| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs11995 | snp | A/G | 0.275464 | 0.2487 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20781764 | TTGGACCCTTTCCTC[A/G]CAACTAACTGTCAAC | 10529 |
| rs67179 | snp | C/T | 0.469839 | 0.119042 | intron-variant | NEBL | GRCh38.p7 | 10:21029963 | CTATCATTATACCTA[C/T]AATCATCCCGAGAGA | 10529 |
| rs106459 | snp | C/G | 0.304438 | 0.244001 | intron-variant | NEBL | GRCh38.p7 | 10:21093259 | AGGATAAGTATTTGG[C/G]AAAGACATGAATGGT | 10529 |
| rs186377 | snp | G/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21122104 | tgggaggtggaggtt[G/T]cagtgagccgagatc | 10529 |
| rs188764 | snp | C/T | 0.484066 | 0.0878235 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21132343 | aaggggtgaatggtg[C/T]tccattgtatagatg | 10529 |
| rs191120 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21122095 | gaggtttcagtgagc[C/T]gagatcgtgccactg | 10529 |
| rs192864 | snp | A/G | 0.3746 | 0.216737 | intron-variant | NEBL | GRCh38.p7 | 10:21098671 | ACAAGATTGTTACAG[A/G]AGCGCATAAATACAC | 10529 |
| rs313787 | snp | C/T | 0.430285 | 0.173197 | intron-variant | NEBL | GRCh38.p7 | 10:21097826 | CAATAAATGAAGACA[C/T]TGGACTTTTTTATGG | 10529 |
| rs313788 | snp | A/C | 0.23846 | 0.249734 | intron-variant | NEBL | GRCh38.p7 | 10:21098447 | GACTCAGGAAACCCA[A/C]TGGTATTTAATAATT | 10529 |
| rs313789 | snp | G/T | 0.478437 | 0.10157 | intron-variant | NEBL | GRCh38.p7 | 10:21124701 | GTCATAGCTGGAATC[G/T]CAGCACTTTGGGAGG | 10529 |
| rs313790 | snp | C/T | 0.478603 | 0.101197 | intron-variant | NEBL | GRCh38.p7 | 10:21124380 | AGACATTGAAGCTAA[C/T]AATATCTTCTCCTCC | 10529 |
| rs313791 | snp | C/T | 0.461259 | 0.133677 | intron-variant | NEBL | GRCh38.p7 | 10:21123751 | TATATCATCTCAAAC[C/T]AATATATTCATAAAA | 10529 |
| rs313792 | snp | C/T | 0.473174 | 0.112665 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21144617 | tgtaatcccagctac[C/T]tcagaggctgagaca | 10529 |
| rs313793 | snp | A/G | 0.462144 | 0.132269 | upstream-variant-2KB, intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21147793 | TTACCTTAGCTACCC[A/G]GCCCCTTCAGCATTC | 10529 |
| rs313794 | snp | G/T | 0.380529 | 0.213219 | intron-variant | NEBL | GRCh38.p7 | 10:21148979 | ttcagaaggggtcct[G/T]ccccatacccaggag | 10529 |
| rs313795 | snp | A/C | 0.380138 | 0.213458 | intron-variant | NEBL | GRCh38.p7 | 10:21149372 | ctcagctcactgcaa[A/C]ctccgcctcctgggt | 10529 |
| rs313796 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEBL | GRCh38.p7 | 10:21149566 | aaagtgctgggatta[C/T]aggcatgagccatcg | 10529 |
| rs473020 | snp | A/G | 0.476833 | 0.105105 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21126884 | GGAGGCTAAGGCAGG[A/G]GAATCGCTTGAACCC | 10529 |
| rs478559 | snp | G/T | 0.482309 | 0.0923707 | intron-variant | NEBL | GRCh38.p7 | 10:21104875 | tttttgtagatgccc[G/T]atatcaggatgaaga | 10529 |
| rs480272 | snp | A/T | 0.478603 | 0.101197 | intron-variant | NEBL | GRCh38.p7 | 10:21105044 | tcttttttaaggtta[A/T]gccaaccctgaattc | 10529 |
| rs491386 | snp | C/T | 0.491473 | 0.0647364 | intron-variant | NEBL | GRCh38.p7 | 10:21052689 | GCTCTTCCTGAGTGT[C/T]GGTGATTTCACTGGA | 10529 |
| rs494226 | snp | C/G | 0.460252 | 0.135255 | intron-variant | NEBL | GRCh38.p7 | 10:21036318 | cagaggtgtacacca[C/G]cacgcctggctaatt | 10529 |
| rs495866 | snp | A/G | 0.497182 | 0.037434 | intron-variant | NEBL | GRCh38.p7 | 10:21042753 | CAGGAAGAATCcaga[A/G]gtttgctggtcaatg | 10529 |
| rs499364 | snp | A/G | 0.463126 | 0.13068 | intron-variant | NEBL | GRCh38.p7 | 10:21048988 | gagtctctctctgtc[A/G]tccaggctggagtgc | 10529 |
| rs500220 | snp | A/G | 0.476833 | 0.105105 | intron-variant | NEBL | GRCh38.p7 | 10:21118103 | GTGTCAGTCTGGCTG[A/G]TGCAGCACCCCACAG | 10529 |
| rs502246 | snp | A/G | 0.466204 | 0.125522 | intron-variant | NEBL | GRCh38.p7 | 10:21163205 | TCTGCTAGAAACCCA[A/G]TTTTTTTTCCTATAA | 10529 |
| rs508282 | snp | A/T | 0.463774 | 0.129618 | intron-variant | NEBL | GRCh38.p7 | 10:21038590 | gactggataaagaaa[A/T]tgtggcacatatgca | 10529 |
| rs515249 | snp | A/C | 0.389152 | 0.207694 | intron-variant | NEBL | GRCh38.p7 | 10:21089156 | ACTCCGCTCAAGCAG[A/C]AAACTCAAATGTCCT | 10529 |
| rs518712 | snp | A/G | 0.462472 | 0.13174 | intron-variant | NEBL | GRCh38.p7 | 10:21035979 | acaagcctggccaac[A/G]tggtgaaatcccatt | 10529 |
| rs522736 | snp | C/T | 0.369142 | 0.219784 | intron-variant | NEBL | GRCh38.p7 | 10:21118210 | ACAGGAACATCTCCT[C/T]CAGCTGACAACTTAT | 10529 |
| rs524176 | snp | A/C | 0.302184 | 0.244493 | intron-variant | NEBL | GRCh38.p7 | 10:21093004 | TCTCTGATGTGGGAA[A/C]AGTTTATGACAAGAG | 10529 |
| rs525350 | snp | A/G | 0.495445 | 0.0475058 | intron-variant | NEBL | GRCh38.p7 | 10:21051250 | tggattacaaatgag[A/G]attacaataaAAAAT | 10529 |
| rs526061 | snp | C/T | 0.419456 | 0.183806 | intron-variant | NEBL | GRCh38.p7 | 10:21025675 | tgctcctaTAAGCAC[C/T]GGAATCTGGATAAAA | 10529 |
| rs534149 | snp | C/T | 0.463666 | 0.129795 | intron-variant | NEBL | GRCh38.p7 | 10:21038005 | TCTGAAGAATCTACT[C/T]TTGATTCTGAAATCT | 10529 |
| rs534865 | snp | C/T | 0.463881 | 0.12944 | intron-variant | NEBL | GRCh38.p7 | 10:21037966 | TATGTCTTATGAAGA[C/T]ATTTTTGCTCGTTCT | 10529 |
| rs536347 | snp | A/T | 0 | 0 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21129121 | aattaaaggaatttg[A/T]tgccaatacacctgc | 10529 |
| rs543011 | snp | A/G | 0.463234 | 0.130503 | intron-variant | NEBL | GRCh38.p7 | 10:21054484 | CTGTACTGCCTCTCG[A/G]ACAGGCATCGGGGAA | 10529 |
| rs550117 | snp | C/G | 0.416545 | 0.186448 | intron-variant | NEBL | GRCh38.p7 | 10:21017393 | TTGCTCAAATGTCGT[C/G]TTCTTTAGAAGCAAT | 10529 |
| rs561415 | snp | A/C | 0.460477 | 0.134905 | intron-variant | NEBL | GRCh38.p7 | 10:21030776 | GGCTCAGGTGCAGAT[A/C]TGGAGTCATGCTCCT | 10529 |
| rs561753 | snp | C/G | 0.493523 | 0.0565391 | intron-variant | NEBL | GRCh38.p7 | 10:21040158 | ggatcacgaggtcag[C/G]agattgagaccatcc | 10529 |
