |
rs374614366 | snp | A/G | 4.9611e-05 | 0.00498026 | intron-variant | HACE1 | GRCh38.p7 | 6:104797036 | CATGACTGTGTGGAA[A/G]TAGAAACAAGTTAAA | 57531 |
rs374629513 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719299 | TTGGAAAACATTTTC[A/G]TGACTAAATGTTTTA | 57531 |
rs374654659 | snp | C/T | 3.66757e-05 | 0.00428212 | intron-variant | HACE1 | GRCh38.p7 | 6:104750514 | ACTTTTCAAAAACCT[C/T]TTACATACTTAATGT | 57531 |
rs374678098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821298 | TGACACAAGTTTACC[C/T]ATGTATCAAACCTGT | 57531 |
rs374681608 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831954 | AGAAGAGAAGAGAAG[A/G]GAAGAGAAGAGAAGA | 57531 |
rs374693960 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756112 | TATCACCACTGACCC[A/C]AAAGAAATATAAACA | 57531 |
rs374727145 | snp | C/G | 3.32602e-05 | 0.00407786 | intron-variant | HACE1 | GRCh38.p7 | 6:104849101 | GTGCCTTGAATAACT[C/G]ATAATACAACTTAAG | 57531 |
rs374738834 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690213 | GGCCTAGGCCCTCTC[C/G]AAGGCTTGTCAGTTT | 57531 |
rs374745153 | snp | A/G | 6.6131e-05 | 0.00574988 | intron-variant | HACE1 | GRCh38.p7 | 6:104849276 | AAAGACAGTTCAGAT[A/G]CATTCAACATACAGC | 57531 |
rs374770046 | in-del | -/A/AA | 0.27278 | 0.24896 | intron-variant | HACE1 | GRCh38.p7 | 6:104734142 | GCAAGACTCTTCCTC[-/A/AA]AAAAAAAAAAAAAAA | 57531 |
rs374780403 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845476 | AAAGCTCTGGGTAAA[C/T]TTTTTTTTTTTTTTT | 57531 |
rs374813736 | snp | A/G | 6.7683e-05 | 0.00581695 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750471 | AGCTGGACGTACTCC[A/G]CCTGTTGAAAAAGAA | 57531 |
rs374818231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836744 | AATTACTGTCTCTAC[A/G]TGCAGACAACATGAC | 57531 |
rs374853183 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834919 | CCCCACTCAACCAGA[C/T]AGAATGCAAGAGGCT | 57531 |
rs374953889 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763031 | CAGTCAAATAAGAAA[A/T]AAACAAATTTCCCAG | 57531 |
rs374959871 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793627 | GAATCAGTTATTTTC[C/T]TAATGAAAATTTCTA | 57531 |
rs374962093 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718565 | TTTTGAATTTTATTA[C/T]AGTTTTTATTAACAA | 57531 |
rs375018138 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695498 | ATGAGGCACAGAGTG[-/TG]AAGAGAAACAGAAAC | 57531 |
rs375062721 | snp | C/T | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777084 | TTGCTTTTGACACAA[C/T]TTCACAGCTACTCCT | 57531 |
rs375064079 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815178 | TTTTGATCAAACTGC[C/T]GATAGTGATATGGAC | 57531 |
rs375071158 | snp | A/C | | | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771215 | TTTTGTGTCACAAGA[A/C]TACTCCCACCCCCAG | 57531 |
rs375102337 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837641 | AACTGATCAATTTGA[C/T]TTCAAAGTTAAAAAA | 57531 |
rs375124919 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832593 | GTAGAGATGGGGTTT[C/T]GCCATGTTGCCCAGG | 57531 |
rs375135634 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757493 | ACACAGAAAGGAAGA[A/G]CATCAACATCAACAA | 57531 |
rs375144785 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848767 | AGTGGCAAAAGATTA[C/G]CAGAAAAAAAGCACA | 57531 |
rs375171828 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736574 | GGCACTACTATAAAT[C/G]TCTTATCTTTAATAC | 57531 |
rs375177941 | in-del | -/AT | 0.112907 | 0.209986 | intron-variant | HACE1 | GRCh38.p7 | 6:104778375 | ACACAGAGTAACACA[-/AT]ATATATATATATATA | 57531 |
rs375196508 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781158 | GAGACTGTGTAATCA[C/T]CCTACCCTTCATCAG | 57531 |
rs375209831 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857823 | TTAGCCGGGCCTGGT[A/G]GCAGGGGCCTGTAGT | 57531 |
rs375211372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846892 | AAGTATTGAATATCA[A/G]GAGTAATCTTTATAG | 57531 |
rs375265621 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812763 | TTAAGAAAACAAAAA[A/C]GGAATAGAGGAATTG | 57531 |
rs375288542 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724893 | CTATGCTTTGCAGAT[G/T]TTCCCATATTAAGTA | 57531 |
rs375332033 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698285 | ATATAGTTTAAATGG[G/T]CAAATTAGGCTGTCG | 57531 |
rs375362211 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685396 | TTGAAATATGGTGGG[-/A]AATTGTAGAAAGAGC | 57531 |
rs375369418 | snp | A/C | 0.000115393 | 0.00759496 | intron-variant | HACE1 | GRCh38.p7 | 6:104796792 | TATCCAGGTTTAAAA[A/C]CAGTCCCTTTTAAAG | 57531 |
rs375375582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848387 | CTTGAACTCGGGAGA[C/T]AGAGGTTGCAGCGAG | 57531 |
rs375505829 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817593 | TAAAATGAATTAATA[C/T]AGAGGAGAAAGAAAG | 57531 |
rs375509131 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857483 | AGCCTTAGAAATGTA[C/T]TGTAGATATTCTTCT | 57531 |
rs375523279 | snp | A/G/T | 5.05753e-05 | 0.00502843 | intron-variant | HACE1 | GRCh38.p7 | 6:104785324 | AATTCCAGAGGCTGA[A/G/T]AGAAACAAAAGTGTT | 57531 |
rs375527845 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831992 | AGAGAGGAAGGAAGG[A/G]AGGAAGGAAGGAAGG | 57531 |
rs375554411 | in-del | -/G | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682763 | CCCTACCACTCTGCA[-/G]AAGCTGACCCGCCTT | 57531 |
rs375563483 | snp | C/T | 3.57379e-05 | 0.00422702 | intron-variant | HACE1 | GRCh38.p7 | 6:104750305 | TAGAGTTTTTTGTTG[C/T]TGTGTTACAACATAA | 57531 |
rs375566760 | in-del | -/TACA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749124 | TTGCTATTTGTTTTT[-/TACA]TACATATAGGTCCAG | 57531 |
rs375588919 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749896 | GAATTATAAAATTAT[A/G]TATATGGCAATATAA | 57531 |
rs375593164 | in-del | -/CCGTCTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782315 | CAGCATGGCAAAATC[-/CCGTCTC]TACAAAAAACACAAA | 57531 |
rs375594388 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826758 | TATACATAATTTTAA[A/G]AGCTATATGCCTAAA | 57531 |
rs375598261 | in-del | -/A | 0.0659589 | 0.169201 | intron-variant | HACE1 | GRCh38.p7 | 6:104784953 | CATCATCTATCAGAG[-/A]AAAAAAAAATAATAA | 57531 |
rs375621587 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804302 | GCCCAAGGTAATTTA[C/T]AGATTCAATGCCATC | 57531 |
rs375652257 | snp | C/G | 0.367297 | 0.220775 | intron-variant | HACE1 | GRCh38.p7 | 6:104742161 | ATACAAAAATCAATT[C/G]AAGATGGATTAAAGA | 57531 |
rs375656932 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809939 | GAGACAATAAGGTTT[A/C]TATTGATTAAGATGA | 57531 |
rs375715605 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853456 | TATATATTACTAAGG[A/G]TCATTTCTCAATTCA | 57531 |
rs375735043 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781866 | CATGTAGACACCCTC[C/G]TCACCCTAGTCAGGC | 57531 |
rs375739054 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104762757 | GCACTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC | 57531 |
rs375768436 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733310 | GATCCTCTAGTTTTA[A/G]CATCTTAATTAAAAT | 57531 |
rs375773009 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762111 | TGGTGGGAGTGTAAA[C/T]TAGTTCAACCATTGT | 57531 |
rs375795792 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844225 | TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT | 57531 |
rs375832178 | snp | C/T | 6.59631e-05 | 0.00574258 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785079 | CATCCTGACAATCTG[C/T]ACTGGCTTCCTGTCT | 57531 |
rs375848681 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800011 | ACTCCTGCCAAAATA[C/T]GGCGCTTTTCCCAAG | 57531 |
rs375852472 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739954 | TAAAAGAACAGAAAT[G/T]ATAACAAACTATCTC | 57531 |
rs375858971 | snp | A/T | 0.000153988 | 0.00877328 | intron-variant | HACE1 | GRCh38.p7 | 6:104777004 | TACATCATCTTCTTT[A/T]ATACCCACCATGCCT | 57531 |
rs375889686 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688536 | ACAGTATTAGTTTCA[C/T]ATTGTTGCTGAGACA | 57531 |
rs375908233 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739910 | AAAATTGACCACATA[C/G]TTGGAAGTAAAGCTC | 57531 |
rs375951672 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739816 | TCTGCACCAAGCGGA[C/T]CTAATAGACATCTAC | 57531 |
rs375953460 | in-del | -/CTAA | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104843152 | TGTACTACACTTTGC[-/CTAA]CTGTCACATTCAATA | 57531 |
rs375963397 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724564 | AAGCCAGGCACAATA[C/G]CATGCAGCTGCAGTC | 57531 |
rs376009293 | snp | A/T | 1.70822e-05 | 0.00292247 | intron-variant | HACE1 | GRCh38.p7 | 6:104796894 | CAGTTTCTATTATAA[A/T]GATAAGGGGCTCAGA | 57531 |
rs376025315 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727588 | ATGTATATGAATACA[C/T]ACACACGTATGTATA | 57531 |
rs376026423 | snp | A/T | 4.99014e-05 | 0.00499482 | intron-variant | HACE1 | GRCh38.p7 | 6:104744117 | GCCATTAAAAGCAGA[A/T]TACATTAAATTATTT | 57531 |
rs376027771 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745510 | GGAGTGCAGTGGCGC[A/G]GCTCACTGCAAGCTC | 57531 |
rs376098085 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705099 | CCATTAAATGGTCCC[C/T]GTTTAAATGGATCTC | 57531 |
rs376142449 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800918 | TAATAACAACTTCTC[C/G]GAGCTAAAGGAGGAT | 57531 |
rs376182011 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697344 | AGAACCCAGCAGTCT[A/G]AAACTAGCTCACCAA | 57531 |
rs376246474 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825947 | TAATGTGTTATGCAC[C/T]ACTCTAAATCAGGAA | 57531 |
rs376250313 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745465 | ATTTCCTTTTTTTTT[G/T]AGACCGAGTCTGGCT | 57531 |
rs376252263 | in-del | -/TGG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826392 | CTGTAGTGTACTAGA[-/TGG]TGATCAGTGCTATCC | 57531 |
rs376262489 | snp | C/T | 3.31549e-05 | 0.0040714 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784987 | AAAACTTTCTTACCC[C/T]GGAGGCATCTGACAA | 57531 |
rs376269563 | snp | A/G | 8.24518e-05 | 0.00642021 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772043 | GTGATCAGGATTTAC[A/G]TAAGAGTTGCTATTA | 57531 |
rs376275846 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104732692 | TTTAAATGATACATT[C/T]TATGATATGCATTTA | 57531 |
rs376277835 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719168 | CTAAATAGATGACAG[A/G]TCAATTAATCAATAG | 57531 |
rs376342947 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732240 | AAAGAACTGAAAGCA[C/T]GGACTCAAAGAAGTA | 57531 |
rs376354679 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786407 | TTAACACCTTTCTAT[A/T]AAAAAAAAAAAAGAT | 57531 |
rs376414150 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796207 | GCTCAACCTCCTGGG[C/T]TCAATCCCTCCTCCC | 57531 |
rs376428689 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812121 | CAGTTGAAAACCTTT[A/T]AAAAAAAAAACTTTC | 57531 |
rs376432282 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793058 | CAGATCACGAGGTCA[A/G]GAGATCGAGACCATC | 57531 |
rs376495256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773029 | GTGTATTTCACCACC[A/G]TAAAAAAAAAGTCTC | 57531 |
rs376505136 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737609 | CCCACCCGAATACTG[C/T]GCTTTTCCGATGGGC | 57531 |
rs376505361 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766216 | CATTTATTACCCTTG[C/T]GGGCATGCTTGCATG | 57531 |
rs376509436 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722644 | GGACACAGAGTTTAC[A/G]TCAAGCCGCCGCGCC | 57531 |
rs376544696 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847564 | GTCAAAGGACTATGC[C/T]CTTCCCCTGTCCAAC | 57531 |
rs376578967 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851649 | CTTGCCAAAAGTTGA[G/T]CCTAGCTATATTAAT | 57531 |
rs376594092 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737535 | CGCAAGGGGTCAGGG[A/G]GTTCCCTTTCTGAGT | 57531 |
rs376619652 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730786 | ATCCCTGGGGCTAGC[A/C]AAATGCCTGGAGTAG | 57531 |
rs376661881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715437 | ATAATGCAGAACAGA[A/G]ACATAAGCATATGTA | 57531 |
rs376664186 | snp | A/C | 3.64166e-05 | 0.00426696 | intron-variant | HACE1 | GRCh38.p7 | 6:104729783 | TAAAAGAAAAATATA[A/C]CACCATTAAACAGGA | 57531 |
rs376682053 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794696 | ATTGCCAGAGCTCAG[G/T]AGTTCAAGACCAGCC | 57531 |
rs376690921 | in-del | -/TAC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807883 | GACTCACAGAAACAC[-/TAC]ATTATAAAACAGTGC | 57531 |
rs376702988 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746980 | TTCATGAATATCACA[G/T]TAATTGTTACGATTT | 57531 |
rs376712504 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104686121 | CATTGAGATATATTG[C/T]CTTTCTCACAAGCTC | 57531 |
rs376749143 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710292 | CTATGGAGGCAGAAA[A/G]TAGATTAGTCGTTGC | 57531 |
rs376766671 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104714744 | TTAGAGCAGAATAAG[C/T]TCCAATAAAACACAA | 57531 |
rs376768350 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739795 | TACCCAGGAATTGAA[C/T]TCAGCTCTGCACCAA | 57531 |
rs376783312 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761548 | ATACAAAAATCAACT[A/C]AAGACGGATGAAAGA | 57531 |
rs376823380 | snp | C/G | 1.66233e-05 | 0.00288295 | intron-variant | HACE1 | GRCh38.p7 | 6:104777336 | GCTCAAAAAATAAGA[C/G]TAAAATATGTTAGCA | 57531 |
rs376841168 | snp | C/T | 6.6346e-05 | 0.00575922 | intron-variant | HACE1 | GRCh38.p7 | 6:104796926 | TATAAATGAAAAACA[C/T]ACCTGTACACATAAA | 57531 |
rs376862321 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722976 | TCTCAGTTTATAGTT[A/C]AATGGTTTTGCAACA | 57531 |
rs376887105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104751559 | TGCTTGAGCCCAGGA[G/T]TTCGAGTCTGCAGTG | 57531 |
rs376912562 | snp | A/T | 5.3615e-05 | 0.00517732 | intron-variant | HACE1 | GRCh38.p7 | 6:104785351 | TGTTTTTTAAACATC[A/T]TTCTTAAACTACAGG | 57531 |
rs376954649 | in-del | -/TTTTTTTTTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745464 | ATTTCCTTTTTTTTT[-/TTTTTTTTTT]GAGACCGAGTCTGGC | 57531 |
rs376984157 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849936 | ATTACAGGCGTAAGC[C/G]ACCACGCCCGTCCTT | 57531 |
rs377006957 | in-del | -/AT | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727747 | TGAATATATACACAC[-/AT]ATATATGTATATGAA | 57531 |
rs377009041 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104740537 | CTACAAACACCTCTA[C/T]GCAAATAAACTAGAA | 57531 |
rs377035926 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705602 | AGTTTTGCCTCGAAC[A/G]ATGGTGCTGGACTCA | 57531 |
rs377053907 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104740080 | CTACTGGGTACATAA[C/T]GAAATGAAGGCAGAA | 57531 |
rs377055294 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832355 | CAAATATTTTGAACA[A/G]ATATAAAAGCACTAT | 57531 |
rs377082054 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712698 | AATTGGTTGAACCCG[C/T]GAGGCGGAGGTTGCA | 57531 |
rs377138485 | snp | A/G | 9.94135e-05 | 0.0070496 | intron-variant | HACE1 | GRCh38.p7 | 6:104795568 | ATTTCCTCTTATTGC[A/G]AAACACTTACCTAAG | 57531 |
rs377178278 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811243 | ATATATTTCTTTATT[C/T]ATACATATATATATA | 57531 |
rs377202781 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744204 | TCTCTCCTCTTGAGT[A/G]ATGTCTTCTACAACT | 57531 |
rs377225368 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767870 | ACCACTTCATCCATT[A/C]CCTGATACCTGCCCC | 57531 |
rs377234104 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838457 | GAACACACATTGGAG[G/T]TAGGGACCATCTCTT | 57531 |
rs377247454 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803891 | AAGAGAAAGAAATAA[C/G]AGTATTCAATTAGGA | 57531 |
rs377255249 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104837119 | AATCAAAATCCCAGC[A/G]AGGTTTTTTTGTAGA | 57531 |
rs377270009 | snp | C/T | 3.34292e-05 | 0.00408821 | intron-variant | HACE1 | GRCh38.p7 | 6:104784503 | GTGGGGGGAAAACAT[C/T]AATCAGAATACACAG | 57531 |
rs377300334 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720638 | CCCGCCCCCCTCCCC[C/G]CCCCCCCAGACGGAG | 57531 |
rs377308464 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104770301 | TCTAACTCCAAATAC[C/T]TCATATAACATATTA | 57531 |
rs377316853 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846556 | CTTCTTTTGGAAAGG[A/G]GGACAATCCAATACA | 57531 |
rs377372004 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794940 | TGTGTGTGTGTGTGT[A/G]TATACATATATACAA | 57531 |
rs377377901 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104752399 | CATGACTATATTTCA[A/G]TTTATGTCTACTCTC | 57531 |
rs377386053 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104738110 | GCAGCTGAGGGTCCT[C/G]TCTGTTAGAAGGAAA | 57531 |
rs377423626 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691803 | GGTGCATGCTTGTAG[A/T]CCCAGCACTTTAGGA | 57531 |
rs377427388 | snp | C/T | 4.96594e-05 | 0.00498269 | intron-variant | HACE1 | GRCh38.p7 | 6:104797037 | ATGACTGTGTGGAAA[C/T]AGAAACAAGTTAAAA | 57531 |
rs377469730 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736368 | CGGCTCACTGCAATC[G/T]CCACCTCCCAGGCTC | 57531 |
rs377471530 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715498 | TCTACAAAAGTCAAA[A/C]TGGAATTCCTGAAGG | 57531 |
rs377477177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836239 | AGCACAGAAGTCTCC[A/G]TAAGAGACTCCTTCA | 57531 |
rs377482670 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830934 | AAACTTAGTGTGGAC[A/T]TCCAAGCAGCATAGT | 57531 |
rs377527561 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722104 | TCTCTGGACACATTT[A/G]AAGTTTGAGATTCCT | 57531 |
rs377550075 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104816027 | GCAGTGAGCCGAGAT[C/T]ACTGCATTGCACTCC | 57531 |
rs377575464 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713704 | GATACAATAATGAAT[A/G]TTTTCATTTCAGGCA | 57531 |
rs377658446 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856299 | AACCATCACATGGAG[A/T]AATTTTTTTAAACAC | 57531 |
rs377672261 | snp | C/T | 1.65187e-05 | 0.00287386 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730349 | TATATGGCACAGCAG[C/T]GATTGTAAAGTTTTG | 57531 |
rs377688723 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720606 | AACTCAGAAATTCCC[A/G]GGCAGCCACGCTCTT | 57531 |
rs377700031 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699648 | CCTCAGTAACGGGAG[A/G]GTTGAATGGTTGGAT | 57531 |
rs377746533 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743101 | CTCATTCATAGGTGG[G/T]AATTGAACAATGAGA | 57531 |
rs386408120 | in-del | -/ATTAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710239 | AGGGCACATCTTATA[-/ATTAT]TTATTCCACTCAAAT | 57531 |
rs386408121 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731870 | AAGAATTCCCATAGA[-/AA]AAAAAAAAAAAATCC | 57531 |
rs386408122 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731881 | TAGAAAAAAAAAAAA[-/AA]ATCCCGATTAAAAAT | 57531 |
rs386408123 | in-del | -/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732716 | CATTTACACACACAC[-/CA]ACAAATGGTTGAAAA | 57531 |
rs386408124 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733847 | CATCTCAAAAAAAAA[-/AA]AGAAAAGAGAAAAAA | 57531 |
rs386704497 | multinucleotide-polymorphism | CCG/TCA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692609 | CTTTAGTTCCCAGTT[CCG/TCA]TGTCTTAAAAGCTGT | 57531 |
rs386704498 | multinucleotide-polymorphism | AT/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705839 | AACTTCATAAATGAC[AT/TA]GTTAATCAAGTGTAA | 57531 |
rs386704499 | multinucleotide-polymorphism | AAG/CAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758608 | ACAAGCCAAACTGTA[AAG/CAA]ACCATCGACGCTATG | 57531 |
rs386704500 | multinucleotide-polymorphism | CA/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771697 | ATAAAAATACACACA[CA/TT]AAAATTGAAAAAAAA | 57531 |
rs386704501 | multinucleotide-polymorphism | AAG/CAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783380 | AGAATCCTCTTAGAG[AAG/CAA]GGAAGTAAGTTTTCT | 57531 |
rs386704502 | multinucleotide-polymorphism | CT/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815881 | AGTTTGAGACCAGCT[CT/TG]GCCAATATGGTGAAT | 57531 |
rs386704503 | multinucleotide-polymorphism | CAATA/TATTG | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860303 | ACAAATCCAAAAGCA[CAATA/TATTG]TGCTTTTGTCTTCAT | 57531 |
rs397697426 | in-del | -/A | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104812131 | CCTTTAAAAAAAAAA[-/A]CTTTCATGGTTTTAT | 57531 |
rs397702228 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809673 | TTTTTTTTTTTTTTT[-/T]AAGATCACTTTGCTG | 57531 |
rs397702767 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771720 | AAAAAAAAAAAAAAA[-/A]GGCTAACTTAACTAG | 57531 |
rs397704969 | in-del | -/A | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851741 | AAAACAAAAAAAAAA[-/A]TTTTTTTAACTTGTT | 57531 |
rs397708563 | in-del | -/A | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104748257 | AAAAAGAAAAAAAAA[-/A]CACAATAGAAAAGTG | 57531 |
rs397716856 | in-del | -/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104777630 | TATTTATTCTCAATT[-/T]CTTTTAAATCCAAGC | 57531 |
rs397751658 | in-del | -/C/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732719 | TTACACACACACACA[-/C/CA]AATGGTTGAAAATAT | 57531 |
rs397766387 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777629 | ATATTTATTCTCAAT[-/T]TCTTTTAAATCCAAG | 57531 |
rs397772232 | in-del | -/A | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104786419 | ATTAAAAAAAAAAAA[-/A]GATGAGGAGAGAATA | 57531 |
rs397785290 | in-del | -/T/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823511 | CTTTTCTATTTTTTT[-/T/TA]AAAAAAAACAGCCCG | 57531 |
rs397796511 | in-del | -/A | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104857974 | AAAAAAAAAAAAAAA[-/A]GGATGTTTTCTAAAC | 57531 |
rs397798824 | in-del | -/TT | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104849664 | CATTTTTTTTTTTTT[-/TT]CTTGAGACAGAGTCT | 57531 |
rs397885953 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731882 | TAGAAAAAAAAAAAA[-/A]TCCCGATTAAAAATG | 57531 |
rs397886852 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854576 | TCAACCATACGTAAT[-/T]ATGTAGTCCTTATCT | 57531 |
rs397887197 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793286 | AAAAAAAAAAAAAAA[-/A]TTAATTTCCTAACTC | 57531 |
rs397887859 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703860 | TGGCTCATGCTTGTA[-/A]GTCCCAGCACTTTGG | 57531 |
rs397888022 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731208 | TGATACAAAAAAAAA[-/A]TTCTATTGCTTTTAA | 57531 |
rs397888835 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737134 | ACTAAAAAAAAAAAA[-/A]TACAAAAATTAGCTG | 57531 |
rs397935188 | in-del | -/AAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751967 | AACAAAAAAAAAAAA[-/AAA]CAGGGGAAAAAAAGA | 57531 |
rs397939454 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733848 | ATCTCAAAAAAAAAA[-/AA]GAAAAGAGAAAAAAA | 57531 |
rs398048717 | in-del | -/A | 0.5 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104798083 | CGAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA | 57531 |
rs398066123 | in-del | -/ATAT | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727695 | TACATACACACATAT[-/ATAT]GTATATGAATATATA | 57531 |
rs398066124 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751966 | CAAACAAAAAAAAAA[-/AA]CAGGGGAAAAAAAGA | 57531 |
rs398072841 | in-del | -/TATATG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727137 | ATGGGTATATATATG[-/TATATG]GGTATATAGATACAC | 57531 |
rs398085197 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798082 | TCGAAAAAAAAAAAA[-/A]AGAAAGAAAGAAAGA | 57531 |
rs398110511 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693639 | TATCAGTTTTTTTTT[-/T]CTTTCCCAAATACTT | 57531 |
rs398110512 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797177 | AATCACAAAAACTTT[-/T]CTCAATGTTAAGCCA | 57531 |
rs527237905 | snp | A/G | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785056 | CCGGTTAGCTGTCAT[A/G]GAAATAACATCCTGA | 57531 |
rs527247912 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855053 | CCTATGAAGTAGGTA[A/C]TATTATCCTCATTTT | 57531 |
rs527273986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690497 | ACTCTAAGGTTAATA[C/T]GGAAAAATGAACAGT | 57531 |
rs527293357 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852601 | AAAGAGCTTAGCTTC[C/T]GGATGTAAAAGGACA | 57531 |
rs527297331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691360 | GAAACAAGGGCTCTT[A/T]TACAGTGTTGTTGGG | 57531 |
rs527297479 | in-del | -/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104807259 | AATCTCTTGACCTCG[-/T]GATCCACCCGCCTCA | 57531 |
rs527298570 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104683118 | GGTGCCCAGCAGAAT[G/T]GCTTCTTACCTTCGT | 57531 |
rs527303443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830661 | GAAAGTTTGTAACCA[A/C]AAAAATAAACAAACT | 57531 |
rs527337258 | in-del | -/CAAT | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104716015 | TATTTAAAATATGAA[-/CAAT]CAGAGTGCAGCTGAT | 57531 |
rs527380925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748842 | AAATAGGCGAATCTC[A/G]TCTATGATTTTAGAA | 57531 |
rs527392089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739778 | CAGAAAGTCAACAAG[C/G]ATACCCAGGAATTGA | 57531 |
rs527402644 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845745 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCTTAA | 57531 |
rs527454436 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104799868 | ACCTGGTCGATCTCA[C/T]TGGGACTGGTTGGAC | 57531 |
rs527461328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851238 | ACAGGCGCATGCCAC[C/T]ACACCCGGCTAATTT | 57531 |
rs527484805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851851 | GTGTAAAGACCCCCT[C/G]ACAAAGCCAAATAAT | 57531 |
rs527485683 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104800177 | GGGGCATCTGCCATT[A/G]CTGGGGCTTGAGTAG | 57531 |
rs527509139 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104800666 | AAGAAAGGAGTAGCA[A/T]CAACATCAACAAAAA | 57531 |
rs527514521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104697328 | TAGAAGTTGCCTGTA[C/T]AGAACCCAGCAGTCT | 57531 |
rs527556569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814477 | AAAAACATGTTTAAC[C/T]ATTTTATAAGATTTT | 57531 |
rs527564955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712312 | CTTTAAATCATATTA[C/T]TAGAGTTTTTGTTCT | 57531 |
rs527570460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761161 | GCTATCTCCATCAAG[C/T]TACCATTCACTTTTT | 57531 |
rs527604831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755982 | CCTTCAAAAAATTCA[A/G]TGAATCCAGGAGCTG | 57531 |
rs527613650 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825992 | AGGAGGTGAGTGGCA[A/G]GCAAGTGAACATCAC | 57531 |
rs527625398 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | HACE1 | GRCh38.p7 | 6:104712750 | GCACTCTAGCCTGGG[C/T]GACAGAGCAAGACTC | 57531 |
rs527651622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719330 | AAAAAGATTTCTGCC[A/G]TAGGACAAAAAAAGC | 57531 |
rs527652813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726759 | CCCTTGCTTTATATT[C/T]GAGTGTTTTATTTCT | 57531 |
rs527662218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813576 | GTCAGGGATGCAGCT[A/G]AATATCCTAAAATTC | 57531 |
rs527688296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767931 | AGCCTGGATGAACTT[C/T]ATGACTAATATTATA | 57531 |
rs527716989 | in-del | -/C | 0.00722274 | 0.0596591 | intron-variant | HACE1 | GRCh38.p7 | 6:104771883 | AAACTGAAAAAAAAA[-/C]AATATAAATAAATGT | 57531 |
rs527733139 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810585 | TGTATATATTTTTAC[A/G]TATGTGTGTGGGTGT | 57531 |
rs527779766 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749644 | AAGCAGCTATATGCT[A/G]TTTAAAATACTGTGC | 57531 |
rs527791809 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746937 | TAAAAATGACTAACA[C/G/T]TATATTCTCTCAAGA | 57531 |
rs527844357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792036 | TCACAGAGAAGCAAT[C/G]GTATAAATCATCATA | 57531 |
rs527886046 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104688158 | ACCTGTCAGCATCTT[C/T]CTTTAGGCCTCAGAT | 57531 |
rs527897503 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104688752 | GGCTGATGGGAAATT[C/T]CAGTCTCTTCTGATC | 57531 |
rs527907029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738213 | TAAAACCACAAAGAT[A/G]GGGAAAAAACAGAAC | 57531 |
rs527907156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731633 | AGACAGTCTTTTCAA[C/T]GAAGTGTGTTGGGAA | 57531 |
rs527931695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746006 | CAAAAGCAGTTGTAA[A/G]GGCCCATTTGTCTTC | 57531 |
rs527974775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850169 | TGGCGAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 57531 |
rs527976655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842473 | TTTTTTTTTTTAACC[A/G]TGATTATCTCAGAGT | 57531 |
rs527991913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737805 | AAGCAGCGGGGAAGC[C/T]CGAACTGGGTGGAGC | 57531 |
rs527995318 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727208 | GAATATATACACATA[C/T]ATGTATACGAATATA | 57531 |
rs528001964 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703265 | AGTAGAAGCCTTCAA[A/T]ATACAGTCTACCTTT | 57531 |
rs528002353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746786 | CCCTGACAGGACTCT[A/G]ATATAGGTTTGCTAA | 57531 |
rs528009567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791312 | TATTTGTAAGAAAAA[C/T]ACAGAAAGCTCACCA | 57531 |
rs528010980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695885 | AGGCGCCCGCCACCA[C/T]ACCCGGGTAATTTTT | 57531 |
rs528011624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843398 | TCAATAACAGCTGAT[A/G]ACATCATAACATCTT | 57531 |
rs528023046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834970 | GAGACAACAGGCACA[C/T]TGAACAAAGAATACC | 57531 |
rs528048426 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716238 | GAAGATTTTAACACG[A/C]CTCAGTGGTTGAAAG | 57531 |
rs528056377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763887 | AAACCTCATTCCTAC[C/T]AAAAATACAAAAATT | 57531 |
rs528068359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819115 | ATCCCTGTTTGCAGA[C/T]GACATAACACTATAT | 57531 |
rs528079156 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764555 | TTTTATAAACTAACA[C/T]GATTTCTTGTTCTGT | 57531 |
rs528159819 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728787 | TTAGGCACATATCAC[A/T]TGAACTTGACATTTT | 57531 |
rs528174711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780667 | ATTTCCTACAAACAA[A/G]GGAATTTTCCTCTAT | 57531 |
rs528189482 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746285 | AGAACTGCTAGTATA[C/G]GGTGTGTTTTAGTCC | 57531 |
rs528204409 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834833 | TCTTGAAAAGAGGTT[G/T]AAAGTTTATTTAATA | 57531 |
rs528219289 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729477 | ATATTTTCTAATTGT[A/G]TCACAAACAGAGAAA | 57531 |
rs528234270 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803426 | AAAAAGAGAATTTTA[C/G]ACCAATATCCTTGAT | 57531 |
rs528243783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735939 | ATAGATCTATAAATT[C/T]AGTAACATATTGCTA | 57531 |
rs528247075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788008 | AGGTGAGTTTACCTA[A/G]GAAGTTTTCTCTTTG | 57531 |
rs528249425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104779048 | AATAAAAACATGAAC[A/G]AAGGTAAAGTTGGAG | 57531 |
rs528270573 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104693062 | GTGTGTGTGTGCACG[C/T]GCGCGCGCGCTGGGG | 57531 |
rs528283228 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685440 | CGAACACAGCTCAGC[A/G]TTCAAAATTTGGCTC | 57531 |
rs528285934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684873 | GTAGTGTGCCAAGTA[A/G]TGTGACATTGCTTGT | 57531 |
rs528307675 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730054 | CTCAGTGCTACTTAC[A/G]GTAGTGTAACTTTAG | 57531 |
rs528373106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751214 | ATTAGAATGTAATCT[C/G]TCTGCAGACAGGAAC | 57531 |
rs528388338 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823338 | ACTTCGGAGGCTGAC[A/G]CAGGAGAATCGCTTG | 57531 |
rs528391276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104796148 | TCACTGTATCGCCCA[A/G]GCTAGAGTGTAGTGG | 57531 |
rs528396138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840052 | TCTCAGTAAGACAGA[C/T]TGTATCAATGTCCAT | 57531 |
rs528401137 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104832313 | ATTAAAACCTATGAA[C/T]TAGAAATAAAATCAA | 57531 |
rs528409910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787236 | TAAGTACAATGTTTC[C/T]TTTTTTAAGAGAAAT | 57531 |
rs528426370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707669 | GCTGCATCCTGACAT[A/G]GCAGAAGAGGTGAAC | 57531 |
rs528440534 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810291 | CTGAATTCTAATACA[C/G]GGTTGTTAAATAGAT | 57531 |
rs528452540 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733428 | AGATCTGATCATGTT[A/G]AGATCATAATTCATC | 57531 |
rs528472164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846695 | ACCAACAAAATGGGA[A/G]GAACTCTACTATGAC | 57531 |
rs528514566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104795103 | AAGGCATTAACTCCA[C/T]GAACTTAGTGATGAT | 57531 |
rs528528418 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104808162 | CTGCACTCCACCCTG[A/G]GCAACAGATTGAGGC | 57531 |
rs528540359 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817263 | CCCGCCAAATCTCAC[A/G]TCAAATTGGAAGAGA | 57531 |
rs528545409 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688701 | AGAAATCTGTTCCTT[A/G/T]TTTCTTCTAACTTCT | 57531 |
rs528555736 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685779 | TTAATAGCAGTACTG[A/G]CATCTTACGAATGCA | 57531 |
rs528556436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104722162 | GTAGGCCACTGTATA[C/T]AGAATCTTGGAATTT | 57531 |
rs528557985 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852908 | ATTATTACAAAAGAA[A/T]TTAGTTTAGAAGCTT | 57531 |
rs528564199 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861106 | AAGTTTCAAAAGAAT[A/C]CCAGAGGCTGGGCGC | 57531 |
rs528566068 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714218 | AGGAGGTTAAGAAAA[C/G]AGAGCCTCACATACA | 57531 |
rs528566356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808686 | TTATCTTAGAGCCCT[A/G]TAATTTGTCCTGGGG | 57531 |
rs528586232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757213 | CTGAAGAGAGCAGTG[C/G]TTCTCCCAGCACAGT | 57531 |
rs528597419 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712711 | CGCGAGGCGGAGGTT[C/G]CAGTGAGCCGAGATC | 57531 |
rs528599490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750173 | ATTAAGCTTAAGAGA[G/T]GCTCATCCATAAATT | 57531 |
rs528653983 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787063 | TTGAAAATATTTTAC[G/T]TACTGAATTTGCAAA | 57531 |
rs528655084 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709074 | ATAAATTGGACTACA[C/T]CAAATTTTAAAATTT | 57531 |
rs528731117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822789 | TTGGACTCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 57531 |
rs528736004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104831457 | GGGTGTGGTGGCACA[C/T]ACCTGTAATCCCAGC | 57531 |
rs528779883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734515 | ATTTAAGATTTTAAA[A/G]AGCTTAAAACTTTCT | 57531 |
rs528798071 | snp | A/G | 0.429688 | 0.173817 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727619 | TGAATACACACACAC[A/G]TATGTATATGAATAC | 57531 |
rs528823571 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770417 | ACATATAGAGGAGAG[G/T]TAATAATAAATAAAA | 57531 |
rs528843418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779725 | ATCCTCACTCTGTGA[C/T]TTACTAGACTTATCT | 57531 |
rs528855830 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772936 | AATAGATAGTGGCCG[A/T]TGGTTGCACAACACT | 57531 |
rs528858365 | in-del | -/G | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104842501 | AGTGCAAGGAATACA[-/G]GGAGTGCTCATTCCC | 57531 |
rs528878835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825131 | GAAAATGGCAGAATA[C/T]ATGGATCAAAATGAT | 57531 |
rs528905351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763345 | CTTGGGACCAGAAGC[A/G]TTTCAAATTTCAAAG | 57531 |
rs528944553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832202 | GATAAAATAAAATAT[G/T]AAGTTTTATTTGCTA | 57531 |
rs528961431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778899 | TTTCCCCATAACCTA[A/C]CCCCACACTCCTAGA | 57531 |
rs529033589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786434 | AGATGAGGAGAGAAT[A/C]AACTATTTCCTATTA | 57531 |
rs529042316 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723476 | ATTGAAGAAATAAGT[A/G]TGTGCCAATTTACAC | 57531 |
rs529047755 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104824258 | AGCAAAAGGTCTAAC[C/G]ACAATAACAAATTAT | 57531 |
rs529100605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691638 | TGATTAAATAAGTGA[C/T]AGCACTTACATGCAA | 57531 |
rs529109904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839177 | TTAGTATAGCCACTA[C/T]GGAAAACAACTGCAT | 57531 |
rs529127314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104787012 | ACCTTCACTGCCACT[C/T]TCAGCCTTTCTTCAG | 57531 |
rs529145585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853736 | AAAATAATATATGCT[C/T]AATATCATATAGTTA | 57531 |
rs529166018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104740936 | GGCAAAACGAATCCA[A/G]CAGCACATCAAAAAG | 57531 |
rs529181465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846364 | ACCTAAGAACACACA[A/G]TAATTTTAAAGCCTC | 57531 |
rs529200203 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775341 | GTGATCCAAGATTGC[A/G]CCACTGCCCTCTAGC | 57531 |
rs529201570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714041 | CAATGTAAAGAATTC[A/G]TAACAACAAAACAGA | 57531 |
rs529232668 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104692366 | GGATCAAGGATGGAG[A/G]AAAACTTGTATTTTT | 57531 |
rs529277346 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104762567 | GGTGGGGGGCTAGAG[A/G]AGGGATAACATTAGG | 57531 |
rs529280972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808002 | GACCAGCCCAGGCAA[A/C]ATGGCAAAACGCCAT | 57531 |
rs529298213 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695889 | GCCCGCCACCACACC[C/T]GGGTAATTTTTTTGT | 57531 |
rs529302029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706947 | GAAATGGAAAAACTC[C/T]TAGAAAATGCAAACA | 57531 |
rs529315980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823125 | CATTAATTTTTTTTT[A/T]AGAGAGAAAAACACT | 57531 |
rs529323815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720679 | GTTGCCCAAACTGGA[A/G]TGTAATGGCGAGATC | 57531 |
rs529350912 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859695 | CCCCACCGGCGGCCT[A/C]CGCGCCCAGAGCCCT | 57531 |
rs529388091 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104713547 | ATTAACTTACCTGTG[A/G]CCGCACAGCTAGTAA | 57531 |
rs529393428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104769729 | GGCCCCAGTTTTGCC[A/G]TTAACTCTTTAGGAT | 57531 |
rs529425128 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104682912 | CTGGAGAAGAATATT[C/T]ACTCTCTTGACAAAG | 57531 |
rs529449155 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776152 | ATGGTTCAATAAGAG[C/G]TTTATAGTAGCCAGG | 57531 |
rs529454093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727332 | ACGAATATATATACA[C/T]ATGTATGTATACGAA | 57531 |
rs529508344 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104788599 | TGAAGTTAAAAGTTT[-/CA]CAATCTTTCTTGGTT | 57531 |
rs529525665 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682287 | ATGATGATTATGATG[A/G]TGGTCCAGGGACCAC | 57531 |
rs529558183 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104769156 | CCTCCCACCTCAGCC[C/T]CCAGAATAGCTAGGA | 57531 |
rs529562303 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104727087 | TTAAAATACTATTTT[A/T]TATATATGCATATGG | 57531 |
rs529580079 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104787676 | GCAAGAAATGACACA[-/G]GCTGATCATGCAGAT | 57531 |
rs529583789 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775620 | ACTCATGACTTCACT[C/G]AACTCGTCATTCACA | 57531 |
rs529590753 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104710271 | AAATGTACACAATAA[A/G]CAAATCTATGGAGGC | 57531 |
rs529606035 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | HACE1 | GRCh38.p7 | 6:104739644 | TATATGCACCCAATA[C/G]AGGAACACCAAGATT | 57531 |
rs529611696 | snp | A/T | 0.000353057 | 0.0132817 | intron-variant | HACE1 | GRCh38.p7 | 6:104784960 | TATCAGAGAAAAAAA[A/T]AATAATAAGCCAAAA | 57531 |
rs529625739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104857693 | GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCCCA | 57531 |
rs529631315 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685539 | ATAGGAATAATAATA[A/C]CTTTCTTAAATGAGC | 57531 |
rs529645492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104703172 | TATAACCACACTAAG[A/G]AAGAGATTTCATTTT | 57531 |
rs529649110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849751 | CCTCCCGGGTTCACG[C/T]CATTCTCCTGCCTCA | 57531 |
rs529660339 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807504 | CTCTAACTAAACCTT[A/G]CTTTTCCTAATAGAA | 57531 |
rs529687077 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798736 | TTCCATTCTTTAACA[C/T]GCCTAAAAATAGAGG | 57531 |
rs529693452 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104754029 | ACAATACAGGAGCTG[A/C]CAGCCACAACAGTCA | 57531 |
rs529714168 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104820513 | AACAACAACCCCATT[A/T]AAAAGTGGGCAAAGG | 57531 |
rs529722245 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104717501 | CCATAAATAAGGCCA[C/T]AAATAAACAAATAAT | 57531 |
rs529796481 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730935 | ATTTGTTTTGTTTTT[C/T]ATAGTGGAAAAACTG | 57531 |
rs529798537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803831 | GCCGTCTCTCACCAC[C/T]CCTATTCAATGTAGT | 57531 |
rs529815955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772879 | GGAGATATTGCTTAA[C/T]GGGTACAGAATTTCT | 57531 |
rs529818045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104724440 | CTGTTATTTATAAAA[A/G]CAACAATATTAGAAA | 57531 |
rs529824793 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820000 | AAGAGTTCGAGACCA[A/C]CCTGACCAACATGGC | 57531 |
rs529840961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760275 | GACCAATATCCCTGA[C/T]GAAAATCAATGCAAA | 57531 |
rs529858004 | snp | A/G/T | 0.00279242 | 0.0372774 | intron-variant | HACE1 | GRCh38.p7 | 6:104766152 | CGGCCTTGGCCCCAC[A/G/T]TGGGGCACAGTGGGG | 57531 |
rs529895177 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689515 | CTATAAAGTTTTAGT[C/T]CCTATTCTAAGTGGA | 57531 |
rs529897018 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715928 | AACAGACCCCTATGA[C/T]ATGAGTTTATCTATA | 57531 |
rs529897420 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104825790 | TGTTTTCAATAAATA[C/T]CTGCTTTTGCTGCTT | 57531 |
rs529909118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834163 | AAAAAAAAAAAAATC[A/G]TTTTAAAATAACTCA | 57531 |
rs529947256 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730500 | TCTAAGTTAGGGTAG[A/G]AATATATCCAACTCT | 57531 |
rs529966701 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | HACE1 | GRCh38.p7 | 6:104737275 | GGGACAGAGTGAGAC[A/T]CTCTCTCAAAAAAAA | 57531 |
rs529978697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104772328 | ATTTTAGAGTACTTT[C/T]GACTGAAATTAGTTG | 57531 |
rs529990650 | snp | C/G | 1.90736e-05 | 0.00308811 | intron-variant | HACE1 | GRCh38.p7 | 6:104729797 | ACCACCATTAAACAG[C/G]AAATCTATAAAATTT | 57531 |
rs529991202 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104826464 | TTATTTTAGCAAATT[C/T]CTTGCCCCTAAAATC | 57531 |
rs529991853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788988 | TAGAGTACCTTGTTA[A/G]TGAAATGGAAATTAG | 57531 |
rs530004432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737423 | CTGAGGTACCGGGTT[C/T]ATCTCATTAGGGAGT | 57531 |
rs530008195 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789960 | GATCAAAATTTTACA[A/G]AGACAGTAAGTCGTC | 57531 |
rs530039252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693903 | GGCAAGTTCTCTTCA[C/T]ACTCTGTTGGTGAGA | 57531 |
rs530046254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104686487 | TGACAGATTCCTCTG[C/T]TCACCAAATCTATTA | 57531 |
rs530050424 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104757544 | CCCCATCTATAGGTC[-/A]CAAACATCAAAGCCA | 57531 |
rs530077279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789731 | TCTAACCCAATTTGA[A/G]TAATATTGACCACAT | 57531 |
rs530087342 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721533 | ATGAGATGACCCCAC[A/G]TCTGTACTTATCTGC | 57531 |
rs530132260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833448 | ACTCCTGGGCTCAAG[A/T]GATCCTCTTGCCTCA | 57531 |
rs530141013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841053 | TTGAACCCGGGAGGT[A/G]GAAGTTGCAGTGAGC | 57531 |
rs530162556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701657 | AGATATTCTGACTTC[C/T]GGCAAAATACTCTAT | 57531 |
rs530203106 | snp | A/C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819080 | AAGGCCAAACAAATA[A/C/G]CAAGAAAAGAAGTCA | 57531 |
rs530240317 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855415 | GCCACTGCACTCTAG[C/G]CTGGGCAACAGAGCG | 57531 |
rs530242308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759091 | GACTTAGACTCCCAC[A/T]CAATAATGGGAGACT | 57531 |
rs530248810 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104840600 | TTGGGTAGCCAAGGC[A/G]GGTGGATCACCTGAG | 57531 |
rs530260399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803436 | TTTTAGACCAATATC[C/T]TTGATGAACATTGAT | 57531 |
rs530261173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796358 | CAAGCAATCCACCCA[C/T]CTCAGCCTCCCAAAG | 57531 |
rs530288463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854718 | CTGTTAATTGTATTG[A/G]CTCTAGTAATGGTAT | 57531 |
rs530331917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700846 | TCTAAGACTTAGAAA[C/T]GATTTTAAATTCCTG | 57531 |
rs530409037 | snp | C/T | 3.31137e-05 | 0.00406887 | intron-variant | HACE1 | GRCh38.p7 | 6:104811433 | GTAAAGCCAGAGGAA[C/T]CAAACAAAAGATACA | 57531 |
rs530432864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759836 | AAAAGAGAGAAGAAT[A/G]AAATACATGCAATAA | 57531 |
rs530448436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710369 | GGGTTTCTTCTGGAT[A/G]ATTAAAATGTTCTAA | 57531 |
rs530497281 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754508 | CCAAGGTCCAAATGA[A/G]AGAAAAGCTGTTAAG | 57531 |
rs530497588 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104759375 | CAGTGCAATCAAATT[A/G]GAACTCAGGATTAAG | 57531 |
rs530507212 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | HACE1 | GRCh38.p7 | 6:104723630 | TGTTAACCTTAAAAG[A/T]GAATTTTGTTGTCTA | 57531 |
rs530536025 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778873 | AGAAATAACTTAAAG[G/T]GGAAAAGCCCTTTCC | 57531 |
rs530563343 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104819916 | AAATGTAAAACCCAG[A/G]CCAGGTGCAGCAGCT | 57531 |
rs530566336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716932 | CAAGATTTTGTAAAT[C/G]TGACAGTCTCAAGTG | 57531 |
rs530568032 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724269 | TAGCCCTAACTGTGC[A/T]GCTGTCCTACCTACC | 57531 |
rs530598006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104686125 | GAGATATATTGCCTT[C/T]CTCACAAGCTCTAAA | 57531 |
rs530603799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104772800 | ATAAAATATCTAGAA[C/T]AGGCAAATTTATAGA | 57531 |
rs530610780 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764794 | TATATTTTTTTGCAT[A/G]TGTAAGGCAGTCAAA | 57531 |
rs530636188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825733 | GTATCCAGAACCTTG[A/G]GCAGCTGCTGGGGCC | 57531 |
rs530648628 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713450 | TGGATGCTTTATATA[C/T]ATTAATTTATTAAAT | 57531 |
rs530674153 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104810719 | TAACTAAACATTTGC[C/T]GAATACATGAATAAG | 57531 |
rs530675609 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716507 | CCAGCCTGGCTAACA[C/T]GGTGAGACCCCGTCT | 57531 |
rs530681514 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104780757 | CCATTTCAAGTCTTG[A/C]CAATTTTCTAATAAT | 57531 |
rs530704005 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732560 | AGGAGGGGGAGTTAG[C/T]GTTTAAAGTACAGTT | 57531 |
rs530715180 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730700 | CTACATTTACAATTA[C/T]TTGCTTTCATGTGGC | 57531 |
rs530738832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788602 | AGTTAAAAGTTTCAC[A/T]ATCTTTCTTGGTTAC | 57531 |
rs530824861 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104736433 | GGGACCACAGGCATG[C/T]GCCACCATGCCCAGA | 57531 |
rs530825133 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845694 | GTGTTAGCCAGGATG[C/G]TCTCGATCTCCTAAC | 57531 |
rs530827077 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104812908 | TATCCAGTTAGTTAC[C/T]ATCCCTCTTTACACT | 57531 |
rs530837529 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728842 | GCAAAAAAATTAACA[C/T]ATTTAAATTATAATT | 57531 |
rs530850870 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779893 | TAATAAATTAGCAAT[A/C]ATTTATTAAGCACCT | 57531 |
rs530885354 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104809648 | CACAAAGTAACAAGA[A/G]CAGATTCTTTTTTTT | 57531 |
rs530903084 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104758542 | CTTGCAAGAGCTCCT[A/G]AAGGAAGCACTAAAC | 57531 |
rs530921071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802685 | AACAAAGACACAACA[C/T]ACCAGAATCTCTGGG | 57531 |
rs530926854 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689221 | TCAATCCAGCAAAGC[A/T]AGTGTTACTGAAATT | 57531 |
rs530928517 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104796179 | GCAGTGACATGATCT[C/T]GGCTCACTGCAGGCT | 57531 |
rs530958491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743104 | ATTCATAGGTGGGAA[C/T]TGAACAATGAGATCA | 57531 |
rs530966831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788098 | TAATTTCTAACTATG[A/G]TAGCAGCCACCAACA | 57531 |
rs530981242 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750881 | TGATTTAAAAATATA[C/G/T]ATATGTGTATATACA | 57531 |
rs530992216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808808 | CAAGATATCACAAGT[A/G]AAATTAAAAGTGTGC | 57531 |
rs531017698 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734259 | GTCAATACTATAAAA[A/G]TATTTAAAAATCACT | 57531 |
rs531024137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854595 | TAGTCCTTATCTGGA[C/T]AGTGATTCAAAAAAA | 57531 |
rs531087700 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104761055 | AATAAGACAGGACAC[A/G]AACAAATGGAAAAAC | 57531 |
rs531099605 | in-del | -/A | 0.499477 | 0.0161657 | intron-variant | HACE1 | GRCh38.p7 | 6:104822204 | AACCCCGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 57531 |
rs531101703 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861263 | AAAAATTAGCCGGGC[A/G]TGGTGGTGTGCCTCT | 57531 |
rs531138480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853827 | CGCAGGGGATACATT[C/G]CAAGACCCCGAGTCA | 57531 |
rs531142819 | in-del | -/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104766247 | ATGGAATCTTGGTGT[-/G]TTGAAGAAAAAATAT | 57531 |
rs531157661 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104707790 | TGAGGGCAAGGCCCT[C/T]ATGACCTAACCACTT | 57531 |
rs531204708 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686773 | GCTGCATTTCATGGA[C/G]CACTGGCAAGGCAAG | 57531 |
rs531207654 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689697 | AGGCCACGTGCTACC[G/T]TAAGCATAGCTTAGG | 57531 |
rs531213913 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727790 | ATATATGTATATGAA[C/T]ATGTACACACATATA | 57531 |
rs531226480 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104836604 | TGTAATCCCAGCTAC[C/T]AGGGTGGCTAAGGCA | 57531 |
rs531239833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793221 | GCAGTAAGCCGAGAT[A/C]GCGCCACTGCACTCC | 57531 |
rs531242826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104784254 | CAGATACACTGACAC[C/T]GAAACAGAAGAAAAA | 57531 |
rs531265072 | in-del | -/AC | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104727411 | TATACAAATATATAT[-/AC]ACACACATGTATATG | 57531 |
rs531288708 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104800815 | ACCTCTTCTCCTCCA[A/G]CTGCTCACAGCTCCT | 57531 |
rs531314168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800062 | AGGAGATTCCATCCC[A/G]TGCCTGGCTCAGCGG | 57531 |
rs531361577 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104844906 | TGATCTCAGGCAATC[C/T]GCCTGCCTCAGCCTC | 57531 |
rs531377248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104760810 | ACCCCATTGTCTCAG[C/T]GCAAAATCTCCTTAA | 57531 |
rs531390805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755944 | TCAGAGGTGAATTGA[A/G]GAAGACAGAGACACA | 57531 |
rs531399382 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805382 | GGATTATAAATCATG[C/T]TACTATAAAGACACA | 57531 |
rs531423225 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718542 | AAAATCAAGGAAATG[C/T]CTTTATATTTTGAAT | 57531 |
rs531433276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851102 | GTTTGTTTGTTTGTT[A/G]AGACAAGAGTCTTGC | 57531 |
rs531446493 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804528 | ATATAGACCAATGGA[A/G]CAGAATAGAGCCCTC | 57531 |
rs531488095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767301 | CAGTTATCCTTGAGT[A/C]CTTCCTCTTTCTCAT | 57531 |
rs531495382 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104844750 | TCACTGCAACCTCTG[C/T]CTCCTGGGTTCAAGC | 57531 |
rs531508886 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104794004 | CTTTTTCCTACCCTG[C/T]TTCTCCTGTCCCACC | 57531 |
rs531514537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814303 | TGATAACATCAGGGA[G/T]AAGAGATTCCAGAGA | 57531 |
rs531542541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850622 | GATAAAAAGAAAATT[C/T]TGGTGAACTGTACCA | 57531 |
rs531560285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104773979 | ATAATAATAGCATAT[A/G]ATATTTATACTTTCT | 57531 |
rs531613790 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718313 | ATTCCACATATTTCT[A/T]ATATATATAAAATCA | 57531 |
rs531659799 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852458 | GAATTTTCCTAACTC[C/T]ATACAAAAAGCGAAA | 57531 |
rs531671841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834907 | GCCAGTAATGGCCCC[C/T]ACTCAACCAGATAGA | 57531 |
rs531684575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737768 | GGGCGCCCGCCATTT[C/T]CCAGGCTTGATTAGG | 57531 |
rs531695537 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746733 | CATAGTCCCTTTGTT[A/G]AAGTTTCGATATTTG | 57531 |
rs531719635 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104828296 | TCTAGACACTGATCT[A/G]TGTACTTTTACAGAA | 57531 |
rs531736473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782317 | GCATGGCAAAATCCC[A/G]TCTCTACAAAAAACA | 57531 |
rs531786963 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768502 | TGTGTTTCTAAAGAT[A/T]TTTAAGAGTTTTATA | 57531 |
rs531804481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104687924 | GCCTAACCCTGGATC[A/G]TTATTAAAGATTTCC | 57531 |
rs531817598 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104745843 | GTACCTTAAATAAGA[C/T]TGATATAAGGCAACA | 57531 |
rs531878021 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835454 | ACAAGGAAAAAAAAC[G/T]CTTGGAAATTAATAC | 57531 |
rs531882364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849053 | CCAAGGTAAATATCA[C/G]GGATGCGGGAGGAAT | 57531 |
rs531898925 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104745267 | AAAATCTCAATCGTA[G/T]AAGTAAAAATGAAAT | 57531 |
rs531899649 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857978 | AAAAAAAAAAAAGGA[G/T]GTTTTCTAAACACAA | 57531 |
rs531918004 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104849701 | TCACCCAGGCTGGAG[G/T]GCAGTGGTGCGATGT | 57531 |
rs531929004 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789980 | AGTAAGTCGTCACTC[C/G]TAACTAGAGCTCAAG | 57531 |
rs531942268 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104687314 | GCTGGGAGTCTGGTT[A/G]TAATCATCATTATTA | 57531 |
rs531944128 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104695854 | CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGACTAC | 57531 |
rs531947498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703053 | TCAAACTTGGGTCTA[C/T]CACAGGTAATGGAGG | 57531 |
rs531975545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704661 | CTTTTTACTAGGATG[A/G]CCAGCCATCTCATCA | 57531 |
rs531975795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850554 | CACCTATGTAAAAAA[C/T]ATAAAGCCAATGACT | 57531 |
rs532012451 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843543 | TTTCATATCATTGGG[A/T]CAAATCACATTCAAA | 57531 |
rs532063921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841562 | ATTTTTACAGGAATT[A/G]TAGATTCCATATAAT | 57531 |
rs532089064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805359 | CCATTACTGGGTATA[C/T]ACCCAATGGATTATA | 57531 |
rs532127481 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709531 | CCACCCCAACTCCAA[A/C]CCCCTGCTTGCTCTG | 57531 |
rs532176266 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104766408 | TTCATGTCAGTACTC[A/G]AAAAGTTTCAGACTC | 57531 |
rs532180152 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819651 | TATACTACAGGGATA[C/T]AGTGAGCAAAACAGT | 57531 |
rs532189614 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713063 | GGGAACAAGTAAGGG[G/T]ATAGAGTGGGATAGC | 57531 |
rs532202731 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754212 | ATAGAGAAAAAGGAA[C/G]AAAAAGGAATGAATA | 57531 |
rs532225460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760675 | CACTCCTATTCAACA[C/T]AGTATTGGAAATTCT | 57531 |
rs532228383 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104711080 | AACGCAGAGCAGAGT[C/G]GTACCTCAAACATTG | 57531 |
rs532253276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773748 | ATCTAGATGCTTAAA[A/T]AGAATAGATAAGGAG | 57531 |
rs532267659 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104769448 | AATAAAGATTCTATG[A/T]CTTCATTACCCTTAA | 57531 |
rs532303626 | snp | C/T | 0.000445492 | 0.014918 | intron-variant | HACE1 | GRCh38.p7 | 6:104796647 | AGCTACTATCACAAA[C/T]ACAATACCATGTTTT | 57531 |
rs532315542 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826720 | CAAGTTAATATACAT[A/G]ATTTTAAGAGCTACG | 57531 |
rs532338001 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766188 | GCTCTTGGCATATGC[A/G]TCCTGCACATGTCAT | 57531 |
rs532351262 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104760322 | CCGGCAAACCAAATC[A/C]AGCAGCACATAAAAA | 57531 |
rs532355132 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849168 | TGCCAAATGAAGGGG[C/T]GTACAGCCTGAAATA | 57531 |
rs532389157 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857747 | CAGATCACGAGGTCA[C/G]GCGATCGAGACCATC | 57531 |
rs532411614 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104782209 | GAAATTGAACTTGTC[A/C]GGGTGTGGTGGCTCA | 57531 |
rs532430251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724556 | TTACAAACAAGCCAG[G/T]CACAATAGCATGCAG | 57531 |
rs532494411 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104725094 | AAACTTGTTTTAAAT[C/T]AAACACACTAAACAA | 57531 |
rs532496682 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846303 | TGAGCTCATAATCAC[C/T]TAAAAAATAAAGAAA | 57531 |
rs532512884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737733 | GACCAAACTGCAAGG[C/T]AGCAGCGAGGCTGGG | 57531 |
rs532524450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730531 | AGGACAATGACAACA[C/T]GACACTTTTTAGTCT | 57531 |
rs532538649 | in-del | -/CA | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104790106 | TACACACTCAACGTG[-/CA]CACACACACACATAC | 57531 |
rs532553391 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826521 | CTGATCTATAAGCCA[G/T]GAAGTCCAAAAAACC | 57531 |
rs532622963 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104797905 | GAAACCCTGTCTCTA[A/T]TAAAAATACAAAATT | 57531 |
rs532623046 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698299 | GTCAAATTAGGCTGT[C/T]GGTCTTGTTATGATA | 57531 |
rs532638944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841176 | TGGGAAGTTTGGAGG[G/T]TGGGGAGGAAGGCCA | 57531 |
rs532671583 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822447 | AGCCCTAGCTACTTG[A/G]GAGGCTGAGGCAGAA | 57531 |
rs532674152 | in-del | -/T | 0.00279162 | 0.0372561 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682373 | AGATAATGTTGTGTG[-/T]TTTAATTTATATAAA | 57531 |
rs532676953 | in-del | -/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861749 | GGAGCAGAAGATAAT[-/G]GAACAGGTAATGCTG | 57531 |
rs532678797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842226 | ATGCTGGATGATTTC[C/T]TGAGCCCAAGAGTTT | 57531 |
rs532687263 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720827 | TTTTTTTAGTGGAAA[C/G]GGGGTTTCACCATGT | 57531 |
rs532706854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853812 | CAGTCCCCACTTATC[C/T]GCAGGGGATACATTC | 57531 |
rs532746466 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694105 | AGCCAAGATTTGGAA[G/T]CAACCTAAGTGTCCA | 57531 |
rs532753544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786930 | GATTATACAACCATA[G/T]TTGGAACCTTAGAAA | 57531 |
rs532761321 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104735204 | CACCAAGAAAACTAT[C/T]TGCAGAGTTAATACC | 57531 |
rs532776084 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826617 | CTTGCTAAAATTAAG[C/T]GCAGTGGCTTACAAT | 57531 |
rs532807894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823295 | AAAAATTAGTTGGGC[A/G]TGGCAGTGGGCACCT | 57531 |
rs532808436 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769978 | CCAATACAACTAACT[G/T]TTGTGCTGTGCTTTT | 57531 |
rs532829863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684716 | ACTGAATTAGAACAA[A/T]CTCTGGAGTAGTCAT | 57531 |
rs532881877 | in-del | -/AGAC | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104791342 | AACTTGCTGTTGATT[-/AGAC]AGAGTTGAGAGGAGA | 57531 |
rs532889051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709569 | CCACGTGACATGCTG[A/G]CTCTCCTTTGCTTTC | 57531 |
rs532922013 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683874 | TTCTTCACAGTGTGA[A/G]GAATCCAGGGGGAAA | 57531 |
rs532926688 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727657 | CGTATGTATATGAAT[A/G]CATACACACGTATGT | 57531 |
rs532948911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845058 | GTATATGTTAAATAC[A/G]TATGTATTGTATACA | 57531 |
rs532976445 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104832034 | GAAGGAAGGAAGGAG[A/G]AAGAAAAGAAAAAGA | 57531 |
rs532977286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706880 | AGAAATAAAAAGCAT[C/T]ACAAAGGAATACTAT | 57531 |
rs532981215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793491 | AGCATTATGTGCAAA[C/T]GCCTCAGTAAATGTT | 57531 |
rs533015370 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756588 | GTTTCCAAGATGGCC[A/G]AATAGGAACAGCTCT | 57531 |
rs533032906 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860051 | TGGGCGTACTCCTAA[A/G]CTTCTGGAAAGGCAT | 57531 |
rs533041336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104740715 | GATGGATTCACAGCC[A/G]AATTCTACCAGAGGT | 57531 |
rs533072006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786274 | TGAACCCAGGAGGCA[A/G]AGGTTGCAGTGAGCT | 57531 |
rs533087457 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104757092 | GTGGCCACTGGAGCT[C/T]AGCAAGGCCTACTGC | 57531 |
rs533090089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838965 | GACACTTCTCAAAAG[C/T]AGACATACAACTGGA | 57531 |
rs533115867 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852496 | GAAGAAGGAGGAAAG[A/G]ATAATGCAGAATACC | 57531 |
rs533128634 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749975 | TTTTTAGAAGTTTAA[C/G]AAGTTAGTATCAGCG | 57531 |
rs533135167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712923 | CCAGACATCAAACTT[A/G]CCAGCTCCTTGATCT | 57531 |
rs533152372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698409 | ACACTCCCATGGGTC[C/T]GTGAGCTCTTGGATT | 57531 |
rs533158515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801227 | ACTATGTGAAAAGAC[C/G]AATCTATGTTTGATT | 57531 |
rs533191457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794222 | TGCTCCTTAGCTTGG[C/T]ACCTGCTTAATAAGT | 57531 |
rs533205459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830441 | AATTCCAGGAAACAG[A/G]AAAAGGATCCTATAA | 57531 |
rs533224836 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822234 | AAAAATACAAAAAAA[G/T]TATCCAGGCGTGGTG | 57531 |
rs533239289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726903 | CAACATATCCATCTA[C/T]ATACAGAAGAAATTG | 57531 |
rs533250521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104768139 | AAGGTATTTTCATCT[A/G]TTTGGTTTCACTTTA | 57531 |
rs533276771 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104800778 | CCAGAGCAGAAAAGC[A/C/T]GAAAATTCTAAAAAC | 57531 |
rs533294765 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | HACE1 | GRCh38.p7 | 6:104727304 | ATACGAATATATATA[C/T]ACATGTATGTATACG | 57531 |
rs533298370 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800888 | AGTTCACAGAAGTAG[C/G]CTTCAGAAGGCTGGT | 57531 |
rs533299045 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719983 | CGAGTAGCTGGGACT[A/C]CAGGTATGCGCCACC | 57531 |
rs533306095 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814632 | ACTAAGATTATTTCT[A/C]GGTTTAGAGGGTGAT | 57531 |
rs533338161 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104815502 | AGGTAGCTGGGATTA[C/T]AGGCGTGCGCCACCA | 57531 |
rs533351949 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861259 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGTGTGC | 57531 |
rs533367211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829818 | TCCCTATAAATCTTC[A/T]GAGAATACAATTGTT | 57531 |
rs533368407 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761847 | GAACTTAAACAAATT[A/T]ACAAGAAAAAAACAA | 57531 |
rs533382969 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104713457 | TTTATATATATTAAT[G/T]TATTAAATGCTTATC | 57531 |
rs533426402 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104688980 | AGGAACTAGAACATG[C/G]ACATGATTGGGGGAC | 57531 |
rs533452549 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104738258 | CTCTAAAAAGCAGAG[C/T]GCCTCTCCTCCTCCA | 57531 |
rs533453334 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104732284 | CAGCATTATTCACAA[C/T]AGCCAAATGGTAGAA | 57531 |
rs533470829 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726332 | TGCTTTGCAGGAATA[C/T]GCACCCATGCACCCA | 57531 |
rs533475620 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104687832 | AGTTTTTGATAACAT[G/T]CCATCCAGATAAAAT | 57531 |
rs533475944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836487 | GGAGGCCGAGGCGGG[C/T]GAATCACCGGAGGTC | 57531 |
rs533507098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822647 | GGATCACTAGAGGTC[A/G]GGAGTTCAAGACCAG | 57531 |
rs533510976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767556 | ACTGAAATTTGATCA[C/T]GTCATTTCCCTCTTT | 57531 |
rs533524296 | snp | A/G/T | 3.47108e-05 | 0.00416584 | intron-variant | HACE1 | GRCh38.p7 | 6:104784225 | AATGAGTAGCATTAA[A/G/T]TGAAATGCAAATTCA | 57531 |
rs533539743 | in-del | -/AATA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727166 | ACATACATGTATACG[-/AATA]TATATACACATATAT | 57531 |
rs533550740 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689611 | AGCCTCCAATGAAGA[C/T]CCCCAAAAAGCATCC | 57531 |
rs533615924 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682202 | TAGATTGCCGGGCCC[A/C]CCTCCAGAGTTTCTG | 57531 |
rs533623947 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773280 | CAAAGAAAAACAAAA[C/G]GTAGAAATGTATTGG | 57531 |
rs533635190 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810720 | AACTAAACATTTGCC[A/G]AATACATGAATAAGT | 57531 |
rs533639241 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104829167 | CTACATGGACACCAG[C/T]TCTGAACAACAAAAA | 57531 |
rs533684889 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104739105 | ATAAAATACTTTACA[C/G]ACAAGCAAATGCTGA | 57531 |
rs533689143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783192 | ACTCCCATCAAAATG[C/T]TGCATATTTTTTCAA | 57531 |
rs533707034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688462 | CAGTATGAACTGACA[C/T]TCCTCATGACAAGAC | 57531 |
rs533737972 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775758 | CATCACAGGGATGAA[G/T]GCCTGCAGCTGCCTA | 57531 |
rs533748726 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836234 | AAGAGAGCACAGAAG[C/T]CTCCGTAAGAGACTC | 57531 |
rs533752308 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104727164 | ACACATACATGTATA[C/T]GAATATATATACACA | 57531 |
rs533806513 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746274 | CAAAAAGTTTTAGAA[A/C]TGCTAGTATAGGGTG | 57531 |
rs533810531 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104799167 | AAAGTCTGACTTAAC[G/T]GTGACACTGTTATAA | 57531 |
rs533828508 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104740408 | AGGATCAACAAAATT[A/G]ATAGACCGCTAGCAA | 57531 |
rs533831848 | in-del | -/AAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802033 | AGCAAACGAAAAGCC[-/AAA]AAAAAAAAAAAAAAA | 57531 |
rs533839093 | snp | A/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791569 | TTCCATTACTGGGGG[A/G]GGATGGACCAATTCG | 57531 |
rs533884042 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104733134 | ATTTCCTATGATGTC[A/G]AATTTCAAATTAAAT | 57531 |
rs533887034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104696344 | GGAGGGGATCACACC[A/G]TCCCCATTGACAACA | 57531 |
rs533896388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857814 | TACAAAAAATTAGCC[A/G]GGCCTGGTGGCAGGG | 57531 |
rs533908599 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851832 | CAGAGCTGACTGGTG[-/T]TAAGTGTAAAGACCC | 57531 |
rs533915332 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104830115 | TGGGCAACAGGTAGG[A/G]TGTGCAAGTCTTAGT | 57531 |
rs533942765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104843960 | CTCCCGGGTTCAAGT[A/G]ATTCTCCTGCCTCAG | 57531 |
rs533958416 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710589 | GGAGCCCAACAAACC[C/T]GGCTTCTCATCTTCT | 57531 |
rs533959182 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743916 | TTTCCAAATTATAAA[A/G]TACAATATACTGATA | 57531 |
rs534006256 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766686 | ATTCACTGCCTTAGT[A/T]AATGAGAAGCCTAGC | 57531 |
rs534008300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760121 | TTCTACCAGAGGTAC[A/G]AAGAGGAGCTGGTAC | 57531 |
rs534016333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738376 | AATTACTCTGAGCTA[C/T]GGGAGGACATTCAAA | 57531 |
rs534018993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717873 | TTTGCCTATCGAGTT[C/T]CCTGTCTTTCTTATC | 57531 |
rs534027007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104698953 | AACTCCTGGCCTCAA[A/G]CAATTCTCCCACCTC | 57531 |
rs534030254 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723759 | ACCAAATTTTTATAT[A/T]TTTTTTATTTTACAG | 57531 |
rs534039566 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750647 | TGAGGAAAAAATTCC[A/G]GGGACTCAATCATCC | 57531 |
rs534055425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842878 | GCACTTTGGGAGGCT[C/G]AGACAGGTGAATCAC | 57531 |
rs534075110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850731 | GATTTACATACAATC[A/C]CAAAGTTAACAGTTT | 57531 |
rs534088441 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104773180 | ACTCATCCATTCAAC[A/C]AACACATAATGAGCT | 57531 |
rs534096359 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714573 | AATCCCCTGTACATT[C/T]CCAAATAAACTGATT | 57531 |
rs534104305 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104737981 | CGCAGCTGGAGATCT[A/G]AGAACGGGCAGACTG | 57531 |
rs534126413 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764879 | CACCATCACTGAACA[C/T]AGTTGCAGGCCAGAG | 57531 |
rs534150538 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104711229 | TTACAAAACCATACC[C/G]TGGAGTCTTGCTAAC | 57531 |
rs534165500 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795966 | ACCTCTAAAACGAAA[C/G]AGAAATTTAAATTCC | 57531 |
rs534218934 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737620 | ACTGCGCTTTTCCGA[G/T]GGGCTTAAAAAACGG | 57531 |
rs534218939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730012 | AATAAGCAATAGGGC[A/T]ATTTAGTTTGAAGTG | 57531 |
rs534228597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849942 | GGCGTAAGCCACCAC[A/G]CCCGTCCTTTTTTTT | 57531 |
rs534240099 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858389 | TCTAAATAGAGACTA[C/G]AGACCATTTTTTCAA | 57531 |
rs534247537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820818 | GAAATACCATTTGAC[C/T]CAGCAATCCCATTAC | 57531 |
rs534251812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826682 | TAAATAGGTGACTGA[C/T]AAATGATTACCTATG | 57531 |
rs534288062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758229 | CTCGAGAAGAGCAAC[C/T]CCAAGACATATAAAA | 57531 |
rs534298657 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736517 | AAACTCCTGAGCTCA[A/T]GTGATCTGCCCACCT | 57531 |
rs534304220 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718418 | ATAGCATTGGTCAAA[C/G]CTTCAGTATCATGTC | 57531 |
rs534306378 | snp | C/T | | | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859382 | GAAAACTCCCACCTG[C/T]CGGGGTGGGAGCGTC | 57531 |
rs534335188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710830 | AATGTAATTTCAGGC[A/G]TTAGGCTTAAATTTC | 57531 |
rs534401190 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104763429 | CACCCAAGTCTCAAC[A/G]TGAATTTGTTTCATT | 57531 |
rs534403164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722534 | TTTTATCCTTTTCAG[C/T]TATTTGCTCAATCAA | 57531 |
rs534421854 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798432 | ATCCTACTACGAATC[C/T]AGTGCCAGAAAACTC | 57531 |
rs534424830 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861597 | CTGTTATCACCATTG[C/T]TCTCTAGGCTGTTGC | 57531 |
rs534428660 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701366 | AAGGTAGATGTCTGT[C/G]AAATTACGCATCTTC | 57531 |
rs534442291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104774122 | TGAGACGGAGTCTCG[C/G]TCTGTCGCCCAGGCT | 57531 |
rs534453539 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773242 | GCTAAAAGAAACAAC[A/G]GATAAACCTAATGAA | 57531 |
rs534464371 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715113 | GAAATTAAGCCCCAC[A/T]TGCCCATAGTGGACA | 57531 |
rs534483937 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727923 | GGCTCAAGCGATCTC[C/G]CACCTAGCCTTCCAA | 57531 |
rs534534235 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860488 | GACAACCTGAAAAAA[A/T]TTTTTCATTTATTTG | 57531 |
rs534555707 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104770684 | AGATCATACCACTGC[A/G]CTCCAGCCTGGGTGA | 57531 |
rs534562794 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854012 | GAATGTGGTCTCTCT[C/T]CCTCTCTCTCAAAAT | 57531 |
rs534603282 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | HACE1 | GRCh38.p7 | 6:104727492 | ATGTATATGAATACA[C/T]ACACACATATGTATA | 57531 |
rs534622800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700467 | CATTCCCAAGGATGG[A/G]AAACGAAATGTTTGT | 57531 |
rs534665244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808487 | TGTATAGCTCTGGTG[C/T]TGGGATTTGAACCTG | 57531 |
rs534697118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838475 | GGGACCATCTCTTCA[A/G]TAAATGGTGCGGGAA | 57531 |
rs534698654 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794450 | CATTTTACAGAATTA[C/T]CTTATTTCACTCTCA | 57531 |
rs534713769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830946 | GACATCCAAGCAGCA[C/T]AGTGCACTACAACCC | 57531 |
rs534744106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104741714 | TAGGAAGAATCATTA[C/T]CGTGAAAATGGCCAT | 57531 |
rs534769258 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845227 | TCATACCATGGATTA[G/T]ATCATATTTCTTTAA | 57531 |
rs534770536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770033 | TTCTGTATGGGAGGT[A/G]TTATTATTCCAATTC | 57531 |
rs534785821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721815 | CCTAGCCATAGCGCT[A/G]TATTGCCCTCTTTTG | 57531 |
rs534792010 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803340 | ATCAATAGAAAAAGA[G/T]GGAATCCTCCCTAAC | 57531 |
rs534800709 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834283 | TGGAGAAAAGGTGTT[-/A]AGATATTTTTCTTTT | 57531 |
rs534827818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816824 | TGCTGAGCCACAGGG[A/G]TGGAGCTACCCAAGG | 57531 |
rs534875864 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807246 | CCAGGATGGTCTCAA[A/T]CTCTTGACCTCGTGA | 57531 |
rs534892784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800435 | TCCCTGACCCCTGTG[G/T]AGCCTAACTAGGAGA | 57531 |
rs534919999 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704423 | AGAGGTCATAAGTCA[A/C]ATTCCTTAAGAGCAA | 57531 |
rs534944084 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | HACE1 | GRCh38.p7 | 6:104823511 | ACTTTTCTATTTTTT[A/T]AAAAAAAACAGCCCG | 57531 |
rs534953150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748555 | TACATGCACAGCCTA[A/T]GTCCCAGCAATTCCA | 57531 |
rs534969161 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780641 | AGTCCCCTATAAACA[C/T]TTAGGCATTTATTTC | 57531 |
rs535009944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104690995 | AAACCACAACATGGA[A/G]AAAAATCGCCCCACG | 57531 |
rs535023359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859167 | CCCCCCGATGCAGCT[C/T]AAAGTAAACAGTATC | 57531 |
rs535028417 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713075 | GGGGATAGAGTGGGA[G/T]AGCAGTGTTGAGAGT | 57531 |
rs535044755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786547 | AAGTCAAGGCTACAG[A/T]GAGCTGTGATCATGT | 57531 |
rs535056648 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104806670 | ATTACTCAACAAATA[A/G]TCATTCTTTATAAAT | 57531 |
rs535072526 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854001 | AAAAGTTATGTGAAT[A/G]TGGTCTCTCTCCCTC | 57531 |
rs535076513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749203 | CCAAGCACAGTACAG[C/G]AAAAGCCATATTGCA | 57531 |
rs535091985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800958 | CATCACAAGGAAGCT[A/G]AAAACCTTGAAAAAA | 57531 |
rs535100115 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695920 | ATTTTTAGTAGAGAC[A/G]GGGTTCCACCATGTT | 57531 |
rs535107642 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104761074 | AAATGGAAAAACATT[-/C]CATGCTTATGGATAG | 57531 |
rs535129095 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104793598 | CCTTAGTTGTCACTA[A/G]TTAACATATATTTGA | 57531 |
rs535131433 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747668 | TAACACATGCTCTAT[A/G]ACCATGAACAAGTTC | 57531 |
rs535139120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104740362 | AAAAACCCTTCAAAA[A/C]ATTAATGAATCCAGG | 57531 |
rs535145735 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104683556 | AACTTCACAGGTTTG[C/T]TATGAAGGCTGATAA | 57531 |
rs535153058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762225 | AAGGATTATAAATCA[C/T]GCTACTATAAAGACA | 57531 |
rs535155083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770011 | TTTTACAAAATGCTA[A/G]TAACAATTCTGTATG | 57531 |
rs535172031 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859810 | CGTCCTGCGTCCGGG[A/G]GCCGGGCTGCTGCCG | 57531 |
rs535188725 | snp | C/T | 0.0314385 | 0.121371 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727662 | GTATATGAATACATA[C/T]ACACGTATGTATATG | 57531 |
rs535219864 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797902 | GGTGAAACCCTGTCT[C/G]TATTAAAAATACAAA | 57531 |
rs535259385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852181 | TAACTTGCCCCAGAA[C/T]ATCTATGTCCAAACT | 57531 |
rs535306312 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728502 | AAAACTTTCAACTTA[C/T]ATGTCTCTCAAACAT | 57531 |
rs535310912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720188 | GTTTGATGTCTTTTT[A/G]CAAATGCACACAGCC | 57531 |
rs535325303 | in-del | -/AT | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104694466 | CACAACAGGGTGACA[-/AT]AGTCAATAATAACTT | 57531 |
rs535330335 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104777907 | TGGGATTGCAGGCAC[A/G]CACCACCACGCCTGG | 57531 |
rs535341375 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733357 | AAACCATTCCTGAAA[C/T]CTTATTCTTTTCCTA | 57531 |
rs535341733 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104824487 | CAAAGGTTAAAACTT[-/A]AGATAGATGAAAATG | 57531 |
rs535381389 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782611 | ACTTCAGCTTACAAA[A/G]AAAAGAGTAGCCATC | 57531 |
rs535384831 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860311 | AAAAGCATATTGTGC[G/T]TTTGTCTTCATTGTA | 57531 |
rs535393614 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807377 | TACTCTAACTGAAAC[A/G]AGTTGCTTCGCAGTA | 57531 |
rs535407903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808362 | TACTCTGCAGCATGC[A/T]TTATAGAAGCCATCA | 57531 |
rs535428498 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844599 | ATCCACCCCCACCCC[C/G]CCAAGCCTCCCAAAG | 57531 |
rs535433225 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748458 | GAGAATGCAGAACAC[A/C]CAGAACTCTCACACC | 57531 |
rs535485705 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833413 | TTGGGGTCTTGCTAT[A/G]TTGTTCAGGTTGGAC | 57531 |
rs535505743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104698490 | ATTTTTGGTTGACAT[A/T]CTGGCTGATTTCTTT | 57531 |
rs535520171 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770637 | GGCAGGAGAATTGCT[C/T]GAACCCAGGAGGCAG | 57531 |
rs535533355 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104713004 | ATTATCCAGACTCAG[A/G]TATTCTGTTATAGCA | 57531 |
rs535617739 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712429 | GGGGGTTGGAGGTCT[A/C]ATGTTTACGTCATGA | 57531 |
rs535618657 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859558 | GCCTGGCCCCGCGAC[C/T]CGGCTCACCCTCGGG | 57531 |
rs535636692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760990 | GAATACAACTTACAA[A/G]GGATGTGAAGAACCC | 57531 |
rs535651699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805654 | GTGGGAATTGAACAA[C/T]GAGAACACTTGGACA | 57531 |
rs535671141 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104755590 | ACAGTCTCTCAGACC[A/G]CAGCACAATCAAATT | 57531 |
rs535710352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821861 | CAGATAATCTAGTAA[C/T]TCCCTACTAAATAAC | 57531 |
rs535746789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719626 | CATTTCTTAAAGAGA[C/T]TGCTTTACTTAATAA | 57531 |
rs535754887 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104733827 | CTGGGCAATAGAGCA[A/C]GACTTCATCTCAAAA | 57531 |
rs535785796 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104690911 | TTGGTCTTGAAACTA[G/T]GTAGAATCTGCTGTA | 57531 |
rs535793030 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822314 | CATGAACCCAGGAGG[C/G]AGAGCTTGCAGTGAG | 57531 |
rs535806985 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804534 | ACCAATGGAACAGAA[C/T]AGAGCCCTCAGAAGT | 57531 |
rs535809771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840792 | AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT | 57531 |
rs535842464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792994 | GTTGCTTTTGCCGGG[C/T]GTGGTGGCTCACGCC | 57531 |
rs535847395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841683 | GGCCTTGAAAACCAG[A/C]ATGGTAAGTAAATAT | 57531 |
rs535871780 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802703 | CAGAATCTCTGGGAC[A/G]CATTTAAAGCAGTGT | 57531 |
rs535873658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689933 | AAGTATTAGGTAGGG[C/T]ATAGTCTCTTAATCC | 57531 |
rs535906652 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756220 | GTTCTAGACCAGCTG[G/T]GCCAGCATGGTGAAA | 57531 |
rs535914434 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701556 | TAGGTATTATTATTA[C/T]CCTTCAGTTCTCTTG | 57531 |
rs535922354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848523 | TCAAAAAATACTTAT[A/T]TTCATTTTAAACATA | 57531 |
rs535942775 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709874 | GTGAAGAAATTGGAA[C/T]TCTCATACATGTAAA | 57531 |
rs535971964 | snp | A/G | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727793 | TATGTATATGAATAT[A/G]TACACACATATATAT | 57531 |
rs535999663 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813452 | CGGGACAATGGGTCT[A/G]TAGCAGTCATCCCCA | 57531 |
rs536006029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702163 | AATGACTTCTGTCAA[C/G]GATAGAAAAAAAATA | 57531 |
rs536016184 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727512 | ACATATGTATATGAA[C/T]ACACACACACGTATG | 57531 |
rs536029463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814706 | GAGGAGGGACCTGGT[A/G]AGAGGTGACCAGAGC | 57531 |
rs536035982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104810844 | TTTTTTGGTTATAGA[C/T]ACAGAGAAAGAAAAG | 57531 |
rs536061084 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810986 | ATAAGTACTTAGTCT[A/G]AAATTGAAGTAATCA | 57531 |
rs536095064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761290 | ATCATGCTACCAGAC[C/T]TCAAACTATACTACA | 57531 |
rs536103555 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700144 | TGGGAGAAAAGACAG[-/A]AAAAAAAAAAAGAAA | 57531 |
rs536128453 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753105 | CCTTCAAACATAATA[A/C]AACAAATTAATATTA | 57531 |
rs536139595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779940 | TTGAAGCACTTTACA[A/G]TGCATTACCACATAC | 57531 |
rs536144433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716516 | CTAACATGGTGAGAC[C/T]CCGTCTCTACTAAAA | 57531 |
rs536174439 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727545 | TATGAATACACACAC[A/G]CGTATGTATATGAAT | 57531 |
rs536180287 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104767490 | ACCGCCCCATTTCAA[C/T]CCATTTTTCACACTC | 57531 |
rs536193844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819334 | ACAACTAAGTAGGGA[A/G]GCGAAAGATCTCTAC | 57531 |
rs536201341 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776505 | GAGACAAGCATTTGG[A/G]AACCAACTGTTTAGA | 57531 |
rs536223456 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734747 | ATTGCTAAGAATGAC[C/T]GTACTATTTAAAGTG | 57531 |
rs536224568 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838727 | TAACCAAAGCAAAAA[C/T]GGACAAATAGGATCA | 57531 |
rs536242561 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789270 | ATTCTTTAACAGTTA[A/T]TACTTATTAATGTGT | 57531 |
rs536243344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685705 | AAGGTTATGCTAAGC[A/C]TTGCCACTTATATTT | 57531 |
rs536247073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833737 | CAAGCCTCTAATCCC[A/G]GAACTTTGGGAGGCT | 57531 |
rs536267207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695075 | CTGCAAGCACCTGAG[A/G]AACCCAGAGCCAGAC | 57531 |
rs536274575 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | HACE1 | GRCh38.p7 | 6:104686702 | ATACACCAGCCACAC[C/T]ACGTGCCTGCCTCCT | 57531 |
rs536275491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781229 | TAGATTCCTGTTTAT[A/G]TTGCCATCATTATTT | 57531 |
rs536281528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745384 | ATATCACAGTTAGAG[A/T]TGCTTACATAGTCAG | 57531 |
rs536320730 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104812446 | AAGACCCCATGCCTT[-/A]AAAAAAAAACAAAAT | 57531 |
rs536352403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797369 | CCTTAACTTGACCAT[C/T]TGCAACTTTAGCCTG | 57531 |
rs536364923 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104788144 | AATTTTAAAATTAAA[A/G]ATAAACCATTGCATA | 57531 |
rs536383711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685076 | TCCGGCAATGTACCA[C/T]ATGTTGGAGGCTCCA | 57531 |
rs536383811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104824844 | TTAGGGAGGCCGAGG[A/C]GGGCAGATCACGACG | 57531 |
rs536402785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855124 | TGTAACAGTGGCATT[A/T]TGTGGCTGATTCCAG | 57531 |
rs536416452 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758795 | AGTGTGCTGTATTCA[A/G/T]GAGACCCATCTCACG | 57531 |
rs536428255 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104847593 | ACCTAGGCAACACTA[C/T]TGCTGTCTTTTTTGC | 57531 |
rs536441880 | snp | C/T | 9.8943e-05 | 0.0070329 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795602 | TTTATGACCATTTGT[C/T]GTAGCAACTTCAGCA | 57531 |