| rs568929 | snp | A/C | 0.463451 | 0.130149 | intron-variant | NEBL | GRCh38.p7 | 10:21053902 | GGGATTACAGGTGCG[A/C]ACCACCATGCCTGGC | 10529 |
| rs579039 | snp | A/G | 0.361684 | 0.223667 | intron-variant | NEBL | GRCh38.p7 | 10:21110398 | AACTTCTACATGAAA[A/G]AGAAAAATTTCTTGA | 10529 |
| rs579249 | snp | C/T | 0.49645 | 0.0419827 | intron-variant | NEBL | GRCh38.p7 | 10:21033929 | atccacccgcctcgg[C/T]ctcccaaaatgctgg | 10529 |
| rs579640 | snp | C/T | 0.474091 | 0.11083 | intron-variant | NEBL | GRCh38.p7 | 10:21153299 | AGGGCCTTTGCAGCC[C/T]TGCTGTATAGTGTGG | 10529 |
| rs581366 | snp | A/C | | | intron-variant | NEBL | GRCh38.p7 | 10:21153461 | cagcctcctgaatag[A/C]tgggattacaggtgc | 10529 |
| rs587211 | snp | C/T | 0.493703 | 0.0557558 | intron-variant | NEBL | GRCh38.p7 | 10:21039634 | aaagttttaaaaaca[C/T]CATTTTAAGTTATGT | 10529 |
| rs589425 | snp | A/G | 0.460589 | 0.13473 | intron-variant | NEBL | GRCh38.p7 | 10:21033514 | AAAACTTAAATCTCT[A/G]TCACTCTCAAAATTC | 10529 |
| rs589483 | snp | A/C | 0.463451 | 0.130149 | intron-variant | NEBL | GRCh38.p7 | 10:21040120 | cacctgcaatcccag[A/C]actttgggaggctga | 10529 |
| rs590763 | snp | A/G | 0.460702 | 0.134554 | intron-variant | NEBL | GRCh38.p7 | 10:21033827 | TATATTGAGAGCCAA[A/G]CGAGAGCCATATCAT | 10529 |
| rs590767 | snp | C/G | 0.195214 | 0.243923 | intron-variant | NEBL | GRCh38.p7 | 10:21036987 | AGGTGGGAACAGCTA[C/G]GGTGGAGAACCTCTG | 10529 |
| rs591652 | snp | C/T | 0.35809 | 0.225425 | intron-variant | NEBL | GRCh38.p7 | 10:21118004 | ATTGAACATCACTCC[C/T]AGCACAGAATAATTA | 10529 |
| rs594599 | snp | A/G | 0.463234 | 0.130503 | intron-variant | NEBL | GRCh38.p7 | 10:21053577 | AAAATAAGCCTACCC[A/G]TTGGATTCTTTATAA | 10529 |
| rs597837 | snp | A/C | 0.431473 | 0.171952 | intron-variant | NEBL | GRCh38.p7 | 10:21013892 | AAACAAAAAGAACCC[A/C]ATGAAGAGCAGAGTC | 10529 |
| rs599087 | snp | A/G | 0.257176 | 0.249897 | intron-variant | NEBL | GRCh38.p7 | 10:21007590 | GGCACAATATCATCC[A/G]GGCGATTGCTTAGTG | 10529 |
| rs600402 | snp | C/G | 0.378372 | 0.214524 | intron-variant | NEBL | GRCh38.p7 | 10:21117064 | AATATTGCTGAGCTT[C/G]AGCTGGGTGCAATAA | 10529 |
| rs602053 | snp | A/G | 0.47517 | 0.10862 | intron-variant | NEBL | GRCh38.p7 | 10:21053774 | AAGTGCTGGGATTAC[A/G]GATTTGAGCCACCAT | 10529 |
| rs602572 | snp | A/G | 0.477345 | 0.103991 | intron-variant | NEBL | GRCh38.p7 | 10:21110940 | cacaagcattcctat[A/G]cagcaataacagaca | 10529 |
| rs603346 | snp | A/G | 0.463126 | 0.13068 | intron-variant | NEBL | GRCh38.p7 | 10:21053519 | TTATCTTTTTCCTTA[A/G]CTACTGATGCTCATT | 10529 |
| rs603790 | snp | C/T | 0.497329 | 0.0364438 | intron-variant | NEBL | GRCh38.p7 | 10:21053419 | ATCATAGATAATATT[C/T]TTGCCTGTTTCCTTT | 10529 |
| rs604251 | snp | C/T | 0.460813 | 0.134379 | intron-variant | NEBL | GRCh38.p7 | 10:21034494 | GCTTATCCTGTGCTC[C/T]AGGATGTCTGGCAAC | 10529 |
| rs604600 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | NEBL | GRCh38.p7 | 10:21163995 | TCCTTCTCACAACTT[C/T]CTGTTTTCATGGTTA | 10529 |
| rs605715 | snp | C/T | 0.465578 | 0.126594 | intron-variant | NEBL | GRCh38.p7 | 10:21088937 | GCAGTTAATGAACCA[C/T]GCGAGGCAGGAAAGA | 10529 |
| rs608788 | snp | C/T | 0.279726 | 0.248226 | intron-variant | NEBL | GRCh38.p7 | 10:20999992 | TTTCCAGCAATGTAG[C/T]CATTTACTACAAAGC | 10529 |
| rs611992 | snp | G/T | 0.491473 | 0.0647364 | intron-variant | NEBL | GRCh38.p7 | 10:21048509 | AGATTTAGCACCACA[G/T]GAGTTTTAAAAATAT | 10529 |
| rs613306 | snp | C/G | 0.497387 | 0.0360476 | intron-variant | NEBL | GRCh38.p7 | 10:21048787 | gatcaccttaggtca[C/G]gagtacgagaccagc | 10529 |
| rs613407 | snp | C/T | 0.4628 | 0.13121 | intron-variant | NEBL | GRCh38.p7 | 10:21048865 | aaaaataaaattagc[C/T]gggcatggtggcagg | 10529 |
| rs618568 | snp | C/G | 0.315273 | 0.241329 | intron-variant | NEBL | GRCh38.p7 | 10:21035401 | AGCATTGTGTACAAC[C/G]TTGTCAACTACTGTG | 10529 |
| rs620853 | snp | A/G | 0.462253 | 0.132093 | intron-variant | NEBL | GRCh38.p7 | 10:21035891 | AAAAGggctgggcac[A/G]gtagcttaggcctgt | 10529 |
| rs621429 | snp | A/G | 0.4021 | 0.198407 | intron-variant | NEBL | GRCh38.p7 | 10:21087760 | TCTCAATTATACCGA[A/G]GTCAGGGCTGCAAAC | 10529 |
| rs623047 | snp | A/G | 0.460813 | 0.134379 | intron-variant | NEBL | GRCh38.p7 | 10:21034468 | GCAACAGGTGCCTGC[A/G]TTACTGTGCTGAGAA | 10529 |
| rs623551 | snp | A/T | 0.460925 | 0.134204 | intron-variant | NEBL | GRCh38.p7 | 10:21034311 | AATTGTGGAAAACTA[A/T]TAATTAACAATAAAA | 10529 |
| rs623634 | snp | C/G | 0.077417 | 0.180873 | intron-variant | NEBL | GRCh38.p7 | 10:21166113 | CCTGCCTCAGCCTCC[C/G]GAGTAGCTGGGACTT | 10529 |
| rs625223 | snp | C/G | 0.481757 | 0.0937492 | missense, intron-variant, utr-variant-3-prime | C10orf113, NEBL | GRCh38.p7 | 10:21125963 | CCCAGTTGCCTGGAT[C/G]TGGTTCAGGAGCTGC | 10529 |
| rs625903 | snp | A/G | 0.483272 | 0.0899109 | intron-variant | NEBL | GRCh38.p7 | 10:21151499 | TGCTTTATTTTTACA[A/G]CCAGCCAAAGTGAAA | 10529 |
| rs627000 | snp | A/G | 0.478685 | 0.10101 | intron-variant | NEBL | GRCh38.p7 | 10:21108458 | ttgttcagtttccac[A/G]tagttgtgcgctttt | 10529 |
| rs627340 | snp | C/T | 0.463234 | 0.130503 | intron-variant | NEBL | GRCh38.p7 | 10:21108499 | attaatcctgagttc[C/T]aatttgattgcactg | 10529 |
| rs631361 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | NEBL | GRCh38.p7 | 10:21047073 | AAAGTCTGCATGGCA[A/G]TAACATTCATCACAT | 10529 |
| rs632551 | snp | G/T | 0.309154 | 0.242901 | intron-variant | NEBL | GRCh38.p7 | 10:21101341 | TCATGCCCAGATCAC[G/T]TGCAGGCAATGTGGT | 10529 |
| rs633714 | snp | A/G | 0.461148 | 0.133852 | intron-variant | NEBL | GRCh38.p7 | 10:21043090 | TATACAGCTCTTCTA[A/G]AGACTTAAATCTGAC | 10529 |
| rs634567 | snp | A/G | 0.314301 | 0.241589 | intron-variant | NEBL | GRCh38.p7 | 10:21043307 | GTCATCCTACAAAAA[A/G]ACAGCCGTCAACATT | 10529 |
| rs634614 | snp | C/T | 0.462909 | 0.131034 | intron-variant | NEBL | GRCh38.p7 | 10:21036769 | TGCTCAGGCGGATGG[C/T]TCACTTTCTGTAGAG | 10529 |
| rs634878 | snp | C/G | 0.490508 | 0.0682328 | intron-variant | NEBL | GRCh38.p7 | 10:21087491 | CTTTTTTCAGACTTT[C/G]TCTTCTCCCAGTTTT | 10529 |
| rs637189 | snp | G/T | 0 | 0 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21143150 | ATGTTCAAAGGGAGG[G/T]TAAACTTTAAGCATG | 10529 |
| rs638548 | snp | C/G | 0.460702 | 0.134554 | intron-variant | NEBL | GRCh38.p7 | 10:21033238 | TTGATATTTTTCAGA[C/G]TATACTCATATCTTA | 10529 |
| rs638597 | snp | A/G | 0.170408 | 0.236992 | intron-variant | NEBL | GRCh38.p7 | 10:21033200 | GAGTCCCAAATCTGC[A/G]TGTGTTTCTCTTGGC | 10529 |
| rs638929 | snp | G/T | 0.460252 | 0.135255 | intron-variant | NEBL | GRCh38.p7 | 10:21029696 | CAATACCCACGGCCA[G/T]ACTGGTCTGAATCAT | 10529 |
| rs640056 | snp | C/T | 0.371177 | 0.218669 | intron-variant | NEBL | GRCh38.p7 | 10:21002402 | AGTTATCCTACGCTG[C/T]AGAATGTTTACCATG | 10529 |
| rs640729 | snp | C/T | 0.46014 | 0.13543 | intron-variant | NEBL | GRCh38.p7 | 10:21030071 | CAAAATAAGCTCGAC[C/T]GGACTGGGAGGTACT | 10529 |
| rs640750 | snp | G/T | 0.459914 | 0.13578 | intron-variant | NEBL | GRCh38.p7 | 10:21030081 | CCTCCAAAGACAAAA[G/T]AAGCTCGACCGGACT | 10529 |
| rs641632 | snp | G/T | 0.459801 | 0.135955 | intron-variant | NEBL | GRCh38.p7 | 10:21040496 | cttctctcctctatt[G/T]ctccttcgctcacca | 10529 |
| rs642446 | snp | A/T | 0.438246 | 0.16451 | intron-variant | NEBL | GRCh38.p7 | 10:21013702 | GGCCAACATGGTGAA[A/T]CCCCATCTCTACTAA | 10529 |
| rs643674 | snp | G/T | 0.462909 | 0.131034 | intron-variant | NEBL | GRCh38.p7 | 10:21049666 | AAGTGAGGAACGGGG[G/T]CAGGGTGGGCGGTTG | 10529 |
| rs649597 | snp | G/T | 0.304688 | 0.243945 | intron-variant | NEBL | GRCh38.p7 | 10:21088438 | GTAGTGGGCTATGAT[G/T]GTACCACTGCACTCC | 10529 |
| rs649734 | snp | C/T | 0.464096 | 0.129085 | intron-variant | NEBL | GRCh38.p7 | 10:21037791 | GGGAGTGTTTTTTGA[C/T]CTCCAATTTATCTTG | 10529 |
| rs652864 | snp | A/G | 0.460027 | 0.135605 | intron-variant | NEBL | GRCh38.p7 | 10:21030470 | TTACCTTTTGGGGCT[A/G]ATCAGTTTTGGTAGA | 10529 |
| rs653028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEBL | GRCh38.p7 | 10:21111945 | tgtcttcctttgaga[A/G]gtgtttgttcatatc | 10529 |
| rs653038 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21111940 | tcctttgagaagtgt[C/T]tgttcatatcctttc | 10529 |
| rs654278 | snp | C/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21039995 | CAAAAATATTCTCTG[C/G]CTGTGTAATCCTATG | 10529 |
| rs654355 | snp | C/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21030860 | GTACAGGTGTTAAGT[C/G]GTTTGAATACCACCC | 10529 |
| rs654717 | snp | A/G | 0.460589 | 0.13473 | intron-variant | NEBL | GRCh38.p7 | 10:21030903 | TCTGATCTTTCAGAT[A/G]CCATTTTTGATTGGT | 10529 |
| rs655438 | snp | C/T | 0.473726 | 0.111565 | intron-variant | NEBL | GRCh38.p7 | 10:21160516 | ATAACCCTTAATTAT[C/T]ACGTGCCTTAAGCAT | 10529 |
| rs655662 | snp | A/G | 0.182933 | 0.240836 | intron-variant | NEBL | GRCh38.p7 | 10:21111357 | CAGCCTGTTTTTACT[A/G]TAGCCTTGTAGTATA | 10529 |
| rs655999 | snp | C/T | 0.47885 | 0.100637 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21126904 | CGCTTGAACCCAGGG[C/T]GGGGAAGTTCTAGTG | 10529 |
| rs656069 | snp | C/T | 0.460589 | 0.13473 | intron-variant | NEBL | GRCh38.p7 | 10:21031233 | GACCCCCATAGGGTT[C/T]ATCATCATCCTCTTT | 10529 |
| rs658096 | snp | A/C | 0.480223 | 0.0974544 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21127316 | aaagaattccaacta[A/C]taaatgcagaaagaa | 10529 |
| rs660859 | snp | A/G | 0.430285 | 0.173197 | intron-variant | NEBL | GRCh38.p7 | 10:21012261 | GCCCCAGAGAGAGAA[A/G]CAGAGTGAAGAGTGA | 10529 |
| rs661860 | snp | C/G | 0.377582 | 0.214995 | upstream-variant-2KB, intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21146985 | TTCACAAGGTCCTCC[C/G]TGCCATAACGCCTCT | 10529 |
| rs661924 | snp | A/G | 0.493658 | 0.0559517 | intron-variant | NEBL | GRCh38.p7 | 10:21024627 | ATTTTCATTTTCAGT[A/G]TAAGGCAGTATGAGT | 10529 |
| rs663661 | snp | A/G | 0.486067 | 0.0822953 | intron-variant | NEBL | GRCh38.p7 | 10:21025654 | CTGGATAAAAAGAGA[A/G]TGTTTCTGGGTTCTC | 10529 |
| rs663759 | snp | A/G | 0.463774 | 0.129618 | intron-variant | NEBL | GRCh38.p7 | 10:21038664 | gtaaatagtgctgca[A/G]taaacatatgtgtgc | 10529 |
| rs664959 | snp | C/T | 0.489409 | 0.12711 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21134566 | GGACTACCTTTTACA[C/T]GGTCGATCCCTAATT | 10529 |
| rs665486 | snp | A/G | 0.465368 | 0.126951 | intron-variant | NEBL | GRCh38.p7 | 10:21039040 | ctgttcatagccttc[A/G]tccactttttgatgg | 10529 |
| rs668045 | snp | A/C | 0.0494327 | 0.149241 | intron-variant | NEBL | GRCh38.p7 | 10:21031644 | TCTGTTCTGTTCTTG[A/C]TGTGGCAGCTTGGAG | 10529 |
| rs669320 | snp | A/G | 0.490508 | 0.0682328 | intron-variant | NEBL | GRCh38.p7 | 10:21038929 | caaatcaaaaccaca[A/G]tgagataccatctca | 10529 |
| rs671024 | snp | C/G | 0.419296 | 0.183954 | intron-variant | NEBL | GRCh38.p7 | 10:21005533 | TGCCCAGGCTGGTCT[C/G]GAACTCTTGGGCTCA | 10529 |
| rs671173 | snp | C/T | 0.460702 | 0.134554 | intron-variant | NEBL | GRCh38.p7 | 10:21032367 | TATCAGGCTTATAGT[C/T]ATTATAATTATGCCT | 10529 |
| rs672500 | snp | A/G | 0.463666 | 0.129795 | intron-variant | NEBL | GRCh38.p7 | 10:21038198 | ataaaaaaaaTATAT[A/G]GAGGGAGTGCATGGG | 10529 |
| rs674276 | snp | A/G | 0.495559 | 0.0469148 | intron-variant | NEBL | GRCh38.p7 | 10:21044382 | AGCCTGGGTGACTGG[A/G]TGACAGAGTAAGAAT | 10529 |
| rs678185 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | NEBL | GRCh38.p7 | 10:21046174 | atccatgaaatctaa[A/G]aaagttgaactcata | 10529 |
| rs679970 | snp | A/T | 0.490727 | 0.0674567 | intron-variant | NEBL | GRCh38.p7 | 10:21151833 | ACCCCCTGCCCAACC[A/T]AGTGAAACTTATCTC | 10529 |
| rs682570 | snp | G/T | 0.460702 | 0.134554 | intron-variant | NEBL | GRCh38.p7 | 10:21032563 | ATTATAAAATTGATG[G/T]TTTGCAACCAGAGGC | 10529 |