rs536451900 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759469 | GTAAATAACGAAAGT[A/C]AGTCAGAAATAAAAA | 57531 |
rs536463987 | in-del | -/CACGTATG | 0.0263992 | 0.111815 | intron-variant | HACE1 | GRCh38.p7 | 6:104727568 | ATATGAATACACACA[-/CACGTATG]TATATGAATACACAC | 57531 |
rs536470915 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833798 | AAGACCATCTTGGCC[A/G]ACATGGTGAAACCTT | 57531 |
rs536493947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751809 | GAGTTAAAAACAATA[C/T]GCTATAGCAGGTATA | 57531 |
rs536528957 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104764124 | CTGTTGCTCAGGCTG[C/G]AGTGCAGTGGCACTG | 57531 |
rs536532192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758200 | GAAATACAGAGAACA[C/T]CACAAAGATACTCCT | 57531 |
rs536532516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720286 | TGTAAAGTACTCCCT[G/T]AATCTTGAGCCCCTG | 57531 |
rs536600411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770898 | TTGCAAATATCTTCA[C/T]TTAAGCTTATATTTC | 57531 |
rs536605298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701128 | CTGTTCATTTTCACT[A/G]TTATTCAGTCATACC | 57531 |
rs536613220 | snp | C/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727692 | GAATACATACACACA[C/T]ATATATGTATATGAA | 57531 |
rs536624035 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855750 | TCTGAACTTCTAAAC[A/C]ATGAGAATTTCCATT | 57531 |
rs536689834 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752359 | ATATTTCATAGTGAT[A/T]ACAGCAGTGATACCT | 57531 |
rs536696684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735609 | GCACTCCAGCCTGGA[C/T]GACAGAGCGAGACTC | 57531 |
rs536725867 | in-del | -/TATATGAATACACACA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727442 | GAATACACACACATG[-/TATATGAATACACACA]TATATGAATACACAC | 57531 |
rs536732274 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104758687 | ATGACAGCATCAAAT[C/T]CACACATAACAATAC | 57531 |
rs536734159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855000 | AGGCACTTTTCTAAA[C/T]ACTTTGCATGTATCA | 57531 |
rs536758891 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736479 | TGTAGAGACGGTTTC[A/G]CCATGTTGCCCAGGC | 57531 |
rs536763993 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779302 | GGCTTTTAGGACACC[A/G]ATAAATTTCTTCATC | 57531 |
rs536766133 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728208 | CATATCTGTAAACAT[C/T]AGTATTATAAGCAGT | 57531 |
rs536815597 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715315 | CAAATAGAACTTCTA[G/T]AAATAAAAAATCATT | 57531 |
rs536815652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722985 | ATAGTTCAATGGTTT[C/T]GCAACATTAGATGCA | 57531 |
rs536863727 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104839447 | TACAATATAGTTCTA[A/T]CTCTGTAACATTCTT | 57531 |
rs536886144 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104742655 | ATCATTAAAAAGTCA[C/G]GAAACAACAGGTGCT | 57531 |
rs536895642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764042 | ACAGAGCAAGATTTT[A/G]TCTCAAACAAACAAA | 57531 |
rs536896887 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774025 | ACTAAGCATTTTCAC[A/G]TATCAGCTAACTGAG | 57531 |
rs536915054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801511 | CATCAGACTAACAGC[A/G]GATCTCTCGGCAGAA | 57531 |
rs536929728 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707344 | CAAGTGGGATTTATC[A/C]AAGTAATGCAAGTTA | 57531 |
rs536939092 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728100 | CCACCACACTCAGTT[A/T]TTTAATATTTTATTA | 57531 |
rs536939488 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104683914 | GAAAAACCAAATCCA[C/G]GGCTGTCCTTCTAAA | 57531 |
rs536951038 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722557 | TCAATCAACAGGTTG[G/T]TCAACTTACTTGTCT | 57531 |
rs536956756 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715200 | TCCCCTACTCCTGTC[C/T]CCTGGGATTACTTCA | 57531 |
rs536958374 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104736472 | GTATTTTTGTAGAGA[C/G]GGTTTCGCCATGTTG | 57531 |
rs536969094 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104741923 | CTATACGACAAGGCT[A/C]CAGTAACCAAAACAG | 57531 |
rs536999194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699535 | ATCCACATGCGGAGA[C/G]GTTGCCCTGCTGATT | 57531 |
rs537017157 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706721 | AATGCCTTCAGGAAT[C/T]TTTGTTTAATTCCTG | 57531 |
rs537025150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848088 | AACTCCTGACCTCAG[A/C]TGATCCGCCCGCCTT | 57531 |
rs537026727 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803527 | CACCACGATCAAGTC[A/G]GCTTCATCCCTGGGA | 57531 |
rs537036587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692391 | ATTTTTTTAAATTTT[G/T]TATCATGTTCACATA | 57531 |
rs537045975 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787493 | GATGAAAAGAACTTA[A/C/T]GTCAGCAAAACTATT | 57531 |
rs537056053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840455 | AGAAAGTCAACAGGT[A/G]ATACCTAAAACCAAA | 57531 |
rs537069080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104832357 | AATATTTTGAACAGA[C/T]ATAAAAGCACTATTT | 57531 |
rs537077227 | snp | A/G | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727709 | TATATGTATATGAAT[A/G]TATACACACATATAT | 57531 |
rs537125937 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104708109 | AATAAGACATTCATA[C/T]TGGAAAAGAAGAAGT | 57531 |
rs537155948 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104795346 | ACAAAATTCTAGACA[C/T]ATATGCCCAAATTCA | 57531 |
rs537182209 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104831749 | ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCCGG | 57531 |
rs537187837 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803041 | GGGGGTATCACCACC[A/C]ATCCTACAGAAATAC | 57531 |
rs537198612 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104698792 | TACGTCCTTGACATC[C/T]GTTTCAAAGTTAGAA | 57531 |
rs537204188 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771557 | AAAGTCTGTTAAATT[A/C]ATTCTGTGTTTCTTT | 57531 |
rs537228769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801409 | CAACCCCAAGACACA[C/T]AACTGTCAGATTTAT | 57531 |
rs537231219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809247 | TAGGGGAGACAGACT[A/G]TAAGAAAGTAAATAA | 57531 |
rs537261336 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699372 | CCATTGTGGAGATCA[G/T]TTACTATTCTATATG | 57531 |
rs537301937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816672 | CATACAGGGCACTGT[C/T]TAGTAGAGCTGTGAG | 57531 |
rs537329051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762716 | TAAAAAAAGGCCGGG[C/T]GCGGTAGCTCACACC | 57531 |
rs537356777 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697852 | TAAAGCGATTCTCCT[C/G]CCTCAGCCTCCAGAG | 57531 |
rs537393078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104800982 | GAAAAAAGGTTAGAC[A/G]AATGGCTAACTGGAA | 57531 |
rs537393181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104808319 | ATGTCAGAACTTAGT[A/G]AGCACCTATCAACTA | 57531 |
rs537394399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714344 | TGTCACAAGGACAGA[A/G]AGCAGGATGCAAAAG | 57531 |
rs537441104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684268 | GACAGCTAAGGTTTC[C/T]CTTGCCTCCAAGCCC | 57531 |
rs537441681 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104778116 | ATGCAGAAATTGGAA[A/C]GTAATTTGTTATCCC | 57531 |
rs537473553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104725649 | ACGAACAAGGCTTCA[A/G]TGAATATCATTGGAC | 57531 |
rs537478434 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104779146 | CAAGTCATGACTGAG[A/G]ATTTGCTTAGCAAAT | 57531 |
rs537522695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794588 | CACCTCACAGATGGC[C/T]TAATGGATGGTACGC | 57531 |
rs537533882 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104752248 | GTCACATACAGGTAC[C/T]TATTATAGAGAGGGA | 57531 |
rs537542894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835138 | CAAGAGTAAATGCCT[A/G]AAGAAATCGACACTG | 57531 |
rs537547677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838569 | CAAACAAAAATTAAT[C/T]AAAAACTTAAATCTA | 57531 |
rs537548862 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690334 | TATAGTTGTTGACTT[C/T]AAGAAAACTCATCTT | 57531 |
rs537557622 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827724 | TTTACATGGCTGTCC[A/G]TAACTGGATGAAAAA | 57531 |
rs537559830 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104786614 | GTCTCCAAAAAAAAA[A/G]AAAAAACAAACAAAC | 57531 |
rs537560923 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104772162 | AAACTAATTCACATA[A/C]AACTTCAGCAAAGCT | 57531 |
rs537586012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104828066 | TAAATCCACGTTATT[C/T]TGAGAAGACTGTAAT | 57531 |
rs537602052 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781047 | CAGAGCATCCTATCA[A/G]CTGGCACACTGCTAT | 57531 |
rs537610923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695539 | TAATTCATCTTCATT[C/T]GGTTTGTATGTGTCC | 57531 |
rs537621087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749389 | AATGAAACTAAATCA[A/C]AATGGACTTCAAAAT | 57531 |
rs537623778 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737152 | CAAAAATTAGCTGGA[C/T]GTGGTGGCAGGCACC | 57531 |
rs537641896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799032 | CTTTAATTTCAGACA[A/C]CATTCATTTGACAAA | 57531 |
rs537663306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845921 | TACATTGTTTAAATG[C/T]GTGATCGTGTGTCTA | 57531 |
rs537715938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104804115 | AACTCCCATTCACAA[C/T]TGCTTCAAAGAGAAT | 57531 |
rs537717728 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733646 | TCACTTGAGATCAGT[A/T]GGGACCAGACTGGCC | 57531 |
rs537723807 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756876 | AGTCTTCGCAACTGG[C/G]AGACCAGGAGATTCC | 57531 |
rs537727793 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852235 | TGTGTGTGTGCGCGC[A/G]TGCGCGTGCACGGGC | 57531 |
rs537735692 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104713742 | AACCTAGTCCGATTG[A/C]CCCTTCCACTAAAAA | 57531 |
rs537737919 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104712629 | ATACAACAATTAGCT[A/G]GGCGCCATGGTGGGT | 57531 |
rs537789721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703426 | GTGTAATTGAAAGCA[C/T]GGCCCCAAATGTCCA | 57531 |
rs537799639 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788275 | AAATATTAGCAGGTT[C/T]CTTGGTACTGTGAAA | 57531 |
rs537805610 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818039 | GGACTAGCATTCTTA[A/T]CAGAAGATTTTAATA | 57531 |
rs537815025 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843899 | TTGAGACAGAGTCTT[C/G]CCAGGCTGGAATGCA | 57531 |
rs537830771 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104812001 | TTAATATATACTTAG[C/T]CCCCTAAGCTCTACT | 57531 |
rs537843239 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846844 | AGTTGTACAAGGCTT[-/C]CCACTCAATAAATAA | 57531 |
rs537863577 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814015 | AGAAGTTTAAAAAGA[A/C]AATGTTCAGGAATTC | 57531 |
rs537875939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775049 | TACAAAAAAGATAAA[C/T]CAAAATGTTTGGCCA | 57531 |
rs537883355 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721325 | CTCCAGCCTGGGCAA[C/T]AGAGCAGGACTCCTT | 57531 |
rs537947122 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719787 | ATTGAGTAGATAGAT[G/T]TTTCTTTTCTTTTTC | 57531 |
rs537953606 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104738330 | GGAGAATGACTTTGA[C/T]GAGCTGAGAGAAGAA | 57531 |
rs537971531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773033 | ATTTCACCACCGTAA[A/C]AAAAAAGTCTCAAAA | 57531 |
rs537973568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765131 | TTTGAGGGAAAATAC[A/G]TGGCAAACACATTAT | 57531 |
rs537995234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704163 | ATTTGAAGTCACAGA[C/T]CTCAACGTTTACGAA | 57531 |
rs538008210 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104849898 | CTCAAGATCCGCCCG[C/T]CTCGGCCTCCCAAAG | 57531 |
rs538008815 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794924 | AAAATAATTGTATAT[A/G]TGTGTGTGTGTGTGT | 57531 |
rs538054103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781099 | GCTTCTCTACTGTAA[A/G]GCACCCTTTTTCTCT | 57531 |
rs538077797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746161 | TGGATTATTTTATGT[A/G]AATAAAATATTTTAC | 57531 |
rs538086919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104729976 | CAGTGGAAGAAAATA[C/T]GTTCCTTTCAGCTTA | 57531 |
rs538097088 | in-del | -/TGTCTG | 0.0101649 | 0.070563 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852196 | CATCTATGTCCAAAC[-/TGTCTG]TGTGTGTGTGTGTGT | 57531 |
rs538120611 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104857784 | AACACGGTGAAACCC[C/G]GTCTCTACTAAAAAT | 57531 |
rs538120684 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104849330 | AAAACAAAATATTCT[A/G]TTAAACACAATTTTC | 57531 |
rs538128639 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760349 | AAAAGCTTATCCACC[A/T]CGATCAAGTCGGCTT | 57531 |
rs538134139 | in-del | -/ACAA | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104808429 | CAGCACTTCCATTTC[-/ACAA]ACAAACAAAGCTTCA | 57531 |
rs538143746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104856624 | TATTTTTAGTAGAGC[C/T]GGGGGTTCACCATGT | 57531 |
rs538164547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789149 | TCCCATGGATGACAA[C/T]GTACAGTTTCTATTT | 57531 |
rs538169147 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698663 | TATATGTGAATGTCA[C/G]AAACAAGTTTCCTAA | 57531 |
rs538202182 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749805 | TACAATAAAGGCAAA[C/T]TAAAGTAGCAAAACC | 57531 |
rs538214285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834587 | CTTCCCTAAACCCCA[C/T]GGAAATGAGAGTAAA | 57531 |
rs538247568 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104687492 | GTATCCATCCAAAAT[A/T]GTCAGTTACAAGATA | 57531 |
rs538251095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835053 | CAAAGCATTCTTCTC[C/T]ATCCAGCACGCAGAC | 57531 |
rs538273641 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690213 | GCCTAGGCCCTCTCC[-/A]AAGGCTTGTCAGTTT | 57531 |
rs538286775 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104831968 | GAGAAGAGAAGAGAA[G/T]AGAAGAGAAGAGAGG | 57531 |
rs538287140 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104857337 | TTATAATCAAAGAAA[A/G]GCAAATGCAAACGAT | 57531 |
rs538296238 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701639 | GACCTAGTACTACAA[C/T]CTAGATATTCTGACT | 57531 |
rs538301660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826581 | ACCTTCTATTTTTAA[A/G]ATTATATGGCTTCTC | 57531 |
rs538336928 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687319 | GAGTCTGGTTGTAAT[C/T]ATCATTATTATTGAT | 57531 |
rs538344565 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104724682 | TCTCTAGATAACGCA[C/G]TTTTTTTAATTAAAA | 57531 |
rs538363386 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104722360 | TTGCTATATGAACAC[A/G]TAACAGTCTCCAAAT | 57531 |
rs538376144 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737660 | AGATTATATCCTGCA[A/C]CTGGCTCGGAGGGTC | 57531 |
rs538398131 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104760264 | AGAGAATTTTAGACC[A/G]ATATCCCTGATGAAA | 57531 |
rs538406371 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702245 | ACATTTTACTTAAAT[A/C]CAACCAAACTGAAGT | 57531 |
rs538430216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104686637 | GAGCTATTAGTTTTC[C/T]GTAGTCATCACTCAG | 57531 |
rs538432889 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104803922 | AAAGAGGAAGTCAAA[C/T]TGTCCCTGTTTGCAG | 57531 |
rs538463008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826009 | CAAGTGAACATCACT[A/G]TCTGAGCTCTGCCTC | 57531 |
rs538467735 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703241 | CAGCCAAGTGGCAGC[A/G]CAGTCTCTAGTAGAA | 57531 |
rs538468994 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786057 | ACTGACTAGCAGGCC[A/G]GAGATGGTGGCTCAC | 57531 |
rs538482230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684423 | CTAGAAGGTACCTAG[C/T]GATCTATCTCATTTG | 57531 |
rs538486310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736693 | AAGCCACAAAAACAA[C/T]ATATTAAATTATTTC | 57531 |
rs538502564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788364 | AGTAACAATGATATG[C/T]CAATCATACATGATT | 57531 |
rs538504209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810911 | TCCCACTGGAAATGA[C/T]CTGGTTACATAACAC | 57531 |
rs538565268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685811 | AAAGTAATAAACATA[C/T]AGATGTTAAGTATAC | 57531 |
rs538593521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104803605 | ATAAAAAGAACCAAC[A/G]GCAAAAACCACATGA | 57531 |
rs538595481 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104811793 | TGGCTAGTGAATTGG[A/T]CCCTATTGCTTTAGA | 57531 |
rs538603389 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104710026 | TTCTACAAAAAAAAA[A/T]GTATATGAGTGTTCA | 57531 |
rs538618142 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793849 | CACTACCAACCCCAA[C/T]AATGAGATATTTACA | 57531 |
rs538627208 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791376 | AAGGTGTGCCTAATT[A/T]TGAAAGTGATATGGG | 57531 |
rs538628341 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750737 | TCTCAATCTTACCTT[A/G]TCTCACTACCTCCAT | 57531 |
rs538632788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781968 | GAAGGGAAAAAGGAA[C/T]AGAAAGTAAAAAGCA | 57531 |
rs538633504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826845 | ATTCCACCCCTTCTC[C/T]CCCCACCAAAAAAAA | 57531 |
rs538662072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737860 | CTGCCTCTGTAGGCT[C/T]CACCTCTGGGGGCAG | 57531 |
rs538670935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782442 | GCAGTGAGCTCAGAT[A/C]AACTATACTCCAGCC | 57531 |
rs538704282 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104849774 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 57531 |
rs538716664 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714548 | ATAGTCCACATACCC[A/C]ACATTTGCAAATCCC | 57531 |
rs538746493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104746075 | AACAGTACCAGTCTT[C/T]CCACTGTTTCTGTTT | 57531 |
rs538768913 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104780889 | TTGATAGTTTTAAAG[A/T]CTGCAGGTCTTTAAA | 57531 |
rs538779299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848735 | AAGCAATTTGCAAAA[A/T]GAGCCATGGAGTTAG | 57531 |
rs538783750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104710509 | AATTCCGTATAACCA[A/G]TGCTTTCTGTAGCCT | 57531 |
rs538786605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825883 | CCACCAGTTTCTTCC[A/G]TCTTTCAACAAAAAT | 57531 |
rs538789328 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761522 | GAAACTGGACCCCTT[C/T]CTTATACTTTATACA | 57531 |
rs538805129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760042 | TAAGAGGTTCTGAAA[C/T]TGAGGCAATAATTAA | 57531 |
rs538812821 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104797419 | CATCCAAGTCTCTAG[C/G]CTTCTTAATCCAAAA | 57531 |
rs538817349 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752732 | ATTATTTCCTCCTAC[A/C]TTTTATTTTTTAATT | 57531 |
rs538832186 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852780 | ATAGGCATCATGTTT[C/T]ATCATACTTACATGT | 57531 |
rs538836998 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817251 | TGGATTTGTGTCCCC[A/G]CCAAATCTCACGTCA | 57531 |
rs538839227 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104717775 | TATTTTAAACTTGCC[-/T]TTTTTGATTTGCATC | 57531 |
rs538844657 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104820532 | AGTGGGCAAAGGACA[C/T]GAACAGACACTTCTC | 57531 |
rs538865298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685748 | ACAAGCCCTGGTACG[A/G]GAAATACAAATTTTT | 57531 |
rs538867963 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824356 | TAATGATGTATTTAT[C/T]GCCTGGTCTTAACAA | 57531 |
rs538872266 | snp | G/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851394 | GCCTAGCTATTCTTC[G/T]GATTCTTCAGGTTTT | 57531 |
rs538879179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104820109 | CTGGGGCAGAAAAAT[C/T]GCTTGAACCCGGGAG | 57531 |
rs538880282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789108 | TTTTACTTGAAATCA[C/T]CCCCACAATGAACAG | 57531 |
rs538894686 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736637 | AAGGGTGGTAAGTTA[C/T]TGACAATTCAGAGTA | 57531 |
rs538904563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751576 | TCGAGTCTGCAGTGA[A/G]CTATGACCGTGCCAC | 57531 |
rs538905994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765716 | TTGCTTGTTTATGAT[C/T]GGCATACCATTAAGT | 57531 |
rs538938655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803002 | AGAGAGAAGAATCAA[A/G]CAGACACAATAAGAA | 57531 |
rs538973546 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796486 | TATTAGCAAAAACTA[A/T]ATTAATTATTATCTA | 57531 |
rs538984041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743499 | GAAATATGTACATTT[A/G]TAATGAAAAAAACCA | 57531 |
rs538995678 | in-del | -/AT | 0.00676609 | 0.0577691 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727775 | TGAATATGTACACAC[-/AT]ATATGTATATGAATA | 57531 |
rs539003477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769319 | GAATACAATTGTTAC[C/T]AGATCTTTCCACTTT | 57531 |
rs539073663 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104696169 | TGGTGGGGGCGGGGG[-/T]GGGGGGTTGTATTAT | 57531 |
rs539089815 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104686542 | GGCTTGTCCATTTGT[G/T]TCACCTTTGTCAAAA | 57531 |
rs539118074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737234 | GGGGCGGAGGTTGCA[G/T]ATCGAGCCACTGCAC | 57531 |
rs539145153 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104771786 | TCTCCTTCAAACCCC[A/G]AATGGCTTACATATA | 57531 |
rs539146056 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104723272 | GGTGTTTCTCTAAAA[G/T]TATTTTTATAATGCA | 57531 |
rs539164961 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776587 | AACTGTGTGAATGCA[C/G]ATAAAAACTCTGAAT | 57531 |
rs539179641 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104768576 | CAACAATTTGATACA[C/G]AATTACTATACTGGT | 57531 |
rs539280592 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775797 | GCAGCCTACTCCCAC[G/T]TGCCTCCCCTAAAAT | 57531 |
rs539294028 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104795770 | CCTATTAAGTATCTT[A/G]AAGCCAATTAGTCTA | 57531 |
rs539317083 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781940 | ACAGATGTTTTTTGA[C/T]TAAATTGTCCAGGAA | 57531 |
rs539318975 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839625 | ACCTACCATGTACAC[A/T]GGTAATAAAACTACA | 57531 |
rs539322336 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104792511 | GTTGATGGTGGTTTT[A/T]TTTTGAAATCTCTAA | 57531 |
rs539324570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719399 | ACGGTATAAAGTTTC[A/G]GTTATGCAAGATAAA | 57531 |
rs539340920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735681 | CTGATAAAAGGAGTA[C/T]ATTCTCTCATTCTCT | 57531 |
rs539343905 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854364 | TAGTTAATAGTATAC[A/G]CAAATGTTAATTTCT | 57531 |
rs539356894 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824214 | GTCTCATTCTCAAAT[A/C]ATCCAGAGTAACAAT | 57531 |
rs539373233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700940 | GGTATGTGCCTGCAA[A/G]CCAGGAAAATAGTTT | 57531 |
rs539378362 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689337 | TACAATTATCTTTGA[A/G]ACATTTTTTACCAAA | 57531 |
rs539420037 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104797010 | TAGGATCTGTGCTGT[A/G]TCTCTCTGACCATGA | 57531 |
rs539421818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858969 | GCTAGCCCACTCAAT[A/G]CTAGTCTGATGAATA | 57531 |
rs539434355 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794635 | TTGGCCAGGCGCATT[A/G]GCGCACGCCTGTAAT | 57531 |
rs539465541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762078 | GGTTGTGGAGAAAGA[A/G]GAACACTTTTACACT | 57531 |
rs539487589 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859908 | GTCCCTCCCGGGCTC[C/G]CGTGGCCTTCTGGGA | 57531 |
rs539508398 | in-del | -/AACTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813689 | ACCAAGTAGTCAACA[-/AACTC]AACTCATGTACACAA | 57531 |
rs539535576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711332 | GTTCAGCTTCTTCCA[A/C]CCAAAGTGTTTAAAT | 57531 |
rs539538917 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703577 | GTAGGATTTGACAAA[C/T]GTACAACAGGATAGG | 57531 |
rs539548716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720230 | ACTACGATCCAGATA[C/T]AGAACATTTTAATCA | 57531 |
rs539550477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822894 | TTTTTATACTGCTTC[A/G]TATTTCTATTTATAC | 57531 |
rs539605601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766800 | TAAAGAAATGCAGTG[C/T]TGTAGTTACAAGCAG | 57531 |
rs539606453 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724239 | TTATAACTTTTTACA[C/T]TCTGGTAGGGCACTT | 57531 |
rs539618055 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718549 | AGGAAATGCCTTTAT[A/G]TTTTGAATTTTATTA | 57531 |
rs539648136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733227 | TAGCACAGTATTTCA[A/G]TATCAATATGATCAA | 57531 |
rs539659324 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803969 | TTTAGAAAACCACAT[C/T]GTCTCAGCCCAAAAT | 57531 |
rs539690427 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104760504 | CAACAGCCTTTCATG[C/T]TAAAAACTCTCAGTA | 57531 |
rs539695417 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104858027 | ACATGATTTTAACTT[G/T]TTAGGGAGGGAAAAA | 57531 |
rs539715504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800284 | CCACTTCTGTGGGCA[C/G]GGCATAGCTGAAAAA | 57531 |
rs539726937 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792942 | GCTCATTAGAAGCAC[A/C/G]GAGCTCTCTTCTTCC | 57531 |
rs539737209 | snp | A/C/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104739289 | CCAGCTAACATCATA[A/C/G]TGACAGGATCAAATT | 57531 |
rs539755011 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725572 | TTCTATTCTAGGGCT[G/T]TAACACATTATTAGT | 57531 |
rs539772266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697569 | AATTCAGAACATCCT[A/G]TTATTGCTGCCACCA | 57531 |
rs539773239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828881 | TATAGCATTTAGCTA[C/T]ATATTCTACAAAGTT | 57531 |
rs539775777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820983 | GAAAATGAGGTACAT[A/G]TACACCACGGAATAC | 57531 |
rs539803751 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787547 | TTCTGAAATGGAAAG[A/C]ACAGGTGGTGATATA | 57531 |
rs539804469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705008 | TGATTTTTCAATAGA[C/G]AGATTTTTATACATT | 57531 |
rs539812908 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711657 | ATGATGTTACAGCAA[C/G]TGGGCTTCAAGTTGC | 57531 |
rs539831140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851341 | CCTGCCTCGGCCTCC[C/T]GAAGTGCTGGGATTA | 57531 |
rs539842275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828045 | TTGACAGTTCTCTAC[A/G]GTTTCTAAATCCACG | 57531 |
rs539864679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705537 | CGTTTTCAGTTTTTA[A/T]AATGTGCGTGTCTTT | 57531 |
rs539904350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760953 | AAATTCACAATTACT[A/T]TTAAGAGAATAAAAT | 57531 |
rs539910170 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719545 | AAATAATAATAAAGA[C/G]ACAGCAGGAAACTTT | 57531 |
rs539936682 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820343 | AAAATTGGAAGTTGG[G/T]ATCTAATTAAACTAA | 57531 |
rs539970958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712379 | GTCCCCTCCAAAACA[C/T]GTGCTGGAAACTTAA | 57531 |
rs539974155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104813432 | AATAAAGAAACAGCC[C/T]AATTCGGGACAATGG | 57531 |
rs539977212 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857230 | ATATTCCTATATGTA[C/T]GATATACTTTAAAGA | 57531 |
rs539985481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805545 | AAGGAGGAGTTCATG[C/T]CCTTTGCAGGGACAC | 57531 |
rs540018393 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104827208 | TCAACTCTCAAAACA[C/G]TGATCAAAGTAAAAA | 57531 |
rs540022113 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104693672 | CATCAGTAGTTGTTT[G/T]TATCAGAGGATGTGG | 57531 |
rs540039211 | in-del | -/TTTTTTTTTTTTTTTT | 0.499382 | 0.017561 | intron-variant | HACE1 | GRCh38.p7 | 6:104774081 | TTATCATCTTTTCTC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTGAGA | 57531 |
rs540041437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821707 | TTGAAGCAGGGATTA[A/G]AACCCAAGTCCATGT | 57531 |
rs540046187 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773580 | AAATATAATCATAAT[C/G]CCAAAAATATAATAT | 57531 |
rs540052324 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104848437 | CTCCAGCCTGGTGAC[A/G]GAGTGAGACCCCATC | 57531 |
rs540058986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813097 | AATCCAGCAGGCAGG[A/C]TTAAAAATCTCAAGT | 57531 |
rs540083605 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104766253 | TCTTGGTGTGTTGAA[A/G]AAAAAATATATATGC | 57531 |
rs540085611 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | HACE1 | GRCh38.p7 | 6:104725041 | GGCAAGAGAGCATTC[C/T]TTTTTTTTTTTTTTA | 57531 |
rs540109492 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104790759 | GGCTCCGTTTCAAAA[A/C]ATAAATACATGAAGA | 57531 |
rs540123544 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104697746 | TATTTTTTATGTTTA[-/T]TTTTTTCTTTGAGGC | 57531 |
rs540132935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834733 | TCAGAATGCTACACC[A/T]GTATTAGAGAAACCC | 57531 |
rs540156468 | snp | C/G | 0.29175 | 0.246489 | intron-variant | HACE1 | GRCh38.p7 | 6:104774152 | TGGAGTGCAGTGGCG[C/G]GATCTCGGCTCACTG | 57531 |
rs540198832 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715937 | CTATGACATGAGTTT[A/G]TCTATATAACAAACC | 57531 |
rs540219255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694795 | AGAGGGCCGCATGCT[C/G]AAAGAGCCCTGCACT | 57531 |
rs540240071 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754925 | ATGACAGGATCAAAT[A/T]CATACATAACAATAC | 57531 |
rs540247629 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104745089 | GGAAAAAGGAGGTAA[C/T]ATAAAAATAGTTACG | 57531 |
rs540249949 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760921 | GACAAACAGAGAGAC[A/C]AATCATGAGTGAACT | 57531 |
rs540251735 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830476 | CCATTTTTCCAACAC[C/T]ATATTAAACATAAGA | 57531 |
rs540329398 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104803689 | CTAGAAACTCTCAAT[A/G]AACTAGGTATTGATG | 57531 |
rs540352335 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104835743 | ATTATCCATCGAAAT[G/T]GATAAAATAAATCCA | 57531 |
rs540361284 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786834 | AATGCTACAAACTAC[A/C]CCATGTGCTACAGAA | 57531 |
rs540380644 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104765198 | AGTTGTTAGGGAATA[A/G]CAAAGTCTTGCAGTC | 57531 |
rs540387445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835155 | AGAAATCGACACTGG[A/G]AAGGTCTAAGAGGCA | 57531 |
rs540415570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702728 | TAAGAAATATTTTCC[A/G]GACTACTAATAGGAC | 57531 |
rs540424045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828110 | AATTCAACACATTTA[C/T]AAATCTTAAAGAAAA | 57531 |
rs540450837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104774372 | TGGGATTACAGGCGT[A/G]AGCCACCGCGCCCGG | 57531 |
rs540463277 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791259 | AAACACTAAATATCT[C/T]TACCCTTAGAATAAA | 57531 |
rs540470307 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104731855 | ATATCCAGAACATAC[A/G]AAGAATTCCCATAGA | 57531 |
rs540488068 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743274 | ATATGTAACTAACCT[A/G]CACAATGTGCACATG | 57531 |
rs540494833 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737715 | GCTAGCACAGCAGTC[A/T]GAGACCAAACTGCAA | 57531 |
rs540554596 | in-del | -/TTAG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795797 | TCTAAATCAAGTCCT[-/TTAG]TTATTTTGTCTTGCA | 57531 |
rs540558184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731336 | AAATTTAAAATACTT[C/T]CTTAAAAATATGATT | 57531 |
rs540584575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849441 | TCCTGGGCTCAAGCA[A/G]TCCTCCCACCTCAGC | 57531 |
rs540588835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104841117 | CAGTGAGACTCTGTC[C/T]CAAAAAAAAAAAAAA | 57531 |
rs540589044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703518 | TAAGGAGTTGTATAA[C/T]ACATGATTAATGCTA | 57531 |
rs540605467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104753833 | TGAAAACTCAAAAAG[C/T]CAGAGTGCCTCTTCT | 57531 |
rs540607367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798427 | ATAGTATCCTACTAC[A/G]AATCTAGTGCCAGAA | 57531 |
rs540611849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786089 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG | 57531 |
rs540621941 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857432 | CGGACTGCTGGTGGA[A/G]CTTTCCAAGGAGTAA | 57531 |
rs540622508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846200 | TACTATTTTCCAGGG[C/T]CTGAATAAGTCAAAT | 57531 |
rs540662100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855183 | GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 57531 |
rs540673933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842061 | ACAGTAATTTTATCT[C/T]TGGGATGCAGAAGTG | 57531 |
rs540675829 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737457 | AGACAGTGGGCGCAG[G/T]TCAGTGGGTGTGCGC | 57531 |
rs540712587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710090 | AATTTTTATTAGCTG[A/G]TAAGTAGATAAAATG | 57531 |
rs540714285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104741966 | ACCAAAACAGAAATA[C/T]AGATCAATGGAACAG | 57531 |
rs540735032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857437 | TGCTGGTGGAACTTT[C/T]CAAGGAGTAAGTTGA | 57531 |
rs540769914 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804188 | CTTCAAGGAGAACTA[A/C]AAACCACTGCTCAAC | 57531 |
rs540782811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853607 | GAAACAAGATATTTA[C/T]ACAGTATCAAGTACC | 57531 |
rs540783017 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762350 | GTGGCACATATACAC[A/C]ATGAAATACTATGCA | 57531 |
rs540792367 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104717336 | TAGAGACGGGGTTTC[C/T]CCATGTTGGTCAGGC | 57531 |
rs540799444 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726921 | ACAGAAGAAATTGTG[G/T]GAATGGAGTAAATTA | 57531 |
rs540799731 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709538 | AACTCCAACCCCCTG[C/T]TTGCTCTGTCTCTTG | 57531 |
rs540809296 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748769 | AACAATATGTATGAT[C/T]CCCACAAACAAAAAC | 57531 |
rs540815483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801556 | AAGAGAGTGGGGGCT[A/G]ATATTTGACATTCTT | 57531 |
rs540839575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713957 | TTTGTTTTTTATAAG[C/G]TCATAGGATACGGGG | 57531 |
rs540858443 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802836 | AACACATTCAAAAGC[C/T]AGCAGAAGGCAAGAA | 57531 |
rs540890786 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831850 | GTGAGCCGAGATGGC[A/G]CCACTGCACTCCAGC | 57531 |
rs540929326 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104724041 | GTTCAGCTCACAAGA[C/G]CATAAATGATCCTTG | 57531 |
rs540936998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716782 | ATCATACAGGTTATA[A/T]TTTTTGCCACAAAGC | 57531 |
rs540946537 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104761828 | AATATCCAGAATCTA[A/C]AAAGAACTTAAACAA | 57531 |
rs540953423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819697 | AAACAGACACATAGA[C/T]CAATGAAACAGAATC | 57531 |
rs540957805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810678 | CTGTATTACACACCT[A/G]CAACAATGCATGACA | 57531 |
rs540978877 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104721287 | AGGCAGAGGTTGCAG[C/T]GAGCCGAGATCACCC | 57531 |
rs540981651 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104838128 | GTCAAAATGTCCATA[C/T]TACTCAAAGCAATCT | 57531 |
rs540981712 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104699741 | TAGACAGTGGTAAAG[C/T]TGATATTAAAGACAT | 57531 |
rs540988767 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769507 | AATAATAAACATGCT[A/G]CAAGGTGAACAATCT | 57531 |
rs540991943 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702169 | TTCTGTCAAGGATAG[-/A]AAAAAAATATTTATA | 57531 |
rs541004668 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104740710 | GACCAGATGGATTCA[C/G]AGCCAAATTCTACCA | 57531 |
rs541014222 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772402 | TATACACATACACAT[-/AC]ACACACACACACACG | 57531 |
rs541017616 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104818236 | TATAAGAAAAACAAG[-/T]TATTTCAGTCACTAT | 57531 |
rs541028601 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857956 | AGTGAGACTCCGTCT[-/C]AAAAAAAAAAAAAAA | 57531 |
rs541039397 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104683817 | GTACACGCCATTCCA[A/C]CCCAATCTCGGGTAC | 57531 |
rs541069713 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838798 | AACAAAGTAAAGAAA[C/G]AACCCATAGAATGGG | 57531 |
rs541073748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104734613 | GGTGAAGCTAGCTCC[A/G]TGTTGTTTCCCCTCA | 57531 |
rs541110802 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706807 | TGTGTAGACTGACAA[A/T]GAAAAAGACTCAAAT | 57531 |
rs541123806 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104739557 | AACCAACAAAGATCA[A/G]AAGAGACAAAGAAGG | 57531 |
rs541146652 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104829642 | CCCTTTACCTGTATA[C/T]GATCATTGCAGGTAA | 57531 |
rs541146779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733580 | GTAATTGGCCAGGCG[C/T]GGTGGCTCACGCCTG | 57531 |
rs541151062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726798 | CCTTATATGAAACTA[C/T]CATGTTTTAAGAATT | 57531 |
rs541162379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722700 | ACCTAAACATATGCT[A/G]TACTGCACAGTTTTT | 57531 |
rs541170179 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104794064 | TTAGAACCTAGAATC[A/C]GCTATTTACTAATGA | 57531 |
rs541197987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690069 | GCTATTTTGCCACCC[A/C]ATGCTGGTTTGCCTG | 57531 |
rs541209158 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860009 | ACGCGGGCGCAGGGC[G/T]GAGTATGCGGGAAGC | 57531 |
rs541222596 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800565 | AGCCTCTGCTGGTGA[C/T]ACCCAGGCAAACAGG | 57531 |
rs541247263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852469 | ACTCTATACAAAAAG[C/T]GAAAAGGAGAGGAAG | 57531 |
rs541249761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807726 | AAATCAATGTGTGCC[C/T]ATATTTTACATGACA | 57531 |
rs541281129 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829356 | AGATAAAACAATACA[A/C]TTATACACTGAGATG | 57531 |
rs541305166 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104687099 | TAGGATAATTTCAAG[C/G]AGAACCCACAAGCCC | 57531 |
rs541316658 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104720458 | CTCGGTATCTGTGGG[C/G]GATTGGTTCTAGGAC | 57531 |
rs541324198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104815327 | TAGAGATCTGTGAAA[C/T]TTTAAACTTGAAAGA | 57531 |
rs541331879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746817 | AAGGGAGTGGGACAG[C/G]CTTTACGCATGTCTT | 57531 |
rs541360380 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778312 | AAGAGCAGTAAAAAC[C/T]CCAAGAACTTGCTAA | 57531 |
rs541366306 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727216 | ACACATACATGTATA[A/C/T]GAATATATATACACA | 57531 |
rs541369796 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104705160 | GTTGTGCCAGCTCTA[A/T]GGCTTCTAGTTCTAA | 57531 |
rs541384436 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830399 | ATAAAAGACAAAAAA[C/T]GCAAATGAACAATGG | 57531 |
rs541400492 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | HACE1 | GRCh38.p7 | 6:104793254 | CCTGGGCGATAGAGC[A/G]AGACTACATCTCAAA | 57531 |
rs541401624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696575 | CAGGAGTTTGGTCTT[C/T]GGAGGGCATAGGGGG | 57531 |
rs541405282 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727536 | ACGTATGTATATGAA[C/T]ACACACACACGTATG | 57531 |
rs541413041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104776023 | TTAGAGAGCTCTCAA[A/G]TATGCCTCACACAAA | 57531 |
rs541427977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706667 | TGGTAGAGAGAAAAC[A/G]GGGAGGTTACATCCT | 57531 |
rs541428537 | snp | C/G | 0.00159617 | 0.0282053 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682733 | ACCTGCCTCTTTCCA[C/G]CAGGAGCCCGTGCTC | 57531 |
rs541451914 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781361 | ACTTTCTTACACAAT[A/G]AGATGTTGCAGGCTT | 57531 |
rs541469168 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735185 | TCTATATTTAACTTT[C/G]ATACACCAAGAAAAC | 57531 |
rs541510107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793127 | AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGCCCA | 57531 |
rs541562363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800531 | AGGAAGGAACAGGCA[A/G]CAATATTTGCTGTTC | 57531 |
rs541577978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768672 | AATGTATAACATTAA[C/T]AATCAAGACCCTGCT | 57531 |
rs541578015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761113 | AATATCATAAAAATG[A/G]CCTTACTGCCCAAAG | 57531 |
rs541578996 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859985 | GTTGGGGGCGCCCAG[G/T]CCACGCCAACGCGGG | 57531 |
rs541597118 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747716 | AGTTTTCTCATCTGT[A/T]AAATGGGGACAATAG | 57531 |
rs541622888 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792715 | AGGATGCTGGCAAAC[A/T]GAAAAACTGCATCTG | 57531 |
rs541630746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689538 | TAAGTGGATTCATTT[C/T]AAATGGCTGTTTTCT | 57531 |
rs541654318 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104739004 | CCAGAAAAGAGTGGG[A/G]GCCAATATTCAACAT | 57531 |
rs541662069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761726 | ACTAAAGAGCTTCTG[G/T]ACAGCAAAAGAAACT | 57531 |
rs541715397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755686 | TGAATGACTCTTGGG[C/T]AAACAACAAAATTAT | 57531 |
rs541757346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799969 | TAGCCAAGGGAAGCC[A/G]TGACAGACTACCTGG | 57531 |
rs541770976 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104775916 | GAATGTAAACATTTG[C/G]GGAGAGAAAAGATTT | 57531 |
rs541775044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727224 | ATGTATACGAATATA[C/T]ATACACATATATGTA | 57531 |
rs541779907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698113 | ATGATAATAATTCAC[C/T]TCCAGGGTCATATAA | 57531 |
rs541794402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748803 | AGCTAAGAAAGCCAG[A/G]TACATTCTATTTACA | 57531 |
rs541799067 | snp | A/G | 5.99994e-05 | 0.00547687 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852392 | TAAAAAAAAACAAAG[A/G]GTTCATTTATCCCCT | 57531 |
rs541821366 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722487 | AATGAATGACTGCCA[C/G]GCATTAGCCTTATTT | 57531 |
rs541843283 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104844934 | CTCCCTAAGTGCTGG[A/G]ATTACAGGCGTGAGC | 57531 |
rs541859937 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806921 | AGTATAAATAGTCCA[C/G]ACAGTTGTAATATTA | 57531 |
rs541881736 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104738141 | ACTAACAAACAGAAA[A/G]GACATCCACACCAAA | 57531 |
rs541893189 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104739647 | ATGCACCCAATACAG[C/G]AACACCAAGATTCAT | 57531 |
rs541914774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706071 | GGACAAAACAGGATA[A/C]AAATAAACTAAAAGA | 57531 |
rs541953693 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104743078 | CAAAAAACCAAACAC[C/T]GCGTATTCTCATTCA | 57531 |
rs541964519 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851756 | ATTTTTTTAACTTGT[C/T]TCAAAATAGTTTCTC | 57531 |
rs541964862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782908 | ACAGTCTGTCCTACA[C/T]ATCTGGCAAATTATT | 57531 |
rs541973665 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850131 | ATTTTTGTATTTTTA[C/G]TAGAGATGGGGTTTC | 57531 |
rs542005853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697027 | GCTTATATTCACAGG[A/G]TTTTGTGTGTGTTTG | 57531 |
rs542063909 | in-del | -/TAAAAG | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854930 | ACAACTTTTTCACTA[-/TAAAAG]TAAAATACTAATAAA | 57531 |
rs542064609 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825451 | CTGATTGGCTGCACA[C/T]AGCAACCAATCAGAC | 57531 |
rs542082306 | in-del | -/C | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104767901 | TCTTACTCTTATCTT[-/C]CTTTTTTTTCTCCAA | 57531 |
rs542104975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797738 | AGAATTGTGTAACTA[C/T]CACTCCAGGGAAATT | 57531 |
rs542110396 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804447 | GCTGGCAGCATCATG[C/G/T]TACCTGACTTCAAAC | 57531 |
rs542122749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711542 | ATACAGCTGAACTCT[A/G]TGTTGACACACACAC | 57531 |
rs542132437 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104754010 | AGCTAAGAATCACAA[A/T]AAAACAATACAGGAG | 57531 |
rs542142351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830302 | TTCCCACATAGAATA[C/T]GTTTTAAATTTAATA | 57531 |
rs542144245 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104822097 | GCGTGGGCCGGGCGC[A/G]GTGGCTCACACCTGT | 57531 |
rs542152526 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699772 | TCTACTAGCACATGG[A/T]AGCTGAGCATTAGCA | 57531 |
rs542163706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703884 | ACTTTGGGAGGTCCA[A/G]GTGGGCAGATCACTC | 57531 |
rs542166366 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749498 | TTAAAGGTATATATC[C/T]GTATCTGTATCCATA | 57531 |
rs542178796 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104836416 | AGACATACAAACTGC[A/G]AAGAAAGAAATAAAG | 57531 |
rs542181401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822579 | TAAAAAAAGTAGGCC[A/G]AGCGCGGTGGCTCAC | 57531 |
rs542194919 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783855 | GAGTTTCATTAAGCT[C/G]CTTTCAGGAAATGTG | 57531 |
rs542221201 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833133 | TGCTGCACAAGGTCA[C/T]GGAGTAGTTCTGTCC | 57531 |
rs542234842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775352 | TTGCGCCACTGCCCT[C/T]TAGCCTGGGTGACAG | 57531 |
rs542254275 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829583 | CTTTATGTTTATATG[A/G]TCATCATAGGTAACG | 57531 |
rs542260050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825631 | TCAGCCTCTGATTGA[C/T]TGCAGGCCACCACTT | 57531 |
rs542288591 | snp | G/T | 6.59065e-05 | 0.00574012 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772003 | CTAATCCCAAGATCT[G/T]CCCAGCAAACCGAAA | 57531 |
rs542291515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840503 | TTAGCATGCTATTTA[G/T]ATATAGAGACAACAT | 57531 |
rs542293887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104844138 | CGCCTCCCAGGTTCA[A/G]GTGATTCTCTTGCCT | 57531 |
rs542294523 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729368 | TAGAATCAGATTTTG[A/C]CTTAATACAATCTTG | 57531 |
rs542307200 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791760 | TGTTTCATATTATAA[G/T]GTAACTGGAGTACAA | 57531 |
rs542311368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104799861 | ATGAGGTACCTGGTC[A/G]ATCTCATTGGGACTG | 57531 |
rs542326254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104707256 | GGTTCCTTGTAAATA[C/T]AAGTTAGAAAATCTT | 57531 |
rs542339532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692927 | TAGTGAAGGCCATAT[C/G]ACAATGAAGATTAAA | 57531 |
rs542402595 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860541 | TGATGACACAGCCTA[A/G]TGGGAAATCCAAAGG | 57531 |
rs542415398 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756320 | AGGAGGCTGAGGCAG[A/G]AGAATTTCTTGAACC | 57531 |
rs542425588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700715 | TTGCATGACTAGGAA[A/G]AGGTCAAAGGGGCAT | 57531 |
rs542456976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848183 | TGTTTAGGCCGGGTG[C/T]GGTGGCTCACGCCTG | 57531 |
rs542461271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743063 | AAACTATCGCAAGAA[C/T]AAAAAACCAAACACC | 57531 |
rs542461769 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104813243 | CTGTAATTCTAAGAC[A/T]TTGGAAAACCAAGGT | 57531 |
rs542507258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809362 | CAGGAACTGCCTTCC[C/T]AAAAAGTTACTTAAT | 57531 |
rs542544871 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808573 | CAAAATTCAAATACA[A/G]AGAAAACAGTTTCAG | 57531 |
rs542549547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805181 | CGCCAGTTAGAATGG[C/T]GATCATTAAGAAGTC | 57531 |
rs542575187 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854265 | GACTAAAGAAACATA[A/C]CTAAAGGCAATGTGG | 57531 |
rs542641795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853738 | AATAATATATGCTCA[A/G]TATCATATAGTTACT | 57531 |
rs542666703 | snp | A/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104743946 | AATCCTAACTGGAGA[A/T]GCTTTTTAATATATT | 57531 |
rs542687615 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104711209 | ACCTATGTGTCCTTA[A/T]GTTATTACAAAACCA | 57531 |
rs542708690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787969 | CTTCAATCATACATA[A/C]ATTAAAACTAAATCC | 57531 |
rs542710353 | snp | A/G | 1.68704e-05 | 0.00290429 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796703 | TTGAATAATAGTCTG[A/G]AAAAGCCTCGGGTGA | 57531 |
rs542711575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779752 | ATCTTAAGGAAATTA[C/T]TAATCCTCACAGAAC | 57531 |
rs542715543 | snp | A/T | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682823 | CTTGGCTCCCTGAGG[A/T]TGAGGCGCTTCTGCC | 57531 |
rs542752367 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104693523 | GTTTGCATATAATCT[A/G]TGCACATTCTCTAAA | 57531 |
rs542752784 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727738 | ATATGTATATGAATA[C/T]ATACACACATATATA | 57531 |
rs542800114 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729467 | CTGTGATTTTATATT[C/T]TCTAATTGTATCACA | 57531 |
rs542818244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104790269 | TTCTTGCAAACTTTA[C/T]TTTTACCTTTTTGCA | 57531 |
rs542818514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838671 | GTAATACCCCTTGAG[C/T]AAATTTCTTGAGTAA | 57531 |
rs542820947 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104796068 | ATTCCTCCACAGAGT[A/C]TTTTCCTCTTGCCAT | 57531 |
rs542839931 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784686 | TTCTCATCAGCAGAC[G/T]ATATCAACAAGTGAC | 57531 |
rs542857210 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812222 | ATGAGGCAATAGGTG[A/G]CTTGAGGCCAGTAGT | 57531 |
rs542876460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793982 | CTATTGTTTTGGTCA[C/T]GGGTTCCTTTTTCCT | 57531 |
rs542913998 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104699949 | GATAAATGAGGGTCT[C/G]TCCCTCCTTATTGTG | 57531 |
rs542934915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698883 | TACCTAAAGTGTTTT[C/T]ATATGTTTGTTTTTG | 57531 |
rs542959278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754716 | AGGAGAAATAAGATC[C/T]TTTTCAGAAAAGCAA | 57531 |
rs542960613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691181 | CAAAAGAAAAAAATG[G/T]GTAAAAATAGTAACT | 57531 |
rs542991209 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832473 | ATCTCAGCTCACTGC[A/C]ACCGCTGACTGCTGA | 57531 |
rs542991263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104743027 | GGGACATGGATGAAA[C/T]TGGAAATCATCGTTC | 57531 |
rs543042086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779588 | TAACAAGCTGGAATA[C/T]AAAGTACTTGAAATT | 57531 |
rs543048807 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104757918 | TAAGCTCCAATAGCC[A/G]ATTCGATCAAGTGGA | 57531 |
rs543066562 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857734 | AGGCCGAGGCGGGCA[A/G]ATCACGAGGTCAGGC | 57531 |
rs543079034 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | HACE1 | GRCh38.p7 | 6:104742035 | ATCTGATCTTTGACA[A/C]ACCTGAGAAAAACAA | 57531 |
rs543082735 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104763605 | GGTTAAAAAAAAAAA[A/G]GGGGCATACCATTAA | 57531 |
rs543129681 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704839 | GCTTCAGATGTGAAA[C/T]GTACTTGCTGGTGGC | 57531 |
rs543133498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847204 | GTCTTATGACTAAGT[C/T]GCCTACTGAAATGAC | 57531 |
rs543161095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770133 | TATAGTTTAAAAAAT[A/G]GCTCAGTGAACATTG | 57531 |
rs543170760 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853708 | AATCAACTGACAAAG[G/T]GTAACATCACCAAAA | 57531 |
rs543172280 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104831348 | CCAGCACTTTGGGAG[A/G]CTGAGGCAGGCAGAT | 57531 |
rs543188911 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814763 | TCTCATGAGAGCTCA[C/T]GGTTTAAAAGTGTGT | 57531 |
rs543198937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104777517 | AATAGTTTGACTACC[C/T]AGAGAAATGTATTTT | 57531 |
rs543213001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757728 | GTAGGCTTCAGAAGG[C/T]TGGTAATAACAAACT | 57531 |
rs543215731 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750607 | ACATCTCAGCAAATC[A/G]GCAAGCCACTATTCA | 57531 |
rs543225557 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845384 | AACTGACAAGTTACT[C/T]TTCTTGCTTTTTGTA | 57531 |
rs543274729 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730748 | CTGATTTGAGGGCCC[A/G]AACAAGTCATATTTA | 57531 |
rs543306165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104740572 | TAGAAGAAATGGATA[A/C]ATTCCTCGACACATA | 57531 |
rs543313546 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766445 | ACTCTGAATTATGGA[C/T]GCTCAACCTGTATAC | 57531 |
rs543352272 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834377 | ATTTTACAAGTAACA[C/T]ATGTATCTTACATAA | 57531 |
rs543353367 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104688581 | AGTGGCCTAAGGCAA[C/G/T]GCAAATTTATTATCT | 57531 |
rs543365404 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734436 | AAAAAGAAAAAAAAT[G/T]TATACTTTTGGTTTT | 57531 |
rs543405834 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692797 | CTAATTAATTTCTAA[C/G]AATTTAATGCCATGT | 57531 |
rs543506789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104734332 | TTTTCAGTAAGGTTG[C/T]GCTAAATTATACTAC | 57531 |
rs543511182 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104802392 | TCTACAGAACTCTCC[A/G]CCCCAAATCAACAGA | 57531 |
rs543522991 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104785626 | AATTTTCAAATGTTT[A/C]GTTTTAAAAGCACAC | 57531 |
rs543560985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690221 | CCCTCTCCAAGGCTT[A/G]TCAGTTTTGTGAACT | 57531 |
rs543580322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683564 | AGGTTTGCTATGAAG[C/G]CTGATAAATAAAAGG | 57531 |
rs543616233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830467 | TATAACCCTCCATTT[C/T]TCCAACACCATATTA | 57531 |
rs543616314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104837972 | TATGACAGCTACAAA[C/T]AAAATAAAATACCTA | 57531 |
rs543621695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691011 | AAAAATCGCCCCACG[G/T]TTCTTTCTTTTCTTC | 57531 |
rs543624859 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774748 | TTACTGGCCCCAAGA[C/T]TGTATCAAAAGAATA | 57531 |
rs543628666 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104845315 | TTAATATTCAATCTT[A/G]TAAGTCAATAGCTAA | 57531 |
rs543658485 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726722 | CCAGATAGTTTCATT[A/G]ATCAGTTTCCTATAA | 57531 |
rs543666495 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800477 | AGGGGCAACAGACAC[C/G]TCATATAGGCGGGTG | 57531 |
rs543674376 | in-del | -/TG | 0.199276 | 0.258862 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852199 | TATGTCCAAACTGTC[-/TG]TGTGTGTGTGTGTGT | 57531 |
rs543695387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697179 | TTTTCTTGCTTATTG[C/T]GTAAATTGCATTCAT | 57531 |
rs543696161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807939 | CGTCTGTAATCCCAG[C/T]ACTTTGGGAGGATGA | 57531 |
rs543703386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706912 | AAAAACCATATACCA[A/G]TAAATTAGATAACTT | 57531 |
rs543718622 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104706082 | GATACAAATAAACTA[A/G]AAGAACAGGGTCCTT | 57531 |
rs543758643 | in-del | -/T | 0.243347 | 0.249911 | intron-variant | HACE1 | GRCh38.p7 | 6:104809656 | AACAAGAGCAGATTC[-/T]TTTTTTTTTTTTTTT | 57531 |
rs543770432 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707854 | TGGAAATTAAGTTTC[A/C]ACATGAATTTGGGAG | 57531 |
rs543783012 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104808615 | TGAATATGATATAAT[A/G]TATTATATCTAGTAA | 57531 |
rs543820774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816313 | TAGGAGGGGAAAATG[C/G]CTTCACAGGCCGGAC | 57531 |
rs543822423 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759535 | TACCAGAATCTCTGG[A/G]ACACATTTAAAGCAA | 57531 |
rs543826352 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821290 | AAGCCCCGTGACACA[A/G]GTTTACCTATGTATC | 57531 |
rs543827908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821027 | AAAAGAACGTGACAA[C/T]GTCCTTTTCAGGGAC | 57531 |
rs543835370 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769668 | ACAATTAATTTTGCA[A/T]ATAGTATGAAGAACA | 57531 |
rs543836631 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762510 | ACAATGAGAAACACA[G/T]GGACACAAGGAGGGG | 57531 |
rs543863528 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771817 | CAGATGGGCTCCAAT[C/G]AAAATAAAAATTATC | 57531 |
rs543875420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770073 | CTGAGTTCGAAGAAT[G/T]GTTAAACATAACCCT | 57531 |
rs543878947 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104812375 | CATTTGAGCCCAGGA[A/G]TTCAAGGCTACTATG | 57531 |
rs543883451 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755512 | ACACTTATTCTGAAA[C/T]TGATCACATAATCAG | 57531 |
rs543887069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104784245 | ATGCAAATTCAGATA[C/T]ACTGACACTGAAACA | 57531 |
rs543901469 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104826944 | TGCGGAGGAACCGCA[A/G]AAGAAAAGCATAGGG | 57531 |
rs543908134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776111 | CAAGCACCATTTCAA[C/T]AAGGAGAGTTAATTA | 57531 |
rs543909446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760225 | CATCCTGATACCAAA[C/G]CCTGGCAGAGACACA | 57531 |
rs543929029 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104823051 | GTCATAGCCTTGTAT[C/T]TGGTTGGTGAAAAAG | 57531 |
rs543962519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687143 | GGATATTTCAAAGTC[A/G]AAAACCATATTTAAT | 57531 |
rs543972783 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715675 | ATATGGAAATAAATA[C/T]AAATGTACAATAAAT | 57531 |
rs543974670 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104699025 | CCTAGCCTTAACATG[-/T]TTTTTTTAATATTGT | 57531 |
rs543975869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739610 | TCAATTCAACAAGAA[C/G]AGCTAACTATCCTAA | 57531 |
rs543979941 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104784893 | ACTTTAAATCAACAA[A/G]TTATTATTTGTTGTT | 57531 |
rs544009536 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682829 | TCCCTGAGGATGAGG[C/T]GCTTCTGCCTAACTT | 57531 |
rs544010546 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842328 | AAGGTTTTATTGGCC[A/G]GGCACAGCAGCTCAC | 57531 |
rs544027540 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687946 | AAGATTTCCATGAAG[G/T]GGGGCTGGTTGGGCA | 57531 |
rs544027703 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809203 | GTAAAATAAACACTA[C/T]TCTTGCTTTCACTGA | 57531 |
rs544048899 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833939 | GCGGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC | 57531 |
rs544065310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104781431 | TTCTCCAAGGAGCCC[C/T]GGTTCATTGAGAATG | 57531 |
rs544069946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797551 | TGTAAGAGAATCTGG[A/G]GAAAAAGGGAACATG | 57531 |
rs544178227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766137 | TGCACAAATGCACAT[C/T]GGCCTTGGCCCCACG | 57531 |
rs544183915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789496 | AAAACATAAAGTCTG[C/G]GTTCTATTTTTTAAA | 57531 |
rs544312722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724875 | ACCAGTTCGTACACT[A/C]ATCTATGCTTTGCAG | 57531 |
rs544333203 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810569 | ACATAATATGTAGGT[C/G]TGTATATATTTTTAC | 57531 |
rs544357599 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811971 | CATATACAGGCTCAA[C/T]TTCACTGATTGCCAT | 57531 |
rs544371963 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851342 | CTGCCTCGGCCTCCC[A/G]AAGTGCTGGGATTAC | 57531 |
rs544386286 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691980 | GAGGAAGGAAGGAAG[A/G]GAGGGAGGGAGGGAA | 57531 |
rs544389754 | snp | C/T | 0.00362159 | 0.042399 | intron-variant | HACE1 | GRCh38.p7 | 6:104784384 | AAAGAGAGGAAAGGC[C/T]AGCAGGGTACTCCAC | 57531 |
rs544403931 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104758922 | CTCTGATAAAACAGA[C/T]GTTAGACCAAAGAAG | 57531 |
rs544456595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737685 | AGGGTCCTACCCCAC[A/G]GAGTCTCGCTGATTG | 57531 |
rs544472420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702439 | TTGTTCCTATGTTGT[C/T]AAATAGACAAGCTTG | 57531 |
rs544481177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744942 | CTTTGGTTTACTTTA[C/T]ATTTTTACAATTCTT | 57531 |
rs544500751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818924 | TATGACAAACTCACA[A/G]CCAGTATCATAATGA | 57531 |
rs544511842 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834744 | CACCAGTATTAGAGA[A/G]ACCCCCCAAAAAATG | 57531 |
rs544518422 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104771027 | AAAATAATCCTTTCT[A/G]ATTCAAAATTTAACA | 57531 |
rs544529250 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728559 | GAGAAAATCTGCATA[C/T]GTCATTCTACAAACA | 57531 |
rs544544068 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760484 | AAAAGGCCTTTGACA[A/G]AATTCAACAGCCTTT | 57531 |
rs544545304 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821787 | AATTCAGATTACTAA[A/G]TAGTATTTATTTAGT | 57531 |
rs544639272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724209 | TTTACTTTCATCACA[C/T]AGCTTTGGCTCCCTT | 57531 |
rs544645831 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826274 | TATGCACGACTCTAG[A/C]TACTCGAGTTACAAC | 57531 |
rs544657702 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729542 | ATGATCCTTTATAAA[C/T]TGGAAGCATCAGCCC | 57531 |
rs544663160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848897 | AGTGAGAATCTAATA[A/T]ATTAATAAATATGAT | 57531 |
rs544664798 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104762564 | GAGGGTGGGGGGCTA[C/G]AGGAGGGATAACATT | 57531 |
rs544666334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104781789 | ACTGGGACCCTCTTC[C/T]ACACAGACACACTTC | 57531 |
rs544682084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703914 | CATGGCCAGGAGTTC[A/G]AGACCAACATGGCAA | 57531 |
rs544683876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104833846 | AAAAATTAGCTGGAC[A/G]TGGTGGTGCGTGCCT | 57531 |
rs544711254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765382 | TGCCTGTTGCACTAG[A/G]ACATCCCTGCACATT | 57531 |
rs544718797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723534 | CAGTACCTAAGACTT[C/T]TACCAAGGACATTCT | 57531 |
rs544725097 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104730248 | TTAGATCTCTGATCA[C/T]TCAAAATTAATCAAA | 57531 |
rs544738827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855324 | GGCAGGCACCTGTAG[G/T]TCCAGCTACTCGGGA | 57531 |
rs544816853 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758858 | ATAGAGGAAGATCTA[A/C]CAAGCAAATGGAAAG | 57531 |
rs544844714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723380 | TCATTTGGTTAACAA[A/G]TATCCCAGAAACCTT | 57531 |
rs544888103 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700746 | ATTCGCTGAGGGTCC[C/T]TCTGGATCAGTGAAA | 57531 |
rs544899725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780299 | ACACACACACACATA[C/T]AAACACCTACACAGC | 57531 |
rs544907953 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729296 | CCTCATATAATATAT[C/G]AGAAATTAGGAGAAA | 57531 |
rs544917468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736970 | ATTAAACACTACTTT[C/T]AAAATAAAAAACACA | 57531 |
rs544919093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825123 | AATGCAAAGAAAATG[A/G]CAGAATATATGGATC | 57531 |
rs544979242 | snp | A/G | 0.000164886 | 0.00907831 | synonymous-codon, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811355 | TGATACATTTGGCCT[A/G]TTAATATCAGCACCA | 57531 |
rs545046400 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737387 | GAGCCACGCAAAAGA[A/C/T]GGTGATTTCTGCATT | 57531 |
rs545050675 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104806418 | AGTGAGTTATGATCA[C/T]GCCACTGCACTCCAG | 57531 |
rs545082294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104825729 | TTCTGTATCCAGAAC[C/T]TTGAGCAGCTGCTGG | 57531 |
rs545099008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772140 | GAAAGATTACTTCGA[A/T]GCAGATAAACTAATT | 57531 |
rs545117516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104687074 | ATCACTCAAATCACA[C/T]AGCACATTTTAGGAT | 57531 |
rs545120844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855191 | GGCTCACGCCTGTAA[C/T]CCCAGCACTTTGGGA | 57531 |
rs545130921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781268 | GCTCAAATTCTTCCA[A/G]ATTTGGTAGTGGGAG | 57531 |
rs545160477 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104734503 | GTTCGAGGTAAAATT[C/T]AAGATTTTAAAAAGC | 57531 |
rs545182231 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711256 | TAACTCAGTTTTTTT[C/G]TTCACTACATTCGAT | 57531 |
rs545190525 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763704 | CAGCTGTTAAACAGA[A/C]GCAACAAACAGCAGG | 57531 |
rs545193341 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104779534 | GCACTGGTGTTATAT[C/G]CATTACTGTGCATAT | 57531 |
rs545201843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817289 | AGAGAGGTCTGGGGG[A/G]AGGTGACTGGATCAT | 57531 |
rs545233789 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104744794 | TGACGCTGATAATCT[C/T]AAATATTATAAGATG | 57531 |
rs545244296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796156 | TCGCCCAGGCTAGAG[A/T]GTAGTGGGCAGTGAC | 57531 |
rs545256427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743079 | AAAAAACCAAACACC[A/G]CGTATTCTCATTCAT | 57531 |
rs545271025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786902 | CTTTCTTTTAAAGAC[C/T]GCCATGGAAGGAGAT | 57531 |
rs545274578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104709226 | CTCAATAATAAAAAC[A/G]ACTCAGCTTTAAAAT | 57531 |
rs545276203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825086 | GACTCCGTCTCAAAA[A/G]AAAAAAAAAAAGAAA | 57531 |
rs545292172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751989 | AAAAAAAGACCAAAA[A/G]AAGGCACTGAGCCAG | 57531 |
rs545296794 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104787110 | GGCCTTCATTTACAC[A/G]TTCAACCAAAAAGCA | 57531 |
rs545303809 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778655 | AAAATGTTTTAATTA[G/T]CCAAGCGTAGTGGTA | 57531 |
rs545314218 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784011 | TGAAGTGTAATAATT[A/G]TTCCACTAAACAGTA | 57531 |
rs545326281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693064 | GTGTGTGTGCACGCG[C/T]GCGCGCGCTGGGGTG | 57531 |
rs545373773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800039 | AAGGTCTTAGTAAAC[A/G]ACACACCAGGAGATT | 57531 |
rs545378742 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758479 | AAGAGAAATAAAATC[A/C/T]TTTCCAGACAAGCAA | 57531 |
rs545413894 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806801 | AAAATTTAACTAATA[A/T]GAAACTTGTGGTGGC | 57531 |
rs545439345 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851056 | TAAAAACATAATAAA[G/T]CAAGTTAACAACTCT | 57531 |
rs545441254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761598 | ACCATAAAAATCCTG[C/T]AAGAAAACCTGGGCA | 57531 |
rs545458418 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104761144 | TCATTTATAGATTCA[A/G]TGCTATCTCCATCAA | 57531 |
rs545462463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758812 | AGACCCATCTCACGT[G/T]CAAAGACACACATAG | 57531 |
rs545465365 | in-del | -/AAAT | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104715405 | AATGAACTGGAAGAC[-/AAAT]AAAAGTATTTTGCAT | 57531 |
rs545521386 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104733627 | GGAGGTCGAGGCTGG[G/T]GGATCACTTGAGATC | 57531 |
rs545524710 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104844337 | ACCACGGTGGCCCAT[C/T]ATAAACATTTTTTTT | 57531 |
rs545537202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104805817 | TATGTAACAAACCCG[C/T]ACGTTGTGCACATGT | 57531 |
rs545542256 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861892 | AACTTTCTGCAATGA[C/T]AGAAATATTCTATAA | 57531 |
rs545592536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775179 | AAACCTCATCTCCAC[A/T]AAAAGAATAGAGAAA | 57531 |
rs545633272 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859892 | CAGCCCCCGCCGCCG[C/T]GTCCCTCCCGGGCTC | 57531 |
rs545647316 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699155 | ATATCAGGAAATGCC[C/T]CTAGTGGTATTATTT | 57531 |
rs545650280 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728305 | AAAATCAAAACATAA[A/G]ACATTATTAGCTTCA | 57531 |
rs545692881 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840890 | ATTGCTTGAACCCGG[C/T]AAGTGGAGGGTGCAG | 57531 |
rs545746939 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705235 | TTGCCTTTCCCTGAG[A/T]TCTGATAAAAACTGC | 57531 |
rs545768842 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | HACE1 | GRCh38.p7 | 6:104741895 | TGGAGGCATCACACT[A/T]CCTGACTTCAAACTA | 57531 |
rs545778587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782212 | ATTGAACTTGTCCGG[A/G]TGTGGTGGCTCATGC | 57531 |
rs545794549 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104732763 | CTATTTGAAATCACT[A/G]ATATGTATACATCCA | 57531 |
rs545805727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755798 | GTTAAGAGGGAAATT[C/T]ATAGCACTAAATGCC | 57531 |
rs545810960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821321 | AAACCTGTATTTGTA[C/T]CCCTGAACTCAAAAT | 57531 |
rs545817207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747745 | AGTACTCACCTCAAG[A/G]GATTTTTTGTGAGCG | 57531 |
rs545840797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814262 | ATCAAAAGACCTTCA[A/G]CGAGGCATGTCAAAG | 57531 |
rs545884027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712561 | GGTGGATCATGAGGT[A/C]AGGAGTTCGAAACCA | 57531 |
rs545903430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719837 | TGAAGTGTAATTTAT[A/G]GAAATCAACTTTACT | 57531 |
rs545906223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761083 | AACATTCCATGCTTA[C/T]GGATAGGAAGAAGCA | 57531 |
rs545920969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731409 | AACCTCAAATAGCCT[A/T]AACAGTCTAGAAAAA | 57531 |
rs545935667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104798479 | GTCTATCACTCTCTT[A/G]ATACTTTATTATTAT | 57531 |
rs545935793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858721 | ACAACCTCCTCCCAA[C/T]CCTTCTCTCACTTGG | 57531 |
rs545940208 | in-del | -/CGC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762716 | TAAAAAAAGGCCGGG[-/CGC]GGTAGCTCACACCTG | 57531 |
rs545950902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857593 | AAAACAGTATTTAGA[A/T]TCAACATTTGTTACA | 57531 |
rs545959528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725315 | ACATAGGCATATGAT[C/T]TGGAGAAACAGGGAA | 57531 |
rs545992003 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104753892 | CAAAAGCACAGAACT[A/G]GTCTGAGGCTGAGAT | 57531 |
rs545997271 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822623 | GCACTTTGGGAGGCC[A/G]AGGCAGTCGGATCAC | 57531 |
rs546026035 | in-del | -/TTAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736264 | GTTAATAGTTATGTC[-/TTAT]TTATTTATTATTTTT | 57531 |
rs546027327 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104790999 | AAGCAATACAAAATA[C/T]TTTAAGAAAATATCT | 57531 |
rs546048443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719134 | GCACAATAGAAACAG[A/G]CCCATGCACAGATGG | 57531 |
rs546086302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724784 | CTTTATGAACTCAAC[C/T]GTGTAAAAAATGAAT | 57531 |
rs546112751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104856521 | CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 57531 |
rs546113477 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828227 | TGCTAAAACTGAAAT[A/T]AAAAAACAACACACT | 57531 |
rs546118291 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720077 | CTCAATCTCCTGACA[C/T]CGTGATCCACCTGCC | 57531 |
rs546160415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703944 | AAGCCCTGTCTCTAC[G/T]AAAAATACAAAAATT | 57531 |
rs546188515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834883 | TCTACCCCTCCCCAA[C/T]TGTGCAAGGCCAGTA | 57531 |
rs546194022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688605 | ATTATCTTACAGTTC[C/T]GAAGGTCAGAAGTCT | 57531 |
rs546201631 | in-del | -/ACA | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104843934 | CACGCTTGGTTCACT[-/ACA]ACATCTGCCTCCCGG | 57531 |
rs546219892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738073 | ACTGACACCTCACAC[G/T]GCAGGGTATTCCAAC | 57531 |
rs546229083 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104835344 | GGAAAAAGGAACCAT[C/G]AATATTCAAGAAAAA | 57531 |
rs546244103 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104695143 | GATAATAAAACGGTT[C/G]CCATGTTCTAAGCCT | 57531 |
rs546270905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745385 | TATCACAGTTAGAGA[G/T]GCTTACATAGTCAGG | 57531 |
rs546278464 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805091 | CAATTATGCAACCAA[C/T]AGACATGAAAAAATG | 57531 |
rs546286192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104812504 | TGGATTGAACACATC[A/T]GTTCATCTTTTTTGC | 57531 |
rs546287829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710455 | GGTAGCAATGCTCTT[C/T]GTTGTGAGGATAATG | 57531 |
rs546298191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711059 | ACTGGTGGTCAATGT[C/T]ACATGAACGCAGAGC | 57531 |
rs546312476 | snp | G/T | 1.64811e-05 | 0.00287059 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849149 | ATAGTTACCCATTTC[G/T]TGCTGCCAAATGAAG | 57531 |
rs546322309 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104799186 | ACACTGTTATAAGCA[C/T]TGTTAAATTAAGCAA | 57531 |
rs546355480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820051 | AATACAAAAATTAGC[C/T]GGGAATGGTGGCACA | 57531 |
rs546358184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695762 | CACCATCTCTAACAT[A/G]GTCTCTAAATACTGA | 57531 |
rs546368109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704409 | CAGCATCCAAAAGTA[A/G]AGGTCATAAGTCACA | 57531 |
rs546377169 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749433 | TTATTCACTATTATA[C/T]TAAGATATACTATGA | 57531 |
rs546394641 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702748 | ACTAATAGGACGCAT[A/G]AAGACTGTGACTCTG | 57531 |
rs546467887 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692710 | ACAGGGGTTTCTTTT[C/G]AGGTTGCAACTGGGT | 57531 |
rs546485913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717948 | TGGACTTAGACATTA[C/T]GGATATCTTTCCCGA | 57531 |
rs546498017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766122 | AAAAGACATGAGTAA[C/T]GCACAAATGCACATC | 57531 |
rs546513433 | snp | A/G | 1.76291e-05 | 0.00296888 | intron-variant | HACE1 | GRCh38.p7 | 6:104811280 | TATATATATGAGCAT[A/G]TATAGCATCTGGAAA | 57531 |
rs546513775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857140 | GATTTGTATCAGTAG[A/G]AATGTTATATATATA | 57531 |
rs546529416 | in-del | -/CTGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689964 | TCTGTAAATTAAATA[-/CTGT]CTAAGAAACAGTTTC | 57531 |
rs546537080 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746287 | AACTGCTAGTATAGG[A/G]TGTGTTTTAGTCCTA | 57531 |
rs546538607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723705 | AAAAAATCTTGACTG[C/T]TGATACACACTGATG | 57531 |
rs546545677 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104686525 | AAAAAAAAAGTAACT[A/C]AGGCTTGTCCATTTG | 57531 |
rs546548913 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772340 | TTTTGACTGAAATTA[C/G]TTGGAAGATCATCAG | 57531 |
rs546552259 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104803756 | AACCCACAGCCAATA[C/T]CATACTGAATGGGCA | 57531 |
rs546583365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767892 | ACCTGCCCCATCTTA[C/T]TCTTATCTTCTTTTT | 57531 |
rs546583806 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104746048 | ACATTAAAGAAATTT[C/G]CAAAACTGTTAAACA | 57531 |
rs546592400 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761435 | CAAATCCGACACACA[C/T]AAGCAATAGGGAAAA | 57531 |
rs546600087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798837 | GTTCTGAGGAATCCA[C/T]CTTATAAAACTGCTG | 57531 |
rs546650007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788235 | CATACCATTTGTTAC[C/T]GAACAATGAGTTAAT | 57531 |
rs546654141 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104787924 | CATTGGACCTTTCTT[C/T]ACTTTTCTCTCTTTT | 57531 |
rs546676139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104857700 | GTGGCTCACGCCTGT[A/G]ATCCCCCAGCACTTT | 57531 |
rs546710615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804531 | TAGACCAATGGAACA[C/G]AATAGAGCCCTCAGA | 57531 |
rs546718520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825794 | TTCAATAAATATCTG[C/T]TTTTGCTGCTTCATT | 57531 |
rs546729754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685746 | CAACAAGCCCTGGTA[C/T]GGGAAATACAAATTT | 57531 |
rs546734438 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104836432 | AAGAAAGAAATAAAG[G/T]CCTGGCGCGGTGGCT | 57531 |
rs546738055 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789018 | GGGATCAATTGCTAC[C/T]TCAGACAAAATGTGG | 57531 |
rs546757274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693187 | CCTCTATACTGGCAG[A/G]TGTTAAACACAAAGG | 57531 |
rs546807789 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846101 | CAGTAATCTATAATG[C/T]TTCCCCTTCCAAAAA | 57531 |
rs546811578 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104765468 | CTTTCTGAGGCAACA[A/G]CAACAAAATAGTGAT | 57531 |
rs546814888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796373 | CCTCAGCCTCCCAAA[A/G]TGCTGGAATTACAGG | 57531 |
rs546840499 | snp | A/G | 0.00155439 | 0.0278349 | intron-variant | HACE1 | GRCh38.p7 | 6:104744471 | CTTACAAAATTAAAC[A/G]GCAAAACTTAACTTC | 57531 |
rs546849219 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700886 | CCTTCCCCTCTGAGT[C/G]AATGTTTAGCCACTT | 57531 |
rs546873603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751536 | AGGGGAGGCTGAGGT[A/G]GAAGCATTGCTTGAG | 57531 |
rs546897841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724448 | TATAAAAGCAACAAT[A/G]TTAGAAATCTAAATG | 57531 |
rs546906935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758617 | ACTGTAAAGACCATC[A/G]ACGCTATGAAGAAAC | 57531 |
rs546923528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764967 | AGCATACACAACATC[C/T]TTCATATTAAACTCC | 57531 |
rs546962612 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823582 | TTTTTAAAGTTTTCA[A/G]TAGCGCACTTGCAGA | 57531 |
rs546998037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737223 | CTTGAACCCAGGGGG[C/T]GGAGGTTGCAGATCG | 57531 |
rs547012675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802841 | ATTCAAAAGCTAGCA[A/G]AAGGCAAGAAATAAC | 57531 |
rs547015508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834210 | TAAGTATACTAAGCT[C/T]CCAATCATCAAATAC | 57531 |
rs547029199 | snp | G/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104683121 | GCCCAGCAGAATGGC[G/T]TCTTACCTTCGTATA | 57531 |
rs547053984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701823 | CTAGCTTTTGAAAAA[C/T]ATATGGCCGTTATTC | 57531 |
rs547061263 | snp | C/G | 1.95345e-05 | 0.0031252 | intron-variant | HACE1 | GRCh38.p7 | 6:104729802 | CATTAAACAGGAAAT[C/G]TATAAAATTTCTGAT | 57531 |
rs547076177 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826031 | CTCTGCCTCCTGTCG[C/G]ATCAGCAGCAACATT | 57531 |
rs547101963 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851240 | AGGCGCATGCCACTA[C/T]ACCCGGCTAATTTTT | 57531 |
rs547128659 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682443 | ATAACAACTTCTAGA[A/C]GGTGTATTAGAAACT | 57531 |
rs547134070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840645 | ATCAGCCTAGCTAAC[C/T]TGGTAAAACCCCGTC | 57531 |
rs547134692 | snp | A/G | 3.29685e-05 | 0.00405995 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785162 | TAGCTCCCAGGTCCT[A/G]GAGGTTCAAATGGAG | 57531 |
rs547134855 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860105 | CTCCTCCAAAGTTGT[A/G]CAGGAGCAGTTTCCT | 57531 |
rs547143586 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104739848 | GAACTCTCCACCCCA[A/G]ATCAACAGAATATAC | 57531 |
rs547236028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851862 | CCCTCACAAAGCCAA[A/C]TAATTGTATTTCATA | 57531 |
rs547242847 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814013 | ACAGAAGTTTAAAAA[A/G]AAAATGTTCAGGAAT | 57531 |
rs547244768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840298 | ACTATGAATAGTTTT[C/T]GTGTACTCAAAAAAA | 57531 |
rs547280206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748844 | ATAGGCGAATCTCGT[C/G]TATGATTTTAGAAGT | 57531 |
rs547294837 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800688 | CAACAAAAAGGACAT[A/C]CACAACAAAACTTAA | 57531 |
rs547301953 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104738019 | TGGGTCCCTGACCCC[C/T]GAGCAGCCTAACTGG | 57531 |
rs547307158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716167 | TATAGCTTGAAGCTA[C/T]AGAAGGTAAAACTTA | 57531 |
rs547317807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756085 | AAACACAATCAGAAA[C/T]GATAAGGTAGATATC | 57531 |
rs547341073 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104830704 | AGTTAATGGTACTGA[C/T]TTTGAGTTGGTTTTG | 57531 |
rs547394592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733727 | AGTGATGTGTGCACC[C/T]GTAATTGGAGGCTAA | 57531 |
rs547419979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761162 | CTATCTCCATCAAGC[A/T]ACCATTCACTTTTTT | 57531 |
rs547440010 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822190 | GATCAACACGGTGAA[A/T]CCCCGTCTCTACTAA | 57531 |
rs547446601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689787 | AACTTCATCTGTGAG[A/G]GAAAATCACCAGCAT | 57531 |
rs547457518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727352 | ATGTATACGAATATA[C/T]ATACACATGTATATG | 57531 |
rs547466483 | in-del | -/AAAATAT | 0.422473 | 0.180978 | intron-variant | HACE1 | GRCh38.p7 | 6:104756424 | CTCAAAAAAAAAAAA[-/AAAATAT]ATATATATATATATA | 57531 |
rs547469840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767994 | TCAATTCTAAATGCT[A/G]GAACTGAAAATATGA | 57531 |
rs547472091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858429 | CCCCAGGCCAGGCGC[A/G]GTGGCTCACATCTGT | 57531 |
rs547481611 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104847302 | CTATGATATTTTTCT[A/G]CATGTAACCTTTTCA | 57531 |
rs547481955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733183 | CAAGATGAGAAAATA[A/G]ATGTTGACATTGATT | 57531 |
rs547482040 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104805454 | GACTTGCAACCAACC[C/G]AAATGTCCATCCGTG | 57531 |
rs547488187 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726053 | ATACAAAAATTGGTC[G/T]GGTGTGATGGTGCAT | 57531 |
rs547493902 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104698233 | ACTATTAATAGCATT[C/T]TTGAAAATAATCTAT | 57531 |
rs547526593 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104810363 | AAGAAGCTAAACAAG[-/A]AAAAAAAGCAGGTCT | 57531 |
rs547539387 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835589 | GGGCTAGTGTGAATA[C/G]GTCTAACATTTAAAT | 57531 |
rs547562690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748212 | TAAAAGACTCTTATA[A/G]AAGAATTCATAAAGA | 57531 |
rs547569529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731653 | TGTGTTGGGAAAACC[A/G]GATATTCACTACAAC | 57531 |
rs547590410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792902 | ATACCAAGGGCTGCA[A/G]AAGCTCAAGGTTGTT | 57531 |
rs547617065 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769646 | ATCAAGTAAGTTCTT[-/C]CTCGACACAATTAAT | 57531 |
rs547629281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688832 | TGATCTCCTGTCCCC[C/T]TCTTCTAAGAATCTT | 57531 |
rs547631338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827878 | AGGGTTCAACTATCA[C/T]TTTATGTTGTTTGTG | 57531 |
rs547655649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737806 | AGCAGCGGGGAAGCC[C/G]GAACTGGGTGGAGCC | 57531 |
rs547657789 | snp | C/T | 0.283947 | 0.247685 | intron-variant | HACE1 | GRCh38.p7 | 6:104774123 | GAGACGGAGTCTCGC[C/T]CTGTCGCCCAGGCTG | 57531 |
rs547658424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836768 | ACATGACTGTCTATG[C/T]AGAAAATCTCAAGCA | 57531 |
rs547658840 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104844960 | TGAGCCACCACACCC[A/G]GCCCCCATCACAACC | 57531 |
rs547691233 | in-del | -/ACAC | 0.00677823 | 0.0578202 | intron-variant | HACE1 | GRCh38.p7 | 6:104727513 | CATATGTATATGAAT[-/ACAC]ACACACGTATGTATA | 57531 |
rs547692258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851244 | GCATGCCACTACACC[C/T]GGCTAATTTTTGTAT | 57531 |
rs547698756 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768921 | AGATTTCATTAAAAT[A/T]CACAAATACAAAAAA | 57531 |
rs547699823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843502 | TGACTCAAAGATAAC[A/G]GGATAAAACAATGAC | 57531 |
rs547704374 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104800178 | GGGCATCTGCCATTA[A/C]TGGGGCTTGAGTAGG | 57531 |
rs547709319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806190 | TTAAGGGCCAGGTGT[C/T]GTGGCTCACATCTGT | 57531 |
rs547712586 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832898 | GTGAGGCCCTGTCTC[-/A]AAAAAAAAAAGTCCA | 57531 |
rs547752572 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104689723 | TTAGGTGGCCTAAAG[A/T]TTATTTCCCTCTGTG | 57531 |
rs547781978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813641 | CCAAAATATCAACAG[C/T]GTTGAGACCAAGAAA | 57531 |
rs547787486 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701389 | GCATCTTCCCCTAAG[A/T]AAATCCTAAATGCAA | 57531 |
rs547792757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834971 | AGACAACAGGCACAT[A/T]GAACAAAGAATACCA | 57531 |
rs547800347 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858746 | ACTTGGGCATAAAGA[C/G]CCAAAAGCTTCTTAG | 57531 |
rs547807756 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858955 | CGTCCTAGTTACCAG[C/G]TAGCCCACTCAATAC | 57531 |
rs547834800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792270 | TATAGGAAATATTTG[C/T]CTACCATGAAAAAAG | 57531 |
rs547849708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104821617 | CGAGGAAGGTGATAT[C/T]CTCTTCACTTTTATA | 57531 |
rs547871682 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852470 | CTCTATACAAAAAGC[A/G]AAAAGGAGAGGAAGA | 57531 |
rs547871897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805851 | CTGGAACTTAAAAGT[A/G]TAATAATAATAAAAC | 57531 |
rs547878453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767429 | TTCATGCATGCTTCC[C/T]CAAACCAAAATGCCA | 57531 |
rs547896654 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723764 | ATTTTTATATTTTTT[A/T]TATTTTACAGAGACA | 57531 |
rs547916666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837244 | GTATTAAGACTTACA[A/G]CTACAGTAATCGAGA | 57531 |
rs547920402 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104792824 | AGCAATAATATGAAG[C/T]TGTGATCAATCAAGC | 57531 |
rs547933455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772344 | GACTGAAATTAGTTG[A/G]AAGATCATCAGAGAC | 57531 |
rs547948573 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747838 | CACTGTATAAATCAA[C/G]ACCATGCCTACAATG | 57531 |
rs547982306 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801623 | GCCAAACTAAGCTTC[A/T]CAAGTGAAGGAGAAA | 57531 |
rs547997126 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799560 | AGTATTCACCCAATT[G/T]TTCAGATGAGAAAAC | 57531 |
rs548013190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828566 | ATTATTAAGAAGTTG[C/T]TATGATTCCTTTCAT | 57531 |
rs548019453 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830909 | CCTGAGAGGTCACCA[C/T]ATTCATGCCAAACTT | 57531 |
rs548027074 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693346 | TTCTTAAAGGCTTGC[C/T]ATTTAACGAATTTCA | 57531 |
rs548047602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695912 | TTTTTTGTATTTTTA[G/T]TAGAGACGGGGTTCC | 57531 |
rs548082930 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860965 | TTCCCTGCCAGTGCC[A/G]TCCTAAATCAGTTCC | 57531 |
rs548096719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805928 | GGAGGATATGTGCTA[G/T]GAGAACAATGGACTG | 57531 |
rs548104486 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732086 | AAGTATTGGCAAGGA[G/T]GTGGAGAAATTGCTG | 57531 |
rs548111077 | snp | A/G | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104688175 | TTTAGGCCTCAGATA[A/G]TTTCAGGCTGTTTCT | 57531 |
rs548119697 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836658 | GCAGAGGTTGCAGTG[A/C]GCTGAGATTGCGCCA | 57531 |
rs548153378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782431 | AGGCAGACGTTGCAG[C/T]GAGCTCAGATCAACT | 57531 |
rs548157446 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792107 | ACTAAACTCTGCCAC[A/T]ATATCCATAATCCCA | 57531 |
rs548179311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104716947 | CTGACAGTCTCAAGT[A/G]CTGGCAAGAATCTAG | 57531 |
rs548200063 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850378 | AATTCAAATACTTCA[A/G]AGAAACCATATGATA | 57531 |
rs548203179 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819993 | CTAGGTCAAGAGTTC[A/G]AGACCACCCTGACCA | 57531 |
rs548206352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829958 | GAAGGCAATTCTAAA[C/T]TTTTAATGCAGCCTG | 57531 |
rs548225009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772254 | AAGTAGAATTGGAAG[G/T]ATAGATGATAATCAT | 57531 |
rs548261123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696685 | ATTTTATAAGAGATG[G/T]CATTAAAAAAAAACT | 57531 |
rs548269989 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104721866 | AGAAACTGAAGGTGG[A/G]TGGCTTGGACAAGGG | 57531 |
rs548281821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738336 | TGACTTTGATGAGCT[A/G]AGAGAAGAAGGCTTC | 57531 |
rs548315420 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104805620 | CAGAAAACTAAACAC[C/T]GCATGTTCTCACTCA | 57531 |
rs548323739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844414 | AGTGATGCGATCTCG[A/G]CTCACTGCAACCTCC | 57531 |
rs548334560 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726119 | AGAATCACTTGAACC[A/C]AGGAGGTGGAGGTTG | 57531 |
rs548350337 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718696 | TTCTCCATTGCTGAA[C/T]CATCACATACTTCTG | 57531 |
rs548358196 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766886 | ACTGGATGGCCCCTG[A/C]ACAAGCAGGCTTGAA | 57531 |
rs548362431 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755145 | TTGCAACCCTAGATT[A/C]TGACAAAAGAGACTT | 57531 |
rs548362903 | in-del | -/ACGT | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104727569 | TATGAATACACACAC[-/ACGT]ATGTATATGAATACA | 57531 |
rs548397504 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104850655 | AAGTACATCCAGGAA[A/G]GACAATCTCCATGTC | 57531 |
rs548436166 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843898 | TTTGAGACAGAGTCT[G/T]GCCAGGCTGGAATGC | 57531 |
rs548436264 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851186 | CCTCCCTGGTTCAAG[A/C]AATTCTCCTGCCTCA | 57531 |
rs548446207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834391 | ACATGTATCTTACAT[A/G]AATAAAGGAGGGTAA | 57531 |
rs548453035 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104813544 | GGGAAAATGCTATTG[C/G]CAGCTAGTGGGTAGA | 57531 |
rs548457939 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703068 | CCACAGGTAATGGAG[A/G]CAGATACTGTTTATG | 57531 |
rs548460939 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822766 | GGAGGCCGAGGCAGG[A/G]GAATTGCTTGGACTC | 57531 |
rs548469547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858330 | AAGTTGGAAAGAAAA[C/T]ATAGAAAAAGTTGAA | 57531 |
rs548475493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104781849 | ACTAGGCCACCACTA[C/T]ACATGTAGACACCCT | 57531 |
rs548489289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849704 | CCCAGGCTGGAGTGC[A/T]GTGGTGCGATGTCAG | 57531 |
rs548490781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805384 | ATTATAAATCATGCT[A/G]CTATAAAGACACATG | 57531 |
rs548498076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711183 | TATGCCTGGGGTCAC[C/T]TGTGTTTGGCACCTA | 57531 |
rs548498357 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753253 | TCACTGGGACCGAGC[G/T]CCGGGGACAAGGGGT | 57531 |
rs548518083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700808 | TGAAATTAAAAACAT[C/T]TTTAGGTCGTCCTCT | 57531 |
rs548529831 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778879 | AACTTAAAGTGGAAA[A/G]GCCCTTTCCCCATAA | 57531 |
rs548533524 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104858090 | TGGTGAAATGACATA[-/T]TTTTTTTCTATTTTT | 57531 |
rs548547764 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104730692 | TTAGTATGCTACATT[G/T]ACAATTATTTGCTTT | 57531 |
rs548561970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763388 | TGGAATATCTGTATA[C/T]ACAAAATGAGTTATC | 57531 |
rs548562260 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775346 | CCAAGATTGCGCCAC[A/T]GCCCTCTAGCCTGGG | 57531 |
rs548566430 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104820768 | TTCAGCCATTGTAGA[A/G]GACAGTGTGGTGATT | 57531 |
rs548573866 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803193 | TCTGAAATTGAGGCA[A/G]TAATTAATAGCCTAC | 57531 |
rs548600294 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104763848 | TGGGGTCAGGATATC[A/G]AGACCAGCCTGGCCA | 57531 |
rs548613840 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104821392 | ACTCTCAACTGGCTC[A/G]GGAGAGATGAAAGCC | 57531 |
rs548623369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731498 | GTAATCAAAACAGTG[A/T]GATACTGCCAAGAAA | 57531 |
rs548631669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104782346 | CACAAAAATTAGCCA[A/G]GTGTGGTGGTATGCA | 57531 |
rs548635939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718327 | TTATATATATAAAAT[C/T]ATAACATCTGCAAAG | 57531 |
rs548639312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789986 | TCGTCACTCCTAACT[A/G]GAGCTCAAGGAAGTG | 57531 |
rs548677227 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104827725 | TTACATGGCTGTCCG[C/T]AACTGGATGAAAAAC | 57531 |
rs548684201 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104725329 | TTTGGAGAAACAGGG[A/G]AAAAAAAGTTACAAA | 57531 |
rs548685145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688020 | TTCTAAAATCCTCCT[A/G]ACTTCTCTCTGCCCC | 57531 |
rs548765492 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727870 | ACAGGCTGGAGTGCA[A/G]TCACATGATCATGTC | 57531 |
rs548771899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695869 | GAGTAGCTGGGACTA[A/C]AGGCGCCCGCCACCA | 57531 |
rs548771976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687368 | GATGGTGTATGAAGT[A/G]GTATAATGATGTGAG | 57531 |
rs548797543 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826926 | TACAGAATAAGAAAC[C/T]ATTGCGGAGGAACCG | 57531 |
rs548803639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834933 | ATAGAATGCAAGAGG[A/C]TTGAAAACAGTCTCT | 57531 |
rs548808576 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770556 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAATT | 57531 |
rs548814800 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104735377 | CTCACGCCTACATGT[A/G]ATCCCAGCATTTTGG | 57531 |
rs548824589 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104722484 | TTTAATGAATGACTG[C/T]CACGCATTAGCCTTA | 57531 |
rs548834428 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104856495 | GCTGGAATGCAGTGG[A/C/T]GCGATCTTGGCTCAC | 57531 |
rs548855433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839218 | TTATCCCAATGTGTA[C/T]CCTGCTGTTTTTAAC | 57531 |
rs548907195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695043 | GGAGAAGTGCTGAGA[C/T]TCCAGCCATAGTTTG | 57531 |
rs548912264 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842168 | AAATATACTAGCCAA[A/G]GGTAGTGAGACACAC | 57531 |
rs548922733 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727354 | GTATACGAATATATA[C/T]ACACATGTATATGTA | 57531 |
rs548937600 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104798679 | TGTTGGTCAAGATGT[G/T]ATAAACAATAGCTAA | 57531 |
rs548940621 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861515 | TCTTGCTTGGCCTCT[C/T]ATGCTATTCAAAAAG | 57531 |
rs548945237 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832207 | AATAAAATATGAAGT[A/T]TTATTTGCTAAAACT | 57531 |
rs548954994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104771134 | AGAATTTAGAGTAAC[C/T]AGCAAACTATCAGGG | 57531 |
rs548964207 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104817786 | TATTACAGTTCACTA[A/C]TTGACTGAGCAGTAA | 57531 |
rs548985701 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823254 | GCCTGGCCAACATGG[C/T]GAAACACTGTCTCTA | 57531 |
rs548988029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699167 | GCCCCTAGTGGTATT[A/G]TTTAGACTTAGTTCA | 57531 |
rs548992435 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820014 | ACCCTGACCAACATG[A/G]CAAAACCCCATCTCT | 57531 |
rs549037015 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751765 | TTATCATTTATATAT[A/T]TTTTAATTAGTTATA | 57531 |
rs549051316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691668 | ATGAAATATTCTTGG[A/C]CAGGCATGGTGGCCT | 57531 |
rs549066657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852124 | TCTTGGAAAATCTTA[C/T]TCCTTATTTCACACA | 57531 |
rs549073079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706353 | GTTTGTTGTTAAACT[C/T]TGAATTCAAATGGCA | 57531 |
rs549128465 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822727 | CCTGGCGTGGTGGTA[C/T]ATGTCTGTAATCCCA | 57531 |
rs549131297 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104692188 | AAAGAAAGAAAAAGA[A/T]TCTACAGTTGTTAAT | 57531 |
rs549132917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801301 | ACACTCTTTAGGATA[C/T]TATCCAGGAGGACTT | 57531 |
rs549144938 | in-del | -/TTTA | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104810652 | CCTTAGGGAATAGAG[-/TTTA]TTTATTACTGTATTA | 57531 |
rs549152281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706066 | GCTGAGGACAAAACA[A/G]GATACAAATAAACTA | 57531 |
rs549154184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683986 | CCTCAGGAAAAATAT[G/T]ACTTCGATTGTGTGA | 57531 |
rs549204742 | snp | C/T | 0.00914312 | 0.0669923 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727666 | ATGAATACATACACA[C/T]GTATGTATATGAATA | 57531 |
rs549248986 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682388 | TTTTAATTTATATAA[A/G]TTGCTCCGTGACTCA | 57531 |
rs549285590 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104720060 | GTATTAGCCAGGATG[A/G]TCTCAATCTCCTGAC | 57531 |
rs549355945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840647 | CAGCCTAGCTAACCT[A/G]GTAAAACCCCGTCTC | 57531 |
rs549377452 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807520 | CTTTTCCTAATAGAA[C/T]AAAAGTTATCTACAA | 57531 |
rs549393383 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104770349 | AAATCTTAAAGTCAT[A/G]TTATGACTTTGAACA | 57531 |
rs549419909 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826618 | TTGCTAAAATTAAGC[A/G]CAGTGGCTTACAATT | 57531 |
rs549430025 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104776690 | ATGTACTGAAATAGT[A/G]TGAAAAATGTGACAA | 57531 |
rs549462528 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104692846 | ACAAGCTAGTTCATA[C/T]CTAATTAATTTTTAG | 57531 |
rs549476124 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104683388 | TAACAAGCATTGTAT[-/A]AAAAAAAGAGCACAG | 57531 |
rs549489062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756710 | GACAGTGGGTGCAGC[A/C]CACGGAGGGCGAGCC | 57531 |
rs549493061 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800869 | ATGGAGAATGACTTT[C/G]ACGAGTTCACAGAAG | 57531 |
rs549508557 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801083 | ATGCACAAGCTTCAA[A/T]AGCCGATTCGATCAA | 57531 |
rs549553046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749866 | AGACGATGGACTCCA[C/T]AGGTTTGAAATAAAG | 57531 |
rs549565222 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104740743 | GGTACAAGGAGGAAC[A/T]GGTACCATTCCTTCT | 57531 |
rs549575983 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734714 | ACTAAATAATAAATA[C/G]CACACCTCTTTTTCA | 57531 |
rs549578093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786280 | CAGGAGGCAGAGGTT[A/G]CAGTGAGCTAAGATC | 57531 |
rs549588238 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853836 | TACATTCCAAGACCC[C/T]GAGTCAATGCCTAAA | 57531 |
rs549657498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683892 | ATCCAGGGGGAAAGA[C/T]CTAATAGAAAAACCA | 57531 |
rs549664453 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104780055 | CTCTAATACTCAATA[A/C]CTAGAATGCTCAATA | 57531 |
rs549667905 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104845701 | CCAGGATGGTCTCGA[A/T]CTCCTAACCTCATAA | 57531 |
rs549685465 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797490 | CTTGTAATACTTTGT[-/A]AAAAAAAAAAAAATT | 57531 |
rs549689664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749053 | AACCCAAAGTTTTAT[A/G]AACTTATTGATATCA | 57531 |
rs549705060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768273 | CAATAGTTCAAAATT[A/G]TAAAGTCGAACTCTA | 57531 |
rs549758787 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797723 | CCTTCTTGTAGAAGT[A/T]GAATTGTGTAACTAT | 57531 |
rs549759431 | snp | C/T | 0.000337439 | 0.0129848 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859651 | TCTCCATCCTCGGCG[C/T]GCCCTCCGCGATCCT | 57531 |
rs549760704 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816704 | AGAGGGCCACCACCC[C/G/T]CCAGACCCAACAATA | 57531 |
rs549776371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748381 | ATTAAAATCTCAAGG[A/G]AAGACCACTACTGAA | 57531 |
rs549787193 | snp | C/T | 0.00597247 | 0.0543191 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727830 | GAATATATACATATA[C/T]ATATTTTTTTTGAGA | 57531 |
rs549796820 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852096 | TATCATAAAATGTTA[C/T]AGCTCATATAGATCT | 57531 |
rs549797315 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706238 | TCTCATTCCCATCTG[G/T]CAACAACTGACTGGT | 57531 |
rs549812441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104824195 | CAGTAGTGTGCAAAA[A/T]GGAGTCTCATTCTCA | 57531 |
rs549834466 | snp | C/T | 0.000798403 | 0.0199641 | splice-acceptor-variant | HACE1 | GRCh38.p7 | 6:104683295 | TAACCACTGGTAACT[C/T]TGGGGACAATGAAGG | 57531 |
rs549843888 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772781 | GGAATATGAATCCAC[-/T]TTTATAAAATATCTA | 57531 |
rs549876474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720605 | AAACTCAGAAATTCC[C/G]GGGCAGCCACGCTCT | 57531 |
rs549887911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691545 | AAAATATTTTCCTAG[C/T]ATACAAAAAAGGGAA | 57531 |
rs549889956 | snp | A/G | 0.00560781 | 0.0526541 | intron-variant | HACE1 | GRCh38.p7 | 6:104831591 | CTCCGTCTCAAAAAA[A/G]AAAAGAAAAGAAAAG | 57531 |
rs549907434 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104761879 | CAACCCCATCAAAAA[A/G]TGGGCAAAGGATATG | 57531 |
rs549909863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837598 | GCAAAGAGTTCTTGA[C/T]ACCAAAAGCATGATC | 57531 |
rs549919969 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756614 | GCTCTGGTCTACAGC[A/T]CCCAGCGAGACTGAC | 57531 |
rs549935660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829890 | CACTTGCTTTAGGTT[A/G]TAAACCATATGGAGT | 57531 |
rs549958288 | in-del | -/AA | 0.0158469 | 0.0875917 | intron-variant | HACE1 | GRCh38.p7 | 6:104693805 | AGAACACAGAAAAGT[-/AA]AAGAGAGGCGGCGTC | 57531 |
rs549963755 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726391 | AGGACCCAAAACTCC[C/T]GACTTCTGCATGAAA | 57531 |
rs549972238 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778631 | ACCCTGTCTCTACCA[-/A]AAAAAAAAAAAATGT | 57531 |
rs549973939 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690750 | AACTGTCAGAACAAC[G/T]GAACAGCCATCTGAG | 57531 |
rs549975806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699147 | TGTCTTGAATATCAG[C/G]AAATGCCCCTAGTGG | 57531 |
rs549996071 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | HACE1 | GRCh38.p7 | 6:104804039 | ACAAAATCAATGGGC[-/A]AAAAATCACAAGCAT | 57531 |
rs550003389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822659 | GTCGGGAGTTCAAGA[A/C]CAGCCTGGCCAACAT | 57531 |
rs550004474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719577 | GGAGGTAATGAACAT[A/G]TTTAAAATCAATTGA | 57531 |
rs550024461 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749983 | AGTTTAAGAAGTTAG[C/T]ATCAGCGCCCTTTAC | 57531 |
rs550035056 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104689140 | TTGACCAAAGTTATG[A/G]TTGAGAGCTGCTGGA | 57531 |
rs550047163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830833 | AAACAGACCAGCATG[A/G]GGGTTGTGACTTGCT | 57531 |
rs550067105 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682211 | GGGCCCACCTCCAGA[A/G]TTTCTGATTCAATGG | 57531 |
rs550079085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821804 | AGTATTTATTTAGTA[A/C]TAACGGCTAATCTGA | 57531 |
rs550083114 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733005 | AAGACCTGGCTATAT[A/C]TCCTTGTAAGTTGAA | 57531 |
rs550109853 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698423 | CCGTGAGCTCTTGGA[A/T]TCTGGAAATGCATAA | 57531 |
rs550110632 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104689617 | CAATGAAGACCCCCA[A/G]AAAGCATCCTAAAGG | 57531 |
rs550140332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801262 | TACCTGAAAGTGTCA[C/G]GGAGAATGGAACCAA | 57531 |
rs550171573 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104739107 | AAAATACTTTACAGA[C/G]AAGCAAATGCTGAGA | 57531 |
rs550173711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792770 | AGTCACGACCCAGGC[A/G]TAAGTATTTCTTGTG | 57531 |
rs550176760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705544 | AGTTTTTAAAATGTG[C/T]GTGTCTTTAGTCATT | 57531 |
rs550190469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849076 | GGAGGAATCATCAAA[C/T]GAAGGCAAAGTGCCT | 57531 |
rs550216047 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104800309 | GAAAAAAAGGCAGCA[C/G]ATAACTTCTGCAGAC | 57531 |
rs550276620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717431 | GGCGTGAGCCACCAC[A/G]CCCGGCCAGCAATAT | 57531 |
rs550326249 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806285 | TGGATGACATACCTT[C/G]ACTTTATTAAAAATA | 57531 |
rs550335706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104825753 | CTGCTGGGGCCAATT[C/T]CCACCCTGTGGAGTA | 57531 |
rs550336504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702054 | TTTTGTTTCAGAACA[C/T]ATACAGTGAGCGTTT | 57531 |
rs550346475 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104727283 | AATATATATACACAT[A/G]TATGTATACGAATAT | 57531 |
rs550359766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822246 | AAATTATCCAGGCGT[A/G]GTGGCAGGAGCCTCT | 57531 |
rs550392050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810791 | ATACAAAAATAACTT[A/C]ATGTATAACAATATC | 57531 |
rs550392922 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104841045 | AGAATCACTTGAACC[C/T]GGGAGGTGGAAGTTG | 57531 |
rs550403121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723648 | ATTTTGTTGTCTAAG[A/G]ACTGTGGAAGTGCAG | 57531 |
rs550412076 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811007 | GAAGTAATCAAGCAA[A/G]TCAAAAGCTCCACAT | 57531 |
rs550418501 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104759433 | TGGAAACTGAACAAC[A/G]CGCTCCTGAATGACT | 57531 |
rs550422583 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104709697 | TTTTCTTTGTAAATT[A/C]TCCAGTCTCAGTTAT | 57531 |
rs550437209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689016 | TTTCAGTTTACTACA[C/T]TGGCTCTCACATGCC | 57531 |
rs550509816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104686362 | CAAGTCACATATATT[A/G]CCCTGCTATTTACTT | 57531 |
rs550511853 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711502 | CTTGACATAGCGTGT[C/G]ACAAGTACTTAGTGG | 57531 |
rs550512657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104819314 | AGAATTAAAAACCTA[A/G]GAATACAACTAAGTA | 57531 |
rs550534336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693109 | ACATTTTTTCTTTTC[A/G]GTTTTAACCCCGATA | 57531 |
rs550556753 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787461 | TTTATGAGCAAAACA[C/T]TGAACCTGCTGTAGA | 57531 |
rs550575500 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793872 | TATTTACAGGCCAAA[A/G]ATGGCCATAAAAATA | 57531 |
rs550579031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710397 | TAAACTTAGATAATC[A/G]TGATGGTTGCATAAC | 57531 |
rs550579357 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816074 | GCAAAACTACAACTC[-/A]AAAAAAAAAAAAGAG | 57531 |
rs550612227 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104795418 | ATCTCTTTAGCAATA[C/G]TTGATTACCCTGGTC | 57531 |
rs550704288 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104796226 | ATCCCTCCTCCCAGC[C/T]CAGCCTCCCAAGTAG | 57531 |
rs550705928 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785543 | ATAATTTAATTTGTA[A/T]GTATGTATTCCTTGT | 57531 |
rs550721284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803538 | AGTCGGCTTCATCCC[C/T]GGGATGCAAGGCTGG | 57531 |
rs550729016 | snp | C/G | 1.65162e-05 | 0.00287365 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729716 | CACAAGAAGTCTGTC[C/G]TTGAGTATTTCTTTA | 57531 |
rs550745921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783126 | TTTACATACTTTTCG[A/G]TCTACATGCTCCAGC | 57531 |
rs550777484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802134 | AAGGACATTACATAA[C/T]GGTAAAGGAATCAAT | 57531 |
rs550787612 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700324 | AAACTCATAACCACT[A/C]CTGAACTGTCGCAGT | 57531 |
rs550791245 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104719613 | TGTGTGTAGGTCTCA[C/T]TTCTTAAAGAGATTG | 57531 |
rs550819885 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104788818 | AATGCTGAAAGAATG[A/G]CTATGTGTTAAGACT | 57531 |
rs550822986 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764880 | ACCATCACTGAACAT[A/C]GTTGCAGGCCAGAGG | 57531 |
rs550827525 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | HACE1 | GRCh38.p7 | 6:104735689 | AGGAGTACATTCTCT[C/G]ATTCTCTACTGACAT | 57531 |
rs550959746 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758647 | CTGCATCAATAAATG[C/G]GCAAAATAACCAGCT | 57531 |
rs550961858 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778811 | AGACCTTATCTCTAC[-/A]AAAAAAAAAAGTAAG | 57531 |
rs550982723 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743169 | GACTGTTGTGGGGTG[A/G]GGGGAGGGGGGAGGG | 57531 |
rs551001331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840556 | GAGAGAGGCCCGTCG[C/T]GGTGGCTCACACCTG | 57531 |
rs551005899 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763288 | CAGAGTAGTAAAAAA[A/C]CAAATCTCATAGTAC | 57531 |
rs551053802 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104773308 | TGGAAAGTGAAATCT[G/T]TAGTCATTTTGACAA | 57531 |
rs551056819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700819 | ACATTTTTAGGTCGT[C/T]CTCTGCTGAATTCTA | 57531 |
rs551068568 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104742629 | ACCGTCTCACACCAG[C/T]TAGAATGGCGATCAT | 57531 |
rs551068702 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751337 | TCAAATTCACTTAAC[A/T]CATACTTAGAACTTG | 57531 |
rs551069136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839336 | CTGGATGGAATACTA[C/T]TCAGCATTATAAAGG | 57531 |
rs551114647 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708783 | ATCTATGGCCAATTG[A/T]TTTTTCAACAAAGGT | 57531 |
rs551122611 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855671 | TTGAAAATACTACAC[A/T]AAGCCTCCCTTGGCA | 57531 |
rs551141488 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727948 | TTCCAACCACAGGCA[A/C]ATGCCACCATGCCCA | 57531 |
rs551169777 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104809700 | GCTGAGGAAAGAAGA[C/G]ATTGGAGGGAAACAA | 57531 |
rs551175820 | in-del | -/CTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736085 | GAAGTGGTTTTTTTT[-/CTC]CTATCTGAATTGTCA | 57531 |
rs551184457 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846918 | TATAGAAACAGAAAG[A/G]CATCCAAATTAAAGA | 57531 |
rs551198034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104763947 | CCTAACTACTTGAGA[A/G]GCTAAGGCAGAACTG | 57531 |
rs551201473 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104722550 | TATTTGCTCAATCAA[C/T]AGGTTGGTCAACTTA | 57531 |
rs551208187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104750909 | ACACATAGATATACA[C/T]GTGTGTGTATGTACA | 57531 |
rs551244112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832331 | GAAATAAAATCAAAA[C/T]GCAAATTACAAATAT | 57531 |
rs551248977 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714352 | GGACAGAGAGCAGGA[G/T]GCAAAAGAACACTTA | 57531 |
rs551288668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761087 | TTCCATGCTTATGGA[C/T]AGGAAGAAGCAATAT | 57531 |
rs551302750 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708808 | AAAGGTGTCAAGATG[A/T]TTCTATGGGGAAAGA | 57531 |
rs551314219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715031 | GGATATGAAAGCTAA[C/T]ACGTAAGTCCCATCT | 57531 |
rs551336146 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104700105 | GTTACCCCACACACC[C/T]TGGCTGTCACACCTT | 57531 |
rs551346197 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727419 | TATATATACACACAC[-/AT]GTATATGAATACACA | 57531 |
rs551354288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764646 | TCTTCATCATCACTA[C/T]TATCACCATCACCTA | 57531 |
rs551382941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716870 | TAATAATTGGGAAAA[C/T]GAAAATTAAAATATA | 57531 |
rs551404820 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104844661 | CAGCCTCCATCACAA[-/C]CTTTTTTTTTTTTTT | 57531 |
rs551414322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803034 | TGATAAAGGGGGTAT[C/T]ACCACCAATCCTACA | 57531 |
rs551461048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707145 | AAAAAAAAAATAGAA[C/T]AAGAGGGAACACTTC | 57531 |
rs551462805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699240 | TAATGTTCTTGGGGG[G/T]AATACAAAATTTATT | 57531 |
rs551484440 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782625 | AAAAAAGAGTAGCCA[C/T]CTTATACAATGGTTA | 57531 |
rs551485204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819141 | TATATTTGGAAAATA[C/T]CACAGTCTCAGCCCA | 57531 |
rs551488380 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104742522 | GAACAGACACTTCTC[A/T]AAAGAAGACATTTAT | 57531 |
rs551505088 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104795104 | AGGCATTAACTCCAC[C/G]AACTTAGTGATGATA | 57531 |
rs551507191 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104685476 | CCACCCTTAATTACA[C/T]AGACAAGTTCCTTAA | 57531 |
rs551509325 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710895 | CAGGAATTGGATTTT[A/T]GCATACTACTATTTC | 57531 |
rs551523612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104824572 | ACACTACCTGAGAGT[A/T]TTAAATTGTATCAAA | 57531 |
rs551527078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816643 | TGCAGACAGGAAATG[C/T]GGAGTTAGAACCCCA | 57531 |
rs551530610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809974 | AAACTGGGGGAAAGG[C/T]TTGAGGAAGAAAATC | 57531 |
rs551626698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695964 | TCGATCTCCTGACCT[C/T]GTGATCCGACCACCT | 57531 |
rs551651668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815720 | GACCTGGCTTATTCT[A/G]AAAGCATTCACTTAC | 57531 |
rs551729332 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696619 | CTCCCATCACTGTTA[C/T]TAGATTATTGAAATA | 57531 |
rs551744037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104741767 | TTCAATGCCATCCCC[A/G]TCAAGCTACCAATGA | 57531 |
rs551744914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788022 | AGGAAGTTTTCTCTT[C/T]GAAGATCTATTCAGA | 57531 |
rs551747317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779068 | TAAAGTTGGAGACAG[A/G]ATAAGGTTCAAGAGA | 57531 |
rs551752107 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812595 | AAGAAAGAAAACAAC[A/C]GCATACTGGATAAGT | 57531 |
rs551792689 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770351 | ATCTTAAAGTCATAT[C/T]ATGACTTTGAACAGT | 57531 |
rs551795393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769827 | AACTCCTGACTTTAT[C/T]TCCAAGAATTCAATC | 57531 |
rs551805069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835797 | ATTTTAGAACACTAA[C/G]GACAAAGTAGATTCT | 57531 |
rs551810095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721586 | TTCCTTGGGGGACAT[C/T]GAACAGGAAGTCGGT | 57531 |
rs551811147 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805361 | ATTACTGGGTATATA[A/C]CCAATGGATTATAAA | 57531 |
rs551843895 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704109 | AAGACTGTCTCAAAA[A/C]AAAAAAAAAAGATAT | 57531 |
rs551846475 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801376 | AGAGAACGCCACAAA[C/G]ATGCTCCTCAAGAAG | 57531 |
rs551862556 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104688281 | CTGCGAGGAAGAATC[C/T]CCACTCCTGATAAGA | 57531 |
rs551863400 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713414 | TAATATATATTGAGC[A/T]CTTAATATTTTCCAT | 57531 |
rs551866366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695995 | CAGCCTCCCAAAGCA[C/T]CGGGATTACAGGCGT | 57531 |
rs551873496 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737916 | GTAACCTCTGCAGAC[A/T]TAAATGTCCCTGTCT | 57531 |
rs551875458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845767 | CAGGCTTAAGCCACC[A/G]CACCCAGCCAACTCT | 57531 |
rs551883677 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104794537 | CTGATTAGACTGTAA[C/T]TTCAACATAGAGATC | 57531 |
rs551925439 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104758007 | AGAGAAAAAAAGAAT[A/G]AAAAGAAACTAACAA | 57531 |
rs551938458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104798976 | GCATGGCAGTTGTCT[C/T]ATAGCATGTACTCAA | 57531 |
rs551947976 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685910 | ATGCAAAAAAAAGCC[A/G]TTAATCCCAATTTGT | 57531 |
rs551966566 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696580 | GTTTGGTCTTTGGAG[G/T]GCATAGGGGGACATC | 57531 |
rs551969818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804717 | TTAATTCAGGATGGA[C/T]TAAAAACTTAAATGT | 57531 |
rs551974873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711889 | AGCAATCCTCCTGCC[C/T]CAGCTTCTTGTGTAG | 57531 |
rs551987322 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104704773 | TGATTCTGAAATTGG[G/T]ACTATTCACGGCAGT | 57531 |
rs551987551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104853094 | CAATTGAGCCATGAG[A/G]GCTCCTCTTTCATGA | 57531 |
rs551992993 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760987 | TAGGAATACAACTTA[C/G]AAGGGATGTGAAGAA | 57531 |
rs552001290 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860239 | CCCTACATGAACTGT[C/T]TTAAGTATGGTATTT | 57531 |
rs552009862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842597 | TTAAAAGAACATAAC[A/G]AAAAACAGCTCTCCA | 57531 |
rs552015094 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797587 | GGGTTATTAGCCAAA[A/G]ATACTATCTAGCTTT | 57531 |
rs552024598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769312 | AGCACTGGAATACAA[C/T]TGTTACTAGATCTTT | 57531 |
rs552038079 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861120 | TACCAGAGGCTGGGC[A/G]CAGTGGCTCATGCCT | 57531 |
rs552045355 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104811977 | CAGGCTCAATTTCAC[C/T]GATTGCCATTAATAT | 57531 |
rs552062590 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727622 | ATACACACACACGTA[C/T]GTATATGAATACATA | 57531 |
rs552065355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713688 | TCATTCGTTTTCTGA[C/T]GATACAATAATGAAT | 57531 |
rs552104985 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693067 | TGTGTGCACGCGCGC[A/G]CGCGCTGGGGTGGGG | 57531 |
rs552112579 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743491 | TCCTAGGAGAAATAT[A/G]TACATTTATAATGAA | 57531 |
rs552138337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717698 | TGCTATATCCTCACT[A/G]AAATTTGGTATTTTC | 57531 |
rs552138966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772969 | GAATGTACTTAAATG[C/T]CACTGAATTGTACAC | 57531 |
rs552140471 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817850 | GTCTAATCAAAACTT[A/G]TAAATCATCATTTAC | 57531 |
rs552151654 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104738280 | CCTCCTCCAAAGGAA[C/T]GCAGTTCCTCACCAG | 57531 |
rs552177938 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104738963 | CATCAGACTAACAGC[A/G]GATCTCTCGGCAGAA | 57531 |
rs552191293 | in-del | -/A | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104846622 | CAAGAGAAATATAGC[-/A]GCCATCTGATGACAG | 57531 |
rs552199719 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760044 | AGAGGTTCTGAAATT[G/T]AGGCAATAATTAATA | 57531 |
rs552212711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780903 | GACTGCAGGTCTTTA[A/G]AACTGACTGCAGGTC | 57531 |
rs552230566 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694847 | CAGTCTTGAGCTTCT[C/T]GATAATTTGTGAACA | 57531 |
rs552255299 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688926 | TTTAATCATATCTGC[A/G]AAGTCCCCTTTGTCT | 57531 |
rs552271258 | snp | A/C | 1.6528e-05 | 0.00287467 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777040 | TCCATGGAACCGTAC[A/C]GCAATCCCTTGCTTT | 57531 |
rs552297760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820120 | AAATCGCTTGAACCC[A/G]GGAGGTGGAGTTTGC | 57531 |
rs552314131 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766517 | ATCTATGGATAAAAG[C/T]CTGTATTTTGTGCTT | 57531 |
rs552336946 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104699089 | ATATAACCTCCAAAA[-/G]TTTGAATTTGAAGCA | 57531 |
rs552345364 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104856442 | CCTTTTATTTATGTG[G/T]TTTTTTTTTGAGACT | 57531 |
rs552346717 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790452 | TATACTCAAACCATT[A/G]TTTAAAGAAATGTAA | 57531 |
rs552348443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760332 | AAATCCAGCAGCACA[C/T]AAAAAGCTTATCCAC | 57531 |
rs552377037 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711106 | CATTGTTATTGACTT[A/T]GCAGTACATTGGGCA | 57531 |
rs552397212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857765 | GATCGAGACCATCCT[A/G]GCTAACACGGTGAAA | 57531 |
rs552415444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754245 | ACCTCCAAGAGATAT[A/G]GGGTTATGTAAAGAG | 57531 |
rs552436189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858275 | ATTCGACTACGAAAA[A/G]TAAGTAAGAGTAGCA | 57531 |
rs552443356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820733 | GGAAGGCTTAAACAC[C/T]GTTGGTGGGAGTAAA | 57531 |
rs552451340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725141 | ATTATGAAAATACTG[C/T]TTATCACTACATAAA | 57531 |
rs552453307 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849312 | TGATGTAGTTCAATT[-/A]AAAAAACAAAATATT | 57531 |
rs552457018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766470 | GTATACTTTTCTAAA[A/G]ATGCATATAAAGAAT | 57531 |
rs552467873 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700398 | AGCACAGAGAAGAGG[C/G]AGTTAAAAAAGAAAA | 57531 |
rs552484672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744384 | TCATATGCACTATTC[C/T]CACAAGAATAATTTG | 57531 |
rs552501026 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104737236 | GGCGGAGGTTGCAGA[C/T]CGAGCCACTGCACTC | 57531 |
rs552501460 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686946 | TGGGAAGCTGAACAC[A/G]TGAGGATCGGCAATG | 57531 |
rs552511449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104841744 | GATTCAAAATATAAA[C/T]ACTATCAAAGGAATG | 57531 |
rs552542012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737372 | TACAGCTCCCAGCGT[A/G]AGCCACGCAAAAGAT | 57531 |
rs552552617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730043 | ATGGTGTGTAACTCA[G/T]TGCTACTTACGGTAG | 57531 |
rs552562811 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684791 | TGTAACTATTATGTA[C/T]TGCAATTTTTTAAAG | 57531 |
rs552572740 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697156 | TACACCATCTATTCC[C/T]AATCATGTTTTCTTG | 57531 |
rs552572775 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736628 | AACAGTGGGAAGGGT[A/G]GTAAGTTATTGACAA | 57531 |
rs552600279 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789927 | CAGCCCTGACAAAAA[C/G]AGTAGGTCAATAATG | 57531 |
rs552608387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737577 | GTGACAGACGGCACC[C/T]AGAAAATCGGGTCAC | 57531 |
rs552613236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827427 | GACTGGTTTACACAT[A/G]TCTTCTCTAAAAACC | 57531 |
rs552614600 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104848430 | CACTGCACTCCAGCC[C/T]GGTGACGGAGTGAGA | 57531 |
rs552637114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797218 | ACGTAGACCAGAATG[C/T]GACCTATTAAATTTT | 57531 |
rs552641790 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104724630 | TGAGTCCAGGAGTTC[A/G]AGTCCAGCCTGGGCA | 57531 |
rs552648844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702181 | TAGAAAAAAAATATT[C/T]ATAATGGGACTTAGG | 57531 |
rs552653400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833797 | CAAGACCATCTTGGC[C/T]GACATGGTGAAACCT | 57531 |
rs552671525 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104840824 | CAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT | 57531 |
rs552672489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104729935 | AAAAAATCTGCTGCA[C/T]TGCAGTTTCTTTCAG | 57531 |
rs552675566 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709884 | TGGAACTCTCATACA[G/T]GTAAAATGCTCTAGC | 57531 |
rs552677355 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687296 | ATTTCCTGAGGGCCA[A/C]ATGCTGGGAGTCTGG | 57531 |
rs552678732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694950 | AAACGGTGATGCAGC[C/T]TCCTCCTTGTTCTCT | 57531 |
rs552701443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849007 | AAAAAAAATATAGAA[A/G]ATAAAATATGCACCA | 57531 |
rs552720615 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810846 | TTTTGGTTATAGATA[C/G]AGAGAAAGAAAAGAC | 57531 |
rs552722865 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721077 | TGGGCCGGGCGCGGT[C/G]GTTCACGCCTGTAAT | 57531 |
rs552743504 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839348 | CTATTCAGCATTATA[A/C]AGGAACAAACTATTG | 57531 |
rs552758471 | in-del | -/ATAT | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104829077 | ATTTTATTCTATAAA[-/ATAT]ATATAATCAGAATTA | 57531 |
rs552758535 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806353 | TATAGTCCCAGCTAC[C/T]TGGGAGGCTGAGATG | 57531 |
rs552759252 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104797933 | ATTAGCTGGGCATGG[G/T]AGCCGGTGCCTGTAA | 57531 |
rs552766551 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104840720 | TGTAATCCCAGCACT[C/T]TGGGAGGCCAAGGCG | 57531 |
rs552781751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841431 | TATGTCATTTCTAGG[A/G]TTTCATAACCCTCTG | 57531 |
rs552782439 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693596 | TTGTTATATTGTATT[C/G]TTTTTGATTTGTATT | 57531 |
rs552785279 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701291 | TTTTAAAAAGTAAAC[A/T]ACCTTCAGTGGATCA | 57531 |
rs552787359 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783729 | CAAAGCCTTTTAACA[C/T]GCTGCCAATGTGATT | 57531 |
rs552803167 | snp | C/G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104855442 | AGCGAGACTCCATCT[C/G/T]GGAAAAAAAAATAAA | 57531 |
rs552818664 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698444 | AAATGCATAACCTTA[A/C]ATTTAGGGTATTTTA | 57531 |
rs552824581 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709662 | GTACAGCCTGCAGAA[A/C/G]CTTGAGCCAAATAAA | 57531 |
rs552893077 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104700959 | GGAAAATAGTTTTAA[C/T]AGGGCCTAATGTTCC | 57531 |
rs552895350 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810614 | GTGGGTGTGACGGCA[C/T]GTGTATAATTATACT | 57531 |
rs552897936 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104686727 | CCTCCTGGTACACAG[A/G]CCAGTTGGAGGCCCC | 57531 |
rs552905328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701899 | CAGACAAATATCAAG[G/T]TAAAAAATTCACATA | 57531 |
rs552907171 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770188 | AAGATGTCTTGGAAT[C/T]ATAATTCAGCTAAAC | 57531 |
rs552911027 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744018 | AATACCAAAATAAAT[A/C]TTTCTTTAATACCTA | 57531 |
rs552924241 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104703104 | TTCTGTGGAGGCAAA[C/T]TTACAGTAAAGAAAT | 57531 |
rs552992351 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104818754 | AATAAATGTAATTCA[A/G]CACATAAGCAGAACT | 57531 |
rs552996673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715458 | AGCATATGTAAAATA[C/T]GAAAAAGGTGGTAGA | 57531 |
rs553002892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855132 | TGGCATTATGTGGCT[A/G]ATTCCAGAGCCTCTA | 57531 |
rs553028468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797377 | TGACCATTTGCAACT[C/T]TAGCCTGACCTTCTT | 57531 |
rs553063184 | snp | C/T | 4.95421e-05 | 0.00497681 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744575 | TTTTATCCAATCACT[C/T]ACATCAATTTCTGGC | 57531 |
rs553078638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722621 | AGCCAGATACCTGAA[A/G]CTGCACTGGACACAG | 57531 |
rs553118972 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684434 | CTAGCGATCTATCTC[A/C]TTTGAATTAAAACAC | 57531 |
rs553130700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104856060 | ATCCAAGAAATACTA[C/T]ACTAAGAAAGGACAG | 57531 |
rs553141178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803567 | GGCTCAACATATGCA[A/C]ATCAATAAACGCAAT | 57531 |
rs553149483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752575 | TTAAAGTGTGACTCA[A/G]TAATCTCTGTGGAAG | 57531 |
rs553174522 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787699 | ATGCAGATGAGCACT[A/G]AGTCTAAACCAACAG | 57531 |
rs553183936 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811120 | CTTAAAAAAGAGATT[G/T]TACTTCCTCTTAAAA | 57531 |
rs553192167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716518 | AACATGGTGAGACCC[C/T]GTCTCTACTAAAAAT | 57531 |
rs553201456 | in-del | -/CT | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104843490 | AAACTGCTTCTATGA[-/CT]CAAAGATAACAGGAT | 57531 |
rs553236033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770907 | TCTTCATTTAAGCTT[A/G]TATTTCTAATCAAAT | 57531 |
rs553243393 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841477 | CACTAAGCATCCTAC[A/G]GATATTCAGAATACA | 57531 |
rs553250100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794642 | GGCGCATTGGCGCAC[A/G]CCTGTAATCCCAGCA | 57531 |
rs553275508 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764131 | TCAGGCTGGAGTGCA[C/G]TGGCACTGTGATCTT | 57531 |
rs553281077 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104774888 | ATTATTATAGATATC[A/G]GGTCTACCCAAACAT | 57531 |
rs553288949 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786784 | CAAATAAATATAAAA[C/G]TTTATCTCACTTTTT | 57531 |
rs553312093 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758801 | CTGTATTCAGGAGAC[C/G]CATCTCACGTGCAAA | 57531 |
rs553319461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814206 | ACTGAAAGACATCAG[G/T]TGCCAGGTTTAAAAG | 57531 |
rs553358393 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104814797 | ACATCCCCCCTCACG[C/G]TCTTTCTCCCTCTCT | 57531 |
rs553385597 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729093 | TTTCATCAACTGTTA[A/G]TATCATCAGTCTAAA | 57531 |
rs553394219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691823 | GCACTTTAGGAGGCC[A/G]AGGCAGGAGGATCTC | 57531 |
rs553420704 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716829 | CACAAATGGCCAGTA[A/T]ATTATAAAAATGCTG | 57531 |
rs553459543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104822522 | CACACCACTACGCTC[C/T]GGCCGGTTCAACAGA | 57531 |
rs553473868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768506 | TTTCTAAAGATTTTT[A/G]AGAGTTTTATATGAA | 57531 |
rs553476419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780057 | CTAATACTCAATACC[C/T]AGAATGCTCAATAAA | 57531 |
rs553497012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692547 | TCAGTAGGCACTAGC[A/T]TGATACACTGCATAT | 57531 |
rs553526859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720193 | ATGTCTTTTTACAAA[G/T]GCACACAGCCATGTG | 57531 |
rs553561546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820374 | AGAGTTTCTGCATAG[C/T]GAAAAAAACTATCAT | 57531 |
rs553562924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836875 | TGAACATGCATAAAC[C/T]CAAATTAAAAACACA | 57531 |
rs553574832 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783493 | CTGCTGTCATTATCT[C/G]CATTTTGTAGATGAA | 57531 |
rs553582733 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | HACE1 | GRCh38.p7 | 6:104756444 | ATATATATATATATA[C/T]ATACACACACACACA | 57531 |
rs553600066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735116 | AATGATAATCAATTT[C/G]GCAATACCGTAATTT | 57531 |
rs553612254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735617 | GCCTGGACGACAGAG[A/C]GAGACTCCGTCTCAA | 57531 |
rs553622335 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693634 | TTGTTATATCAGTTT[C/T]TTTTTCTTTCCCAAA | 57531 |
rs553627112 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104802235 | GTCCTTAGAGACATA[A/C]AAAGAGACTTAGACT | 57531 |
rs553636248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775781 | GCTGCCTAGCTCTAC[C/T]GCAGCCTACTCCCAC | 57531 |
rs553637475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700363 | TTCATACCTGTTTCT[C/T]GTGTTCCCAAATGTC | 57531 |
rs553668480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846065 | AAAAAAGTGTTTATG[A/G]TAGGGGTTGTTGAAG | 57531 |
rs553683752 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845068 | AATACATATGTATTG[G/T]ATACATATTATATAA | 57531 |
rs553706238 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104736975 | CACTACTTTTAAAAT[-/A]AAAAAACACAGTTTT | 57531 |
rs553706635 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104719782 | TGTGAATTGAGTAGA[C/T]AGATTTTTCTTTTCT | 57531 |
rs553707171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838674 | ATACCCCTTGAGCAA[A/G]TTTCTTGAGTAAATT | 57531 |
rs553735812 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104741938 | ACAGTAACCAAAACA[C/G]CATGGTACTGGGACC | 57531 |
rs553756458 | in-del | -/TGAGA | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104806726 | TTTTTTAATATTGAT[-/TGAGA]TAATACTCTCTTCAA | 57531 |
rs553778846 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764925 | CACAATTGTGTCTTT[A/T]CTCACTGTGTTCCAA | 57531 |
rs553800296 | snp | C/G | 0.0305496 | 0.119756 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859486 | AGTTAGTTTTTCCAC[C/G]CGACCTTGACGCGGC | 57531 |
rs553813021 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821974 | GGGCTTTGGGAGACC[A/C]AAGTGGGAGGAGTGC | 57531 |
rs553817251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104764915 | GCCAGGCATGCACAA[C/T]TGTGTCTTTACTCAC | 57531 |
rs553820775 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104760130 | AGGTACAAAGAGGAG[C/T]TGGTACCATTCCTTC | 57531 |
rs553869124 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827662 | CTACCTACCTTTGTG[C/T]CTCAAGGCTGAATCT | 57531 |
rs553877040 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788935 | CCACTCATTCTTAAT[A/G]GAAAACCCATTAGTT | 57531 |
rs553915204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850757 | AGTTTAGAGACAGAA[C/T]GGATAGCACACCACG | 57531 |
rs553934783 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720014 | ACGCCCGGCTAATTT[C/T]TTGTATCTTTAGTAG | 57531 |
rs553943551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773550 | CTTTGTGAGATAAAG[C/G]CAGACTTCAAAGACA | 57531 |
rs553948212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857460 | TAAGTTGAGAAACTG[A/G]TATGTTGAGCCTTAG | 57531 |
rs553950454 | in-del | -/TGTATACGAATATATATACACATG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727312 | ATATATACACATGTA[-/TGTATACGAATATATATACACATG]TATGTATACGAATAT | 57531 |
rs553957682 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770919 | CTTATATTTCTAATC[-/A]AATTTCTCAAAATGC | 57531 |
rs553957959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804218 | CCAAATAAAAGAGGA[C/T]ACAAACAAATGGAAG | 57531 |
rs553979727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829260 | CAACTTATGGAAAGA[G/T]ATACAAATGGTTTTT | 57531 |
rs554001656 | snp | A/T | 0.0341408 | 0.126114 | intron-variant | HACE1 | GRCh38.p7 | 6:104731883 | AGAAAAAAAAAAAAA[A/T]CCCGATTAAAAATGG | 57531 |
rs554013859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104732732 | ACAAATGGTTGAAAA[C/T]ATGCACCAGGATTGT | 57531 |
rs554023079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696345 | GAGGGGATCACACCA[A/T]CCCCATTGACAACAG | 57531 |
rs554035391 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688505 | GTGCTCTCATCAGAA[A/C]TTTGGTCACTGTTTG | 57531 |
rs554059624 | in-del | -/AT | 0.00517822 | 0.0506191 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727801 | TGAATATGTACACAC[-/AT]ATATATGTATATGAA | 57531 |
rs554094361 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829088 | TAAAATATATATAAT[C/G]AGAATTATGTAAGCT | 57531 |
rs554121342 | in-del | -/ATG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795841 | AGCTAATATAGAGAT[-/ATG]ATGATACATAATAAA | 57531 |
rs554127806 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104835278 | AAACATCTGATAAAC[C/G]CATCTAATTTGAAAG | 57531 |
rs554132215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772682 | TCTAATGGCAAACAA[C/T]TAAGTTTAAACAATT | 57531 |
rs554135470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849973 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTGTGTC | 57531 |
rs554136373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724064 | GATCCTTGACATAGC[C/T]GAACTATACAATATA | 57531 |
rs554144512 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798448 | AGTGCCAGAAAACTC[C/T]GCAACGTTATTATAG | 57531 |
rs554145673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799172 | CTGACTTAACGGTGA[A/C]ACTGTTATAAGCATT | 57531 |
rs554164165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104825094 | CTCAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA | 57531 |
rs554184150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821883 | CTAAATAACTATTAC[A/G]GAGTCAAGCTTAAGT | 57531 |
rs554240278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843024 | GGCTGAGGCACAAGA[A/G]TCGCTTGAACCAGGA | 57531 |
rs554244368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704306 | TACAAGCAGGTAATA[A/G]AAGAAAGTCGGCATT | 57531 |
rs554246961 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104775059 | ATAAATCAAAATGTT[G/T]GGCCAGACGTAGTAG | 57531 |
rs554252133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857845 | GCCTGTAGTCCCAAC[C/T]ACTGGGAAGGCTGAG | 57531 |
rs554281890 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703945 | AGCCCTGTCTCTACG[-/A]AAAATACAAAAATTA | 57531 |
rs554310982 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687673 | AGAAAGCACAAATTG[A/C]CATAAAGGCAGCTTC | 57531 |
rs554332278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703563 | TGCTTGAAGGACAAG[C/T]AGGATTTGACAAATG | 57531 |
rs554430571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104726359 | CCCAATATTGTCAGA[C/T]TGTCTCACTGCTCAA | 57531 |
rs554441417 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104798400 | AATTAAAGTTTTTTT[A/T]AAAAAAACTTAATAG | 57531 |
rs554459579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104739262 | AACTATATCAACTAA[C/T]GAACAAAATAACCAG | 57531 |
rs554478515 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104790590 | AAGCCCCATCTCTAA[C/G]AAAAAATACAAAAAT | 57531 |
rs554495011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773190 | TCAACAAACACATAA[A/T]GAGCTCATGCTATAT | 57531 |
rs554500738 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718253 | TACTGCTGATAAAGA[C/T]GAATGCTATCATTCT | 57531 |
rs554572101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841985 | GCAAAGAAAGTGGTA[C/T]GGCAAAATGGCCAAT | 57531 |
rs554585544 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767026 | ACATCAAACAGTGCC[A/T]AGCACATTATAAAAA | 57531 |
rs554602381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754316 | GAGAATGGAACCAAG[C/T]TGGAAAACATACTTC | 57531 |
rs554613053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773061 | AAAAAAAAATACTAC[C/T]AGTTAAAAGTTAAAA | 57531 |
rs554617970 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833979 | ACACAGTAAGACTCC[A/G]TCTCAAAAAAAAAAA | 57531 |
rs554659273 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834181 | TTAAAATAACTCATA[A/G]TGGTTCAAAACAGTA | 57531 |
rs554705818 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707053 | AATTTACCATGAAGA[A/C]AATCTCAGGACCAGA | 57531 |
rs554741949 | in-del | -/A/AA/GA | 0.209765 | 0.256577 | intron-variant | HACE1 | GRCh38.p7 | 6:104731869 | AAAGAATTCCCATAG[-/A/AA/GA]AAAAAAAAAAAAATC | 57531 |
rs554742704 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104842686 | GTGACAAAGGCTAGG[A/G]GAATAAGCTTCAAAA | 57531 |
rs554751379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811123 | AAAAAAGAGATTGTA[C/T]TTCCTCTTAAAAGAC | 57531 |
rs554783162 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795228 | AAGGTTAAACAGTAG[C/T]TTGTACCTAATTTTA | 57531 |
rs554815886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737337 | GGAGCCAAGATGGCC[A/G]AATAGGAACAGCTCC | 57531 |
rs554818029 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762176 | ACTAGAAATACCATT[G/T]GACCCAGTGATCCCA | 57531 |
rs554842839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703480 | AACATTGCATGAAAG[A/G]AGCTTTTCATAGTGC | 57531 |
rs554852542 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821864 | ATAATCTAGTAACTC[C/T]CTACTAAATAACTAT | 57531 |
rs554868236 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857800 | GTCTCTACTAAAAAT[A/T]CAAAAAATTAGCCGG | 57531 |
rs554868334 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849371 | TCAGACAGTCTTGCT[C/G]TGTCGCCCATGCTGG | 57531 |
rs554918703 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780333 | ATGGTACATTTTTGT[A/G]TGTAAACTTTCTAGA | 57531 |
rs554923491 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104812020 | CTAAGCTCTACTCCT[C/G]TAATCATTTGACTCA | 57531 |
rs554937038 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104824851 | GGCCGAGGCGGGCAG[A/C]TCACGACGTCAGGAG | 57531 |
rs554939258 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729326 | AACACCCTTTTAACA[A/C]GACAGTTACATAGCA | 57531 |
rs554940062 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760096 | CAGGACCAGTGGATT[C/G]ACAGCCAAATTCTAC | 57531 |
rs554960460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804168 | ACAAGGGATGTGAAG[A/G]ACCTCTTCAAGGAGA | 57531 |
rs554968656 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104753815 | GAATCAACACAAAAA[A/T]GCTGAAAACTCAAAA | 57531 |
rs554971629 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853501 | TTTATGTTTTTTAAT[A/G]AATTATTTACAAAGA | 57531 |
rs554978671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857617 | TGTTACATGCATCCT[A/G]TGAAATTCTGAAGTC | 57531 |
rs555008155 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795126 | GTGATGATAAAACCA[A/C]AGGATCTTTTAGAAA | 57531 |
rs555011230 | in-del | -/AATA | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104770718 | GTGAGACTTCGTCTC[-/AATA]AATAAATAAATAAAT | 57531 |
rs555051044 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104762787 | CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 57531 |
rs555074340 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748453 | CTAGTGAGAATGCAG[A/G]ACACCCAGAACTCTC | 57531 |
rs555077181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820236 | CCCAAAACCATAAAA[C/T]CCTGGAAAACAATGT | 57531 |
rs555086542 | snp | A/G | 1.67829e-05 | 0.00289675 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750389 | GGGTGGAATGAACAT[A/G]TGAAAGCCCTGTAAA | 57531 |
rs555122241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717865 | TTTGTCCATTTGCCT[A/G]TCGAGTTTCCTGTCT | 57531 |
rs555122306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710056 | ATTGCACCATTATCC[A/G]TAGTAGCCAAATAAT | 57531 |
rs555153143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104826056 | AACATTTGATTCTCA[C/T]AGGAGCATGAACTCT | 57531 |
rs555180714 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860368 | TGTTTTTCCTGCCGG[G/T]CGGCTTTATGAGGGC | 57531 |
rs555189272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723932 | CTATTCATAAAGACA[A/G]CTATTACACACTCTG | 57531 |
rs555240956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819630 | TCACGCTACCCAACT[C/T]AAAACTATACTACAG | 57531 |
rs555256788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833624 | TGAGGCAAGAGGATT[A/G]CTTGAAGCAACGAGT | 57531 |
rs555258329 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104727475 | TATGAATACACACAC[A/G]TATGTATATGAATAC | 57531 |
rs555263682 | in-del | -/CAT | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104701336 | TAATGGTTTCAGTCA[-/CAT]CATCATAAAATTAAG | 57531 |
rs555316454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825580 | TGCTTCCCACAACCA[A/G]TCAGATGTTTGCATA | 57531 |
rs555329841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845197 | ACTATTTATTCAACT[A/G]GATCATAAATATCTT | 57531 |
rs555411847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770017 | AAAATGCTAATAACA[A/G]TTCTGTATGGGAGGT | 57531 |
rs555424466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807688 | AAGACTTAAAGGTGT[A/G]TAAAGATGGCAGGGG | 57531 |
rs555437139 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104707400 | CAGTGTAATAAACCA[C/T]ATAAACAGAATAAAT | 57531 |
rs555442274 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104844600 | TCCACCCCCACCCCC[A/C]CAAGCCTCCCAAAGT | 57531 |
rs555461796 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104713931 | TGCACTGATCCTTGA[G/T]GACCCTGGCTTTTGT | 57531 |
rs555480134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816771 | AAGCCACACGTACTC[A/C]ATGTCAGCCTGTGGA | 57531 |
rs555505761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814711 | GGGACCTGGTGAGAG[A/G]TGACCAGAGCATGGG | 57531 |
rs555507192 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104837677 | GCTCTTCAAAAGACC[C/G]TCTTAACACCACTAT | 57531 |
rs555518415 | snp | A/G | 0.000164764 | 0.00907495 | intron-variant | HACE1 | GRCh38.p7 | 6:104850893 | AGTTTAACTCAAAAT[A/G]TCTTTAGTCTTACTT | 57531 |
rs555522595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706769 | CACATAAAAGTCCTA[C/T]AGATAAATTACTACT | 57531 |
rs555535016 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707401 | AGTGTAATAAACCAT[A/G]TAAACAGAATAAATG | 57531 |
rs555550372 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860473 | GAAGATATGAATGAT[A/G]ACAACCTGAAAAAAT | 57531 |
rs555554875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822946 | ACAATTTATTCATTA[A/G]ACTAACATACTCCTC | 57531 |
rs555574207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713062 | AGGGAACAAGTAAGG[A/G]GATAGAGTGGGATAG | 57531 |
rs555584580 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104697822 | TCGGCTCAGTGCAAC[C/T]TCCATCTCCCGAGTT | 57531 |
rs555609721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727232 | GAATATATATACACA[C/T]ATATGTATACGAATA | 57531 |
rs555614570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104704175 | AGATCTCAACGTTTA[C/T]GAAAATAAAACTAAG | 57531 |
rs555614636 | in-del | -/CAAA | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104850365 | AAGTATTTGAGAAAT[-/CAAA]TCAAATACTTCAAAG | 57531 |
rs555642759 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104823497 | TCATAAATCTTTCTA[C/T]TTTTCTATTTTTTTA | 57531 |
rs555656426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859063 | TTTAAGAGTACCTGT[C/T]TGATGTTTGACAACC | 57531 |
rs555661722 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104712450 | TACGTCATGAGGGCT[A/C]TGCCTTTGTGAGTGA | 57531 |
rs555663022 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104726448 | ACTCATTCAAAATTT[C/T]AGAAACAGTATGACA | 57531 |
rs555673007 | in-del | -/TCCT | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104848501 | TATAAGTTCTTCAAG[-/TCCT]GAATCAAAAAATACT | 57531 |
rs555679558 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682664 | CCACTCAATTTCTAC[G/T]TGCCTGCCTTGTCGT | 57531 |
rs555681188 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690952 | AATGAATTTGACTAT[A/T]CAATATTTTTAATTT | 57531 |
rs555692585 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104806430 | TCACGCCACTGCACT[C/T]CAGCCTGGGTGGCAG | 57531 |
rs555703162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806878 | ACTTTGGACTCTTTC[A/T]TCCTTATAAATTTGA | 57531 |
rs555755439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104784563 | TTGATAAATATATAC[G/T]GAACTGGACTGGCTT | 57531 |
rs555764991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690052 | CTAGGCACAAAGCCC[A/G]CGCTATTTTGCCACC | 57531 |
rs555796926 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104806648 | TCAGTTTAAATAACT[-/A]AAAAAAATTACTCAA | 57531 |
rs555802603 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833709 | ATTAGCTGGGCAGCC[A/G]GGCACGGTAGCTCAA | 57531 |
rs555805305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768600 | TACTGGTAACATTAG[A/G]AAAAAAAGGCTCAAT | 57531 |
rs555840401 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104769324 | CAATTGTTACTAGAT[A/C]TTTCCACTTTGTCAT | 57531 |
rs555844271 | in-del | -/AA | 0.000299244 | 0.0122284 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851029 | TGAGGAATCAAGTGT[-/AA]AAAAAGTTTTTAAAA | 57531 |
rs555876105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762095 | AACACTTTTACACTG[C/T]TGGTGGGAGTGTAAA | 57531 |
rs555879564 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743860 | TATACAAATATTAAA[A/G]ATTTGGCTACTATCA | 57531 |
rs555886575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755596 | TCTCAGACCACAGCA[C/T]AATCAAATTAGAACT | 57531 |
rs555888034 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807661 | TTTGAAATATTGGTA[C/G]AAGTCATATAAAAGA | 57531 |
rs555894088 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800395 | TTTGAGCTCTGAGAA[C/T]GGACAGACTGCCTCC | 57531 |
rs555912849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756893 | GACCAGGAGATTCCC[C/T]TCTGTGCCTGGCTCA | 57531 |
rs555915970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775868 | GGAAGCAATCAGAAG[C/T]TACAATTAATGAAGC | 57531 |
rs555923821 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861716 | CATTGCATCTCATGC[C/T]GGTCACTGTTCACCA | 57531 |
rs555929211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713745 | CTAGTCCGATTGACC[C/G]TTCCACTAAAAACAC | 57531 |
rs555934595 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104793021 | CGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCGA | 57531 |
rs555946095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747700 | ATATCTTCTTTGGCC[C/T]AGTTTTCTCATCTGT | 57531 |
rs555960529 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705145 | ATATTTACACATCCA[A/G]TTGTGCCAGCTCTAA | 57531 |
rs555989853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761295 | GCTACCAGACTTCAA[A/G]CTATACTACAAGGCT | 57531 |
rs556058054 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682605 | CTTTTACTAACCAAA[C/T]CTTAACCAGTTGAGT | 57531 |
rs556063623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767505 | CCCATTTTTCACACT[C/T]CAAGCTGAGTTTGGT | 57531 |
rs556074436 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104733231 | ACAGTATTTCAATAT[C/G]AATATGATCAATCTA | 57531 |
rs556081008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775340 | AGTGATCCAAGATTG[C/T]GCCACTGCCCTCTAG | 57531 |
rs556082290 | in-del | -/TCCATCTTGGGATGGCCGAATATGAACA | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104799761 | TCTCAAGACTCCCAT[-/TCCATCTTGGGATGGCCGAATATGAACA]TCCAAGATGGCCGAA | 57531 |
rs556102245 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104761026 | AGGAGAACTACAAAC[C/T]GCTGCTTTAAGGAAA | 57531 |
rs556104074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713309 | TTGTTTTAAGAGAAA[C/T]AATAATATACACTTA | 57531 |
rs556138049 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104747587 | TGATTACTCATGCCA[A/C]CAAGCAGCAGACTGG | 57531 |
rs556173950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721084 | GGCGCGGTGGTTCAC[A/G]CCTGTAATCCCAGCA | 57531 |
rs556188449 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745050 | CTAAACAAGGGGAAA[C/G]TCATCAAGAAATCAT | 57531 |
rs556195948 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765064 | TATTTATTCTTCACT[C/G]ATCTAATGTGACTGA | 57531 |
rs556210350 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104814868 | CTTCCACCATGATTG[C/T]AAGTTTCCTGAGGCC | 57531 |
rs556211244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739310 | GGATCAAATTCACAC[A/G]TAACAATATTAACCA | 57531 |
rs556226614 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761719 | TAATTAAACTAAAGA[C/G]CTTCTGTACAGCAAA | 57531 |
rs556263706 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849471 | CCTCCCAAGTAGCTG[A/G]GACTTACAGGCATGA | 57531 |
rs556276872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755458 | ACAGAACTTCCCACC[A/G]AAATTCAACAGAATA | 57531 |
rs556317378 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104844531 | GTGTATTTTAGTAAA[C/G]ACACGGTTTCACCAT | 57531 |
rs556321261 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104702956 | CATAAAGGTAAAAAG[-/A]AAAAAAAGCAATCCA | 57531 |
rs556334975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859347 | CAGCAGCGGAACCCC[C/G]ACCAACCCAGTTTCC | 57531 |
rs556347805 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699205 | CTTATCATTCATTTC[C/G]TAGACACATAATACT | 57531 |
rs556357170 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104741110 | GACAAAATTCAACAA[-/C]CCTTCATGCTAAAAA | 57531 |
rs556372206 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822549 | CAGAGTGAAACCCTG[A/T]CTCTAAATAAAAAAT | 57531 |
rs556380124 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104783790 | ATTTCCCAAATGTAT[C/T]TGGGGGCTAAAATCC | 57531 |
rs556387108 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857232 | ATTCCTATATGTATG[A/C]TATACTTTAAAGAGC | 57531 |
rs556397529 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104727210 | ATATATACACATACA[C/T]GTATACGAATATATA | 57531 |
rs556416348 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818845 | CATCGATTTATGTTT[-/A]AAAAAAAAAACTCTT | 57531 |
rs556435086 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722567 | GGTTGGTCAACTTAC[C/T]TGTCTCTAAATCTAG | 57531 |
rs556504756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760954 | AATTCACAATTACTA[C/T]TAAGAGAATAAAATA | 57531 |
rs556507945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689849 | GATCAGTGTCACATG[C/G]GAAAAGAATTTAACG | 57531 |
rs556531653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738632 | AAAAAAGAATAAAAA[C/G]AAATGAGCAAAGCCT | 57531 |
rs556579545 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802522 | AAACTGTCTCTCAGA[C/G]CACAGTGCAATCAAA | 57531 |
rs556588803 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859136 | TAAAAAATAACAAAA[A/G]TAAAAGCCCGCCTGG | 57531 |
rs556608049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855009 | TCTAAACACTTTGCA[C/T]GTATCATTGCTTTTC | 57531 |
rs556622170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836316 | TATTTACAAAGCTGA[A/G]AGAGACCTTGGAATT | 57531 |
rs556623430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850773 | GGATAGCACACCACG[C/T]GCTCAAACAGGATAA | 57531 |
rs556662994 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104828289 | TAAAGGGTCTAGACA[A/C]TGATCTGTGTACTTT | 57531 |
rs556670180 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727458 | ATATGAATACACACA[G/T]ATATGAATACACACA | 57531 |
rs556683217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799236 | AGACTGTCACTATAC[C/T]TTTGAGTTCCTCTGT | 57531 |
rs556698110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788391 | GATTTATAAGCATTT[A/T]AAGTCATATTTCAAA | 57531 |
rs556714837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854107 | GTTCTTGCCAAAAAT[A/G]CATAACTTCAATCTA | 57531 |
rs556719074 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810651 | TCCTTAGGGAATAGA[A/G]TTTATTTATTACTGT | 57531 |
rs556720323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799799 | AGCTCCGGTCTGCAG[C/T]TCCTAGCATGACTGA | 57531 |
rs556723732 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775942 | GATTTTTAGGAAAAA[A/C]AAGCGACTGTGCAAA | 57531 |
rs556758307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711419 | ATCAACTCAGGGAAG[C/T]TATTCCAGGAGGATC | 57531 |
rs556797897 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104805092 | AATTATGCAACCAAC[A/G]GACATGAAAAAATGC | 57531 |
rs556806902 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104838335 | ATAGTAACCAAAACA[A/G]CATGTTACTGGTATA | 57531 |
rs556811972 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761054 | AAATAAGACAGGACA[C/T]GAACAAATGGAAAAA | 57531 |
rs556815881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766877 | ACAGAGAAGACTGGA[C/T]GGCCCCTGCACAAGC | 57531 |
rs556853288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104809325 | CGATCAAAAATCTGG[A/G]GAACGACCTGCTTAG | 57531 |
rs556861173 | snp | A/G | 0.29175 | 0.246489 | intron-variant | HACE1 | GRCh38.p7 | 6:104774153 | GGAGTGCAGTGGCGG[A/G]ATCTCGGCTCACTGC | 57531 |
rs556886827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823646 | AAAATAAAAAAACAG[A/T]GAAAAACCTACTTCC | 57531 |
rs556894534 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734612 | GGGTGAAGCTAGCTC[C/T]GTGTTGTTTCCCCTC | 57531 |
rs556907262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685063 | CCCTGTCAGAGGGTC[C/T]GGCAATGTACCATAT | 57531 |
rs556942587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840735 | TTGGGAGGCCAAGGC[A/G]GGCAGATCACCTGAG | 57531 |
rs557013183 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861675 | TGTGGGCAGGGGTAG[A/G]AGCCCCCAGCAGCCT | 57531 |
rs557028122 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104693426 | AAGTCATCCCTCTGT[C/G]TTCTCGAGGGATTGG | 57531 |
rs557031871 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691778 | TATTTAAAGAGTTGC[C/G]AGGTGGGGTGGTGCA | 57531 |
rs557037177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701138 | TCACTATTATTCAGT[C/T]ATACCATTCCTGCTT | 57531 |
rs557050313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104831753 | AAAAAATTAGCCGGG[C/T]GTGGTGGCCGGTCCC | 57531 |
rs557053060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751716 | TACAGAGAGAGAAAG[A/G]GTATGTGCCTGTATA | 57531 |
rs557091482 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104795981 | GAGAAATTTAAATTC[C/T]GCAATTTTTCTAAGA | 57531 |
rs557119402 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810204 | TTTCTAGCCAAGCAA[C/G]CAAATCATAAATATA | 57531 |
rs557146137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794601 | GCCTAATGGATGGTA[C/T]GCCCTCAAAAATATG | 57531 |
rs557147775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758692 | AGCATCAAATTCACA[C/T]ATAACAATACAAACC | 57531 |
rs557164962 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699427 | AATGAAGTCTATAAG[A/C]TACAAAATGTTGGCC | 57531 |
rs557167974 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714984 | TGGAAGCACAGGGAC[A/G]TTGTCATCCCTGGGG | 57531 |
rs557186719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762922 | GTGAACCTGGGAGGT[A/G]GAGCTTGCAGTGAGC | 57531 |
rs557204131 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802428 | CATTCTTCTCAGCAC[C/G]ACATCACACTTATTC | 57531 |
rs557206140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104780425 | GCATTTGTACAGCAA[C/T]ACAAAATGTTTCTCC | 57531 |
rs557209537 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789271 | TTCTTTAACAGTTAA[A/T]ACTTATTAATGTGTT | 57531 |
rs557216811 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104778210 | CTTTTGTTCATCTGC[C/T]AGGTAAGCAAACTGT | 57531 |
rs557219928 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801031 | TCTTAAATGACCTGA[G/T]GGAGCTGAAAACCAT | 57531 |
rs557251125 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698102 | TGTAAATGTTGATGA[C/T]AATAATTCACTTCCA | 57531 |
rs557258989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801439 | TCAAGGTTGAAATGA[A/G]GGAAAAAATATTAAG | 57531 |
rs557263927 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104845926 | TGTTTAAATGTGTGA[A/T]CGTGTGTCTATACCT | 57531 |
rs557283178 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104779385 | AATTCTTAATAAAAA[-/C]AATATGATCGATGAG | 57531 |
rs557283285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750989 | CTTCTCATGACATCT[A/G]GAGTAACATCCAAAT | 57531 |
rs557290512 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104753782 | ACAAAGGTAGATTAA[A/G]GCCAAAAAGATGAGA | 57531 |
rs557298595 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838662 | CTTTCTTGAGTAATA[C/G]CCCTTGAGCAAATTT | 57531 |
rs557305231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779170 | AGCAAATGATACAGA[C/T]GGCAAGAAAAGTCAA | 57531 |
rs557309005 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735580 | AGCTTACAGTGAGCC[A/G]AGATGGCGCCAGTGC | 57531 |
rs557325937 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104706561 | TTTGATTAGATGTTG[G/T]AATATGAGATCAAAA | 57531 |
rs557373569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770104 | TTTTAAAATAATCCA[C/T]ATTTTACTAAATCTA | 57531 |
rs557409090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104833560 | AATCAAGAACTCAGT[A/G]GGGCTCCAAGTGGTG | 57531 |
rs557442964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758241 | AACCCCAAGACATAT[A/G]AAATGTCAGATTCAC | 57531 |
rs557461242 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104846323 | AAATAAAGAAAAACT[-/C]TTCTTTCAAAACTGA | 57531 |
rs557462338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847108 | TTGTTTCTAAAAAAC[A/G]GTACATGAAAATTCT | 57531 |
rs557466838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787516 | AAACTATTTAGCTTT[A/G]TATCAGAAAATGAAC | 57531 |
rs557469569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750535 | TACTTAATGTTAATA[G/T]AATTATTTCTTATTT | 57531 |
rs557484691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104795809 | CCTTTAGTTATTTTG[C/T]CTTGCATAAGTTTAA | 57531 |
rs557489179 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690441 | CAACAGGAATATTTA[C/G]AATGAAACCAGCTGA | 57531 |
rs557524000 | snp | A/C | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729154 | CTAAAAAAATCATTG[A/C]AATATAGAATACACT | 57531 |
rs557541980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734333 | TTTCAGTAAGGTTGC[A/G]CTAAATTATACTACA | 57531 |
rs557574078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854039 | AAATATTGTGCTGTG[C/T]CTCCCGCAACTGAAA | 57531 |
rs557597896 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832181 | AATTGAGGCTTAACA[A/G]CAAAAGATAAAATAA | 57531 |
rs557599831 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104741913 | TGACTTCAAACTATA[C/T]GACAAGGCTACAGTA | 57531 |
rs557638159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845343 | TAAAATTCTCATTGA[C/T]TGAATAAAACTTTTT | 57531 |
rs557645325 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104721856 | TTGCAGTCTGAGAAA[C/T]TGAAGGTGGGTGGCT | 57531 |
rs557648190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757380 | CTGTTCTGCAGCCTC[C/T]GCTGGTGATACCCAG | 57531 |
rs557653551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804909 | AAGAAACTACCATCA[C/G]AGTGAACAGGCAACC | 57531 |
rs557655686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762889 | CAGCTACTCGGGAGG[C/G]TGAGGCAGGAAAATG | 57531 |
rs557669542 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855182 | GGGTGCAGTGGCTCA[C/G]GCCTGTAATCCCAGC | 57531 |
rs557688030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838485 | CTTCAATAAATGGTG[C/T]GGGAAAACTGGATAT | 57531 |
rs557691462 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104853237 | CACACTGTTGGACTT[A/C]CCAGCTTCCAGAACT | 57531 |
rs557722027 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712702 | GGTTGAACCCGCGAG[A/G]CGGAGGTTGCAGTGA | 57531 |
rs557722966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734309 | TCAACAATTGGAACA[C/T]GTTTGATTTTTCAGT | 57531 |
rs557766192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847810 | GAGAAGTTTTTTGGG[G/T]TTTTTTTTGTTGTTT | 57531 |
rs557786742 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715129 | TGCCCATAGTGGACA[A/T]TATCTAAGGCACTCT | 57531 |
rs557806934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763443 | CATGAATTTGTTTCA[C/T]TGAACCATCAGAAAG | 57531 |
rs557813956 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700516 | TGAACCTCAGGCAAA[A/G]CCCAGACTGGCTCCC | 57531 |
rs557838739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707462 | CAGTAAAAGTATTGT[A/G]TCTAACAAAGTCCAA | 57531 |
rs557847838 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104708059 | TTCAACATCATAATG[G/T]AGGTTCTAGCCAGGG | 57531 |
rs557900550 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807432 | TAGCCCTTTCTGTCT[A/C]TAGTAGAGACCTCTA | 57531 |
rs557910230 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699782 | CATGGAAGCTGAGCA[A/T]TAGCATTGTACATAG | 57531 |
rs557940243 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104817971 | AAGTTTAGAAAGTTG[A/C]AAATTGTTGCCTCTG | 57531 |
rs557966128 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104793607 | TCACTAATTAACATA[C/T]ATTTGAATCAGTTAT | 57531 |
rs557966484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706411 | AACTTAGAATACGTC[C/T]ATGAAGTAAAGTGAA | 57531 |
rs557993385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769607 | ATTATAATCTTCTAG[A/G]GCTTAACATGACTTA | 57531 |
rs557995655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721306 | CCGAGATCACCCCAC[C/T]GCACTCCAGCCTGGG | 57531 |
rs558000612 | snp | G/T | 0.046775 | 0.145601 | intron-variant | HACE1 | GRCh38.p7 | 6:104740383 | TGAATCCAGGAGGTG[G/T]TTTTTTGAAAGGATC | 57531 |
rs558009816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684200 | AGGTGATTTCATTCT[A/G]TTTTCATGTGATGGG | 57531 |
rs558023556 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806709 | TTTTGAGATAGTCTC[A/C]ATTTTTTAATATTGA | 57531 |
rs558028170 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684855 | TTATTTTGGATCTAC[A/G]TAGTAGTGTGCCAAG | 57531 |
rs558042280 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705768 | GTATCACTTCAATTT[A/C]TAGCTGAGTAGAAGG | 57531 |
rs558045542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778054 | ATGAGCCACTGCGCC[C/T]GGCCTCTTACTCCTA | 57531 |
rs558061502 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706473 | GCTGGAGTCAGTAGT[A/G]CTACACGAGATTGGG | 57531 |
rs558087819 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710089 | AAATTTTTATTAGCT[G/T]ATAAGTAGATAAAAT | 57531 |
rs558090192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830987 | GGCAAAGGGATCTCT[C/G]CACCTAATCTTGACC | 57531 |
rs558092978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835083 | CTGTTAACATCTTCC[A/G]GGCAGTTGGAAGAGT | 57531 |
rs558128153 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749855 | GAGGATGGCAAAGAC[A/G]ATGGACTCCATAGGT | 57531 |
rs558134030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104724822 | GAAGAAAATATAACA[C/T]AATTGTTGGGTAGTA | 57531 |
rs558178039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822998 | GAGACAAACTTGAAG[C/T]AAATCATAGAAAAAA | 57531 |
rs558191408 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724550 | AAATGTTTACAAACA[A/G]GCCAGGCACAATAGC | 57531 |
rs558205263 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777275 | AATCTGGCTGTCCTG[A/C]ATGCAAATGTTCATA | 57531 |
rs558228282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695477 | CAATGTGAAGAGCCT[A/G]ATTGAATGAGGCACA | 57531 |
rs558251049 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784034 | AAACAGTATTAGAAT[C/T]TTAGAAATTAATTTC | 57531 |
rs558269351 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731698 | ACCCTTACTTTACAC[A/T]AAGTTACTTAAAAAC | 57531 |
rs558282442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748662 | GCCTGAAACTGAAAA[A/G]TACCCACTAAATGTT | 57531 |
rs558290245 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712543 | CATTGGGAGGCTAAG[A/G]CAGGTGGATCATGAG | 57531 |
rs558318378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104820373 | AAGAGTTTCTGCATA[A/G]CGAAAAAAACTATCA | 57531 |
rs558328332 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761566 | GACGGATGAAAGACT[C/T]AAACGTAAGACCTAG | 57531 |
rs558330219 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734977 | AATCAAAATAAGGTC[C/T]GGATGGTTTAAAAAT | 57531 |
rs558357068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703315 | TGATTGCAATAAAGT[C/T]TAGAAATTTTTTTCA | 57531 |
rs558380461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756752 | GGGTGTCGTTTCACC[C/T]GGGAAGCGCAAGGGG | 57531 |
rs558381532 | in-del | -/CCT | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104737996 | AGAACGGGCAGACTG[-/CCT]CCTCAAGTGGGTCCC | 57531 |
rs558401314 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859171 | CCGATGCAGCTTAAA[A/G]TAAACAGTATCTTTG | 57531 |
rs558421106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803621 | GCAAAAACCACATGA[C/T]TATCTCAATAGATGC | 57531 |
rs558435888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851541 | CACTTGGATAATCCT[A/G]TGTTACCTGCTCTTA | 57531 |
rs558460386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800451 | AGCCTAACTAGGAGA[C/T]ACCTCCTAGTAGGGG | 57531 |
rs558461656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761426 | GCTCTTTGACAAATC[C/T]GACACACATAAGCAA | 57531 |
rs558487585 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737389 | GCCACGCAAAAGATG[A/C/G]TGATTTCTGCATTTC | 57531 |
rs558509344 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813841 | ACTCAGAATAACAAA[A/G]ACAGTAAAGGGAACC | 57531 |
rs558525850 | in-del | -/AAT | | | utr-variant-3-prime, nc-transcript-variant, cds-indel, intron-variant | HACE1 | GRCh38.p7 | 6:104728531 | ATTACTGGCAAACAC[-/AAT]GACTGCTTATGAGAA | 57531 |
rs558539389 | in-del | -/TT | 0.313141 | 0.280162 | intron-variant | HACE1 | GRCh38.p7 | 6:104856441 | CCTTTTATTTATGTG[-/TT]TTTTTTTTTTGAGAC | 57531 |
rs558563618 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773328 | CATTTTGACAATAAT[G/T]CACTCTGTGTTTCAC | 57531 |
rs558585429 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104848760 | AGTTAGGAGTGGCAA[A/T]AGATTAGCAGAAAAA | 57531 |
rs558591825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771815 | TACAGATGGGCTCCA[A/G]TCAAAATAAAAATTA | 57531 |
rs558609268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104797461 | GTCAGAACAAAAGTA[C/T]ATTTTATGGCACACT | 57531 |
rs558614088 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104844720 | CAGGCTGGAGTGCAA[C/T]GGCACAATTTAGGCT | 57531 |
rs558629315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687530 | AAGATAGTGGCCAGA[A/G]AAAGGAATTCCAAAA | 57531 |
rs558640207 | in-del | -/AGAC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719544 | AAAATAATAATAAAG[-/AGAC]AGCAGGAAACTTTGG | 57531 |
rs558645838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737667 | ATCCTGCACCTGGCT[C/T]GGAGGGTCCTACCCC | 57531 |
rs558661651 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736887 | GTATCTCTGAATAGT[-/G]GGGATCACTTAACAT | 57531 |
rs558665196 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796488 | TTAGCAAAAACTATA[C/T]TAATTATTATCTAAT | 57531 |
rs558668376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758825 | GTGCAAAGACACACA[C/T]AGGCTCAACATAAAG | 57531 |
rs558673818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772414 | ACATACACACACACA[C/G]ACGCACATATACACA | 57531 |
rs558717721 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824685 | AGAAATTTTCAGCAA[C/T]AGATACAAACAGATA | 57531 |
rs558724367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781989 | GTAAAAAGCAGAGAC[A/G]GTATTAGGTTGGTGC | 57531 |
rs558736477 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104744815 | TTATAAGATGTGGAG[A/G]TGTTTCCACATTGAT | 57531 |
rs558756398 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820986 | AATGAGGTACATATA[C/T]ACCACGGAATACTAT | 57531 |
rs558784409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764266 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATAT | 57531 |
rs558787948 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786383 | CAAATTCTTAATTCC[A/T]AGTAAAGATTAACAC | 57531 |
rs558793389 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818428 | AAAAGCCCAGGACCA[C/G]ATGAATTCACAGCTG | 57531 |
rs558793447 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851419 | GGTTTTGTCCCACAC[C/T]CACCACAAAATACTG | 57531 |
rs558798384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745498 | GTCACCCAGGCTGGA[A/G]TGCAGTGGCGCGGCT | 57531 |
rs558814233 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710605 | GGCTTCTCATCTTCT[C/T]CACTTTGAGCATCCC | 57531 |
rs558861491 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104856377 | TATTAAACAAACTGC[A/T]TTCACTATATAGTAG | 57531 |
rs558882344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819488 | TATATAGATTCAATG[C/T]TATTCCTATTAAACT | 57531 |
rs558900043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104857169 | TATTTACATATATAT[A/G]TTTATTTACATATAT | 57531 |
rs558931530 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104752743 | CTACATTTTATTTTT[A/T]AATTAATTTTTACAA | 57531 |
rs558940744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787894 | GAGAAAAAAAATAAG[A/G]TAAGTAATAAACCAC | 57531 |
rs558949479 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104717127 | CAAAGCAATATTGGG[G/T]TTTTTTTGTGGTTTG | 57531 |
rs558977586 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718771 | TTCACTAGAATTTTC[A/T]TAAGCATATCTGTAA | 57531 |
rs558985905 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803392 | ATCCTGATACCAAAG[C/G]CTGGCAGAGACACAA | 57531 |
rs558993013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825985 | ACACAGCAGGAGGTG[A/T]GTGGCAGGCAAGTGA | 57531 |
rs558999552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104685235 | CATAATCCAGCCTAC[C/T]CTACTGATGCCACAT | 57531 |
rs559009496 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104825041 | GAGCTGAGATGCGCC[-/A]ACTGCACTCCAGCCT | 57531 |
rs559014860 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | HACE1 | GRCh38.p7 | 6:104782805 | AATTAGTTCATAGCT[A/T]AACTTCTGAAAGGAC | 57531 |
rs559050535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736943 | TCTCCATTTTCCAAA[C/T]TTTCTACAATGATTA | 57531 |
rs559052346 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728751 | CCAAAAATTCAAAAA[C/T]CCACCAACATCCAAG | 57531 |
rs559072454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692109 | AAAGGAGGAAGCTAG[A/G]AAGGGAGGGAGAAAA | 57531 |
rs559081887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685752 | GCCCTGGTACGGGAA[A/G]TACAAATTTTTTTAA | 57531 |
rs559090328 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792333 | ATTAAATTAACATAA[A/T]CTCACTTTTACTGAT | 57531 |
rs559096293 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736662 | AGAGTAATAATTCCT[C/T]GTTTTAGTTATCTCT | 57531 |
rs559117271 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104840002 | CAGAGCGAGACTCTG[C/T]CTCAAAAAAATAAAA | 57531 |
rs559136311 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727057 | ATCTATATTTTAAAA[C/T]ATTCAAATTGATGGT | 57531 |
rs559137731 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684393 | ATTTACACCTTCCTG[A/T]TTTACAAAAACAATC | 57531 |
rs559140326 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735905 | CTAAAAATAAAACTA[C/G]ATAGCCATTAAAAAT | 57531 |
rs559154737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840532 | ATTTTAAAATCCATT[A/C]AAATAGCTGAGAGAG | 57531 |