| rs683469 | snp | C/G | 0.460477 | 0.134905 | intron-variant | NEBL | GRCh38.p7 | 10:21032756 | TGACTGCCCTTTAGA[C/G]AGCCAGGGGTTTGGA | 10529 |
| rs684390 | snp | C/T | 0.460702 | 0.134554 | intron-variant | NEBL | GRCh38.p7 | 10:21032961 | TCTAGGTGACATGTT[C/T]CAATAGCCGATAAGC | 10529 |
| rs685192 | snp | C/T | 0.460702 | 0.134554 | intron-variant | NEBL | GRCh38.p7 | 10:21033101 | TTGTTTGTGTATTCC[C/T]GTGATCAATATCAGC | 10529 |
| rs688247 | snp | C/T | 0.256061 | 0.249927 | intron-variant | NEBL | GRCh38.p7 | 10:21094273 | TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG | 10529 |
| rs694004 | snp | G/T | 0.463343 | 0.130326 | intron-variant | NEBL | GRCh38.p7 | 10:21054498 | ACAAACAAAAACAAT[G/T]CCCCGATGCCTGTCC | 10529 |
| rs697160 | snp | C/T | 0.369754 | 0.219451 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20872023 | CATTCATATGAAAAC[C/T]GCAGGGGGGAAATGT | 10529 |
| rs697161 | snp | A/G | 0.198014 | 0.244535 | intron-variant | NEBL | GRCh38.p7 | 10:20889645 | CATATATAATAAAAT[A/G]TATGAAGCATACATA | 10529 |
| rs703087 | snp | C/G | 0.046775 | 0.145601 | intron-variant | NEBL | GRCh38.p7 | 10:20827990 | CGATTATTTTGTCAC[C/G]CAGGTGTTAAGCCTA | 10529 |
| rs703088 | snp | A/C | 0.160938 | 0.233598 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20851326 | TGTTAATGATAATTC[A/C]ACCCAAGAGAAATTT | 10529 |
| rs703089 | snp | C/T | 0.0564523 | 0.15824 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20852540 | CCGTACGGGCAAGTG[C/T]GTACCTGACTTTGGA | 10529 |
| rs703090 | snp | C/G | 0.131464 | 0.220378 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20852923 | TATTCACAACACCAG[C/G]GTGTGGCAACGGAAA | 10529 |
| rs703091 | snp | A/T | 0.0901694 | 0.192235 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20854539 | CACCCCCCAGGAAGG[A/T]CATGAAAATGTTCAT | 10529 |
| rs703092 | snp | A/G | 0.130694 | 0.219696 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20855857 | AAAACAATAGCTACT[A/G]TGACAAATGGATAAT | 10529 |
| rs703093 | snp | C/T | 0.374 | 0.217081 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20858489 | CATTCAGTAGTAAAT[C/T]AGCACCATCTAGTGG | 10529 |
| rs703094 | snp | C/G | 0.498369 | 0.0285077 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860086 | GCACTAAAATACCAA[C/G]ATTTTTAAATGTCAG | 10529 |
| rs703095 | snp | C/T | 0.120674 | 0.21395 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860567 | TTTTTTTTTTTTTTT[C/T]TTTTTGTAGTGAACT | 10529 |
| rs703096 | snp | A/G | 0.127944 | 0.218179 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860982 | TCCATTTGATAATAA[A/G]AAATTTCTGATATTC | 10529 |
| rs703097 | snp | A/C | 0.151668 | 0.229849 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20870307 | TTCCAAACTGGGCAA[A/C]AGAGTGGGACTTTAT | 10529 |
| rs703098 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20872499 | GTGTAGGAATCTGTG[C/T]GAGAAGCCATGTTGC | 10529 |
| rs703099 | snp | A/G | 0.128632 | 0.218563 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20874758 | tttttttcttttttg[A/G]agatgaagtcttgct | 10529 |
| rs703100 | snp | C/T | 0.200492 | 0.245049 | intron-variant | NEBL | GRCh38.p7 | 10:20888016 | AGCGTTTTAATAAAA[C/T]GTTTTCATCATGGGT | 10529 |
| rs703101 | snp | A/G | 0.378962 | 0.21417 | intron-variant | NEBL | GRCh38.p7 | 10:20889032 | GAATGAAATCAGTAC[A/G]TTTTCTTTCATTAAG | 10529 |
| rs703102 | snp | A/T | 0.229723 | 0.249176 | intron-variant | NEBL | GRCh38.p7 | 10:20890231 | CCTGTTTACCCAGCC[A/T]GCCCAGTGCAATTAG | 10529 |
| rs703106 | snp | C/T | 0.463343 | 0.130326 | intron-variant | NEBL | GRCh38.p7 | 10:21038347 | aaaggggagagacag[C/T]attaggagaaatacc | 10529 |
| rs735680 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NEBL | GRCh38.p7 | 10:21063148 | CAGGGGTCTTGCTGT[A/G]TGTGTTTTCAGTCCT | 10529 |
| rs735681 | snp | C/G | 0.0341408 | 0.126114 | intron-variant | NEBL | GRCh38.p7 | 10:21062279 | ACTGCAGAAGTTAAG[C/G]GGAGGGGAAAGAAGA | 10529 |
| rs764147 | snp | G/T | 0.0748431 | 0.178382 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20899016 | AATTGCCTCAAGCAT[G/T]CTGAACTTGGAAACC | 10529 |
| rs787801 | snp | A/C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004537 | gagacggggtttcac[A/C/T]gtgttagccagggtg | 10529 |
| rs787802 | snp | A/C | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004487 | gtgatctgcccgcct[A/C]ggcctccgaaagtac | 10529 |
| rs787803 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21073460 | ctgcctaatttttgt[A/G]tttttagtagagacg | 10529 |
| rs787804 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21073446 | tgtttttagtagaga[C/T]ggggtttcaccatgt | 10529 |
| rs787805 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21073388 | ctcaagtgatccacc[C/T]gccttggcctcccaa | 10529 |
| rs788487 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004447 | tcacctgggccgggc[A/G]cggtggctcacgcct | 10529 |
| rs788488 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004461 | cgcggtggctcacgc[C/T]tgtaatcccagtact | 10529 |
| rs788489 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004473 | cgcttgtaatcccag[C/T]actttcggaggccga | 10529 |
| rs788490 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004502 | gagacaggcggatca[C/T]gaggtcaggagatcg | 10529 |
| rs788492 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004548 | acacagtgaaacccc[A/G]tctctactaaaaata | 10529 |
| rs788948 | snp | C/T | 0.129664 | 0.219133 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20867788 | gctaatccaacttct[C/T]cccactgacttgaat | 10529 |
| rs788949 | snp | C/T | 0.384017 | 0.211044 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20874940 | AGATGAGGTTTATCA[C/T]GTTGGCCAGGTTGGT | 10529 |
| rs788950 | snp | A/C | 0.129664 | 0.219133 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20875818 | TCAGTTTAACCTTCA[A/C]AGGGTTCTGGGTCAG | 10529 |
| rs788951 | snp | C/G | 0.371582 | 0.218444 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20876232 | TCCTAAATGATAAGC[C/G]ATTCTGGCCATAACT | 10529 |