rs559159334 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796574 | GCAAAATTACTAAGC[A/T]AAGCACATTTGTAAA | 57531 |
rs559162566 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756376 | GAGATCACACCACTG[C/T]ACCCCAGCCTGAGTG | 57531 |
rs559181528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104779825 | CTTCAAGAGCTGTTA[A/G]GATTAAATAATTCAA | 57531 |
rs559185027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104708364 | AGAATAAACTTAACA[A/G]AAGAAATGCAACACT | 57531 |
rs559196335 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729181 | CACTGTGGCAAAATA[C/T]GTATTTGTGGCTTTA | 57531 |
rs559232911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847329 | TTCAAGACCTTTGTC[A/G]ATACCCTATCAACAC | 57531 |
rs559236609 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778775 | GTGCTCACTTTGTCA[C/T]TCCAGCCTGAGTGAC | 57531 |
rs559255570 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104824749 | CACTCCACTTAAAGA[C/T]ACAAAAGGAAAAAAA | 57531 |
rs559303150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723477 | TTGAAGAAATAAGTA[C/T]GTGCCAATTTACACC | 57531 |
rs559306151 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104693305 | GCATTTTGTCAAGGA[A/T]ATTAGAAAGTCATAT | 57531 |
rs559316620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832446 | TCACCCAGGCTGGAG[C/T]ATAGTGGCACAATCT | 57531 |
rs559316695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840331 | ATAACACACAAAAAT[G/T]ATCTAACTAAAATTA | 57531 |
rs559349863 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805373 | ATACCCAATGGATTA[C/T]AAATCATGCTACTAT | 57531 |
rs559366157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104809493 | TTGCATTTAAGGAAC[A/G]CAAAGAGAATCACTG | 57531 |
rs559384688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714207 | CCAAATAAGATAGGA[A/G]GTTAAGAAAAGAGAG | 57531 |
rs559420249 | snp | C/T | 3.29462e-05 | 0.00405857 | intron-variant | HACE1 | GRCh38.p7 | 6:104833193 | GAAGCCATTTAGTTA[C/T]TTAACATTTGTGTAA | 57531 |
rs559429619 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104742327 | GGATCTAATTAAACT[A/G]AAGAGCTTCTGCACA | 57531 |
rs559436112 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819087 | AACAAATAGCAAGAA[A/T]AGAAGTCAAACTATC | 57531 |
rs559452938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743074 | AGAACAAAAAACCAA[A/C]CACCGCGTATTCTCA | 57531 |
rs559474336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853780 | CTGAAAGGGGACACA[C/T]CACTTTTGCAGTACA | 57531 |
rs559478003 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104823217 | GCCAGGTGGATCACC[C/T]GAGGTCAGGAGTTCA | 57531 |
rs559478923 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685435 | CAGAGCGAACACAGC[A/T]CAGCATTCAAAATTT | 57531 |
rs559485315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788462 | CAAGAAGTGCTGAAA[C/T]GAGGAATGAATTTGG | 57531 |
rs559492760 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712834 | CTCTTCTGCCATGTA[A/C]GGAACAGCATTTCCC | 57531 |
rs559501243 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733084 | ATTAATAACGTGACC[A/G]AACATAAAAAGGGAT | 57531 |
rs559524745 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | HACE1 | GRCh38.p7 | 6:104693025 | TGTCCAAAGAGTGGT[A/G]TGTGTGTGTGTGTGT | 57531 |
rs559531917 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104801895 | GCTAAATGCCCCAAT[G/T]AAAAGACAGACTGGT | 57531 |
rs559551557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823903 | ACAGACAACCTGAAT[C/G]ACAGTTTTAAGAAAC | 57531 |
rs559560481 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796143 | GAGCATCACTGTATC[A/G]CCCAGGCTAGAGTGT | 57531 |
rs559596496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787995 | AATCCCAACCTTGAG[A/G]TGAGTTTACCTAGGA | 57531 |
rs559606852 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104682969 | GGGGCCAGGGCCACA[C/T]TGGGAACTGAGTACT | 57531 |
rs559641163 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104751198 | CTCACTGAAATGTCT[C/T]ATTAGAATGTAATCT | 57531 |
rs559668250 | snp | C/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104795087 | TAAATTCAAGTAATA[C/T]AAGGCATTAACTCCA | 57531 |
rs559673970 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711881 | TGGGTTCAAGCAATC[A/C]TCCTGCCTCAGCTTC | 57531 |
rs559681525 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727608 | ACGTATGTATATGAA[C/T]ACACACACACGTATG | 57531 |
rs559683943 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861803 | CTGCAATATGATGCC[G/T]TCTCCCAATAGCTCT | 57531 |
rs559724146 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104805796 | CCAACATGGCACATG[C/T]ATACCTATGTAACAA | 57531 |
rs559766921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757922 | CTCCAATAGCCGATT[C/T]GATCAAGTGGAAGAA | 57531 |
rs559780561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711067 | TCAATGTTACATGAA[C/T]GCAGAGCAGAGTGGT | 57531 |
rs559796144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813453 | GGGACAATGGGTCTA[G/T]AGCAGTCATCCCCAA | 57531 |
rs559816298 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104831423 | AACCCCATCTCTACT[A/G]AAAATACAAAAAGTA | 57531 |
rs559852105 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710743 | TTTATTTGCTGATCC[A/G]CCACAGATAAGTTGG | 57531 |
rs559871217 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104711714 | ATCAACAGTATGCTT[C/G]ATTCTCCTAGATGAA | 57531 |
rs559876792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858659 | AAAGAGAGTTTTGAA[A/G]AAGTAAGATAAACTA | 57531 |
rs559889795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104831818 | GAATGGCATGAACCC[A/G]GGAGGCGGAGCTTGC | 57531 |
rs559890883 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737394 | GCAAAAGATGGTGAT[G/T]TCTGCATTTCCATCT | 57531 |
rs559902633 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792468 | TATTGAATCTAATAA[C/T]ATATCTTTAAACACA | 57531 |
rs559906231 | snp | A/G | 0.00716266 | 0.059414 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727765 | TATATGTATATGAAT[A/G]TGTACACACATATAT | 57531 |
rs559916348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778547 | TGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 57531 |
rs559932350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763166 | GTTTTCATGTTTTCA[C/T]TGTTGACAGGAAGAT | 57531 |
rs559954375 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104767150 | ACATAAAGAACATGG[A/T]TCAGATACATGAAAC | 57531 |
rs559956128 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718890 | CACATCCCCTCTTTT[A/G]TGGAATAACTTGAAT | 57531 |
rs559957361 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812521 | TTCATCTTTTTTGCC[A/G]CTTTTAAACAAAGTA | 57531 |
rs559957602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104812511 | AACACATCTGTTCAT[C/T]TTTTTTGCCGCTTTT | 57531 |
rs560012565 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104782184 | AACAGTATCATACAG[A/T]GTAGGTTAAGAAATT | 57531 |
rs560037539 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778469 | CAATGAAGCCAATCC[A/G]AGAGATACTACTTCT | 57531 |
rs560048460 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692779 | AAACGTGCTAGTTAA[C/G]ATCTAATTAATTTCT | 57531 |
rs560049192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828158 | TTTAATTTATGGTCC[A/T]AAAAGCGTTAATAAA | 57531 |
rs560064650 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768396 | AACAAACCAAAAATC[A/C]ATAGTATTTCCAAGA | 57531 |
rs560079834 | in-del | -/ATA | 0.00137533 | 0.0261873 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851048 | AAAGTTTTTAAAAAC[-/ATA]ATAAATCAAGTTAAC | 57531 |
rs560100709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104766032 | TCACTGTTACCCACA[A/G]GGGTATCTGCAGGCC | 57531 |
rs560103872 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104735499 | AGCCATGCATGGTGG[C/T]GGGTGCCTATAGTCC | 57531 |
rs560110836 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104774381 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTCTCTTT | 57531 |
rs560123501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104790850 | CACCCAAAAAAACAT[C/T]AACAAGAGCAATTAT | 57531 |
rs560129610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781721 | CACTGATCAGCTGCA[A/G]CCACCGCCAACATGG | 57531 |
rs560135069 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104821296 | CGTGACACAAGTTTA[C/T]CTATGTATCAAACCT | 57531 |
rs560153229 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717960 | TTATGGATATCTTTC[C/T]CGATCTGCCATCTTC | 57531 |
rs560153731 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754957 | AACATTAAATGTAAA[C/T]GGGTTAAATGCCCCA | 57531 |
rs560175709 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687766 | TGGGACCCAGCCTAG[A/T]TTATAGGTCAGAAAG | 57531 |
rs560191458 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104753178 | CCCAGTAACATTTCA[A/G]GTGTTCATGTTGTGT | 57531 |
rs560237063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858220 | ATTCAAACTAGACAA[C/T]ATAAATTATACATGT | 57531 |
rs560241591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789825 | ATCATGGGTAGATTC[A/C]GTCACTAACAAAGTG | 57531 |
rs560243321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745637 | TAGTAGAGATGAGGT[C/T]TCACCGTGTTAGCCA | 57531 |
rs560253290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820623 | TTAGAGAAATGCAAA[C/T]CAAAACCACAATGAG | 57531 |
rs560297771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759759 | AAATCAATAAATCCA[A/G]GAACTAGTTTTTTGA | 57531 |
rs560303337 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | HACE1 | GRCh38.p7 | 6:104737716 | CTAGCACAGCAGTCT[A/G]AGACCAAACTGCAAG | 57531 |
rs560309813 | in-del | -/CCC | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104720634 | CTTCCCCGCCCCCCT[-/CCC]CCCCCCCCCAGACGG | 57531 |
rs560318816 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104766382 | CAGGTATGGGATTTA[C/T]CACTTATGGCTTCAT | 57531 |
rs560324108 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746069 | CTGTTAAACAGTACC[A/G]GTCTTCCCACTGTTT | 57531 |
rs560337299 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720000 | AGGTATGCGCCACCA[C/T]GCCCGGCTAATTTTT | 57531 |
rs560343238 | in-del | -/TT | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104727001 | ATATTAACTACACTC[-/TT]ATTTTAAAAATGTGA | 57531 |
rs560373812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764495 | TTTCCTCCAGGGTTA[C/T]CTGCCTCATTAACAA | 57531 |
rs560376607 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104725055 | CCTTTTTTTTTTTTT[A/T]AACTGTTTACAAAGA | 57531 |
rs560395154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849498 | ATGAGCCACCACAAT[C/T]GGGTAATTTTTTTTT | 57531 |
rs560429274 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848777 | GATTAGCAGAAAAAA[A/G]GCACACTAAAATAGA | 57531 |
rs560450194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803472 | AATCCTCAATAAAAT[A/G]CCAGAAAACCAAATG | 57531 |
rs560493621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730526 | ACTCTAGGACAATGA[C/T]AACACGACACTTTTT | 57531 |
rs560498840 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104717380 | CCAACCTCAGGTGAT[C/T]CACCTTCTTCGGCCT | 57531 |
rs560504094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834751 | ATTAGAGAAACCCCC[C/T]AAAAAATGTGATTCA | 57531 |
rs560522294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702743 | AGACTACTAATAGGA[C/T]GCATAAAGACTGTGA | 57531 |
rs560569688 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852149 | CACACACACAAAATT[A/G]TAACAGAAAAGTTAA | 57531 |
rs560580382 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104841136 | AAAAAAAAAAAAAAA[C/T]AGCTGAGAGAAGTTG | 57531 |
rs560604235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848977 | ACAATATCATCAATA[A/G]TATCTTTGAGAGACA | 57531 |
rs560626904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104797892 | TGGCCAACATGGTGA[A/C]ACCCTGTCTCTATTA | 57531 |
rs560637807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811189 | ATACACAGAAACGTG[C/T]GTGTCTAGAAATAGA | 57531 |
rs560638805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819483 | CAATTTATATAGATT[C/T]AATGCTATTCCTATT | 57531 |
rs560644118 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709560 | TGTCTCTTGCCACGT[A/G]ACATGCTGGCTCTCC | 57531 |
rs560659548 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104694868 | TTTGTGAACAAGGGG[C/G]CCACATTTTCACCTT | 57531 |
rs560665125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820376 | AGTTTCTGCATAGCG[A/G]AAAAAACTATCATCA | 57531 |
rs560666535 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104855430 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCGGA | 57531 |
rs560670460 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104765333 | GATTGAGAACACAGG[C/T]TTTTGCCTATCATGG | 57531 |
rs560675944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814138 | AAAGAAAAGAAAGGG[A/G]GTGAGGGACCAAAGG | 57531 |
rs560740510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826437 | CAGGATTTTCTATGA[C/T]TTGGATTCAATTTAT | 57531 |
rs560743179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803699 | TCAATAAACTAGGTA[C/T]TGATGGAACGTATCT | 57531 |
rs560747842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810685 | ACACACCTACAACAA[C/T]GCATGACACAGTGAG | 57531 |
rs560748071 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104819713 | CAATGAAACAGAATC[G/T]AAAACCCACAAATAA | 57531 |
rs560750280 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715773 | CCACCATTGAGGTAT[C/G]TTAAAAAGAAGGCTG | 57531 |
rs560796374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724989 | GAGAGAGCTAAAAAC[A/G]GTGCTAATTATCAGG | 57531 |
rs560803905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716823 | ATGAAGCACAAATGG[C/G]CAGTAAATTATAAAA | 57531 |
rs560841492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104694736 | TAAAGTATGGTTAGA[A/G]TGACACCATATGACT | 57531 |
rs560847368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789576 | GTATTGACTGTGTAG[A/G]TAGAAAACTAACATT | 57531 |
rs560855533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687177 | CTCTGGGGCCAAGGC[A/C]GGGACACAGTAAAGG | 57531 |
rs560900070 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104812476 | TAGTTTGAAATTAGA[C/T]GCTTATTACTTCTGG | 57531 |
rs560924689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857655 | CTATTGAAGAATACA[A/G]AAAAAAAAAAACATT | 57531 |
rs560925921 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104857000 | TTTACAAGTTTAATA[-/G]TTTGTTGTAATTAGA | 57531 |
rs560931948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731255 | GCTTTTTGGATAAAT[C/T]AGAAAAATGACAAAG | 57531 |
rs560942210 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764655 | TCACTATTATCACCA[C/T]CACCTACACTCAGAA | 57531 |
rs560945965 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702427 | TTGTGAGCAGGTTTG[C/T]TCCTATGTTGTCAAA | 57531 |
rs560947922 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104782101 | TTTTGCACCAACCTA[C/T]ATTAAAAACAGCAGA | 57531 |
rs560976211 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693815 | AAAGTAAAAGAGAGG[C/T]GGCGTCACAGGAAAC | 57531 |
rs560984006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804468 | GACTTCAAACTATAC[G/T]ACAAGGCTACAGTAA | 57531 |
rs560990746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833356 | TTTTTCCTTTTTTAA[A/G]TTTGTTTAAGTTTTA | 57531 |
rs560995205 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818811 | AACAGATGCAGAAAA[C/G]GCTTTTGATAAAATT | 57531 |
rs561031670 | in-del | -/AG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816095 | AAAAAAAGAGGAAAC[-/AG]AACACAAAGTTTGGA | 57531 |
rs561086840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772871 | GGGATATGGGAGATA[C/T]TGCTTAACGGGTACA | 57531 |
rs561100139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104803653 | GAAAAGGCCTTCGAC[A/G]AAATTCAACAGCCCT | 57531 |
rs561125997 | in-del | -/GAGAC | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851102 | GTTTGTTTGTTTGTT[-/GAGAC]AAGAGTCTTGCTCTG | 57531 |
rs561131711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730441 | TATATCTTAATACAT[G/T]GTAATCATGAAAGAA | 57531 |
rs561148082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724348 | TTCTATGACCACAGA[A/G]CAATTGATGGACATT | 57531 |
rs561158953 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702644 | TCCATTAATCTCCCC[C/G]CTGTTATCAAGTGTC | 57531 |
rs561183937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700839 | GCTGAATTCTAAGAC[C/T]TAGAAATGATTTTAA | 57531 |
rs561194552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104802777 | GAAAGATCTAAAATC[A/G]ACACCCTAACAGCAC | 57531 |
rs561199407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737418 | TCCATCTGAGGTACC[A/G]GGTTCATCTCATTAG | 57531 |
rs561200662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771085 | TTATCTGCTATGATA[C/T]TGTAATAGTAAAAGT | 57531 |
rs561208105 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751472 | TACTTAAAATTTAAC[C/G/T]GGTAATAAGCAGAGG | 57531 |
rs561210355 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848373 | AGGCAGGAGAATCAC[G/T]TGAACTCGGGAGATA | 57531 |
rs561233765 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712412 | ACCTATGCAACAGTG[C/T]TGGGGGTTGGAGGTC | 57531 |
rs561241570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833988 | GACTCCGTCTCAAAA[A/G]AAAAAATTAGCTGGC | 57531 |
rs561242541 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104848922 | TATGATAGCTATTTT[G/T]AAATTGAATATAATG | 57531 |
rs561260397 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789563 | CTCTATTATGTCTGT[A/G]TTGACTGTGTAGGTA | 57531 |
rs561285764 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104809721 | AGGGAAACAACATAG[C/G]AATCAGGGAGACCAG | 57531 |
rs561287703 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744993 | TAAGGAGACAGTATT[C/G]TCAACATGAAAGTGA | 57531 |
rs561289090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763787 | AGGCTCAGTGGCTCA[C/T]GCCTATAATCCCAGC | 57531 |
rs561300315 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743083 | AACCAAACACCGCGT[A/G]TTCTCATTCATAGGT | 57531 |
rs561387698 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786154 | AGCCTGGCCAACATG[A/G]TGAATTGAAATCCCA | 57531 |
rs561393562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104709314 | GTACATGAAAAGATG[C/T]TCATCCAATGATATA | 57531 |
rs561401802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759006 | AGAAGAGCTAAATGA[C/T]CTAAATATGTATGCA | 57531 |
rs561418330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803399 | TACCAAAGCCTGGCA[A/G]AGACACAACAAAAAA | 57531 |
rs561439523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818362 | GATGGAAAGTAGCAA[C/T]GGTGTTCACTACTGT | 57531 |
rs561449200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723434 | TCTCCAATTTTCTCA[C/T]CTGTAAAGTGAAGGG | 57531 |
rs561478434 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752244 | ACAAGTCACATACAG[C/G]TACTTATTATAGAGA | 57531 |
rs561504656 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104845202 | TTATTCAACTAGATC[A/G]TAAATATCTTCATAC | 57531 |
rs561534417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722773 | TATTTCCTTTAAGGG[C/T]AAATACTGGGTCACA | 57531 |
rs561552570 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762713 | TTTTAAAAAAAGGCC[A/G]GGCGCGGTAGCTCAC | 57531 |
rs561557333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104690464 | CCAGCTGATTCTAAG[A/G]TTAATATGGAAAAAT | 57531 |
rs561562565 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838086 | CAAAATGGAAAAATA[G/T]TCCTAAGGGTTGGAA | 57531 |
rs561575894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810610 | GGGTGTGGGTGTGAC[A/G]GCATGTGTATAATTA | 57531 |
rs561608362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756518 | CTGATAAAAATCCTA[C/T]TACTTCAGCTTCCTT | 57531 |
rs561622011 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104739741 | TAACACCCCACTGTC[A/C]ACATTAGACAGATCA | 57531 |
rs561643142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698126 | ACTTCCAGGGTCATA[C/T]AAAACTTACAAATAA | 57531 |
rs561655123 | in-del | -/GTGA | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104699826 | TCTACAGCAGTAGGC[-/GTGA]GTATGAATAAAGGGT | 57531 |
rs561664688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104845546 | ACAGTGGCACGATCT[C/T]GGCTCACTGCAAGCT | 57531 |
rs561676136 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748821 | CATTCTATTTACATA[A/C]TTCTAAAATAGGCGA | 57531 |
rs561684791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733709 | CAAAAATTAGCCAGG[C/T]GAAGTGATGTGTGCA | 57531 |
rs561684979 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104740628 | GAAGTTGAATCTCTG[A/G]ATAGACCAATAACAG | 57531 |
rs561687472 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852485 | GAAAAGGAGAGGAAG[A/G]AGGAGGAAAGAATAA | 57531 |
rs561691987 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768782 | AAACTGAGAAACAAA[A/C]GTTTCAAGCTCTTTA | 57531 |
rs561692277 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104766651 | AAACATACTAAATTT[C/G]TATTTGCTACTTTGT | 57531 |
rs561719990 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859404 | GGGAGCGTCGGGCCA[C/G]GGGAGTTCGGGGCCC | 57531 |
rs561720235 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837263 | CAGTAATCGAGACAG[A/T]GTGGTATTAGCAGAG | 57531 |
rs561743059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732815 | ATCCAATATGAAAGA[A/G]TCCCTAAAAACAGCA | 57531 |
rs561776664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852424 | CTTTGTGCAAGGGGT[C/G]ATACTTAAGATTAGT | 57531 |
rs561780872 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104806948 | ATTATTGGGAATGGC[A/G]TATGAAACAGATCAT | 57531 |
rs561805847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104719884 | AGTCTCACTCTGTTG[C/T]CCAGGCTGGAGTGCA | 57531 |
rs561809938 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771706 | ACACACAAAAATTGA[-/A]AAAAAAAAAAAAAAG | 57531 |
rs561820706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815199 | TGATATGGACAATGA[C/T]GTCCAGGCTGAGGTG | 57531 |
rs561821914 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825856 | TCAAAATGCCAAGAA[A/T]CTGGACACCCTCCAC | 57531 |
rs561852902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712721 | AGGTTGCAGTGAGCC[A/G]AGATCATGCCACTGC | 57531 |
rs561881055 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104738860 | CAACTCCAAGACACA[C/T]AACTGTCAGATTCAC | 57531 |
rs561906923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104720342 | CAGTAATTTGGCCTT[C/T]TCTAAAATGTCATAC | 57531 |
rs561912609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705334 | TCAGGAAGGAAATCT[C/T]AAGAAAGGTATCAGG | 57531 |
rs561925918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829598 | ATCATCATAGGTAAC[A/G]ATCCAGAAAATAATC | 57531 |
rs561949927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705394 | AGGGCTCAGAAACTC[C/T]TAAGGGAGCAAAATG | 57531 |
rs561965545 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738143 | TAACAAACAGAAAGG[A/C]CATCCACACCAAAAA | 57531 |
rs561980127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822602 | TGGCTCACACCTGTA[A/T]TCCTAGCACTTTGGG | 57531 |
rs561980429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814456 | TCAAATAGATGGTTA[G/T]AAATAAAAAACATGT | 57531 |
rs562002522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711596 | CACTGCATTTAGTCT[C/G]GTAGAGGAGCACACT | 57531 |
rs562012588 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703201 | TTAGGGGCAGAGATT[C/T]ACTCACAGTAAAGCC | 57531 |
rs562016748 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104849742 | CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT | 57531 |
rs562046348 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836419 | CATACAAACTGCGAA[G/T]AAAGAAATAAAGGCC | 57531 |
rs562088940 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750883 | ATTTAAAAATATATA[G/T]ATGTGTATATACACA | 57531 |
rs562095453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822106 | GGGCGCGGTGGCTCA[C/T]ACCTGTAATCCCAGC | 57531 |
rs562108606 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104800061 | CAGGAGATTCCATCC[C/T]GTGCCTGGCTCAGCG | 57531 |
rs562145772 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104800509 | CCCTCTGGGATGAAG[C/G]TTCCAGAGGAAGGAA | 57531 |
rs562152052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799795 | GAACAGCTCCGGTCT[A/G]CAGCTCCTAGCATGA | 57531 |
rs562154843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688737 | CTGTGGGCTTTTCCC[A/G]GCTGATGGGAAATTC | 57531 |
rs562162729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792608 | AGCAGGATTAACTTT[A/G]TATGTTGGAGGCCAA | 57531 |
rs562166999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104689509 | TATTTACTATAAAGT[C/T]TTAGTCCCTATTCTA | 57531 |
rs562178288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835525 | TAATATTGAGGAAGT[C/G]TCCCTAAAAGTACAA | 57531 |
rs562213299 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104847401 | AATGAATGATTTACT[-/C]TATGACCTTGGGTGT | 57531 |
rs562219732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805819 | TGTAACAAACCCGCA[C/G]GTTGTGCACATGTAC | 57531 |
rs562230577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104805182 | GCCAGTTAGAATGGC[A/G]ATCATTAAGAAGTCA | 57531 |
rs562278924 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104791816 | AGAACAGTTTAACAG[A/G]AAGTTACATTATTTA | 57531 |
rs562322308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767749 | TGGTTTCCCAAAGCA[A/T]GCTCTGTCACCTCTG | 57531 |
rs562326081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705286 | CAGGATGTGGTCAGA[A/G]GCGTCGTTCCTCCTC | 57531 |
rs562370681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104727202 | GTATACGAATATATA[C/T]ACATACATGTATACG | 57531 |
rs562379869 | in-del | -/TGTT | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104706178 | GAATATCCAGATTTA[-/TGTT]TGTTTGTTTGTTTGT | 57531 |
rs562387082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754028 | AACAATACAGGAGCT[A/G]ACAGCCACAACAGTC | 57531 |
rs562419907 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104695874 | GCTGGGACTACAGGC[A/G]CCCGCCACCACACCC | 57531 |
rs562428874 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104747756 | CAAGAGATTTTTTGT[C/G]AGCGTTTTTAAAGTT | 57531 |
rs562477803 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797216 | CTACGTAGACCAGAA[A/T]GTGACCTATTAAATT | 57531 |
rs562486977 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841472 | CGTGTCACTAAGCAT[C/G]CTACGGATATTCAGA | 57531 |
rs562491746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748739 | ATTAAAATGAACAAA[C/T]TACCAACTGCATGCA | 57531 |
rs562491756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104739127 | AAATGCTGAGAGATT[C/T]TGTCACCACCAGGCC | 57531 |
rs562494554 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104822071 | CATAATTTTTTTTTT[A/T]AATTATCCAGGCGTG | 57531 |
rs562507128 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104792776 | GACCCAGGCATAAGT[A/T]TTTCTTGTGATTAGG | 57531 |
rs562522082 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746592 | GGTTCAGGCTCCCAC[A/G]GGGCTCTTCACAGTA | 57531 |
rs562523482 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858743 | CTCACTTGGGCATAA[A/C]GAGCCAAAAGCTTCT | 57531 |
rs562540979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737633 | GATGGGCTTAAAAAA[C/T]GGCGCACCACGAGAT | 57531 |
rs562559923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704783 | ATTGGGACTATTCAC[A/G]GCAGTCCCAATTTTA | 57531 |
rs562560537 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104773772 | TAAGGAGACTTTTTT[A/T]AAAAAAAAAAAGGAA | 57531 |
rs562579673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814290 | AAGTGAAATTTCATG[A/G]TAACATCAGGGATAA | 57531 |
rs562586670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754999 | AAGAATGGCAAGCTG[G/T]ATGAAGAGCCAAGAC | 57531 |
rs562616012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851080 | CAACTCTTTAGCTGC[A/T]CTGTTTGTTTGTTTG | 57531 |
rs562649395 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713563 | CCGCACAGCTAGTAA[A/C]TATTAGAGCCAAGTT | 57531 |
rs562665473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813505 | GGAACATGAGGCAAC[C/T]TTTTTATTTTCATGA | 57531 |
rs562676962 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834917 | GCCCCCACTCAACCA[A/G]ATAGAATGCAAGAGG | 57531 |
rs562687531 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858278 | CGACTACGAAAAATA[A/C]GTAAGAGTAGCACTT | 57531 |
rs562702888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745153 | CAATTCTGGAATAAT[C/T]TGGATCCTGTAAAGT | 57531 |
rs562718298 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104719845 | AATTTATAGAAATCA[A/G]CTTTACTTTTTTTTT | 57531 |
rs562734284 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847647 | AAATTTGGCCTCGGA[C/T]TGATGTAATGGACAA | 57531 |
rs562736376 | snp | C/T | 0.0659589 | 0.169201 | intron-variant | HACE1 | GRCh38.p7 | 6:104738080 | CCTCACACGGCAGGG[C/T]ATTCCAACAGACCTG | 57531 |
rs562747502 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712039 | CCTCATCCTCCCAAA[A/C]TGCTGAGATTATAGA | 57531 |
rs562764483 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104745842 | TGTACCTTAAATAAG[A/G]TTGATATAAGGCAAC | 57531 |
rs562857863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827486 | AATTCTTACATAGTA[A/T]CCGGCAAAAATCATT | 57531 |
rs562867655 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791708 | AAATTACATATTAAA[A/T]TACTTATTTTAAAAC | 57531 |
rs562882977 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771578 | GTGTTTCTTTCACAT[C/T]GTTACAATGTAATCT | 57531 |
rs562892483 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104753247 | GGTATCTCACTGGGA[C/T]CGAGCTCCGGGGACA | 57531 |
rs562928545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695853 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 57531 |
rs562937921 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702771 | TGACTCTGACAATAC[C/T]GTTAGATAAATAAAA | 57531 |
rs562956753 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766656 | TACTAAATTTGTATT[C/T]GCTACTTTGTTCACA | 57531 |
rs562966005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770405 | TTTTTAAATAATACA[C/T]ATAGAGGAGAGGTAA | 57531 |
rs562973537 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834896 | AACTGTGCAAGGCCA[G/T]TAATGGCCCCCACTC | 57531 |
rs562990617 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832477 | CAGCTCACTGCAACC[A/G]CTGACTGCTGAGCTC | 57531 |
rs563021088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687909 | TAAAAATAAACAAAA[A/G]CCTAACCCTGGATCG | 57531 |
rs563028762 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829924 | TTATACTTATACCAC[C/T]TAATTTTCAGTAACT | 57531 |
rs563034092 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737767 | GGGGCGCCCGCCATT[G/T]TCCAGGCTTGATTAG | 57531 |
rs563035354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804400 | AAAAAAGTGCCCTCA[C/T]TGCCAAGACAATCCT | 57531 |
rs563042668 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104760206 | TATTTTATGAGGCCA[A/G]CATCATCCTGATACC | 57531 |
rs563076911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798559 | TAATTTATTCTAGAA[A/G]AATCAAAAAATAAAT | 57531 |
rs563078122 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104849641 | AGCCGCCATGCCTGG[C/T]CTTAAACACATTTTT | 57531 |
rs563080631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104849021 | AAATAAAATATGCAC[C/T]ATTATTTTAGTTTTT | 57531 |
rs563120164 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694985 | CACTCATGTCGGAGA[A/G]TTAAAGCCACCCTAG | 57531 |
rs563150669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803766 | CAATATCATACTGAA[G/T]GGGCAAAAACTGGAA | 57531 |
rs563164279 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104742111 | CTGGCTAGCCATATG[G/T]AGAAAGCTGAAACTG | 57531 |
rs563165415 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104710354 | TACTAATGGATACCT[C/G]GGTTTCTTCTGGATG | 57531 |
rs563193196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852534 | TTTCAGAATTTACGA[C/T]AGTGAAGAATCTTTC | 57531 |
rs563200735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714740 | AAGCTTAGAGCAGAA[C/T]AAGCTCCAATAAAAC | 57531 |
rs563212343 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104720277 | TGTCCTTTTGTAAAG[-/TA]TACTCCCTTAATCTT | 57531 |
rs563259217 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803149 | TAAACCAGGAAGAAG[C/T]TGAATCTCTGAACAC | 57531 |
rs563283934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104832518 | CCCACTTCAGCCTCC[A/G]GAACAGCTGGGACTA | 57531 |
rs563294249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735814 | AATCAGACTGTCCCA[C/T]AAGGATAGAAGCACA | 57531 |
rs563295607 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697263 | AATGCATCGATTTCC[A/G]TTGCTACAGCCCTAG | 57531 |
rs563305053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685299 | CAGACCTCTGTAACT[G/T]GTAGAGGTCAGGGAA | 57531 |
rs563308396 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728639 | ATAACAAATCCTTCC[A/G]TTAGCATTTCTTCGT | 57531 |
rs563325940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721420 | TGACTCAGTCCCCAG[C/T]AGTTTTCAACTCCCA | 57531 |
rs563325992 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104713522 | AGAAAACCAAGACAA[C/T]TGGAGGTTGATTAAC | 57531 |
rs563360416 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691713 | TTGGGAGCTCAATGC[A/G]TAGTTCAAGACCAGC | 57531 |
rs563364363 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104692059 | GGAAGGGAAGGGGGG[A/G]AGGGGTAGAAGGAGG | 57531 |
rs563376451 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684812 | TTTTTTAAAGCTAAC[A/G]TGTATTTATTTTAAG | 57531 |
rs563378272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832168 | ATCTAATCTCCAAAA[C/T]TGAGGCTTAACAGCA | 57531 |
rs563378343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104692836 | AGTGACATAAACAAG[C/T]TAGTTCATATCTAAT | 57531 |
rs563390998 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774932 | AAATTCTTGATTCCT[A/G]TATGTAATTCTCTTT | 57531 |
rs563425040 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104787946 | CTCTCTTTTCTTACC[G/T]TTTATTTCTTCAATC | 57531 |
rs563446579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801656 | AAATCCTTTACAGAC[A/C]TGCAAATGCCGAGAG | 57531 |
rs563476275 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753615 | AAACCAAGGCAACTG[A/G]GGTCTGGAGAGGACC | 57531 |
rs563483847 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794926 | AATAATTGTATATAT[C/G]TGTGTGTGTGTGTGT | 57531 |
rs563516500 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694805 | ATGCTCAAAGAGCCC[C/T]GCACTTGGTATAATG | 57531 |
rs563528774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699874 | CCTCGGCTGAGGCAG[A/G]CCTGCTTGAGAATGA | 57531 |
rs563541179 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778618 | TGGGCAACAGTGAGA[C/T]CCTGTCTCTACCAAA | 57531 |
rs563604176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757744 | TGGTAATAACAAACT[C/T]CTCCAAATTAAAGGA | 57531 |
rs563621082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707516 | TACCAAACTGGGAAT[A/G]GAATAGAAGATGCCT | 57531 |
rs563658389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690241 | TTTTGTGAACTTGAG[A/G]AATAAGAAATGTTTT | 57531 |
rs563663966 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710401 | CTTAGATAATCGTGA[C/T]GGTTGCATAACTCCA | 57531 |
rs563676367 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729049 | TTCATACAATATAGC[A/G]TAAGCTTTCATATAT | 57531 |
rs563729033 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733677 | AACATGGTGAAACCC[A/C]GTCTCTACTAAAAAT | 57531 |
rs563737333 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104727328 | GTATACGAATATATA[C/T]ACACATGTATGTATA | 57531 |
rs563752676 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104777712 | TAATTTTTCATGAAA[A/G]TAATCTCTTACACCT | 57531 |
rs563784275 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706954 | AAAAACTCCTAGAAA[A/C]TGCAAACACAAAACA | 57531 |
rs563796689 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104844856 | TTTAGTAGAGACTGG[G/T]TTTCACCACGTTGGC | 57531 |
rs563800138 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683700 | GGATGCCTTATCACG[C/T]ACTTCGGAAAGATAC | 57531 |
rs563806343 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104748482 | TCACACCTCCTAATG[G/T]GAGTGTAAACTGATG | 57531 |
rs563817366 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855829 | AAACTTAAATCAAGA[A/T]AAACTTTAAATCAAG | 57531 |
rs563818221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793205 | CCGGGAGGTGGAGCT[C/T]GCAGTAAGCCGAGAT | 57531 |
rs563828331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837086 | CCCCAAATTGACCTA[C/T]CAGTTTAAAGCAACT | 57531 |
rs563854650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104784901 | TCAACAAATTATTAT[C/T]TGTTGTTTTTGAAAT | 57531 |
rs563868704 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104786139 | CAGGAATTCGAGATC[A/T]GCCTGGCCAACATGG | 57531 |
rs563888699 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776115 | CACCATTTCAACAAG[A/C/G]AGAGTTAATTATCTG | 57531 |
rs563900686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104809529 | CAAGTACAGTGAGCT[A/G]AACAGGAGTGAAATC | 57531 |
rs563971119 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836540 | CAACAAGGTGTAACC[A/C]CGTCTCTATTAAAAA | 57531 |
rs563991590 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704309 | AAGCAGGTAATAAAA[G/T]AAAGTCGGCATTGGA | 57531 |
rs564007254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739637 | CTAAATATATATGCA[C/T]CCAATACAGGAACAC | 57531 |
rs564017877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794213 | ATATTCGAATGCTCC[C/T]TAGCTTGGTACCTGC | 57531 |
rs564036634 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685425 | GCCAGGCTTTCAGAG[C/T]GAACACAGCTCAGCA | 57531 |
rs564050236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691383 | TTGTTGGGAAGGTGA[C/T]TAGAACAATCTTTAT | 57531 |
rs564060543 | in-del | -/AG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700155 | GACAGAAAAAAAAAA[-/AG]AAAGCTGTCACTGGT | 57531 |
rs564060958 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | HACE1 | GRCh38.p7 | 6:104742002 | AGCCCTCAGAAATAA[C/T]GCCACGTATCTACAA | 57531 |
rs564068430 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104831484 | CAGCTACTTAGGAGG[C/T]TGAGGCACAAGGATC | 57531 |
rs564068517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838805 | TAAAGAAACAACCCA[C/T]AGAATGGGAGAAAAT | 57531 |
rs564084165 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860017 | GCAGGGCTGAGTATG[A/C]GGGAAGCCACGCAGC | 57531 |
rs564086899 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727633 | CGTATGTATATGAAT[A/G]CATACACACGTATGT | 57531 |
rs564090106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756573 | AGTGATCGAAGAGTC[A/G]TTTCCAAGATGGCCG | 57531 |
rs564105120 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104832033 | GGAAGGAAGGAAGGA[A/G]AAAGAAAAGAAAAAG | 57531 |
rs564124061 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104735177 | TGGAAATCTCTATAT[C/T]TAACTTTGATACACC | 57531 |
rs564130594 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801147 | ATTAATGACATAAAG[G/T]GAAAAGACAAGATTA | 57531 |
rs564144281 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691984 | AAGGAAGGAAGGGAG[A/G]GAGGGAGGGAAGGAG | 57531 |
rs564157006 | in-del | -/A | 0.0119091 | 0.0762411 | intron-variant | HACE1 | GRCh38.p7 | 6:104763627 | ACCATTAATACAGTG[-/A]AAAAAAATCACATGT | 57531 |
rs564181056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838154 | AATCTATAGATTCAA[C/T]GTAATCTCTATCAAA | 57531 |
rs564185648 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104800643 | ACCTGACTGTTAGAA[C/G]GAAAACTAAGAAAGG | 57531 |
rs564238283 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104794728 | GGGCAACATGGCAAA[A/C]CCCCATCTCTACTGA | 57531 |
rs564239554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807762 | AATGAGTTAATTAGT[C/T]ATATAGTTTACATGA | 57531 |
rs564283455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713979 | GATACGGGGATACAA[A/G]GCAAAGTCCAGGGCC | 57531 |
rs564284014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822639 | AGGCAGTCGGATCAC[C/T]AGAGGTCGGGAGTTC | 57531 |
rs564300196 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | HACE1 | GRCh38.p7 | 6:104769016 | ATGCAAGCATAAATA[C/T]AGATATACCTCATAC | 57531 |
rs564313195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706861 | AGATCACTATCAATC[G/T]TACAGAAATAAAAAG | 57531 |
rs564319456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698335 | ATTCCTTATGTTATG[C/T]CTACTTTCCACTCCA | 57531 |
rs564325622 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | HACE1 | GRCh38.p7 | 6:104687670 | CTCAGAAAGCACAAA[C/T]TGCCATAAAGGCAGC | 57531 |
rs564338291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836483 | TTTGGGAGGCCGAGG[C/T]GGGTGAATCACCGGA | 57531 |
rs564353020 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803003 | GAGAGAAGAATCAAA[C/T]AGACACAATAAGAAG | 57531 |
rs564354440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732954 | AAGACACTAATGCAT[A/G]AACAATTCCTATTAA | 57531 |
rs564362844 | snp | A/C/G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104703943 | AAAGCCCTGTCTCTA[A/C/G/T]GAAAAATACAAAAAT | 57531 |
rs564400325 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696604 | GGACATCTCCCTCAA[A/C]TCCCATCACTGTTAT | 57531 |
rs564447392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830430 | TGTCCAGAAAAAATT[C/T]CAGGAAACAGAAAAA | 57531 |
rs564447798 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104844314 | TGCAGGGATTACAGG[C/T]GTGAGTCACCACGGT | 57531 |
rs564473912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739090 | ATAAGCGAAGGAGAA[A/G]TAAAATACTTTACAG | 57531 |
rs564476457 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768474 | TAACAATTTTAAGCA[A/C]GGTAAAATGTGATGT | 57531 |
rs564498729 | in-del | -/CTCT | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104840144 | AAAAGTGCAGGGCAA[-/CTCT]CTCTCTCTATTATTT | 57531 |
rs564525127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775549 | ATATAAAGAGAAGAA[A/G]TAAGTCTAAAATATA | 57531 |
rs564525248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104784858 | CTAGATTAGTATGAG[C/T]ATCTTAAAACAAGGA | 57531 |
rs564530569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724217 | CATCACACAGCTTTG[G/T]CTCCCTTTATAACTT | 57531 |
rs564594022 | snp | C/T | 9.88957e-05 | 0.00703122 | missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104850952 | ACACGTCCGAATGCA[C/T]AATTGACATCAAATT | 57531 |
rs564610068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776061 | ATAACTAATTCCATT[G/T]AGTCTACAACAGCAA | 57531 |
rs564615606 | snp | C/T | 0.000399281 | 0.0141238 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682761 | CTCCCTACCACTCTG[C/T]AGAAGCTGACCCGCC | 57531 |
rs564625932 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | HACE1 | GRCh38.p7 | 6:104822195 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAA | 57531 |
rs564642209 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104768079 | TAATATATATACATC[C/T]GCCTATATTGCTTGT | 57531 |
rs564662219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826316 | CAGACAAAAAAACCT[A/G]CCTTCAAGAAGTTTA | 57531 |
rs564667570 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104747724 | CATCTGTAAAATGGG[A/G]ACAATAGTACTCACC | 57531 |
rs564711811 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835382 | TTAATACTGTCAGAG[A/G]GAGAACATACTGATT | 57531 |
rs564743592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732460 | CAAAAGGACAAATAT[C/T]GTATGATTCCATGTA | 57531 |
rs564806900 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759434 | GGAAACTGAACAACG[C/T]GCTCCTGAATGACTA | 57531 |
rs564824431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688863 | TGTGTTACATCAGAC[C/T]CATCTGGATAATCCA | 57531 |
rs564828682 | snp | C/T | | | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858517 | CCAGCCTGGGGAACA[C/T]AGTGAGACCTCATCT | 57531 |
rs564833024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707839 | TTAATACCATTACAA[C/T]GGAAATTAAGTTTCA | 57531 |
rs564839150 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104738238 | CAGAACAGAAAAACC[A/G]GAAACTCTAAAAAGC | 57531 |
rs564855084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104819212 | GAATACAAAACCAAC[A/G]TGGAAAAATCACTAG | 57531 |
rs564857404 | snp | A/G | 0.000313814 | 0.0125223 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730350 | ATATGGCACAGCAGC[A/G]ATTGTAAAGTTTTGC | 57531 |
rs564900844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802666 | GTTCTTTGAAACCAA[C/T]GAGAACAAAGACACA | 57531 |
rs564901231 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104717419 | GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC | 57531 |
rs564938669 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803204 | GGCAATAATTAATAG[A/C]CTACCAACCAAAAAA | 57531 |
rs564951545 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808748 | CTTTCATTTATCAGA[A/T]ATAACACATTGGGAA | 57531 |
rs564969997 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825732 | TGTATCCAGAACCTT[A/G]AGCAGCTGCTGGGGC | 57531 |
rs564980936 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845667 | TATTTTTAGTAGAGA[A/C]GGGGTTTCACCGTGT | 57531 |
rs565001851 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846432 | AATCCCCCTGTACAA[C/G]GAAGCAACTATATTC | 57531 |
rs565002153 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104817585 | ATATCAGGTAAAATG[-/A]ATTAATATAGAGGAG | 57531 |
rs565020315 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843867 | ATAAAATTTGCCATC[A/G]TAACTTTTTTTTTTT | 57531 |
rs565053623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685478 | ACCCTTAATTACACA[A/G]ACAAGTTCCTTAAAC | 57531 |
rs565087299 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716332 | AGCTTTACCTGTTGA[C/T]GTATATAGAACATTT | 57531 |
rs565088056 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737012 | TTATAGGCCAGGCAC[A/G]GTGGCTCACACCTGT | 57531 |
rs565095241 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104780698 | AACTAGATAACAACC[A/G]TCAAAATCAGAAATT | 57531 |
rs565112911 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104847434 | CACATTACAAGATAT[C/G]TAACATGGCTAATTA | 57531 |
rs565137172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796158 | GCCCAGGCTAGAGTG[C/T]AGTGGGCAGTGACAT | 57531 |
rs565159340 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104743098 | ATTCTCATTCATAGG[C/T]GGGAATTGAACAATG | 57531 |
rs565183521 | in-del | -/ACGGAGTCA | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104816885 | CCCTGGATATGAGAC[-/ACGGAGTCA]ACGGAAATTATTTTA | 57531 |
rs565187967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840552 | AGCTGAGAGAGGCCC[C/G]TCGCGGTGGCTCACA | 57531 |
rs565189073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104778662 | TTTAATTAGCCAAGC[A/G]TAGTGGTATGCGCCT | 57531 |
rs565258622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855254 | TCAAGACCATCCTGG[C/T]TAACAAGGTGAAACC | 57531 |
rs565261018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708496 | GATGGCAAAAGTCCT[C/T]AAATTTATCTACAAA | 57531 |
rs565262665 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104761210 | CTAATTTAATCTTCA[C/T]ATGGAACCAAAAAAG | 57531 |
rs565314606 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104763278 | TAAAAGTTTTCAGAG[C/T]AGTAAAAAAACAAAT | 57531 |
rs565318771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762719 | AAAAAGGCCGGGCGC[A/G]GTAGCTCACACCTGT | 57531 |
rs565334634 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861915 | TTCTATAATCTGCAA[C/T]GTCCAAAATAGCATC | 57531 |
rs565343473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715002 | GTCATCCCTGGGGCA[A/G]TCTTTGATTGATGGG | 57531 |
rs565360380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758217 | ACAAAGATACTCCTC[A/G]AGAAGAGCAACCCCA | 57531 |
rs565379568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758500 | AGACAAGCAAATGCT[A/G]AGAGACTTTGTCACC | 57531 |
rs565384102 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104789317 | TTTTACAATTAGTGT[C/T]TTACAAAATGGAAGT | 57531 |
rs565424923 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104734113 | AGCCGAGTGAGATCC[A/T]GCCTGAGAAACAGAG | 57531 |
rs565437597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825091 | CGTCTCAAAAAAAAA[A/G]AAAAAAGAAAGAAAG | 57531 |
rs565461512 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801367 | AGGAAATACAGAGAA[C/T]GCCACAAAGATGCTC | 57531 |
rs565475504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763428 | ACACCCAAGTCTCAA[C/T]ATGAATTTGTTTCAT | 57531 |
rs565477253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770261 | GCTACTTGTAAGCAA[C/T]AGAACTAGAATTCAT | 57531 |
rs565520823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818308 | TCCTCTGATCATTGA[C/T]CTAGAAGTGGTGTCT | 57531 |
rs565527881 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104811615 | GAATTATCAGTGTAA[C/T]AGAAACTGTGTTAAT | 57531 |
rs565530647 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787114 | TTCATTTACACGTTC[A/C]ACCAAAAAGCAGAAA | 57531 |
rs565540370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716208 | AAGCAAAAATATATA[C/T]GTACCAGTAAAGCTG | 57531 |
rs565551714 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104688433 | TATGAAGAAGACAAA[A/C/G]TCATTAAAGTATTCA | 57531 |
rs565556088 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727888 | ACATGATCATGTCTC[A/G]TTACAGCCTCGATCT | 57531 |
rs565560932 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854003 | AAGTTATGTGAATGT[C/G]GTCTCTCTCCCTCTC | 57531 |
rs565581292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802249 | ACAAAGAGACTTAGA[C/T]TCCCACACAATAATA | 57531 |
rs565604024 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727780 | ATGTACACACATATA[G/T]GTATATGAATATGTA | 57531 |
rs565634432 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104809122 | TTTCATAGTGATGCA[G/T]TCATTCAAAAACATC | 57531 |
rs565638428 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818493 | ATTCCCATTCAAACT[A/C]TTCCAAAAAATTGAG | 57531 |
rs565643463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104839227 | TGTGTACCCTGCTGT[C/T]TTTAACAGCTTTACT | 57531 |
rs565656354 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751790 | GTTATAAGTGAAACT[C/T]TGTGAGTTAAAAACA | 57531 |
rs565658632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715094 | CTCTTCAAAAGGTCC[C/T]GATGAAATTAAGCCC | 57531 |
rs565669623 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861580 | TCAGCTTCTCTCAGC[C/T]GCTGTTATCACCATT | 57531 |
rs565723424 | in-del | -/TA | 0.00551423 | 0.0522179 | intron-variant | HACE1 | GRCh38.p7 | 6:104744661 | TTTAGGGAAAAAAGT[-/TA]TTATATTTAAGTGGT | 57531 |
rs565747162 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770030 | CAATTCTGTATGGGA[C/G]GTATTATTATTCCAA | 57531 |
rs565749212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104721750 | GACAACAGCTAATAG[A/G]GTCAAAGCTGGAGTT | 57531 |
rs565799050 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104706366 | CTTTGAATTCAAATG[C/G]CATGAACAAAATAGA | 57531 |
rs565843273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104831668 | GGAGGCCGAGGCAGG[C/T]GGATCATGAGGTCGG | 57531 |
rs565850291 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104787150 | AACAAAACCAACAAA[A/C]CCACCACTACTACAA | 57531 |
rs565861606 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832238 | GAGAACAGAATGAAC[A/T]TTATAAATGTTAAAA | 57531 |
rs565877582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779022 | GACAGTGATGCAGCT[C/G]AGACACTGAAAATAA | 57531 |
rs565892486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104815688 | GAAATTTCTAACCAG[A/C]AAAGCATTCAAGATG | 57531 |
rs565910255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684861 | TGGATCTACATAGTA[C/G]TGTGCCAAGTAGTGT | 57531 |
rs565923106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104698538 | TTTGTTGAAACTAAA[C/T]CTGGATCTTAATCAT | 57531 |
rs565928265 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | HACE1 | GRCh38.p7 | 6:104691712 | TTTGGGAGCTCAATG[C/T]GTAGTTCAAGACCAG | 57531 |
rs565936932 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727373 | CATGTATATGTATAC[A/G]AATATATATACACAT | 57531 |
rs565941191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104741588 | GAATAAAATACCTAG[A/G]AATCCAACTTACAAG | 57531 |
rs565949680 | in-del | -/AC | 0.00359999 | 0.0422733 | intron-variant | HACE1 | GRCh38.p7 | 6:104727515 | TATGTATATGAATAC[-/AC]ACACACGTATGTATA | 57531 |
rs565964232 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104786530 | GATTGCTTGAGTCTC[A/G]GAAGTCAAGGCTACA | 57531 |
rs565989091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104690975 | TTTAATTTCTACATG[C/T]AAAGAAACCACAACA | 57531 |
rs565994325 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684021 | ATCTTTCACAGAGCA[G/T]GCAAGAGCACTGCCG | 57531 |
rs566020601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800871 | GGAGAATGACTTTGA[C/T]GAGTTCACAGAAGTA | 57531 |
rs566042755 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104749126 | GCTATTTGTTTTTTA[C/T]ATACATATAGGTCCA | 57531 |
rs566051438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104822751 | AATCCCAGCTACTCA[A/G]GAGGCCGAGGCAGGA | 57531 |
rs566053308 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104814735 | GCATGGGAGCAGATT[A/T]CCCCCTTGCTGCTCT | 57531 |
rs566083305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794402 | AAATTATAACCATCA[C/T]CACCTCTACTATATA | 57531 |
rs566090045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104695031 | AAGAGCCCAGATGGA[A/G]AAGTGCTGAGACTCC | 57531 |
rs566100959 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807686 | AAAAGACTTAAAGGT[G/T]TGTAAAGATGGCAGG | 57531 |
rs566108884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703979 | AGGCATGGTGGTGCA[A/C]ACCTGTAATCCCAGC | 57531 |
rs566114848 | in-del | -/C | 0.00953873 | 0.0683987 | intron-variant | HACE1 | GRCh38.p7 | 6:104792653 | GATCAACTCAGTATA[-/C]CCACTGGAGGCTATA | 57531 |
rs566145951 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104808126 | AGGAGGCAGAGATTG[C/T]AGTGAGCCAAGATCA | 57531 |
rs566163831 | snp | C/G | 0.00676609 | 0.0577691 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859739 | GCCCGTCCAGCAGGC[C/G]GAGACGCGGGCTTGC | 57531 |
rs566196078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703240 | TCAGCCAAGTGGCAG[C/T]GCAGTCTCTAGTAGA | 57531 |
rs566209451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852733 | CTGTAGCTTTAACAA[C/T]TGAAATTTCTTTTAC | 57531 |
rs566210267 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804611 | AAGAAATAGGGAAAG[A/G]ATTCCCTATTTGATA | 57531 |
rs566236263 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800495 | TATAGGCGGGTGCCC[-/T]CTCTGGGATGAAGCT | 57531 |
rs566249919 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731306 | ACTAAATACATACTT[A/G]CAAACATCTGAATAA | 57531 |
rs566281968 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732257 | GACTCAAAGAAGTAT[C/T]TGCGCATACAGCAGC | 57531 |
rs566312667 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798953 | GTAGGCTTGTTCCAT[A/T]GCACCAAGCATGGCA | 57531 |
rs566323160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709949 | TTAAATATAGGGTTA[C/T]TACTAATATATGACC | 57531 |
rs566326106 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757662 | GAACACAACTCCTGG[A/C]CAGCAATGGAACAAA | 57531 |
rs566336281 | in-del | -/AAAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782488 | ACCCTGTGTCAAAAA[-/AAAT]AAATAAATAAAATAA | 57531 |
rs566338217 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755130 | AGAAAAAAGCAGGAG[C/T]TGCAACCCTAGATTC | 57531 |
rs566352538 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696362 | CCCATTGACAACAGA[A/T]TATACTCTCCTTCAG | 57531 |
rs566355840 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746046 | AGACATTAAAGAAAT[C/T]TGCAAAACTGTTAAA | 57531 |
rs566361318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776394 | AAACATTTAATTCAA[A/C]AAATGTAGACTCAAG | 57531 |
rs566363792 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786017 | TTTAAAACAAGAGAT[A/G]CAATTACCAAACTTC | 57531 |
rs566389832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727344 | ACACATGTATGTATA[C/T]GAATATATATACACA | 57531 |
rs566399995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769255 | GCCCAGGCTTGTCTC[A/G]AACTCCTGGCCTCAA | 57531 |
rs566428386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737634 | ATGGGCTTAAAAAAC[A/G]GCGCACCACGAGATT | 57531 |
rs566436717 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104721870 | ACTGAAGGTGGGTGG[C/T]TTGGACAAGGGTAAT | 57531 |
rs566448871 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104695255 | CATGAGTTCTTAATC[G/T]TTTGCGTGCAATAAA | 57531 |
rs566451486 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104820056 | AAAAATTAGCCGGGA[A/G]TGGTGGCACATGCCT | 57531 |
rs566521080 | snp | C/T | 0.000148352 | 0.00861127 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849234 | CAAAACCAAGCATTC[C/T]ACCGATCCACAACTA | 57531 |
rs566531001 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712377 | TTGTCCCCTCCAAAA[C/T]ACGTGCTGGAAACTT | 57531 |
rs566538007 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104717595 | ATAGGTACATACATA[C/T]TGAATTTCACTAAAC | 57531 |
rs566541658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104798323 | GAAACTTAAAAAACA[A/G]AACACTATTCATTCT | 57531 |
rs566572740 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | HACE1 | GRCh38.p7 | 6:104754153 | AAGCAGAGGAAAGAA[C/T]CTCAGAGCTTGAAGA | 57531 |
rs566575120 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763688 | ACCAGAATATCTGTG[C/T]CAGCTGTTAAACAGA | 57531 |
rs566585315 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761485 | GGTTTTGGGAAAACT[A/G]GCTAGCCATATGCAG | 57531 |
rs566602233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772901 | AGAATTTCTGCTTGG[G/T]GTGATGAAAAAGCTC | 57531 |
rs566616290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780078 | GCTCAATAAATAGAT[A/G]CTGTTCTTATTATCA | 57531 |
rs566646122 | in-del | -/TC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787930 | ACCTTTCTTTACTTT[-/TC]TCTCTTTTCTTACCT | 57531 |
rs566663965 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792792 | TTTCTTGTGATTAGG[A/T]ACATCTGAAGCCTGT | 57531 |
rs566679015 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851393 | GGCCTAGCTATTCTT[C/G]TGATTCTTCAGGTTT | 57531 |
rs566689732 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765669 | TGAAAAGTCAGAGTT[C/G]CCTTCAATTTTCACT | 57531 |
rs566697002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760006 | TAAACCAGGAAGCAG[C/T]TGAATCTCTGAATAT | 57531 |
rs566700543 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803898 | AGAAATAACAGTATT[A/C]AATTAGGAAAAGAGG | 57531 |
rs566788409 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826498 | CAAATACTTCTGTGA[A/G]AAATGCACTGATCTA | 57531 |
rs566789704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717055 | GATGTACATTAACTA[C/T]GACTCAGCAATTCCA | 57531 |
rs566822347 | snp | A/T | 1.96084e-05 | 0.00313111 | intron-variant | HACE1 | GRCh38.p7 | 6:104729803 | ATTAAACAGGAAATC[A/T]ATAAAATTTCTGATT | 57531 |
rs566829411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744360 | CAAAAATGATTTCAT[A/G]CAAAGCTTTCATATG | 57531 |
rs566845259 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716902 | AGCGATACCAGTTGA[C/T]ACCAACTGTATTGGC | 57531 |
rs566857670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825806 | CTGCTTTTGCTGCTT[C/T]ATTACTTGTTTGTGT | 57531 |
rs566876432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104723713 | TTGACTGCTGATACA[C/T]ACTGATGTACCTTAA | 57531 |
rs566876757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104686528 | AAAAAAGTAACTCAG[G/T]CTTGTCCATTTGTTT | 57531 |
rs566888163 | snp | A/G | 1.66891e-05 | 0.00288864 | intron-variant | HACE1 | GRCh38.p7 | 6:104744492 | ACTTAACTTCATTCT[A/G]AGCTCTAGAGAAATT | 57531 |
rs566955524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797155 | GAGAATATGAAATAC[A/G]TCTTCATAATCACAA | 57531 |
rs566966305 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730841 | AGATTAATATTCGAT[C/T]GACTAATTCAAGCAA | 57531 |
rs566966322 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709678 | CTTGAGCCAAATAAA[A/C]CTCTTTTCTTTGTAA | 57531 |
rs566984302 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855800 | TCATAAAAAACACTG[G/T]TATTTGTGGGTTTAA | 57531 |
rs566996101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709733 | TATAGCGATGCAAAT[A/G]GACTAACACAACCAA | 57531 |
rs567009444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737224 | TTGAACCCAGGGGGC[A/G]GAGGTTGCAGATCGA | 57531 |
rs567009757 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729135 | ATATTAAAATATTAA[A/G]ATGCTAAAAAAATCA | 57531 |
rs567016671 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757764 | AAATTAAAGGAGCAT[A/G]TTCTAACCCATCACC | 57531 |
rs567021294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796390 | GCTGGAATTACAGGC[A/G]TGAGATACCACGCCC | 57531 |
rs567042475 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820143 | GAGTTTGCAGTGAGC[C/G]GAGATTGTGCCACTG | 57531 |
rs567049856 | in-del | -/ACTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698130 | CCAGGGTCATATAAA[-/ACTT]ACAAATAATGTCTGA | 57531 |
rs567071843 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104848515 | GTCCTGAATCAAAAA[A/G]TACTTATTTTCATTT | 57531 |
rs567077062 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695775 | ATGGTCTCTAAATAC[G/T]GACTTCAAGTGATCC | 57531 |
rs567080941 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104848588 | ATAAAAACTAATGTT[A/G]GCACTAAAAGGAGTA | 57531 |
rs567110717 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854804 | TTATAGGGGAAATGG[A/G]AAAAAGTTATCAATA | 57531 |
rs567121182 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805621 | AGAAAACTAAACACC[A/G]CATGTTCTCACTCAT | 57531 |
rs567134003 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | HACE1 | GRCh38.p7 | 6:104700424 | GAAAAAAAAAAAAAA[A/G]AGAGAGAAACTAAAA | 57531 |
rs567135191 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802990 | ATAAAGAAGAAGAGA[G/T]AGAAGAATCAAACAG | 57531 |
rs567197362 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703141 | GGGCTAGATTTATTA[A/T]GAAAGAATGAAAACT | 57531 |
rs567202275 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847859 | GTTTCCCTCTGTTGT[C/G]CAGGCTGGAATGCAA | 57531 |
rs567230153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818674 | CAGCACATCAAAAAG[C/T]TCATACACCATAATC | 57531 |
rs567230192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825780 | AGTATACTTTTGTTT[C/T]CAATAAATATCTGCT | 57531 |
rs567230800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104797360 | CTCTCTCCACCTTAA[C/T]TTGACCATTTGCAAC | 57531 |
rs567271253 | in-del | -/AGAC | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104711304 | GTGTTTCTATAGACT[-/AGAC]AGAGTTAGAGTTCAG | 57531 |
rs567292991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104694365 | TGGTTACCAGAGGCT[A/G]GGAAGGGTAATAGGG | 57531 |
rs567295116 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104759926 | CTATAAACATCTCTA[C/T]GCAAATAAACTAGAA | 57531 |
rs567297176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857089 | AGAGAGATCTCAGAG[C/T]TTCCATTCAGCTCTT | 57531 |
rs567309287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844014 | GGCGTGTGCCACCAC[A/G]CCAGCTAATTTTTGT | 57531 |
rs567314755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798138 | TAAGTTGTACAGTTT[A/G]GAAGAGCATGAATCC | 57531 |
rs567314837 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104789264 | TAATAAATTCTTTAA[C/T]AGTTAATACTTATTA | 57531 |
rs567343854 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104810236 | TGCAAGAAAATGGCT[A/G]GAATCAGAAAGATCT | 57531 |
rs567351542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104685642 | AGAGAATCTGACAAT[A/G]GGCAGCACAAAAGCA | 57531 |
rs567368793 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754825 | TGTTACCAGCCACTA[C/T]AAAAATACACTGAAG | 57531 |
rs567370335 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104758693 | GCATCAAATTCACAC[A/C]TAACAATACAAACCT | 57531 |
rs567374242 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104692486 | ATCCATTGTCAGCAC[C/G]ACTGAGCCTTGTTGA | 57531 |
rs567374794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803553 | TGGGATGCAAGGCTG[G/T]CTCAACATATGCAAA | 57531 |
rs567407117 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104823337 | TACTTCGGAGGCTGA[C/T]GCAGGAGAATCGCTT | 57531 |
rs567408507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104796265 | ACAGATGCATGCCAC[C/T]ACACTTAGCTAATTT | 57531 |
rs567408961 | in-del | -/TTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785607 | TCACAATCTTTCTTC[-/TTT]TAATTTTCAAATGTT | 57531 |
rs567434121 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104736766 | GCAAGAGAAGTACCT[C/T]GCCCAGCCTATTTAT | 57531 |
rs567435313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685075 | GTCCGGCAATGTACC[A/G]TATGTTGGAGGCTCC | 57531 |
rs567437329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693140 | AAGAAGTTATTCTTT[C/T]TCTTTGAGTAATTCA | 57531 |
rs567481436 | snp | C/T | 1.81082e-05 | 0.00300895 | intron-variant | HACE1 | GRCh38.p7 | 6:104729781 | TTTAAAAGAAAAATA[C/T]ACCACCATTAAACAG | 57531 |
rs567489836 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104719700 | CAGACAGATGTAACA[A/C]ACTTCCTTTTCTAGC | 57531 |
rs567490452 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104764884 | TCACTGAACATAGTT[C/G]CAGGCCAGAGGTTGT | 57531 |
rs567515824 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686685 | AAAGCCATAAAACTT[-/C]CATACACCAGCCACA | 57531 |
rs567561518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771636 | ATTATAAACTTCAAA[A/T]ATGCCAATTATCTTA | 57531 |
rs567576559 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763312 | ATAGTACAGATTGAG[A/T]ATCCCTTATCCAAAA | 57531 |
rs567580826 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820131 | ACCCGGGAGGTGGAG[C/T]TTGCAGTGAGCCGAG | 57531 |
rs567585184 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104723031 | CACCAAGTATGCTTG[A/G]AATTAAACATTTTTA | 57531 |
rs567599650 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764074 | AAAAAAAAAGTACTG[A/C]ACACTTTTTATTTTT | 57531 |
rs567630641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832847 | AAGGCTGCAGTGAGC[C/T]AGGATCCCACCACTG | 57531 |
rs567639951 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104801482 | GAAAGGTCAGTTACC[C/T]ACAAAGGGAAGCCCA | 57531 |
rs567644716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104828239 | AATTAAAAAACAACA[C/T]ACTGGGCCCAGCTTC | 57531 |
rs567662699 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104832383 | TATTTTCCTGTTTTT[C/T]GTTGTTGTTGTTGTT | 57531 |
rs567742407 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | HACE1 | GRCh38.p7 | 6:104742638 | CACCAGTTAGAATGG[C/T]GATCATTAAAAAGTC | 57531 |
rs567749714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822380 | AGAGCAGGACTCCAT[C/T]TCAGAAAAAAAAAAA | 57531 |
rs567759456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772749 | AGTTACCAATTACTA[C/T]GAAAATCCAGTGCAA | 57531 |
rs567764448 | in-del | -/GTAT | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727571 | TGAATACACACACAC[-/GTAT]GTATATGAATACACA | 57531 |
rs567766501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689181 | AAGCCATTGACAAAT[A/G]AGGCTCCTGCAGAGA | 57531 |
rs567777198 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783689 | ATTAACAAAGCTAAA[C/T]CACTATTTTTACTGA | 57531 |
rs567814419 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736348 | AGAGTGCAGTGGTGC[A/T]ATCTCGGCTCACTGC | 57531 |
rs567815996 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750922 | CATGTGTGTGTATGT[A/G]CATGTAAATAACTCA | 57531 |
rs567820593 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104757399 | GGTGATACCCAGGCA[A/G]ATGGGGTCTGGAGTG | 57531 |
rs567835550 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104718869 | TAAAATGAGTCACCA[C/G]TTTTCCACATCCCCT | 57531 |
rs567836952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707343 | CCAAGTGGGATTTAT[C/T]CAAGTAATGCAAGTT | 57531 |
rs567841426 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693356 | CTTGCTATTTAACGA[A/G]TTTCATATGAAAACT | 57531 |
rs567845421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846952 | GGTCATGAATTCTTT[C/T]TATTCCTTTTCTTCT | 57531 |
rs567872435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799594 | GGCTCAAGAGTATAA[C/T]GGAGTTGCTCGAGAT | 57531 |
rs567895842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104700329 | CATAACCACTACTGA[A/C]CTGTCGCAGTTGGTA | 57531 |
rs567910203 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861436 | AAAGAAATACCAGAC[A/G]TTATGGACCAGTCTA | 57531 |
rs567959967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792361 | GATCAGAAAGCCCTT[C/G]AGAATCCCACAGTTA | 57531 |
rs567970694 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808877 | CAACAATGATTTTTT[G/T]GTTTCACATTTCATC | 57531 |
rs567973861 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775635 | GAACTCGTCATTCAC[A/G/T]AAGACACCAAATTCA | 57531 |
rs567984360 | in-del | -/G | 0.0115465 | 0.0750994 | intron-variant | HACE1 | GRCh38.p7 | 6:104831591 | TCCGTCTCAAAAAAA[-/G]AAAAGAAAAGAAAAG | 57531 |
rs567993303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758135 | CTCTTCAGGATATTA[C/T]CCAGGAGAACTTCCC | 57531 |
rs568014503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104733078 | TAAAAAATTAATAAC[A/G]TGACCAAACATAAAA | 57531 |
rs568070815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104836700 | CCTGGGTGACAGAGT[A/G]AGACTCTGTCTAAAT | 57531 |
rs568076273 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725042 | CAAGAGAGCATTCCT[-/T]TTTTTTTTTTTTTAA | 57531 |
rs568098765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697282 | CTACAGCCCTAGCTA[C/T]ATATTTATTATCTGT | 57531 |
rs568127018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748137 | GAACTATGTTAAACC[C/T]CAAAATTTTTATTCA | 57531 |
rs568131576 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695516 | AGAGAAACAGAAACT[G/T]ATTCACCTAATTCAT | 57531 |
rs568135387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844415 | GTGATGCGATCTCGG[A/C]TCACTGCAACCTCCG | 57531 |
rs568141761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738342 | TGATGAGCTGAGAGA[A/G]GAAGGCTTCAGACGA | 57531 |
rs568155154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104829111 | TGTAAGCTCCTAAGC[C/T]TAAAAATAAAATATT | 57531 |
rs568187859 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807443 | GTCTCTAGTAGAGAC[C/T]TCTAAAACTCCATTA | 57531 |
rs568204935 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739188 | ACATGGAAAGGAACA[A/C]CTGGTACCAGCCACT | 57531 |
rs568247525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104843958 | GCCTCCCGGGTTCAA[A/G]TGATTCTCCTGCCTC | 57531 |
rs568249147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851228 | AGCCAGGACTACAGG[C/T]GCATGCCACTACACC | 57531 |
rs568270108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737777 | CCATTTTCCAGGCTT[C/G]ATTAGGTAAACAAAG | 57531 |
rs568283729 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104805414 | GGATACATATGTTTA[C/T]TGCAGTACTATTCAC | 57531 |
rs568291461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800112 | TTCCTCACTGCTAGC[A/G]CAGCAGTCTGAGATA | 57531 |
rs568319368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704176 | GATCTCAACGTTTAC[A/G]AAAATAAAACTAAGA | 57531 |
rs568323074 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104849929 | TGCTAGGATTACAGG[C/T]GTAAGCCACCACGCC | 57531 |
rs568335158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754330 | GTTGGAAAACATACT[C/T]CAGGATATCATATAG | 57531 |
rs568338229 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857726 | ACTTTGGGAGGCCGA[C/G]GCGGGCAGATCACGA | 57531 |
rs568347695 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104746265 | TCCTAAGACCAAAAA[C/G]TTTTAGAACTGCTAG | 57531 |
rs568350047 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794232 | CTTGGTACCTGCTTA[A/G]TAAGTGATGAAGGTA | 57531 |
rs568393421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104737352 | AAATAGGAACAGCTC[C/T]GGTCTACAGCTCCCA | 57531 |
rs568395547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745327 | TTTCCAAGGGAAAAG[A/G]GGACATGAAAAGAGC | 57531 |
rs568454385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718358 | AATTTCAATTTCATC[C/T]CTTCATTTCCAATCC | 57531 |
rs568465757 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104857810 | AAAATACAAAAAATT[A/G]GCCGGGCCTGGTGGC | 57531 |
rs568474573 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | HACE1 | GRCh38.p7 | 6:104804877 | TCTAATTAAACTAAA[C/G]AGCTTCTGCACAGCA | 57531 |
rs568482340 | snp | A/G | 7.97162e-05 | 0.00631282 | intron-variant | HACE1 | GRCh38.p7 | 6:104772094 | TGAAATAAATACAAA[A/G]TAATATATTATTAAG | 57531 |
rs568572924 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104782365 | TGGTGGTATGCACCT[A/G]TAGTCCCAGCTACTT | 57531 |
rs568594682 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104730773 | TATTTACATCTATAT[C/T]CCTGGGGCTAGCAAA | 57531 |
rs568630299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696644 | GAAATACATGGACTT[C/T]ACAGTTTGGGGGATA | 57531 |
rs568637462 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827319 | AAAAAAAGTGTCCTT[A/G]CTTTTTTTATTAAAA | 57531 |
rs568640052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791270 | ATCTCTACCCTTAGA[A/T]TAAAACACCAATGGA | 57531 |
rs568649568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773145 | TTTCTGTGATGGTCA[C/T]TAATTCATATTACAA | 57531 |
rs568653618 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724696 | ACTTTTTTTAATTAA[A/T]AAAGTTTTAATGACA | 57531 |
rs568655069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104835092 | TCTTCCGGGCAGTTG[C/G]AAGAGTCTTCTCTGA | 57531 |
rs568655080 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | HACE1 | GRCh38.p7 | 6:104751044 | AAATGATCTGGCCTC[C/T]GCCTTGCTCTCTGAT | 57531 |
rs568673376 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104804752 | CCTAAAGCCATAAAA[A/C]CCCTAGAAGAAAACC | 57531 |
rs568674714 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104856498 | GGAATGCAGTGGCGC[A/G]ATCTTGGCTCACTGC | 57531 |
rs568676082 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830721 | TTGAGTTGGTTTTGT[G/T]GTTGTTATTATGGTC | 57531 |
rs568697487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104688101 | ATTCTCATTCTCTGT[C/T]TCTGAAAATATTCTG | 57531 |
rs568701694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820314 | AGATGCTAAAAGCAA[C/T]TGGAACAAGAGTAAA | 57531 |
rs568703564 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827748 | TGAAAAACTTGGAAG[C/G]TGGCTAAAGATACCA | 57531 |
rs568708161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104841644 | TGTTTTTCTATACCT[C/T]ATTCCCCAATTTTTA | 57531 |
rs568717344 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738307 | CCAGCAACGGAACAA[A/T]GCTGGATGGAGAATG | 57531 |
rs568723930 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104686692 | TAAAACTTCCATACA[A/C]CAGCCACACCACGTG | 57531 |
rs568744711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834437 | CCTATAAGTCTACCA[C/T]TCAAAGATAATCAAT | 57531 |
rs568759643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799007 | TACATTCAATGAATT[A/G]TATTATAGGCTTTAA | 57531 |
rs568769525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783324 | ATGTTGTAGTTACTA[G/T]TTTATACATATGTTT | 57531 |
rs568779748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732507 | TAGTCAAATTCGTAG[A/G]CATAAAATTGGTGGT | 57531 |
rs568785071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687382 | TAGTATAATGATGTG[A/G]GCTTTTGGTGTGCAA | 57531 |
rs568793385 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104731727 | ACTAACTCAAAATGG[A/G]TTGAAGACCTAAATC | 57531 |
rs568807173 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768806 | CTCTTTAATATTAAA[A/G]TAGTATTCCCACCTC | 57531 |
rs568822710 | in-del | -/A | 0.219947 | 0.248187 | intron-variant | HACE1 | GRCh38.p7 | 6:104778630 | GACCCTGTCTCTACC[-/A]AAAAAAAAAAAAATG | 57531 |
rs568829613 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846671 | AAGCTGGCCCCAAAA[C/T]GCAGACTGACCAACA | 57531 |
rs568850408 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104843110 | GCGAGACTCTGTCTC[-/A]AAAAAAAAGTAACTT | 57531 |
rs568889764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842628 | AGAATGAACACATAA[C/T]ACACCTCAGCAGAGA | 57531 |
rs568919331 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104791410 | AAACCAAACTTACAA[C/G]CTGTTCATGAGCTTT | 57531 |
rs568923954 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850599 | CATATAAAATCTCAT[A/C]TTGCTGGGATAAAAA | 57531 |
rs568957244 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104746158 | TAATGGATTATTTTA[C/T]GTGAATAAAATATTT | 57531 |
rs568969425 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844807 | AGCTGGGATTACAGG[C/T]GCCCGCCACCATGCC | 57531 |
rs568978429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737930 | CTTAAATGTCCCTGT[C/T]TCACAGCTTTGAGGA | 57531 |
rs569018453 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747106 | AATGTACATATTAAG[A/C]AAAATATTTTAAGCC | 57531 |
rs569044811 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754298 | GTACCTGAAAGAGAC[A/G]AGGAGAATGGAACCA | 57531 |
rs569047816 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104849893 | CTGACCTCAAGATCC[A/G]CCCGCCTCGGCCTCC | 57531 |
rs569062355 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761860 | TTTACAAGAAAAAAA[C/G]AAACAACCCCATCAA | 57531 |
rs569105137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710711 | GAAATCTTGCTCATA[A/C]TAGTTTCAAAACTCT | 57531 |
rs569112390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781094 | GCTAAGCTTCTCTAC[C/T]GTAAGGCACCCTTTT | 57531 |
rs569125651 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788126 | ACAAAAAGGATTCAA[A/G]TAAATTTTAAAATTA | 57531 |
rs569143832 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104718306 | TCTGCTCATTCCACA[C/T]ATTTCTTATATATAT | 57531 |
rs569155859 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819846 | CTATAGGAAAACAAC[C/T]GAAACCCTTCCTTAC | 57531 |
rs569183653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820742 | AAACACCGTTGGTGG[A/G]AGTAAATTATTTCAG | 57531 |
rs569191366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104743627 | AATCATCTAGTTTTC[C/T]AATATCTATTATATT | 57531 |
rs569193442 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104752325 | TCTGGAGTCCAACCC[A/G]GGAAATAACATATAT | 57531 |
rs569210743 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696287 | CTCTGCTGCGTGTTC[C/T]ATATGCATTACCCCA | 57531 |
rs569211846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687306 | GGCCACATGCTGGGA[G/T]TCTGGTTGTAATCAT | 57531 |
rs569305397 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769390 | TAGTATTCACAGATA[A/C]GAATCATGTTTATGG | 57531 |
rs569328566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104841476 | TCACTAAGCATCCTA[C/T]GGATATTCAGAATAC | 57531 |
rs569335854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834349 | TAGCAATGCTATATT[C/T]CTTACTTCCTGTATT | 57531 |
rs569337881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104825989 | AGCAGGAGGTGAGTG[A/G]CAGGCAAGTGAACAT | 57531 |
rs569352285 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104789973 | CAAAGACAGTAAGTC[A/G]TCACTCCTAACTAGA | 57531 |
rs569376486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737595 | AAAATCGGGTCACTC[C/T]CACCCGAATACTGCG | 57531 |
rs569376895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826541 | TCCAAAAAACCTAAC[A/G]ATTGTGATTTACAAT | 57531 |
rs569394485 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104856456 | GTTTTTTTTTTGAGA[C/T]TGAGTTTCGCTCTTG | 57531 |
rs569405346 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104769367 | GGAGTGACAAACCTC[A/T]CCAGATATAGTATTC | 57531 |
rs569446470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770004 | CTTTTCATTTTACAA[A/G]ATGCTAATAACAATT | 57531 |
rs569448228 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853112 | TCCTCTTTCATGAAT[A/G]GATTAATTCTGTTAA | 57531 |
rs569448475 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773390 | TTAACCTGCTGACTA[A/G]TTTATTTAGATATAA | 57531 |
rs569449873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833617 | GGGAAGTTGAGGCAA[G/T]AGGATTGCTTGAAGC | 57531 |
rs569459192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104729945 | CTGCATTGCAGTTTC[C/T]TTCAGCATGCAAATG | 57531 |
rs569479288 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104686615 | TCCTTTCTTATTTGC[A/G]CTTCCAGAGCTATTA | 57531 |
rs569489712 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848434 | GCACTCCAGCCTGGT[C/G]ACGGAGTGAGACCCC | 57531 |
rs569510859 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104797310 | CTAGTCAGGCTTCTG[C/T]TTTTTTTTTTTTTCT | 57531 |
rs569572278 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840722 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGGCGGG | 57531 |
rs569576434 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104856487 | ATGTCCAGGCTGGAA[C/T]GCAGTGGCGCGATCT | 57531 |
rs569579103 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104770251 | ACCAGAAGCTGCTAC[A/T]TGTAAGCAACAGAAC | 57531 |
rs569583134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808341 | TATCAACTACTAAGT[A/G]TTGAATACTCTGCAG | 57531 |
rs569596310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749092 | CAAGGCAAAGTTTTC[A/G]TCAATTATTTTTGTT | 57531 |
rs569598780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104739375 | ACACAGACTGGCAAA[C/T]TGGATAAAGAGGCAA | 57531 |
rs569660947 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | HACE1 | GRCh38.p7 | 6:104740118 | TGTTCTTTGAAACCA[A/G]TGAGAACAACGACAC | 57531 |
rs569661685 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104817682 | TTTTATAGGAGCATA[C/T]AGATGAAGAAACGCT | 57531 |
rs569678689 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714490 | CTTTTACCTTTAAAA[C/T]CTTCCCTTTGCCTTA | 57531 |
rs569705631 | in-del | -/ACACACACACAC | 0.0252325 | 0.109451 | intron-variant | HACE1 | GRCh38.p7 | 6:104688354 | ACTTTTCCTTTGTAA[-/ACACACACACAC]ACACACACACACACA | 57531 |
rs569728559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104777755 | TTATTTTGGTTTATT[A/G]TTGTAGTTGTTGTTG | 57531 |
rs569730161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852103 | AAATGTTACAGCTCA[C/T]ATAGATCTTGGAAAA | 57531 |
rs569770234 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104823357 | GAGAATCGCTTGAAC[A/C]TGGGAGGCAGAGGTT | 57531 |
rs569803101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845144 | TGGTTTTTGCCATTA[C/T]TTTGAATGGCAGAGT | 57531 |
rs569803763 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859036 | AATATATTGTGTTTA[C/T]CCATACAGTACTTTA | 57531 |
rs569840665 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859687 | ATCAGCCGCCCCACC[C/G]GCGGCCTCCGCGCCC | 57531 |
rs569841937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851446 | ACTGCACTATTCTCT[C/T]AGTATGTTAGCCAGC | 57531 |
rs569843151 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703946 | GCCCTGTCTCTACGA[A/G]AAATACAAAAATTAC | 57531 |
rs569845148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830888 | TCTCCTTAAGCTATC[C/T]GGCATCCTGAGAGGT | 57531 |
rs569879474 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782027 | TTGCGGTTTTTGCTA[-/T]TTTTAATTTGACAAT | 57531 |
rs569921087 | snp | A/C | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104689866 | AAAAGAATTTAACGC[A/C]TTTCTGAAGGGGTCT | 57531 |
rs569921532 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724692 | ACGCACTTTTTTTAA[C/T]TAAAAAAGTTTTAAT | 57531 |
rs569922570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104720004 | ATGCGCCACCACGCC[C/T]GGCTAATTTTTTGTA | 57531 |
rs569950336 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772829 | GATAGGTAAAGTAGA[C/T]TAGTAGTTACCTAAG | 57531 |
rs569952218 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793522 | TATTATCTTTAGCAA[A/G]TATTCCTGAAATCAG | 57531 |
rs569994036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807172 | GAGACTACAGGCGTG[A/C]GCCACAATGCCCAGC | 57531 |
rs570003491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756621 | TCTACAGCTCCCAGC[G/T]AGACTGACACAGAAG | 57531 |
rs570009591 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761274 | GAACAAAGCTGGAGG[A/C]ATCATGCTACCAGAC | 57531 |
rs570016508 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694186 | CTATTCAGCCACACA[-/C]AAAAAAAAAGATTCT | 57531 |
rs570026282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800324 | GATAACTTCTGCAGA[C/T]TGAAATGTCACTGTC | 57531 |
rs570073296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806408 | TGGAGGTTGCAGTGA[A/G]TTATGATCACGCCAC | 57531 |
rs570075144 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737476 | GTGGGTGTGCGCACC[A/G]TGCGCGAGCCGAAGC | 57531 |
rs570106229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104697809 | CAACGGCATGATCTC[A/G]GCTCAGTGCAACCTC | 57531 |
rs570112401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800829 | AACTGCTCACAGCTC[C/T]TTGCCAGCAATGGAA | 57531 |
rs570132243 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861781 | TGTGAATTGTCAGTT[C/T]CAAATTCTGCAATAT | 57531 |
rs570225766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104727035 | AAATAAATCCTAAAA[C/T]AAGCAGATCTATATT | 57531 |
rs570227978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813847 | AATAACAAAGACAGT[A/G]AAGGGAACCAAAGAA | 57531 |
rs570237868 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104776521 | AACCAACTGTTTAGA[C/G]GAACAAATGTTAGAC | 57531 |
rs570240244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696822 | AAACATATAGGGTCC[A/G]CTTGCCCCTACTTGC | 57531 |
rs570250418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760955 | ATTCACAATTACTAT[A/T]AAGAGAATAAAATAC | 57531 |
rs570258364 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779937 | TTTTTGAAGCACTTT[A/G]CAATGCATTACCACA | 57531 |
rs570280716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768253 | TTAGCAAGTCATTTA[A/G]GTTTCAATAGTTCAA | 57531 |
rs570351670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822813 | AGTGAGCGGAGATCG[C/T]GCCACTGCACTCCAG | 57531 |
rs570360086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775001 | ATTTTAATTTATTAA[C/T]ACTATGACACCAAAG | 57531 |
rs570366207 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804504 | ACAGCATGGTACTGG[G/T]ACCAAGAGATATAGA | 57531 |
rs570384968 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794376 | GGTTAAATGGTATTA[C/T]AGGGTACTTAAAATT | 57531 |
rs570385838 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836479 | GCATTTTGGGAGGCC[A/G]AGGCGGGTGAATCAC | 57531 |
rs570390722 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104815721 | ACCTGGCTTATTCTG[A/G]AAGCATTCACTTACA | 57531 |
rs570392487 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104775610 | AAATAATTAAACTCA[C/T]GACTTCACTGAACTC | 57531 |
rs570396345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767481 | GACTCTAGTACCGCC[C/T]CATTTCAACCCATTT | 57531 |
rs570400576 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756138 | AAACAACCTGCCAGG[A/C]ACGGTGGCTCATGCC | 57531 |
rs570408945 | snp | A/C | 0.000798403 | 0.0199641 | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682454 | TAGACGGTGTATTAG[A/C]AACTATGCAAACTGA | 57531 |
rs570412653 | in-del | -/CT | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104823261 | CAACATGGTGAAACA[-/CT]GTCTCTACTAAAAAT | 57531 |
rs570416317 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104727382 | GTATACGAATATATA[C/T]ACACATGTATATGTA | 57531 |
rs570432965 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823785 | AAGATGTTTGCTGGC[A/G]GTTTTCTTTTTGTAA | 57531 |
rs570479341 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104720945 | CGCCCGGCCCAGCGA[C/T]GCTCTTATACAAACA | 57531 |
rs570503537 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104740025 | AACTCACTCAAAACC[A/G]CTCAACTACATGGAA | 57531 |
rs570514478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104739283 | AAATAACCAGCTAAC[A/G]TCATACTGACAGGAT | 57531 |
rs570517553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104792906 | CAAGGGCTGCAGAAG[C/T]TCAAGGTTGTTGCTG | 57531 |
rs570534688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104837443 | ATTCATAGGCAGAAA[A/G]AAAAGAGTAAACCTT | 57531 |
rs570536226 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723800 | CTCACTATGTTGCCC[A/G]GGCTGCTCTTGAACT | 57531 |
rs570573543 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808192 | TCTGTCTCAAAAATT[-/A]AAAAAAAAAAAAAGT | 57531 |
rs570592655 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692576 | ATGCACAGCAGGTAT[C/T]TGGAGTGAGAAGATG | 57531 |
rs570600426 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104689800 | AGGGAAAATCACCAG[C/G]ATGGTAAGCTTAACA | 57531 |