| rs788952 | snp | A/G | 0.081446 | 0.184634 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20877481 | ataaaaagcagcccc[A/G]aagtctttttctttt | 10529 |
| rs788953 | snp | C/T | 0.371987 | 0.218218 | intron-variant, downstream-variant-500B | NEBL, LOC102725112 | GRCh38.p7 | 10:20880163 | GTCAGGAGCTCAAGA[C/T]CAGCCTGGCCTAGAT | 10529 |
| rs788954 | snp | A/C | 0.127599 | 0.217986 | intron-variant, downstream-variant-500B | NEBL, LOC102725112 | GRCh38.p7 | 10:20880186 | gcctagatggtgaaa[A/C]cccgtctctactaaa | 10529 |
| rs788955 | snp | C/T | 0.127599 | 0.217986 | intron-variant, downstream-variant-500B | NEBL, LOC102725112 | GRCh38.p7 | 10:20880229 | aggccggtgtggtgg[C/T]gggcacctgtaatcc | 10529 |
| rs788956 | snp | A/G | 0.3744 | 0.216852 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20882111 | TGATCCCAGGAGGTC[A/G]AGGCTGCAGTGAGCC | 10529 |
| rs788957 | snp | C/T | 0.193028 | 0.243422 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20882925 | ATAAGGCCACATAGA[C/T]GCAGCTAGGGGGAGA | 10529 |
| rs788958 | snp | A/C | 0.373397 | 0.217424 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20884253 | TCCATCTCTAAAATA[A/C]ATGAATAAATAAGTA | 10529 |
| rs788959 | snp | C/T | 0.169435 | 0.236663 | intron-variant, nc-transcript-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20884764 | GTTCCAATGCCTGAG[C/T]AGCGTGAATTGCTTC | 10529 |
| rs788960 | snp | A/G | 0.376394 | 0.215696 | intron-variant | NEBL | GRCh38.p7 | 10:20886104 | GGGTTCATATTAAAT[A/G]GGTGCAGCAAATCAC | 10529 |
| rs788961 | snp | G/T | 0.377582 | 0.214995 | intron-variant | NEBL | GRCh38.p7 | 10:20886874 | TTCTAAGGATATGCT[G/T]CCTTTTACATAGTTT | 10529 |
| rs788962 | snp | A/T | 0.388964 | 0.20782 | intron-variant | NEBL | GRCh38.p7 | 10:20891107 | TCAAATCAGGCTTGC[A/T]TATGGGAAAATCTCC | 10529 |
| rs788963 | snp | A/G | 0.236434 | 0.249632 | intron-variant | NEBL | GRCh38.p7 | 10:20891958 | TAACAGGAAATGATC[A/G]TTGAAAGGGAACTAT | 10529 |
| rs788964 | snp | C/T | 0.198324 | 0.244601 | intron-variant | NEBL | GRCh38.p7 | 10:20892616 | CAAAATTGATGACTT[C/T]ATGATCATTAAGATG | 10529 |
| rs788965 | snp | C/T | 0.371582 | 0.218444 | intron-variant | NEBL | GRCh38.p7 | 10:20892774 | TCCATGTCTGTCATC[C/T]GATTTCAGCCTTTAG | 10529 |
| rs788966 | snp | C/T | 0.377385 | 0.215112 | intron-variant | NEBL | GRCh38.p7 | 10:20893368 | ATAATACTATTATTT[C/T]CTCAGATATATTTTC | 10529 |
| rs788967 | snp | A/G | 0.291493 | 0.246533 | intron-variant | NEBL | GRCh38.p7 | 10:20894435 | ctgcagtcacatgac[A/G]gaactccagcctggg | 10529 |
| rs788968 | snp | C/T | 0.155987 | 0.23165 | intron-variant | NEBL | GRCh38.p7 | 10:20894585 | GTATAGAATTCTATT[C/T]GGAAGCAAAATGTGA | 10529 |
| rs788969 | snp | A/C | 0.14933 | 0.228835 | intron-variant | NEBL | GRCh38.p7 | 10:20895952 | CTGAGGGATGGAGCC[A/C]AGCCAGGTTCCATAA | 10529 |
| rs788970 | snp | A/G | 0.425277 | 0.178263 | intron-variant | NEBL | GRCh38.p7 | 10:20896732 | GCAAAACTCATAAGG[A/G]ACAGGATTCTGGATT | 10529 |
| rs788971 | snp | G/T | 0.141258 | 0.225111 | intron-variant | NEBL | GRCh38.p7 | 10:20896892 | TATTATGTTATAGAG[G/T]CATAGAGCTGTGGGG | 10529 |
| rs788972 | snp | C/T | 0.157311 | 0.232183 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20898376 | ACTTAGAATGACATA[C/T]TATTTTTAATAAATT | 10529 |
| rs788973 | snp | C/T | 0.42666 | 0.176893 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20898817 | CTATCTTTTTTTTAA[C/T]CATACCCACTACCCC | 10529 |
| rs788974 | snp | C/G | 0.271432 | 0.24908 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20898869 | GAAATATGACCGACT[C/G]CTTAGGGAAACATTG | 10529 |
| rs788975 | snp | A/T | 0.317692 | 0.240661 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20899023 | TCAAGCATGCTGAAC[A/T]TGGAAACCACAACTC | 10529 |
| rs788976 | snp | A/T | 0.427119 | 0.176434 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20899268 | GCAAATTTCTAGGAG[A/T]GTAGGGAGAAAATCT | 10529 |
| rs788977 | snp | C/G | 0.426201 | 0.177351 | intron-variant | NEBL | GRCh38.p7 | 10:20900218 | TTCTACTTTAGTACT[C/G]TACGCATGCCTTGAT | 10529 |
| rs788978 | snp | C/T | 0.406641 | 0.194842 | intron-variant | NEBL | GRCh38.p7 | 10:20900561 | GGGTGCGGTGGTTCA[C/T]GCCTGTAATCCTAGC | 10529 |
| rs788979 | snp | A/G | 0.317692 | 0.240661 | intron-variant | NEBL | GRCh38.p7 | 10:20900633 | GTTCGAGACCAGCCT[A/G]GGCAACATGGTGAAA | 10529 |
| rs788980 | snp | A/T | 0.400325 | 0.199756 | intron-variant | NEBL | GRCh38.p7 | 10:20900694 | AAAAAATTAGCCGAG[A/T]GTGATGGCAGTAGAT | 10529 |
| rs788981 | snp | A/G | 0.235854 | 0.249599 | intron-variant | NEBL | GRCh38.p7 | 10:20900794 | AGGTTGCAGTGAGCC[A/G]AGATCCTGCCACTGC | 10529 |
| rs788982 | snp | A/G | 0.317933 | 0.240593 | intron-variant | NEBL | GRCh38.p7 | 10:20900855 | ATCCCGAAAAAAAAA[A/G]AAAAAAGAAAAAAAT | 10529 |
| rs788983 | snp | G/T | 0.3752 | 0.216391 | intron-variant | NEBL | GRCh38.p7 | 10:20901032 | TAAAAAAAATAAAAA[G/T]AAAAAGCACCTTAAA | 10529 |
| rs788984 | snp | A/G | 0.206336 | 0.246157 | intron-variant | NEBL | GRCh38.p7 | 10:20901324 | GGTAATTCAAGTCTC[A/G]GAGACACAGCCGTGG | 10529 |
| rs788985 | snp | C/T | 0.206336 | 0.246157 | intron-variant | NEBL | GRCh38.p7 | 10:20901764 | TTTTGTTTTGATGAC[C/T]GTCTTCCGGAAGGTT | 10529 |
| rs788986 | snp | A/G | 0.146314 | 0.227484 | intron-variant | NEBL | GRCh38.p7 | 10:20901868 | GAACAGAACTTTACT[A/G]ATGGACGAGGCAAGA | 10529 |
| rs788987 | snp | C/T | 0.377977 | 0.21476 | intron-variant | NEBL | GRCh38.p7 | 10:20901874 | AACTTTACTGATGGA[C/T]GAGGCAAGATAAATC | 10529 |
| rs788988 | snp | A/T | 0.219349 | 0.248114 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20852054 | TGCTAGAGAGAAGAT[A/T]TTTTTTAAGTTTATT | 10529 |
| rs788989 | snp | A/G | 0.294576 | 0.245994 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20861469 | CAGGCGTGAGCCACC[A/G]CGCCCAGCCACAGTC | 10529 |