rs570610087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845046 | ACAATACAGTGTGTA[C/T]ATGTTAAATACATAT | 57531 |
rs570637948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836847 | AAAACCAAAAACCAA[C/T]TGCATTTCCATCTGA | 57531 |
rs570649725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760950 | CTTAAATTCACAATT[A/G]CTATTAAGAGAATAA | 57531 |
rs570696786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104844500 | AGACATGCACCACCA[C/T]GCCAGGCTAATTTTT | 57531 |
rs570724805 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104705509 | TATCTCTAGCTCCAA[A/T]ACAAATAGCACTCGT | 57531 |
rs570744183 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797542 | TAAAACCAATGTAAG[A/G]GAATCTGGGGAAAAA | 57531 |
rs570779565 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767423 | TAATTCTTCATGCAT[A/G]CTTCCCCAAACCAAA | 57531 |
rs570782619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834982 | ACATTGAACAAAGAA[C/T]ACCACACTAAAAAGG | 57531 |
rs570799882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104761190 | TTTCACAGAAATGGA[A/G]AAAACTAATTTAATC | 57531 |
rs570806955 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104767435 | CATGCTTCCCCAAAC[C/T]AAAATGCCACAGCCT | 57531 |
rs570816788 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858943 | TCTTTGCAGATGCGT[C/T]CTAGTTACCAGCTAG | 57531 |
rs570820495 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104814585 | ATAGAAGATATGGAA[A/T]CTAGAATATGGAGAT | 57531 |
rs570830136 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104712867 | CTGGTGGAGGACACA[A/G]CATTCAAGGTGTCAC | 57531 |
rs570831399 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701462 | ACACTGTTTATATTC[A/C]TATAGCCCTTTCTGT | 57531 |
rs570836640 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703430 | AATTGAAAGCATGGC[C/T]CCAAATGTCCATTAA | 57531 |
rs570840768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850758 | GTTTAGAGACAGAAC[A/G]GATAGCACACCACGC | 57531 |
rs570863014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704993 | GATGTAAAAGCACTT[C/T]GATTTTTCAATAGAG | 57531 |
rs570893250 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104726110 | CTGAGGAGCAGAATC[A/C]CTTGAACCCAGGAGG | 57531 |
rs570899646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806191 | TAAGGGCCAGGTGTC[A/G]TGGCTCACATCTGTA | 57531 |
rs570928773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104855749 | ATCTGAACTTCTAAA[C/T]CATGAGAATTTCCAT | 57531 |
rs570967962 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752338 | CCGGGAAATAACATA[C/T]ATAAAATATTTCATA | 57531 |
rs570988951 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773761 | AAAAGAATAGATAAG[A/G]AGACTTTTTTAAAAA | 57531 |
rs570990165 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709302 | AATGGCCACTAAGTA[C/T]ATGAAAAGATGTTCA | 57531 |
rs570992788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821690 | CAACACATAAGTAAA[C/T]ATTGAAGCAGGGATT | 57531 |
rs571023966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820957 | TGCCCATCGATGGTA[A/G]ACTGGATAAAGAAAA | 57531 |
rs571035580 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | HACE1 | GRCh38.p7 | 6:104737817 | AGCCCGAACTGGGTG[G/T]AGCCCACCACAGCTC | 57531 |
rs571040291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766760 | CAGTTACAAGTTTTG[G/T]GCCCTCGGGCAGTTA | 57531 |
rs571040448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718492 | TCCCCATTAACAAGA[C/T]ATTTGCTGAAGAATT | 57531 |
rs571057290 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant | HACE1 | GRCh38.p7 | 6:104803799 | ATTCCCTTTGAAAAC[A/C/T]GACACAAGAGAAGGA | 57531 |
rs571066106 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838034 | TCTAAAAGAAAACTA[C/T]AGAAAAAGATGCAAG | 57531 |
rs571070759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104774874 | AAGTTCTTTAAAAAA[C/T]TATTATAGATATCGG | 57531 |
rs571105410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722554 | TGCTCAATCAACAGG[C/T]TGGTCAACTTACTTG | 57531 |
rs571135608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827935 | TAATAAGGTTTATTC[A/T]GATAAAAGTGAAATT | 57531 |
rs571149072 | snp | A/G | 0.243061 | 0.249904 | intron-variant | HACE1 | GRCh38.p7 | 6:104774151 | CTGGAGTGCAGTGGC[A/G]GGATCTCGGCTCACT | 57531 |
rs571160587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709668 | CCTGCAGAACCTTGA[G/T]CCAAATAAACCTCTT | 57531 |
rs571168580 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848059 | GTTTCACCACGTTGG[C/T]CAGACTGGTCTCAAA | 57531 |
rs571173836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832348 | CAAATTACAAATATT[A/T]TGAACAGATATAAAA | 57531 |
rs571179057 | in-del | -/TTTTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774103 | TTTTTTTTTTTTTTT[-/TTTTT]GAGACGGAGTCTCGC | 57531 |
rs571202876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104796577 | AAATTACTAAGCTAA[A/G]CACATTTGTAAAATG | 57531 |
rs571242946 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728049 | AAGCAATTCTCCCAC[C/T]TCAGCCTCTCGAAAT | 57531 |
rs571275101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764040 | TGACAGAGCAAGATT[C/T]TATCTCAAACAAACA | 57531 |
rs571291475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716440 | CTCACACCTGTAATC[C/T]CCACACTTTGGGAGG | 57531 |
rs571301760 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803518 | AAGCTTATCCACCAC[C/G]ATCAAGTCGGCTTCA | 57531 |
rs571307728 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700985 | GTTCCCTGCAGGCTT[A/G]TGTGTTTTCTCAAGC | 57531 |
rs571339007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775605 | GGCCTAAATAATTAA[A/T]CTCATGACTTCACTG | 57531 |
rs571384553 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802099 | AGACGTTAGACGAAG[C/G]AAGATCAAAACAGAC | 57531 |
rs571428601 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840870 | CAGGAGGCTGAAGCA[C/G]GAGAATTGCTTGAAC | 57531 |
rs571437071 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696431 | AGCAGGGATGCTGAT[C/G]CAAAACTATACACAG | 57531 |
rs571444825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838524 | AAAAAATGAAACTAG[A/G]CTCCTATATCTCTTG | 57531 |
rs571445397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818565 | CCTGACACCAAAACC[C/T]GGCAGAGATACAATA | 57531 |
rs571452045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104824621 | CAACATAATTCAAGA[C/G]AATAAATTCTGGATT | 57531 |
rs571475333 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104716141 | AAAATTCCAAACTAA[G/T]TTCTAAATAATATAG | 57531 |
rs571476191 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684934 | TGCCTGCTCCTGTGA[A/C]GTTGGGCAGGGCCAA | 57531 |
rs571485345 | snp | A/C/T | 6.61883e-05 | 0.00575243 | synonymous-codon, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771328 | ATTATCTAAAATCCA[A/C/T]TGCAAATTTTTCGCA | 57531 |
rs571529946 | in-del | -/AC | 0.0770498 | 0.180522 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727741 | TGTATATGAATATAT[-/AC]ACACATATATATGTA | 57531 |
rs571545433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801379 | GAACGCCACAAAGAT[A/G]CTCCTCAAGAAGAGC | 57531 |
rs571558998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779073 | TTGGAGACAGGATAA[A/G]GTTCAAGAGATGAAA | 57531 |
rs571579869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104742542 | AAGACATTTATGCAG[C/G]CAAAAAACACATGAA | 57531 |
rs571597149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770777 | TATCAAAAGGTCGAA[A/C]AAACTTACTGGATCC | 57531 |
rs571598068 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104684206 | TTTCATTCTATTTTC[A/G]TGTGATGGGCTATTA | 57531 |
rs571605314 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845793 | ACTCTGGGTAAACTT[A/T]TAAGATAAAACATTT | 57531 |
rs571620349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807554 | GAAAATACCTGAAAA[C/T]CATTATACATCCCAA | 57531 |
rs571659052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794014 | CCCTGTTTCTCCTGT[C/T]CCACCAACCACCCCT | 57531 |
rs571668874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853813 | AGTCCCCACTTATCC[A/G]CAGGGGATACATTCC | 57531 |
rs571754383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104846803 | CAGGAAGTACTCAAG[C/T]CACTTAGCAAACATT | 57531 |
rs571758058 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756985 | GTCGCTGGACCTTGG[C/T]GGGGAGAGGGGCGTC | 57531 |
rs571766969 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104853099 | GAGCCATGAGGGCTC[A/C]TCTTTCATGAATGGA | 57531 |
rs571799880 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762059 | AAACAACAGATGCTG[C/G]AGAGGTTGTGGAGAA | 57531 |
rs571815823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707163 | GAGGGAACACTTCCC[A/G]ACTCATTCTATGAGG | 57531 |
rs571864725 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785378 | CAGGATTAAAAAAAA[A/C]AAAACAAAACACAAC | 57531 |
rs571876937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713735 | GTATTACAACCTAGT[C/T]CGATTGACCCTTCCA | 57531 |
rs571910331 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733579 | AGTAATTGGCCAGGC[A/G]CGGTGGCTCACGCCT | 57531 |
rs571923104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762250 | AAGACACACGCACAC[A/G]TATGTTTACTGCAGC | 57531 |
rs571942545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104698936 | TGTCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA | 57531 |
rs571948059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762681 | TCTGCACATGTAACC[C/T]AGAACTTAAAGTATA | 57531 |
rs571962198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104801555 | GAAGAGAGTGGGGGC[C/T]AATATTTGACATTCT | 57531 |
rs572010400 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756759 | GTTTCACCCGGGAAG[A/C]GCAAGGGGTCAGGGG | 57531 |
rs572035348 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104761773 | GGCAGCCTACAGAAT[A/G]GGAGAAAATTTCTGC | 57531 |
rs572038271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852445 | TAAGATTAGTTTAGA[A/G]TTTTCCTAACTCTAT | 57531 |
rs572055018 | in-del | -/GGAAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702135 | CGTACTTTTCTAGTT[-/GGAAAA]GGAAATTAATGACTT | 57531 |
rs572056140 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725199 | AAAAAACCTATTAAT[A/G]ATACTTCTTTTCTGG | 57531 |
rs572068657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748761 | CTGCATGCAACAATA[C/T]GTATGATTCCCACAA | 57531 |
rs572072260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104733518 | TTAGATTATACAGTA[C/T]AAAATTACAGTAAAC | 57531 |
rs572076663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764974 | ACAACATCCTTCATA[C/T]TAAACTCCCTTTGAA | 57531 |
rs572092527 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846157 | TAGGAGAGAAATATA[A/T]CCTATCTTTCTATTG | 57531 |
rs572095989 | snp | A/G | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104837730 | AGCTAGAGCAATCAG[A/G]CAAAAGAAAGAAATA | 57531 |
rs572137168 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685787 | AGTACTGGCATCTTA[A/C]GAATGCAGAAAGTAA | 57531 |
rs572139487 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853544 | AACCCCCACTCAGCC[C/T]TTTAAAAGTTAATGC | 57531 |
rs572160043 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104831763 | CCGGGCGTGGTGGCC[A/G]GTCCCTGTAGTCCCA | 57531 |
rs572174835 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | HACE1 | GRCh38.p7 | 6:104807705 | AAAGATGGCAGGGGG[A/G]AAAAAAAATCAATGT | 57531 |
rs572198293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104714524 | ACTTTGGATATGACT[C/G]TGGTCCCCATAGTCC | 57531 |
rs572200232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104845611 | GCCTCCTGAGTAGCT[A/G]GGACTACAGGCACCC | 57531 |
rs572202302 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722950 | ACTACATATAGTAAT[A/C]GTCATTAGATTCTCA | 57531 |
rs572208004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104739531 | CCTAGTCTCTGATAA[A/G]ACAGACTTTAAACCA | 57531 |
rs572210047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104732853 | CTTCTATCTGGGAAG[C/T]CGTCTGGTTTGGTTT | 57531 |
rs572246172 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104857058 | AGCAAAAAAAATCTG[-/ATT]ATTTTCTAAATTTAG | 57531 |
rs572255171 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104808193 | TCTGTCTCAAAAATT[A/T]AAAAAAAAAAAAGTG | 57531 |
rs572264802 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803514 | CAAAAAGCTTATCCA[A/C/T]CACGATCAAGTCGGC | 57531 |
rs572286767 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104713952 | TGGCTTTTGTTTTTT[A/G]TAAGGTCATAGGATA | 57531 |
rs572293453 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104720417 | GTTGCCTGTATCTTT[A/T]TATTGCTGAATAGTA | 57531 |
rs572306547 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104705666 | ATGTCAAATTGCCCA[A/G]GATGCTTCTTTATGG | 57531 |
rs572329403 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683492 | TTATTTTCTTACCTA[G/T]GAAATAGAAGGAAAA | 57531 |
rs572332560 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104769459 | TATGACTTCATTACC[C/G]TTAATTGAGGGTAGG | 57531 |
rs572335957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830352 | ACTAATGAGAAGAAT[A/G]TACTTGAAAACACTG | 57531 |
rs572380460 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750924 | TGTGTGTGTATGTAC[A/G]TGTAAATAACTCAGA | 57531 |
rs572421270 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104689519 | AAAGTTTTAGTCCCT[A/T]TTCTAAGTGGATTCA | 57531 |
rs572433348 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104712491 | CAATAAAAGGGCTGT[C/T]GGCTGGGCGCGGTGG | 57531 |
rs572438213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104784618 | GTTTTGAATCTTCTT[C/T]GTAAGTTTAGGAAAC | 57531 |
rs572464764 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730191 | ATTCCAAAATCCTGG[A/C]GAGAGATCACAGCTG | 57531 |
rs572490648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834570 | TGCATCAGTCTCTAC[C/T]TCTTCCCTAAACCCC | 57531 |
rs572491817 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748484 | ACACCTCCTAATGGG[A/T]GTGTAAACTGATGCA | 57531 |
rs572503355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799905 | TGCAGCCCACGGAGG[A/G]TGAGCACCTCACTTG | 57531 |
rs572511935 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802808 | AATTAAAAGAACTAG[A/G]GAAGCAAGAGCAAAC | 57531 |
rs572520638 | snp | C/T | 0.00199481 | 0.0315187 | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682713 | CTTGGTCCCAGTCCA[C/T]GAAGACCTGCCTCTT | 57531 |
rs572527345 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724139 | TGTGTCATAAAGATA[A/C]GTTTCCTCCCCTGTT | 57531 |
rs572548690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783980 | CATGCAATCATTCCT[C/T]TTACAACAGAATGTC | 57531 |
rs572555636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806500 | GAATAATTTTTTAAA[A/T]AGATTTAAAAACAAT | 57531 |
rs572567797 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774292 | AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG | 57531 |
rs572572497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104684797 | TATTATGTATTGCAA[C/T]TTTTTAAAGCTAACA | 57531 |
rs572577157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104747703 | TCTTCTTTGGCCTAG[G/T]TTTCTCATCTGTAAA | 57531 |
rs572588651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104736952 | TCCAAATTTTCTACA[A/G]TGATTAAACACTACT | 57531 |
rs572627175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104756246 | TGAAACGTCATCTTT[A/G]CTAAAAACACAAAAA | 57531 |
rs572642099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800396 | TTGAGCTCTGAGAAC[A/G]GACAGACTGCCTCCT | 57531 |
rs572643550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858591 | CCACATTTCTTTCAT[A/G]ACCGTCTGCCAAGGT | 57531 |
rs572650059 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104754802 | AACTAAATATGGAAA[G/T]AAAAAATTGTTACCA | 57531 |
rs572663820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755610 | ACAATCAAATTAGAA[C/G]TCAAGATTAAGAAAT | 57531 |
rs572705140 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104702242 | TAAACATTTTACTTA[A/C]ATCCAACCAAACTGA | 57531 |
rs572705657 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841710 | ATATTCAATATTATT[A/C]TTTATTCAAAAATTA | 57531 |
rs572715492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840543 | CATTAAAATAGCTGA[C/G]AGAGGCCCGTCGCGG | 57531 |
rs572772408 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830284 | GACATTTCACATCTT[C/T]TTTTCCCACATAGAA | 57531 |
rs572797685 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783765 | ATTTCCAAAGGGCAT[A/G]TGTTATGTAATTTCC | 57531 |
rs572801034 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790463 | CATTGTTTAAAGAAA[C/T]GTAAGTTGGCTGGGT | 57531 |
rs572802230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772740 | AGGGCAATAAGTTAC[C/T]AATTACTATGAAAAT | 57531 |
rs572830290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104709225 | ACTCAATAATAAAAA[C/T]GACTCAGCTTTAAAA | 57531 |
rs572837633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744655 | ATTTTCTTTAGGGAA[A/C]AAAGTTATTATATTT | 57531 |
rs572876819 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781949 | TTTTGACTAAATTGT[A/C]CAGGAAGGGAAAAAG | 57531 |
rs572886719 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | HACE1 | GRCh38.p7 | 6:104703607 | GGTTAGTTTTCCAGA[C/T]AGAAGAGAGACGAAA | 57531 |
rs572889900 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104809518 | TCACTGTGGTTCAAG[G/T]ACAGTGAGCTAAACA | 57531 |
rs572890395 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685781 | AATAGCAGTACTGGC[A/G]TCTTACGAATGCAGA | 57531 |
rs572899147 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737386 | TGAGCCACGCAAAAG[A/T]TGGTGATTTCTGCAT | 57531 |
rs572903164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104803604 | CATAAAAAGAACCAA[C/T]GGCAAAAACCACATG | 57531 |
rs572950242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104789307 | ACTAGCTGAGTTTTA[C/T]AATTAGTGTTTTACA | 57531 |
rs572967915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744046 | CTAAAACAGTGGAAA[A/G]GGTGGTAAGTTACTG | 57531 |
rs572992136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104797416 | ACACATCCAAGTCTC[C/T]AGGCTTCTTAATCCA | 57531 |
rs573001762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104693602 | TATTGTATTGTTTTT[G/T]ATTTGTATTATTTTT | 57531 |
rs573049696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752729 | CCTATTATTTCCTCC[C/T]ACATTTTATTTTTTA | 57531 |
rs573068757 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104787715 | AGTCTAAACCAACAG[C/T]GATCCTATTTTCAAA | 57531 |
rs573083929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104856245 | CTGTTAACAAAAAAA[A/G]GGTGCTCAGAGTAAT | 57531 |
rs573103104 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779453 | GAAAAGAATAAATGC[C/T]ACCTTTTTAAAGTTA | 57531 |
rs573107953 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | HACE1 | GRCh38.p7 | 6:104803166 | GAATCTCTGAACACA[C/T]CAATAATAGGCTCTG | 57531 |
rs573121610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848188 | AGGCCGGGTGCGGTG[A/G]CTCACGCCTGTAATC | 57531 |
rs573126178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758810 | GGAGACCCATCTCAC[A/G]TGCAAAGACACACAT | 57531 |
rs573170009 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764245 | ACCATGCCCAGCTAA[G/T]TTTTGTATTTTTAGT | 57531 |
rs573174409 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104716553 | AAGTAAGCTGGTTGT[A/G]GTGGTGGGCATCTGT | 57531 |
rs573181866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786868 | CTCACCTTTAAAATA[C/T]TTCAAGGAAAGAAAT | 57531 |
rs573213143 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104734842 | CTTAGTACTAAAAAA[C/T]TTGAATAACTGATTT | 57531 |
rs573262655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825039 | AGTGAGCTGAGATGC[A/G]CCACTGCACTCCAGC | 57531 |
rs573266331 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825477 | CAGACTAACTGAAGG[C/T]AGTTATGTGCAAGCA | 57531 |
rs573275110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770947 | TGCATATGCCCAATT[C/T]ATACTATCAGCTGAA | 57531 |
rs573288031 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104758467 | CTTCATAAGTGAAAG[A/C]GAAATAAAATCCTTT | 57531 |
rs573328318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722630 | CCTGAAGCTGCACTG[A/G]ACACAGAGTTTACAT | 57531 |
rs573336705 | in-del | -/A | 0.32153 | 0.239548 | intron-variant | HACE1 | GRCh38.p7 | 6:104712771 | GCAAGACTCGGTCTC[-/A]AAAAAAAAAAAAAAA | 57531 |
rs573343046 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823934 | TCTCCAGTCATTTCT[A/C]TGAGGACAGCAAGTA | 57531 |
rs573351706 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728302 | CAAAAAATCAAAACA[G/T]AAAACATTATTAGCT | 57531 |
rs573362585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848179 | AAAGTGTTTAGGCCG[A/G]GTGCGGTGGCTCACG | 57531 |
rs573369259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104832406 | TTGTTGTTGTTGTTG[C/T]TGTTTGATACAGGCT | 57531 |
rs573401423 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104763691 | AGAATATCTGTGCCA[C/G]CTGTTAAACAGAAGC | 57531 |
rs573406804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735857 | TTCATAAATAGGAAA[A/G]TTTAGCAATAAAGAA | 57531 |
rs573418971 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705011 | TTTTCAATAGAGAGA[-/T]TTTTTATACATTTAT | 57531 |
rs573456787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691858 | GCACAGGAGTTTGAG[G/T]GGGCAGTGAGCTATA | 57531 |
rs573459324 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104742961 | ATGTGGCACATAAAC[A/C]CCATGGAATACTATG | 57531 |
rs573471238 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104741943 | AACCAAAACAGCATG[C/G]TACTGGGACCAAAAC | 57531 |
rs573477140 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104815245 | GAGGAACTTATTGGC[A/G]ACTGGAGTAAAGATC | 57531 |
rs573506036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104831834 | GGAGGCGGAGCTTGC[A/G]GTGAGCCGAGATGGC | 57531 |
rs573524815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847298 | AGTACTATGATATTT[C/T]TCTACATGTAACCTT | 57531 |
rs573532441 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834415 | AGGGTAAAAAATATA[C/T]AAAACACCTATAAGT | 57531 |
rs573533553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104693491 | ATGCTCAAATCCCTG[A/G]TATAAAATGGCATAG | 57531 |
rs573537429 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684371 | TCAAATTGACACCTG[A/C]GAGTTAATTTACACC | 57531 |
rs573537979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104838689 | ATTTCTTGAGTAAAT[C/T]TGCTTTTAAGTAAAA | 57531 |
rs573573026 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757329 | GTGCCCCTCTGGGAC[A/G]AAGCTTCCAGAAGAA | 57531 |
rs573582661 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694139 | ACAAATGAATGGATG[A/G]AGAGAATGTGGTACA | 57531 |
rs573582833 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698275 | TTATACATGCATATA[A/G]TTTAAATGGTCAAAT | 57531 |
rs573609750 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805315 | TTCCTCCAGGATCTA[A/T]AACTAGAAATACATT | 57531 |
rs573612230 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104839937 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 57531 |
rs573613312 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781796 | CCCTCTTCTACACAG[A/T]CACACTTCTTAATCA | 57531 |
rs573626066 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726783 | TATTTCTGTTTTCTT[C/T]CTTATATGAAACTAC | 57531 |
rs573627710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104839604 | ATATTGACTATGGTG[C/G]TGAAAACCTACCATG | 57531 |
rs573628818 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701161 | TCCTGCTTTCCATGT[A/T]TTGAGAGCTCACAGT | 57531 |
rs573629341 | snp | C/T | 0.000535858 | 0.0163598 | intron-variant | HACE1 | GRCh38.p7 | 6:104780345 | TGTATGTAAACTTTC[C/T]AGAGTACCTGCATTT | 57531 |
rs573634221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104715373 | ACAAAAGAATAGATA[C/G]AGTATAAGAAAGAAT | 57531 |
rs573651206 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104722041 | TGAGACAGGAAAGAC[A/T]GGGATGGGGTGACAG | 57531 |
rs573675328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104787964 | TATTTCTTCAATCAT[A/G]CATACATTAAAACTA | 57531 |
rs573677842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104824795 | AAATGCAAAGAAGGC[C/T]GGGCACGGTGGCTCA | 57531 |
rs573717518 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104685960 | ACAGGAGTTGTAATA[C/T]AGATAAAAGACAACA | 57531 |
rs573725155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104840483 | AAAAAACCAGGAAGT[A/G]GCATTTAGCATGCTA | 57531 |
rs573778459 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708280 | TCTATGTACTAGCAG[C/T]AAGCATTCTGAAAGT | 57531 |
rs573785248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803086 | GAATACTATAAACAC[C/T]TCTATGCAAATAAAC | 57531 |
rs573792503 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104700691 | AGAGAAAAAGCAGGA[A/T]GAGGGTAATTGCATG | 57531 |
rs573797746 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783517 | AGATGAAGAAACCAA[A/G]GGCTCAAGGATATTA | 57531 |
rs573803951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823662 | GAAAAACCTACTTCC[C/T]TTAGAATTAGGATAA | 57531 |
rs573853192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794633 | ATTTGGCCAGGCGCA[C/T]TGGCGCACGCCTGTA | 57531 |
rs573866189 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838363 | ATAAAAACAGACACA[C/T]AGACCAATGGGACAG | 57531 |
rs573877079 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861682 | AGGGGTAGGAGCCCC[A/C]AGCAGCCTCCATGGT | 57531 |
rs573878602 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707589 | AATTTATAAACAATA[A/C]AAATTTATTTCTCAC | 57531 |
rs573913583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104758404 | AATATTCAGTATTCT[A/T]AAAGAAAAGAATTTT | 57531 |
rs573915227 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104795982 | AGAAATTTAAATTCC[A/G]CAATTTTTCTAAGAC | 57531 |
rs573933404 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104683705 | CCTTATCACGTACTT[A/C]GGAAAGATACTTATG | 57531 |
rs573935285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104691814 | GTAGTCCCAGCACTT[C/T]AGGAGGCCAAGGCAG | 57531 |
rs573946383 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816987 | TGTTTTGGCCAATTT[A/C]TCCCACTTGGAGCAT | 57531 |
rs573979162 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104763599 | CTTAATGGTTAAAAA[A/C]AAAAAAGGGGCATAC | 57531 |
rs573982604 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104808623 | ATATAATATATTATA[A/T]CTAGTAATACTTATC | 57531 |
rs574050234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104831754 | AAAAATTAGCCGGGC[A/G]TGGTGGCCGGTCCCT | 57531 |
rs574066705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104778232 | GCAAACTGTGAGTTA[C/T]CTACAATTTTTGATT | 57531 |
rs574085919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813389 | CTGTAAAGCAAGACC[C/T]TATCTCTAAAAAGAA | 57531 |
rs574090141 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104821915 | CCTAGACAGCTACTT[A/G]TGTATGGTTTTAAAG | 57531 |
rs574093693 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762942 | TTGCAGTGAGCTGAG[A/G]TCGCGCCACTGAACT | 57531 |
rs574110265 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711628 | TTGTGTGTGGTGATG[A/T]CAATTCATGTTTAAT | 57531 |
rs574118306 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734435 | AAAAAAGAAAAAAAA[A/T]TTATACTTTTGGTTT | 57531 |
rs574119360 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727719 | TGAATATATACACAC[A/G]TATATATGTATATGA | 57531 |
rs574141223 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754523 | AAGAAAAGCTGTTAA[C/G/T]GGCAGCCAGAGATAA | 57531 |
rs574146175 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747612 | GACTGGCAACAGTGA[C/T]GGTATCTGGGGTCAG | 57531 |
rs574201827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104777481 | TCAATAACTATTTAC[A/G]AAAAGACAGAACTTA | 57531 |
rs574203131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821271 | TGAAATAATCTGTAC[A/G]ACAAAGCCCCGTGAC | 57531 |
rs574212475 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104845362 | ATAAAACTTTTTAGA[A/G]AAAAACAACTGACAA | 57531 |
rs574219506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104786665 | TAGGATATTTTTAAT[A/C]CCAAATAAAGATTAA | 57531 |
rs574231056 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777978 | TAGCCAGGCTGGTTT[C/T]GAACTCCTGACCTCA | 57531 |
rs574251174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791488 | TCTTCCTAACAATGC[C/T]ATATACTTTTCTCAC | 57531 |
rs574265895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104842715 | AATAAACAAAAGTCA[C/T]AAACTTAAAAAGGAG | 57531 |
rs574277220 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730437 | AGTTTATATCTTAAT[A/G]CATTGTAATCATGAA | 57531 |
rs574304092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104718866 | TCATAAAATGAGTCA[C/T]CACTTTTCCACATCC | 57531 |
rs574338103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104715034 | TATGAAAGCTAATAC[A/G]TAAGTCCCATCTTTC | 57531 |
rs574339688 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104688325 | AAGTTTATACCAATT[G/T]CCCTTTGAATATTAC | 57531 |
rs574365086 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104801529 | TCTCTCGGCAGAAAC[C/T]CTACAAGCCAGAAGA | 57531 |
rs574380709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104749436 | TTCACTATTATACTA[A/C]GATATACTATGAATG | 57531 |
rs574381496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858101 | ACATATTTTTTTCTA[C/T]TTTTCTTTATTTTCC | 57531 |
rs574389984 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104740459 | TCAAATAGATGCACT[A/G]AAAAATGATAAAGGG | 57531 |
rs574401917 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104712704 | TTGAACCCGCGAGGC[A/G]GAGGTTGCAGTGAGC | 57531 |
rs574403344 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805209 | GTCAAGAAACAACAA[C/G]TGCTGGAGAGGATGT | 57531 |
rs574409190 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760674 | CCACTCCTATTCAAC[A/G]TAGTATTGGAAATTC | 57531 |
rs574420933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828074 | CGTTATTCTGAGAAG[A/G]CTGTAATTAACATTT | 57531 |
rs574432573 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104846017 | AATGGCAAAATAAAT[A/C]ATTAGGTAGGAATGA | 57531 |
rs574435285 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104774285 | TTAGTAGAGACGGGG[G/T]TTCACCGTTTTAGCC | 57531 |
rs574456206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725013 | TATCAGGCAACGTGG[A/G]AACAACTTTGTGGGC | 57531 |
rs574497415 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760606 | CTGAATAGGGAAAAA[A/C]ACGGGAAGCATTCTC | 57531 |
rs574521754 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788583 | CCACAAGATAAGATC[C/T]TGAAGTTAAAAGTTT | 57531 |
rs574528972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835154 | AAGAAATCGACACTG[A/G]AAAGGTCTAAGAGGC | 57531 |
rs574540684 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104782155 | TCTTTCACCTATTAT[C/G]TCATTTGCCCCAGAA | 57531 |
rs574544433 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104761056 | ATAAGACAGGACACG[A/C]ACAAATGGAAAAACA | 57531 |
rs574561108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104827145 | CTGTGCCCAATACAC[C/T]GATAAATTACAAAGC | 57531 |
rs574604625 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737249 | GATCGAGCCACTGCA[C/T]TCCAGCCTGGGGGAC | 57531 |
rs574622772 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104740099 | ATGAAGGCAGAAATA[A/C]AGATGTTCTTTGAAA | 57531 |
rs574633433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745585 | AGCTAGGACTACAGG[C/T]GCCTGCCACCATGCC | 57531 |
rs574634370 | in-del | -/AGGAAGGG | 0.0115144 | 0.0749975 | intron-variant | HACE1 | GRCh38.p7 | 6:104692016 | AAGAGCAGGAGTGGA[-/AGGAAGGG]AGGAAGGGAGGAAGG | 57531 |
rs574648584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104731329 | CTGAATAAAATTTAA[A/G]ATACTTTCTTAAAAA | 57531 |
rs574652670 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737971 | TCTCCCATCACGCAG[C/G]TGGAGATCTGAGAAC | 57531 |
rs574666448 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104764355 | AGTGCTGGGATTACA[A/G]GTGTGAGCCACTATG | 57531 |
rs574696101 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821922 | AGCTACTTGTGTATG[A/G]TTTTAAAGTAATGCT | 57531 |
rs574698066 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804177 | GTGAAGGACCTCTTC[A/C]AGGAGAACTACAAAC | 57531 |
rs574701385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765154 | CACATTATTTTTGAT[A/G]AGAATTTCAGCTGGA | 57531 |
rs574724747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104834704 | TATCTTGTCAGATTA[C/T]ACTTGTTGACTTGTC | 57531 |
rs574727232 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768371 | ACAGAATGTATAAGC[-/A]AAAAAAAAGAACAAA | 57531 |
rs574742443 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104703499 | TTTTCATAGTGCATC[A/G]GTGTAAGGAGTTGTA | 57531 |
rs574765413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702705 | AATTTTGTTCTGTTT[C/T]GATGTAGTAAGAAAT | 57531 |
rs574767298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104753817 | ATCAACACAAAAATG[C/G]TGAAAACTCAAAAAG | 57531 |
rs574784704 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104737710 | TGATTGCTAGCACAG[C/T]AGTCTGAGACCAAAC | 57531 |
rs574789175 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795478 | AAATTTTTATAACAT[C/T]GTTATCACTGACAAA | 57531 |
rs574801554 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792759 | ATGCTGAGGGCAGTC[A/G]CGACCCAGGCATAAG | 57531 |
rs574804394 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745059 | GGGAAAGTCATCAAG[A/T]AATCATTATCATGAG | 57531 |
rs574828920 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851793 | TTCTTCTTCTTATAT[A/C]AAAAAATTCAATGGC | 57531 |
rs574835177 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787229 | GTCGGGTTAAGTACA[A/G]TGTTTCCTTTTTTAA | 57531 |
rs574888183 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104724029 | GCTAAGTTCCTAGTT[C/G]AGCTCACAAGAGCAT | 57531 |
rs574891082 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104753025 | TACTTGAAAGAGCTG[C/T]GTTTAATGGAAAAAT | 57531 |
rs574895303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104803667 | CAAAATTCAACAGCC[C/G]TTCATGCTAGAAACT | 57531 |
rs574905985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849433 | CCTTGACCTCCTGGG[C/T]TCAAGCAATCCTCCC | 57531 |
rs574910505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104772498 | TCATCTGTATGTGCC[A/G]GTGCAGTAAGTATTT | 57531 |
rs574913810 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835130 | GACCAGTTCAAGAGT[A/C]AATGCCTAAAGAAAT | 57531 |
rs574917404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725613 | CTGATAGACACTGAA[A/G]TTATTCTGTTTTCCT | 57531 |
rs575004159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104833708 | AATTAGCTGGGCAGC[C/T]GGGCACGGTAGCTCA | 57531 |
rs575007266 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104811136 | TACTTCCTCTTAAAA[G/T]ACAGCATATTTGTGG | 57531 |
rs575012000 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710078 | CCAAATAATACAAAT[G/T]TTTATTAGCTGATAA | 57531 |
rs575018538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104781200 | ATTCATTAACTTTTT[C/T]CAGTACAGACTCATA | 57531 |
rs575019871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848942 | TGAATATAATGACCC[C/T]AGATCCACTATAAAG | 57531 |
rs575036054 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104826935 | AGAAACTATTGCGGA[A/G]GAACCGCAAAAGAAA | 57531 |
rs575036522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104716763 | CTAATTTTAAAGGAT[C/T]GATATCATACAGGTT | 57531 |
rs575058258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798391 | ACCAATTGGAATTAA[A/G]GTTTTTTTAAAAAAA | 57531 |
rs575080848 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104819654 | ACTACAGGGATATAG[C/T]GAGCAAAACAGTATG | 57531 |
rs575092726 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824952 | GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC | 57531 |
rs575106170 | in-del | -/A/AA | 0.225 | 0.256431 | intron-variant | HACE1 | GRCh38.p7 | 6:104825081 | GCAAGACTCCGTCTC[-/A/AA]AAAAAAAAAAAAAAA | 57531 |
rs575110963 | in-del | -/A | 0.0433465 | 0.140692 | intron-variant, splice-acceptor-variant | HACE1 | GRCh38.p7 | 6:104824909 | AACCCCGTCTCTACT[-/A]AAAAAAAAAAAAAAA | 57531 |
rs575113098 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104833896 | AGGCTGAGGCAGGGG[A/C]ATCACTTGAACCCAG | 57531 |
rs575157824 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104825611 | GGGGTGTGACCTTTG[C/T]AACTTCAGCCTCTGA | 57531 |
rs575209157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104848212 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGTG | 57531 |
rs575219370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819008 | ATCTCTCACCACCCC[C/T]ATTCAACACAGTATT | 57531 |
rs575243340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104701403 | GAAAATCCTAAATGC[A/G]ATATATTTAAAGTAG | 57531 |
rs575289004 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717128 | AAAGCAATATTGGGG[-/T]TTTTTTGTGGTTTGT | 57531 |
rs575321363 | snp | C/T | 0.29175 | 0.246489 | intron-variant | HACE1 | GRCh38.p7 | 6:104774155 | AGTGCAGTGGCGGGA[C/T]CTCGGCTCACTGCAA | 57531 |
rs575351798 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737055 | TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG | 57531 |
rs575367296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104737392 | ACGCAAAAGATGGTG[A/T]TTTCTGCATTTCCAT | 57531 |
rs575388165 | in-del | -/AAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811870 | AAAACTAAGCACCAG[-/AAT]AATAACTTTCCCAAA | 57531 |
rs575397449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104790402 | GTGGCACATAAAAAC[A/G]TTTATATCACTTTTT | 57531 |
rs575404794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104771024 | ATCAAAATAATCCTT[C/T]CTAATTCAAAATTTA | 57531 |
rs575404942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104780249 | GTGGAACATTAAAAG[G/T]TACAAACTGCTACCT | 57531 |
rs575419695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104702293 | CGTTAATTTTGACAT[C/T]ATTTACTGAATATAA | 57531 |
rs575436663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104687116 | GAACCCACAAGCCCA[A/G]TAACATGCAGAGGAT | 57531 |
rs575442045 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104760310 | CTCAATAAAATACCG[G/T]CAAACCAAATCCAGC | 57531 |
rs575445772 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104842326 | AAAAGGTTTTATTGG[C/T]CGGGCACAGCAGCTC | 57531 |
rs575449029 | in-del | -/A/AAA | 0.24932 | 0.249999 | intron-variant | HACE1 | GRCh38.p7 | 6:104751955 | CAAAAAAAACCAAAC[-/A/AAA]AAAAAAAAAAAACAG | 57531 |
rs575476831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849327 | TAAAAAACAAAATAT[C/T]CTATTAAACACAATT | 57531 |
rs575479968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104745511 | GAGTGCAGTGGCGCG[A/G]CTCACTGCAAGCTCC | 57531 |
rs575493535 | in-del | -/AAAC | 0.0689305 | 0.172377 | intron-variant | HACE1 | GRCh38.p7 | 6:104761838 | ATCTACAAAGAACTT[-/AAAC]AAATTTACAAGAAAA | 57531 |
rs575516191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104779570 | AAATATCTCATTTTC[A/G]GTTAACAAGCTGGAA | 57531 |
rs575591225 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104709282 | CTCCAAAAGAAGAGA[G/T]ATAAAATGGCCACTA | 57531 |
rs575602749 | in-del | -/TA | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104784852 | CTAGATCTAGATTAG[-/TA]TGAGTATCTTAAAAC | 57531 |
rs575616504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104744830 | ATGTTTCCACATTGA[C/T]ACAATTTCATTAAAA | 57531 |
rs575627418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800529 | AGAGGAAGGAACAGG[C/T]AGCAATATTTGCTGT | 57531 |
rs575646347 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691977 | AGGGAGGAAGGAAGG[A/G]AGGGAGGGAGGGAGG | 57531 |
rs575651877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104819555 | TTTAAAATTCATATG[A/G]AACCAAAAAAGAGCC | 57531 |
rs575658884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104818908 | AATAATATGAACCAT[C/T]TATGACAAACTCACA | 57531 |
rs575673723 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104855272 | ACAAGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 57531 |
rs575675671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104784237 | TAAGTGAAATGCAAA[C/T]TCAGATACACTGACA | 57531 |
rs575678440 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765053 | ACAAAGTGTTATATT[A/T]ATTCTTCACTGATCT | 57531 |
rs575686704 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104764307 | GGTCTGAAACTCCTG[A/C]CCTCAGGTGATCCAC | 57531 |
rs575704313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104717142 | GTTTTTTTGTGGTTT[A/G]TTTGTTTGTTTGTTG | 57531 |
rs575714402 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825481 | CTAACTGAAGGTAGT[C/T]ATGTGCAAGCAATCG | 57531 |
rs575740569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104752106 | AAACCCTGTGTGGCT[C/T]CTTTTATAATTTAAC | 57531 |
rs575793646 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104829574 | AAGCATTCCCTTTAT[A/G]TTTATATGATCATCA | 57531 |
rs575801008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104775913 | AAAGAATGTAAACAT[C/T]TGGGGAGAGAAAAGA | 57531 |
rs575804026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104840386 | AGGCTAATGTGCTTA[C/T]ACACCACAGGGCGGG | 57531 |
rs575832655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104788362 | ATAGTAACAATGATA[C/T]GCCAATCATACATGA | 57531 |
rs575836333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104761347 | TACTGGTACCAAAAC[A/G]ATATATAGAACAATG | 57531 |
rs575841564 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104768662 | GAAAGCTGAGAATGT[A/G]TAACATTAATAATCA | 57531 |
rs575849621 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104685262 | ACATCAGAAATTCTT[C/G]CCTCAACAATGTTCC | 57531 |
rs575870054 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104789379 | GAAATAGTAGTTGTC[A/C]ATGCTGTAGAAAGCA | 57531 |
rs575870283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104722652 | AGTTTACATCAAGCC[A/G]CCGCGCCAATGTTTC | 57531 |
rs575877850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104735729 | TCTAGAAGATAAATG[A/G]ATATATATCAAGATT | 57531 |
rs575886618 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104825529 | TCAAATGCACAGAAG[G/T]GCAACTTTGTAACTT | 57531 |
rs575985488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104807666 | AATATTGGTAGAAGT[C/T]ATATAAAAGACTTAA | 57531 |
rs575998264 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738713 | GACCTGAAAGTGATG[C/G]GGAGAATGGAACCAA | 57531 |
rs576006000 | in-del | -/AAAAT | 0.00318978 | 0.0398085 | intron-variant | HACE1 | GRCh38.p7 | 6:104840009 | AGACTCTGTCTCAAA[-/AAAAT]AAAATAAAATAAAAC | 57531 |
rs576030281 | in-del | -/ACC | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859351 | GCGGAACCCCCACCA[-/ACC]ACCCAGTTTCCTCCC | 57531 |
rs576050241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104833031 | CTTAAAGTCCTCATG[A/G]CTCAACTTACCGTCT | 57531 |
rs576051398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761720 | AATTAAACTAAAGAG[C/T]TTCTGTACAGCAAAA | 57531 |
rs576059345 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765339 | GAACACAGGCTTTTG[C/G]CTATCATGGCAAATT | 57531 |
rs576063651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806892 | CATCCTTATAAATTT[G/T]AGAATTTGGCATAAG | 57531 |
rs576078130 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767762 | CATGCTCTGTCACCT[A/C]TGTGCCTTCCTGTAA | 57531 |
rs576087777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850842 | ATATTGTGTGATAAT[A/G]CTGTTCAAAGCTTAC | 57531 |
rs576088184 | snp | A/C | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727926 | TCAAGCGATCTCGCA[A/C]CTAGCCTTCCAACCA | 57531 |
rs576092619 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104815936 | AAATTAGCCAGGCGT[C/G]GTGGCAGGGACCTGT | 57531 |
rs576119211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762135 | CCATTGTGGAAGACA[A/G]TGTGGCGATTCCTCA | 57531 |
rs576119731 | in-del | -/GA | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104812642 | GATAGCAAGCAAATG[-/GA]GAAATAGTAACTGAC | 57531 |
rs576120721 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104746562 | ATGGCTACCATCAGG[G/T]GGCCCCTCCTTGGTG | 57531 |
rs576121144 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691323 | GGTGAAAAACAAAAA[C/T]GTGATGACACATTAG | 57531 |
rs576132192 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720452 | ATTACACTCGGTATC[-/TG]TGGGGGATTGGTTCT | 57531 |
rs576132901 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104738092 | GGGTATTCCAACAGA[A/C]CTGCAGCTGAGGGTC | 57531 |
rs576142919 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855803 | TAAAAAACACTGTTA[C/T]TTGTGGGTTTAAACT | 57531 |
rs576159655 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857238 | ATATGTATGATATAC[C/T]TTAAAGAGCCAAGCT | 57531 |
rs576210947 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838899 | CATAGTAAAAAAAAA[-/A]AAAAAAAAAAAAAAA | 57531 |
rs576240706 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836920 | TATGCCAAAGAAAAT[C/G]AAACAGTTATATGCT | 57531 |
rs576241496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104713349 | AAGGGCAATGAAAGA[A/G]TAGATTGGCTCAAAG | 57531 |
rs576241522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851742 | AAACAAAAAAAAAAA[A/T]TTTTTTAACTTGTTT | 57531 |
rs576246400 | snp | G/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854649 | AGACAATTTTTGAGA[G/T]GAGGACAAACTGTAT | 57531 |
rs576252276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858464 | CCAACACTTTGGGGG[A/G]AGCAGGGTGCGGATC | 57531 |
rs576255537 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825408 | ACTTCACTTCAGCCT[C/G/T]GGATTGGTTGCACAC | 57531 |
rs576256142 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726699 | TTGGATAACTTAATC[A/T]ACTCTGCCCAGATAG | 57531 |
rs576265714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104719852 | AGAAATCAACTTTAC[C/T]TTTTTTTTTTTGACG | 57531 |
rs576275290 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762481 | GCATGTTCTCACTCA[-/C]AAGTGAGAGTTGAAC | 57531 |
rs576284532 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104822578 | ATAAAAAAAGTAGGC[C/T]GAGCGCGGTGGCTCA | 57531 |
rs576365823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104858068 | TGGTAACACTGTTTA[C/T]AACTGGATGGTGAAA | 57531 |
rs576365976 | snp | A/C | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104718703 | TTGCTGAACCATCAC[A/C]TACTTCTGAACTCAA | 57531 |
rs576374957 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | HACE1 | GRCh38.p7 | 6:104836397 | GGCAAGAAACAAATA[C/T]AAAAGACATACAAAC | 57531 |
rs576402842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783839 | GCCTTATAGAACTAA[A/G]GAGTTTCATTAAGCT | 57531 |
rs576441972 | snp | A/G | 4.9731e-05 | 0.00498629 | intron-variant | HACE1 | GRCh38.p7 | 6:104843313 | CCTGAAAAGAAAAAA[A/G]AGTCATGGATAACTG | 57531 |
rs576443982 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734614 | GTGAAGCTAGCTCCG[C/T]GTTGTTTCCCCTCAG | 57531 |
rs576446624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104830295 | TCTTTTTTTCCCACA[C/T]AGAATACGTTTTAAA | 57531 |
rs576454519 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104705021 | GAGAGATTTTTATAC[A/G]TTTATTGGCATTCTC | 57531 |
rs576467205 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104806798 | ACAAAAATTTAACTA[A/G]TAAGAAACTTGTGGT | 57531 |
rs576469548 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802597 | ATGGAAACTGAACAA[C/T]CTGCTCCTGAATGAC | 57531 |
rs576499649 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104791733 | TAAAACATTTTCATC[A/C]CACTGACCATCTGTT | 57531 |
rs576535412 | in-del | -/GG | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104737570 | AAAGGGGTGACAGAC[-/GG]GGCACCTAGAAAATC | 57531 |
rs576547903 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104689384 | TTCATTCTCTGTTCA[A/C]TCTAAACTTATAATT | 57531 |
rs576551590 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818678 | ACATCAAAAAGCTCA[C/T]ACACCATAATCAAGT | 57531 |
rs576558412 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104711498 | AACTCTTGACATAGC[A/G]TGTCACAAGTACTTA | 57531 |
rs576570173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104696519 | CCTCCTTGAAAAGCT[C/T]CTTCTGCAGAAGAGG | 57531 |
rs576570563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104704549 | CCTGGGAGGAATGGC[A/G]GCAAAAGAGAATGAC | 57531 |
rs576587607 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104840734 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACCTGA | 57531 |
rs576591225 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104754680 | AATTTCATATCTGGA[C/T]AAACTAAGCTTTATA | 57531 |
rs576594541 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104774417 | TTGAGACGGAGTCTC[A/G]CCCTGTCACCAGGCT | 57531 |
rs576596471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104783561 | AAGTTCACATAGCTG[A/G]TAAGGAGCAAAACAA | 57531 |
rs576628034 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104821022 | CATAAAAAAGAACGT[A/G]ACAATGTCCTTTTCA | 57531 |
rs576634090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104775152 | TTTGAGGCCAGCCTC[A/G]GCAGCATGGCGAAAC | 57531 |
rs576647020 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104812354 | AGGAGGCTGAGGTGG[C/G]AGGATCATTTGAGCC | 57531 |
rs576668653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760208 | TTTTATGAGGCCAAC[A/G]TCATCCTGATACCAA | 57531 |
rs576673443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104813218 | TTCATCCAGACATGG[C/T]GGCTCATGCCTGTAA | 57531 |
rs576696089 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | HACE1 | GRCh38.p7 | 6:104760572 | AGCTATTTATGACAA[A/C]CCCACAGCCAATATC | 57531 |
rs576709210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104710947 | TCTTCTGTTAAATTC[C/T]CGAGTCCATTCAGAA | 57531 |
rs576741813 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104799242 | TCACTATACTTTTGA[G/T]TTCCTCTGTAACAAA | 57531 |
rs576780887 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104713263 | CTAGGTGTTATTTGA[C/G]AATGACCTCCTCTTA | 57531 |
rs576827337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104821996 | GAGGAGTGCTTGAGG[C/T]CAGGAGTTCAAGACC | 57531 |
rs576856974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104767651 | TCTTTCAGAATTTGG[C/T]CACTTTCTCCCTTCC | 57531 |
rs576866520 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791577 | CTGGGGGAGGATGGA[C/T]CAATTCGAAAGACGT | 57531 |
rs576871536 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789000 | TTAATGAAATGGAAA[G/T]TAGGGATCAATTGCT | 57531 |
rs576872612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104822526 | CCACTACGCTCCGGC[C/T]GGTTCAACAGAGTGA | 57531 |
rs576872974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858661 | AGAGAGTTTTGAAAA[A/G]GTAAGATAAACTACT | 57531 |
rs576878190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760382 | TCCCTGGGATGCAAG[A/G]CTGGTTCAACATACA | 57531 |
rs576894139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104761071 | AACAAATGGAAAAAC[A/G]TTCCATGCTTATGGA | 57531 |
rs576909596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859194 | TATCTTTGGATCATC[A/T]CTATCCCCAGCTACT | 57531 |
rs576912143 | in-del | -/AATGGA | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104748404 | CTACTGAATTACCAG[-/AATGGA]AATGAAAAAGATGGA | 57531 |
rs576921112 | snp | A/G/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859891 | GCAGCCCCCGCCGCC[A/G/T]CGTCCCTCCCGGGCT | 57531 |
rs576922704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104753862 | CTCCTCCAAATGACC[A/G]CAACACCTCTCCAGC | 57531 |
rs576940340 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104829344 | ACATGCAACTCAAGA[C/T]AAAACAATACACTTA | 57531 |
rs576946824 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765010 | TCCACAATTACAATT[C/T]TGTTCACTGATGCTA | 57531 |
rs576947195 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737481 | TGTGCGCACCGTGCG[C/T]GAGCCGAAGCAGGGC | 57531 |
rs576947312 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104755746 | ATGAGAACAAAGAGA[A/C]AATGTACCAGAATCT | 57531 |
rs577009619 | in-del | -/ATATATATGTATATGAATATATACACACAT | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727719 | TGAATATATACACAC[lengthTooLong]ATATATGTATATGAA | 57531 |
rs577012585 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721887 | TGGACAAGGGTAATA[A/G]AAGTTGGCTAATTTA | 57531 |
rs577038151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104760142 | GAGCTGGTACCATTC[C/T]TTCTGAAACTATTCC | 57531 |
rs577049886 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104738045 | ACTGGGAGGCACCCC[C/G]CAGCAGGGGCACACT | 57531 |
rs577071012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104725938 | GGTGTGGTGACATAA[C/T]CCCAGCACTTTGGGG | 57531 |
rs577100646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104730941 | TTTGTTTTTTATAGT[A/G]GAAAAACTGAAAAAT | 57531 |
rs577108851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104828164 | TTATGGTCCAAAAAG[C/T]GTTAATAAATTATAC | 57531 |
rs577116405 | snp | C/T | 0 | 0 | intron-variant | HACE1 | GRCh38.p7 | 6:104799180 | ACGGTGACACTGTTA[C/T]AAGCATTGTTAAATT | 57531 |
rs577125848 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768667 | CTGAGAATGTATAAC[A/G]TTAATAATCAAGACC | 57531 |
rs577131258 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795845 | AATATAGAGATATGA[A/T]GATACATAATAAAAT | 57531 |
rs577159693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104835331 | GCAAAAAGTAGGGGG[A/C]AAAAGGAACCATGAA | 57531 |
rs577187932 | snp | C/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860221 | GTGCCTTTGTTTCAG[C/G]TACCCTACATGAACT | 57531 |
rs577232604 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104740457 | AATCAAATAGATGCA[A/C]TAAAAAATGATAAAG | 57531 |
rs577249140 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104836243 | CAGAAGTCTCCGTAA[C/G]AGACTCCTTCAAGAC | 57531 |
rs577262627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104849499 | TGAGCCACCACAATT[A/G]GGTAATTTTTTTTTT | 57531 |
rs577277380 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726515 | CCAACTTGTGAGCTA[C/T]CCTTTAAAGCTTGCG | 57531 |
rs577282694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104798471 | TATTATAGGTCTATC[A/G]CTCTCTTGATACTTT | 57531 |
rs577296670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104850014 | GAAAGCAGTGGCACA[A/G]TCTTGGCTCACTGCA | 57531 |
rs577303423 | in-del | -/TTG | 0.00215827 | 0.0327792 | intron-variant | HACE1 | GRCh38.p7 | 6:104832384 | TTTTCCTGTTTTTTG[-/TTG]TTGTTGTTGTTGTTG | 57531 |
rs577314120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104750561 | TATTTAAGAGGTAAA[A/G]GTTTAAAATAAAATT | 57531 |
rs577324530 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104843087 | CCTCACTCTAGCCTG[A/G]GTGACAGAGCGAGAC | 57531 |
rs577326327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104751031 | TCTCTAAGGCCCTAA[A/G]TGATCTGGCCTCTGC | 57531 |
rs577374624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104857542 | AGAGGCAGACTATGT[A/C]TTAAATACAAAGCTG | 57531 |
rs577379967 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860514 | ATTTGGTACAATGCT[A/G]AAGTGTCTATGTGAT | 57531 |
rs577415878 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853618 | TTTACACAGTATCAA[A/G]TACCTCTCAAAAATA | 57531 |
rs577419605 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861654 | GTGAGGACCAAGCCT[A/G]GAGTTTGTGGGCAGG | 57531 |
rs577428804 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104805066 | TGAACAGACACTTCT[C/G]AAAAGAAGACAATTA | 57531 |
rs577442520 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | HACE1 | GRCh38.p7 | 6:104826734 | TAATTTTAAGAGCTA[C/T]GCTACATTTATACAT | 57531 |
rs577446213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854297 | ATCCTGAATTGGATC[C/T]GTAAATGACATTAGT | 57531 |
rs577456975 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104773250 | AAACAACGGATAAAC[C/G]TAATGAAATAGCATC | 57531 |
rs577458114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104765337 | GAGAACACAGGCTTT[C/T]GCCTATCATGGCAAA | 57531 |
rs577472302 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798621 | CTTTACCGGCATCAA[A/G]CAAGAAGTCCTCATC | 57531 |
rs577479633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104820339 | AGTAAAAATTGGAAG[C/T]TGGGATCTAATTAAA | 57531 |
rs577495123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104766109 | AGCAAAAGAAAAGAA[A/C]AGACATGAGTAATGC | 57531 |
rs577499058 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104717383 | ACCTCAGGTGATCCA[C/T]CTTCTTCGGCCTCCC | 57531 |
rs577525195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104795929 | AAAATCACCAAGTAT[A/G]GTTTTGGAAATTTAA | 57531 |
rs577539051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104804267 | ATAGGAAGAATCAAT[A/G]TCGTGAAAATGGCCA | 57531 |
rs577618483 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702353 | GCATCCAAGCTTCCT[A/G]TGGGATCAAAAGGAA | 57531 |
rs577634247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104708097 | GCAAGAAAAATAAAT[A/G]AGACATTCATATTGG | 57531 |
rs577634720 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104721362 | CAAAAGGGGAGGAGA[A/G]GGGAGTGATGGTGGG | 57531 |
rs577652916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104846269 | AAAATATTATGTAAC[A/G]CATGGGCCCTACCCT | 57531 |
rs577673338 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104742005 | CCTCAGAAATAACGC[C/T]ACGTATCTACAACTA | 57531 |
rs577681235 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725307 | AGAAAATAACATAGG[C/T]ATATGATTTGGAGAA | 57531 |
rs577687395 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104794901 | CGAGACTCTGTCTCA[A/T]AAAAAAAAAAATAAT | 57531 |
rs577693075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104691996 | GAGGGAGGGAGGGAA[A/G]GAGGAAGAGCAGGAG | 57531 |
rs577694050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104847126 | ACATGAAAATTCTTT[G/T]CAGCAGACCAAGAAC | 57531 |
rs577733919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104805166 | TGAGATACCATCTCA[C/T]GCCAGTTAGAATGGC | 57531 |
rs577754948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104692698 | GGGACAAATAAGACA[A/G]GGGTTTCTTTTGAGG | 57531 |
rs577777246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104707477 | ATCTAACAAAGTCCA[A/G]CAACCCTTCTGGATA | 57531 |
rs577779993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104699862 | ACATCAGGCCTCCCT[C/T]GGCTGAGGCAGGCCT | 57531 |
rs577782504 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | HACE1 | GRCh38.p7 | 6:104705488 | AAAAGATCAAAAGGG[A/G]TATTCTATCTCTAGC | 57531 |
rs577820092 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724993 | GAGCTAAAAACAGTG[C/G]TAATTATCAGGCAAC | 57531 |
rs577825414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104816296 | TCAGAGGCCTGGAGG[C/T]CTAGGAGGGGAAAAT | 57531 |
rs577834503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104823525 | TTAAAAAAAACAGCC[C/T]GATGAAGATCCTCAA | 57531 |
rs577837223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104802362 | CAGCTCTGGACCAAG[C/T]GGACCTAATAGACAT | 57531 |
rs577839569 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803120 | AAAATCCAGAAGAAA[C/T]GAATAAATTGGACTA | 57531 |
rs577854001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104762491 | ACTCACAAGTGAGAG[C/T]TGAACAATGAGAAAC | 57531 |
rs577888892 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733950 | TTGAGGTCAGGAGAT[C/T]GAGACCAGCCTGGCC | 57531 |
rs577893010 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | HACE1 | GRCh38.p7 | 6:104714008 | CCTGCCCAAGCCGGG[G/T]AGTCTAATAAGAGAC | 57531 |
rs577899469 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | HACE1 | GRCh38.p7 | 6:104762900 | GAGGCTGAGGCAGGA[A/G]AATGGTGTGAACCTG | 57531 |
rs577991994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104770065 | ACAGAAAACTGAGTT[C/T]GAAGAATTGTTAAAC | 57531 |
rs578052085 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778171 | GAAGAATAAGATCTC[C/T]TGAATAGCAAAGAGA | 57531 |
rs578072762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104778112 | ATACATGCAGAAATT[A/G]GAACGTAATTTGTTA | 57531 |
rs578080842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104793148 | GGCAGGCCCATGTAG[C/T]CCCAGCTACTTGGGA | 57531 |
rs578085842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104734315 | ATTGGAACACGTTTG[A/G]TTTTTCAGTAAGGTT | 57531 |
rs578088387 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104739586 | GGCCATTACATAATG[A/G]TAAAGGGATCAATTC | 57531 |
rs578091002 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755349 | GGCTTTAACAGCCCA[C/T]TAACAATATTAGACA | 57531 |
rs578093022 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687758 | AGGCATTTTGGGACC[C/T]AGCCTAGATTATAGG | 57531 |
rs578127822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104785610 | CAATCTTTCTTCTTT[C/T]AATTTTCAAATGTTT | 57531 |
rs578139076 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712588 | ACCAGCCTGGCCAAG[A/G]TGGTGAAATCCTGTC | 57531 |
rs578139994 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753468 | CAGGGGTCTCCAGCC[A/T]CCTCTTATAGGTGCA | 57531 |
rs578153391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | HACE1 | GRCh38.p7 | 6:104793622 | TATTTGAATCAGTTA[C/T]TTTCTTAATGAAAAT | 57531 |
rs578197730 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840222 | AAGACAATCATTAAC[C/T]ACAGGGAAAATAAAA | 57531 |
rs578204826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104800460 | AGGAGACACCTCCTA[A/G]TAGGGGCAACAGACA | 57531 |
rs578228105 | in-del | -/TATG | 0.00438332 | 0.0466095 | intron-variant | HACE1 | GRCh38.p7 | 6:104725240 | GTGGATGTTTATATA[-/TATG]TATGTGTATATACAT | 57531 |
rs578252234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | HACE1 | GRCh38.p7 | 6:104748680 | CCCACTAAATGTTCA[C/T]CAAGAGTAGAAAAGA | 57531 |
rs745324844 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792114 | TCTGCCACTATATCC[A/G]TAATCCCATATCCCC | 57531 |
rs745327770 | snp | C/G | 1.65075e-05 | 0.00287289 | intron-variant | HACE1 | GRCh38.p7 | 6:104776703 | GTGTGAAAAATGTGA[C/G]AAGTTGCAGAAAAAG | 57531 |
rs745334971 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756070 | TGAGAAGAATGAAGT[A/G]AACACAATCAGAAAT | 57531 |
rs745380035 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775764 | AGGGATGAATGCCTG[A/C]AGCTGCCTAGCTCTA | 57531 |
rs745380889 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772014 | ATCTGCCCAGCAAAC[C/T]GAAAATAGTTCAAGT | 57531 |
rs745392895 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793400 | TTTCTCTGTTCATTT[A/C]CACATTGTTAACTAC | 57531 |
rs745394044 | in-del | -/C | 4.95978e-05 | 0.0049796 | frameshift-variant, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730377 | TGCAATCCACTTCCA[-/C]CCCATGATATTAGCA | 57531 |
rs745437083 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689363 | CCAAAAATGAATCAA[C/T]CATGATTCATTCTCT | 57531 |
rs745485507 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833266 | CAGCTGGGCGTGATT[C/T]GCACATGCAAATCTA | 57531 |
rs745497754 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688381 | CACACACACACACAC[-/AT]GTGTACACCTACAGA | 57531 |
rs745499861 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757381 | TGTTCTGCAGCCTCC[A/G]CTGGTGATACCCAGG | 57531 |
rs745513860 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785854 | AGAATCCCTAAAGAA[C/G]CTAATGAACAGCTTT | 57531 |
rs745515108 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785380 | GGATTAAAAAAAAAA[A/C]AACAAAACACAACTA | 57531 |
rs745535026 | snp | C/T | 9.98461e-05 | 0.00706492 | intron-variant | HACE1 | GRCh38.p7 | 6:104771914 | CTGCAGAAATAATAA[C/T]AGAGCCATACCAAGA | 57531 |
rs745543093 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716759 | TCAACTAATTTTAAA[G/T]GATTGATATCATACA | 57531 |
rs745560442 | snp | A/T | 1.66327e-05 | 0.00288376 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785312 | GAGTGCCAAAGCAAT[A/T]CCAGAGGCTGAGAGA | 57531 |
rs745570489 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852925 | TAGTTTAGAAGCTTT[C/T]ATGAAAGAGCACTGA | 57531 |
rs745586151 | snp | C/T | 1.65603e-05 | 0.00287747 | intron-variant | HACE1 | GRCh38.p7 | 6:104843209 | AAACATCAGATGAAA[C/T]TGATAGCACTTACTG | 57531 |
rs745588308 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817694 | ATATAGATGAAGAAA[C/T]GCTGATTCATACAAA | 57531 |
rs745607210 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782929 | GCAAATTATTTTCTA[A/T]AACTTTGCCAGAATT | 57531 |
rs745619932 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822964 | TAACATACTCCTCTA[A/C]TGTTCTCATCAAACT | 57531 |
rs745635265 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840151 | CAGGGCAACTCTCTC[C/T]CTCTATTATTTCTTA | 57531 |
rs745676350 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766617 | CTAGCAATAAAACCA[A/T]ATTAAAATGAAATCG | 57531 |
rs745677925 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, missense, synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833053 | TTACCGTCTTGTGAC[C/T]GTTCTGGCAGGCAAC | 57531 |
rs745688269 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795524 | TAAACTACTCAGGAG[A/G]TGAAGCCAACAGACA | 57531 |
rs745694980 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765717 | TGCTTGTTTATGATC[A/G]GCATACCATTAAGTG | 57531 |
rs745729363 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729073 | CATATATAAATTATA[A/T]GTCATTTCATCAACT | 57531 |
rs745780688 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714985 | GGAAGCACAGGGACG[C/T]TGTCATCCCTGGGGC | 57531 |
rs745781309 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824392 | ATTTAACAACGGAGT[G/T]TCAAGACTCCACATA | 57531 |
rs745782118 | snp | A/C | 0.000195867 | 0.0098942 | intron-variant | HACE1 | GRCh38.p7 | 6:104780305 | ACACACATACAAACA[A/C]CTACACAGCCAAATG | 57531 |
rs745785582 | snp | C/T | | | nc-transcript-variant, downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682673 | TTCTACTTGCCTGCC[C/T]TGTCGTCTCAGCTGA | 57531 |
rs745787717 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744206 | TCTCCTCTTGAGTAA[C/T]GTCTTCTACAACTTC | 57531 |
rs745815621 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702506 | GGACCTTTTTCCAAC[C/T]GACAAGCAGACAACT | 57531 |
rs745862119 | snp | C/T | 1.65149e-05 | 0.00287353 | intron-variant | HACE1 | GRCh38.p7 | 6:104777182 | TGTGCTTCACACATA[C/T]ATCAGTTTCTTTGTT | 57531 |
rs745874740 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754906 | ATAACCAGCTAGCAT[C/T]GTCATGACAGGATCA | 57531 |
rs745884235 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819398 | AGAGATGACACAAAC[A/C]AATGGAAAAACATCC | 57531 |
rs745901938 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849160 | TTTCTTGCTGCCAAA[C/T]GAAGGGGTGTACAGC | 57531 |
rs745926307 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719608 | TTATATGTGTGTAGG[A/T]CTCATTTCTTAAAGA | 57531 |
rs745974644 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760020 | GTTGAATCTCTGAAT[A/C]TATCAATAAGAGGTT | 57531 |
rs745986353 | in-del | -/CG | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727617 | ATGAATACACACACA[-/CG]CGTATGTATATGAAT | 57531 |
rs745990731 | snp | A/T | 3.29576e-05 | 0.00405928 | intron-variant | HACE1 | GRCh38.p7 | 6:104850856 | TGCTGTTCAAAGCTT[A/T]CTGATCCTTGCCCTA | 57531 |
rs745998629 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706749 | CTGTATTAAAGCAAA[A/C]TCTACACATAAAAGT | 57531 |
rs746016595 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747361 | CTTCTGTCTACAATG[C/G]ATGACTACACCTCCA | 57531 |
rs746018759 | snp | C/T | 1.64765e-05 | 0.00287019 | missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849203 | GATAGTTAGGATTTG[C/T]TCCTTTCTTTAACAG | 57531 |
rs746071135 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798043 | ACTGCACTCCAGCCT[C/G]GGTAACAAGAGCAAA | 57531 |
rs746080042 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695929 | AGAGACGGGGTTCCA[C/T]CATGTTAGCAAGGAT | 57531 |
rs746105971 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821719 | TTAAAACCCAAGTCC[A/G]TGTTCATAATCACTA | 57531 |
rs746113041 | snp | A/T | 0.000117779 | 0.00767304 | intron-variant | HACE1 | GRCh38.p7 | 6:104784956 | CATCTATCAGAGAAA[A/T]AAAAAATAATAAGCC | 57531 |
rs746115683 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856042 | TGGTGCTAGAAGAAG[A/C]CTATCCAAGAAATAC | 57531 |
rs746140662 | in-del | -/G | 1.70243e-05 | 0.00291751 | intron-variant | HACE1 | GRCh38.p7 | 6:104796899 | CTATTATAAAGATAA[-/G]GGGGCTCAGAATATA | 57531 |
rs746163527 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799393 | TGATTTCTCTACTTT[C/G]CTTCCATATTCAGCC | 57531 |
rs746190172 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764801 | TTTTGCATATGTAAG[A/G]CAGTCAAACATCATT | 57531 |
rs746260547 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732493 | CGAAGTTCTTAGAGT[A/G]GTCAAATTCGTAGAC | 57531 |
rs746263100 | snp | G/T | 6.61693e-05 | 0.00575155 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784440 | AAAGCATTTTAAAAC[G/T]TCATCATGTTTGCAG | 57531 |
rs746316020 | snp | C/T | 9.81672e-05 | 0.00700528 | intron-variant | HACE1 | GRCh38.p7 | 6:104796798 | GGTTTAAAAACAGTC[C/T]CTTTTAAAGTTCATA | 57531 |
rs746337300 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686183 | AGATGAATTTCTTAA[C/T]AAAAATTCAATTTGT | 57531 |
rs746369953 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845682 | AGGGGTTTCACCGTG[C/T]TAGCCAGGATGGTCT | 57531 |
rs746382977 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804768 | CCCTAGAAGAAAACC[C/T]AGGCAGTACCATTCA | 57531 |
rs746388579 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793904 | GATTCTATAAAGCAC[-/T]TGGAAGGTAGCACCA | 57531 |
rs746397616 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775309 | GGGTCCCTTGAGCCC[A/G]GGAGGTCAAGGCTGC | 57531 |
rs746414393 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687629 | AAAAGGCTTCTCTCT[C/T]GAAGGCCTTTCCCAC | 57531 |
rs746424315 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707968 | TAATGATGAAAGACT[A/G]AATGCTTTCCCCATA | 57531 |
rs746431171 | snp | A/C | 6.33092e-05 | 0.00562588 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859557 | AGCCTGGCCCCGCGA[A/C]CCGGCTCACCCTCGG | 57531 |
rs746445508 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838890 | AAACAACTCCATAGT[-/A]AAAAAAAAAAAAAAA | 57531 |
rs746452761 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789941 | AGAGTAGGTCAATAA[C/T]GTAGATCAAAATTTT | 57531 |
rs746465158 | in-del | -/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851381 | CCACCCCACCCGGCC[-/T]TAGCTATTCTTCTGA | 57531 |
rs746466974 | snp | C/T | 1.65195e-05 | 0.00287393 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730362 | AGCGATTGTAAAGTT[C/T]TGCAATCCACTTCCA | 57531 |
rs746470794 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834930 | CAGATAGAATGCAAG[A/G]GGCTTGAAAACAGTC | 57531 |
rs746472051 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795590 | TTACCTAAGCAGTTT[A/G]TGACCATTTGTTGTA | 57531 |
rs746481211 | in-del | -/GTGTGTGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693025 | TGTCCAAAGAGTGGT[-/GTGTGTGT]GTGTGTGTGTGTGTG | 57531 |
rs746500975 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744722 | TGTAAAACTGATATA[C/T]TTTTGTGACAGTTCC | 57531 |
rs746521977 | snp | C/T | 3.67884e-05 | 0.00428869 | intron-variant | HACE1 | GRCh38.p7 | 6:104729786 | AAGAAAAATATACCA[C/T]CATTAAACAGGAAAT | 57531 |
rs746545869 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724178 | GGAGACTGGAGGTTG[C/G]CAATGATTAAAATAA | 57531 |
rs746555932 | snp | C/T | 1.71073e-05 | 0.00292461 | intron-variant | HACE1 | GRCh38.p7 | 6:104796891 | TTCCAGTTTCTATTA[C/T]AAAGATAAGGGGCTC | 57531 |
rs746616581 | snp | C/T | 0.000515951 | 0.0160533 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104859610 | GCGCAGCGAGCGCGT[C/T]AGGCGGTTGAGTTGC | 57531 |
rs746642855 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836670 | GTGAGCTGAGATTGC[A/G]CCACTGCACTGTAGC | 57531 |
rs746644802 | snp | A/G | 3.29973e-05 | 0.00406172 | intron-variant | HACE1 | GRCh38.p7 | 6:104776735 | CATCTAGACTGTACA[A/G]CTTACCATCAGCTGA | 57531 |
rs746672319 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808273 | AAATGAGGACAACAC[A/G]ACTTTATGCTCACTG | 57531 |
rs746674095 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712287 | TTCAGGTTTTAAGGT[A/C]TTTCCAATGCTTTAA | 57531 |
rs746709280 | in-del | -/AAAAAAAAAAAAAGGGGGAAAAAAAAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726191 | AGAGTTAAAAAAAAA[-/AAAAAAAAAAAAAGGGGGAAAAAAAAAA]AAAAAAAAAAAAAAG | 57531 |
rs746715484 | in-del | -/AAAA | 2.3758e-05 | 0.00344651 | intron-variant | HACE1 | GRCh38.p7 | 6:104784953 | CATCATCTATCAGAG[-/AAAA]AAAAAATAATAAGCC | 57531 |
rs746716752 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791536 | TTGGAGTTTTATTCC[C/G]ATTGTAGCCCATATC | 57531 |
rs746716845 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712024 | CAAGTGATCCTCCTG[C/T]CTCATCCTCCCAAAA | 57531 |
rs746738255 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821482 | AAAGAAATTTTAACA[A/T]AATATACTATTTATA | 57531 |
rs746740833 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717876 | GCCTATCGAGTTTCC[-/TG]TCTTTCTTATCACTA | 57531 |
rs746777314 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767547 | GTTTTCTTAACTGAA[A/G]TTTGATCATGTCATT | 57531 |
rs746779830 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826128 | TGTGAGAATCTAATG[C/T]CTGATGATCTGAAGT | 57531 |
rs746792618 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730733 | TCTATTGAAGTGGGG[C/T]TGATTTGAGGGCCCA | 57531 |
rs746805628 | snp | A/G | 1.70003e-05 | 0.00291545 | intron-variant | HACE1 | GRCh38.p7 | 6:104785384 | TAAAAAAAAAAAAAC[A/G]AAACACAACTAGACA | 57531 |
rs746832923 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768749 | GCAATTAAACAAAAT[A/G]TAAATATATATAGTA | 57531 |
rs746837321 | in-del | -/ATCTAGTATTTGATAGCAC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694435 | GAAAGAATAAAAAAG[-/ATCTAGTATTTGATAGCAC]AACAGGGTGACAATA | 57531 |
rs746843492 | snp | A/G | 1.64923e-05 | 0.00287156 | intron-variant | HACE1 | GRCh38.p7 | 6:104849137 | TAAGAAAACTAAATA[A/G]TTACCCATTTCTTGC | 57531 |
rs746858787 | snp | C/T | 1.65512e-05 | 0.00287669 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104843268 | GACATCAGCGCTATA[C/T]TCTAATAATTTACTC | 57531 |
rs746859981 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716392 | TGAAACAGTAATTTA[C/T]AAAAATTGAACACAT | 57531 |
rs746897669 | snp | A/C | 2.16265e-05 | 0.00328828 | intron-variant | HACE1 | GRCh38.p7 | 6:104744657 | TTTCTTTAGGGAAAA[A/C]AGTTATTATATTTAA | 57531 |
rs746911075 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704023 | GAGGCACAAGAATCA[A/C]TTGAACCTGGGAGGC | 57531 |
rs746915238 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835082 | ACTGTTAACATCTTC[C/T]GGGCAGTTGGAAGAG | 57531 |
rs746921953 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705144 | CATATTTACACATCC[A/T]GTTGTGCCAGCTCTA | 57531 |
rs746938746 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764782 | AACTCTGAAGGTATA[-/T]TTTTTTTGCATATGT | 57531 |
rs746943753 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810395 | TCAACCTAAAACCAA[C/T]TTCCAATAAAATGAT | 57531 |
rs747027193 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817286 | GGAAGAGAGGTCTGG[A/G]GGGAGGTGACTGGAT | 57531 |
rs747039144 | in-del | -/GC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696165 | CCCATGGTGGGGGCG[-/GC]GGGGGGGGGGTTGTA | 57531 |
rs747081619 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800930 | CTCCGAGCTAAAGGA[A/G]GATGTTCTAACCCAT | 57531 |
rs747084941 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760766 | CAAATTGTCCCTGTT[G/T]GCAGATGGCATGATT | 57531 |
rs747094541 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707707 | CCTCAAATGGTAGAA[C/G]GTAGAAGGGCAAAAA | 57531 |
rs747137022 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856224 | CACTACAGTTTCAAA[A/G]CCCAACTGTTAACAA | 57531 |
rs747163701 | snp | C/T | 1.68766e-05 | 0.00290483 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852270 | AGTACACATTTAGAA[C/T]AATGTATGCTTCTTA | 57531 |
rs747173672 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697162 | ATCTATTCCCAATCA[C/T]GTTTTCTTGCTTATT | 57531 |
rs747217216 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849951 | CACCACGCCCGTCCT[-/T]TTTTTTTTTTTTTTT | 57531 |
rs747228166 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819100 | AAAAGAAGTCAAACT[A/G]TCCCTGTTTGCAGAT | 57531 |
rs747229773 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720616 | TTCCCGGGCAGCCAC[C/G]CTCTTCCCCGCCCCC | 57531 |
rs747231078 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840339 | CAAAAATGATCTAAC[C/T]AAAATTACAATAATT | 57531 |
rs747231465 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104858137 | TTCTACAATGAAACT[A/G]TATTACTTTTAAAAC | 57531 |
rs747290122 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847345 | ATACCCTATCAACAC[A/G]TGGAATAATGTACCT | 57531 |
rs747290599 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | HACE1 | GRCh38.p7 | 6:104850891 | AGAGTTTAACTCAAA[A/G]TATCTTTAGTCTTAC | 57531 |
rs747294147 | snp | C/T | 4.94319e-05 | 0.00497127 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771262 | TTCCATTGCTCCAAA[C/T]ACATCAGTCTCAACA | 57531 |
rs747313886 | in-del | -/A | 1.66424e-05 | 0.0028846 | intron-variant | HACE1 | GRCh38.p7 | 6:104771914 | TGCAGAAATAATAAT[-/A]AGAGCCATACCAAGA | 57531 |
rs747325760 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830510 | TGTCACCTTTGCCTA[C/T]TATCTTGAAGAAGTC | 57531 |
rs747380117 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734827 | CCACCTAAGAGACAA[C/T]TTAGTACTAAAAAAC | 57531 |
rs747382683 | snp | A/G | | | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791552 | ATTGTAGCCCATATC[A/G]ATTCCATTACTGGGG | 57531 |
rs747389143 | snp | A/G | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785131 | AGATTCCCTTGTGCC[A/G]GTGGACAGATTTTCA | 57531 |
rs747411958 | snp | A/T | 1.72095e-05 | 0.00293333 | intron-variant | HACE1 | GRCh38.p7 | 6:104750486 | GCCTGTTGAAAAAGA[A/T]GTTTTCATGATGACT | 57531 |
rs747444450 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687733 | TCAAAATGCTGAAGA[C/T]CAGAGCTGCAGGCAT | 57531 |
rs747462598 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794246 | ATAAGTGATGAAGGT[-/A]AAACTTAAAAACATA | 57531 |
rs747514346 | snp | A/G | 3.39046e-05 | 0.00411718 | intron-variant | HACE1 | GRCh38.p7 | 6:104811274 | TATATATATATATAT[A/G]AGCATATATAGCATC | 57531 |
rs747531125 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760098 | GGACCAGTGGATTCA[C/T]AGCCAAATTCTACCA | 57531 |
rs747573498 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816356 | TGCTCTGTGCAGCTT[C/T]GGGACTTAGTGCTCT | 57531 |
rs747615801 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785382 | TTAAAAAAAAAAAAA[-/C]CAAAACACAACTAGA | 57531 |
rs747635027 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781375 | TAAGATGTTGCAGGC[A/T]TATTTTATACTTTCC | 57531 |
rs747638788 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763821 | TTGGGAGGCCGAGGT[G/T]GGCAGATCACTTGGG | 57531 |
rs747657119 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838373 | ACACACAGACCAATG[C/G]GACAGAACAGAGAAC | 57531 |
rs747685719 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859093 | CCTTTGTTTGCCTGT[C/T]ATCAAAACAAGGCAG | 57531 |
rs747691758 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765007 | CCTTCCACAATTACA[A/G]TTCTGTTCACTGATG | 57531 |
rs747700715 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727030 | TGAAAAAATAAATCC[C/T]AAAATAAGCAGATCT | 57531 |
rs747732687 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736355 | AGTGGTGCAATCTCG[A/G]CTCACTGCAATCTCC | 57531 |
rs747770803 | snp | A/G | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796994 | TGGCTCCTCGTAATA[A/G]TAGGATCTGTGCTGT | 57531 |
rs747780778 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805700 | CACACACCAGGGCTT[C/G]TCGGGAAGTCAGGGG | 57531 |
rs747781162 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753231 | CTAAGGACAGCGCTT[G/T]GGTATCTCACTGGGA | 57531 |
rs747815905 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822583 | AAAAGTAGGCCGAGC[A/G]CGGTGGCTCACACCT | 57531 |
rs747820866 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834599 | CCACGGAAATGAGAG[G/T]AAAGAGTATTTCCTT | 57531 |
rs747822285 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734189 | GTCTGATTCTTAAGG[A/G]ATAATGAAACAGTAA | 57531 |
rs747825941 | snp | C/T | 1.65822e-05 | 0.00287938 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730396 | ATGATATTAGCAAAC[C/T]CACCATGTGGGACCC | 57531 |
rs747852839 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701352 | ATCATCATAAAATTA[A/C]GGTAGATGTCTGTGA | 57531 |
rs747854934 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719520 | AAGTGTTCTTACCAC[-/A]AAAAAATAAAAATAA | 57531 |
rs747873295 | snp | G/T | 1.69931e-05 | 0.00291483 | intron-variant | HACE1 | GRCh38.p7 | 6:104776967 | AAAGGCATTTCAATC[G/T]TTCTTTACATACAGT | 57531 |
rs747876459 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807431 | TTAGCCCTTTCTGTC[C/T]CTAGTAGAGACCTCT | 57531 |
rs747889125 | in-del | -/A | 1.68755e-05 | 0.00290473 | intron-variant | HACE1 | GRCh38.p7 | 6:104744474 | ACAAAATTAAACGGC[-/A]AAACTTAACTTCATT | 57531 |
rs747905449 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815608 | TCTCAAGTGATCCAC[C/T]CACCTTGGCCTCCTA | 57531 |
rs747909897 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811812 | TATTGCTTTAGATAC[A/T]TGAATTTAAATTGCT | 57531 |
rs747918832 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776778 | TGCATAATCAGGATT[A/G]ACTATCTCATTGGAC | 57531 |
rs747926697 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717414 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCA | 57531 |
rs747957746 | snp | A/C/G | 5.00015e-05 | 0.00499987 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791651 | ATCATAATTGCTAGA[A/C/G]AGGCTGAAAATAAAA | 57531 |
rs747981334 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745160 | GGAATAATTTGGATC[C/G]TGTAAAGTCAATTTT | 57531 |
rs747983679 | in-del | -/AC/C | 0.00722274 | 0.0596591 | intron-variant | HACE1 | GRCh38.p7 | 6:104771882 | AAACTGAAAAAAAAA[-/AC/C]CAATATAAATAAATG | 57531 |
rs747990032 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796009 | AGACTAAAACTATCA[C/T]AAACACATAGCTGAG | 57531 |
rs747996468 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717435 | TGAGCCACCACGCCC[A/G]GCCAGCAATATTGTT | 57531 |
rs747998184 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758736 | GGCTAAATGACCCAA[C/T]TAAAAGACACAGACT | 57531 |
rs748011108 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791566 | CAATTCCATTACTGG[C/G]GGAGGATGGACCAAT | 57531 |
rs748042380 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694196 | ACACACAAAAAAAAA[G/T]ATTCTGTCATTTGCA | 57531 |
rs748052334 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836845 | GCAAAACCAAAAACC[A/T]ATTGCATTTCCATCT | 57531 |
rs748073977 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693123 | CAGTTTTAACCCCGA[C/T]AAAGAAGTTATTCTT | 57531 |
rs748087446 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693953 | CTATAGAGAACAATT[C/T]GGAGGTTCCACAAAC | 57531 |
rs748101723 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797454 | CTCAAGAGTCAGAAC[A/G]AAAGTACATTTTATG | 57531 |
rs748152144 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779958 | CATTACCACATACAA[C/T]CCTCACAACACTATG | 57531 |
rs748166393 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802212 | GAGCACGCAGACTCA[C/T]AAAGCAAGTCCTTAG | 57531 |
rs748183103 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786514 | GAGGTTGAAGGGGGA[A/G]GATTGCTTGAGTCTC | 57531 |
rs748192174 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841969 | ACATAAACTTATTTT[C/T]GCAAAGAAAGTGGTA | 57531 |
rs748198025 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794974 | CTTGCAGGCTAAGAA[-/AT]AATAAGACAATAATC | 57531 |
rs748212749 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784561 | ACTTGATAAATATAT[A/T]CTGAACTGGACTGGC | 57531 |
rs748219004 | snp | G/T | 1.66394e-05 | 0.00288434 | intron-variant | HACE1 | GRCh38.p7 | 6:104744496 | AACTTCATTCTAAGC[G/T]CTAGAGAAATTTTAC | 57531 |
rs748274096 | snp | C/G | 0.00017484 | 0.00934824 | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104780398 | GACTGATTATAGAGG[C/G]TCCTCTTAATAGCAT | 57531 |
rs748308873 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730884 | CATGTAATCCAAATG[A/G]TTTCCTTGTTTGTGA | 57531 |
rs748316084 | snp | A/C | 6.59935e-05 | 0.0057439 | intron-variant | HACE1 | GRCh38.p7 | 6:104777199 | TCAGTTTCTTTGTTA[A/C]GCATACCTCTGTGAA | 57531 |
rs748342957 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842084 | CAGAAGTGAAAGGAT[A/T]GCTTGAGGCCAAGAG | 57531 |
rs748351361 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826259 | CTCTAAATTATGTGC[G/T]ATGCACGACTCTAGA | 57531 |
rs748361461 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684343 | CTTCCTGTCATTTGC[C/T]TCGTGGGCTCGTTCA | 57531 |
rs748377417 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810535 | TTACTATAGTATTCT[A/G]TAACTACATTTACAT | 57531 |
rs748378138 | snp | C/T | 5.06043e-05 | 0.00502987 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796688 | TTCATTCTGTGTCAT[C/T]TGAATAATAGTCTGA | 57531 |
rs748380849 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704230 | AGAACTGGAAAGCAA[A/C]ATGAAGTGGAGTAAG | 57531 |
rs748381389 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769035 | TATACCTCATACACA[G/T]TTTTTTTTCTTTTTT | 57531 |
rs748398844 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746990 | TCACATTAATTGTTA[C/T]GATTTTTTTTCAAGA | 57531 |
rs748433332 | snp | A/G | 0.00021462 | 0.0103568 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852422 | TACTTTGTGCAAGGG[A/G]TGATACTTAAGATTA | 57531 |
rs748437322 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843057 | CAGAGATTGCAGTGA[A/G]CACAGATTAGACCAC | 57531 |
rs748470970 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816496 | GTGTTGGGCCTGCAG[A/G]TGTGCAGAAGGCAAG | 57531 |
rs748500141 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754132 | GTATCAATAGCAGAA[C/G/T]AGACCAAGCAGAGGA | 57531 |
rs748506476 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775687 | GTTACAGAGTTAAAG[C/T]AGGCAGTTCCATGTT | 57531 |
rs748507545 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736438 | CACAGGCATGCGCCA[C/T]CATGCCCAGATAATT | 57531 |
rs748510356 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722655 | TTACATCAAGCCGCC[A/G]CGCCAATGTTTCTGT | 57531 |
rs748520103 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685465 | TGGCTCTGAAACCAC[A/C]CTTAATTACACAGAC | 57531 |
rs748526110 | snp | C/G | 1.65157e-05 | 0.0028736 | intron-variant | HACE1 | GRCh38.p7 | 6:104771441 | TTTGCCTTCCCTTAT[C/G]TATTTAATGGTAAAA | 57531 |
rs748557587 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776466 | GGACTGATAAGAAAC[A/C]TCTTTGGGCCAACAC | 57531 |
rs748559640 | snp | A/C | 1.67624e-05 | 0.00289498 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852296 | TCTTAAAAAGCAAAA[A/C]TTTTTGGAACAAGCA | 57531 |
rs748565227 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708960 | TAAGAGCTAAAACTA[A/T]AAAATTCAGAAGAAT | 57531 |
rs748578236 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771448 | TCCCTTATCTATTTA[A/T]TGGTAAAATACTGCC | 57531 |
rs748585677 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829443 | ATGAACACAGATTTG[G/T]AGAACTATACTTCAG | 57531 |
rs748598523 | snp | C/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727916 | TCTCCTGGGCTCAAG[C/T]GATCTCGCACCTAGC | 57531 |
rs748609049 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762555 | GGGCCTGCTGAGGGT[C/G/T]GGGGGCTAGAGGAGG | 57531 |
rs748630309 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817420 | CTCTCTCCTGCTGCC[A/G]TGTGAAGAAGCTGTC | 57531 |
rs748636379 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797125 | GAAGAGTATCACTTT[C/T]AAAAATTAAGACAAG | 57531 |
rs748644944 | snp | C/G | 4.94539e-05 | 0.00497238 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785157 | TTTCATAGCTCCCAG[C/G]TCCTGGAGGTTCAAA | 57531 |
rs748654343 | in-del | -/AC | 6.80156e-05 | 0.00583123 | intron-variant | HACE1 | GRCh38.p7 | 6:104811269 | TATATATATATATAT[-/AC]ATATGAGCATATATA | 57531 |
rs748659354 | in-del | -/A | 8.41161e-05 | 0.00648467 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852378 | TTTCATTATCTGAGT[-/A]AAAAAAAACAAAGAG | 57531 |
rs748683111 | snp | A/C/T | 0.000197946 | 0.00994666 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785249 | TCTGTTGAGTCTCTT[A/C/T]TGTTTTTCATCAATT | 57531 |
rs748697342 | snp | A/G | | | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858475 | GGGGGAGCAGGGTGC[A/G]GATCACTTGAGCCCA | 57531 |
rs748703199 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710370 | GGTTTCTTCTGGATG[A/G]TTAAAATGTTCTAAA | 57531 |
rs748718780 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766482 | AAAGATGCATATAAA[A/G]AATCCACTTTAAGTC | 57531 |
rs748726281 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824205 | CAAAATGGAGTCTCA[C/T]TCTCAAATAATCCAG | 57531 |
rs748769775 | snp | A/G | 1.65059e-05 | 0.00287275 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785269 | TTTCATCAATTCTGT[A/G]GCTATTAAAACTAGC | 57531 |
rs748775168 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856601 | ACCACATCCAGCTAA[-/T]TTTTTTGTATTTTTA | 57531 |
rs748792445 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701517 | TTCATTTGATATTCT[C/T]AGTAACTGTGTGATG | 57531 |
rs748794979 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713665 | GGCTTTCTGAATTAC[A/G]GGAAATTTCATTCGT | 57531 |
rs748807134 | in-del | -/T | 1.83616e-05 | 0.00302993 | intron-variant | HACE1 | GRCh38.p7 | 6:104750512 | GACTTTTCAAAAACC[-/T]TTTTACATACTTAAT | 57531 |
rs748812965 | in-del | -/CT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720260 | ATTCTAGAAAGTCCC[-/CT]GTGTCCTTTTGTAAA | 57531 |
rs748820378 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754514 | TCCAAATGAAAGAAA[A/C]GCTGTTAAGGGCAGC | 57531 |
rs748823375 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790381 | TCCTAACTAGTTTTC[A/G]AGGAAGTGGCACATA | 57531 |
rs748845549 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687876 | GCTTGAGGACCAGCT[A/G]CACTCCAGAGCTACT | 57531 |
rs748852078 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714885 | TGGTAGTGCTTTGCA[C/G]TTATTTCTTGCTCTG | 57531 |
rs748879860 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755940 | AAGATCAGAGGTGAA[C/T]TGAAGAAGACAGAGA | 57531 |
rs748881846 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734986 | AAGGTCCGGATGGTT[G/T]AAAAATTGGAATGTA | 57531 |
rs748901937 | snp | A/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785171 | GGTCCTGGAGGTTCA[A/G]ATGGAGGAATGGAAG | 57531 |
rs748902584 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848966 | TATAAAGAAGAACAA[C/T]ATCATCAATAATATC | 57531 |
rs748925813 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831842 | AGCTTGCAGTGAGCC[A/G]AGATGGCGCCACTGC | 57531 |
rs748981416 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832105 | AGTAGAAAAATAGGA[C/T]AACCTGACTCATACT | 57531 |
rs749005577 | snp | A/G | 5.08703e-05 | 0.00504307 | intron-variant | HACE1 | GRCh38.p7 | 6:104811291 | GCATATATAGCATCT[A/G]GAAATATAAAATATC | 57531 |
rs749013729 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830291 | CACATCTTTTTTTCC[A/C]ACATAGAATACGTTT | 57531 |
rs749030886 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836981 | CTGTACAAAATTCTA[A/G]TGAATAAAATCAAAG | 57531 |
rs749038700 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791688 | ATATGAGATTAGAGT[A/G]AAACAAATTACATAT | 57531 |
rs749046238 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797696 | CCATATGCCTCATTC[C/T]CTGATTGCCCTCCTT | 57531 |
rs749053775 | snp | A/T | 1.68069e-05 | 0.00289882 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730415 | CATGTGGGACCCTGG[A/T]ACTAAGAGTTTATAT | 57531 |
rs749059247 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854267 | CTAAAGAAACATAAC[C/T]AAAGGCAATGTGGTA | 57531 |
rs749075377 | snp | A/G | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744166 | ACTGCTTACCTGCCC[A/G]TAACAAACTGTAAGA | 57531 |
rs749091292 | snp | C/T | 1.67733e-05 | 0.00289592 | intron-variant | HACE1 | GRCh38.p7 | 6:104777138 | CATTGGTTAATTTTA[C/T]ATATTAAAATTTATA | 57531 |
rs749094102 | in-del | -/TTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832378 | AGCACTATTTTCCTG[-/TTT]TTTGTTGTTGTTGTT | 57531 |
rs749149699 | snp | C/T | | | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729693 | CCATAGCTGCCACAA[C/T]GTAGTGCCACAAGAA | 57531 |
rs749186637 | snp | A/G/T | 0.000119813 | 0.00773899 | intron-variant | HACE1 | GRCh38.p7 | 6:104811287 | ATGAGCATATATAGC[A/G/T]TCTGGAAATATAAAA | 57531 |
rs749189164 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838463 | ACATTGGAGGTAGGG[A/G]CCATCTCTTCAATAA | 57531 |
rs749227159 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815038 | ACACTCCTATAAAGA[C/T]ACTTGAAAATGTGGA | 57531 |
rs749264444 | in-del | -/A | 1.66676e-05 | 0.00288679 | intron-variant | HACE1 | GRCh38.p7 | 6:104797055 | AAACAAGTTAAAAAT[-/A]CAATCTTTTTAAAGT | 57531 |
rs749269060 | snp | A/T | 1.67874e-05 | 0.00289714 | intron-variant | HACE1 | GRCh38.p7 | 6:104791660 | GCTAGAGAGGCTGAA[A/T]ATAAAAATTAAAATA | 57531 |
rs749300809 | in-del | -/C | 1.66324e-05 | 0.00288374 | intron-variant | HACE1 | GRCh38.p7 | 6:104744120 | ATTAAAAGCAGAATA[-/C]ATTAAATTATTTCCA | 57531 |
rs749306912 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765347 | GCTTTTGCCTATCAT[A/G]GCAAATTTACACTTA | 57531 |
rs749318198 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825998 | TGAGTGGCAGGCAAG[C/T]GAACATCACTATCTG | 57531 |
rs749342313 | snp | C/T | 1.67579e-05 | 0.00289459 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750458 | AAGTTCAGTAACAAG[C/T]TGGACGTACTCCGCC | 57531 |
rs749348621 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104828426 | AAAATTATATCTCCA[G/T]TTGAATAACCAAACT | 57531 |
rs749372738 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770499 | CGAGGCAGACAGATC[A/T]CCTGAGGTCAGGAGT | 57531 |
rs749378007 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725253 | TATATGTATGTGTAT[A/G]TACATACACACACAC | 57531 |
rs749379930 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733228 | AGCACAGTATTTCAA[C/T]ATCAATATGATCAAT | 57531 |
rs749403278 | snp | A/G | 1.65795e-05 | 0.00287914 | intron-variant | HACE1 | GRCh38.p7 | 6:104843315 | TGAAAAGAAAAAAGA[A/G]TCATGGATAACTGGT | 57531 |
rs749435938 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685851 | ATGATAGAGAGGGAT[C/T]TATTTATTTACTCAA | 57531 |
rs749444888 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809888 | GAGAGAGAGAGAAAT[-/A]AAAAAATAACCTAAT | 57531 |
rs749510870 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699854 | AAGGGTTAACATCAG[A/G]CCTCCCTCGGCTGAG | 57531 |
rs749512378 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702188 | AAAATATTTATAATG[G/T]GACTTAGGGGCAGGA | 57531 |
rs749516165 | in-del | -/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796510 | TTATCTAATTCACAC[-/TT]ATCCTATAATGCAGA | 57531 |
rs749526274 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706498 | ATTGGGCAAAGACAC[C/T]AAAGAAACACACACA | 57531 |
rs749529307 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758846 | CAACATAAAGGGATA[C/G]AGGAAGATCTACCAA | 57531 |
rs749545803 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818579 | CTGGCAGAGATACAA[C/T]AAAAAAAAATGTCAG | 57531 |
rs749564368 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796189 | GATCTCGGCTCACTG[C/T]AGGCTCAACCTCCTG | 57531 |
rs749570400 | snp | C/G | 1.70515e-05 | 0.00291984 | intron-variant | HACE1 | GRCh38.p7 | 6:104784073 | GAATAAAAAGATGAA[C/G]AAAAATTTCTACCTG | 57531 |
rs749576241 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762053 | GTCAGGAAACAACAG[A/G]TGCTGGAGAGGTTGT | 57531 |
rs749586790 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813710 | ACTCATGTACACAAC[A/G]CTTCCAGCCAACATT | 57531 |
rs749627409 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807976 | CAGATCACCTGAGGT[C/T]GGGAGTTCGAGACCA | 57531 |
rs749633828 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802539 | ACAGTGCAATCAAAC[C/T]AGAACTCAGGATTAA | 57531 |
rs749642305 | snp | A/G | 0.000100862 | 0.00710078 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859553 | GGCCAGCCTGGCCCC[A/G]CGACCCGGCTCACCC | 57531 |
rs749644565 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723908 | AAAATTTCATTATTA[A/G]CTAAGCACCTATTCA | 57531 |
rs749691461 | snp | C/T | 3.37405e-05 | 0.0041072 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796701 | ATTTGAATAATAGTC[C/T]GAAAAAGCCTCGGGT | 57531 |
rs749699661 | snp | A/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858887 | GGAACCCTGGCACGC[A/T]GAACTAAAAGTCCTG | 57531 |
rs749700529 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763667 | CTACAGCAGCACAGA[G/T]GCATCACCAGAATAT | 57531 |
rs749701107 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731150 | CAAAAAGAAAATTAA[C/T]ATTTCTTCTAAAGTT | 57531 |
rs749711186 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698757 | ATGACATCAAGAACC[A/G]TGTTGAAGAAGGGAG | 57531 |
rs749750023 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842157 | AAAAAAATATAAAAT[A/G]TACTAGCCAAGGGTA | 57531 |
rs749765097 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822340 | GTGAGCCGCGACCAC[A/G]CCACTGCACCCCAGC | 57531 |
rs749789601 | snp | G/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860519 | GTACAATGCTAAAGT[G/T]TCTATGTGATGACAC | 57531 |
rs749791606 | snp | A/G | 1.6477e-05 | 0.00287024 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771997 | TCAACGCTAATCCCA[A/G]GATCTGCCCAGCAAA | 57531 |
rs749798387 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767902 | CTTACTCTTATCTTC[-/C]TTTTTTTTCTCCAAG | 57531 |
rs749802893 | snp | A/C | 3.4497e-05 | 0.00415299 | intron-variant | HACE1 | GRCh38.p7 | 6:104771889 | AAAAAAAAACAATAT[A/C]AATAAATGTCTGCAG | 57531 |
rs749805602 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699755 | GTTGATATTAAAGAC[A/C]TTCTACTAGCACATG | 57531 |
rs749817163 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684618 | ATCCAGCTAACAAAC[A/G]AGTCATTATAAATAG | 57531 |
rs749831094 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781155 | TCTGAGACTGTGTAA[-/T]CATCCTACCCTTCAT | 57531 |
rs749842747 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812873 | AACAGACTCTCCCCC[-/T]AGGACCTTTCTTCCC | 57531 |
rs749861513 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843976 | ATTCTCCTGCCTCAG[A/C]CTTCCGAGTAGCTGG | 57531 |
rs749864291 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849478 | AGTAGCTGGGACTTA[A/C]AGGCATGAGCCACCA | 57531 |
rs749873039 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827140 | ACCACCTGTGCCCAA[C/T]ACACTGATAAATTAC | 57531 |
rs749916941 | snp | C/G | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791612 | AAACATTCTCACAAT[C/G]CTTAAAAGGCTCTTC | 57531 |
rs749921145 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768638 | GAGAAATGTTTATAT[A/T]AAAAAAATGAAAGCT | 57531 |
rs749924511 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829252 | TCAGTGTTCAACTTA[C/T]GGAAAGATATACAAA | 57531 |
rs749953516 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772640 | ATGATTAGAAAATCA[C/T]CTCAGTCCACAAGGT | 57531 |
rs749964357 | snp | A/G | 1.64991e-05 | 0.00287215 | intron-variant | HACE1 | GRCh38.p7 | 6:104849250 | ACCGATCCACAACTA[A/G]AACAATATTAAAAGA | 57531 |
rs749968429 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791504 | ATATACTTTTCTCAC[C/T]TTGAACACCTGGCTT | 57531 |
rs749973881 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758452 | TCCAGCCAAACTAAG[C/T]TTCATAAGTGAAAGA | 57531 |
rs749974094 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769342 | TCCACTTTGTCATAT[A/G]TATCTGAAAGGAGTG | 57531 |
rs750006823 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746386 | ATTCTCTAGCTTCCT[C/T]TGCACTGCAGACTGG | 57531 |
rs750020844 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718633 | CAATTGATGTAATCA[C/T]AGGATTTCTCCCTAT | 57531 |
rs750076739 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704898 | TACTGGTATGTAAAA[C/T]GTACAGCTCAATTGC | 57531 |
rs750088137 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814540 | AGCTACTGAAGCATA[A/T]CCTCCTCCAAAGAAA | 57531 |
rs750095227 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721383 | TGATGGTGGGGAGGC[C/T]TGAAAACACGTTTCC | 57531 |
rs750107983 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794762 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGTGT | 57531 |
rs750124576 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807704 | AAAGATGGCAGGGGG[-/A]AAAAAAAAATCAATG | 57531 |
rs750127495 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705940 | TTTATATTAAAGGGC[A/G]GAAGATAATAACTTT | 57531 |
rs750128492 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818123 | TACCCCAACATGAAT[C/T]CTATAATCTATGTAA | 57531 |
rs750129842 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692523 | TAATGAAGAATTTTG[C/T]GCTGAAATTCAGTAG | 57531 |
rs750132370 | in-del | -/AAC | 3.57309e-05 | 0.0042266 | intron-variant | HACE1 | GRCh38.p7 | 6:104750307 | AGTTTTTTGTTGTTG[-/AAC]TGTTACAACATAAGA | 57531 |
rs750134011 | in-del | -/AATAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743840 | ATATTAAAATATTAA[-/AATAA]TATACAAATATTAAA | 57531 |
rs750136860 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857723 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA | 57531 |
rs750168126 | snp | C/T | 1.65051e-05 | 0.00287267 | intron-variant | HACE1 | GRCh38.p7 | 6:104744638 | AGAAAAATATTTCAA[C/T]AATTTTCTTTAGGGA | 57531 |
rs750187073 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800801 | CTAAAAACCAGAGCA[C/T]CTCTTCTCCTCCAAC | 57531 |
rs750203573 | snp | C/T | | | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730404 | AGCAAACCCACCATG[C/T]GGGACCCTGGAACTA | 57531 |
rs750217022 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761547 | TATACAAAAATCAAC[C/T]CAAGACGGATGAAAG | 57531 |
rs750217284 | in-del | -/T | 1.65045e-05 | 0.00287263 | intron-variant | HACE1 | GRCh38.p7 | 6:104849256 | CCACAACTAAAACAA[-/T]ATTAAAAGACAGTTC | 57531 |
rs750218485 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801576 | TTGACATTCTTAAAG[A/C]AAATAATTTTCAACT | 57531 |
rs750235571 | in-del | -/CCTCCGCGAT | 0.000168364 | 0.00917354 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859654 | CCATCCTCGGCGCGC[-/CCTCCGCGAT]CCTCCGCGATCAGCC | 57531 |
rs750238687 | snp | A/C | 1.73315e-05 | 0.00294371 | intron-variant | HACE1 | GRCh38.p7 | 6:104784224 | GAATGAGTAGCATTA[A/C]GTGAAATGCAAATTC | 57531 |
rs750339154 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715992 | ATAAAAGTTTAAAAA[A/T]ATATATATATTTAAA | 57531 |
rs750344933 | snp | C/G | 1.65531e-05 | 0.00287686 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729644 | GCATCAGTAGTCAGA[C/G]GAGTTTTCCAGACTT | 57531 |
rs750362950 | snp | A/C/T | 0.0001642 | 0.00905954 | intron-variant | HACE1 | GRCh38.p7 | 6:104796769 | ACCCTAAAAACAAGA[A/C/T]CTAAAATTATCCAGG | 57531 |
rs750371878 | snp | A/G | 1.69614e-05 | 0.00291211 | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796666 | ATACCATGTTTTCTC[A/G]GAGGTCTTCATTCTG | 57531 |
rs750408718 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688759 | GGGAAATTCCAGTCT[C/T]TTCTGATCTCTCATT | 57531 |
rs750418750 | snp | A/C | 1.89102e-05 | 0.00307486 | intron-variant | HACE1 | GRCh38.p7 | 6:104771394 | TACAGGAATACCTAA[A/C]AAATGCAAACATACA | 57531 |
rs750430110 | snp | A/G | 0.000106729 | 0.00730433 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859471 | GTTTTCTCAGCTTTC[A/G]GTTAGTTTTTCCACC | 57531 |
rs750432750 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842994 | GCGCATACCTGTAAT[A/C]CCAGATACTTGGGTG | 57531 |
rs750442159 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785775 | CACTCAACATTTTCT[A/G]TATTAATATGATCAA | 57531 |
rs750459875 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755319 | GACTGAGACTCCCAC[A/T]CAATAATAGTGAGAG | 57531 |
rs750464348 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848531 | TACTTATTTTCATTT[G/T]AAACATAATTCCAAT | 57531 |
rs750517576 | snp | A/G | 4.95021e-05 | 0.0049748 | intron-variant | HACE1 | GRCh38.p7 | 6:104771173 | CAAACAATGGTTAAG[A/G]TAAAAACTGAAATAC | 57531 |
rs750562092 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703384 | GGTTCTCTTTGACAG[C/T]AGCAATTTGGGGAAA | 57531 |
rs750596260 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825728 | ATTCTGTATCCAGAA[C/T]CTTGAGCAGCTGCTG | 57531 |
rs750631829 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690107 | GCCACAACAGATGTG[C/T]CACTGGTTTCCAGGA | 57531 |
rs750649658 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785083 | CTGACAATCTGCACT[A/G]GCTTCCTGTCTCCCT | 57531 |
rs750686165 | snp | C/T | 5.06308e-05 | 0.00503119 | intron-variant | HACE1 | GRCh38.p7 | 6:104797072 | AATCTTTTTAAAGTC[C/T]TTCTCTATGAATTAT | 57531 |
rs750697682 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783107 | TCTGCTGCAATACTG[C/T]AGTTTTACATACTTT | 57531 |
rs750714714 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833848 | AAATTAGCTGGACGT[A/G]GTGGTGCGTGCCTGT | 57531 |
rs750727619 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817187 | TTGTATTTTCCAATA[C/T]GAGAAGAACATGAGA | 57531 |
rs750735655 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839618 | GGTGAAAACCTACCA[C/T]GTACACAGGTAATAA | 57531 |
rs750739815 | snp | C/T | 1.84446e-05 | 0.00303677 | intron-variant | HACE1 | GRCh38.p7 | 6:104730466 | AAAGAAAGATATTTG[C/T]GACAGATAAATTTCA | 57531 |
rs750740254 | in-del | -/AG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709198 | ATTGAAGATATATAA[-/AG]AGCTCTTTCAACTCA | 57531 |
rs750789508 | in-del | -/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765569 | TGAATTTCACCACTG[-/TT]TTGTGATCAGCAGAT | 57531 |
rs750830019 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767127 | GAGGCTGTTACAGGA[A/C]ATGAGAAACATAAAG | 57531 |
rs750838672 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721361 | ACAAAAGGGGAGGAG[-/A]GGGGAGTGATGGTGG | 57531 |
rs750841143 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823313 | GCAGTGGGCACCTGT[A/G]ATCCCAGCTACTTCG | 57531 |
rs750866398 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728151 | ACTTGCAAAAAAAAC[G/T]AATATGACAAAGCCA | 57531 |
rs750886035 | snp | C/T | 1.65425e-05 | 0.00287593 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777079 | ACAATTTGCTTTTGA[C/T]ACAACTTCACAGCTA | 57531 |
rs750904282 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749209 | ACAGTACAGGAAAAG[C/G]CATATTGCAGTCAGG | 57531 |
rs750927741 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841257 | ACATGAATAATTTTG[C/T]TAAATAAAAATTTTA | 57531 |
rs750941565 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847090 | TTCTCTGTGCCACTT[C/T]ATTTGTTTCTAAAAA | 57531 |
rs750952911 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807142 | GATTCTCCTGCCTCA[C/G]CCTCTGGAGTAGCTG | 57531 |
rs750960157 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766506 | TTAAGTCAATAATCT[A/G]TGGATAAAAGTCTGT | 57531 |
rs750999433 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752061 | TCAGAGCTACAGAAG[C/T]GTCACAGTAGATTCC | 57531 |
rs751025231 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813358 | GCCATGCATGGTGCT[A/G]CATGCAAGACGCTAT | 57531 |
rs751061505 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815021 | TCAGTACCAGGAGTG[C/G]GACACTCCTATAAAG | 57531 |
rs751093676 | snp | G/T | 3.32342e-05 | 0.00407627 | intron-variant | HACE1 | GRCh38.p7 | 6:104795562 | CTATTGATTTCCTCT[G/T]ATTGCGAAACACTTA | 57531 |
rs751136654 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706163 | TTTGGAGGTTTCCCA[C/T]GAATATCCAGATTTA | 57531 |
rs751151882 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707018 | CTGTAACAGATAAAA[A/C]GCGTAAGTTACTAAT | 57531 |
rs751159938 | snp | A/G | 1.64944e-05 | 0.00287175 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791633 | AAGGCTCTTCATTTG[A/G]GCATCATAATTGCTA | 57531 |
rs751164289 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797975 | TGGGAGGCTAAGGCA[A/G]GAGAATCACTTGAAC | 57531 |
rs751164465 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759682 | AAAGCTAGCAGAATA[C/T]AAGAAATAACTAAGA | 57531 |
rs751195577 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810306 | GGGTTGTTAAATAGA[C/T]GATCTGAATTGGTCT | 57531 |
rs751203579 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843950 | CAACATCTGCCTCCC[A/G]GGTTCAAGTGATTCT | 57531 |
rs751223455 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694043 | AGGAAATCAGTATAT[C/T]GAAGAGATATCTGCA | 57531 |
rs751261083 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798599 | CTTTGAAAGCAACAA[A/T]AATCAGCTTTACCGG | 57531 |
rs751266052 | snp | A/G | 1.65236e-05 | 0.00287429 | intron-variant | HACE1 | GRCh38.p7 | 6:104771159 | TCAGGGCCAAGTTAC[A/G]AACAATGGTTAAGGT | 57531 |
rs751269312 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781165 | TGTAATCATCCTACC[C/G]TTCATCAGACTTTCC | 57531 |
rs751332809 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851362 | GCTGGGATTACAGGC[A/G]TGAGCCACCCCACCC | 57531 |
rs751343844 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787660 | GGAGGTAAGGCCTAA[C/T]GCAAGAAATGACACA | 57531 |
rs751344733 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751149 | AAAACACAAGCTTGT[C/T]CGGGCCCCAATGTGT | 57531 |
rs751362911 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861017 | GTGGTGCCACAGGCA[C/T]GGGGAAGACCTCTGT | 57531 |
rs751364562 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843473 | ACTTGACGCAAGATA[C/G]AAAACTGCTTCTATG | 57531 |
rs751394124 | in-del | -/CAGGAATAAAGCTT | 6.20713e-05 | 0.00557062 | intron-variant | HACE1 | GRCh38.p7 | 6:104796607 | GTCATATATGCTGAG[-/CAGGAATAAAGCTT]CTTCATTTACAAGCT | 57531 |
rs751396057 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752405 | TATATTTCAGTTTAT[A/G]TCTACTCTCACTAAA | 57531 |
rs751401777 | snp | C/G/T | 3.29784e-05 | 0.00406058 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785041 | AATGACAGCACTTAG[C/G/T]CGGTTAGCTGTCATA | 57531 |
rs751403205 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717261 | TCTCCTGCCTCAGCC[A/T]CCCGAGTAACTGAGA | 57531 |
rs751431511 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827537 | AAGTAACAGTGGTAA[C/G]AGAACTTTCTACTAT | 57531 |
rs751433182 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684135 | GCACAAAATTAAAAT[A/G]CCAAAATTAAAAATC | 57531 |
rs751462723 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699361 | TCCCAGAGTTACCAT[G/T]GTGGAGATCAGTTAC | 57531 |
rs751493086 | in-del | -/TTT | 8.23825e-05 | 0.00641751 | intron-variant | HACE1 | GRCh38.p7 | 6:104833016 | ACAAACACATGCAGC[-/TTT]TTAAAGTCCTCATGG | 57531 |
rs751496530 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699077 | AACTCTTGGAAGATA[C/T]AACCTCCAAAAGTTT | 57531 |
rs751532771 | in-del | -/AACA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755570 | AAGAAATGAAATCAT[-/AACA]AACAGTCTCTCAGAC | 57531 |
rs751534476 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794705 | GCTCAGGAGTTCAAG[A/T]CCAGCCTGGGCAACA | 57531 |
rs751562678 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776266 | CTTGGGTTTTCCTAA[C/T]CAATATATTTTAAAA | 57531 |
rs751569979 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834010 | TTAGCTGGCCATGGT[A/G]GCATACACCTATGGT | 57531 |
rs751577510 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743906 | AGCAAAAAGATTTCC[A/G]AATTATAAAGTACAA | 57531 |
rs751582378 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692075 | AGGGGTAGAAGGAGG[A/G]TAAGGAAGGGAAGGA | 57531 |
rs751585859 | snp | A/G | 1.65397e-05 | 0.00287569 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796933 | GAAAAACACACCTGT[A/G]CACATAAATCCAGAG | 57531 |
rs751617979 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761635 | TTCAGGACATAGGCA[A/T]GGGCAAAGACTTCAT | 57531 |
rs751632392 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723658 | CTAAGAACTGTGGAA[A/G]TGCAGGAGAACAGAG | 57531 |
rs751656938 | snp | C/T | 3.2962e-05 | 0.00405954 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771971 | GTAAATATTGACCAG[C/T]TGCCTGTGGTTCAAC | 57531 |
rs751687101 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778721 | TGGGAGAAAACTTTA[A/T]CCCAGGAGTTCAAGG | 57531 |
rs751699378 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803827 | GGATGCCGTCTCTCA[A/C]CACTCCTATTCAATG | 57531 |
rs751712035 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848684 | TGTACAATATATTAA[A/G]TCTGTGTATAATTCC | 57531 |
rs751712682 | snp | A/C/G | 0.000117638 | 0.00766858 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852420 | CCTACTTTGTGCAAG[A/C/G]GGTGATACTTAAGAT | 57531 |
rs751726472 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822385 | AGGACTCCATCTCAG[-/A]AAAAAAAAAAAAAAA | 57531 |
rs751738323 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763211 | TCAAACCCACCTAAT[A/T]ACACACACGTATACT | 57531 |
rs751760021 | snp | A/C | 4.00096e-05 | 0.00447249 | intron-variant | HACE1 | GRCh38.p7 | 6:104785358 | TAAACATCATTCTTA[A/C]ACTACAGGATTAAAA | 57531 |
rs751781445 | snp | A/C | 2.07084e-05 | 0.00321773 | intron-variant | HACE1 | GRCh38.p7 | 6:104771409 | AAAATGCAAACATAC[A/C]GCAGTTATAGTCTGG | 57531 |
rs751800248 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805876 | TAAAACAAAAAAAAA[-/C]AATTTAGTACTCAAA | 57531 |
rs751807243 | in-del | -/TGAGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710180 | ATTGCTAAACATGGA[-/TGAGT]TATCAGAACATTATG | 57531 |
rs751809418 | in-del | -/TG | | | frameshift-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776752 | TTACCATCAGCTGAC[-/TG]GGTAAACAATGCATA | 57531 |
rs751814024 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698248 | CTTGAAAATAATCTA[G/T]TGTTAATGAAGTTAT | 57531 |
rs751817607 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819180 | TTAAGCCAATTAACA[A/G]CCTCAACAAAGTCTC | 57531 |
rs751828336 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776529 | GTTTAGAGGAACAAA[C/T]GTTAGACTGAGTCAG | 57531 |
rs751837323 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711518 | ACAAGTACTTAGTGG[A/C]ATAAGTACATACAGC | 57531 |
rs751848467 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801669 | ACATGCAAATGCCGA[C/G]AGATTTTGTCACCAC | 57531 |
rs751860051 | in-del | -/A | 5.11526e-05 | 0.00505704 | intron-variant | HACE1 | GRCh38.p7 | 6:104784073 | AATAAAAAGATGAAG[-/A]AAAAATTTCTACCTG | 57531 |
rs751882947 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785232 | GTAAAATAGAAGTGA[C/T]CTCTGTTGAGTCTCT | 57531 |
rs751883005 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant, synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833138 | CACAAGGTCATGGAG[C/T]AGTTCTGTCCGCCCA | 57531 |
rs751893449 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825416 | TCAGCCTCGGATTGG[C/T]TGCACACAGCAACCA | 57531 |
rs751919874 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767178 | AACACAAAGCACTCA[A/G]TAAGTAGTAATTATT | 57531 |
rs751926764 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857775 | ATCCTAGCTAACACG[A/G]TGAAACCCCGTCTCT | 57531 |
rs751935958 | snp | A/G | 1.65701e-05 | 0.00287833 | intron-variant | HACE1 | GRCh38.p7 | 6:104811439 | CCAGAGGAATCAAAC[A/G]AAAGATACAATTACC | 57531 |
rs751937767 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702249 | TTTACTTAAATCCAA[A/C]CAAACTGAAGTGTCA | 57531 |
rs751968580 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788796 | AGGCACTAGATAAAC[A/T]TCTCTTAATGCTGAA | 57531 |
rs751987782 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700409 | AGGGAGTTAAAAAAG[-/AA]AAAAAAAAAAAAAAA | 57531 |
rs752006153 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755722 | AAATCAAGAATTTAT[C/T]TGAAACTAATGAGAA | 57531 |
rs752022515 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756979 | ACCTGGGTCGCTGGA[C/T]CTTGGCGGGGAGAGG | 57531 |
rs752039257 | snp | C/G | 1.65359e-05 | 0.00287536 | intron-variant | HACE1 | GRCh38.p7 | 6:104744267 | TTAGCTCATATTTCA[C/G]AGCAATTGTAGACTT | 57531 |
rs752060255 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850709 | AACAAAGACAAGAGG[C/G]ACATGAGATTTACAT | 57531 |
rs752079106 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848592 | AAACTAATGTTAGCA[C/T]TAAAAGGAGTAAACT | 57531 |
rs752089146 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703637 | AAAACACCTCTACTC[C/T]TTTCCCATTCTAACT | 57531 |
rs752092152 | snp | C/T | 3.32662e-05 | 0.00407824 | intron-variant | HACE1 | GRCh38.p7 | 6:104744120 | ATTAAAAGCAGAATA[C/T]ATTAAATTATTTCCA | 57531 |
rs752095793 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690293 | CTGCCTCTGTAAAAT[A/G]AGAATATTATTAATG | 57531 |
rs752100694 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834066 | GGAGGATCCCTTGAG[C/T]CCAGGAGTTTGAGGC | 57531 |
rs752125192 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722331 | GAAAAATGTAGAGCC[A/G]TCTCCAAATATGATT | 57531 |
rs752134207 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780212 | GAAATAAAAACAAAT[C/G]GAACCTTTTCAAGTA | 57531 |
rs752159309 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855515 | ACCCAGTATATACCA[A/C]ATAACCAGAAGGTCT | 57531 |
rs752205662 | snp | G/T | 1.65419e-05 | 0.00287588 | intron-variant | HACE1 | GRCh38.p7 | 6:104744274 | ATATTTCAGAGCAAT[G/T]GTAGACTTCTCAATA | 57531 |
rs752238930 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782524 | AAAGAAATTGAACTT[G/T]AGAACCAGACAGACT | 57531 |
rs752241771 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746969 | ATTTGAAGCACTTCA[C/T]GAATATCACATTAAT | 57531 |
rs752249845 | in-del | -/T | 1.695e-05 | 0.00291114 | frameshift-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795682 | CTCCAGAACTTGCCG[-/T]TAACTAAATTTTTTA | 57531 |
rs752254680 | snp | C/T | 8.2498e-05 | 0.00642201 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777264 | CACCATATCTGAATC[C/T]GGCTGTCCTGAATGC | 57531 |
rs752262666 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696726 | TATTTTGTGCCCCAT[A/C]AGGCCTCCCATCAGA | 57531 |
rs752266775 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839945 | CAGGAGGCGGAGGTT[A/G]CAGTGAGCTGAGATT | 57531 |
rs752276869 | snp | A/T | 1.66291e-05 | 0.00288345 | intron-variant | HACE1 | GRCh38.p7 | 6:104777116 | AAAATAGAATCTAAA[A/T]ATGTAGCATTGGTTA | 57531 |
rs752304160 | in-del | -/AG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692697 | AGGGACAAATAAGAC[-/AG]GGGTTTCTTTTGAGG | 57531 |
rs752304848 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748681 | CCACTAAATGTTCAT[A/C]AAGAGTAGAAAAGAC | 57531 |
rs752311908 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695280 | AATAAACAAGAGAGG[C/T]GCAAGTAAGGACAGG | 57531 |
rs752326427 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766789 | TATTTAACGTCTAAA[A/G]AAATGCAGTGTTGTA | 57531 |
rs752329130 | snp | A/G | 1.92236e-05 | 0.00310023 | intron-variant | HACE1 | GRCh38.p7 | 6:104796639 | CATTTACAAGCTACT[A/G]TCACAAATACAATAC | 57531 |
rs752364879 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846601 | GAGAAAAATGCTAAA[C/G]CAAGCCAAGAGAAAT | 57531 |
rs752369607 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839194 | GAAAACAACTGCATT[A/C]CTGGACATTTATCCC | 57531 |
rs752413153 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730084 | GTGATACTTGAACTA[C/T]AGTCAATTAAATTGT | 57531 |
rs752417348 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794669 | AGCACTTTGGGAGGC[C/T]GAGATGAGCGGATTG | 57531 |
rs752433781 | in-del | -/TAAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743836 | CAAATATTAAAATAT[-/TAAAA]TAAAATAATATACAA | 57531 |
rs752456491 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813463 | GTCTATAGCAGTCAT[C/G]CCCAACCAAGGTTAA | 57531 |
rs752457180 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840626 | CTGAGGTCAGGAGTT[C/T]GAGATCAGCCTAGCT | 57531 |
rs752459020 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771832 | CAAAATAAAAATTAT[C/G]TCATCCAAAATACTA | 57531 |
rs752472625 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829698 | TAAATCCTGTTGGCC[A/G]TTACATAATCAACCA | 57531 |
rs752477147 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734396 | TAAACTAATACAGAA[C/T]ACAGAATACAGAATC | 57531 |
rs752524759 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733003 | AGAAGACCTGGCTAT[A/G]TCTCCTTGTAAGTTG | 57531 |
rs752560221 | snp | C/T | 1.65688e-05 | 0.00287821 | intron-variant | HACE1 | GRCh38.p7 | 6:104849288 | GATACATTCAACATA[C/T]AGCCATACTTGATGT | 57531 |
rs752662838 | snp | A/G | 1.65121e-05 | 0.00287329 | intron-variant | HACE1 | GRCh38.p7 | 6:104771167 | AAGTTACAAACAATG[A/G]TTAAGGTAAAAACTG | 57531 |
rs752672855 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820950 | ACCTAAATGCCCATC[A/G]ATGGTAGACTGGATA | 57531 |
rs752679575 | snp | A/G | 1.65795e-05 | 0.00287914 | intron-variant | HACE1 | GRCh38.p7 | 6:104784376 | CTGTAAGTAAAGAGA[A/G]GAAAGGCTAGCAGGG | 57531 |
rs752681271 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848436 | ACTCCAGCCTGGTGA[C/T]GGAGTGAGACCCCAT | 57531 |
rs752716928 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815231 | TCTCAGATGGAGATG[A/G]GGAACTTATTGGCAA | 57531 |
rs752729914 | in-del | -/G | 1.70515e-05 | 0.00291984 | intron-variant | HACE1 | GRCh38.p7 | 6:104784950 | TTTCATCATCTATCA[-/G]AGAAAAAAAAAATAA | 57531 |
rs752740922 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751251 | TTACCAGGATATATA[C/T]CAACTTCTAAAAAGT | 57531 |
rs752787314 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860006 | CCAACGCGGGCGCAG[A/G]GCTGAGTATGCGGGA | 57531 |
rs752791373 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780538 | TAGAGGAGGACAATC[C/T]CCAAGTTACAGAAAA | 57531 |
rs752791442 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763484 | ACTATCTCAGCCACC[C/T]GTGTAGACACAATCT | 57531 |
rs752801360 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805037 | ACAACCCCATCAAAA[C/T]TGGGCAAAGGATATG | 57531 |
rs752844233 | snp | C/T | 3.3036e-05 | 0.0040641 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729681 | GCCATTGTGTAACCA[C/T]AGCTGCCACAATGTA | 57531 |
rs752851571 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821170 | AGAGGGGAACAATAT[A/G]CACTGAGGCCTTTCA | 57531 |
rs752897081 | snp | C/T | 2.87105e-05 | 0.00378872 | intron-variant | HACE1 | GRCh38.p7 | 6:104772100 | AAATACAAAATAATA[C/T]ATTATTAAGAATCTA | 57531 |
rs752935752 | snp | C/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861084 | GGCAACAAGGTGGTA[C/G]AGGTCAAAGTTTCAA | 57531 |
rs752944979 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699677 | ATGAAGGGATAGATG[G/T]CTAGATCTCTATCTC | 57531 |
rs752945609 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712624 | TAAAAATACAACAAT[G/T]AGCTAGGCGCCATGG | 57531 |
rs752962055 | snp | C/G | 0.000218126 | 0.0104411 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859544 | CAGCCCCGCGGCCAG[C/G]CTGGCCCCGCGACCC | 57531 |
rs752962543 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806568 | TAGGGGCTCAAGTGC[C/G]TCACCTGTAATTCAA | 57531 |
rs752986068 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793118 | TAAAAATACAAAAAA[G/T]TAGCCGGGCGTGGTG | 57531 |
rs753001792 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700567 | GGTCAGGTCCCAGCC[A/C]AGTCAGAGTGGAGGA | 57531 |
rs753013753 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688771 | TCTCTTCTGATCTCT[C/T]ATTTCAATCTCTTGC | 57531 |
rs753021756 | snp | A/G | 0.000131815 | 0.00811728 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771985 | GCTGCCTGTGGTTCA[A/G]CGCTAATCCCAAGAT | 57531 |
rs753022289 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845324 | AATCTTGTAAGTCAA[C/T]AGCTAAAATTCTCAT | 57531 |
rs753054834 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757057 | TATAAACAAAGAGGC[A/G]GGGAAGCTTGAACTG | 57531 |
rs753061720 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690634 | GAACAGAACAATAGA[G/T]CACAACAGGGAGTCC | 57531 |
rs753065978 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747828 | TTATTATTATCACTG[C/T]ATAAATCAAGACCAT | 57531 |
rs753067593 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851101 | TGTTTGTTTGTTTGT[C/T]GAGACAAGAGTCTTG | 57531 |
rs753074968 | in-del | -/GTTTTTTGTTGTT | 3.58584e-05 | 0.00423413 | intron-variant | HACE1 | GRCh38.p7 | 6:104750294 | ATTACATCAACTAGA[-/GTTTTTTGTTGTT]GTGTTACAACATAAG | 57531 |
rs753088992 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810982 | GTTAATAAGTACTTA[A/G]TCTAAAATTGAAGTA | 57531 |
rs753097742 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813897 | GTAACTGATAACCTC[A/G]AACAGAAAAGAAATT | 57531 |
rs753105828 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758087 | TTGGTGTGCCTGAGA[A/G]TGACGGGGAGAATGG | 57531 |
rs753107708 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744070 | GTTACTGACAATTCA[C/G]AGTAATAATTCCTTA | 57531 |
rs753113465 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716632 | ACCCGGGAGGCGGAG[A/G]TTGCAGTGAGCTGAG | 57531 |
rs753118772 | snp | C/T | 1.65074e-05 | 0.00287288 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744563 | GTATTCTGTATTTTT[C/T]ATCCAATCACTCACA | 57531 |
rs753139425 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant | HACE1 | GRCh38.p7 | 6:104833181 | CAATGTATCTGTGAA[A/G]CCATTTAGTTACTTA | 57531 |
rs753160751 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745583 | GTAGCTAGGACTACA[A/G]GCGCCTGCCACCATG | 57531 |
rs753161679 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725362 | GGGAGAAGTCCATCC[A/C]ACTATACAACTCATT | 57531 |
rs753164720 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704836 | GTTGCTTCAGATGTG[A/C]AATGTACTTGCTGGT | 57531 |
rs753175100 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692937 | CATATGACAATGAAG[-/A]TTAAATAGACCCCTC | 57531 |
rs753177784 | in-del | -/GA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823226 | ATCACCTGAGGTCAG[-/GA]GTTCAAGATCAGCCT | 57531 |
rs753209519 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723773 | TTTTTTTTATTTTAC[A/G]GAGACAGGGGTCTCA | 57531 |
rs753211059 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836147 | AAAGCAAGAAAAAAG[C/G]AAAAGGAATCCCCAG | 57531 |
rs753221632 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834262 | GACTCTATGCATAGT[G/T]TGTCTCTGGAGAAAA | 57531 |
rs753230765 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857609 | TCAACATTTGTTACA[C/T]GCATCCTATGAAATT | 57531 |
rs753287489 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697821 | CTCGGCTCAGTGCAA[C/T]CTCCATCTCCCGAGT | 57531 |
rs753293485 | snp | A/G | 1.64773e-05 | 0.00287026 | intron-variant | HACE1 | GRCh38.p7 | 6:104833019 | AAACACATGCAGCTT[A/G]AAGTCCTCATGGCTC | 57531 |
rs753317242 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785662 | TACTATATATAATCA[C/T]CCTTAACATTTACTG | 57531 |
rs753323750 | snp | C/G | | | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682590 | CCTGAGAACCCTAGC[C/G]TTTTACTAACCAAAT | 57531 |
rs753362703 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783926 | GTAGGCACTCAGTAC[A/G]TATTTCTTGAAGAAA | 57531 |
rs753365803 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825681 | CCAAGTGGCCAATGG[A/G]AAACATATATGGGGT | 57531 |
rs753370387 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768485 | AGCAAGGTAAAATGT[A/G]ATGTGTTTCTAAAGA | 57531 |
rs753372936 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750046 | TGTAGAATACTGTGT[A/G]TATAGGAAGACTGGC | 57531 |
rs753387866 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728919 | AGTAATGAAAAGAAA[C/T]GTGGTAAAATACATT | 57531 |
rs753388037 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801519 | TAACAGCGGATCTCT[C/T]GGCAGAAACTCTACA | 57531 |
rs753405224 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734163 | AAAAAAAAAAAAAAA[-/G]AAATCATCAAGTCTG | 57531 |
rs753408804 | snp | G/T | 1.7192e-05 | 0.00293185 | intron-variant | HACE1 | GRCh38.p7 | 6:104744618 | AGTAGCTCCTTGGGG[G/T]AAGAAGAAAAATATT | 57531 |
rs753416097 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767392 | TTTCTCCATCTTCAC[C/T]GCCACTTGCCTTACA | 57531 |
rs753418019 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750238 | TTTGTCTCATTTATA[-/C]CATTATTTCATTCAT | 57531 |
rs753418261 | in-del | -/G | 1.65712e-05 | 0.00287843 | intron-variant | HACE1 | GRCh38.p7 | 6:104784381 | AGTAAAGAGAGGAAA[-/G]GCTAGCAGGGTACTC | 57531 |
rs753442722 | snp | C/T | 1.75019e-05 | 0.00295815 | intron-variant | HACE1 | GRCh38.p7 | 6:104730443 | TATCTTAATACATTG[C/T]AATCATGAAAGAAAG | 57531 |
rs753470173 | snp | C/T | 1.71261e-05 | 0.00292622 | intron-variant | HACE1 | GRCh38.p7 | 6:104784212 | AATGGACAGGAAGAA[C/T]GAGTAGCATTAAGTG | 57531 |
rs753484137 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104683530 | ATCGTAGCAATGGTG[C/T]GTGGCTTATCAACTT | 57531 |
rs753491983 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723851 | CTGCCTTGGTTTCCC[A/C]AAATGCCAGGATTAC | 57531 |
rs753511544 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832538 | AGCTGGGACTACGGA[G/T]GCATGCCACCATACC | 57531 |
rs753527207 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826931 | AATAAGAAACTATTG[C/T]GGAGGAACCGCAAAA | 57531 |
rs753651448 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688356 | TTTTCCTTTGTAAAC[-/AC]ACACACACACACACA | 57531 |
rs753741977 | in-del | -/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849950 | CCACCACGCCCGTCC[-/TT]TTTTTTTTTTTTTTT | 57531 |
rs753744840 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749007 | CAAGCTATACATTTA[C/T]GATGTGTGTCCTTTT | 57531 |
rs753766627 | snp | A/G | 1.66081e-05 | 0.00288163 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851025 | AAAATGAGGAATCAA[A/G]TGTAAAAAAAGTTTT | 57531 |
rs753807497 | snp | C/T | 2.05565e-05 | 0.0032059 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852398 | AAAACAAAGAGTTCA[C/T]TTATCCCCTACTTTG | 57531 |
rs753831083 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840071 | ATCAATGTCCATGTC[C/T]TTACTGTAATATTAT | 57531 |
rs753873181 | snp | A/C | 1.67231e-05 | 0.00289159 | intron-variant | HACE1 | GRCh38.p7 | 6:104797060 | AGTTAAAAATACAAT[A/C]TTTTTAAAGTCTTTC | 57531 |
rs753922100 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700622 | TCTGAAGTAGGCGCT[A/G]CACAATTTAAACCAC | 57531 |
rs753949125 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730722 | TCATGTGGCTCTCTA[G/T]TGAAGTGGGGCTGAT | 57531 |
rs753978357 | snp | A/T | 1.697e-05 | 0.00291285 | intron-variant | HACE1 | GRCh38.p7 | 6:104784940 | TATCACTGCTTTTCA[A/T]CATCTATCAGAGAAA | 57531 |
rs753985740 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808526 | AACTAGGTTCTTTCC[C/T]CTGTATCTTAATACC | 57531 |
rs754007858 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778224 | CAGGTAAGCAAACTG[-/T]TGAGTTATCTACAAT | 57531 |
rs754023734 | in-del | -/TTTG | | | frameshift-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785248 | CTCTGTTGAGTCTCT[-/TTTG]TTTTTCATCAATTCT | 57531 |
rs754026335 | snp | C/T | 1.65252e-05 | 0.00287443 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730338 | AAGATTTGGAGTATA[C/T]GGCACAGCAGCGATT | 57531 |
rs754049034 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831123 | CAAGGTAGAAAATTA[C/T]AGCAAAGCAGAAATT | 57531 |
rs754055564 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734541 | TTTCTCAGTTTGAAC[G/T]CAAAATATAGAGCTC | 57531 |
rs754059627 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702064 | GAACATATACAGTGA[A/G]CGTTTCAATCTATTA | 57531 |
rs754068043 | snp | C/G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846817 | GTCACTTAGCAAACA[C/G/T]TGAGCACCTCTAAGT | 57531 |
rs754082375 | snp | A/T | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796940 | ACACCTGTACACATA[A/T]ATCCAGAGGAGTTAC | 57531 |
rs754107439 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841733 | AAAAATTAAAAGATT[A/C]AAAATATAAATACTA | 57531 |
rs754125919 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779339 | AAATTAAATAGGTTT[G/T]TTTTAAAAGATTCAA | 57531 |
rs754135714 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745633 | GTTTTAGTAGAGATG[A/C]GGTTTCACCGTGTTA | 57531 |
rs754142649 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758457 | CCAAACTAAGCTTCA[C/T]AAGTGAAAGAGAAAT | 57531 |
rs754162396 | snp | C/T | 1.77995e-05 | 0.00298319 | intron-variant | HACE1 | GRCh38.p7 | 6:104772114 | ATATTATTAAGAATC[C/T]ATATGCAGAAGAAAG | 57531 |
rs754178269 | snp | C/T | 5.03706e-05 | 0.00501824 | intron-variant | HACE1 | GRCh38.p7 | 6:104776849 | TTCAAGAAATAAAAT[C/T]AAGCATCAACAGAAA | 57531 |
rs754197351 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827949 | CTGATAAAAGTGAAA[-/T]TTATTTTTAAATAAA | 57531 |
rs754213401 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769572 | CAAATCATATAGGTT[G/T]AAAAATTAAGTGTTT | 57531 |
rs754216122 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853669 | AAGAAAATTTATAGT[A/G]AAGAACCCAGCAGAC | 57531 |
rs754238287 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782236 | CTCATGCCCATAATC[C/T]CAACACTTTGGGAGG | 57531 |
rs754245158 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725548 | ATTCTTTATACATAC[A/C]AATTAGTATTCTATT | 57531 |
rs754260004 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780701 | TAGATAACAACCATC[A/T]AAATCAGAAATTAAC | 57531 |
rs754279180 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685203 | CCACTGAGATATTAG[C/G]GTTGCTTATACCACA | 57531 |
rs754283080 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | HACE1 | GRCh38.p7 | 6:104791484 | TCTATCTTCCTAACA[A/C]TGCCATATACTTTTC | 57531 |
rs754292150 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712051 | AAAATGCTGAGATTA[C/T]AGATGTGAACTACCA | 57531 |
rs754334754 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764487 | TTTAAATGTTTCCTC[C/T]AGGGTTATCTGCCTC | 57531 |
rs754349113 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705585 | GCTTTAAACATGTTG[-/AC]AGTTTTGCCTCGAAC | 57531 |
rs754350187 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819597 | GGCAATCCTAAGCAG[A/T]AAGAAAAGTTGGAGG | 57531 |
rs754373075 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821866 | AATCTAGTAACTCCC[C/T]ACTAAATAACTATTA | 57531 |
rs754383071 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820621 | CATTAGAGAAATGCA[A/C]ATCAAAACCACAATG | 57531 |
rs754426067 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852696 | AGTATGGTAGCCCGC[A/G]CATCATCATCCAAAA | 57531 |
rs754432975 | snp | A/C/T | 4.96441e-05 | 0.00498197 | intron-variant | HACE1 | GRCh38.p7 | 6:104849119 | AATACAACTTAAGCC[A/C/T]CTTAAGAAAACTAAA | 57531 |
rs754434939 | in-del | -/TTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832380 | ACTATTTTCCTGTTT[-/TTT]TTTGTTGTTGTTGTT | 57531 |
rs754444508 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824910 | AACCCCGTCTCTACT[-/A]AAAAAAAAAAAAAAT | 57531 |
rs754448860 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725682 | ATATCCTTATATACA[C/T]GAACAAGTGGATGCC | 57531 |
rs754456998 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684959 | GGCCAAGTGAAATGC[-/T]TTAGACAAGGACATG | 57531 |
rs754473498 | in-del | -/TTTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751892 | GCCCTCTTCCTTTAT[-/TTTT]TTTTCTTTTTTTGGC | 57531 |
rs754491933 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745942 | TCTGTATGAGGTTGA[A/G]TTTTCTTCATATATT | 57531 |
rs754494339 | in-del | -/ATATA | 1.692e-05 | 0.00290856 | intron-variant | HACE1 | GRCh38.p7 | 6:104784532 | AGGCAAAAGTTTGTG[-/ATATA]ATATAGCGAACTTGA | 57531 |
rs754506121 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693818 | GTAAAAGAGAGGCGG[C/T]GTCACAGGAAACTGG | 57531 |
rs754508303 | snp | A/G | 4.95814e-05 | 0.00497878 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730371 | AAAGTTTTGCAATCC[A/G]CTTCCACCCATGATA | 57531 |
rs754515931 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836756 | TACGTGCAGACAACA[C/T]GACTGTCTATGTAGA | 57531 |
rs754586580 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853994 | CTGTAATAAAAGTTA[C/T]GTGAATGTGGTCTCT | 57531 |
rs754593149 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798614 | TAATCAGCTTTACCG[A/G]CATCAAGCAAGAAGT | 57531 |
rs754594811 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695172 | CTTAAAGTTTTAGGC[A/T]GATTTTTTACAAAAC | 57531 |
rs754595178 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764224 | CTGGGATTACAGGCA[C/T]GCACTACCATGCCCA | 57531 |
rs754601004 | snp | G/T | 1.79438e-05 | 0.00299526 | intron-variant | HACE1 | GRCh38.p7 | 6:104776875 | AGAAATATGTTATAT[G/T]GGGAAATTTTTTTCT | 57531 |
rs754622083 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781223 | GACTCATAGATTCCT[C/G]TTTATGTTGCCATCA | 57531 |
rs754711400 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764833 | CTTTCACTTGACATA[A/C]AGAATCCTTCAAAGT | 57531 |
rs754711725 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773209 | CTCATGCTATATACT[A/T]CTATTGTAAATGCCT | 57531 |
rs754727726 | snp | C/T | 1.65132e-05 | 0.00287339 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791637 | CTCTTCATTTGAGCA[C/T]CATAATTGCTAGAGA | 57531 |
rs754732990 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778644 | CCAAAAAAAAAAAAA[-/T]GTTTTAATTAGCCAA | 57531 |
rs754748394 | snp | A/G | 3.30677e-05 | 0.00406605 | intron-variant | HACE1 | GRCh38.p7 | 6:104849278 | AGACAGTTCAGATAC[A/G]TTCAACATACAGCCA | 57531 |
rs754761488 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707021 | TAACAGATAAAAAGC[A/G]TAAGTTACTAATTTT | 57531 |
rs754772999 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732882 | TTACTGATGAAATTC[A/T]TGAGCTTACTTTAAT | 57531 |
rs754806754 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844429 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 57531 |
rs754816505 | snp | C/T | 1.67013e-05 | 0.0028897 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750441 | ATGGCTCTTGTCATT[C/T]GAAGTTCAGTAACAA | 57531 |
rs754817630 | in-del | -/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727309 | ATATATATACACATG[-/TA]TATGTATACGAATAT | 57531 |
rs754825243 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718593 | CAAGAGGGGCTGAAG[-/T]TTTATCAAGTGTTTA | 57531 |
rs754829728 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777580 | TGATAAATTTGGTTA[-/TG]TCTCAGAACTTAATA | 57531 |
rs754854340 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685570 | ACCTACAAGCAAAAT[A/G]CCTTTCACATAATTT | 57531 |
rs754857768 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845265 | AGTAGTAAGCATAGC[C/G]AGGCTCATAGTAGCT | 57531 |
rs754875683 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813385 | CTATCTGTAAAGCAA[A/G]ACCCTATCTCTAAAA | 57531 |
rs754913277 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719998 | ACAGGTATGCGCCAC[C/G]ACGCCCGGCTAATTT | 57531 |
rs754930823 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811551 | ATGGCTGAGCAAATT[C/G]AACTTTTTGTAAGCT | 57531 |
rs754930840 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769984 | CAACTAACTTTTGTG[C/T]TGTGCTTTTCATTTT | 57531 |
rs754975348 | in-del | -/C | 4.96134e-05 | 0.00498039 | intron-variant | HACE1 | GRCh38.p7 | 6:104771150 | AGCAAACTATCAGGG[-/C]CAAGTTACAAACAAT | 57531 |
rs755004202 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846061 | GCCCAAAAAAGTGTT[G/T]ATGGTAGGGGTTGTT | 57531 |
rs755010577 | snp | C/G | 2.1959e-05 | 0.00331346 | intron-variant | HACE1 | GRCh38.p7 | 6:104744659 | TCTTTAGGGAAAAAA[C/G]TTATTATATTTAAGT | 57531 |
rs755021580 | in-del | -/A | 0.303347 | 0.246218 | intron-variant | HACE1 | GRCh38.p7 | 6:104785369 | TTAAACTACAGGATT[-/A]AAAAAAAAAAAAACA | 57531 |
rs755030858 | snp | C/T | 1.70017e-05 | 0.00291558 | intron-variant | HACE1 | GRCh38.p7 | 6:104784535 | CAAAAGTTTGTGATA[C/T]AATATAGCGAACTTG | 57531 |
rs755048247 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104828997 | GATTTATCATCCATG[A/C]CTCTTTGAAAAGAGC | 57531 |
rs755050421 | in-del | -/A | 0.099723 | 0.199792 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851029 | TGAGGAATCAAGTGT[-/A]AAAAAAGTTTTTAAA | 57531 |
rs755059473 | snp | A/T | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727831 | AATATATACATATAT[A/T]TATTTTTTTTGAGAC | 57531 |
rs755063992 | snp | A/G | 1.68835e-05 | 0.00290542 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796683 | AGGTCTTCATTCTGT[A/G]TCATTTGAATAATAG | 57531 |
rs755089947 | snp | C/T | 0.00210526 | 0.0323759 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859485 | CAGTTAGTTTTTCCA[C/T]CCGACCTTGACGCGG | 57531 |
rs755100527 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750487 | CCTGTTGAAAAAGAA[A/G]TTTTCATGATGACTT | 57531 |
rs755135755 | snp | A/G | 1.64811e-05 | 0.00287059 | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771973 | AAATATTGACCAGCT[A/G]CCTGTGGTTCAACGC | 57531 |
rs755141174 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710055 | CATTGCACCATTATC[C/T]GTAGTAGCCAAATAA | 57531 |
rs755158500 | in-del | -/ATACAGCG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716883 | AATGAAAATTAAAAT[-/ATACAGCG]ATACCAGTTGACACC | 57531 |
rs755222378 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751185 | CTTCTAGATCATTCT[C/T]ACTGAAATGTCTCAT | 57531 |
rs755250395 | snp | C/T | 2.26544e-05 | 0.00336552 | intron-variant | HACE1 | GRCh38.p7 | 6:104771422 | ACAGCAGTTATAGTC[C/T]GGTTTTGCCTTCCCT | 57531 |
rs755267381 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715572 | TGGATGAATTTTCCA[G/T]ATTGAATGACTCAAA | 57531 |
rs755275946 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843497 | TTCTATGACTCAAAG[A/G]TAACAGGATAAAACA | 57531 |
rs755288999 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755830 | ACATCAAAAAGCTAG[A/G]AAGATCTCAAGTTAA | 57531 |
rs755305409 | snp | C/T | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785234 | AAAATAGAAGTGATC[C/T]CTGTTGAGTCTCTTT | 57531 |
rs755305769 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714285 | ACATATGCCTGTAAC[A/G]AAAACTTTTGCCAAG | 57531 |
rs755343687 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702274 | GTGTCAGCACAATTC[C/T]ATTCGTTAATTTTGA | 57531 |
rs755360953 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689203 | CTGCAGAGACAGAAC[A/T]CTTCAATCCAGCAAA | 57531 |
rs755367639 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848600 | GTTAGCACTAAAAGG[A/G]GTAAACTACCCTAGT | 57531 |
rs755422139 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832803 | ACTCGTGAGGCTGAG[A/G]TGGAAGGATCATTTG | 57531 |
rs755432067 | snp | C/T | 0.000214311 | 0.0103494 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785137 | CCTTGTGCCAGTGGA[C/T]AGATTTTCATAGCTC | 57531 |
rs755432702 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731418 | AGCCTAAACAGTCTA[-/G]GAAAAAAAAGAACAA | 57531 |
rs755445037 | snp | A/T | 0.000361958 | 0.013448 | intron-variant | HACE1 | GRCh38.p7 | 6:104811275 | ATATATATATATATG[A/T]GCATATATAGCATCT | 57531 |
rs755450390 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850717 | CAAGAGGGACATGAG[A/T]TTTACATACAATCCC | 57531 |
rs755464650 | snp | A/G | 1.65679e-05 | 0.00287814 | intron-variant | HACE1 | GRCh38.p7 | 6:104811441 | AGAGGAATCAAACAA[A/G]AGATACAATTACCAC | 57531 |
rs755492842 | in-del | -/GT | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852230 | TGTGTGTGTGTGTGC[-/GT]GCGCGTGCGCGTGCA | 57531 |
rs755494303 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722481 | CAATTTAATGAATGA[A/C]TGCCACGCATTAGCC | 57531 |
rs755511573 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817385 | AAAAGTGTGTGGCAC[A/T]TCCCCCTTGCACACA | 57531 |
rs755557549 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727466 | CACACATATATGAAT[-/AC]ACACACACATATGTA | 57531 |
rs755564263 | snp | A/T | 1.64749e-05 | 0.00287005 | intron-variant | HACE1 | GRCh38.p7 | 6:104833033 | TAAAGTCCTCATGGC[A/T]CAACTTACCGTCTTG | 57531 |
rs755569583 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783428 | ACCATTTATTGAGCA[C/T]ATATCACAGTCATTC | 57531 |
rs755584175 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814765 | TCATGAGAGCTCATG[G/T]TTTAAAAGTGTGTGG | 57531 |
rs755586468 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713550 | AACTTACCTGTGACC[G/T]CACAGCTAGTAAATA | 57531 |
rs755590443 | in-del | -/TAGG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818868 | AAACTCTTAAAAAAC[-/TAGG]TATTGAAGGAACATA | 57531 |
rs755594445 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776378 | ATTAATTTATGAAAT[A/C]AAACATTTAATTCAA | 57531 |
rs755615218 | snp | A/G | 3.31005e-05 | 0.00406807 | intron-variant | HACE1 | GRCh38.p7 | 6:104744277 | TTTCAGAGCAATTGT[A/G]GACTTCTCAATACCA | 57531 |
rs755639786 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748781 | GATTCCCACAAACAA[A/T]AACTTGAGCTAAGAA | 57531 |
rs755660224 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716859 | GCTTAACTTTTTAAT[A/G]ATTGGGAAAATGAAA | 57531 |
rs755691095 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728683 | TACTTCCTGTTCAAA[C/T]ATATGCTGTAACTAT | 57531 |
rs755702718 | in-del | -/AA | 3.56834e-05 | 0.00422379 | intron-variant | HACE1 | GRCh38.p7 | 6:104750309 | TTTTTTGTTGTTGTG[-/AA]TTACAACATAAGAAC | 57531 |
rs755725353 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825581 | GCTTCCCACAACCAA[G/T]CAGATGTTTGCATAG | 57531 |
rs755746299 | in-del | -/TTTA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696848 | CTTGCACAAAATGTC[-/TTTA]TTTGTCTCTAGACCT | 57531 |
rs755754567 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766338 | ATGTTGTATGCTTGT[G/T]TTCTGAGTGCCCCCT | 57531 |
rs755772070 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818087 | AGACATAGTATTCAC[-/AT]GTCTATTTAAATTTA | 57531 |
rs755781815 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783893 | GTTCTGTTGTTTTTG[C/T]ACAGACCTCTGTACA | 57531 |
rs755793999 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808631 | TATTATATCTAGTAA[C/T]ACTTATCAACCAATA | 57531 |
rs755800735 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798314 | GATTTCTCAGAAACT[A/T]AAAAAACAAAACACT | 57531 |
rs755805919 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754164 | AGAACCTCAGAGCTT[A/G]AAGACTGTCCAAAAT | 57531 |
rs755806085 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767224 | AATTAATGATAATGA[G/T]GTTGATGAAGAGTAT | 57531 |
rs755820095 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786101 | GCACTTTGGGAGGCC[A/G]AGGTGGGTAGATCAC | 57531 |
rs755825485 | snp | A/T | 3.57705e-05 | 0.00422894 | intron-variant | HACE1 | GRCh38.p7 | 6:104730457 | GTAATCATGAAAGAA[A/T]GATATTTGTGACAGA | 57531 |
rs755838916 | in-del | -/C | | | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104780361 | AGAGTACCTGCATTT[-/C]CATAAATAATTCACA | 57531 |
rs755859387 | in-del | -/CCTCCGCGAT | 0.000168364 | 0.00917354 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859653 | CCATCCTCGGCGCGC[-/CCTCCGCGAT]CCTCCGCGATCCTCC | 57531 |
rs755860416 | snp | C/T | 1.66355e-05 | 0.002884 | intron-variant | HACE1 | GRCh38.p7 | 6:104777118 | AATAGAATCTAAATA[C/T]GTAGCATTGGTTAAT | 57531 |
rs755877890 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795622 | CAACTTCAGCAAGGC[C/T]TGTTAGAATCTTTAG | 57531 |
rs755881968 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719310 | TTTCATGACTAAATG[C/T]TTTAAAAAAGATTTC | 57531 |
rs755900153 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686502 | CTCACCAAATCTATT[-/A]AAAAAAAAAAAAAAA | 57531 |
rs755908767 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727269 | CATGTATGTATACGA[-/AT]ATATATACACATATA | 57531 |
rs755937411 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720480 | TTCTAGGACCCCCAA[G/T]GACCTCAAAATCTGT | 57531 |
rs755939100 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706437 | GTGAATTTCTGAATT[C/G]TGATAATTTAAAATA | 57531 |
rs755959298 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687236 | CTCCAGTGCTTCAGG[C/G]TGGAAGTCACCAAAC | 57531 |
rs755960410 | snp | A/T | 0.000112026 | 0.00748334 | intron-variant | HACE1 | GRCh38.p7 | 6:104795737 | GTAATCCATTAAATC[A/T]TATCAAACAATTAAG | 57531 |
rs755974163 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854262 | GGAGACTAAAGAAAC[A/G]TAACTAAAGGCAATG | 57531 |
rs756004805 | snp | C/T | 1.65457e-05 | 0.00287621 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851008 | AGACCTATGCCAAAA[C/T]AAAAATGAGGAATCA | 57531 |
rs756015921 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798737 | TCCATTCTTTAACAC[G/T]CCTAAAAATAGAGGC | 57531 |
rs756020604 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813499 | CCCCTGGGAACATGA[A/G]GCAACTTTTTTATTT | 57531 |
rs756023772 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694215 | CTGTCATTTGCAACA[A/G]CATGAATGGAACTGG | 57531 |
rs756044478 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831984 | AGAAGAGAAGAGAGG[-/A]AGGAAGGAAGGAAGG | 57531 |
rs756048314 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842372 | GCACTTTGGGAGGCC[A/G]GCGGGTGGATCACCT | 57531 |
rs756052044 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772661 | TCCACAAGGTAACCA[A/C]GTCTTTCTAATGGCA | 57531 |
rs756055603 | snp | C/T | 1.65963e-05 | 0.0028806 | intron-variant | HACE1 | GRCh38.p7 | 6:104849294 | TTCAACATACAGCCA[C/T]ACTTGATGTAGTTCA | 57531 |
rs756064283 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759889 | CTAATCCTACAGAAA[C/T]ACAAACTACCATCAG | 57531 |
rs756065707 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838400 | GAACCCAGAAATAAA[A/T]CCACACATCTACAGT | 57531 |
rs756065744 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855561 | TCTTAATATGTAAAA[C/T]AGACTCTGTTTTATC | 57531 |
rs756067127 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770072 | ACTGAGTTCGAAGAA[C/T]TGTTAAACATAACCC | 57531 |
rs756092826 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746453 | GGTTTGGGTTTGGAG[C/G]CTGGGAAACATAGGC | 57531 |
rs756100921 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704324 | GAAAGTCGGCATTGG[-/A]AAAACATACATCCTC | 57531 |
rs756159609 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752909 | GCCAATTAAGTAATT[A/C]AAATGTGGATGGCAG | 57531 |
rs756160487 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746978 | ACTTCATGAATATCA[A/C]ATTAATTGTTACGAT | 57531 |
rs756182941 | snp | A/C | 1.6507e-05 | 0.00287284 | intron-variant | HACE1 | GRCh38.p7 | 6:104771170 | TTACAAACAATGGTT[A/C]AGGTAAAAACTGAAA | 57531 |
rs756191472 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711937 | GGCCACCACCCCTGG[C/T]TAATTTACTTATTTT | 57531 |
rs756207103 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104740415 | ACAAAATTGATAGAC[C/T]GCTAGCAAGACTAAA | 57531 |
rs756218512 | snp | G/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861132 | GGCGCAGTGGCTCAT[G/T]CCTGTAATCCCAGCA | 57531 |
rs756221853 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764329 | GTGATCCACTCACCT[C/T]GGCCTCCCAAAGTGC | 57531 |
rs756232056 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698711 | ACTGGATCAGATCAA[A/G]GGCTTCCCCAGCTTA | 57531 |
rs756240109 | snp | C/T | 1.6534e-05 | 0.00287519 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796934 | AAAAACACACCTGTA[C/T]ACATAAATCCAGAGG | 57531 |
rs756240153 | snp | A/C/G | 8.28842e-05 | 0.00643709 | intron-variant | HACE1 | GRCh38.p7 | 6:104784377 | TGTAAGTAAAGAGAG[A/C/G]AAAGGCTAGCAGGGT | 57531 |
rs756242631 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699735 | AGAAAATAGACAGTG[A/G]TAAAGTTGATATTAA | 57531 |
rs756266267 | snp | A/G | 1.65094e-05 | 0.00287305 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729694 | CATAGCTGCCACAAT[A/G]TAGTGCCACAAGAAG | 57531 |
rs756300692 | snp | C/T | 0.00020536 | 0.010131 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859549 | CCGCGGCCAGCCTGG[C/T]CCCGCGACCCGGCTC | 57531 |
rs756337701 | in-del | -/AA | 1.65124e-05 | 0.00287331 | intron-variant | HACE1 | GRCh38.p7 | 6:104849260 | AACTAAAACAATATT[-/AA]AAGACAGTTCAGATA | 57531 |
rs756338941 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726582 | GCTGTGTTCAGCAGA[-/T]TATTTCCAAGCTGGG | 57531 |
rs756388935 | snp | G/T | 1.77215e-05 | 0.00297665 | intron-variant | HACE1 | GRCh38.p7 | 6:104772109 | ATAATATATTATTAA[G/T]AATCTATATGCAGAA | 57531 |
rs756441971 | snp | A/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771987 | TGCCTGTGGTTCAAC[A/G]CTAATCCCAAGATCT | 57531 |
rs756443416 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723818 | CTGCTCTTGAACTCC[C/T]GGCCTTCAGCAATCC | 57531 |
rs756484254 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692355 | TGTACATTTTAGGAT[A/C]AAGGATGGAGGAAAA | 57531 |
rs756490315 | snp | C/T | 0.000356316 | 0.0133428 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858455 | TCTGTAATCCCAACA[C/T]TTTGGGGGGAGCAGG | 57531 |
rs756498110 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690850 | ATGAAGCCATTAAAA[G/T]TGCTAAAAGGAAATA | 57531 |
rs756554381 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855781 | AAGTCACCCCATAAT[-/A]AAGTCATAAAAAACA | 57531 |
rs756562179 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818543 | CATTCTATAAAGCCA[G/T]CATCATCCTGACACC | 57531 |
rs756615777 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802246 | CATACAAAGAGACTT[A/T]GACTCCCACACAATA | 57531 |
rs756630910 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836438 | GAAATAAAGGCCTGG[C/T]GCGGTGGCTCACACC | 57531 |
rs756644697 | in-del | -/TCT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785818 | TCAATTAAACAAATG[-/TCT]TTTTTCAATTAAAAA | 57531 |
rs756648178 | snp | A/C | 1.6473e-05 | 0.00286988 | intron-variant | HACE1 | GRCh38.p7 | 6:104833183 | ATGTATCTGTGAAGC[A/C]ATTTAGTTACTTAAC | 57531 |
rs756681842 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779157 | TGAGAATTTGCTTAG[C/T]AAATGATACAGACGG | 57531 |
rs756756443 | snp | A/G | | | downstream-variant-500B | HACE1 | GRCh38.p7 | 6:104682642 | TCTGTCTCTAGCTTA[A/G]GCACTTCCACTCAAT | 57531 |
rs756758401 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842322 | TAAAAAAAGGTTTTA[C/T]TGGCCGGGCACAGCA | 57531 |
rs756800473 | snp | A/T | 7.67195e-05 | 0.00619305 | intron-variant | HACE1 | GRCh38.p7 | 6:104785368 | TCTTAAACTACAGGA[A/T]TAAAAAAAAAAAAAC | 57531 |
rs756806753 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716670 | CACTGCACTCCAGCC[C/T]GGGCAACAGATCAAG | 57531 |
rs756807307 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825686 | TGGCCAATGGGAAAC[A/G]TATATGGGGTATTTA | 57531 |
rs756833997 | snp | A/G | 1.72961e-05 | 0.00294071 | intron-variant | HACE1 | GRCh38.p7 | 6:104744620 | TAGCTCCTTGGGGGA[A/G]GAAGAAAAATATTTC | 57531 |
rs756861682 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715891 | ACTAAGCTTAGCACC[C/T]GGGTGATGAAATAAT | 57531 |
rs756889299 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755964 | ACAGAGACACAAAAC[A/C]ACCCTTCAAAAAATT | 57531 |
rs756900438 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849085 | ATCAAACGAAGGCAA[A/G]GTGCCTTGAATAACT | 57531 |
rs756914581 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703841 | TTATAATGGGCTGGG[C/T]GCGGTGGCTCATGCT | 57531 |
rs756927008 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant | HACE1 | GRCh38.p7 | 6:104833209 | TTAACATTTGTGTAA[C/T]AGTGTTTTATATAAA | 57531 |
rs756933590 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825294 | AGCGACCTTTGCAAA[-/C]CCCCCACCTCTTTGC | 57531 |
rs756954721 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843952 | ACATCTGCCTCCCGG[C/G]TTCAAGTGATTCTCC | 57531 |
rs756964139 | in-del | -/A | 0.000945188 | 0.0217187 | intron-variant | HACE1 | GRCh38.p7 | 6:104796880 | AATTTTTACCATTCC[-/A]GTTTCTATTATAAAG | 57531 |
rs756968525 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707815 | CCACTTTCCAAAAGG[C/T]TTCATCTCTTAATAC | 57531 |
rs756990531 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851269 | TTGTATTTTTAGTAG[A/G]GAGGGGGTTTCACCA | 57531 |
rs757001610 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724868 | GCTTTTTACCAGTTC[A/G]TACACTAATCTATGC | 57531 |
rs757001640 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760596 | CAATATCATACTGAA[C/T]AGGGAAAAAAACGGG | 57531 |
rs757065112 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695828 | GCTGGGATTACAGGC[A/G]TGCCATTCTCCTGCC | 57531 |
rs757067168 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851378 | TGAGCCACCCCACCC[A/G]GCCTAGCTATTCTTC | 57531 |
rs757084666 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857370 | CATTTTTGCCTATGT[A/G]GAAAAGTTTTACTTT | 57531 |
rs757094836 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821485 | GAAATTTTAACAAAA[C/T]ATACTATTTATAAAA | 57531 |
rs757097017 | snp | C/T | 1.70676e-05 | 0.00292122 | splice-donor-variant | HACE1 | GRCh38.p7 | 6:104796654 | ATCACAAATACAATA[C/T]CATGTTTTCTCGGAG | 57531 |
rs757107912 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732708 | ATGATATGCATTTAC[-/AC]ACACACACACAAATG | 57531 |
rs757121448 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726182 | CTGGGCAACAGAGTT[-/A]AAAAAAAAAAAAAAA | 57531 |
rs757132615 | snp | G/T | 1.67089e-05 | 0.00289035 | intron-variant | HACE1 | GRCh38.p7 | 6:104777148 | TTTTACATATTAAAA[G/T]TTATAATAAAAAGCA | 57531 |
rs757141556 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855897 | TAAGGTTCACAATGG[C/T]TGTACTTGTAAGGTT | 57531 |
rs757148297 | snp | A/T | 2.10471e-05 | 0.00324393 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852402 | CAAAGAGTTCATTTA[A/T]CCCCTACTTTGTGCA | 57531 |
rs757162332 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783945 | TTCTTGAAGAAAACT[C/T]ACTCCTCATATTAAA | 57531 |
rs757171684 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799216 | AACAGGAGGCCATTA[G/T]CCTGAGACTGTCACT | 57531 |
rs757191364 | in-del | -/TAAC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769587 | TAAAAATTAAGTGTT[-/TAAC]TATTATAATCTTCTA | 57531 |
rs757198782 | in-del | -/A | 3.31439e-05 | 0.00407073 | intron-variant | HACE1 | GRCh38.p7 | 6:104843306 | CTTCTGCCTGAAAAG[-/A]AAAAAAGAGTCATGG | 57531 |
rs757214008 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824217 | TCATTCTCAAATAAT[A/C]CAGAGTAACAATATT | 57531 |
rs757215689 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783099 | ACAAAATTTCTGCTG[C/T]AATACTGCAGTTTTA | 57531 |
rs757215955 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841016 | TTCCCAGCTACTCGG[A/G]AGGCTGAGGCAGGAG | 57531 |
rs757221111 | snp | C/T | 1.64958e-05 | 0.00287187 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795651 | AGGTACTGGCTTTCA[C/T]TTTGCTGAGACAAAT | 57531 |
rs757225746 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777411 | CCTTTTCTACAAATA[A/C]TCATTCTTAGATCTT | 57531 |
rs757248867 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699098 | CCAAAAGTTTGAATT[A/T]GAAGCATATCTTATT | 57531 |
rs757259655 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800766 | GATGGAGAGAAACCA[C/G]AGCAGAAAAGCCGAA | 57531 |
rs757288919 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729040 | TGCAAATAATTCATA[C/T]AATATAGCGTAAGCT | 57531 |
rs757296063 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727585 | CGTATGTATATGAAT[-/AC]ACACACACGTATGTA | 57531 |
rs757322269 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794858 | TGCAGTGAGCCAAGA[C/T]TGTGCTGCCTGGGTA | 57531 |
rs757323758 | snp | C/T | 1.64917e-05 | 0.00287151 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785076 | TAACATCCTGACAAT[C/T]TGCACTGGCTTCCTG | 57531 |
rs757359456 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753860 | TTCTCCTCCAAATGA[A/C]CGCAACACCTCTCCA | 57531 |
rs757365960 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831252 | AATAACAGGAAAGCA[C/T]TGTCATAAAACAAAT | 57531 |
rs757369895 | snp | A/G | 1.70513e-05 | 0.00291982 | intron-variant | HACE1 | GRCh38.p7 | 6:104784950 | TTTCATCATCTATCA[A/G]AGAAAAAAAAAATAA | 57531 |
rs757383847 | snp | C/T | 8.4064e-05 | 0.00648266 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750463 | CAGTAACAAGCTGGA[C/T]GTACTCCGCCTGTTG | 57531 |
rs757405232 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687423 | TTCATTGACTTTACT[C/T]GCAAATCTCCACAGA | 57531 |
rs757414835 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791159 | CTGTGCATTTTATTT[C/T]CTTACTAATAAGAAA | 57531 |
rs757421072 | snp | A/G | 1.65045e-05 | 0.00287263 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796948 | ACACATAAATCCAGA[A/G]GAGTTACTCCATTTT | 57531 |
rs757422416 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734584 | ATGTTGAAAGGTGAA[A/T]TCTTCAATCCAAGGG | 57531 |
rs757448304 | snp | G/T | 1.67452e-05 | 0.0028935 | intron-variant | HACE1 | GRCh38.p7 | 6:104797062 | TTAAAAATACAATCT[G/T]TTTAAAGTCTTTCTC | 57531 |
rs757461173 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772808 | TCTAGAATAGGCAAA[C/T]TTATAGATAGGTAAA | 57531 |
rs757467953 | snp | A/C | 1.65239e-05 | 0.00287431 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730341 | ATTTGGAGTATATGG[A/C]ACAGCAGCGATTGTA | 57531 |
rs757476097 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720551 | ATATGGACTTGGTGC[A/G]CAGCAAATGCACTGC | 57531 |
rs757542782 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848744 | GCAAAATGAGCCATG[C/G]AGTTAGGAGTGGCAA | 57531 |
rs757563414 | snp | G/T | | | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104780414 | TCCTCTTAATAGCAT[G/T]TGTACAGCAATACAA | 57531 |
rs757563583 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761346 | GTACTGGTACCAAAA[C/T]GATATATAGAACAAT | 57531 |
rs757576956 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857979 | AAAAAAAAAAAGGAT[C/G]TTTTCTAAACACAAA | 57531 |
rs757646288 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699828 | TACAGCAGTAGGCGT[A/G]AGTATGAATAAAGGG | 57531 |
rs757651656 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788982 | TAGCATTAGAGTACC[C/T]TGTTAATGAAATGGA | 57531 |
rs757657198 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753516 | TAAGTACCTACCCCC[-/T]GGGACAGAGCTTCCA | 57531 |
rs757658153 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697449 | TTTCTCTACTGGGAA[-/G]GCCCCTGACATCTGA | 57531 |
rs757671478 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695878 | GGACTACAGGCGCCC[A/G]CCACCACACCCGGGT | 57531 |
rs757675835 | snp | A/C | 0.000199568 | 0.00998719 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859554 | GCCAGCCTGGCCCCG[A/C]GACCCGGCTCACCCT | 57531 |
rs757680738 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694022 | CTAGCTATATACCCC[A/C]AAGAAAGGAAATCAG | 57531 |
rs757687596 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764645 | ATCTTCATCATCACT[A/G]TTATCACCATCACCT | 57531 |
rs757696330 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861432 | GAAGAAAGAAATACC[A/G]GACGTTATGGACCAG | 57531 |
rs757720567 | snp | C/T | 3.66993e-05 | 0.00428349 | intron-variant | HACE1 | GRCh38.p7 | 6:104772116 | ATTATTAAGAATCTA[C/T]ATGCAGAAGAAAGAT | 57531 |
rs757775202 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772001 | CGCTAATCCCAAGAT[C/T]TGCCCAGCAAACCGA | 57531 |
rs757853931 | in-del | -/GAAA | 1.76499e-05 | 0.00297063 | intron-variant | HACE1 | GRCh38.p7 | 6:104730450 | ATACATTGTAATCAT[-/GAAA]GAAAGATATTTGTGA | 57531 |
rs757856739 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744460 | GTGCTGAAAAGCTTA[C/T]AAAATTAAACGGCAA | 57531 |
rs757889187 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834253 | ATAATCCTGGACTCT[A/G]TGCATAGTTTGTCTC | 57531 |
rs757903278 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant | HACE1 | GRCh38.p7 | 6:104791490 | TTCCTAACAATGCCA[C/T]ATACTTTTCTCACCT | 57531 |
rs757906927 | in-del | -/CATG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727438 | ATATGAATACACACA[-/CATG]TATATGAATACACAC | 57531 |
rs757943201 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758616 | AACTGTAAAGACCAT[C/T]GACGCTATGAAGAAA | 57531 |
rs757944180 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769552 | AAAATATTTTCACTC[A/G]CTGGCAAATCATATA | 57531 |
rs757948319 | snp | A/T | 1.6501e-05 | 0.00287232 | intron-variant | HACE1 | GRCh38.p7 | 6:104776722 | TTGCAGAAAAAGTCA[A/T]CTAGACTGTACAACT | 57531 |
rs757950354 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704000 | TAATCCCAGCTACTC[A/G]GGAGTCTGAGGCACA | 57531 |
rs757950761 | snp | C/T | 4.94262e-05 | 0.00497098 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791613 | AACATTCTCACAATC[C/T]TTAAAAGGCTCTTCA | 57531 |
rs757956007 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811187 | AAATACACAGAAACG[C/T]GTGTGTCTAGAAATA | 57531 |
rs757963374 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739248 | CAAGACTAGGAAGAA[A/C]CTATATCAACTAACG | 57531 |
rs757978093 | in-del | -/GT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693031 | AAGAGTGGTGTGTGT[-/GT]GTGTGTGTGTGTGTG | 57531 |
rs758002774 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852539 | GAATTTACGATAGTG[A/C]AGAATCTTTCATCCC | 57531 |
rs758013293 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794942 | TGTGTGTGTGTGTGT[A/G]TACATATATACAATT | 57531 |
rs758048388 | snp | A/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851363 | CTGGGATTACAGGCG[A/T]GAGCCACCCCACCCG | 57531 |
rs758053144 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766894 | GCCCCTGCACAAGCA[A/G]GCTTGAAATTTACAG | 57531 |
rs758054766 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692524 | AATGAAGAATTTTGC[A/G]CTGAAATTCAGTAGG | 57531 |
rs758068376 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797140 | TAAAAATTAAGACAA[A/G]AGAATATGAAATACA | 57531 |
rs758117312 | snp | A/C | 1.67231e-05 | 0.00289159 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750394 | GAATGAACATATGAA[A/C]GCCCTGTAAAAAAGC | 57531 |
rs758141431 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745720 | TGCTGGGATTACAGG[C/T]GTGAACCACCGTGCC | 57531 |
rs758148777 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836614 | GCTACTAGGGTGGCT[A/G]AGGCAGGAGAATTGC | 57531 |
rs758157377 | snp | C/T | 1.89363e-05 | 0.00307698 | intron-variant | HACE1 | GRCh38.p7 | 6:104744642 | AAATATTTCAATAAT[C/T]TTCTTTAGGGAAAAA | 57531 |
rs758212523 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696869 | TGTCTCTAGACCTGG[A/C]TGTCATTTGGTTCCA | 57531 |
rs758221562 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846355 | CAAAACACAACCTAA[C/G]AACACACAATAATTT | 57531 |
rs758229584 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732855 | TCTATCTGGGAAGTC[A/G]TCTGGTTTGGTTTAC | 57531 |
rs758232213 | snp | C/T | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104682787 | CCGCCTTTTTAGGGT[C/T]GAGTCATGGGTCGTC | 57531 |
rs758253554 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784952 | CATCATCTATCAGAG[-/A]AAAAAAAAAATAATA | 57531 |
rs758260163 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698040 | CAGCAAGATAGATGT[A/C]GTATTAGAAAAGTAA | 57531 |
rs758261432 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709941 | CAAAAAAGTTAAATA[C/T]AGGGTTACTACTAAT | 57531 |
rs758282605 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841386 | ATTCAACCATCATGC[C/T]TAAACTGGTTAGTGT | 57531 |
rs758301162 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825864 | CCAAGAATCTGGACA[C/G]CCTCCACCAGTTTCT | 57531 |
rs758327385 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717534 | TGTCCCCCTATGAAC[-/AT]GTGTAAAATTCCTCT | 57531 |
rs758332319 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753027 | CTTGAAAGAGCTGTG[-/T]TTAATGGAAAAATCT | 57531 |
rs758339954 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724398 | ATATTATCCCTCCTA[A/G]ACTATAAGCAGTTTT | 57531 |
rs758360393 | in-del | -/AA | 1.84211e-05 | 0.00303483 | intron-variant | HACE1 | GRCh38.p7 | 6:104795703 | AAATTTTTTACAAAT[-/AA]AAAAATGTGATTACA | 57531 |
rs758430306 | snp | A/G | 0.000182665 | 0.00955506 | intron-variant | HACE1 | GRCh38.p7 | 6:104780335 | GGTACATTTTTGTAT[A/G]TAAACTTTCTAGAGT | 57531 |
rs758436222 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775488 | CTAATGATTCCACAC[C/T]AAATCTGTTTTTCAG | 57531 |
rs758457880 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768655 | AAAAAATGAAAGCTG[A/G]GAATGTATAACATTA | 57531 |
rs758489644 | snp | A/G | 1.6623e-05 | 0.00288292 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851027 | AATGAGGAATCAAGT[A/G]TAAAAAAAGTTTTTA | 57531 |
rs758491182 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708691 | AAGGCTACAGTAATC[A/G]AGACAATACAAGACT | 57531 |
rs758500369 | in-del | -/GGGTGACA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831560 | ACTGCACTCCAGCCT[-/GGGTGACA]GAGCGAGCCTCCGTC | 57531 |
rs758523679 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745685 | TGACCTTGTGATCCA[-/C]CCACCTCAGCCTCCA | 57531 |
rs758525627 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721172 | CAACATGGTGACACC[C/T]GGTCTCTACTAAAAA | 57531 |
rs758531683 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735678 | GTGCTGATAAAAGGA[A/G]TACATTCTCTCATTC | 57531 |
rs758534543 | snp | C/T | 1.93325e-05 | 0.003109 | intron-variant | HACE1 | GRCh38.p7 | 6:104771398 | GGAATACCTAAAAAA[C/T]GCAAACATACAGCAG | 57531 |
rs758536260 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817190 | TATTTTCCAATACGA[A/G]AAGAACATGAGATTT | 57531 |
rs758583351 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776137 | AATTATCTGTTTTAT[A/G]TGGTTCAATAAGAGC | 57531 |
rs758617427 | snp | A/G | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785118 | GAGCATCTGGTTTAG[A/G]TTCCCTTGTGCCAGT | 57531 |
rs758654132 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766013 | ATGCTCCCTCTTTTC[C/T]CTGTCACTGTTACCC | 57531 |
rs758654920 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856085 | GGACAGAATACAATT[G/T]GTTGCCAGATACTTC | 57531 |
rs758662808 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761558 | CAACTCAAGACGGAT[C/G]AAAGACTTAAACGTA | 57531 |
rs758705376 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754000 | AATGCAAAGAAGCTA[A/C]GAATCACAATAAAAC | 57531 |
rs758711525 | snp | C/G | 5.55078e-05 | 0.0052679 | intron-variant | HACE1 | GRCh38.p7 | 6:104730467 | AAGAAAGATATTTGT[C/G]ACAGATAAATTTCAA | 57531 |
rs758714129 | in-del | -/T | 0.000161567 | 0.00898651 | intron-variant | HACE1 | GRCh38.p7 | 6:104750294 | TTACATCAACTAGAG[-/T]TTTTTTGTTGTTGTG | 57531 |
rs758717518 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783728 | TCAAAGCCTTTTAAC[A/G]TGCTGCCAATGTGAT | 57531 |
rs758742710 | snp | G/T | 1.68835e-05 | 0.00290542 | intron-variant | HACE1 | GRCh38.p7 | 6:104797073 | ATCTTTTTAAAGTCT[G/T]TCTCTATGAATTATG | 57531 |
rs758781571 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700863 | ATTTTAAATTCCTGA[A/G]AGCAACTCCTTCCCC | 57531 |
rs758799425 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789966 | AATTTTACAAAGACA[A/G]TAAGTCGTCACTCCT | 57531 |
rs758832664 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702202 | GGGACTTAGGGGCAG[A/G]AGCTTTGCAATTAAA | 57531 |
rs758865323 | snp | A/C/T | 3.29811e-05 | 0.00406075 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796971 | TCCATTTTTATCTGG[A/C/T]AGATATTTGGCTCCT | 57531 |
rs758872457 | snp | C/T | 1.65181e-05 | 0.00287381 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730352 | ATGGCACAGCAGCGA[C/T]TGTAAAGTTTTGCAA | 57531 |
rs758884328 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807348 | CTCTTTTATATGGCT[A/G]CTTTGATTTTGAATA | 57531 |
rs758927632 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831502 | AGGCACAAGGATCAC[C/T]TAAACCTGGGAGGCA | 57531 |
rs758927930 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752620 | TGAAGCATGAAAATA[A/C]AAGATTTATGACTTG | 57531 |
rs758931446 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751892 | AGCCCTCTTCCTTTA[-/T]TTTTCTTTTTTTGGC | 57531 |
rs758966034 | snp | C/T | 4.94214e-05 | 0.00497074 | intron-variant | HACE1 | GRCh38.p7 | 6:104791458 | GCTTTGTCAAATTCA[C/T]CTCTTTTACGTCTAT | 57531 |
rs758998672 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692940 | ATGACAATGAAGATT[A/T]AATAGACCCCTCAGC | 57531 |
rs759011050 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755401 | ACAAAGATATTCTGG[A/T]CCTGAACTCAGCTCT | 57531 |
rs759017961 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857629 | CCTATGAAATTCTGA[A/C]GTCATTAAGCCTATT | 57531 |
rs759018367 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720065 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACATCGT | 57531 |
rs759030279 | snp | C/T | 8.60252e-05 | 0.00655784 | intron-variant | HACE1 | GRCh38.p7 | 6:104776867 | GCATCAACAGAAATA[C/T]GTTATATTGGGAAAT | 57531 |
rs759037515 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815056 | TTGAAAATGTGGAAG[C/T]GACTTTGGAACTGGG | 57531 |
rs759048154 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708181 | AAATCCTAAGGAATT[C/T]ACAAAAAGCTATTGG | 57531 |
rs759055641 | snp | C/T | 2.04397e-05 | 0.00319678 | intron-variant | HACE1 | GRCh38.p7 | 6:104796619 | GAGCAGGAATAAAGC[C/T]TCTTCATTTACAAGC | 57531 |
rs759056324 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855435 | GCAACAGAGCGAGAC[C/T]CCATCTCGGAAAAAA | 57531 |
rs759063208 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832346 | TGCAAATTACAAATA[C/T]TTTGAACAGATATAA | 57531 |
rs759096676 | in-del | -/TAAAATAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743837 | CAAATATTAAAATAT[-/TAAAATAA]TATACAAATATTAAA | 57531 |
rs759111224 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707120 | AATACCAATTCTTTG[C/T]AGTTTTCTAAAAAAA | 57531 |
rs759136842 | snp | C/G | 1.67116e-05 | 0.0028906 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852362 | AATGTATAAACAGCA[C/G]TTTCATTATCTGAGT | 57531 |
rs759190298 | snp | C/T | 3.29674e-05 | 0.00405988 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104850955 | CGTCCGAATGCATAA[C/T]TGACATCAAATTTTG | 57531 |
rs759201829 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765600 | TGCTCTATTGCCACA[A/C]ATCTTTAAAAAATGA | 57531 |
rs759260592 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857063 | AAAAAATCTGATTAT[A/T]TTCTAAATTTAGAGA | 57531 |
rs759272071 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803205 | GCAATAATTAATAGC[C/T]TACCAACCAAAAAAA | 57531 |
rs759321837 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835615 | TAAATAATAGGAGTT[A/G]GGGAAAAAATAAAAC | 57531 |
rs759327615 | in-del | -/GA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811274 | TATATATATATATAT[-/GA]GCATATATAGCATCT | 57531 |
rs759353330 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687030 | ATTCAGCCAAACTTC[A/T]ACTGGGGAAAAAGTA | 57531 |
rs759405289 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712570 | TGAGGTCAGGAGTTC[A/G]AAACCAGCCTGGCCA | 57531 |
rs759435055 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771586 | TTCACATTGTTACAA[C/T]GTAATCTTTCTTTGA | 57531 |
rs759441946 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735339 | TAAATTATATGAAAG[G/T]AAAAATGGGCCGGGT | 57531 |
rs759443756 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779071 | AGTTGGAGACAGGAT[-/A]AGGTTCAAGAGATGA | 57531 |
rs759454343 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700366 | ATACCTGTTTCTCGT[A/G]TTCCCAAATGTCACT | 57531 |
rs759485076 | snp | A/C | 1.6489e-05 | 0.00287128 | missense, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811358 | TACATTTGGCCTGTT[A/C]ATATCAGCACCACTG | 57531 |
rs759507774 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701607 | AATTACCATAAGAAC[C/G]CAGAAAGTTGTTAAC | 57531 |
rs759510771 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745551 | GTTCACGCCATTCTC[C/T]CACCTCAGCCTCCCA | 57531 |
rs759522987 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705664 | GAATGTCAAATTGCC[C/T]AGGATGCTTCTTTAT | 57531 |
rs759528199 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846541 | GGAAGCTTAATGGGG[C/T]TTCTTTTGGAAAGGA | 57531 |
rs759529274 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734312 | ACAATTGGAACACGT[C/T]TGATTTTTCAGTAAG | 57531 |
rs759531771 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805761 | CCTAATGTAAATGAC[A/G]AGTTGATGGGTGCAG | 57531 |
rs759532481 | snp | C/T | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104688208 | AGTGCAATCACCAGT[C/T]CTCCGTGGCTTCTTC | 57531 |
rs759539529 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775883 | CTACAATTAATGAAG[C/T]ATTCTCTCCTGATAA | 57531 |
rs759548241 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847785 | AACGCATTTGTATAC[C/T]GTGTCCATAGAGAAG | 57531 |
rs759555988 | in-del | -/TTTTGTA | 5.74193e-05 | 0.00535783 | intron-variant | HACE1 | GRCh38.p7 | 6:104772100 | AATACAAAATAATAT[-/TTTTGTA]ATTATTAAGAATCTA | 57531 |
rs759561403 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790493 | TGCAGTGGCTCACGC[C/T]TGCAATCCCAGCACT | 57531 |
rs759567828 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725089 | CAATTAAACTTGTTT[C/T]AAATTAAACACACTA | 57531 |
rs759569576 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709768 | ATCGGCCACGAGAGA[A/C]ATGCAAATCAAAACC | 57531 |
rs759580178 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835813 | GACAAAGTAGATTCT[A/G]TAAGTTTCTAGAGAG | 57531 |
rs759600959 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692108 | GAAAGGAGGAAGCTA[A/G]GAAGGGAGGGAGAAA | 57531 |
rs759613812 | snp | A/G/T | 5.01068e-05 | 0.00500513 | intron-variant | HACE1 | GRCh38.p7 | 6:104797058 | CAAGTTAAAAATACA[A/G/T]TCTTTTTAAAGTCTT | 57531 |
rs759641985 | snp | A/G | 1.64732e-05 | 0.0028699 | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791584 | AGGATGGACCAATTC[A/G]AAAGACGTGACAAAA | 57531 |
rs759644081 | snp | C/T | 4.50999e-05 | 0.00474846 | intron-variant | HACE1 | GRCh38.p7 | 6:104772088 | TCCTATTGAAATAAA[C/T]ACAAAATAATATATT | 57531 |
rs759654057 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693645 | GTTTTTTTTTCTTTC[C/T]CAAATACTTTCCATC | 57531 |
rs759655144 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857349 | AAAAGCAAATGCAAA[C/T]GATGCCATTTTTGCC | 57531 |
rs759682082 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790125 | ACACACACATACATA[C/T]ATGGCTAAAAACTGT | 57531 |
rs759690027 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746459 | GGTTTGGAGCCTGGG[A/T]AACATAGGCAGTTAG | 57531 |