| rs788990 | snp | C/T | 0.224116 | 0.248656 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20861984 | aactcccttagccta[C/T]agctaggcaaaatca | 10529 |
| rs788991 | snp | C/T | 0.225005 | 0.248747 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20862159 | ttaaacagtcttaaa[C/T]tgaaccaCTAGAAG | 10529 |
| rs788992 | snp | C/T | 0.373799 | 0.217195 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20862517 | TGTCTGTGTAGTTGG[C/T]GAGTGAACAAGTCCG | 10529 |
| rs788993 | snp | A/G | 0.373397 | 0.217424 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20862862 | AAATTAATAAAAAAA[A/G]GTGATAAATATTGGG | 10529 |
| rs788994 | snp | A/G | 0.373799 | 0.217195 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20863101 | ACTTGGAGAAAACAC[A/G]GATACTGTTAAGCTA | 10529 |
| rs788995 | snp | C/T | 0.372995 | 0.217652 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20863608 | TTCCTTGCAAAATAA[C/T]GTCTTACTGACTTTG | 10529 |
| rs788996 | snp | C/T | 0.127254 | 0.217792 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20863893 | GAGTCAGGAACATGA[C/T]ATTTGAGCTGATACT | 10529 |
| rs788997 | snp | A/G | 0.130351 | 0.219509 | intron-variant, nc-transcript-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20865342 | TTAACCTTCACAGCA[A/G]CCCTGAGAAGTAAAT | 10529 |
| rs788998 | snp | G/T | 0.372592 | 0.217879 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20865811 | AACAATTACTATGAG[G/T]CACAATTGCATTTGG | 10529 |
| rs788999 | snp | C/T | 0.139564 | 0.224285 | intron-variant | NEBL | GRCh38.p7 | 10:20842781 | AAGTGCACTATATAC[C/T]ATCTTCACCACACTG | 10529 |
| rs789000 | snp | C/T | 0.123105 | 0.215401 | intron-variant | NEBL | GRCh38.p7 | 10:20834047 | GTTGAGATCCCATTA[C/T]ACATTTCCCTTGCAG | 10529 |
| rs805252 | snp | C/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004453 | gatcacaggcgtgag[C/G]caccgtgcccggccc | 10529 |
| rs805253 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NEBL | GRCh38.p7 | 10:21073433 | gatggggtttcacca[C/T]gttggccaggctggt | 10529 |
| rs805254 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21073394 | cctgacctcaagtga[C/T]ccacccgccttggcc | 10529 |
| rs809309 | snp | C/T | 0.32768 | 0.237625 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20865223 | TCTAAAAATGTAGAA[C/T]AGAAAACTATTTTGA | 10529 |
| rs809806 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004503 | tcgatctcctgacct[C/T]gtgatctgcccgcct | 10529 |
| rs811506 | snp | A/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21094532 | aaaaaaaaaaaaaaa[A/T]ttagccagatgtggt | 10529 |
| rs812557 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21082441 | tgaggaaacatcatt[C/T]tggcaacttactttc | 10529 |
| rs812558 | snp | C/G/T | 0.0341408 | 0.126114 | intron-variant | NEBL | GRCh38.p7 | 10:21073501 | gcctcctgagtagct[C/G/T]ggattacaggtgtgt | 10529 |
| rs813112 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004572 | ccactacgcctggct[A/G]attttttgtattttt | 10529 |
| rs813113 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21073422 | accacgttggccagg[C/T]tggtctcaaactcct | 10529 |
| rs813121 | snp | C/T | 0.462363 | 0.131916 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21143442 | gaaaagagtgaaact[C/T]catctcaaaaaaaaa | 10529 |
| rs813710 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21082482 | aggaataaaaatGTT[C/T]TTTGTAGTGTACTGA | 10529 |
| rs813711 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21073510 | cctgtcttggcctcc[C/T]gagtagctgggatta | 10529 |
| rs893880 | snp | C/T | 0.221141 | 0.248329 | intron-variant | NEBL | GRCh38.p7 | 10:21063084 | GCATCCCCATGCTGA[C/T]ATCACTTTGGCCTTC | 10529 |
| rs893881 | snp | C/T | 0.480382 | 0.097079 | intron-variant | NEBL | GRCh38.p7 | 10:21060439 | AACAAGCAATCCAGA[C/T]GATTCTGATACACGC | 10529 |
| rs893882 | snp | A/T | 0.478271 | 0.101943 | intron-variant | NEBL | GRCh38.p7 | 10:21060243 | ATGTATTACAGGCAG[A/T]TGTGCTGTGGGGAGT | 10529 |
| rs946861 | snp | A/C | 0.030278 | 0.119257 | intron-variant | NEBL | GRCh38.p7 | 10:20992322 | CTCTCACCAGGTTGA[A/C]GTTATAGATACTTTC | 10529 |
| rs951804 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NEBL | GRCh38.p7 | 10:20974219 | CAATTCAAATACTTC[A/G]TAAACTTCAAAGACC | 10529 |
| rs952182 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | NEBL | GRCh38.p7 | 10:20975022 | AAGGACAAATATAAT[C/T]GTACCTGTAACACCA | 10529 |
| rs952183 | snp | A/G | 0.404733 | 0.196361 | intron-variant | NEBL | GRCh38.p7 | 10:20975004 | ACCTGTAACACCATG[A/G]AATTATATCGAATCA | 10529 |
| rs952738 | snp | A/G | 0.474544 | 0.10991 | intron-variant | NEBL | GRCh38.p7 | 10:20935190 | GGTGGATGCTTCCTC[A/G]GGGTGACTTTTATAA | 10529 |
| rs960941 | snp | A/G | 0.408359 | 0.193449 | intron-variant | NEBL | GRCh38.p7 | 10:20982224 | AGAAAATTCGGAAAC[A/G]TCGTCAAATGTTGTT | 10529 |
| rs968949 | snp | A/G | 0.039522 | 0.134904 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21127695 | caatccagaatgtgg[A/G]acatgctataaggca | 10529 |
| rs1006362 | snp | C/T | 0.494358 | 0.0528145 | intron-variant, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20819318 | CAGTATTTGGTTTTA[C/T]GTTCCTGTGTTAGTT | 10529 |
| rs1006363 | snp | C/T | 0.372658 | 0.217842 | intron-variant, synonymous-codon, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20819448 | CTGCTCCTGGTTTCG[C/T]CTCACTCTCTCTATC | 10529 |
| rs1043121 | snp | C/G | 0.493247 | 0.0577133 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20782262 | TGTTTGTCTAGTATG[C/G]TCTTGGAAAGAAAAC | 10529 |
| rs1062669 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20783755 | GCAATATTTTTGCAA[A/T]AAAATCTGTCGTTAA | 10529 |
| rs1062670 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20783311 | CAAGATGTTGCATGC[G/T]CTTGAGGCCATAATT | 10529 |
| rs1062671 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20783203 | TAAAACCAAAGTGCT[A/G]TTTTTAAAAGCATCA | 10529 |
| rs1062672 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20781260 | AACATTGAATGTTTT[A/G]CAAATGAAGGGGCTT | 10529 |