rs759696945 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | HACE1 | GRCh38.p7 | 6:104791465 | CAAATTCATCTCTTT[C/T]ACGTCTATCTTCCTA | 57531 |
rs759705445 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714516 | CCTTAACCACTTTGG[-/AT]ATGACTCTGGTCCCC | 57531 |
rs759708433 | snp | C/T | | | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104853235 | GCCACACTGTTGGAC[C/T]TCCCAGCTTCCAGAA | 57531 |
rs759774396 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711540 | ACATACAGCTGAACT[C/G]TGTGTTGACACACAC | 57531 |
rs759796069 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, synonymous-codon, missense, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833141 | AAGGTCATGGAGTAG[C/T]TCTGTCCGCCCATTC | 57531 |
rs759799751 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837223 | TGAGAGGAATTATTC[C/T]ACCTGGTATTAAGAC | 57531 |
rs759815127 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762850 | AAAAAATTAGCCTGG[C/T]ATGATGGTGGACACC | 57531 |
rs759817372 | in-del | -/AATGCACTTAATGCCACAAAAGTGTACACTTAAAAATTGTTTA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732638 | TCACACATTAATGTG[lengthTooLong]AATGATACATTTTAT | 57531 |
rs759818728 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837256 | ACAGCTACAGTAATC[A/G]AGACAGTGTGGTATT | 57531 |
rs759829648 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861026 | CAGGCACGGGGAAGA[C/T]CTCTGTAATCTTCAC | 57531 |
rs759832046 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843764 | CAATAAAATGCATGT[C/T]TATGCATCCCTCTAC | 57531 |
rs759850659 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768230 | TTTACAAAGGCCCTC[A/T]AACAAGTTTAGCAAG | 57531 |
rs759867491 | snp | A/G | 1.65836e-05 | 0.0028795 | intron-variant | HACE1 | GRCh38.p7 | 6:104843318 | AAAGAAAAAAGAGTC[A/G]TGGATAACTGGTACT | 57531 |
rs759875774 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781802 | TCTACACAGACACAC[C/T]TCTTAATCACATCCA | 57531 |
rs759890829 | snp | A/T | 1.66774e-05 | 0.00288763 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784144 | CATTCAAGGAGAAAG[A/T]GAAAGTGGTCAAATA | 57531 |
rs759902165 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787195 | GTTCACTCACTCAAC[A/C]AGTACTATGCACTAG | 57531 |
rs759903580 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769281 | CTCAAGCAATCCCCC[C/T]GCCTTAGTCTCCCAA | 57531 |
rs759905673 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756998 | GGCGGGGAGAGGGGC[A/G]TCCACCATTGCTGAG | 57531 |
rs759961098 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790068 | AGGTGGCACAATAAG[-/A]AAAAAAAAAAAAGAA | 57531 |
rs760015476 | snp | C/G | 3.38158e-05 | 0.00411178 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796713 | GTCTGAAAAAGCCTC[C/G]GGTGATATTGAATTA | 57531 |
rs760015521 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813004 | AGACACACAGGTAGA[A/G]CAAAGATGAGGAGCC | 57531 |
rs760022503 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704693 | GTGCAATGTACACAT[C/T]GAGGATTTACACCAT | 57531 |
rs760055675 | snp | A/G | 1.65323e-05 | 0.00287505 | intron-variant | HACE1 | GRCh38.p7 | 6:104744268 | TAGCTCATATTTCAG[A/G]GCAATTGTAGACTTC | 57531 |
rs760056019 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718111 | CCATAATTCCTTTAA[A/G]TAGTTTCAAGGTTTT | 57531 |
rs760103402 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762718 | AAAAAAGGCCGGGCG[C/T]GGTAGCTCACACCTG | 57531 |
rs760145400 | snp | C/T | 4.94956e-05 | 0.00497447 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777254 | CTGGCCTGTGCACCA[C/T]ATCTGAATCTGGCTG | 57531 |
rs760175401 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708253 | AATATACAAAAATTG[G/T]TTGTATTTATTTCTA | 57531 |
rs760183863 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761373 | CAATGGAACAGAACA[C/G]AGCCCTCAGAAGTAA | 57531 |
rs760205926 | snp | C/T | 5.06026e-05 | 0.00502978 | intron-variant | HACE1 | GRCh38.p7 | 6:104784186 | TTTCTAAAAGAAAAA[C/T]ATTTTGTTTAAATGG | 57531 |
rs760217292 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817928 | AGAGCCATGGAAGCT[C/T]GTTATTTGGAAATAC | 57531 |
rs760217918 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801498 | ACAAAGGGAAGCCCA[A/T]CAGACTAACAGCGGA | 57531 |
rs760224628 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709503 | TTGTTGCTTAAAAGA[A/G]CATGGCACCTTCCCA | 57531 |
rs760224876 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722979 | CAGTTTATAGTTCAA[C/T]GGTTTTGCAACATTA | 57531 |
rs760279600 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697805 | AGCACAACGGCATGA[C/T]CTCGGCTCAGTGCAA | 57531 |
rs760350466 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809112 | ATAAGATATTTTTCA[G/T]AGTGATGCATTCATT | 57531 |
rs760386982 | snp | C/T | 1.65748e-05 | 0.00287874 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729618 | AAATTACTTCTGCCA[C/T]TCTGAATTGTGCATC | 57531 |
rs760392084 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790816 | ACACATTTTTCTAAA[A/G]TCTGTTACTTTAAAA | 57531 |
rs760392141 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859217 | CAGCTACTGTTAAAT[A/G]ACCCGCAATTATGAT | 57531 |
rs760409587 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750507 | CATGATGACTTTTCA[A/C]AAACCTTTTACATAC | 57531 |
rs760414272 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735345 | ATATGAAAGTAAAAA[C/T]GGGCCGGGTGCGGTG | 57531 |
rs760436438 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848006 | ACAGGCATGTGCCAC[C/T]ATGCCTGGATTATTT | 57531 |
rs760447614 | in-del | -/AATTTTTCTTC | 1.64849e-05 | 0.00287092 | intron-variant | HACE1 | GRCh38.p7 | 6:104784210 | AAATGGACAGGAAGA[-/AATTTTTCTTC]ATGAGTAGCATTAAG | 57531 |
rs760464438 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730173 | CATAATTACTCATCA[A/G]TGATTCCAAAATCCT | 57531 |
rs760494910 | snp | A/G | 2.05181e-05 | 0.00320291 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852391 | GTAAAAAAAAACAAA[A/G]AGTTCATTTATCCCC | 57531 |
rs760498964 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734467 | GAATGACAAGTACTA[C/T]ACCTATACTAATGAC | 57531 |
rs760508005 | in-del | -/AC | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727685 | TGTATATGAATACAT[-/AC]ACACATATATATGTA | 57531 |
rs760514166 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775113 | TTGGGAGGCCGAGGC[A/G]GGTAGATAACCTGAG | 57531 |
rs760521886 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755032 | ATCAGTATGCTGTCC[G/T]CAAGAGACCCATCTC | 57531 |
rs760531820 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799615 | GCTCGAGATGAACAG[-/T]TTACATGGCAGACCA | 57531 |
rs760585422 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688487 | CAAGACTCATTCACT[C/T]CTGTGCTCTCATCAG | 57531 |
rs760590352 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792486 | ATCTTTAAACACAGT[A/G]TTTTTGTTGGTTGAT | 57531 |
rs760591663 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785186 | AATGGAGGAATGGAA[A/G]CAGCATCTTGATCTT | 57531 |
rs760596927 | snp | C/T | 1.73147e-05 | 0.00294228 | intron-variant | HACE1 | GRCh38.p7 | 6:104785343 | AACAAAAGTGTTTTT[C/T]AAACATCATTCTTAA | 57531 |
rs760618070 | snp | C/T | 1.69137e-05 | 0.00290802 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771361 | TTCTGGATCAATGGA[C/T]GCCACATCTTGGTAA | 57531 |
rs760674890 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732148 | AAAACAGTATGCAAG[C/T]TCCTCAACAAAATTA | 57531 |
rs760683542 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832485 | TGCAACCGCTGACTG[C/T]TGAGCTCAAGCAATT | 57531 |
rs760703696 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775809 | CACTTGCCTCCCCTA[A/G]AATCATCCTTCTGAT | 57531 |
rs760718054 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747578 | AAGTCCCTCTGATTA[C/T]TCATGCCACCAAGCA | 57531 |
rs760726742 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, synonymous-codon, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833075 | GCAGGCAACATGCAG[C/T]GCTGTCTGCCCCATG | 57531 |
rs760745649 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778377 | ACAGAGTAACACAAT[-/AT]ATATATATATATAAT | 57531 |
rs760768397 | snp | C/T | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730316 | ACCATGTGCTTGAAG[C/T]TGGTAAAAGATTTGG | 57531 |
rs760776635 | in-del | -/A | 3.51099e-05 | 0.00418972 | intron-variant | HACE1 | GRCh38.p7 | 6:104744624 | CCTTGGGGGAAGAAG[-/A]AAAAATATTTCAATA | 57531 |
rs760787263 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758185 | AACATTCAAATTCAG[A/G]AAATACAGAGAACAC | 57531 |
rs760846785 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765748 | GCAAGTGTTCACTGT[C/T]AGGCTGACAAATCCA | 57531 |
rs760871474 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809509 | CAAAGAGAATCACTG[C/T]GGTTCAAGTACAGTG | 57531 |
rs760888256 | snp | A/C | 3.30644e-05 | 0.00406585 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776820 | CCACTCACGCACAAC[A/C]CCTTGACCCTGAATT | 57531 |
rs760895420 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758101 | AGTGACGGGGAGAAT[C/G]GAACCAAGTTAGAAA | 57531 |
rs760937835 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718021 | AAAAAAAAAACCCTT[A/G]ATTTTGTAGTAATCA | 57531 |
rs761011792 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791591 | ACCAATTCGAAAGAC[A/G]TGACAAAACATTCTC | 57531 |
rs761034766 | snp | A/G | 9.95372e-05 | 0.00705398 | intron-variant | HACE1 | GRCh38.p7 | 6:104843321 | GAAAAAAGAGTCATG[A/G]ATAACTGGTACTTAA | 57531 |
rs761043653 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766767 | AAGTTTTGTGCCCTC[A/G]GGCAGTTATTTAACG | 57531 |
rs761050646 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770971 | AGCTGAAGTGCTCTC[A/G]ATTTTTTAGGAACCA | 57531 |
rs761053023 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766518 | TCTATGGATAAAAGT[C/G]TGTATTTTGTGCTTG | 57531 |
rs761077926 | snp | C/T | 1.72121e-05 | 0.00293356 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750341 | GATGTTTTTCCTTAC[C/T]AATTCATATTCATCA | 57531 |
rs761086584 | snp | A/G/T | 4.94428e-05 | 0.00497186 | stop-gained, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849228 | TAACAGCAAAACCAA[A/G/T]CATTCCACCGATCCA | 57531 |
rs761096361 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694757 | CCATATGACTTTCAT[A/G]GGCATCAGACCTATG | 57531 |
rs761101965 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759529 | ACAACGTACCAGAAT[A/C]TCTGGGACACATTTA | 57531 |
rs761112901 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718303 | CAGTCTGCTCATTCC[A/G]CATATTTCTTATATA | 57531 |
rs761133017 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798254 | TCTTTCCACAATAAC[A/G]TTACCTAAAGAGGCA | 57531 |
rs761133092 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841303 | TATTCCACCTCCCTT[A/G]AAGTACAGGAAGGAA | 57531 |
rs761142410 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814687 | AAAATCTCCTGTTGA[A/G]TTGGAGGAGGGACCT | 57531 |
rs761143953 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700729 | AAAGGTCAAAGGGGC[A/T]TATTCGCTGAGGGTC | 57531 |
rs761149414 | in-del | -/AAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756411 | GCCAGATTCCATCTC[-/AAAA]AAAAAAAAAAAAAAA | 57531 |
rs761156470 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745264 | CACAAAATCTCAATC[A/G]TATAAGTAAAAATGA | 57531 |
rs761171758 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800075 | CCGTGCCTGGCTCAG[C/T]GGGTCCCATGCCCAC | 57531 |
rs761202080 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693935 | TGTAAATTAGCACAA[G/T]GACTATAGAGAACAA | 57531 |
rs761216337 | in-del | -/TAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836711 | GAGTGAGACTCTGTC[-/TAAA]TAAATAAATAAACAA | 57531 |
rs761223507 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706792 | TTACTACTGTAATTT[C/T]GTGTAGACTGACAAA | 57531 |
rs761223780 | snp | A/T | 1.66032e-05 | 0.0028812 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784478 | CAATGAAACGAGGTG[A/T]AGTCATTCTGTGGGG | 57531 |
rs761224057 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746507 | TCTCTGCTCCCCCAC[C/T]GCTTCAGCATCTCTT | 57531 |
rs761233617 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753367 | TCCCCTTCAACACAG[-/C]ACATGTGCTCTACCA | 57531 |
rs761265633 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752021 | AAGTTCTATATGACT[G/T]CTAGCTATGAATTCT | 57531 |
rs761267137 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801525 | CGGATCTCTCGGCAG[-/A]AACTCTACAAGCCAG | 57531 |
rs761270140 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860821 | AGCTTCTCTTCCTCA[A/G]AGAGACAAAGCTGTT | 57531 |
rs761295159 | snp | G/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855050 | CACCCTATGAAGTAG[G/T]TACTATTATCCTCAT | 57531 |
rs761297846 | snp | A/G | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744564 | TATTCTGTATTTTTT[A/G]TCCAATCACTCACAT | 57531 |
rs761309328 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780567 | AACTTCTAAGTACAG[C/T]AGAGTACAAAGTATT | 57531 |
rs761336527 | snp | A/G | 0.000132404 | 0.00813539 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784988 | AAACTTTCTTACCCC[A/G]GAGGCATCTGACAAG | 57531 |
rs761348740 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699042 | TTTTTTAATATTGTT[A/G]TCTTTTTTCAGTAGA | 57531 |
rs761371892 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711157 | AGCAATGTACTCCTG[C/T]CTCCTTCACATATGC | 57531 |
rs761396355 | in-del | -/TGATA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840057 | TAAGACAGATTGTAT[-/TGATA]CAATGTCCATGTCCT | 57531 |
rs761403268 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685200 | AAGCCACTGAGATAT[C/T]AGGGTTGCTTATACC | 57531 |
rs761412785 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731634 | GACAGTCTTTTCAAC[A/G]AAGTGTGTTGGGAAA | 57531 |
rs761444288 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826977 | TTTTCATATGGCCTT[C/G]AAGAGATCCTTAAGA | 57531 |
rs761470029 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755741 | AACTAATGAGAACAA[A/G]GAGACAATGTACCAG | 57531 |
rs761474592 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793756 | ACATAAATCAGCAGG[A/G]GGAAACAATTTGTAT | 57531 |
rs761482530 | snp | A/G | 0.000170838 | 0.00924066 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859659 | CTCGGCGCGCCCTCC[A/G]CGATCCTCCGCGATC | 57531 |
rs761495495 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716889 | AATTAAAATATACAG[C/T]GATACCAGTTGACAC | 57531 |
rs761533509 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723149 | CACTAGCTTGTTGTG[A/G]CACAGTGAGAGAGAA | 57531 |
rs761538337 | in-del | -/AAATAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748172 | AAAGACCTGAGTAGA[-/AAATAT]TCATAATACATATAT | 57531 |
rs761584723 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709699 | TTCTTTGTAAATTAT[A/C]CAGTCTCAGTTATTC | 57531 |
rs761597622 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788527 | GTACATTGATATCCT[A/G]TTAGTCTGACTATTC | 57531 |
rs761606378 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761503 | TAGCCATATGCAGAA[A/C]ACTGAAACTGGACCC | 57531 |
rs761606413 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826903 | TAGAATGGGGTTCCC[-/T]TCCTCCTTACAGAAT | 57531 |
rs761608313 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778216 | TTCATCTGCCAGGTA[A/G]GCAAACTGTGAGTTA | 57531 |
rs761628007 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772138 | AAGAAAGATTACTTC[A/G]ATGCAGATAAACTAA | 57531 |
rs761633389 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721864 | TGAGAAACTGAAGGT[G/T]GGTGGCTTGGACAAG | 57531 |
rs761641588 | snp | C/T | 8.637e-05 | 0.00657096 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796742 | TAATACTTCACAAGT[C/T]TCTCCATATCCACCC | 57531 |
rs761656057 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818028 | GGTGGTTTAAGGGAC[C/T]AGCATTCTTATCAGA | 57531 |
rs761703540 | snp | A/G | 3.29783e-05 | 0.00406055 | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771949 | GCTTGTAGAAGGATC[A/G]TGTGAAGTAAATATT | 57531 |
rs761712161 | snp | C/T | 3.3117e-05 | 0.00406908 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729639 | ATTGTGCATCAGTAG[C/T]CAGAGGAGTTTTCCA | 57531 |
rs761720374 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686955 | GAACACGTGAGGATC[A/G]GCAATGGAATTCCCA | 57531 |
rs761728651 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730082 | TAGTGATACTTGAAC[A/T]ATAGTCAATTAAATT | 57531 |
rs761752201 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767058 | CTAATAAATGTCAAA[C/T]GTTTTAATATTAAGG | 57531 |
rs761770762 | snp | A/G | 3.29897e-05 | 0.00406125 | synonymous-codon, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811382 | ACCACTGTCTAGCAA[A/G]CACTGCACTGTCTGA | 57531 |
rs761788230 | snp | C/T | 9.4304e-05 | 0.00686609 | intron-variant | HACE1 | GRCh38.p7 | 6:104785393 | AAAAACAAAACACAA[C/T]TAGACAAATATTATA | 57531 |
rs761804952 | snp | A/G | 6.59261e-05 | 0.00574097 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772034 | ATAGTTCAAGTGATC[A/G]GGATTTACATAAGAG | 57531 |
rs761808499 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762883 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 57531 |
rs761808585 | in-del | -/CTGGCCGCCCCCAGCCCCG | 4.5881e-05 | 0.00478941 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859518 | GGAGCTCCTGCCCCA[-/CTGGCCGCCCCCAGCCCCG]CGGCCAGCCTGGCCC | 57531 |
rs761811461 | snp | G/T | 1.65206e-05 | 0.00287403 | intron-variant | HACE1 | GRCh38.p7 | 6:104744252 | ACAAGAACAAAAAAC[G/T]TAGCTCATATTTCAG | 57531 |
rs761825190 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818838 | AATTCAACATCGATT[A/T]ATGTTTAAAAAAAAA | 57531 |
rs761840774 | in-del | -/GA | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852232 | TGTGTGTGTGTGCGC[-/GA]GCGTGCGCGTGCACG | 57531 |
rs761858926 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801520 | AACAGCGGATCTCTC[A/G]GCAGAAACTCTACAA | 57531 |
rs761916623 | in-del | -/GAGAGAAGTTGTTTAGG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841141 | AAAAAAAAAATAGCT[-/GAGAGAAGTTGTTTAGG]GAGTGGGAAGTTTGG | 57531 |
rs761929232 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715257 | ATATGAATAAGGAAC[A/G]AGAGACTATAAAACA | 57531 |
rs761936681 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825265 | AACTTTCCACGCCTA[A/C]GTAACAAAAGGACCA | 57531 |
rs762030393 | in-del | -/AAAAC | 0.00482191 | 0.0488641 | intron-variant | HACE1 | GRCh38.p7 | 6:104785379 | AGGATTAAAAAAAAA[-/AAAAC]AAAACACAACTAGAC | 57531 |
rs762052090 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703327 | AGTTTAGAAATTTTT[C/T]TCATTGATATAAATT | 57531 |
rs762055877 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850426 | TTTCGTAAGCCAAAT[C/T]ATTCATGAAAAATTA | 57531 |
rs762065043 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746790 | GACAGGACTCTGATA[C/T]AGGTTTGCTAAAAGG | 57531 |
rs762101794 | in-del | -/AAAAAAAAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838891 | AAACAACTCCATAGT[-/AAAAAAAAAA]AAAAAAAAAAAAAAA | 57531 |
rs762104831 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689860 | CATGGGAAAAGAATT[C/T]AACGCCTTTCTGAAG | 57531 |
rs762112164 | snp | A/G | 3.36831e-05 | 0.00410371 | intron-variant | HACE1 | GRCh38.p7 | 6:104776851 | CAAGAAATAAAATTA[A/G]GCATCAACAGAAATA | 57531 |
rs762125916 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798449 | GTGCCAGAAAACTCT[A/G]CAACGTTATTATAGG | 57531 |
rs762143711 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792709 | AAATGCAGGATGCTG[A/G]CAAACTGAAAAACTG | 57531 |
rs762147663 | snp | G/T | 1.6528e-05 | 0.00287467 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777070 | TAGCTTTGCACAATT[G/T]GCTTTTGACACAACT | 57531 |
rs762170807 | in-del | -/ACAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104741665 | GAAATAAAAGAGGAT[-/ACAA]ACAAATGGAAGAACA | 57531 |
rs762173469 | in-del | -/ATAT | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727719 | TGAATATATACACAC[-/ATAT]ATATGTATATGAATA | 57531 |
rs762285351 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799773 | CCATTCCAAGATGGC[C/T]GAATATGAACAGCTC | 57531 |
rs762289121 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708047 | TCACCACTTCTATTC[A/T]ACATCATAATGGAGG | 57531 |
rs762302937 | snp | A/T | 1.73459e-05 | 0.00294494 | intron-variant | HACE1 | GRCh38.p7 | 6:104791689 | TATGAGATTAGAGTA[A/T]AACAAATTACATATT | 57531 |
rs762322391 | in-del | -/A | 1.65236e-05 | 0.00287429 | intron-variant | HACE1 | GRCh38.p7 | 6:104811402 | CACTGTCTGAGGGGG[-/A]AAAAAATAATTAAAA | 57531 |
rs762356026 | snp | A/C/T | 4.94257e-05 | 0.004971 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791611 | AAAACATTCTCACAA[A/C/T]CCTTAAAAGGCTCTT | 57531 |
rs762361335 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685324 | AGGGAAGGGGTCAAG[A/G]GGCAGAGCTGTAAAG | 57531 |
rs762400674 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839534 | AGGACAAAGGGAAAG[A/G]TATGGTTATAAAAGG | 57531 |
rs762415117 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823203 | CAGCACTCTGGGAGG[C/T]CAGGTGGATCACCTG | 57531 |
rs762419841 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765839 | CATTAACTTCTTTTC[A/G]TCAGTTTTGGCACAG | 57531 |
rs762422944 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845893 | ACAAACCAGATAGTC[C/G]CATTAAAATAAATAC | 57531 |
rs762447119 | snp | C/T | 2.03963e-05 | 0.00319339 | intron-variant | HACE1 | GRCh38.p7 | 6:104750520 | CAAAAACCTTTTACA[C/T]ACTTAATGTTAATAT | 57531 |
rs762467930 | snp | C/T | 1.65081e-05 | 0.00287293 | intron-variant | HACE1 | GRCh38.p7 | 6:104849258 | ACAACTAAAACAATA[C/T]TAAAAGACAGTTCAG | 57531 |
rs762497394 | snp | A/G | 4.94409e-05 | 0.00497172 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104850945 | TCTTTTCACACGTCC[A/G]AATGCATAATTGACA | 57531 |
rs762513195 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788629 | TTACCAAAATTTCCA[A/G]ATTGTAAGTCTATGA | 57531 |
rs762524185 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815780 | GGAATATGTTTAAAA[-/G]GGAAACAGAGGGCCA | 57531 |
rs762573253 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829263 | CTTATGGAAAGATAT[A/G]CAAATGGTTTTTAAT | 57531 |
rs762583678 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759587 | CACTAAACGCCCACA[A/G]GAGAAAGCAGGAGAG | 57531 |
rs762609275 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814847 | GATGCTTGCTTCCCC[C/T]TTTGCCTTCCACCAT | 57531 |
rs762610404 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780241 | TAATTCAAGTGGAAC[A/G]TTAAAAGGTACAAAC | 57531 |
rs762633803 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797548 | AATGTAAGAGAATCT[-/G]GGGGAAAAAGGGAAC | 57531 |
rs762635810 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773290 | CAAAAGGTAGAAATG[C/T]ATTGGAAAGTGAAAT | 57531 |
rs762636485 | in-del | -/A | 8.63055e-05 | 0.00656851 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852408 | GTTCATTTATCCCCT[-/A]CTTTGTGCAAGGGGT | 57531 |
rs762644570 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769718 | GCTTGGGTTTTGGCC[A/C]CAGTTTTGCCATTAA | 57531 |
rs762735109 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699247 | CTTGGGGGGAATACA[A/G]AATTTATTTTAATAT | 57531 |
rs762762031 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773245 | AAAAGAAACAACGGA[G/T]AAACCTAATGAAATA | 57531 |
rs762767807 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803563 | GGCTGGCTCAACATA[C/T]GCAAATCAATAAACG | 57531 |
rs762836595 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724799 | TGTGTAAAAAATGAA[A/T]TGCTATAGAAGAAAA | 57531 |
rs762837428 | snp | C/T | 1.67265e-05 | 0.00289188 | intron-variant | HACE1 | GRCh38.p7 | 6:104784506 | GGGGGAAAACATCAA[C/T]CAGAATACACAGGCA | 57531 |
rs762847892 | snp | C/T | 1.65291e-05 | 0.00287476 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729665 | TTCCAGACTTCATTA[C/T]GCCATTGTGTAACCA | 57531 |
rs762889077 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711328 | TAGAGTTCAGCTTCT[C/T]CCACCCAAAGTGTTT | 57531 |
rs762914862 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820386 | TAGCGAAAAAAACTA[C/T]CATCAGAATGAACAG | 57531 |
rs762918010 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712437 | GAGGTCTAATGTTTA[C/T]GTCATGAGGGCTCTG | 57531 |
rs762927963 | snp | A/C | 1.66067e-05 | 0.00288151 | intron-variant | HACE1 | GRCh38.p7 | 6:104796923 | GAATATAAATGAAAA[A/C]CACACCTGTACACAT | 57531 |
rs762936975 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752376 | CAGCAGTGATACCTG[C/T]ATTAGCACATGACTA | 57531 |
rs762943720 | snp | A/G | 3.55278e-05 | 0.00421457 | intron-variant | HACE1 | GRCh38.p7 | 6:104730275 | CAAAACAATTTGTAA[A/G]GCATTTAAATAAACC | 57531 |
rs763000669 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851209 | CTGCCTCAGCCTCCC[A/G]AGTAGCCAGGACTAC | 57531 |
rs763020414 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703521 | GGAGTTGTATAATAC[A/G]TGATTAATGCTACCA | 57531 |
rs763104813 | snp | C/T | 1.64735e-05 | 0.00286993 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833107 | CATCCTCAACATCAA[C/T]ATCACTGACATGCTG | 57531 |
rs763151869 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833916 | CTTGAACCCAGGAGG[C/T]GGCAGTTGCGGTGAG | 57531 |
rs763169518 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847878 | GCTGGAATGCAATGG[C/T]GCAATCTCCACTCAC | 57531 |
rs763170120 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835402 | ACATACTGATTGCAT[C/T]CCTGAAATGAGAAAA | 57531 |
rs763177911 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745333 | AGGGAAAAGAGGACA[G/T]GAAAAGAGCTTGTCC | 57531 |
rs763195821 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728232 | AAGCAGTGTAATATT[A/G]AAGGTGGTTATCTAT | 57531 |
rs763204667 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840448 | ATCTTCCAGAAAGTC[A/C]ACAGGTGATACCTAA | 57531 |
rs763230295 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704104 | GAGCAAGACTGTCTC[-/A]AAAAAAAAAAAAAAA | 57531 |
rs763232610 | snp | A/C | 1.6557e-05 | 0.00287719 | intron-variant | HACE1 | GRCh38.p7 | 6:104811432 | AGTAAAGCCAGAGGA[A/C]TCAAACAAAAGATAC | 57531 |
rs763263917 | snp | A/C | 4.97055e-05 | 0.00498501 | splice-donor-variant | HACE1 | GRCh38.p7 | 6:104744510 | CTCTAGAGAAATTTT[A/C]CCTGAATAACTGGAT | 57531 |
rs763317369 | snp | C/T | 1.65241e-05 | 0.00287433 | intron-variant | HACE1 | GRCh38.p7 | 6:104744258 | ACAAAAAACTTAGCT[C/T]ATATTTCAGAGCAAT | 57531 |
rs763324143 | snp | C/T | | | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785006 | GGCATCTGACAAGAA[C/T]AGCACATGTAAAAAG | 57531 |
rs763326565 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727308 | GAATATATATACACA[-/TG]TATGTATACGAATAT | 57531 |
rs763331446 | in-del | -/AT | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727719 | TGAATATATACACAC[-/AT]ATATATGTATATGAA | 57531 |
rs763382378 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826559 | TGTGATTTACAATGA[C/T]GGTCATACCTTCTAT | 57531 |
rs763404649 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703219 | TCACAGTAAAGCCAC[A/G]GCAATTCAGCCAAGT | 57531 |
rs763416464 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697779 | AGTTTCACTCTTGTC[A/G]TCCAGGCTGGAGCAC | 57531 |
rs763420822 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840578 | TCACACCTGTAATCC[C/G]AGCACTTTGGGTAGC | 57531 |
rs763421862 | in-del | -/A | 1.66026e-05 | 0.00288115 | intron-variant | HACE1 | GRCh38.p7 | 6:104777331 | GCTAGCTCAAAAAAT[-/A]AAGAGTAAAATATGT | 57531 |
rs763427782 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790723 | TTGTGCCACTGCATT[A/C]CAGCCTAGGCAACAG | 57531 |
rs763431334 | snp | A/G | 1.66225e-05 | 0.00288287 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852341 | TCAGCCATAACCATT[A/G]GCATTAATGTATAAA | 57531 |
rs763434333 | snp | A/G | 1.64953e-05 | 0.00287182 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777225 | GTGAACCAGCAGGAT[A/G]TCATTTTCATTCACT | 57531 |
rs763451827 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750035 | TTCAGAAATAATGTA[G/T]AATACTGTGTATATA | 57531 |
rs763459849 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715427 | AGTATTTTGCATAAT[A/G]CAGAACAGAGACATA | 57531 |
rs763506245 | snp | C/G | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683277 | ACAGGAAGTCCGGGT[C/G]TGTAACCACTGGTAA | 57531 |
rs763511922 | in-del | -/AA/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785370 | TAAACTACAGGATTA[-/AA/T]AAAAAAAAAAAACAA | 57531 |
rs763521978 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767913 | TCTTCTTTTTTTTCT[C/T]CAAGCCTGGATGAAC | 57531 |
rs763531979 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104729965 | GCATGCAAATGCAGT[A/G]GAAGAAAATACGTTC | 57531 |
rs763567551 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809510 | AAAGAGAATCACTGT[A/G]GTTCAAGTACAGTGA | 57531 |
rs763575907 | snp | A/G | 1.68057e-05 | 0.00289872 | intron-variant | HACE1 | GRCh38.p7 | 6:104795533 | CAGGAGGTGAAGCCA[A/G]CAGACACTGCTACCT | 57531 |
rs763636275 | snp | A/T | 1.6473e-05 | 0.00286988 | intron-variant | HACE1 | GRCh38.p7 | 6:104833187 | ATCTGTGAAGCCATT[A/T]AGTTACTTAACATTT | 57531 |
rs763638109 | snp | A/G | 1.70182e-05 | 0.00291699 | intron-variant | HACE1 | GRCh38.p7 | 6:104784205 | TTGTTTAAATGGACA[A/G]GAAGAATGAGTAGCA | 57531 |
rs763662146 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827503 | CGGCAAAAATCATTA[A/T]CATCTGGTTGTGTTA | 57531 |
rs763677431 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817995 | GCCTCTGGTGATCAT[C/G]ACTTAACAAAGAGGA | 57531 |
rs763683301 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797769 | AATGTTAACAGCTGA[C/T]TCTTAAGAAATGCCC | 57531 |
rs763749675 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785420 | TATAGAAGAGAAAAT[G/T]TACTCTAGTCATTTC | 57531 |
rs763754468 | snp | A/G | 1.66117e-05 | 0.00288194 | intron-variant | HACE1 | GRCh38.p7 | 6:104777335 | AGCTCAAAAAATAAG[A/G]GTAAAATATGTTAGC | 57531 |
rs763758087 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825583 | TTCCCACAACCAATC[A/C]GATGTTTGCATAGGG | 57531 |
rs763808488 | snp | A/G | 1.83646e-05 | 0.00303018 | intron-variant | HACE1 | GRCh38.p7 | 6:104796650 | TACTATCACAAATAC[A/G]ATACCATGTTTTCTC | 57531 |
rs763837043 | snp | A/T | | | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730382 | ATCCACTTCCACCCA[A/T]GATATTAGCAAACCC | 57531 |
rs763867101 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753150 | ATTTTACTATGAACA[C/T]CCACTACTGTTGCCC | 57531 |
rs763883945 | snp | C/T | 0.000767754 | 0.0195777 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858555 | AGAAAGGAAAGAAAA[C/T]TATCGCCAAAGTACC | 57531 |
rs763892377 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731490 | AAGCTGTGGTAATCA[A/G]AACAGTGTGATACTG | 57531 |
rs763949593 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831064 | GTACATTCTATTACC[A/G]ATAATGTTAAATGTT | 57531 |
rs763954378 | snp | A/T | 1.73216e-05 | 0.00294287 | intron-variant | HACE1 | GRCh38.p7 | 6:104785344 | ACAAAAGTGTTTTTT[A/T]AACATCATTCTTAAA | 57531 |
rs763966255 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761374 | AATGGAACAGAACAG[A/G]GCCCTCAGAAGTAAC | 57531 |
rs763995860 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775849 | ATTTGCTGCTAGTTT[C/G]GTTGGAAGCAATCAG | 57531 |
rs764006245 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832535 | AACAGCTGGGACTAC[A/G]GATGCATGCCACCAT | 57531 |
rs764018891 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713341 | TTCAATCAAAGGGCA[A/G]TGAAAGAGTAGATTG | 57531 |
rs764054562 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803733 | AATAATAAGAGCTAT[C/T]TATGACAAACCCACA | 57531 |
rs764060978 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708271 | GTATTTATTTCTATG[C/T]ACTAGCAGTAAGCAT | 57531 |
rs764069637 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760369 | CAAGTCGGCTTCATC[C/T]CTGGGATGCAAGGCT | 57531 |
rs764080768 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735588 | GTGAGCCGAGATGGC[A/G]CCAGTGCACTCCAGC | 57531 |
rs764082227 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721711 | CCTAACAGCTCATCT[C/T]TCTCCCAGCTCAGCT | 57531 |
rs764091093 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714202 | CAAACCCAAATAAGA[C/T]AGGAGGTTAAGAAAA | 57531 |
rs764124015 | in-del | -/TAAT | 1.65282e-05 | 0.00287469 | intron-variant | HACE1 | GRCh38.p7 | 6:104811409 | CTGAGGGGGAAAAAA[-/TAAT]TAAAAGTAAAGCCAG | 57531 |
rs764135887 | snp | C/T | 1.69232e-05 | 0.00290883 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771363 | CTGGATCAATGGATG[C/T]CACATCTTGGTAATT | 57531 |
rs764171417 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846640 | CATCTGATGACAGCT[A/G]AGGGAACAAAACAAA | 57531 |
rs764191455 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712660 | GCCTGTAATCCCAGC[C/T]ACTTGGGAGGCTGAG | 57531 |
rs764205784 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821657 | TTGAGTGTCAAAGAG[A/T]TCATGTAATTTGTAC | 57531 |
rs764240735 | snp | A/G | 1.66754e-05 | 0.00288746 | intron-variant | HACE1 | GRCh38.p7 | 6:104776840 | GACCCTGAATTCAAG[A/G]AATAAAATTAAGCAT | 57531 |
rs764246498 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700617 | CCATATCTGAAGTAG[A/G]CGCTGCACAATTTAA | 57531 |
rs764248259 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836477 | CAGCATTTTGGGAGG[C/T]CGAGGCGGGTGAATC | 57531 |
rs764248917 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734495 | GACTGGGAGTTCGAG[A/G]TAAAATTTAAGATTT | 57531 |
rs764263948 | snp | A/T | 1.65375e-05 | 0.0028755 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730328 | AAGTTGGTAAAAGAT[A/T]TGGAGTATATGGCAC | 57531 |
rs764265456 | in-del | -/GGTG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721861 | GTCTGAGAAACTGAA[-/GGTG]GGTGGCTTGGACAAG | 57531 |
rs764289829 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702026 | TATTTCTAACAGTTC[A/G]CTAAGCTCCAAATTT | 57531 |
rs764297436 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806882 | TGGACTCTTTCATCC[C/T]TATAAATTTGAGAAT | 57531 |
rs764310470 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759533 | CGTACCAGAATCTCT[A/G]GGACACATTTAAAGC | 57531 |
rs764323737 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765768 | TGACAAATCCACTCT[C/T]TAAATACACAATTGA | 57531 |
rs764336252 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806443 | CTCCAGCCTGGGTGG[C/T]AGAACAAGACCCTGT | 57531 |
rs764338170 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833670 | GCAATGTAGCAAGAA[C/T]CTGTCTCTACAAAAA | 57531 |
rs764357653 | snp | A/T | 3.29462e-05 | 0.00405857 | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791594 | AATTCGAAAGACGTG[A/T]CAAAACATTCTCACA | 57531 |
rs764359475 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692953 | TTAAATAGACCCCTC[A/G]GCTGCAGCAGACAAA | 57531 |
rs764404317 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796825 | CATATTCTTCACACA[A/G]TAAAAATCTTTGCAC | 57531 |
rs764429846 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710263 | CTCAAATGAAATGTA[C/T]ACAATAAGCAAATCT | 57531 |
rs764446022 | in-del | -/AGAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817599 | GAATTAATATAGAGG[-/AGAA]AGAAAGATGGAACTG | 57531 |
rs764465996 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697591 | CTGCCACCATCATGA[A/G]TGTATGTCACACAGC | 57531 |
rs764546120 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790825 | TCTAAAATCTGTTAC[C/T]TTAAAATGTCACCCA | 57531 |
rs764571580 | in-del | -/TAGA | 0.000318893 | 0.0126232 | intron-variant | HACE1 | GRCh38.p7 | 6:104784052 | AGAAATTAATTTCAT[-/TAGA]TAGAATAAAAAGATG | 57531 |
rs764584746 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746712 | TAACACTGCCCATAC[C/G]TCTGTCATAGTCCCT | 57531 |
rs764584810 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725456 | TATATTCTATTTCAC[A/G]TTAGTCATTCTTCTA | 57531 |
rs764638580 | in-del | -/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696959 | AGGCTGGGCCATATC[-/TT]TTATGAGGGTGATGT | 57531 |
rs764642325 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860257 | AAGTATGGTATTTTC[A/G]TATGTCAAACTTAAA | 57531 |
rs764651547 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842918 | GAAGTTAGAAACCAG[C/G]CTGGCCAACATGGTG | 57531 |
rs764665339 | snp | C/T | 1.71384e-05 | 0.00292727 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750344 | GTTTTTCCTTACCAA[C/T]TCATATTCATCAAAA | 57531 |
rs764702666 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104683735 | GTTCCAGCCTGCACA[A/G]ATAGTAGGGATTTGT | 57531 |
rs764736153 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723995 | GTAAGTCTAAGTTTT[G/T]GAAACGTTATAAATG | 57531 |
rs764743744 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827035 | TAACCTTTCAAGTGA[C/T]AAAACAATATCCTGA | 57531 |
rs764769167 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753500 | CAGGCCAACAACAGG[-/T]TAAGTACCTACCCCC | 57531 |
rs764801481 | in-del | -/AA | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728435 | ACATTTAGAAAAGAC[-/AA]GAGAATAAGAGAATC | 57531 |
rs764822344 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824053 | AAGGTCTACTTAGTG[C/T]TAGGCGAGGGGACAG | 57531 |
rs764825430 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752713 | TTTTTACCAATTAAT[C/T]CCTATTATTTCCTCC | 57531 |
rs764834049 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829144 | AACTTACATGCACTG[A/G]TATATGTCTACATGG | 57531 |
rs764834135 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810991 | TACTTAGTCTAAAAT[C/T]GAAGTAATCAAGCAA | 57531 |
rs764853644 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725899 | AGTGAAGCATGCTGG[A/G]CTAAGAAAATGGCGA | 57531 |
rs764879398 | snp | A/G | 1.84446e-05 | 0.00303677 | intron-variant | HACE1 | GRCh38.p7 | 6:104744637 | AAGAAAAATATTTCA[A/G]TAATTTTCTTTAGGG | 57531 |
rs764896081 | in-del | -/T | 1.64732e-05 | 0.0028699 | intron-variant | HACE1 | GRCh38.p7 | 6:104791495 | AACAATGCCATATAC[-/T]TTTCTCACCTTGAAC | 57531 |
rs764900341 | snp | C/T | 0.000181982 | 0.00953719 | intron-variant | HACE1 | GRCh38.p7 | 6:104849120 | ATACAACTTAAGCCA[C/T]TTAAGAAAACTAAAT | 57531 |
rs764904109 | snp | C/T | 3.29576e-05 | 0.00405928 | intron-variant | HACE1 | GRCh38.p7 | 6:104850862 | TCAAAGCTTACTGAT[C/T]CTTGCCCTAGATCAG | 57531 |
rs764906408 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787345 | ATTTGGAGTCCCTGA[A/G]CTGCTTAAAGAAGGG | 57531 |
rs764910539 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820801 | TCAAAGACCTAAAGA[C/T]AGAAATACCATTTGA | 57531 |
rs764919428 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769341 | TTCCACTTTGTCATA[C/T]ATATCTGAAAGGAGT | 57531 |
rs764938294 | in-del | -/ATAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727375 | TGTATATGTATACGA[-/ATAT]ATATACACATGTATA | 57531 |
rs764939524 | snp | A/C | 1.71799e-05 | 0.00293081 | intron-variant | HACE1 | GRCh38.p7 | 6:104784217 | ACAGGAAGAATGAGT[A/C]GCATTAAGTGAAATG | 57531 |
rs764945313 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700764 | TGGATCAGTGAAACA[A/G]GAGGAAAGAAAAGCA | 57531 |
rs764958110 | snp | C/G | 1.66693e-05 | 0.00288693 | intron-variant | HACE1 | GRCh38.p7 | 6:104784494 | AGTCATTCTGTGGGG[C/G]GAAAACATCAATCAG | 57531 |
rs764993313 | snp | A/C | 1.80107e-05 | 0.00300084 | intron-variant | HACE1 | GRCh38.p7 | 6:104796764 | TATCCACCCTAAAAA[A/C]AAGATCTAAAATTAT | 57531 |
rs765017159 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803234 | AAGTCCAGGAACAGA[C/T]GGATTCACAGCCGAA | 57531 |
rs765046327 | snp | C/G | 1.6557e-05 | 0.00287719 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729642 | GTGCATCAGTAGTCA[C/G]AGGAGTTTTCCAGAC | 57531 |
rs765054820 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833762 | GAGGCTGAGGCAGGC[A/G]GATCACAAGGTCAGG | 57531 |
rs765072235 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761518 | AACTGAAACTGGACC[C/G]CTTCCTTATACTTTA | 57531 |
rs765076310 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778339 | CTAAAAACTGTTTAA[C/T]AGAGTTAAAGAGATG | 57531 |
rs765077216 | snp | C/T | 1.67318e-05 | 0.00289234 | intron-variant | HACE1 | GRCh38.p7 | 6:104796913 | AAGGGGCTCAGAATA[C/T]AAATGAAAAACACAC | 57531 |
rs765083894 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723154 | GCTTGTTGTGGCACA[A/G]TGAGAGAGAAGAAAT | 57531 |
rs765085489 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857403 | CTAATAATACTCTAG[C/T]TTCTGGGCACTCTCG | 57531 |
rs765093777 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709742 | GCAAATGGACTAACA[C/T]AACCAACCTCATCGG | 57531 |
rs765113726 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750976 | AACCCTATAATGACT[C/T]CTCATGACATCTGGA | 57531 |
rs765122604 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707150 | AAAAATAGAACAAGA[A/G]GGAACACTTCCCAAC | 57531 |
rs765153335 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735350 | AAAGTAAAAATGGGC[C/T]GGGTGCGGTGGCTCA | 57531 |
rs765185604 | in-del | -/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790108 | CACACTCAACGTGCA[-/CA]CACACACACATACAT | 57531 |
rs765195061 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779533 | AGCACTGGTGTTATA[C/T]GCATTACTGTGCATA | 57531 |
rs765199077 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688524 | GTCACTGTTTGACAG[-/T]TATTAGTTTCATATT | 57531 |
rs765202775 | in-del | -/TTTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104858103 | ATATTTTTTTCTATT[-/TTTC]TTTATTTTCCAAATT | 57531 |
rs765203805 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831141 | CAAAGCAGAAATTCA[A/G]TCTAAAATCTTAAGC | 57531 |
rs765284800 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695466 | CAATGGTGCATCAAT[A/G]TGAAGAGCCTAATTG | 57531 |
rs765288556 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803550 | CCCTGGGATGCAAGG[C/T]TGGCTCAACATATGC | 57531 |
rs765296661 | snp | C/T | 0.000137732 | 0.0082974 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859424 | GTTCGGGGCCCGGGG[C/T]CGCCTCTCAGCTCTG | 57531 |
rs765339184 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808551 | AATACCATTCTAAAT[G/T]TAATTGCAAAATTCA | 57531 |
rs765359328 | snp | A/G | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785189 | GGAGGAATGGAAGCA[A/G]CATCTTGATCTTGGC | 57531 |
rs765359734 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688736 | GCTGTGGGCTTTTCC[C/T]GGCTGATGGGAAATT | 57531 |
rs765381337 | snp | A/T | 1.81493e-05 | 0.00301236 | intron-variant | HACE1 | GRCh38.p7 | 6:104730462 | CATGAAAGAAAGATA[A/T]TTGTGACAGATAAAT | 57531 |
rs765386728 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825312 | CCCACCTCTTTGCGA[A/G]GCAGATGGGAAATTG | 57531 |
rs765395499 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850479 | CCTGAAAAGAGGATA[A/G]GTACCAATTAGTTAA | 57531 |
rs765399543 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839693 | AAAATACATAAACAT[-/AC]ACACACACACATACA | 57531 |
rs765402902 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760770 | TTGTCCCTGTTTGCA[A/G]ATGGCATGATTGTGT | 57531 |
rs765406141 | snp | C/T | 1.68761e-05 | 0.00290478 | intron-variant | HACE1 | GRCh38.p7 | 6:104797071 | CAATCTTTTTAAAGT[C/T]TTTCTCTATGAATTA | 57531 |
rs765410158 | snp | A/G | 3.30366e-05 | 0.00406413 | intron-variant | HACE1 | GRCh38.p7 | 6:104811401 | TGCACTGTCTGAGGG[A/G]GAAAAAATAATTAAA | 57531 |
rs765431700 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689943 | TAGGGCATAGTCTCT[G/T]AATCCTCTGTAAATT | 57531 |
rs765448507 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776003 | TGGAATATGTCTTTA[G/T]TAAGTTAGAGAGCTC | 57531 |
rs765454964 | snp | C/T | | | intron-variant, missense, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833155 | GTTCTGTCCGCCCAT[C/T]CACAGCCAGCCAATG | 57531 |
rs765455997 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747747 | TACTCACCTCAAGAG[A/G]TTTTTTGTGAGCGTT | 57531 |
rs765517532 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855343 | AGCTACTCGGGAGGT[C/T]GAGGTAGGAGAATGG | 57531 |
rs765519227 | in-del | -/GAGAAG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716598 | AGGAAGCTGAGGTAG[-/GAGAAG]GAGAATTGCTTGAAC | 57531 |
rs765554803 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735579 | CAGCTTACAGTGAGC[C/T]GAGATGGCGCCAGTG | 57531 |
rs765566155 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747802 | CCTGGCAAATACTAA[A/G]TGCTTAATAATTATT | 57531 |
rs765568061 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726527 | CTATCCTTTAAAGCT[G/T]GCGTTTCCCGATACC | 57531 |
rs765605291 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716514 | GCTAACATGGTGAGA[-/C]CCCCGTCTCTACTAA | 57531 |
rs765609483 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764815 | GGCAGTCAAACATCA[-/T]TTCTTTCACTTGACA | 57531 |
rs765642616 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765865 | CACAGAACGTCAACA[A/G]TTTATTCTTTTGTTT | 57531 |
rs765646713 | snp | A/G | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728060 | CCACCTCAGCCTCTC[A/G]AAATGCTGAGATTAC | 57531 |
rs765651848 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694980 | TGGAACACTCATGTC[A/G]GAGAGTTAAAGCCAC | 57531 |
rs765657633 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782353 | ATTAGCCAGGTGTGG[C/T]GGTATGCACCTGTAG | 57531 |
rs765661314 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843851 | TTGTGGTAAAATACA[C/T]ATAAAATTTGCCATC | 57531 |
rs765667457 | in-del | -/G | 3.58941e-05 | 0.00423624 | intron-variant | HACE1 | GRCh38.p7 | 6:104750292 | GAATTACATCAACTA[-/G]AGTTTTTTGTTGTTG | 57531 |
rs765670890 | snp | A/C/G | 5.05475e-05 | 0.00502709 | intron-variant | HACE1 | GRCh38.p7 | 6:104776852 | AAGAAATAAAATTAA[A/C/G]CATCAACAGAAATAT | 57531 |
rs765686378 | snp | C/T | 3.30639e-05 | 0.00406581 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777073 | CTTTGCACAATTTGC[C/T]TTTGACACAACTTCA | 57531 |
rs765709886 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782210 | AAATTGAACTTGTCC[A/G]GGTGTGGTGGCTCAT | 57531 |
rs765710660 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783641 | GTACACATCTGGTAG[A/G]GGAAAGGTGGTCAGG | 57531 |
rs765715029 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839599 | TCAGAATATTGACTA[C/T]GGTGGTGAAAACCTA | 57531 |
rs765737771 | snp | C/G | 3.53251e-05 | 0.00420253 | intron-variant | HACE1 | GRCh38.p7 | 6:104791692 | GAGATTAGAGTAAAA[C/G]AAATTACATATTAAA | 57531 |
rs765757479 | in-del | -/ATTCTTAATAA | 6.04175e-05 | 0.00549592 | intron-variant | HACE1 | GRCh38.p7 | 6:104772102 | TACAAAATAATATAT[-/ATTCTTAATAA]TATTAAGAATCTATA | 57531 |
rs765765014 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718739 | ATTCATCATTGTTGG[A/G]TTCAATTAGCCAATA | 57531 |
rs765772042 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714397 | TCCACTAAAGAACTG[A/T]CTTCGACTCCTGAAA | 57531 |
rs765791203 | in-del | -/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718563 | TATTTTGAATTTTAT[-/TA]TAGTTTTTATTAACA | 57531 |
rs765804130 | snp | C/T | 1.67242e-05 | 0.00289168 | intron-variant | HACE1 | GRCh38.p7 | 6:104795550 | AGACACTGCTACCTA[C/T]TGATTTCCTCTTATT | 57531 |
rs765859242 | snp | A/G | 1.64836e-05 | 0.0028708 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104850951 | CACACGTCCGAATGC[A/G]TAATTGACATCAAAT | 57531 |
rs765885832 | in-del | -/AGCAGCA | 1.71465e-05 | 0.00292796 | intron-variant | HACE1 | GRCh38.p7 | 6:104784213 | TGGACAGGAAGAATG[-/AGCAGCA]AGTAGCATTAAGTGA | 57531 |
rs765909605 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750646 | TTGAGGAAAAAATTC[C/T]AGGGACTCAATCATC | 57531 |
rs765928533 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775658 | CAAATTCACCTCAGA[A/G]CAAAGAATTAAAGGT | 57531 |
rs765931812 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813118 | AATCTCAAGTAGAAG[A/G]AATTAAAAGCTTCCT | 57531 |
rs765953878 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848196 | TGCGGTGGCTCACGC[C/G]TGTAATCCCAGCACT | 57531 |
rs765956137 | in-del | -/ATTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689368 | AATGAATCAATCATG[-/ATTC]ATTCTCTGTTCACTC | 57531 |
rs765963417 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791630 | TAAAAGGCTCTTCAT[C/T]TGAGCATCATAATTG | 57531 |
rs765973838 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830680 | AATAAACAAACTTTG[C/T]ATCCTTGTAGTTAAT | 57531 |
rs765990302 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814920 | AGCCAGCAGAACTCT[A/G]AGTCAATTAAACATC | 57531 |
rs766004270 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854060 | CAACTGAAACCTCGG[-/TT]AAAGCAAAGCTGCAG | 57531 |
rs766042175 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798454 | AGAAAACTCTGCAAC[A/G]TTATTATAGGTCTAT | 57531 |
rs766080530 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746839 | GCATGTCTTACAATT[A/C]ATGAGTTTAATCCTT | 57531 |
rs766082739 | in-del | -/AAC | 0.00101696 | 0.0225266 | intron-variant | HACE1 | GRCh38.p7 | 6:104785381 | GATTAAAAAAAAAAA[-/AAC]AAAACACAACTAGAC | 57531 |
rs766084047 | snp | A/G | 1.66974e-05 | 0.00288936 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750407 | AAAGCCCTGTAAAAA[A/G]GCATTGATCTGAGGC | 57531 |
rs766090783 | snp | G/T | 1.65321e-05 | 0.00287502 | intron-variant | HACE1 | GRCh38.p7 | 6:104849273 | TTAAAAGACAGTTCA[G/T]ATACATTCAACATAC | 57531 |
rs766105771 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751143 | ATTCCCAAAACACAA[A/G]CTTGTCCGGGCCCCA | 57531 |
rs766119131 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737679 | CTCGGAGGGTCCTAC[-/G]CCCACGGAGTCTCGC | 57531 |
rs766127881 | in-del | -/CCGCGATCCTCCGCGATCAGCCGCCCCAC | 7.303e-05 | 0.00604232 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859657 | TCCTCGGCGCGCCCT[lengthTooLong]CGGCGGCCTCCGCGC | 57531 |
rs766136458 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832772 | GGTGCAGTGGTTCAC[A/G]CATGTAATCCCAGCT | 57531 |
rs766137032 | snp | A/T | 1.67806e-05 | 0.00289656 | intron-variant | HACE1 | GRCh38.p7 | 6:104784517 | TCAATCAGAATACAC[A/T]GGCAAAAGTTTGTGA | 57531 |
rs766138426 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819166 | AGCCCAAAAGCTTCT[G/T]AAGCCAATTAACAAC | 57531 |
rs766141661 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763870 | GCCTGGCCAACATGG[C/T]GAAACCTCATTCCTA | 57531 |
rs766144219 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800612 | CAGGAAACTCCAACA[C/G]ACCTGCAGCTGAGGG | 57531 |
rs766153040 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760308 | TACTCAATAAAATAC[C/T]GGCAAACCAAATCCA | 57531 |
rs766161512 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751896 | TCTTCCTTTATTTTT[-/C]CTTTTTTTGGCACTA | 57531 |
rs766186516 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772731 | AAAATGGCAAGGGCA[A/G]TAAGTTACCAATTAC | 57531 |
rs766205493 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843464 | ACAAACACTACTTGA[C/T]GCAAGATACAAAACT | 57531 |
rs766212021 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699274 | ATATTTATGGTCTAG[A/G]ATATAATAAAATACA | 57531 |
rs766230905 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831004 | ACCTAATCTTGACCT[C/G]TCCACCTCAGCCTCC | 57531 |
rs766233516 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788731 | TCCCCATGTTCACTG[C/T]GCTTCAAAAATAAAA | 57531 |
rs766284913 | snp | A/C | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860970 | TGCCAGTGCCGTCCT[A/C]AATCAGTTCCAGCTA | 57531 |
rs766298616 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700319 | AACTCAAACTCATAA[A/C]CACTACTGAACTGTC | 57531 |
rs766312420 | snp | A/G | 1.68672e-05 | 0.00290402 | intron-variant | HACE1 | GRCh38.p7 | 6:104730292 | CATTTAAATAAACCA[A/G]GTCAACATACCATGT | 57531 |
rs766351522 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732803 | AAACATTTAACAATC[C/T]AATATGAAAGAATCC | 57531 |
rs766352235 | in-del | -/AAC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722362 | GCTATATGAACACAT[-/AAC]AGTCTCCAAATCATG | 57531 |
rs766372748 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845022 | TCCAGTGAGTAAACA[C/G]TAATACATACAATAC | 57531 |
rs766378417 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812816 | ATAGGAATGGTTATG[A/T]AGAGCTAAAAATAGG | 57531 |
rs766400256 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690187 | ATCAAGTATATAAGG[A/G]AGACCATCTGGGCCT | 57531 |
rs766410176 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685409 | GGAAATTGTAGAAAG[A/C]GCCAGGCTTTCAGAG | 57531 |
rs766414567 | in-del | -/GTG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841978 | ATTTTTGCAAAGAAA[-/GTG]GTGGTATGGCAAAAT | 57531 |
rs766416104 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743706 | TATTTTTTAGGCCAT[G/T]AATCTTGACACTTTA | 57531 |
rs766463594 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833925 | AGGAGGCGGCAGTTG[C/T]GGTGAGCTGAGATCG | 57531 |
rs766469176 | snp | A/C | 1.64811e-05 | 0.00287059 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771968 | GAAGTAAATATTGAC[A/C]AGCTGCCTGTGGTTC | 57531 |
rs766486544 | snp | G/T | 1.81529e-05 | 0.00301266 | intron-variant | HACE1 | GRCh38.p7 | 6:104785353 | TTTTTTAAACATCAT[G/T]CTTAAACTACAGGAT | 57531 |
rs766510710 | snp | C/T | 4.36719e-05 | 0.00467269 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852409 | TTCATTTATCCCCTA[C/T]TTTGTGCAAGGGGTG | 57531 |
rs766521365 | in-del | -/TAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775682 | TAAAGGTTACAGAGT[-/TAAA]GCAGGCAGTTCCATG | 57531 |
rs766528409 | in-del | -/T | 1.65048e-05 | 0.00287265 | intron-variant | HACE1 | GRCh38.p7 | 6:104744640 | AAAATATTTCAATAA[-/T]TTTTCTTTAGGGAAA | 57531 |
rs766538464 | snp | A/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854878 | TGAAAAACAATTTAG[A/T]CCTTGGCAACATTCA | 57531 |
rs766542223 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763099 | TTTATAGGTTTGGTA[A/G]TTTTTAAAGTTAATT | 57531 |
rs766545946 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835731 | TAGGGTCTCAATATT[A/G]TCCATCGAAATGGAT | 57531 |
rs766548858 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776197 | AATGACTGAAAATAA[A/G]GTTAGTATACATAAA | 57531 |
rs766563587 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857304 | AAGATAAATTAAATT[C/T]AAGGAACAAAATGAA | 57531 |
rs766611532 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785229 | TCAGTAAAATAGAAG[C/T]GATCTCTGTTGAGTC | 57531 |
rs766618313 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840588 | AATCCGAGCACTTTG[A/G]GTAGCCAAGGCGGGT | 57531 |
rs766635358 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794107 | AGGTTTATTTATTAG[C/G]TTGGCAAATCATTTA | 57531 |
rs766640002 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818707 | GTAGGCTTCAACCTA[A/G]GGATGCAAGGTTGGT | 57531 |
rs766646092 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767806 | CTTCTTCCCATCCTT[-/A]ACTCCTACTCGACCA | 57531 |
rs766725695 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739182 | CGCTAAACATGGAAA[A/G]GAACAACTGGTACCA | 57531 |
rs766732901 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841458 | TCTGTTGCACGTACC[A/G]TGTCACTAAGCATCC | 57531 |
rs766733045 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823587 | AAAGTTTTCAATAGC[A/G]CACTTGCAGATAAAA | 57531 |
rs766783857 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715536 | AAGGAAATTTTGAGG[A/C]AACAATATTCAAAGA | 57531 |
rs766784306 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716697 | AAGACTCCGTCTCGA[-/G]GGAAAAAAAAAAAAA | 57531 |
rs766844206 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768150 | ATCTATTTGGTTTCA[C/G]TTTATAATCACCAAA | 57531 |
rs766901240 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104707225 | AAGCATCACAAAAAA[G/T]AAAACTATAAGCCAA | 57531 |
rs766913612 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815214 | CGTCCAGGCTGAGGT[C/G]ATCTCAGATGGAGAT | 57531 |
rs766915902 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703618 | CAGACAGAAGAGAGA[C/T]GAAAAAACACCTCTA | 57531 |
rs766962324 | in-del | -/AGGG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691978 | GGGAGGAAGGAAGGA[-/AGGG]AGGGAGGGAGGGAAG | 57531 |
rs766999698 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767961 | AAAGTGATGCTAACA[-/T]TTTAAACCCCTACAG | 57531 |
rs767008500 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792892 | TACCCAATAAATACC[A/T]AGGGCTGCAGAAGCT | 57531 |
rs767028363 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708193 | ATTCACAAAAAGCTA[C/T]TGGAAATAACAAATG | 57531 |
rs767040232 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700805 | CATTGAAATTAAAAA[A/C]ATTTTTAGGTCGTCC | 57531 |
rs767060211 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800358 | CAGCTCAGAAGAGAG[C/T]AGTGGTTCTCCCACC | 57531 |
rs767109457 | in-del | -/TTG | 1.78947e-05 | 0.00299116 | intron-variant | HACE1 | GRCh38.p7 | 6:104750299 | ATCAACTAGAGTTTT[-/TTG]TTGTTGTGTTACAAC | 57531 |
rs767117543 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816727 | CAACAATAGGAGACC[C/T]ACTGACAGCTTGCAT | 57531 |
rs767125120 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772179 | ACTTCAGCAAAGCTA[A/G]GGTTACATTATGTAT | 57531 |
rs767147337 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769988 | TAACTTTTGTGCTGT[A/G]CTTTTCATTTTACAA | 57531 |
rs767165120 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783786 | TGTAATTTCCCAAAT[A/G]TATTTGGGGGCTAAA | 57531 |
rs767221749 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104728517 | CATGTCTCTCAAACA[A/T]TACTGGCAAACACAA | 57531 |
rs767230193 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784726 | ATCTTGAAATTTGGT[G/T]CATTTCTGCTCTACA | 57531 |
rs767238906 | snp | C/T | 1.65378e-05 | 0.00287552 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851002 | AGAAACAGACCTATG[C/T]CAAAATAAAAATGAG | 57531 |
rs767247506 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748543 | ACTGAAATGGGGTAC[A/G]TGCACAGCCTATGTC | 57531 |
rs767300655 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749879 | CATAGGTTTGAAATA[A/T]AGAATTATAAAATTA | 57531 |
rs767316187 | snp | A/C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798251 | TACTCTTTCCACAAT[A/C/G]ACATTACCTAAAGAG | 57531 |
rs767323118 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748187 | AAATATTCATAATAC[A/T]TATATCTGATAAAAG | 57531 |
rs767361405 | in-del | -/A | 0.000116205 | 0.00762161 | intron-variant | HACE1 | GRCh38.p7 | 6:104843324 | AAAAGAGTCATGGAT[-/A]ACTGGTACTTAAAAA | 57531 |
rs767372302 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700538 | CTGGCTCCCAAGAGG[G/T]CAGTGCCCTTGATGG | 57531 |
rs767377915 | in-del | -/ACACT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104739879 | ATTTTTTTCAGCACC[-/ACACT]ACACCTATTCCAAAA | 57531 |
rs767379827 | in-del | -/GC | 2.57935e-05 | 0.00359111 | frameshift-variant, upstream-variant-2KB, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104859586 | GGGCAACTCCACGGT[-/GC]GCGCGCGGCGCAGCG | 57531 |
rs767411043 | snp | A/G | 5.02685e-05 | 0.00501316 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771356 | GCATATTCTGGATCA[A/G]TGGATGCCACATCTT | 57531 |
rs767413249 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845311 | ATTATTAATATTCAA[C/T]CTTGTAAGTCAATAG | 57531 |
rs767415845 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789130 | AATGAACAGGAGATC[A/T]GATTCCCATGGATGA | 57531 |
rs767425609 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687135 | CATGCAGAGGATATT[C/T]CAAAGTCGAAAACCA | 57531 |
rs767431471 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846594 | TGGCAAAGAGAAAAA[C/T]GCTAAAGCAAGCCAA | 57531 |
rs767439437 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719136 | ACAATAGAAACAGAC[A/C]CATGCACAGATGGAC | 57531 |
rs767440402 | in-del | -/TACTGACT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830697 | CCTTGTAGTTAATGG[-/TACTGACT]TACTGACTTTGAGTT | 57531 |
rs767464194 | snp | C/T | 3.30295e-05 | 0.0040637 | intron-variant | HACE1 | GRCh38.p7 | 6:104771165 | CCAAGTTACAAACAA[C/T]GGTTAAGGTAAAAAC | 57531 |
rs767487235 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734371 | AGAAAGATACTTCAG[A/T]ATCTAAATATAAACT | 57531 |
rs767489715 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713471 | TTTATTAAATGCTTA[C/T]CACAAGCCTATGCAG | 57531 |
rs767494325 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730158 | GGGCACAAAAAACTA[C/T]ATAATTACTCATCAG | 57531 |
rs767519260 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830857 | ACTTGCTGTTTCTGA[A/C]CTGTTCTGGTTCACC | 57531 |
rs767608850 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737769 | GGCGCCCGCCATTTT[C/T]CAGGCTTGATTAGGT | 57531 |
rs767610402 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764076 | AAAAAAAGTACTGCA[C/T]ACTTTTTATTTTTTG | 57531 |
rs767622257 | snp | C/T | 1.65277e-05 | 0.00287464 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729667 | CCAGACTTCATTATG[C/T]CATTGTGTAACCATA | 57531 |
rs767622763 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726330 | AATGCTTTGCAGGAA[C/T]ATGCACCCATGCACC | 57531 |
rs767637716 | snp | A/C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819304 | TGCCACAAAAAGAAT[A/C/T]AAAAACCTAGGAATA | 57531 |
rs767639076 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823431 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 57531 |
rs767655856 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821167 | TACAGAGGGGAACAA[C/T]ATACACTGAGGCCTT | 57531 |
rs767657784 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805026 | AGAAAAAACAAACAA[C/G]CCCATCAAAATTGGG | 57531 |
rs767663580 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752653 | CATGTGAACGTTACC[C/T]ATTTTAATTGCATTC | 57531 |
rs767685049 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809075 | GTCTCTATTTTAACT[A/G]TTATAAATGGCATTG | 57531 |
rs767695795 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763467 | CAGAAAGTAAAGGGA[C/T]CACTATCTCAGCCAC | 57531 |
rs767771147 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841164 | TTGTTTAGGGAGTGG[G/T]AAGTTTGGAGGTTGG | 57531 |
rs767771258 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711607 | GTCTGGTAGAGGAGC[A/G]CACTCTTGTGTGTGG | 57531 |
rs767802964 | snp | A/T | 1.67829e-05 | 0.00289675 | intron-variant | HACE1 | GRCh38.p7 | 6:104785362 | CATCATTCTTAAACT[A/T]CAGGATTAAAAAAAA | 57531 |
rs767833540 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810933 | ACATAACACAGTAAA[C/T]GATGGGAATTACCAG | 57531 |
rs767865394 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684578 | TGCTGGTTACTTTTA[A/C]ATCTACCTCTATCTC | 57531 |
rs767884356 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703821 | ATTAAACACTTAAAA[G/T]ATATTTATAATGGGC | 57531 |
rs767898789 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809979 | GGGGGAAAGGTTTGA[A/G]GAAGAAAATCTGAAG | 57531 |
rs767925997 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757056 | GTATAAACAAAGAGG[C/T]AGGGAAGCTTGAACT | 57531 |
rs767955549 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716860 | CTTAACTTTTTAATA[A/G]TTGGGAAAATGAAAA | 57531 |
rs767976657 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104692226 | AGATAGCTCTAGGTG[C/T]GCTGAATGAGCTCCA | 57531 |
rs767979450 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744061 | GGGTGGTAAGTTACT[C/G]ACAATTCAGAGTAAT | 57531 |
rs767982277 | snp | A/G | 1.6473e-05 | 0.00286988 | intron-variant, missense, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104833149 | GGAGTAGTTCTGTCC[A/G]CCCATTCACAGCCAG | 57531 |
rs768017013 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852063 | ATACTTAGTATTTCA[A/G]TATTCATTAAGAAAA | 57531 |
rs768024971 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723715 | GACTGCTGATACACA[C/T]TGATGTACCTTAAAT | 57531 |
rs768031443 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744557 | ACTTGTGTATTCTGT[A/G]TTTTTTATCCAATCA | 57531 |
rs768032594 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745574 | GCCTCCCAAGTAGCT[A/G]GGACTACAGGCGCCT | 57531 |
rs768052901 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766395 | TACCACTTATGGCTT[C/G]ATGTCAGTACTCGAA | 57531 |
rs768058391 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856683 | CAGGTGATCCACCCA[C/T]GTCGGCCTCCCAAAG | 57531 |
rs768067874 | in-del | -/G | | | frameshift-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744208 | CCTCTTGAGTAATGT[-/G]CTTCTACAACTTCCC | 57531 |
rs768078440 | snp | C/T | | | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796657 | ACAAATACAATACCA[C/T]GTTTTCTCGGAGGTC | 57531 |
rs768078693 | snp | A/G | 1.6684e-05 | 0.00288821 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784152 | GAGAAAGTGAAAGTG[A/G]TCAAATATAATTTTG | 57531 |
rs768092339 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794637 | GGCCAGGCGCATTGG[C/T]GCACGCCTGTAATCC | 57531 |
rs768095791 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779699 | TTGAAGTCAGATAAA[C/G]ATGGTTTGAAATCCT | 57531 |
rs768144827 | snp | A/G/T | 9.99124e-05 | 0.00706734 | intron-variant | HACE1 | GRCh38.p7 | 6:104784490 | GTGAAGTCATTCTGT[A/G/T]GGGGGAAAACATCAA | 57531 |
rs768155288 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711115 | TGACTTAGCAGTACA[C/T]TGGGCACAGATCAAG | 57531 |
rs768179797 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757812 | GAAAAAAGGTTAAAC[A/G]AATGGCTAACTAGAA | 57531 |
rs768191042 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834962 | CTAGATAAGAGACAA[C/T]AGGCACATTGAACAA | 57531 |
rs768195480 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787207 | AACCAGTACTATGCA[C/T]TAGGTAGTCGGGTTA | 57531 |
rs768217806 | snp | A/C | 0.000168563 | 0.00917895 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859643 | CATCGCTCTCTCCAT[A/C]CTCGGCGCGCCCTCC | 57531 |
rs768238585 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751703 | AAAATGAATTATATA[C/T]AGAGAGAGAAAGAGT | 57531 |
rs768314021 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791547 | TTCCCATTGTAGCCC[A/T]TATCAATTCCATTAC | 57531 |
rs768315293 | in-del | -/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772545 | TCAGGAGTAGAACAC[-/TA]TGAGAATAACTAAAA | 57531 |
rs768350759 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850106 | AGGCGCACGCCATCA[C/T]GCCGAGCTGATTTTT | 57531 |
rs768352043 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818725 | ATGCAAGGTTGGTTC[A/T]ACATACACAAATCAA | 57531 |
rs768355360 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712294 | TTTAAGGTCTTTCCA[A/G]TGCTTTAAATCATAT | 57531 |
rs768377593 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810486 | AGGCCTAAATAAATA[G/T]TACAATTCATATAAT | 57531 |
rs768439023 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833415 | GGGGTCTTGCTATGT[C/T]GTTCAGGTTGGACTC | 57531 |
rs768442356 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746823 | GTGGGACAGGCTTTA[C/T]GCATGTCTTACAATT | 57531 |
rs768456211 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805498 | AGAAAATGTGGCACA[G/T]ATACACCATGGAATA | 57531 |
rs768469264 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737030 | GGCTCACACCTGTAA[C/T]CCTAGCACTTTGGGA | 57531 |
rs768488919 | snp | A/C | 1.65704e-05 | 0.00287836 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729623 | ACTTCTGCCATTCTG[A/C]ATTGTGCATCAGTAG | 57531 |
rs768512262 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723082 | GACTACCCATGATCT[A/G]TGATCTGACAATACA | 57531 |
rs768518315 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815115 | GGGCTCTGAAGAAGA[C/G]AGTAAGATGTGGGAA | 57531 |
rs768576065 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842840 | ACACAGGCCAGGTGC[A/G]GTGGCTCACGCCTAT | 57531 |
rs768581814 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749324 | ATGCTAACTGAAGCC[A/G]TTAACTGTACAGCTT | 57531 |
rs768586079 | in-del | -/ATAT | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727666 | TGAATACATACACAC[-/ATAT]GTATGTATATGAATA | 57531 |
rs768595012 | snp | G/T | 1.65625e-05 | 0.00287766 | missense, utr-variant-5-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104843294 | TACTCATACATTTCT[G/T]CTGCCTGAAAAGAAA | 57531 |
rs768599762 | snp | A/T | 3.49375e-05 | 0.00417942 | intron-variant | HACE1 | GRCh38.p7 | 6:104785385 | AAAAAAAAAAAAACA[A/T]AACACAACTAGACAA | 57531 |
rs768600026 | snp | A/C | 1.65116e-05 | 0.00287324 | intron-variant | HACE1 | GRCh38.p7 | 6:104777191 | CACATATATCAGTTT[A/C]TTTGTTAAGCATACC | 57531 |
rs768600728 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689688 | TGGAGAGCAAGGCCA[C/T]GTGCTACCTTAAGCA | 57531 |
rs768611461 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795766 | AGTACCTATTAAGTA[C/T]CTTAAAGCCAATTAG | 57531 |
rs768623577 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826205 | AAACTTGTCTTCCAT[-/G]AAACTGGGCCCTAGT | 57531 |
rs768632038 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703435 | AAAGCATGGCCCCAA[A/G]TGTCCATTAAAACTT | 57531 |
rs768675848 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783342 | TATACATATGTTTAT[G/T]ATCTCCCCAGCCAGA | 57531 |
rs768705196 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757523 | AAAAGGACATCCACA[A/C]CAAAACCCCATCTAT | 57531 |
rs768715773 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778643 | CCAAAAAAAAAAAAA[-/AT]TGTTTTAATTAGCCA | 57531 |
rs768724960 | snp | C/G | 1.66081e-05 | 0.00288163 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795673 | GAGACAAATGCTCCA[C/G]AACTTGCCGTAACTA | 57531 |
rs768738282 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826016 | ACATCACTATCTGAG[C/T]TCTGCCTCCTGTCGG | 57531 |
rs768779734 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766140 | ACAAATGCACATCGG[C/T]CTTGGCCCCACGTGG | 57531 |
rs768814699 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768623 | GGCTCAATTTATTGT[A/G]AGAAATGTTTATATA | 57531 |
rs768821517 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696024 | GTGAGCCACCGTGCC[G/T]GGCCCTCCTTTTGCA | 57531 |
rs768827544 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839371 | AACTATTGATAAGTA[C/T]AACCTAGATAAGTCT | 57531 |
rs768827613 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856324 | AAACACAATTATCCC[A/C]ATCACATATGCTAAA | 57531 |
rs768861137 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824757 | TTAAAGATACAAAAG[A/G]AAAAAAAGTGACAAA | 57531 |
rs768869556 | snp | A/G | | | nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104683015 | GGCGGATGGCAGGAA[A/G]AGGGGAGCATTCACA | 57531 |
rs768880347 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849753 | TCCCGGGTTCACGCC[-/A]TTCTCCTGCCTCAGC | 57531 |
rs768887712 | snp | C/G | 1.65261e-05 | 0.0028745 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777051 | GTACAGCAATCCCTT[C/G]CTTTAGCTTTGCACA | 57531 |
rs768893834 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784406 | GTACTCCACAAACCC[A/G]GAAAGCTTACCTATT | 57531 |
rs768981373 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687775 | GCCTAGATTATAGGT[C/T]AGAAAGACCAGGCTG | 57531 |
rs768986019 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715138 | TGGACAATATCTAAG[A/G]CACTCTTGTGTTGGC | 57531 |
rs768989863 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830516 | CTTTGCCTACTATCT[C/T]GAAGAAGTCCAATAT | 57531 |
rs768992721 | snp | G/T | 3.48499e-05 | 0.00417417 | intron-variant | HACE1 | GRCh38.p7 | 6:104750497 | AAGAAGTTTTCATGA[G/T]GACTTTTCAAAAACC | 57531 |
rs769008566 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773200 | CATAATGAGCTCATG[C/T]TATATACTACTATTG | 57531 |
rs769013851 | snp | C/T | 1.68476e-05 | 0.00290233 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852273 | ACACATTTAGAACAA[C/T]GTATGCTTCTTAAAA | 57531 |
rs769041973 | in-del | -/AAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785370 | TTAAACTACAGGATT[-/AAA]AAAAAAAAAACAAAA | 57531 |
rs769047341 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847424 | TTGGGTGTGACACAT[G/T]ACAAGATATCTAACA | 57531 |
rs769053546 | in-del | -/ACAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104741520 | ATACACCAACAACAG[-/ACAA]ACAGAGAGCCAAATC | 57531 |
rs769067740 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721293 | AGGTTGCAGTGAGCC[A/G]AGATCACCCCACTGC | 57531 |
rs769069938 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848104 | TGATCCGCCCGCCTT[A/G]GCCTCCCAAAAGGCT | 57531 |
rs769076273 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799500 | TGAATTGTTTTTCAT[C/T]TAAATAAACTTTAAA | 57531 |
rs769076847 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751605 | ACCACACTCCAACCC[A/G]GGCAACAGGGCAAGA | 57531 |
rs769077282 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814753 | CCCTTGCTGCTCTCA[C/T]GAGAGCTCATGGTTT | 57531 |
rs769096930 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760801 | ATTTAGAACACCCCA[A/T]TGTCTCAGCGCAAAA | 57531 |
rs769113091 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838378 | CAGACCAATGGGACA[-/G]AACAGAGAACCCAGA | 57531 |
rs769159103 | snp | A/C | 1.67293e-05 | 0.00289212 | intron-variant | HACE1 | GRCh38.p7 | 6:104784972 | AAAAAATAATAAGCC[A/C]AAACTTTCTTACCCC | 57531 |
rs769169079 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777916 | AGGCACGCACCACCA[C/T]GCCTGGCTAATTTTT | 57531 |
rs769199038 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861870 | CTTATCACCTCCTGT[C/T]CAACAGAACTTTCTG | 57531 |
rs769223413 | in-del | -/T | 3.77751e-05 | 0.00434581 | intron-variant | HACE1 | GRCh38.p7 | 6:104811263 | ATATATATATATATA[-/T]ATATATATATGAGCA | 57531 |
rs769226897 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765137 | GGAAAATACATGGCA[A/T]ACACATTATTTTTGA | 57531 |
rs769229028 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752080 | ACAGTAGATTCCATA[A/C]AGCTCTCCCGAAACC | 57531 |
rs769256709 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725256 | ATGTATGTGTATATA[C/T]ATACACACACACATA | 57531 |
rs769260701 | in-del | -/TTTCAACTTCTTAGAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827556 | ACTTTCTACTATTTG[-/TTTCAACTTCTTAGAAA]TGATTAAAGGAGAAT | 57531 |
rs769290703 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814288 | CAAAGTGAAATTTCA[G/T]GATAACATCAGGGAT | 57531 |
rs769323276 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712398 | CTGGAAACTTAATCA[C/T]CTATGCAACAGTGTT | 57531 |
rs769340925 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708018 | ATGTCCATCCAAGAA[C/T]AGGATGTCCACTCTC | 57531 |
rs769343894 | snp | A/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860855 | GAAATGAATGGGCAC[A/G]TGTACGTTGATGATG | 57531 |
rs769346313 | snp | C/T | 3.29734e-05 | 0.00406025 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796995 | GGCTCCTCGTAATAG[C/T]AGGATCTGTGCTGTA | 57531 |
rs769360751 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771077 | TAAACGTTTTATCTG[C/T]TATGATACTGTAATA | 57531 |
rs769370676 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733748 | TGGAGGCTAAGGAAG[A/G]AGAATCGCTTGAACC | 57531 |
rs769374156 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686334 | ACATGAGTTGACCCA[A/G]ATTTTTTTCTCTCAA | 57531 |
rs769374479 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700198 | GCCTCCCCATGATGA[C/T]GATCCTGAATCTTTT | 57531 |
rs769384607 | snp | C/T | 3.47162e-05 | 0.00416616 | intron-variant | HACE1 | GRCh38.p7 | 6:104811283 | ATATATGAGCATATA[C/T]AGCATCTGGAAATAT | 57531 |
rs769393225 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701372 | GATGTCTGTGAAATT[A/C]CGCATCTTCCCCTAA | 57531 |
rs769401432 | snp | C/G/T | 3.34971e-05 | 0.00409238 | synonymous-codon, missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730412 | CACCATGTGGGACCC[C/G/T]GGAACTAAGAGTTTA | 57531 |
rs769424869 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753255 | ACTGGGACCGAGCTC[C/T]GGGGACAAGGGGTGA | 57531 |
rs769452510 | snp | A/T | 1.69876e-05 | 0.00291436 | intron-variant | HACE1 | GRCh38.p7 | 6:104776969 | AGGCATTTCAATCTT[A/T]CTTTACATACAGTGA | 57531 |
rs769454071 | in-del | -/A | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729140 | AAATATTAAAATGCT[-/A]AAAAAAATCATTGCA | 57531 |
rs769469454 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805807 | CATGTATACCTATGT[A/T]ACAAACCCGCACGTT | 57531 |
rs769501448 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709663 | TACAGCCTGCAGAAC[C/T]TTGAGCCAAATAAAC | 57531 |
rs769534668 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856095 | CAATTTGTTGCCAGA[C/T]ACTTCCTTGTCTACT | 57531 |
rs769536420 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796020 | ATCACAAACACATAG[C/G]TGAGTAAACTAGTGA | 57531 |
rs769538583 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835368 | AGAAAAAACTATATT[A/T]AATACTGTCAGAGGG | 57531 |
rs769548644 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851687 | AAATAAAGAAAATCA[A/G]ACAAAAAACATTTTT | 57531 |
rs769551393 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818955 | ATGGGCAAAACCTGT[A/G]AGCATTACCTTGAAA | 57531 |
rs769568508 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767717 | CTAAGCTAAGCTCCA[C/T]AACTCTGATCTACTT | 57531 |
rs769587922 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780007 | CCCCATTTTACCAAA[G/T]AGAAAAATACATTAA | 57531 |
rs769602764 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790277 | AACTTTATTTTTACC[C/T]TTTTGCAAAAATTTT | 57531 |
rs769619903 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840233 | TAACTACAGGGAAAA[C/T]AAAATGTTATGCAAG | 57531 |
rs769638812 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853034 | TCATGTGTTGGAAAT[C/T]TGGTTGCTATTATGG | 57531 |
rs769650018 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737188 | TCCCAACTACTTGGG[A/G]GGCTGAGGCAGGAGA | 57531 |
rs769686144 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711271 | CTTCACTACATTCGA[C/T]GTAATTTTCACATCA | 57531 |
rs769705888 | in-del | -/CA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693058 | GTGTGTGTGTGTGTG[-/CA]CGCGCGCGCGCGCTG | 57531 |
rs769707771 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836861 | ATTGCATTTCCATCT[A/G]AACATGCATAAACTC | 57531 |
rs769721636 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730958 | AAAAACTGAAAAATT[A/C]TTTATGTTCCTCTTT | 57531 |
rs769724644 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746190 | ACATTTCTGTTTTAA[A/T]TTCAAGTAAATATCC | 57531 |
rs769729775 | snp | C/G | 1.66103e-05 | 0.00288182 | intron-variant | HACE1 | GRCh38.p7 | 6:104744500 | TCATTCTAAGCTCTA[C/G]AGAAATTTTACCTGA | 57531 |
rs769731342 | snp | C/T | 1.6507e-05 | 0.00287284 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776788 | GGATTGACTATCTCA[C/T]TGGACAGAATATCAA | 57531 |
rs769736205 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791574 | TTACTGGGGGAGGAT[A/G]GACCAATTCGAAAGA | 57531 |
rs769737529 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842098 | TTGCTTGAGGCCAAG[A/G]GTTCAAGACTAGCCT | 57531 |
rs769748683 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763822 | TGGGAGGCCGAGGTG[A/G]GCAGATCACTTGGGG | 57531 |
rs769758829 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104748717 | AAACTGAAATGCTAT[-/A]ACAGCAATTAAAATG | 57531 |
rs769762375 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833085 | TGCAGTGCTGTCTGC[C/T]CCATGGCATCCTCAA | 57531 |
rs769765234 | snp | A/G | 0.000172846 | 0.00929479 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104859691 | GCCGCCCCACCGGCG[A/G]CCTCCGCGCCCAGAG | 57531 |
rs769794325 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781436 | CAAGGAGCCCTGGTT[C/T]ATTGAGAATGGCACT | 57531 |
rs769800896 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720927 | TACAGGCCTGAGCCA[C/T]CGCGCCCGGCCCAGC | 57531 |
rs769858994 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104821744 | TCACTATTCTATTTA[C/T]CAAAAAGTAGGCATT | 57531 |
rs769863397 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712403 | AACTTAATCACCTAT[G/T]CAACAGTGTTGGGGG | 57531 |
rs769873358 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819517 | CTACAATTGATGTTC[-/T]TCACAGAACTAGAGA | 57531 |
rs769877045 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849337 | AATATTCTATTAAAC[A/G]CAATTTTCTTTTTGT | 57531 |
rs769914242 | in-del | -/CG | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727593 | ATGAATACACACACA[-/CG]CGTATGTATATGAAT | 57531 |
rs769914423 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104743513 | TATAATGAAAAAAAC[A/C]AAACTACATTTTCAT | 57531 |
rs769918490 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725877 | GGCCAGGAAGATAAC[A/G]TAGAGTAGTGAAGCA | 57531 |
rs769950029 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751150 | AAACACAAGCTTGTC[C/T]GGGCCCCAATGTGTT | 57531 |
rs769965719 | snp | G/T | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683252 | GGCGCCAGACCACCA[G/T]CGGCGCCTCACAGGA | 57531 |
rs769993255 | in-del | -/TG | 1.65086e-05 | 0.00287298 | splice-acceptor-variant | HACE1 | GRCh38.p7 | 6:104797027 | CTCTCTGACCATGAC[-/TG]TGTGGAAATAGAAAC | 57531 |
rs770007113 | snp | C/T | 3.30437e-05 | 0.00406457 | intron-variant | HACE1 | GRCh38.p7 | 6:104744253 | CAAGAACAAAAAACT[C/T]AGCTCATATTTCAGA | 57531 |
rs770008059 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708054 | TTCTATTCAACATCA[C/T]AATGGAGGTTCTAGC | 57531 |
rs770018567 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684424 | TAGAAGGTACCTAGC[A/G]ATCTATCTCATTTGA | 57531 |
rs770060186 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793895 | TAAAAATAAGATTCT[A/G]TAAAGCACTTGGAAG | 57531 |
rs770064537 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826372 | AAGATGTAAATAAAC[A/G]AAATCTGTAGTGTAC | 57531 |
rs770071310 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704245 | AATGAAGTGGAGTAA[A/G]TGACTTTCAGAAAAG | 57531 |
rs770083188 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810609 | TGGGTGTGGGTGTGA[C/T]GGCATGTGTATAATT | 57531 |
rs770093170 | snp | C/T | 0.000176538 | 0.0093935 | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104780408 | AGAGGCTCCTCTTAA[C/T]AGCATTTGTACAGCA | 57531 |
rs770100394 | snp | G/T | 3.34913e-05 | 0.00409201 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852298 | TTAAAAAGCAAAAAT[G/T]TTTGGAACAAGCACT | 57531 |
rs770104907 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757698 | ATGGAGAATGAGTTT[A/G]ATGAACTGACAGAAG | 57531 |
rs770112016 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842099 | TGCTTGAGGCCAAGA[A/G]TTCAAGACTAGCCTG | 57531 |
rs770146580 | snp | A/C | 1.6498e-05 | 0.00287206 | splice-donor-variant | HACE1 | GRCh38.p7 | 6:104777205 | TCTTTGTTAAGCATA[A/C]CTCTGTGAACCAGCA | 57531 |
rs770146581 | snp | C/T | 3.372e-05 | 0.00410595 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796696 | GTGTCATTTGAATAA[C/T]AGTCTGAAAAAGCCT | 57531 |
rs770148241 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722657 | ACATCAAGCCGCCGC[A/G]CCAATGTTTCTGTAG | 57531 |
rs770162517 | in-del | -/AGAAGAGAAGAGAAGAGAAGAGAAG/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831918 | AGAAAGAAAAGAGAA[-/AGAAGAGAAGAGAAGAGAAGAGAAG/G]AGAAGAGAAGAGAAG | 57531 |
rs770169193 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812075 | AAAATCTTAAAAATA[C/T]ATATCTGTTGATTAA | 57531 |
rs770183744 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799789 | GAATATGAACAGCTC[C/T]GGTCTGCAGCTCCTA | 57531 |
rs770199309 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709031 | TTAGATACAATGCCA[A/C]AAGCATAAGTAACAG | 57531 |
rs770211571 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856634 | AGAGCCGGGGGTTCA[A/C]CATGTTAGCCAGCTG | 57531 |
rs770233908 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817434 | CATGTGAAGAAGCTG[C/T]CTGATTCCCCTTAAC | 57531 |
rs770237221 | snp | A/C | 5.2621e-05 | 0.0051291 | intron-variant | HACE1 | GRCh38.p7 | 6:104771883 | AAACTGAAAAAAAAA[A/C]AATATAAATAAATGT | 57531 |
rs770269925 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801062 | GGCTAGAGAACTTCA[C/T]AATGCATGCACAAGC | 57531 |
rs770290209 | snp | A/T | 1.65004e-05 | 0.00287227 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771311 | CCCAGATCACTTATA[A/T]CATTATCTAAAATCC | 57531 |
rs770303848 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802167 | AACAAGAAGAGCTAA[C/G]TATCCTAAATATATA | 57531 |
rs770321749 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749667 | TACTGTGCTTTATTA[A/C]GATTTAGACAACTCA | 57531 |
rs770359688 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754640 | CAATATTCAACATTC[C/T]TAAAGAAAAGAATTT | 57531 |
rs770387585 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840555 | TGAGAGAGGCCCGTC[A/G]CGGTGGCTCACACCT | 57531 |
rs770394660 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104808715 | GGTTAACTTGTTCTA[C/T]TTCCTATATTCCTTT | 57531 |
rs770405568 | snp | C/T | 1.66197e-05 | 0.00288263 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852349 | AACCATTGGCATTAA[C/T]GTATAAACAGCAGTT | 57531 |
rs770421238 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832151 | TGCTCACTTTCCTCA[C/G]TATCTAATCTCCAAA | 57531 |
rs770431549 | in-del | -/AATAAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751641 | TCTCTTAAAGAAAAA[-/AATAAT]AATAATAACTGGTAA | 57531 |
rs770433927 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689301 | TTTCCTTATGATGCA[A/T]AAATGTGAAATAAAT | 57531 |
rs770435421 | in-del | -/ATT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725579 | CTAGGGCTGTAACAC[-/ATT]ATTAGTCAGCCCCCT | 57531 |
rs770445440 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839669 | CAAGTAATAAAAATG[A/C]ATAGAACTTAAAATA | 57531 |
rs770452802 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104701537 | ACTGTGTGATGTGGT[A/G]AGATAGGTATTATTA | 57531 |
rs770462250 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791745 | ATCCCACTGACCATC[C/T]GTTTCATATTATAAT | 57531 |
rs770473727 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777747 | TTATTTATTTATTTT[G/T]GTTTATTGTTGTAGT | 57531 |
rs770511186 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816535 | TTTTGAAACCTCTGC[C/T]TAGATTTCAGAGAAT | 57531 |
rs770531794 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721444 | ACTCCCAGCTCTCCC[C/T]CTTCACCCTCCTCCC | 57531 |
rs770534550 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790474 | GAAATGTAAGTTGGC[C/T]GGGTGCAGTGGCTCA | 57531 |
rs770557937 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735003 | AAAATTGGAATGTAA[A/G]AACAGAAATTATAAA | 57531 |
rs770589292 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747313 | CACAAGCAGCACAGT[A/G]TGGAAGAACAGTCCA | 57531 |
rs770596378 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702304 | ACATTATTTACTGAA[C/T]ATAATCCCCTTAAGT | 57531 |
rs770607475 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854298 | TCCTGAATTGGATCC[A/G]TAAATGACATTAGTG | 57531 |
rs770663890 | snp | C/T | 3.30836e-05 | 0.00406702 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785296 | TAGCCATTCATCTAA[C/T]GAGTGCCAAAGCAAT | 57531 |
rs770684803 | snp | C/G | 1.64972e-05 | 0.00287199 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744192 | TAAGAGAAGAACTCT[C/G]TCCTCTTGAGTAATG | 57531 |
rs770686757 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837171 | ATTTATATGGAAAGG[C/T]AAAGGAATCAGAATG | 57531 |
rs770716775 | snp | A/G | 1.64741e-05 | 0.00286998 | intron-variant, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833043 | ATGGCTCAACTTACC[A/G]TCTTGTGACCGTTCT | 57531 |
rs770732988 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775733 | ATACTCAAAGTGTAT[A/C]CACGAAACCCATCAC | 57531 |
rs770758397 | in-del | -/AAGAGAAGAGAGGAAGGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831971 | AAGAGAAGAGAAGAG[-/AAGAGAAGAGAGGAAGGA]AGGAAGGAAGGAAGG | 57531 |
rs770776355 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838990 | ACTGGAAAACAGGTA[C/T]ATAAAAAGGTGCTCA | 57531 |
rs770796988 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822754 | CCCAGCTACTCAGGA[A/G]GCCGAGGCAGGAGAA | 57531 |
rs770810996 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726052 | AATACAAAAATTGGT[C/T]GGGTGTGATGGTGCA | 57531 |
rs770811226 | snp | A/G | 1.7182e-05 | 0.00293099 | intron-variant | HACE1 | GRCh38.p7 | 6:104730429 | GAACTAAGAGTTTAT[A/G]TCTTAATACATTGTA | 57531 |
rs770845513 | snp | C/T | 1.67849e-05 | 0.00289692 | intron-variant | HACE1 | GRCh38.p7 | 6:104811298 | TAGCATCTGGAAATA[C/T]AAAATATCATACCTG | 57531 |
rs770856841 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757923 | TCCAATAGCCGATTC[A/G]ATCAAGTGGAAGAAA | 57531 |
rs770920433 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705633 | CCATGGGCATGTTTT[C/T]CAAGCCATTTTCTAT | 57531 |
rs770920758 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104766515 | TAATCTATGGATAAA[A/T]GTCTGTATTTTGTGC | 57531 |
rs770929061 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807752 | TGACAGAAGGAATGA[A/G]TTAATTAGTTATATA | 57531 |
rs770937910 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770640 | AGGAGAATTGCTCGA[A/G]CCCAGGAGGCAGAGG | 57531 |
rs770950763 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727513 | CATATGTATATGAAT[-/AC]ACACACACGTATGTA | 57531 |
rs770993059 | snp | G/T | 1.64765e-05 | 0.00287019 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849177 | AAGGGGTGTACAGCC[G/T]GAAATATCTTGATAG | 57531 |
rs771026817 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816267 | GTCAGAGACCTTCAC[C/T]GCAGCCCCACATGTC | 57531 |
rs771028140 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747685 | CCATGAACAAGTTCC[A/G]TATCTTCTTTGGCCT | 57531 |
rs771040519 | snp | C/T | 1.658e-05 | 0.00287919 | intron-variant | HACE1 | GRCh38.p7 | 6:104843316 | GAAAAGAAAAAAGAG[C/T]CATGGATAACTGGTA | 57531 |