| rs1085866 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004589 | gctgggcatggtggc[A/G]ggtgcctgtagtccc | 10529 |
| rs1085867 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004636 | gaggcaggagaatgg[C/T]gtgaacccgggaggt | 10529 |
| rs1085868 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21004644 | agaatggcgtgaacc[C/T]gggaggtggagcttg | 10529 |
| rs1091609 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21073586 | tctgtcacccaggct[A/G]gagtgcagtggcgcg | 10529 |
| rs1123710 | snp | C/G | 0.329317 | 0.237084 | intron-variant | NEBL | GRCh38.p7 | 10:21084359 | CGAGAGAGAAACAAA[C/G]TATAGACTCTTGCCC | 10529 |
| rs1123796 | snp | A/G | 0.493837 | 0.055168 | intron-variant | NEBL | GRCh38.p7 | 10:21082087 | atattcaggttaggc[A/G]tggttggcagggatt | 10529 |
| rs1124487 | snp | A/G | 0.375996 | 0.215928 | intron-variant | NEBL | GRCh38.p7 | 10:20821023 | GTCACAAGAATCTGC[A/G]TAACATCTCAAACTA | 10529 |
| rs1142683 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NEBL | GRCh38.p7 | 10:21039361 | tttatggttttgggt[C/T]ttacgtttaagtctt | 10529 |
| rs1312754 | snp | C/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21166192 | gccactgcactccag[C/G]ctgggcgacagagcg | 10529 |
| rs1340291 | snp | C/T | 0.405082 | 0.196086 | intron-variant | NEBL | GRCh38.p7 | 10:20907388 | TCATTAATGAAATGA[C/T]GTAAAGTCCCACTAG | 10529 |
| rs1340292 | snp | G/T | 0.405082 | 0.196086 | intron-variant | NEBL | GRCh38.p7 | 10:20907471 | GAATAATAAACATTC[G/T]ATAATTCTCTATCTA | 10529 |
| rs1340293 | snp | A/G | 0.479014 | 0.100263 | intron-variant | NEBL | GRCh38.p7 | 10:20910236 | GCTCAAGGTTCATAC[A/G]AAAGCAGTATTTCTT | 10529 |
| rs1361452 | snp | A/C | 0.15665 | 0.231917 | intron-variant | NEBL | GRCh38.p7 | 10:20981867 | CTCTTAGCAGCCTTG[A/C]CCTAATGCCAGTTTC | 10529 |
| rs1406112 | snp | A/G | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860321 | ACCCAGGACATTTCA[A/G]AAAATGTAATTCCTA | 10529 |
| rs1406113 | snp | A/G | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860265 | TATAGGAAATGATGA[A/G]AAAAACTGTGGTACA | 10529 |
| rs1409272 | snp | A/G | 0.484771 | 0.0859212 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20858591 | AAATTACTTTATTCT[A/G]TTGACATTACCCTTC | 10529 |
| rs1409273 | snp | A/T | 0.497959 | 0.0318836 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20858441 | TGTCCATTTACCACT[A/T]AATAGTCCTACTTTA | 10529 |
| rs1409348 | snp | C/T | 0.494896 | 0.0502595 | intron-variant | NEBL | GRCh38.p7 | 10:20826403 | ATTTGTCTATAGTTT[C/T]GGTTTGCTTTTAGAA | 10529 |
| rs1417184 | snp | C/T | 0.383439 | 0.21141 | intron-variant | NEBL | GRCh38.p7 | 10:20963266 | CTGGCACATTCTCAG[C/T]GTTTAATGCCTAACT | 10529 |
| rs1417185 | snp | C/T | 0.29278 | 0.246313 | intron-variant | NEBL | GRCh38.p7 | 10:20987785 | GGAGATTTTCCAGGG[C/T]TCCTTCTGTACCAGC | 10529 |
| rs1418075 | snp | A/G | 0.114036 | 0.209795 | intron-variant | NEBL | GRCh38.p7 | 10:20953122 | ATGAATTTTGGGGTG[A/G]TACACAGTTCAGTCC | 10529 |
| rs1440295 | snp | A/G | 0.414245 | 0.188477 | intron-variant | NEBL | GRCh38.p7 | 10:21065469 | GCTTAATTCATTTTC[A/G]GCACTGTGGGTGGAA | 10529 |
| rs1440296 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | NEBL | GRCh38.p7 | 10:21056738 | TATTTTGCTTTTGAG[A/G]TGCATCCATACAGCT | 10529 |
| rs1440297 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NEBL | GRCh38.p7 | 10:21078909 | CAGATCCAGGGGATG[A/G]GTGTATCCACTGATC | 10529 |
| rs1470118 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21054859 | TTAACTCTCAAGTTT[C/T]ATGAAATTGAAAAAT | 10529 |
| rs1475354 | snp | C/T | 0.185472 | 0.241529 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20868099 | TCAGAATTATATAAA[C/T]GTCATGCAACTTCTG | 10529 |
| rs1527042 | snp | C/T | 0.429987 | 0.173507 | intron-variant | NEBL | GRCh38.p7 | 10:21164868 | ACTGTCATCCTGTCA[C/T]GTCAGATACTGTGTC | 10529 |
| rs1528181 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20830523 | GTATATTTGACAAAT[C/T]TAAATTTTACCAAGA | 10529 |
| rs1528182 | snp | C/T | 0.000913057 | 0.021347 | intron-variant, synonymous-codon, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20828578 | TTCTACCATAGCAGA[C/T]ACTCCTGAAATTCAG | 10529 |
| rs1536310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20861025 | AAACTGATTTTAAGT[A/G]ATCAGCAAGAACTCT | 10529 |
| rs1536553 | snp | A/G | 0.184203 | 0.241186 | intron-variant | NEBL | GRCh38.p7 | 10:21121183 | ATCTCAAATGGCTTC[A/G]GTTCAAAGAAGGAAA | 10529 |
| rs1536554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEBL | GRCh38.p7 | 10:21079353 | ATCTTTGGTAGGCTC[C/T]CATTTCTGTGATTTA | 10529 |
| rs1539210 | snp | G/T | 0.480853 | 0.0959518 | intron-variant | NEBL | GRCh38.p7 | 10:20947270 | CAGAGAGCATTAGGG[G/T]AGTTGTAGGGTAACT | 10529 |
| rs1539211 | snp | A/G | 0.474363 | 0.110278 | intron-variant | NEBL | GRCh38.p7 | 10:20947399 | ATGAGGGCAGGCTAG[A/G]AAGTGTCAAACTCAC | 10529 |
| rs1543829 | snp | C/T | 0.461923 | 0.132621 | intron-variant | NEBL | GRCh38.p7 | 10:21056960 | TTTAAATTGAATGCA[C/T]AGTTTAAAGAATCAT | 10529 |
| rs1543830 | snp | C/T | 0.495291 | 0.0482933 | intron-variant | NEBL | GRCh38.p7 | 10:21056896 | AAGAAAGGGATTAGC[C/T]GTACTGCATGGAGCC | 10529 |
| rs1543831 | snp | C/T | 0.462363 | 0.131916 | intron-variant | NEBL | GRCh38.p7 | 10:21056783 | TAATCTGCATGTGGA[C/T]GATTTTGTGATTTGC | 10529 |
| rs1545202 | snp | A/T | 0.157311 | 0.232183 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21137676 | GGTGGCTCATGACTG[A/T]AATCCCAGCACTTTG | 10529 |
| rs1556996 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NEBL | GRCh38.p7 | 10:20910821 | TTGTTTGGTGTTTTT[C/T]GTTTTTGTTTTTTTT | 10529 |
| rs1675503 | snp | C/G | 0.468949 | 0.12067 | intron-variant | NEBL | GRCh38.p7 | 10:21151860 | TCTCTTCCCCTGCTC[C/G]ATTTTTCTCTATAGA | 10529 |
| rs1675504 | snp | C/T | 0.381891 | 0.212379 | intron-variant | NEBL | GRCh38.p7 | 10:21151906 | ATATTTTACTGATTG[C/T]TTGGTTTTGGGTTTT | 10529 |