rs771051556 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845045 | TACAATACAGTGTGT[A/T]TATGTTAAATACATA | 57531 |
rs771054858 | in-del | -/A | 2.26042e-05 | 0.00336179 | intron-variant | HACE1 | GRCh38.p7 | 6:104772090 | TATTGAAATAAATAC[-/A]AAAATAATATATTAT | 57531 |
rs771062392 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713679 | CGGGAAATTTCATTC[C/G]TTTTCTGACGATACA | 57531 |
rs771069923 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774768 | TCAAAAGAATAGCAG[C/T]CAAGATTCTCACCAT | 57531 |
rs771141564 | snp | C/T | | | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104853210 | GGGATGACTCTTACT[C/T]GATGCTGGTGCCACA | 57531 |
rs771172568 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812350 | ACTCAGGAGGCTGAG[A/G]TGGGAGGATCATTTG | 57531 |
rs771179803 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697786 | CTCTTGTCGTCCAGG[C/T]TGGAGCACAACGGCA | 57531 |
rs771191918 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799498 | CATGAATTGTTTTTC[A/C]TTTAAATAAACTTTA | 57531 |
rs771198514 | in-del | -/G | 2.66663e-05 | 0.00365136 | intron-variant | HACE1 | GRCh38.p7 | 6:104784953 | ATCATCTATCAGAGA[-/G]AAAAAAAAATAATAA | 57531 |
rs771202003 | snp | A/C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693432 | TCCCTCTGTCTTCTC[A/C/G]AGGGATTGGATCCAG | 57531 |
rs771220956 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780316 | AACACCTACACAGCC[A/C]AATGGTACATTTTTG | 57531 |
rs771231645 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746317 | AGTCACAGTGTTATA[C/G]AATCCTTTTCCTAGA | 57531 |
rs771232008 | snp | G/T | 1.7842e-05 | 0.00298675 | intron-variant | HACE1 | GRCh38.p7 | 6:104750309 | GTTTTTTGTTGTTGT[G/T]TTACAACATAAGAAC | 57531 |
rs771252638 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858914 | CCTGATCCTCAGGGA[C/G]CATGCCTTATTCCTC | 57531 |
rs771260639 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813824 | TACAACTGAAAAATG[A/G]AACTCAGAATAACAA | 57531 |
rs771280996 | snp | G/T | 1.65405e-05 | 0.00287576 | intron-variant | HACE1 | GRCh38.p7 | 6:104784411 | CCACAAACCCAGAAA[G/T]CTTACCTATTAACAA | 57531 |
rs771285089 | snp | A/G | 1.65102e-05 | 0.00287312 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744548 | TTCATAGCCACTTGT[A/G]TATTCTGTATTTTTT | 57531 |
rs771313052 | snp | A/G | 1.94539e-05 | 0.00311875 | intron-variant | HACE1 | GRCh38.p7 | 6:104796795 | CCAGGTTTAAAAACA[A/G]TCCCTTTTAAAGTTC | 57531 |
rs771313667 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797737 | TAGAATTGTGTAACT[A/G]TCACTCCAGGGAAAT | 57531 |
rs771315853 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787973 | AATCATACATACATT[A/G]AAACTAAATCCCAAC | 57531 |
rs771340845 | snp | C/G | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860521 | ACAATGCTAAAGTGT[C/G]TATGTGATGACACAG | 57531 |
rs771372357 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802546 | AATCAAACTAGAACT[C/G]AGGATTAACAAACTC | 57531 |
rs771401297 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826588 | ATTTTTAAAATTATA[C/T]GGCTTCTCATTTACT | 57531 |
rs771407610 | snp | G/T | 1.67379e-05 | 0.00289287 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784100 | CCTGTGCTTTTATGA[G/T]ATGCATGAATCTTGA | 57531 |
rs771411262 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684754 | CTGGTCCTTAGGAAT[C/G]GGTCTAGGGAACTCT | 57531 |
rs771425260 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734279 | TAAAAATCACTTTTT[G/T]TATTAATTCTTGGTT | 57531 |
rs771427898 | in-del | -/AAAAAAAAAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822204 | AACCCCGTCTCTACT[-/AAAAAAAAAAA]AAAAAAAAATACAAA | 57531 |
rs771432373 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830016 | CTTAGTAATTCTTGC[G/T]TCTATACTGGTTCAA | 57531 |
rs771489172 | snp | A/C | 4.14611e-05 | 0.00455289 | intron-variant | HACE1 | GRCh38.p7 | 6:104795727 | TGATTACATAGTAAT[A/C]CATTAAATCTTATCA | 57531 |
rs771501264 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786103 | ACTTTGGGAGGCCGA[-/G]GTGGGTAGATCACTT | 57531 |
rs771514911 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762498 | AGTGAGAGTTGAACA[A/G]TGAGAAACACATGGA | 57531 |
rs771517402 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802058 | AAAAAAAAAGCAGGG[G/T]TTGCAATCCAGGTCT | 57531 |
rs771548710 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751511 | GCACATGCCTGTACT[C/G]CTAGTTACTAGGGGA | 57531 |
rs771553063 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731300 | TAGGTTACTAAATAC[A/G]TACTTGCAAACATCT | 57531 |
rs771555313 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834732 | GTCAGAATGCTACAC[C/T]AGTATTAGAGAAACC | 57531 |
rs771561621 | snp | G/T | 1.69069e-05 | 0.00290743 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796715 | CTGAAAAAGCCTCGG[G/T]TGATATTGAATTAAT | 57531 |
rs771564145 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817783 | CGTTATTACAGTTCA[C/T]TACTTGACTGAGCAG | 57531 |
rs771568425 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736666 | TAATAATTCCTCGTT[A/T]TAGTTATCTCTAAGC | 57531 |
rs771586100 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722865 | TTTCTGCACTAACTA[C/T]ATATCCAGCACCCAC | 57531 |
rs771614944 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704344 | CATACATCCTCCTCC[-/T]TTACCCTGTGAGCAG | 57531 |
rs771743852 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691016 | TCGCCCCACGGTTCT[A/T]TCTTTTCTTCTTGTA | 57531 |
rs771764573 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715003 | TCATCCCTGGGGCAA[A/T]CTTTGATTGATGGGA | 57531 |
rs771782254 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709280 | TTCTCCAAAAGAAGA[C/G]ATATAAAATGGCCAC | 57531 |
rs771782366 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724100 | ATAGCAAGTGCTCAA[A/G]TGCTGAGTCCTGTGA | 57531 |
rs771785256 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818618 | CCTTGATGAAATTGA[C/T]GCAAAAATCCCTAAC | 57531 |
rs771798096 | snp | A/G | 1.64776e-05 | 0.00287028 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772015 | TCTGCCCAGCAAACC[A/G]AAAATAGTTCAAGTG | 57531 |
rs771818409 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761315 | ACTACAAGGCTACAG[A/T]AACCAAAACAGAATG | 57531 |
rs771822961 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857123 | ATGTAAGCACAAATG[C/T]GGATTTGTATCAGTA | 57531 |
rs771831766 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824468 | GAAAACTGTTCATGT[A/G]TGCCCAAAGGTTAAA | 57531 |
rs771851244 | snp | A/C | 1.65924e-05 | 0.00288027 | intron-variant | HACE1 | GRCh38.p7 | 6:104771919 | GAAATAATAATAGAG[A/C]CATACCAAGAATGTG | 57531 |
rs771859527 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785381 | GATTAAAAAAAAAAA[A/C]ACAAAACACAACTAG | 57531 |
rs771879376 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720192 | GATGTCTTTTTACAA[A/T]TGCACACAGCCATGT | 57531 |
rs771892064 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763183 | GTTGACAGGAAGATA[-/C]CAAAAAGATCATTCA | 57531 |
rs771894143 | in-del | -/TTG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844358 | CATTTTTTTTTTTTT[-/TTG]AGACGGAGTTTCACT | 57531 |
rs771906017 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713624 | GTGCTCTGATAATGA[-/T]GTGATGCTAATAATG | 57531 |
rs771923611 | snp | C/T | 3.29772e-05 | 0.00406048 | missense, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811363 | TTGGCCTGTTAATAT[C/T]AGCACCACTGTCTAG | 57531 |
rs771946729 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793266 | GCGAGACTACATCTC[-/A]AAAAAAAAAAAAAAA | 57531 |
rs771947906 | snp | A/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859119 | GGCAGTGCCCCACAT[A/T]TTAAAAAATAACAAA | 57531 |
rs771992216 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787511 | CAGCAAAACTATTTA[C/G]CTTTATATCAGAAAA | 57531 |
rs772013547 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853302 | CAGTCTGTGGTATTG[C/T]TGTATCAGCAGAAAA | 57531 |
rs772021855 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706766 | CTACACATAAAAGTC[C/G]TATAGATAAATTACT | 57531 |
rs772027934 | snp | C/T | 1.68046e-05 | 0.00289862 | intron-variant | HACE1 | GRCh38.p7 | 6:104791662 | TAGAGAGGCTGAAAA[C/T]AAAAATTAAAATATG | 57531 |
rs772070353 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746464 | GGAGCCTGGGAAACA[C/T]AGGCAGTTAGTCTGG | 57531 |
rs772070626 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770918 | GCTTATATTTCTAAT[A/C]AAATTTCTCAAAATG | 57531 |
rs772072673 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745076 | ATCATTATCATGAGG[A/G]AAAAGGAGGTAATAT | 57531 |
rs772091827 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756087 | ACACAATCAGAAATG[A/G]TAAGGTAGATATCAC | 57531 |
rs772094294 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847786 | ACGCATTTGTATACC[A/G]TGTCCATAGAGAAGT | 57531 |
rs772107623 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798114 | AAGAGAAGAAAAGAA[A/G]TGCCCAAATAAGTTG | 57531 |
rs772114456 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694120 | GCAACCTAAGTGTCC[A/C]TCAACAAATGAATGG | 57531 |
rs772127875 | snp | C/T | 1.65165e-05 | 0.00287367 | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776806 | GACAGAATATCAAAC[C/T]ACTCACGCACAACAC | 57531 |
rs772131070 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767511 | TTTCACACTCCAAGC[C/T]GAGTTTGGTTGTTTC | 57531 |
rs772142603 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844662 | AGCCTCCATCACAAC[C/T]TTTTTTTTTTTTTTT | 57531 |
rs772180296 | in-del | -/ATATATATACACATGTATGTATACGAAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727321 | CATGTATGTATACGA[-/ATATATATACACATGTATGTATACGAAT]ATATATACACATGTA | 57531 |
rs772201876 | in-del | -/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774388 | GCCACCGCGCCCGGC[-/TT]CTCTCTTTTTTTTTT | 57531 |
rs772230767 | snp | G/T | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791588 | TGGACCAATTCGAAA[G/T]ACGTGACAAAACATT | 57531 |
rs772237191 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816224 | AATGTTAATAACCAA[C/G]ACAACAGGAAAAATG | 57531 |
rs772277964 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695931 | AGACGGGGTTCCACC[A/G]TGTTAGCAAGGATGG | 57531 |
rs772301448 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822980 | TGTTCTCATCAAACT[G/T]GTGAGACAAACTTGA | 57531 |
rs772305945 | snp | A/G | 1.76599e-05 | 0.00297147 | intron-variant | HACE1 | GRCh38.p7 | 6:104750319 | GTTGTGTTACAACAT[A/G]AGAACTGATGTTTTT | 57531 |
rs772314243 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826612 | ATTTACTTGCTAAAA[G/T]TAAGCGCAGTGGCTT | 57531 |
rs772327153 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799453 | GGAAGAGCTCTCTCA[C/T]CCGCTTCTGATTCTG | 57531 |
rs772335573 | snp | A/C | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854689 | GTATTTTATTTCAAG[A/C]TAATACAATATTACT | 57531 |
rs772338048 | in-del | -/AAG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747002 | TTACGATTTTTTTTC[-/AAG]AAGAAGAAAAAGAAA | 57531 |
rs772357540 | snp | A/C | 3.29571e-05 | 0.00405924 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849216 | TGCTCCTTTCTTTAA[A/C]AGCAAAACCAAGCAT | 57531 |
rs772358978 | in-del | -/AAGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782060 | TAATTTGGCAATTAA[-/AAGT]AACTGCCAAAAACCG | 57531 |
rs772390928 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699984 | AAAAAAAAACAACAA[A/C]AAAAACCCAGGTCGA | 57531 |
rs772396204 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781908 | CCCTCTCTGGGTCAA[C/T]AAAGTGGATACCTAA | 57531 |
rs772400789 | snp | G/T | 1.69663e-05 | 0.00291253 | splice-acceptor-variant | HACE1 | GRCh38.p7 | 6:104750474 | TGGACGTACTCCGCC[G/T]GTTGAAAAAGAAGTT | 57531 |
rs772410684 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838900 | ATAGTAAAAAAAAAA[-/AA]AAAAAAAAAAAAAAA | 57531 |
rs772414060 | snp | C/T | 0.00016581 | 0.00910371 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784471 | ACAAATTCAATGAAA[C/T]GAGGTGAAGTCATTC | 57531 |
rs772445694 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753154 | TACTATGAACACCCA[C/T]TACTGTTGCCCAGTA | 57531 |
rs772451256 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783027 | ATCTGGAAATCAAGG[C/T]TCATCATTGGATGAC | 57531 |
rs772451438 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104861602 | ATCACCATTGCTCTC[C/T]AGGCTGTTGCTCCAT | 57531 |
rs772476906 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772940 | GATAGTGGCCGATGG[A/T]TGCACAACACTGTGA | 57531 |
rs772482886 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814109 | AAGGGAGACATACTG[C/T]AGAAAATAAGAATAA | 57531 |
rs772486233 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104828599 | GATCATTATTAAATA[C/T]GGATAGAAGTAGTTT | 57531 |
rs772502695 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830438 | AAAAATTCCAGGAAA[C/G]AGAAAAAGGATCCTA | 57531 |
rs772506220 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686208 | ATTTGTAGGGTTTAG[A/G]TATTATTTACTTCTT | 57531 |
rs772528569 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732580 | AAAGTACAGTTTCAG[C/T]TGGGAAAGATGAAAA | 57531 |
rs772542178 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700205 | CATGATGACGATCCT[A/G]AATCTTTTTGCTGTG | 57531 |
rs772567597 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812560 | GTAAAATAATAAAAC[G/T]AAACACCCAAAGGAA | 57531 |
rs772575370 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718132 | TCAAGGTTTTATCTG[C/T]AGATTTTTTTGTGTG | 57531 |
rs772593100 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806045 | AACTCTGTACCATAT[A/G]TAACAAAAAAGGATA | 57531 |
rs772611916 | in-del | -/TG | 4.20796e-05 | 0.00458672 | intron-variant | HACE1 | GRCh38.p7 | 6:104811272 | ATATATATATATATA[-/TG]TGAGCATATATAGCA | 57531 |
rs772617238 | in-del | -/TATGTATATGGG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727116 | GGGTGTGTGTATATA[-/TATGTATATGGG]TATATATATGGGTAT | 57531 |
rs772652041 | snp | A/G | 1.65105e-05 | 0.00287315 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771316 | ATCACTTATATCATT[A/G]TCTAAAATCCATTGC | 57531 |
rs772659242 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702824 | ATTCACTAGCTAGCA[C/T]AATAGCAAAATAGAA | 57531 |
rs772664705 | snp | C/T | 1.64844e-05 | 0.00287087 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785167 | CCCAGGTCCTGGAGG[C/T]TCAAATGGAGGAATG | 57531 |
rs772700096 | in-del | -/A | 8.41161e-05 | 0.00648467 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852377 | TTTCATTATCTGAGT[-/A]AAAAAAAAACAAAGA | 57531 |
rs772771531 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104728334 | CAGTTACTATAAATA[A/G]AGCATCCGAATCTTA | 57531 |
rs772773287 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104805167 | GAGATACCATCTCAC[A/G]CCAGTTAGAATGGCG | 57531 |
rs772802953 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845865 | GAAATAAATATTCAA[G/T]AATCATGAGACCACA | 57531 |
rs772871860 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788611 | TTTCACAATCTTTCT[C/T]GGTTACCAAAATTTC | 57531 |
rs772890597 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784993 | TTCTTACCCCGGAGG[C/T]ATCTGACAAGAACAG | 57531 |
rs772902946 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104687840 | ATAACATGCCATCCA[A/G]ATAAAATTGTGCCTC | 57531 |
rs772935329 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790375 | TTTCAATCCTAACTA[C/G]TTTTCAAGGAAGTGG | 57531 |
rs772935492 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771086 | TATCTGCTATGATAC[C/T]GTAATAGTAAAAGTT | 57531 |
rs772938238 | snp | A/T | 1.81965e-05 | 0.00301628 | intron-variant | HACE1 | GRCh38.p7 | 6:104730261 | CATTCAAAATTAATC[A/T]AAACAATTTGTAAAG | 57531 |
rs772943575 | in-del | -/TT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750501 | AGTTTTCATGATGAC[-/TT]TTCAAAAACCTTTTA | 57531 |
rs772974938 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731997 | TTTACTAGGGAAATG[A/C]CAATCAAAACCACTT | 57531 |
rs772985979 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689098 | GTGAAATTGCCAAAC[-/T]TGCAAAAGATGAATG | 57531 |
rs773012435 | snp | C/G | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104797003 | GTAATAGTAGGATCT[C/G]TGCTGTATCTCTCTG | 57531 |
rs773019055 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836968 | AATCCCCACTGTGCT[A/G]TACAAAATTCTAATG | 57531 |
rs773092137 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819028 | AACACAGTATTGGAG[A/G]TTCTGGCCAGGGCCA | 57531 |
rs773104513 | snp | A/T | 1.65097e-05 | 0.00287308 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776796 | TATCTCATTGGACAG[A/T]ATATCAAACCACTCA | 57531 |
rs773116156 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716078 | CTTTAAGGCAAAAGA[C/T]AATGAAACTAAATAA | 57531 |
rs773136742 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857204 | CATATATATTTACAT[-/AT]ATATATATATATATT | 57531 |
rs773145766 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859158 | CCCGCCTGGCCCCCC[A/G]ATGCAGCTTAAAGTA | 57531 |
rs773201515 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787668 | GGCCTAACGCAAGAA[A/C]TGACACAGGCTGATC | 57531 |
rs773201957 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843496 | CTTCTATGACTCAAA[A/G]ATAACAGGATAAAAC | 57531 |
rs773207980 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769057 | TTCTTTTTTAAGTGA[C/T]AGGATCTTGCTCTGT | 57531 |
rs773238393 | in-del | -/AGCAGAATAGACCA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754125 | ATCACAAGTATCAAT[-/AGCAGAATAGACCA]AGCAGAGGAAAGAAC | 57531 |
rs773250917 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793947 | GAGCACAGTTTAGCA[A/G]AGTAATTTTTTAAAA | 57531 |
rs773253866 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747124 | AATATTTTAAGCCCC[A/T]ATCAATTTTTTTAAT | 57531 |
rs773295379 | snp | A/T | 1.76736e-05 | 0.00297262 | intron-variant | HACE1 | GRCh38.p7 | 6:104785349 | AGTGTTTTTTAAACA[A/T]CATTCTTAAACTACA | 57531 |
rs773333047 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691855 | TGAGCACAGGAGTTT[C/G]AGGGGGCAGTGAGCT | 57531 |
rs773333407 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767875 | TTCATCCATTCCCTG[A/G]TACCTGCCCCATCTT | 57531 |
rs773337212 | snp | C/T | 0.00014871 | 0.00862165 | intron-variant | HACE1 | GRCh38.p7 | 6:104744256 | GAACAAAAAACTTAG[C/T]TCATATTTCAGAGCA | 57531 |
rs773342935 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860964 | TTTCCCTGCCAGTGC[C/T]GTCCTAAATCAGTTC | 57531 |
rs773346273 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770938 | TTCTCAAAATGCATA[C/T]GCCCAATTTATACTA | 57531 |
rs773382627 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756924 | GAGGGTCGCATGCCC[A/G]TGGAGCCTTGCTTGC | 57531 |
rs773386410 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856785 | TAAAGTAATTTCTTA[C/T]TCTTCACCTCTTTTT | 57531 |
rs773399090 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719336 | TTTCTGCCATAGGAC[-/A]AAAAAAAGCACTAAC | 57531 |
rs773399290 | snp | C/T | 3.31395e-05 | 0.00407046 | intron-variant | HACE1 | GRCh38.p7 | 6:104744509 | GCTCTAGAGAAATTT[C/T]ACCTGAATAACTGGA | 57531 |
rs773403752 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850484 | AAAGAGGATAGGTAC[A/C]AATTAGTTAACTGAT | 57531 |
rs773440121 | in-del | -/A | 1.65074e-05 | 0.00287288 | frameshift-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744563 | TATTCTGTATTTTTT[-/A]ATCCAATCACTCACA | 57531 |
rs773441436 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817672 | GGAAGAGATATTTTA[C/T]AGGAGCATATAGATG | 57531 |
rs773450439 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705569 | GTCATTTCCCAGGAT[A/G]GCTTTAAACATGTTG | 57531 |
rs773502716 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794267 | TAAAAACATAGATAC[A/C]TCAAAACATAAATGC | 57531 |
rs773504579 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815986 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 57531 |
rs773518397 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812076 | AAATCTTAAAAATAC[A/G]TATCTGTTGATTAAG | 57531 |
rs773560868 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799790 | AATATGAACAGCTCC[A/G]GTCTGCAGCTCCTAG | 57531 |
rs773570180 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104729980 | GGAAGAAAATACGTT[C/T]CTTTCAGCTTAAAAT | 57531 |
rs773570685 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104696576 | AGGAGTTTGGTCTTT[C/G]GAGGGCATAGGGGGA | 57531 |
rs773577410 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801243 | AATCTATGTTTGATT[C/G]GTGTACCTGAAAGTG | 57531 |
rs773588715 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697771 | TGAGGCGGAGTTTCA[C/T]TCTTGTCGTCCAGGC | 57531 |
rs773594228 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104812531 | TTGCCGCTTTTAAAC[A/T]AAGTACAATGTCAGT | 57531 |
rs773653787 | snp | G/T | 3.2993e-05 | 0.00406145 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777218 | TACCTCTGTGAACCA[G/T]CAGGATATCATTTTC | 57531 |
rs773670190 | snp | A/G | | | splice-donor-variant | HACE1 | GRCh38.p7 | 6:104688143 | CTGGATGTCTCACTA[A/G]CCTGTCAGCATCTTC | 57531 |
rs773674472 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830683 | AAACAAACTTTGTAT[C/G]CTTGTAGTTAATGGT | 57531 |
rs773679192 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826650 | ACTAAATGCAAACAC[A/G]TAAAAGCATGCCAAC | 57531 |
rs773714940 | in-del | -/AAG/C | 0.000435437 | 0.0147492 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852385 | TCTGAGTAAAAAAAA[-/AAG/C]ACAAAGAGTTCATTT | 57531 |
rs773733547 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790491 | GGTGCAGTGGCTCAC[A/G]CCTGCAATCCCAGCA | 57531 |
rs773750574 | snp | A/G | 1.66546e-05 | 0.00288566 | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852321 | CAAGCACTCACCTGT[A/G]TTGATCAGCCATAAC | 57531 |
rs773782069 | snp | C/T | 3.54717e-05 | 0.00421125 | intron-variant | HACE1 | GRCh38.p7 | 6:104795694 | GCCGTAACTAAATTT[C/T]TTACAAATAAAAAAA | 57531 |
rs773795064 | snp | A/G | 1.6788e-05 | 0.00289719 | intron-variant | HACE1 | GRCh38.p7 | 6:104771903 | TAAATAAATGTCTGC[A/G]GAAATAATAATAGAG | 57531 |
rs773798442 | in-del | -/TGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693032 | AGAGTGGTGTGTGTG[-/TGT]GTGTGTGTGTGTGTG | 57531 |
rs773806386 | snp | C/G | 0.000406421 | 0.0142494 | intron-variant, utr-variant-5-prime | HACE1 | GRCh38.p7 | 6:104858492 | ATCACTTGAGCCCAG[C/G]AGTTCAAGACCAGCC | 57531 |
rs773827939 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761918 | TTCTCAAAAGAAGAC[-/A]ATTTATGCACCCAAC | 57531 |
rs773831084 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731925 | AAAAGACATTTCTCC[-/A]AAAAAAAAGATAAAC | 57531 |
rs773861483 | snp | A/G | 1.662e-05 | 0.00288266 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852352 | CATTGGCATTAATGT[A/G]TAAACAGCAGTTTCA | 57531 |
rs773890518 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703169 | ACTTATAACCACACT[A/G]AGGAAGAGATTTCAT | 57531 |
rs773906976 | snp | C/T | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683263 | ACCAGCGGCGCCTCA[C/T]AGGAAGTCCGGGTCT | 57531 |
rs773960951 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830612 | CCAGATTCCACTAGG[A/G]ATTCTCCCTTCTCCC | 57531 |
rs773965000 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104791953 | GGCAACAACTTCAAG[A/G]CAACTCCTAAATTTT | 57531 |
rs773970072 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721532 | AATGAGATGACCCCA[C/G]GTCTGTACTTATCTG | 57531 |
rs774003088 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695272 | TTGCGTGCAATAAAC[-/AA]GAGAGGCGCAAGTAA | 57531 |
rs774005554 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763987 | GAGAGGCAAAGGTTG[C/T]AGTGGGCCGAGATCC | 57531 |
rs774017617 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775737 | TCAAAGTGTATCCAC[A/G]AAACCCATCACAGGG | 57531 |
rs774025738 | snp | C/T | 1.65839e-05 | 0.00287953 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771336 | AAATCCATTGCAAAT[C/T]TTTCGCATATTCTGG | 57531 |
rs774040094 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689333 | ATCATACAATTATCT[C/T]TGAAACATTTTTTAC | 57531 |
rs774068390 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747895 | CAACTTAGTAAAGTC[A/G]GAGTCCAAGACAAAC | 57531 |
rs774086461 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771916 | GCAGAAATAATAATA[C/G]AGCCATACCAAGAAT | 57531 |
rs774087108 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708151 | CTTCACAGATAATAC[A/G]AACTTGTGCATATAA | 57531 |
rs774101301 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816615 | CCTTCATGGAGAACC[C/T]CTACTAGGGCAGTGC | 57531 |
rs774105553 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807970 | GACAGCCAGATCACC[C/T]GAGGTCGGGAGTTCG | 57531 |
rs774113073 | snp | A/C | 1.65789e-05 | 0.0028791 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785305 | ATCTAACGAGTGCCA[A/C]AGCAATTCCAGAGGC | 57531 |
rs774132999 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822765 | AGGAGGCCGAGGCAG[A/G]AGAATTGCTTGGACT | 57531 |
rs774176403 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799887 | GACTGGTTGGACAGT[A/G]GGTGCAGCCCACGGA | 57531 |
rs774199145 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806313 | ATAAAAATTGAAAAA[C/T]TAGTTCAGTATGGTG | 57531 |
rs774218775 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757917 | ATAAGCTCCAATAGC[C/T]GATTCGATCAAGTGG | 57531 |
rs774236122 | snp | A/G | 3.2969e-05 | 0.00405998 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785178 | GAGGTTCAAATGGAG[A/G]AATGGAAGCAGCATC | 57531 |
rs774249698 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765590 | GATCAGCAGATGCTC[C/T]ATTGCCACAAATCTT | 57531 |
rs774280865 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781774 | ACCCACATGACTCAC[A/G]CTGGGACCCTCTTCT | 57531 |
rs774286036 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734045 | TAATCCCAGCGACTC[G/T]GGAGGGCTTAGGCAG | 57531 |
rs774288726 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104788758 | AAAAATGATCTTCTC[A/C]TTCAAATGCTCCAAA | 57531 |
rs774289142 | in-del | -/G | 1.69308e-05 | 0.00290949 | intron-variant | HACE1 | GRCh38.p7 | 6:104744471 | CTTACAAAATTAAAC[-/G]GCAAAACTTAACTTC | 57531 |
rs774303244 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753439 | ATTCCTTGTGACTTG[C/T]TAAGATCTCCCAGCA | 57531 |
rs774306799 | snp | C/T | 1.71973e-05 | 0.0029323 | intron-variant | HACE1 | GRCh38.p7 | 6:104730431 | ACTAAGAGTTTATAT[C/T]TTAATACATTGTAAT | 57531 |
rs774341766 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104856946 | ATAGTTTCAACCTTT[C/G]CAACAAAATTAATTT | 57531 |
rs774345937 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744079 | AATTCAGAGTAATAA[G/T]TCCTTATTTTAGTTA | 57531 |
rs774370540 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686980 | TTCCCAGTGAGTTGT[A/G]CCTCCTGAATGACCT | 57531 |
rs774398691 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757931 | CCGATTCGATCAAGT[A/G]GAAGAAAGGATGTCA | 57531 |
rs774403688 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700343 | AACTGTCGCAGTTGG[C/T]AATCTTCATACCTGT | 57531 |
rs774416061 | snp | C/T | 1.66946e-05 | 0.00288912 | intron-variant | HACE1 | GRCh38.p7 | 6:104797056 | AACAAGTTAAAAATA[C/T]AATCTTTTTAAAGTC | 57531 |
rs774417720 | snp | G/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851934 | GAACACAAAAATAAG[G/T]AGCACATAAGGGAAA | 57531 |
rs774418890 | snp | C/T | 1.64765e-05 | 0.00287019 | intron-variant | HACE1 | GRCh38.p7 | 6:104791461 | TTGTCAAATTCATCT[C/T]TTTTACGTCTATCTT | 57531 |
rs774420781 | snp | A/C | 1.65831e-05 | 0.00287945 | intron-variant | HACE1 | GRCh38.p7 | 6:104843317 | AAAAGAAAAAAGAGT[A/C]ATGGATAACTGGTAC | 57531 |
rs774433508 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835760 | ATAAAATAAATCCAA[A/G]GCAAGACATAATAAT | 57531 |
rs774440220 | snp | C/T | 1.65091e-05 | 0.00287303 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772053 | TTTACATAAGAGTTG[C/T]TATTAGGCTGAAAAG | 57531 |
rs774442856 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726056 | CAAAAATTGGTCGGG[A/T]GTGATGGTGCATGCC | 57531 |
rs774453977 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759363 | TCTCTCAGAGCACAG[A/T]GCAATCAAATTAGAA | 57531 |
rs774459097 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104690348 | TCAAGAAAACTCATC[C/T]TAAAATTCAGAGGAA | 57531 |
rs774492588 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849186 | ACAGCCTGAAATATC[C/T]TGATAGTTAGGATTT | 57531 |
rs774511478 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698858 | ATTACAGAAAAACAA[C/T]TAATGGACTTACCTA | 57531 |
rs774584427 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725008 | CTAATTATCAGGCAA[C/T]GTGGAAACAACTTTG | 57531 |
rs774584690 | snp | C/G | 4.01357e-05 | 0.00447953 | intron-variant | HACE1 | GRCh38.p7 | 6:104744650 | CAATAATTTTCTTTA[C/G]GGAAAAAAGTTATTA | 57531 |
rs774592160 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837201 | GGCTAACACAATCTT[A/G]ACAAAGTGAGAGGAA | 57531 |
rs774598066 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104796600 | GTAAAATGTCATATA[G/T]GCTGAGCAGGAATAA | 57531 |
rs774606440 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694502 | TCACACTTTAAATAA[C/G]TAAACAATTGAATTG | 57531 |
rs774619642 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820280 | CAGGACTTAGGCACA[A/G]GCAAAGATTTCCTGA | 57531 |
rs774651038 | snp | C/T | | | intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104780405 | TATAGAGGCTCCTCT[C/T]AATAGCATTTGTACA | 57531 |
rs774677060 | in-del | -/TATATT | 9.73094e-05 | 0.00697461 | intron-variant | HACE1 | GRCh38.p7 | 6:104811266 | ATATATATATATATA[-/TATATT]TATATATGAGCATAT | 57531 |
rs774701790 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716798 | TTTTTGCCACAAAGC[A/G]CTTCATAGAATGAAG | 57531 |
rs774710080 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842862 | CACGCCTATAATCCC[A/G]GCACTTTGGGAGGCT | 57531 |
rs774711204 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104683465 | GCTTGGCCAAACACC[C/T]AGAGCCTCCATTTAT | 57531 |
rs774749455 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768198 | GGGAATAAGGGACTC[C/T]CCCATGTGGAGATCA | 57531 |
rs774752459 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704586 | TATTTTTCTATATGC[C/T]GCAATGTGACAATGT | 57531 |
rs774770072 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769198 | CAAAACTAGGCCTGG[C/G]TAATTTTTTTATTTT | 57531 |
rs774810108 | snp | G/T | 1.67284e-05 | 0.00289205 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104784167 | GTCAAATATAATTTT[G/T]GGATTTCTAAAAGAA | 57531 |
rs774817528 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849758 | GGTTCACGCCATTCT[A/C]CTGCCTCAGCCTCCC | 57531 |
rs774835136 | in-del | -/AGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723671 | AGTGCAGGAGAACAG[-/AGA]AGAAACATGTTTCAC | 57531 |
rs774888955 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697787 | TCTTGTCGTCCAGGC[C/T]GGAGCACAACGGCAT | 57531 |
rs774929498 | snp | G/T | 3.43348e-05 | 0.00414321 | intron-variant | HACE1 | GRCh38.p7 | 6:104796881 | ATTTTTACCATTCCA[G/T]TTTCTATTATAAAGA | 57531 |
rs774956209 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757500 | AAGGAAGAGCATCAA[C/T]ATCAACAAAAAGGAC | 57531 |
rs774965483 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715004 | ATCCCTGGGGCAATC[-/T]TTTGATTGATGGGAT | 57531 |
rs774982768 | snp | A/G | 5.08255e-05 | 0.00504085 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796720 | AAAGCCTCGGGTGAT[A/G]TTGAATTAATACTTC | 57531 |
rs774984488 | snp | G/T | 6.06778e-05 | 0.00550774 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859561 | TGGCCCCGCGACCCG[G/T]CTCACCCTCGGGCAA | 57531 |
rs775039952 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708227 | TCAACAAGTTTGCAA[C/G]ACTTGAGATGAATAT | 57531 |
rs775046184 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784226 | ATGAGTAGCATTAAG[C/T]GAAATGCAAATTCAG | 57531 |
rs775095169 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709342 | ATAGTTTGAATGTTT[G/T]TCCCCTCCAAATCTC | 57531 |
rs775109321 | snp | A/G | 0.000570288 | 0.0168766 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858541 | CTCATCTCTATAAAA[A/G]AAAGGAAAGAAAATT | 57531 |
rs775110132 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777581 | GATAAATTTGGTTAT[A/G]TCTCAGAACTTAATA | 57531 |
rs775122972 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816738 | GACCCACTGACAGCT[A/T]GCATAGTGCACCTGA | 57531 |
rs775135557 | in-del | -/AGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764404 | TTATGTTTTAAGGTG[-/AGA]AGAAGCAGTTGAGAG | 57531 |
rs775136817 | in-del | -/TCCAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797680 | GAATGAACTCTCCTA[-/TCCAT]ATGCCTCATTCCCTG | 57531 |
rs775141580 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817867 | AAATCATCATTTACC[A/G]TAACAAGAAATGATT | 57531 |
rs775153789 | in-del | -/C | 1.64936e-05 | 0.00287168 | frameshift-variant, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811379 | AGCACCACTGTCTAG[-/C]AAGCACTGCACTGTC | 57531 |
rs775155049 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801410 | AACCCCAAGACACAT[A/G]ACTGTCAGATTTATC | 57531 |
rs775162649 | snp | A/G | 4.08722e-05 | 0.00452045 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852389 | GAGTAAAAAAAAACA[A/G]AGAGTTCATTTATCC | 57531 |
rs775184640 | snp | A/G | 1.6585e-05 | 0.00287962 | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729614 | TCCCAAATTACTTCT[A/G]CCATTCTGAATTGTG | 57531 |
rs775188894 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104858970 | CTAGCCCACTCAATA[C/T]TAGTCTGATGAATAA | 57531 |
rs775211236 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797593 | TTAGCCAAAAATACT[A/C]TCTAGCTTTCGATCT | 57531 |
rs775222377 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704368 | GAGCAGACCTTACTT[-/A]ATATGCGTGAGAAAG | 57531 |
rs775232445 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697797 | CAGGCTGGAGCACAA[C/T]GGCATGATCTCGGCT | 57531 |
rs775280348 | snp | C/T | | | missense, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104850959 | CGAATGCATAATTGA[C/T]ATCAAATTTTGAATT | 57531 |
rs775291620 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790733 | GCATTCCAGCCTAGG[C/G]AACAGAGTGAGGCTC | 57531 |
rs775299318 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772125 | ATCTATATGCAGAAG[-/AA]AAAGATTACTTCGAT | 57531 |
rs775303598 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844663 | GCCTCCATCACAACC[-/T]TTTTTTTTTTTTTTT | 57531 |
rs775309908 | snp | C/T | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772020 | CCAGCAAACCGAAAA[C/T]AGTTCAAGTGATCAG | 57531 |
rs775345361 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824650 | TTAAACTTTTAAAAT[A/C]CCTAAGGATTCTCAA | 57531 |
rs775376004 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104847879 | CTGGAATGCAATGGC[A/G]CAATCTCCACTCACT | 57531 |
rs775398896 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763233 | CGTATACTCAACATG[-/A]AAAAAACTGTAGACT | 57531 |
rs775400818 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806160 | GTTCAGTTGGCATTT[C/T]ATTTCAAAAACAGAT | 57531 |
rs775426176 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104737330 | TGGGGGAGGAGCCAA[G/T]ATGGCCAAATAGGAA | 57531 |
rs775439989 | in-del | -/AAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723512 | CAGTAGGCAGGTTAC[-/AAT]AACTCAGTACCTAAG | 57531 |
rs775445820 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104735340 | AAATTATATGAAAGT[A/G]AAAATGGGCCGGGTG | 57531 |
rs775462554 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727377 | TATATGTATACGAAT[-/AT]ATATACACATGTATA | 57531 |
rs775486183 | snp | C/T | 1.65312e-05 | 0.00287495 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104777035 | TCTTCTCCATGGAAC[C/T]GTACAGCAATCCCTT | 57531 |
rs775488985 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790653 | CAGCTACTGGGGAGG[G/T]TGAGGTGGGAGCATC | 57531 |
rs775562937 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703171 | TTATAACCACACTAA[C/G]GAAGAGATTTCATTT | 57531 |
rs775563328 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688449 | TCATTAAAGTATTCA[A/G]TATGAACTGACACTC | 57531 |
rs775580552 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104837399 | TGTAGGAAGGACAGC[A/C]TTTTCAACAAACAGT | 57531 |
rs775607098 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793401 | TTCTCTGTTCATTTC[C/T]ACATTGTTAACTACC | 57531 |
rs775641513 | in-del | -/CTTG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721622 | CTCCCCTTTTAGCCT[-/CTTG]CTTATCCCATCACAG | 57531 |
rs775646467 | snp | A/T | 1.71711e-05 | 0.00293006 | intron-variant | HACE1 | GRCh38.p7 | 6:104750485 | CGCCTGTTGAAAAAG[A/T]AGTTTTCATGATGAC | 57531 |
rs775788650 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104686250 | AATTTGTGAGCCTTA[C/T]CCAACGTGGCTACAT | 57531 |
rs775828320 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705835 | ATCCAACTTCATAAA[C/T]GACTAGTTAATCAAG | 57531 |
rs775864203 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104830499 | ACATAAGACAATGTC[A/G]CCTTTGCCTACTATC | 57531 |
rs775874421 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845529 | GTCGCCCAGGCTGGA[A/G]TACAGTGGCACGATC | 57531 |
rs775883601 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693816 | AAGTAAAAGAGAGGC[A/G]GCGTCACAGGAAACT | 57531 |
rs775888642 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852233 | TGTGTGTGTGTGCGC[A/G]CGTGCGCGTGCACGG | 57531 |
rs775907125 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104819681 | TATGGTACTGGTACA[A/G]AAACAGACACATAGA | 57531 |
rs775916067 | snp | A/G | | | stop-gained, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796702 | TTTGAATAATAGTCT[A/G]AAAAAGCCTCGGGTG | 57531 |
rs775917937 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104769314 | CACTGGAATACAATT[A/G]TTACTAGATCTTTCC | 57531 |
rs775933614 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104759519 | GAACAAAGACACAAC[A/G]TACCAGAATCTCTGG | 57531 |
rs775936263 | snp | A/G | 1.65891e-05 | 0.00287998 | intron-variant | HACE1 | GRCh38.p7 | 6:104843320 | AGAAAAAAGAGTCAT[A/G]GATAACTGGTACTTA | 57531 |
rs775937835 | in-del | -/TTTC | 0.000115568 | 0.00760069 | intron-variant | HACE1 | GRCh38.p7 | 6:104777188 | TCACACATATATCAG[-/TTTC]TTTGTTAAGCATACC | 57531 |
rs775977189 | snp | C/T | 0.000104838 | 0.00723935 | intron-variant | HACE1 | GRCh38.p7 | 6:104750328 | CAACATAAGAACTGA[C/T]GTTTTTCCTTACCAA | 57531 |
rs776038574 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720935 | TGAGCCACCGCGCCC[A/G]GCCCAGCGACGCTCT | 57531 |
rs776051313 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772793 | CACTTTTATAAAATA[-/T]CTAGAATAGGCAAAT | 57531 |
rs776053475 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718269 | GAATGCTATCATTCT[C/T]ATCTCCCAACAGTTC | 57531 |
rs776058340 | snp | A/C | 1.69994e-05 | 0.00291538 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750355 | CCAATTCATATTCAT[A/C]AAAAAGCTGTATGAG | 57531 |
rs776071702 | snp | C/T | 4.94629e-05 | 0.00497283 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796987 | AGATATTTGGCTCCT[C/T]GTAATAGTAGGATCT | 57531 |
rs776098232 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104754171 | CAGAGCTTGAAGACT[A/G]TCCAAAATAAGACAG | 57531 |
rs776139885 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842471 | TTTTTTTTTTTTTAA[C/T]CGTGATTATCTCAGA | 57531 |
rs776147040 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823328 | AATCCCAGCTACTTC[A/G]GAGGCTGACGCAGGA | 57531 |
rs776204331 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104801172 | AGATTAGAGAAAAAA[-/A]GAGCAAAAAGAAATG | 57531 |
rs776205415 | snp | A/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104853442 | TTTGAATTGATTTTT[A/G]TATATTACTAAGGGT | 57531 |
rs776219286 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689730 | GCCTAAAGATTATTT[A/C]CCTCTGTGGCCTAAA | 57531 |
rs776271036 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818799 | CATGATTATCTCAAC[A/C]GATGCAGAAAAGGCT | 57531 |
rs776287457 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104803495 | ACCAAATGCAGCAGC[A/G]TATCAAAAAGCTTAT | 57531 |
rs776310733 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699998 | AAAAAAACCCAGGTC[A/G]AGGGATCTGCGAGCT | 57531 |
rs776312616 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685159 | GCAGTTTAGACAAAT[A/G]ACAAGCAATAAGTCT | 57531 |
rs776313518 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851591 | CTGGCTTTAGCTTTC[C/T]TTAGATTCTTGAGAA | 57531 |
rs776328765 | snp | A/C/G | 5.05338e-05 | 0.00502641 | intron-variant | HACE1 | GRCh38.p7 | 6:104796907 | AAAGATAAGGGGCTC[A/C/G]GAATATAAATGAAAA | 57531 |
rs776346604 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732617 | GAAGATGGATGGTGG[C/T]GATAGTCACACATTA | 57531 |
rs776346831 | snp | C/G | 1.64819e-05 | 0.00287066 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104772033 | AATAGTTCAAGTGAT[C/G]AGGATTTACATAAGA | 57531 |
rs776378239 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731564 | AGAAATAACCCCTCA[C/T]ATACATAATGAAATG | 57531 |
rs776378559 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792681 | ATATGAGTAAACAGC[C/G]AACTGTTCTCATAAA | 57531 |
rs776404107 | snp | A/C | 7.02062e-05 | 0.00592437 | intron-variant | HACE1 | GRCh38.p7 | 6:104785388 | AAAAAAAAAACAAAA[A/C]ACAACTAGACAAATA | 57531 |
rs776421501 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850314 | ATAGTAAACATTCTC[C/T]ACTTTCAAGATGGTC | 57531 |
rs776435179 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850272 | CACATTATTTTTACC[C/T]ATAATTTGATTTAAC | 57531 |
rs776443771 | snp | A/T | 3.87589e-05 | 0.00440204 | intron-variant | HACE1 | GRCh38.p7 | 6:104729799 | CACCATTAAACAGGA[A/T]ATCTATAAAATTTCT | 57531 |
rs776461444 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724352 | ATGACCACAGAGCAA[C/T]TGATGGACATTTCAA | 57531 |
rs776481339 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810525 | AAAAGAAGAATTACT[A/G]TAGTATTCTATAACT | 57531 |
rs776482517 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778213 | TTGTTCATCTGCCAG[A/G]TAAGCAAACTGTGAG | 57531 |
rs776506073 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793595 | ACACCTTAGTTGTCA[C/G]TAATTAACATATATT | 57531 |
rs776508050 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833423 | GCTATGTTGTTCAGG[C/T]TGGACTCAAACTCCT | 57531 |
rs776559313 | in-del | -/G | 2.00282e-05 | 0.00316445 | intron-variant | HACE1 | GRCh38.p7 | 6:104744649 | CAATAATTTTCTTTA[-/G]GGGAAAAAAGTTATT | 57531 |
rs776592343 | in-del | -/GTGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688382 | CACACACACACACAC[-/GTGT]ACACCTACAGACACA | 57531 |
rs776598443 | snp | A/T | 1.6492e-05 | 0.00287154 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771947 | GTGCTTGTAGAAGGA[A/T]CGTGTGAAGTAAATA | 57531 |
rs776601549 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780283 | AAGCTCAGATCAAAC[-/AC]ACACACACACACATA | 57531 |
rs776624383 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104784498 | ATTCTGTGGGGGGAA[A/G]ACATCAATCAGAATA | 57531 |
rs776633060 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807019 | TTAAGTGTAAGAATT[-/C]TTTTTTTTTTTTTTT | 57531 |
rs776638202 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720678 | TGTTGCCCAAACTGG[A/G]GTGTAATGGCGAGAT | 57531 |
rs776666577 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736886 | ATGTATCTCTGAATA[A/G]TGGGATCACTTAACA | 57531 |
rs776677878 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767667 | CACTTTCTCCCTTCC[C/T]CACATCATCTTTTTC | 57531 |
rs776703286 | snp | A/G | 4.96274e-05 | 0.00498109 | intron-variant | HACE1 | GRCh38.p7 | 6:104744241 | AACCACTAACAACAA[A/G]AACAAAAAACTTAGC | 57531 |
rs776708282 | snp | A/T | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683217 | AGCAACGAGAAAGCC[A/T]GGCAACTTCACCAGC | 57531 |
rs776719547 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104823195 | TGCAATCCCAGCACT[C/T]TGGGAGGCCAGGTGG | 57531 |
rs776729974 | snp | C/T | 1.64912e-05 | 0.00287147 | missense, intron-variant, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104811369 | TGTTAATATCAGCAC[C/T]ACTGTCTAGCAAGCA | 57531 |
rs776748476 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729570 | CCCTGCCTATGGGTT[A/G]CATTTAGGCTGCTTT | 57531 |
rs776761017 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104718208 | CTATTATAGGTAGCA[C/T]CTAATTTCCAATTAC | 57531 |
rs776776917 | in-del | -/TATAT | 2.7627e-05 | 0.00371655 | intron-variant | HACE1 | GRCh38.p7 | 6:104772098 | ATAAATACAAAATAA[-/TATAT]TATTAAGAATCTATA | 57531 |
rs776798535 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840516 | TAGATATAGAGACAA[C/T]ATTTTAAAATCCATT | 57531 |
rs776802100 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721432 | CAGTAGTTTTCAACT[C/T]CCAGCTCTCCCCCTT | 57531 |
rs776819533 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767028 | ATCAAACAGTGCCTA[C/G]CACATTATAAAAACC | 57531 |
rs776832068 | snp | C/T | 3.3018e-05 | 0.00406299 | intron-variant | HACE1 | GRCh38.p7 | 6:104777193 | CATATATCAGTTTCT[C/T]TGTTAAGCATACCTC | 57531 |
rs776849696 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104831984 | AGAAGAGAAGAGAGG[A/G]AGGAAGGAAGGAAGG | 57531 |
rs776958071 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747726 | TCTGTAAAATGGGGA[A/C]AATAGTACTCACCTC | 57531 |
rs776965042 | snp | G/T | 1.67548e-05 | 0.00289432 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795677 | CAAATGCTCCAGAAC[G/T]TGCCGTAACTAAATT | 57531 |
rs776967677 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814781 | TTTAAAAGTGTGTGG[C/T]ACATCCCCCCTCACG | 57531 |
rs776986191 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816463 | GGGTGCAAGCCCAAG[C/T]CTTGAAGCTTCCACG | 57531 |
rs776993750 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705840 | ACTTCATAAATGACT[A/T]GTTAATCAAGTGTAA | 57531 |
rs776995224 | in-del | -/ATATA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104794305 | TTACTGTGGAAGTAT[-/ATATA]ATATGACAAATATTT | 57531 |
rs777018650 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771871 | CTAGTTTTCCTCAAA[C/T]TGAAAAAAAAACAAT | 57531 |
rs777053637 | in-del | -/TTGAACACATTC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716714 | GAAAAAAAAAAAAAA[-/TTGAACACATTC]TGGGCCGTGAAACGA | 57531 |
rs777075021 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706983 | CAAGACTCAAGAAGA[A/C]ATAGAAAATCTCAGT | 57531 |
rs777109899 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720819 | TTTTTTTTTTTTTTT[-/A]GTGGAAACGGGGTTT | 57531 |
rs777121354 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104845240 | TATATCATATTTCTT[C/T]AATCAACTCAGTAGT | 57531 |
rs777123437 | snp | A/G | | | downstream-variant-500B, intron-variant | HACE1 | GRCh38.p7 | 6:104727899 | TCTCATTACAGCCTC[A/G]ATCTCCTGGGCTCAA | 57531 |
rs777124057 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773220 | TACTACTATTGTAAA[C/T]GCCTGGGCTAAAAGA | 57531 |
rs777142884 | snp | C/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791600 | AAAGACGTGACAAAA[C/T]ATTCTCACAATCCTT | 57531 |
rs777143335 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747721 | TCTCATCTGTAAAAT[C/G]GGGACAATAGTACTC | 57531 |
rs777152093 | snp | A/C | 3.56487e-05 | 0.00422174 | intron-variant | HACE1 | GRCh38.p7 | 6:104750510 | GATGACTTTTCAAAA[A/C]CCTTTTACATACTTA | 57531 |
rs777202394 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764647 | TTCATCATCACTATT[-/A]ATCACCATCACCTAC | 57531 |
rs777257043 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104855114 | TAACAAGCTGTGTAA[C/G]AGTGGCATTATGTGG | 57531 |
rs777257955 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840040 | AAACTGAGGAAATCT[C/T]AGTAAGACAGATTGT | 57531 |
rs777269342 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694779 | AGACCTATGAAATCA[C/T]AGAGGGCCGCATGCT | 57531 |
rs777271297 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708023 | CATCCAAGAATAGGA[C/T]GTCCACTCTCACCAC | 57531 |
rs777277931 | snp | C/T | 1.65004e-05 | 0.00287227 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785263 | TTTGTTTTTCATCAA[C/T]TCTGTGGCTATTAAA | 57531 |
rs777315813 | snp | C/G | 1.6513e-05 | 0.00287336 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104744162 | AAATACTGCTTACCT[C/G]CCCGTAACAAACTGT | 57531 |
rs777344264 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702275 | TGTCAGCACAATTCT[A/T]TTCGTTAATTTTGAC | 57531 |
rs777345102 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839425 | AAGCCAATCCCCAAA[C/G]GTTCCATACAATATA | 57531 |
rs777352459 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842083 | GCAGAAGTGAAAGGA[C/T]TGCTTGAGGCCAAGA | 57531 |
rs777354116 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767231 | GATAATGAGGTTGAT[A/G]AAGAGTATGATGGCA | 57531 |
rs777386067 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104744470 | GCTTACAAAATTAAA[C/T]GGCAAAACTTAACTT | 57531 |
rs777405870 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104755855 | AGTTAACAATCTGAC[A/C]TCTCAACTAAAATAA | 57531 |
rs777430415 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839286 | AAATGTCTTTTAACA[G/T]GTGAACAGTCCAACA | 57531 |
rs777480392 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722656 | TACATCAAGCCGCCG[C/T]GCCAATGTTTCTGTA | 57531 |
rs777480925 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797573 | GGGAACATGAAGTGG[G/T]GTTATTAGCCAAAAA | 57531 |
rs777482549 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104853064 | GCAGTGTGAAGAGGT[A/G]AGGCTTTGGGGAGGC | 57531 |
rs777506841 | in-del | -/AC/ACACATGTATGTATACGAATATATATAC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727252 | TATACGAATATATAT[lengthTooLong]ACATGTATGTATACG | 57531 |
rs777513785 | in-del | -/AATCC | 6.08612e-05 | 0.00551606 | intron-variant | HACE1 | GRCh38.p7 | 6:104795724 | ATGTGATTACATAGT[-/AATCC]ATTAAATCTTATCAA | 57531 |
rs777529999 | in-del | -/AATT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104768936 | ACACAAATACAAAAA[-/AATT]AATAATATTTTAAAA | 57531 |
rs777536040 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104781574 | CCATTTTGTAACTCC[G/T]TTCTCCAACAACGAG | 57531 |
rs777563731 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714824 | AATCAAACCCCAAAA[G/T]ACATCAAGTAGTGCA | 57531 |
rs777598892 | snp | C/T | 1.64866e-05 | 0.00287106 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795639 | GTTAGAATCTTTAGG[C/T]ACTGGCTTTCACTTT | 57531 |
rs777600854 | snp | C/T | 1.68046e-05 | 0.00289862 | intron-variant | HACE1 | GRCh38.p7 | 6:104776989 | ACATACAGTGATTTC[C/T]ACATCATCTTCTTTT | 57531 |
rs777643779 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702166 | ACTTCTGTCAAGGAT[-/A]AGAAAAAAAATATTT | 57531 |
rs777650323 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750291 | TGAATTACATCAACT[A/G]GAGTTTTTTGTTGTT | 57531 |
rs777650509 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773771 | TAAGGAGACTTTTTT[-/A]AAAAAAAAAAAAGGA | 57531 |
rs777656023 | snp | A/G | 1.6674e-05 | 0.00288734 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791652 | TCATAATTGCTAGAG[A/G]GGCTGAAAATAAAAA | 57531 |
rs777676414 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104694260 | AGTGGAGTAAGACAG[A/G]CACAGAGAGATGAAC | 57531 |
rs777676965 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699737 | AAAATAGACAGTGGT[A/G]AAGTTGATATTAAAG | 57531 |
rs777677920 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813579 | AGGGATGCAGCTAAA[C/T]ATCCTAAAATTCAGA | 57531 |
rs777682413 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790010 | GGAAGTGGTACGTGA[A/C]AAGCCACATGAATTA | 57531 |
rs777685890 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848445 | GGTGACGGAGTGAGA[-/C]CCCCATCTCAAAAAA | 57531 |
rs777696083 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104798978 | ATGGCAGTTGTCTTA[C/T]AGCATGTACTCAATA | 57531 |
rs777697606 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843687 | ACATTGTATCCTACA[A/T]TCTTGACAGCAAAAC | 57531 |
rs777709749 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104809495 | GCATTTAAGGAACGC[-/AA]AGAGAATCACTGTGG | 57531 |
rs777727866 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695695 | AGCTGGGATTACAGG[A/T]GCCCACCACCATGCC | 57531 |
rs777733826 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724652 | GCCTGGGCAACATAT[A/G]CAGAGAGACCTCCAT | 57531 |
rs777734029 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838440 | TTCTACAAAGGTGCC[A/G]AGAACACACATTGGA | 57531 |
rs777734688 | snp | A/C | 1.66004e-05 | 0.00288096 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851022 | ATAAAAATGAGGAAT[A/C]AAGTGTAAAAAAAGT | 57531 |
rs777734820 | in-del | -/CT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721611 | TCGGTGACTTCTCCC[-/CT]CTTTTAGCCTCTTGC | 57531 |
rs777807510 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774562 | GTTAATTTTTGTATT[G/T]TCAGTTAGAGATGGG | 57531 |
rs777818174 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776476 | GAAACCTCTTTGGGC[C/G]AACACTAGTCCTTGA | 57531 |
rs777931614 | snp | A/G | 3.3942e-05 | 0.00411945 | intron-variant | HACE1 | GRCh38.p7 | 6:104784939 | GTATCACTGCTTTTC[A/G]TCATCTATCAGAGAA | 57531 |
rs777981659 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104772720 | AGGTGAAAGTAAAAA[C/T]GGCAAGGGCAATAAG | 57531 |
rs777984024 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776699 | AATAGTGTGAAAAAT[G/T]TGACAAGTTGCAGAA | 57531 |
rs777986046 | snp | C/G/T | 3.30274e-05 | 0.0040636 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729713 | TGCCACAAGAAGTCT[C/G/T]TCCTTGAGTATTTCT | 57531 |
rs778004968 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104828190 | TATACCTACAGAGAA[C/T]AGTGTTAGGTTTTAC | 57531 |
rs778005763 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770440 | AAATAAAAATAAGGC[C/T]GAGAGTGGTGGCTCA | 57531 |
rs778053479 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104752971 | AAATCCTAGCTATCA[A/T]AAACACTTAATTTTT | 57531 |
rs778054315 | in-del | -/TTTTTTTTTTTTTTTTT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774081 | TTATCATCTTTTCTC[-/TTTTTTTTTTTTTTTTT]TTTTTTTTTTGAGAC | 57531 |
rs778056795 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786604 | TGAGATACTGTCTCC[-/A]AAAAAAAAAAAAAAA | 57531 |
rs778080891 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799481 | CTGAGTGCTGCCTGA[C/T]TCATGAATTGTTTTT | 57531 |
rs778081571 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719338 | TTCTGCCATAGGACA[A/T]AAAAAGCACTAACAC | 57531 |
rs778088090 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104829747 | TGTACCCCTCCTCCT[C/T]TACTCTGTCTGCAAA | 57531 |
rs778104349 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733476 | AGAAAAATAAATAAA[-/AC]AGTCTTTGGTTGAAT | 57531 |
rs778112208 | in-del | -/AAAAGAAATGAGAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104835542 | CCTAAAAGTACAAAG[-/AAAAGAAATGAGAAA]AAAAGAAATGAGAAA | 57531 |
rs778146974 | snp | A/C | 6.79325e-05 | 0.00582766 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859552 | CGGCCAGCCTGGCCC[A/C]GCGACCCGGCTCACC | 57531 |
rs778170881 | snp | A/G/T | 6.23194e-05 | 0.0055818 | intron-variant | HACE1 | GRCh38.p7 | 6:104785365 | CATTCTTAAACTACA[A/G/T]GATTAAAAAAAAAAA | 57531 |
rs778180912 | snp | C/T | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860465 | GCTCTGGGGAAGATA[C/T]GAATGATGACAACCT | 57531 |
rs778195314 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104712041 | TCATCCTCCCAAAAT[C/G]CTGAGATTATAGATG | 57531 |
rs778209302 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802472 | ATAATTCGAAGTAAA[G/T]CACTCCTCAGCAAAT | 57531 |
rs778209912 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818563 | ATCCTGACACCAAAA[A/C]CTGGCAGAGATACAA | 57531 |
rs778236508 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779316 | CAATAAATTTCTTCA[C/T]CTGAGCTAAATTAAA | 57531 |
rs778246842 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689195 | TGAGGCTCCTGCAGA[A/G]ACAGAACTCTTCAAT | 57531 |
rs778256172 | in-del | -/AGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855972 | TAACCTAAAGAAAAA[-/AGT]AGGTCACATACATTA | 57531 |
rs778261621 | in-del | -/AACTT | 0.000168481 | 0.00917671 | intron-variant | HACE1 | GRCh38.p7 | 6:104744476 | AAAATTAAACGGCAA[-/AACTT]AACTTCATTCTAAGC | 57531 |
rs778358730 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789621 | AATCATTTAAATCAC[C/T]TATAGAGAGGCTACT | 57531 |
rs778374265 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104763626 | ATACCATTAATACAG[C/T]GAAAAAAATCACATG | 57531 |
rs778377669 | snp | C/T | 1.73192e-05 | 0.00294267 | intron-variant | HACE1 | GRCh38.p7 | 6:104771886 | CTGAAAAAAAAACAA[C/T]ATAAATAAATGTCTG | 57531 |
rs778393998 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698730 | TTCCCCAGCTTAGAA[C/T]TGCATCTGATGATGA | 57531 |
rs778411552 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810136 | CAACATGATTACAGG[A/G]AATCAAATGATGATA | 57531 |
rs778427326 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751339 | AAATTCACTTAACAC[A/G]TACTTAGAACTTGGT | 57531 |
rs778465862 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792125 | ATCCATAATCCCATA[A/T]CCCCTTCCCACCACA | 57531 |
rs778469294 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104691002 | AACATGGAGAAAAAT[C/T]GCCCCACGGTTCTTT | 57531 |
rs778475252 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104833022 | CACATGCAGCTTAAA[C/G]TCCTCATGGCTCAAC | 57531 |
rs778496760 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104715924 | GTACAACAGACCCCT[A/G]TGACATGAGTTTATC | 57531 |
rs778499150 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734129 | GCCTGAGAAACAGAG[A/C]AAGACTCTTCCTCAA | 57531 |
rs778503101 | snp | C/T | 1.64732e-05 | 0.0028699 | intron-variant | HACE1 | GRCh38.p7 | 6:104791495 | AACAATGCCATATAC[C/T]TTTCTCACCTTGAAC | 57531 |
rs778533402 | in-del | -/ATCT | 1.69726e-05 | 0.00291308 | intron-variant | HACE1 | GRCh38.p7 | 6:104784942 | TCACTGCTTTTCATC[-/ATCT]ATCAGAGAAAAAAAA | 57531 |
rs778558995 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104855955 | ACATCTTAAGTCACA[C/T]CTAACCTAAAGAAAA | 57531 |
rs778590087 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764236 | GCACGCACTACCATG[C/T]CCAGCTAATTTTTGT | 57531 |
rs778638494 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695915 | TTTGTATTTTTAGTA[A/G]AGACGGGGTTCCACC | 57531 |
rs778674680 | snp | A/G | 1.65712e-05 | 0.00287843 | intron-variant | HACE1 | GRCh38.p7 | 6:104843180 | TCAATATCATTTTCT[A/G]AAACATACTTTTAAA | 57531 |
rs778693113 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104703843 | ATAATGGGCTGGGCG[C/T]GGTGGCTCATGCTTG | 57531 |
rs778739360 | in-del | -/C | | | | | GRCh38.p7 | 6:104771434 | GTCTGGTTTTGCCTT[-/C]CCTTATCTATTTAAT | 57531 |
rs778755643 | snp | C/T | | | | | GRCh38.p7 | 6:104839019 | CAACATCACTGATCA[C/T]CAAAGAAATGCAAAC | 57531 |
rs778756132 | snp | A/G | | | | | GRCh38.p7 | 6:104851305 | GCCAAGATGATCTCA[A/G]TCTCTTGACCTCGTG | 57531 |
rs778770990 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104824366 | TTTATTGCCTGGTCT[C/T]AACAACTGGAATTTA | 57531 |
rs778773900 | in-del | -/AAGAGAGTCT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778180 | ATCTCTTGAATAGCA[-/AAGAGAGTCT]AAGAGAGTCTCTCCC | 57531 |
rs778797459 | snp | C/T | 1.64741e-05 | 0.00286998 | intron-variant, missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104833046 | GCTCAACTTACCGTC[C/T]TGTGACCGTTCTGGC | 57531 |
rs778804301 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104719414 | AGTTATGCAAGATAA[A/T]TAAGTTCTGGAGATC | 57531 |
rs778806206 | snp | C/T | 1.66344e-05 | 0.0028839 | intron-variant | HACE1 | GRCh38.p7 | 6:104849298 | ACATACAGCCATACT[C/T]GATGTAGTTCAATTA | 57531 |
rs778821682 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104850307 | GACACAAATAGTAAA[-/C]ATTCTCTACTTTCAA | 57531 |
rs778823748 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799362 | GCAAACACACACATA[A/C]GGGTAGTCAGTTGGG | 57531 |
rs778843369 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789767 | CCTGATTTGATTTTA[C/T]ATTCATCATTACTGA | 57531 |
rs778857086 | snp | A/G | 1.6516e-05 | 0.00287362 | intron-variant | HACE1 | GRCh38.p7 | 6:104777181 | TTGTGCTTCACACAT[A/G]TATCAGTTTCTTTGT | 57531 |
rs778897210 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104782917 | CCTACATATCTGGCA[A/G]ATTATTTTCTAAAAC | 57531 |
rs778899481 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104844621 | CTCCCAAAGTGCTGG[G/T]ATTACAGGCGTGAGC | 57531 |
rs778935768 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104730479 | TGTGACAGATAAATT[G/T]CAAGTTCTAAGTTAG | 57531 |
rs778937522 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753785 | AGGTAGATTAAGGCC[-/A]AAAAAGATGAGAAAG | 57531 |
rs778942229 | in-del | -/AAACAATATAAATAAATGTCTGCAG | 0.0016995 | 0.0291009 | intron-variant | HACE1 | GRCh38.p7 | 6:104771879 | CTCAAACTGAAAAAA[-/AAACAATATAAATAAATGTCTGCAG]AAACAATATAAATAA | 57531 |
rs778943809 | snp | C/T | 1.69798e-05 | 0.00291369 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796665 | AATACCATGTTTTCT[C/T]GGAGGTCTTCATTCT | 57531 |
rs778947018 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770774 | AAATATCAAAAGGTC[A/G]AACAAACTTACTGGA | 57531 |
rs778951161 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846967 | TTATTCCTTTTCTTC[C/T]TGCTGAATAGCTATG | 57531 |
rs778970676 | in-del | -/TA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713443 | TAAATCTGGATGCTT[-/TA]TATATATATTAATTT | 57531 |
rs779000722 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104706734 | ATTTTTGTTTAATTC[C/T]TGTATTAAAGCAAAC | 57531 |
rs779022162 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104846137 | TGCAAAAGGTACAGG[C/G]AATGTAGGAGAGAAA | 57531 |
rs779026250 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104815185 | CAAACTGCTGATAGT[G/T]ATATGGACAATGACG | 57531 |
rs779055135 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760010 | CCAGGAAGCAGTTGA[A/C]TCTCTGAATATATCA | 57531 |
rs779061406 | in-del | -/AATA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800996 | CGAATGGCTAACTGG[-/AATA]AATAGTGTAGAGAAG | 57531 |
rs779121465 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104783465 | ATTTATTCTGGACAA[C/T]AGTTCTATGAGGCTG | 57531 |
rs779128196 | snp | A/G | 1.65021e-05 | 0.00287241 | intron-variant | HACE1 | GRCh38.p7 | 6:104771172 | ACAAACAATGGTTAA[A/G]GTAAAAACTGAAATA | 57531 |
rs779139811 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834148 | TGACAACCTATTTCC[-/A]AAAAAAAAAAAATCG | 57531 |
rs779183005 | snp | C/T | 1.65386e-05 | 0.00287559 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729734 | GAGTATTTCTTTACT[C/T]GGGTATTCAGGTAAC | 57531 |
rs779187641 | snp | A/G | 5.04409e-05 | 0.00502175 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104750464 | AGTAACAAGCTGGAC[A/G]TACTCCGCCTGTTGA | 57531 |
rs779188921 | snp | A/C | | | upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104860537 | TATGTGATGACACAG[A/C]CTAGTGGGAAATCCA | 57531 |
rs779198302 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104747349 | ATCTCTTGATGCCTT[C/G]TGTCTACAATGGATG | 57531 |
rs779209481 | snp | C/G | 3.91558e-05 | 0.00442452 | intron-variant | HACE1 | GRCh38.p7 | 6:104796797 | AGGTTTAAAAACAGT[C/G]CCTTTTAAAGTTCAT | 57531 |
rs779212253 | in-del | -/TGTGTGTGT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693032 | AGAGTGGTGTGTGTG[-/TGTGTGTGT]GTGTGTGTGTGTGTG | 57531 |
rs779223062 | snp | A/C | 0.000119772 | 0.00773769 | intron-variant | HACE1 | GRCh38.p7 | 6:104784954 | ATCATCTATCAGAGA[A/C]AAAAAAAATAATAAG | 57531 |
rs779223914 | in-del | -/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104826204 | AAAACTTGTCTTCCA[-/TG]AAACTGGGCCCTAGT | 57531 |
rs779233321 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854308 | GATCCGTAAATGACA[C/T]TAGTGGGAAAGCTGG | 57531 |
rs779245864 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685332 | GGTCAAGGGGCAGAG[C/G]TGTAAAGGGATATAT | 57531 |
rs779250646 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104806979 | ATTTTCTAAAGGTCC[A/G]TTCCTATGCTGAAAG | 57531 |
rs779276252 | snp | A/G | 1.65026e-05 | 0.00287246 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796951 | CATAAATCCAGAGGA[A/G]TTACTCCATTTTTAT | 57531 |
rs779305882 | snp | A/G | 1.65097e-05 | 0.00287308 | intron-variant | HACE1 | GRCh38.p7 | 6:104776701 | TAGTGTGAAAAATGT[A/G]ACAAGTTGCAGAAAA | 57531 |
rs779309604 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852545 | ACGATAGTGAAGAAT[C/G]TTTCATCCCCTCCAC | 57531 |
rs779356323 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793016 | GCTCACGCCTGTAAT[-/C]CCAGCACTTTGGGAG | 57531 |
rs779360824 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689989 | AACAGTTTCTGGAAG[G/T]TCTCACAGATAGGAA | 57531 |
rs779370563 | snp | G/T | 3.24733e-05 | 0.00402934 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104859555 | CCAGCCTGGCCCCGC[G/T]ACCCGGCTCACCCTC | 57531 |
rs779374852 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104713354 | CAATGAAAGAGTAGA[C/T]TGGCTCAAAGGTAAC | 57531 |
rs779398605 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764747 | ACCTTTTCAATATCC[A/C]CTTCTTTCAGTTCAC | 57531 |
rs779403594 | in-del | -/A | 1.80247e-05 | 0.003002 | intron-variant | HACE1 | GRCh38.p7 | 6:104730460 | TCATGAAAGAAAGAT[-/A]ATTTGTGACAGATAA | 57531 |
rs779407108 | snp | C/T | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854941 | ACTATAAAAGTAAAA[C/T]ACTAATAAATCCTAT | 57531 |
rs779437952 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822095 | AGGCGTGGGCCGGGC[A/G]CGGTGGCTCACACCT | 57531 |
rs779444077 | in-del | -/AAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698630 | ATTGTATTTGGAGAA[-/AAT]AATAAAAGGAAAAAA | 57531 |
rs779461738 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852579 | TTATCCCTTTTACAT[C/G]ATTACAAAAGAGCTT | 57531 |
rs779496350 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104814916 | GTTAAGCCAGCAGAA[-/C]TCTGAGTCAATTAAA | 57531 |
rs779509294 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104786244 | TACTCGGGAGGCTGA[C/G]GCAGGACGATCACTT | 57531 |
rs779532959 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104779560 | CATATAAATTAAATA[C/T]CTCATTTTCAGTTAA | 57531 |
rs779536304 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104753121 | AACAAATTAATATTA[A/T]CTTGACAATACAAAT | 57531 |
rs779571660 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705115 | GTTTAAATGGATCTC[C/T]TTACTTGGCAAAACA | 57531 |
rs779586844 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795380 | AAGTATGCTCTATTT[C/T]TAGTCTCTTTAGAGA | 57531 |
rs779587370 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722541 | CTTTTCAGTTATTTG[C/T]TCAATCAACAGGTTG | 57531 |
rs779590455 | in-del | -/TGTT | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851082 | ACTCTTTAGCTGCTC[-/TGTT]TGTTTGTTTGTTTGT | 57531 |
rs779599334 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733449 | ATAATTCATCAGGCA[C/T]AAGTATATATGAGAA | 57531 |
rs779635587 | in-del | -/TCAATTGC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104789007 | AATGGAAATTAGGGA[-/TCAATTGC]TACCTCAGACAAAAT | 57531 |
rs779646384 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104724155 | GTTTCCTCCCCTGTT[C/G]TTGGGTAGGAGACTG | 57531 |
rs779660375 | snp | G/T | 1.65026e-05 | 0.00287246 | intron-variant | HACE1 | GRCh38.p7 | 6:104849131 | GCCACTTAAGAAAAC[G/T]AAATAGTTACCCATT | 57531 |
rs779662237 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104698095 | TTGTCTCTGTAAATG[C/T]TGATGATAATAATTC | 57531 |
rs779676233 | in-del | -/AAA | 3.55897e-05 | 0.00421825 | intron-variant | HACE1 | GRCh38.p7 | 6:104750313 | TTGTTGTTGTGTTAC[-/AAA]AACATAAGAACTGAT | 57531 |
rs779692476 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104858017 | ACTATATGCAACATG[A/G]TTTTAACTTGTTAGG | 57531 |
rs779701134 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841453 | AACCCTCTGTTGCAC[A/G]TACCGTGTCACTAAG | 57531 |
rs779701546 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104711053 | GATTCTACTGGTGGT[A/C]AATGTTACATGAACG | 57531 |
rs779706113 | snp | C/T | 1.73918e-05 | 0.00294883 | intron-variant | HACE1 | GRCh38.p7 | 6:104776870 | TCAACAGAAATATGT[C/T]ATATTGGGAAATTTT | 57531 |
rs779708881 | in-del | -/AAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104751644 | CTTAAAGAAAAAAAT[-/AAT]AATAATAACTGGTAA | 57531 |
rs779721781 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825939 | CCTCTAGATAATGTG[C/T]TATGCACTACTCTAA | 57531 |
rs779746830 | in-del | -/CAGGCAA | | | nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104683215 | AAGCAACGAGAAAGC[-/CAGGCAA]CAGGCAACTTCACCA | 57531 |
rs779752458 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785908 | TATAATTCCTAGAAT[C/T]TGGATAATTTTTGAC | 57531 |
rs779756339 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811247 | TTTCTTTATTTATAC[-/AT]ATATATATATATATA | 57531 |
rs779757526 | snp | C/T | 1.6501e-05 | 0.00287232 | intron-variant | HACE1 | GRCh38.p7 | 6:104776723 | TGCAGAAAAAGTCAT[C/T]TAGACTGTACAACTT | 57531 |
rs779760527 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702150 | GGAAAAGGAAATTAA[C/T]GACTTCTGTCAAGGA | 57531 |
rs779765706 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716945 | ATCTGACAGTCTCAA[A/G]TGCTGGCAAGAATCT | 57531 |
rs779787803 | in-del | -/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816593 | AAGTCTGCTGCAGGA[-/G]GTAGAGCCTTCATGG | 57531 |
rs779805211 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756110 | GATATCACCACTGAC[C/T]CCAAAGAAATATAAA | 57531 |
rs779876884 | snp | C/T | 8.32688e-05 | 0.00645194 | intron-variant | HACE1 | GRCh38.p7 | 6:104744495 | TAACTTCATTCTAAG[C/T]TCTAGAGAAATTTTA | 57531 |
rs779880535 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104770167 | CTTATAGTTAAATTG[A/C]TTCTGAAGATGTCTT | 57531 |
rs779902500 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836649 | ATCCAGGAGGCAGAG[G/T]TTGCAGTGAGCTGAG | 57531 |
rs779904752 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104818624 | TGAAATTGATGCAAA[A/C]ATCCCTAACAAAAAC | 57531 |
rs779905439 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104704001 | AATCCCAGCTACTCG[A/G]GAGTCTGAGGCACAA | 57531 |
rs779970264 | snp | C/T | 1.65529e-05 | 0.00287683 | missense, utr-variant-5-prime, nc-transcript-variant, intron-variant, synonymous-codon | HACE1 | GRCh38.p7 | 6:104843225 | TGATAGCACTTACTG[C/T]TGTAAGGCCTTCATT | 57531 |
rs779993731 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104816294 | TGTCAGAGGCCTGGA[A/G]GCCTAGGAGGGGAAA | 57531 |
rs780013804 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104799478 | ATTCTGAGTGCTGCC[C/T]GATTCATGAATTGTT | 57531 |
rs780036274 | snp | C/T | 2.05556e-05 | 0.00320584 | intron-variant | HACE1 | GRCh38.p7 | 6:104771408 | AAAAATGCAAACATA[C/T]AGCAGTTATAGTCTG | 57531 |
rs780048247 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757436 | CAGCAAACTCCAACA[C/G]ACCTGCAGCTAAGGG | 57531 |
rs780064386 | snp | C/G | 3.31835e-05 | 0.00407316 | intron-variant | HACE1 | GRCh38.p7 | 6:104784367 | TAGATGAAACTGTAA[C/G]TAAAGAGAGGAAAGG | 57531 |
rs780066982 | snp | A/C | 5.0197e-05 | 0.00500959 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104851046 | AAAAAGTTTTTAAAA[A/C]CATAATAAATCAAGT | 57531 |
rs780067324 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104760690 | TAGTATTGGAAATTC[G/T]GGCCAGGGCAATCAG | 57531 |
rs780070978 | in-del | -/ACCCAAGA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104709988 | CATTCTTAGGGATAT[-/ACCCAAGA]GAAATGAAAACAAAC | 57531 |
rs780072681 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104842592 | AGTATTTAAAAGAAC[A/G]TAACGAAAAACAGCT | 57531 |
rs780073680 | in-del | -/CTA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104757100 | GGAGCTCAGCAAGGC[-/CTA]CTACTGCCTCTCTAG | 57531 |
rs780087954 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104717225 | GCTCACTGCAACCTC[A/C]ACCTCCCGGGTTCAA | 57531 |
rs780106170 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104832680 | ACAGCTGTGAGCCAC[A/G]GCTCCCAGCCCAAAA | 57531 |
rs780177625 | in-del | -/A | 9.91719e-05 | 0.00704103 | intron-variant | HACE1 | GRCh38.p7 | 6:104797034 | ACCATGACTGTGTGG[-/A]AATAGAAACAAGTTA | 57531 |
rs780195508 | in-del | -/CATACAGC | 1.65449e-05 | 0.00287614 | intron-variant | HACE1 | GRCh38.p7 | 6:104849284 | TTCAGATACATTCAA[-/CATACAGC]CATACTTGATGTAGT | 57531 |
rs780196329 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817262 | CCCCGCCAAATCTCA[C/T]GTCAAATTGGAAGAG | 57531 |
rs780215033 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104722308 | CTTTCAAGAAGCCAA[C/T]CTTCTGAGAAAAATG | 57531 |
rs780237607 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104749128 | TATTTGTTTTTTACA[C/T]ACATATAGGTCCAGC | 57531 |
rs780251216 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807717 | GGGAAAAAAAAATCA[A/G]TGTGTGCCTATATTT | 57531 |
rs780268698 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756744 | GCAGGGCAGGGTGTC[A/G]TTTCACCCGGGAAGC | 57531 |
rs780282703 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104729303 | TAATATATCAGAAAT[C/T]AGGAGAAAACACCCT | 57531 |
rs780284155 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800853 | AATGGAACAAAGTTG[A/G]ATGGAGAATGACTTT | 57531 |
rs780286708 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104825783 | ATACTTTTGTTTTCA[A/G]TAAATATCTGCTTTT | 57531 |
rs780288781 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104750263 | ATTCATCATAATACT[C/T]CACAATTATTTCTGA | 57531 |
rs780298760 | snp | C/T | 3.2956e-05 | 0.00405918 | intron-variant | HACE1 | GRCh38.p7 | 6:104850867 | GCTTACTGATCCTTG[C/T]CCTAGATCAGAGTTT | 57531 |
rs780304597 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761563 | CAAGACGGATGAAAG[A/T]CTTAAACGTAAGACC | 57531 |
rs780317697 | in-del | -/AAAAAAAAA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104838892 | AACAACTCCATAGTA[-/AAAAAAAAA]AAAAAAAAAAAAAAA | 57531 |
rs780329596 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104710981 | GGAAAGAGAGAGATG[C/T]CTAGATTCCAAAATA | 57531 |
rs780333703 | snp | A/G | 3.29745e-05 | 0.00406031 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785126 | GGTTTAGATTCCCTT[A/G]TGCCAGTGGACAGAT | 57531 |
rs780343474 | snp | A/G | 1.64765e-05 | 0.00287019 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771231 | TACTCCCACCCCCAG[A/G]TTTCAAAGGCACCTC | 57531 |
rs780344934 | snp | A/G | 1.67905e-05 | 0.00289741 | intron-variant | HACE1 | GRCh38.p7 | 6:104784965 | GAGAAAAAAAAAATA[A/G]TAAGCCAAAACTTTC | 57531 |
rs780353692 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104699826 | TCTACAGCAGTAGGC[A/G]TGAGTATGAATAAAG | 57531 |
rs780354089 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104700907 | TTAGCCACTTTAATG[C/T]GCTTTACCTGGGAGT | 57531 |
rs780366032 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104840317 | TACTCAAAAAAATAA[C/T]AACACACAAAAATGA | 57531 |
rs780411257 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736253 | GTCTATAACCTGTTA[A/G]TAGTTATGTCTTATT | 57531 |
rs780458430 | snp | A/C | 3.5926e-05 | 0.00423813 | intron-variant | HACE1 | GRCh38.p7 | 6:104811264 | TATATATATATATAT[A/C]TATATATATGAGCAT | 57531 |
rs780472993 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849408 | GTGGCACCATCACAG[C/T]TCACTGTAGCCTTGA | 57531 |
rs780528215 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104702211 | GGGCAGGAGCTTTGC[A/C]ATTAAAAATACCATT | 57531 |
rs780536522 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104777756 | TATTTTGGTTTATTG[C/T]TGTAGTTGTTGTTGT | 57531 |
rs780536567 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104807376 | ATACTCTAACTGAAA[C/T]GAGTTGCTTCGCAGT | 57531 |
rs780560956 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104714004 | AGGGCCTGCCCAAGC[C/T]GGGGAGTCTAATAAG | 57531 |
rs780568397 | snp | G/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104773015 | TGGTAAATTTATATG[G/T]GTATTTCACCACCGT | 57531 |
rs780576704 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104734819 | AGGAGCAGCCACCTA[A/T]GAGACAACTTAGTAC | 57531 |
rs780583215 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104689014 | TATTTCAGTTTACTA[C/T]ACTGGCTCTCACATG | 57531 |
rs780646593 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104810616 | GGGTGTGACGGCATG[C/T]GTATAATTATACTGA | 57531 |
rs780661677 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822577 | AATAAAAAAAGTAGG[C/G]CGAGCGCGGTGGCTC | 57531 |
rs780671045 | snp | C/G | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104854008 | ATGTGAATGTGGTCT[C/G]TCTCCCTCTCTCTCA | 57531 |
rs780693144 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104725685 | TCCTTATATACATGA[A/G]CAAGTGGATGCCTAA | 57531 |
rs780720534 | snp | A/G | 1.65176e-05 | 0.00287376 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730356 | CACAGCAGCGATTGT[A/G]AAGTTTTGCAATCCA | 57531 |
rs780728644 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104721179 | GTGACACCTGGTCTC[C/T]ACTAAAAATGAAAAA | 57531 |
rs780733356 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685756 | TGGTACGGGAAATAC[A/C]AATTTTTTTAATAGC | 57531 |
rs780741905 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104797413 | CACACACATCCAAGT[A/C]TCTAGGCTTCTTAAT | 57531 |
rs780744057 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104836799 | ATTTGCCCAAAGTCC[A/C]CCAGAACTAATAAGT | 57531 |
rs780777458 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104764862 | GTCACACATTTGCTC[A/G]TCACCATCACTGAAC | 57531 |
rs780801648 | snp | A/C | 1.65963e-05 | 0.0028806 | missense, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104777108 | TACTCCTAAAAATAG[A/C]ATCTAAATATGTAGC | 57531 |
rs780841332 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104746327 | TTATAGAATCCTTTT[C/G]CTAGATGAAGACAGT | 57531 |
rs780842070 | in-del | -/GAG | 4.96656e-05 | 0.004983 | utr-variant-3-prime, nc-transcript-variant, cds-indel, intron-variant | HACE1 | GRCh38.p7 | 6:104729642 | GTGCATCAGTAGTCA[-/GAG]GAGTTTTCCAGACTT | 57531 |
rs780853712 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104820038 | CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCGG | 57531 |
rs780900462 | snp | A/G | 1.65553e-05 | 0.00287705 | synonymous-codon, nc-transcript-variant, intron-variant | HACE1 | GRCh38.p7 | 6:104730389 | TCCACCCATGATATT[A/G]GCAAACCCACCATGT | 57531 |
rs780915268 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104793091 | GGCTACACAGTGAAA[C/T]CCCGTCTCTACTAAA | 57531 |
rs780936637 | in-del | -/AAGAT | 1.70927e-05 | 0.00292336 | intron-variant | HACE1 | GRCh38.p7 | 6:104796893 | CCAGTTTCTATTATA[-/AAGAT]AAGGGGCTCAGAATA | 57531 |
rs780973191 | snp | C/T | 3.29995e-05 | 0.00406185 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104776763 | TGACTGGGTAAACAA[C/T]GCATAATCAGGATTG | 57531 |
rs780989191 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104705389 | TGTTAAGGGCTCAGA[A/G]ACTCTTAAGGGAGCA | 57531 |
rs781016225 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104795271 | GTGGTCAAGATTCCT[A/G]AACTTTCTCAATTCT | 57531 |
rs781028974 | snp | C/T | 1.6546e-05 | 0.00287624 | intron-variant | HACE1 | GRCh38.p7 | 6:104849281 | CAGTTCAGATACATT[C/T]AACATACAGCCATAC | 57531 |
rs781077941 | snp | C/G | 8.23866e-05 | 0.00641767 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104849165 | TGCTGCCAAATGAAG[C/G]GGTGTACAGCCTGAA | 57531 |
rs781088333 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685598 | TTTCTCAAACTGTAG[C/G]TGCTATTTTTATCAT | 57531 |
rs781099793 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104791548 | TCCCATTGTAGCCCA[C/T]ATCAATTCCATTACT | 57531 |
rs781108809 | in-del | -/CT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104765553 | TTGGCAAATTCCTCA[-/CT]GAATTTCACCACTGT | 57531 |
rs781111652 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780472 | CCTGAAAACCACCAA[A/C]AGAAGAAGAAGTCAA | 57531 |
rs781120469 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104839993 | CCTGGGCAACAGAGC[A/G]AGACTCTGTCTCAAA | 57531 |
rs781131682 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104827751 | AAAACTTGGAAGCTG[A/G]CTAAAGATACCAAGA | 57531 |
rs781144635 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813438 | GAAACAGCCCAATTC[A/G]GGACAATGGGTCTAT | 57531 |
rs781217301 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104800966 | GGAAGCTAAAAACCT[C/T]GAAAAAAGGTTAGAC | 57531 |
rs781232339 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104767440 | TTCCCCAAACCAAAA[C/T]GCCACAGCCTCCTCT | 57531 |
rs781254522 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104758702 | TCACACATAACAATA[C/T]AAACCTTAAATGTAA | 57531 |
rs781287270 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104787733 | TCCTATTTTCAAATA[C/T]TGACAATGTGTAAAA | 57531 |
rs781311491 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104745967 | TATATTTCAACCAAA[A/C]AACATACCAAAACAG | 57531 |
rs781343189 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785370 | TTAAACTACAGGATT[-/A]AAAAAAAAAAAACAA | 57531 |
rs781356358 | snp | A/C | 1.83522e-05 | 0.00302915 | intron-variant | HACE1 | GRCh38.p7 | 6:104796773 | TAAAAACAAGATCTA[A/C]AATTATCCAGGTTTA | 57531 |
rs781356489 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104697274 | TTCCGTTGCTACAGC[C/T]CTAGCTATATATTTA | 57531 |
rs781376241 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727475 | TATGAATACACACAC[-/AT]ATGTATATGAATACA | 57531 |
rs781412738 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716452 | ATCCCCACACTTTGG[A/G]AGGCCGAGGCGGGCG | 57531 |
rs781414623 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104731957 | AATGCCCAATAAGCA[C/T]ATGAAAAGATGCTCA | 57531 |
rs781424992 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104849060 | AAATATCAGGGATGC[A/G]GGAGGAATCATCAAA | 57531 |
rs781428891 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104723192 | TATTAATCACTCTTA[A/C]GTATCAGCTTATTAA | 57531 |
rs781456262 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104841938 | ATCCCATACCACCTC[C/T]ATGTGATTCAAAAAT | 57531 |
rs781480828 | snp | C/T | 1.68764e-05 | 0.00290481 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104796684 | GGTCTTCATTCTGTG[C/T]CATTTGAATAATAGT | 57531 |
rs781498916 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104834254 | TAATCCTGGACTCTA[A/T]GCATAGTTTGTCTCT | 57531 |
rs781520291 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104684304 | AACGTAGTCCTCTCT[A/G]CTGGAGAAATTTCTC | 57531 |
rs781532948 | snp | C/T | 1.65053e-05 | 0.0028727 | intron-variant | HACE1 | GRCh38.p7 | 6:104771432 | TAGTCTGGTTTTGCC[C/T]TCCCTTATCTATTTA | 57531 |
rs781538226 | snp | A/G | 1.64974e-05 | 0.00287201 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852421 | CTACTTTGTGCAAGG[A/G]GTGATACTTAAGATT | 57531 |
rs781545181 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761472 | TTTTTAAATAAATGG[A/T]TTTGGGAAAACTGGC | 57531 |
rs781582710 | snp | C/G | 3.31675e-05 | 0.00407218 | intron-variant | HACE1 | GRCh38.p7 | 6:104811443 | AGGAATCAAACAAAA[C/G]ATACAATTACCACAA | 57531 |
rs781584464 | snp | C/G | 1.64868e-05 | 0.00287109 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104771298 | AGTTAGTTCTAGACC[C/G]AGATCACTTATATCA | 57531 |
rs781586315 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785248 | CTCTGTTGAGTCTCT[C/T]TTGTTTTTCATCAAT | 57531 |
rs781604025 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104848858 | TAATGAACTTCCACA[C/T]ATAATATTTTCAAGA | 57531 |
rs781617861 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104843504 | ACTCAAAGATAACAG[C/G]ATAAAACAATGACAC | 57531 |
rs781626759 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104817400 | TTCCCCCTTGCACAC[A/T]CTCTCTCTCTCCTGC | 57531 |
rs781648853 | snp | C/T | 5.05233e-05 | 0.00502585 | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852275 | ACATTTAGAACAATG[C/T]ATGCTTCTTAAAAAG | 57531 |
rs781663123 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104736243 | TATATTTTTAGTCTA[C/T]AACCTGTTAATAGTT | 57531 |
rs781666822 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104802088 | TCTGATAAAACAGAC[A/G]TTAGACGAAGGAAGA | 57531 |
rs781672263 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104685148 | AAGTTGGACACGCAG[-/T]TTAGACAAATGACAA | 57531 |
rs781681072 | snp | C/G/T | 3.38766e-05 | 0.00411551 | intron-variant | HACE1 | GRCh38.p7 | 6:104791676 | ATAAAAATTAAAATA[C/G/T]GAGATTAGAGTAAAA | 57531 |
rs781687827 | snp | C/T | 1.64844e-05 | 0.00287087 | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104785153 | AGATTTTCATAGCTC[C/T]CAGGTCCTGGAGGTT | 57531 |
rs781721123 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104775671 | GAGCAAAGAATTAAA[A/G]GTTACAGAGTTAAAG | 57531 |
rs781745716 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104804500 | CAAAACAGCATGGTA[C/G]TGGTACCAAGAGATA | 57531 |
rs781747868 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104776456 | ATTTTACAAAGGACT[A/G]ATAAGAAACCTCTTT | 57531 |
rs781770641 | snp | A/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104708956 | GATGTAAGAGCTAAA[A/T]CTATAAAATTCAGAA | 57531 |
rs781772022 | in-del | -/A | | | intron-variant | HACE1 | GRCh38.p7 | 6:104857654 | CCTATTGAAGAATAC[-/A]AAAAAAAAAAAACAT | 57531 |
rs796111330 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104771882 | CAAACTGAAAAAAAA[-/AC]AATATAAATAAATGT | 57531 |
rs796117024 | in-del | -/GTA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822724 | TAGCCTGGCGTGGTG[-/GTA]CATGTCTGTAATCCC | 57531 |
rs796171233 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852200 | TATGTCCAAACTGTC[-/TG]TGTGTGTGTGTGTGT | 57531 |
rs796175414 | in-del | -/GC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104693057 | TGTGTGTGTGTGTGT[-/GC]ACGCGCGCGCGCGCT | 57531 |
rs796196294 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104695079 | AAGCACCTGAGAAAC[A/C]CAGAGCCAGACCTAC | 57531 |
rs796214453 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104792123 | ATATCCATAATCCCA[C/T]ATCCCCTTCCCACCA | 57531 |
rs796245532 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785382 | ATTAAAAAAAAAAAA[-/AC]AAAACACAACTAGAC | 57531 |
rs796254974 | in-del | -/GT/GTGT | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852198 | CTATGTCCAAACTGT[-/GT/GTGT]CTGTGTGTGTGTGTG | 57531 |
rs796285552 | snp | C/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104761751 | GAAACTATCATCAGA[C/G]TGAACAGGCAGCCTA | 57531 |
rs796314861 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104732707 | TTATGATATGCATTT[-/AC]ACACACACACAAATG | 57531 |
rs796316910 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | HACE1 | GRCh38.p7 | 6:104852388 | TGAGTAAAAAAAAAC[-/AA]AGAGTTCATTTATCC | 57531 |
rs796362812 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104811209 | CTAGAAATAGAGTAT[-/T]ATATACATCTGGAAA | 57531 |
rs796445722 | in-del | -/CC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104720634 | CTTCCCCGCCCCCCT[-/CC]CCCCCCCCCCAGACG | 57531 |
rs796527463 | in-del | -/AC | | | intron-variant | HACE1 | GRCh38.p7 | 6:104688380 | CACACACACACACAC[-/AC]GTGTACACCTACAGA | 57531 |
rs796530420 | in-del | -/AA | | | intron-variant | HACE1 | GRCh38.p7 | 6:104785370 | TTAAACTACAGGATT[-/AA]AAAAAAAAAAACAAA | 57531 |
rs796531716 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104778376 | ACACAGAGTAACACA[-/AT]ATATATATATATAAT | 57531 |
rs796550108 | in-del | -/AAAAAAT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756422 | ATCTCAAAAAAAAAA[-/AAAAAAT]ATATATATATATATA | 57531 |
rs796554790 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104716467 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 57531 |
rs796637880 | in-del | -/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104813344 | AAATTTTAAAATTAG[-/C]CATGCATGGTGCTGC | 57531 |
rs796650846 | snp | C/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774332 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 57531 |
rs796673829 | in-del | -/GG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104727137 | TATGGGTATATATAT[-/GG]GTATATAGATACACA | 57531 |
rs796745128 | snp | A/G | | | missense, nc-transcript-variant | HACE1 | GRCh38.p7 | 6:104795618 | GTAGCAACTTCAGCA[A/G]GGCTTGTTAGAATCT | 57531 |
rs796796191 | in-del | -/AT | | | intron-variant | HACE1 | GRCh38.p7 | 6:104790118 | CGTGCACACACACAC[-/AT]ACATATATGGCTAAA | 57531 |
rs796814387 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104733112 | GATAAAAATCAAGTC[A/G]TTCTGAATTTCCTAT | 57531 |
rs796847637 | in-del | -/T | | | intron-variant | HACE1 | GRCh38.p7 | 6:104756428 | AAAAAAAAAAAAAAA[-/T]ATATATATATATATA | 57531 |
rs796873447 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104774370 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 57531 |
rs796958249 | multinucleotide-polymorphism | CA/TG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104762003 | CCACAATAAGATACT[CA/TG]CTCACACCATTTAGA | 57531 |
rs796968132 | in-del | -/ATG | | | intron-variant | HACE1 | GRCh38.p7 | 6:104822717 | AAAAATTAGCCTGGC[-/ATG]GTGGTGGTACATGTC | 57531 |
rs796995747 | snp | A/C | | | intron-variant | HACE1 | GRCh38.p7 | 6:104780172 | GATATTAAACTATAT[A/C]ATTTATCTATGAAAT | 57531 |
rs796996390 | snp | A/G | | | intron-variant | HACE1 | GRCh38.p7 | 6:104726358 | ACCCAATATTGTCAG[A/G]TTGTCTCACTGCTCA | 57531 |