| rs1726223 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | NEBL | GRCh38.p7 | 10:21158626 | TGATTCCAGTGTTTC[A/C]GTTCCAGGACCACAT | 10529 |
| rs1726224 | snp | C/T | 0.478188 | 0.10213 | intron-variant | NEBL | GRCh38.p7 | 10:21150304 | TTCTCATCAACTTTC[C/T]GACAAATTCTGCTCA | 10529 |
| rs1726226 | snp | A/G | 0.487933 | 0.0767327 | intron-variant | NEBL | GRCh38.p7 | 10:21152111 | GCATTTCCGCTATCC[A/G]GAAATGGGACAGAGA | 10529 |
| rs1751913 | snp | C/T | 0.424968 | 0.178567 | intron-variant | NEBL | GRCh38.p7 | 10:21150272 | AGGATTTATATCGAA[C/T]GGTTGGAAGCTTTCG | 10529 |
| rs1751915 | snp | C/T | 0.363568 | 0.222716 | intron-variant | NEBL | GRCh38.p7 | 10:21155674 | TTGTTTGAGCTGTAG[C/T]AATGCAGTGATTACC | 10529 |
| rs1751916 | snp | A/G | 0.471768 | 0.115407 | intron-variant | NEBL | GRCh38.p7 | 10:21158844 | AAATAGGAATTGCAT[A/G]AAAGCTAAATAGGAT | 10529 |
| rs1830297 | snp | C/G | 0.401924 | 0.198543 | intron-variant | NEBL | GRCh38.p7 | 10:20820684 | TACAAAATGAGCCAG[C/G]CATGGTGGTTTGCAT | 10529 |
| rs1832677 | snp | C/T | 0.355311 | 0.226737 | intron-variant | NEBL | GRCh38.p7 | 10:20981551 | CACCCTGACTTGCTT[C/T]TGAAAACTCAGCACT | 10529 |
| rs1832678 | snp | C/T | 0.355525 | 0.226637 | intron-variant | NEBL | GRCh38.p7 | 10:20981713 | GTGATAGGGGCCTCT[C/T]TTCCACTGGACTGAC | 10529 |
| rs1837534 | snp | G/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21063775 | TCACGCCATTCTCCT[G/T]CCTCAGCTTCCCAAG | 10529 |
| rs1837537 | snp | C/T | 0.251014 | 0.249998 | intron-variant | NEBL | GRCh38.p7 | 10:21069496 | TCTCCTGGCGGGCGC[C/T]GTGGTGTCAAAACAG | 10529 |
| rs1856762 | snp | G/T | 0.424814 | 0.178718 | intron-variant | NEBL | GRCh38.p7 | 10:20950948 | ATTCTAAGGATGCAA[G/T]GATACAAAGCTTAAT | 10529 |
| rs1870706 | snp | A/C | 0.472147 | 0.114677 | intron-variant | NEBL | GRCh38.p7 | 10:21088839 | CCTGAAGCTTGGACT[A/C]TCTGACTCTGTAGAA | 10529 |
| rs1887459 | snp | C/T | 0.102014 | 0.201495 | intron-variant | NEBL | GRCh38.p7 | 10:21155699 | AAACAATTGACACAC[C/T]TGAAAAGACCAGAAG | 10529 |
| rs1926206 | snp | A/G | | | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20854683 | AATCTTCCCATCTTA[A/G]CCTCCCAAGTAGCTG | 10529 |
| rs1926207 | snp | G/T | 0.477937 | 0.102688 | intron-variant | NEBL | GRCh38.p7 | 10:20789611 | CCAGCACTTTGGAAG[G/T]CCAAAGCAGGAGGAC | 10529 |
| rs1934678 | snp | C/T | 0.41441 | 0.188333 | intron-variant | NEBL | GRCh38.p7 | 10:20916799 | AGTTCCTCAAGGCAA[C/T]AGGCTATTTTATACT | 10529 |
| rs1934679 | snp | A/T | 0.474272 | 0.110462 | intron-variant | NEBL | GRCh38.p7 | 10:20917209 | TACCATTTTGTCCTC[A/T]CCCAGCATACACACA | 10529 |
| rs1954224 | snp | G/T | 0.416382 | 0.186593 | intron-variant | NEBL | GRCh38.p7 | 10:20920459 | CTGGAGCTGTCAAAA[G/T]GTATAAGGCAGATTT | 10529 |
| rs1954225 | snp | A/C | 0.404035 | 0.196909 | intron-variant | NEBL | GRCh38.p7 | 10:20920546 | AGAGTGTGTACTGTA[A/C]ATTACCATTTGGTTA | 10529 |
| rs1969903 | snp | A/G | 0.499784 | 0.0103811 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20861854 | tcaacttatgatggg[A/G]ttgcatctcagtaaa | 10529 |
| rs1969941 | snp | C/T | 0.474992 | 0.108989 | intron-variant | NEBL | GRCh38.p7 | 10:21120991 | TACATTTTCAGGCTT[C/T]ATACAATAACTTCTG | 10529 |
| rs1974057 | snp | C/T | 0.0221141 | 0.102801 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20899521 | AAACACCACGTGCAA[C/T]GTGAACACAAATTTT | 10529 |
| rs1977449 | snp | A/T | 0.260227 | 0.249791 | intron-variant | NEBL | GRCh38.p7 | 10:21089669 | GGCTGCTCTCAATGA[A/T]TGATAGGTGAATGGG | 10529 |
| rs1977450 | snp | G/T | 0.0741063 | 0.177655 | intron-variant | NEBL | GRCh38.p7 | 10:21037872 | GTAGACAAATTCATT[G/T]AATACGAGGTTCAGA | 10529 |
| rs1979486 | snp | C/T | 0.476314 | 0.106217 | intron-variant | NEBL | GRCh38.p7 | 10:21166444 | TAGTGCGAAAAACTT[C/T]GGTATAAACCTTTTA | 10529 |
| rs1979487 | snp | A/T | 0.295599 | 0.245806 | intron-variant | NEBL | GRCh38.p7 | 10:21167926 | GAAACATAAAAGCTT[A/T]TGAAAACATGGCACG | 10529 |
| rs2000065 | snp | C/T | 0.135825 | 0.222405 | intron-variant | NEBL | GRCh38.p7 | 10:20907968 | TCATCCAAGCTATGC[C/T]GACATTTTTTGGGAA | 10529 |
| rs2025847 | snp | A/C/T | 0.0748431 | 0.178382 | intron-variant | NEBL | GRCh38.p7 | 10:21057696 | ctgggactacaggag[A/C/T]gcaccagcacaccca | 10529 |
| rs2038914 | snp | C/T | 0.4944 | 0.0526182 | intron-variant | NEBL | GRCh38.p7 | 10:20825851 | CCAGTCTAAAGGTTA[C/T]TGGAAGCTAAGTTAT | 10529 |
| rs2038915 | snp | C/G | 0.47614 | 0.106587 | intron-variant | NEBL | GRCh38.p7 | 10:20789138 | GGCACTGGCTACTCA[C/G]GGTATTTCCAATTAA | 10529 |
| rs2039858 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | NEBL | GRCh38.p7 | 10:20951913 | CTAGTCTTTGTTAGA[C/T]TTTCCCTGTGTCCTG | 10529 |
| rs2078155 | snp | C/T | 0.490618 | 0.0678448 | intron-variant | NEBL | GRCh38.p7 | 10:21082603 | GAATAAATGGTCCAA[C/T]TCAGCAATGGGCTAT | 10529 |
| rs2083444 | snp | C/T | 0.206642 | 0.246211 | intron-variant | NEBL | GRCh38.p7 | 10:21103809 | ataaagtcaatgtat[C/T]catttttttcattta | 10529 |
| rs2094403 | snp | C/T | 0.183568 | 0.241012 | intron-variant | NEBL | GRCh38.p7 | 10:21103764 | atgcgattattagta[C/T]cttttgaaaagaaaa | 10529 |
| rs2094404 | snp | C/T | 0.488965 | 0.0734569 | intron-variant | NEBL | GRCh38.p7 | 10:21116353 | ttctcacacggtaca[C/T]gcaaaaaaggtaatc | 10529 |
| rs2103287 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEBL | GRCh38.p7 | 10:20890253 | GGAGCGAGATGGCAC[A/G]TGCTTGCTAATTGCA | 10529 |
| rs2119239 | snp | A/G | 0.475081 | 0.108804 | intron-variant | NEBL | GRCh38.p7 | 10:21056291 | TTTGAAGTACTCTAT[A/G]TTAGGTTTTATGAAC | 10529 |
| rs2119240 | snp | A/T | 0.463018 | 0.130857 | intron-variant | NEBL | GRCh38.p7 | 10:21056002 | AGTTCACTGGTCTGC[A/T]TTGGGATGAACCTCC | 10529 |
| rs2119241 | snp | C/T | 0.461703 | 0.132974 | intron-variant | NEBL | GRCh38.p7 | 10:21055946 | AACAAAGCATTTGCC[C/T]GTGTAGCCTCAGGGC | 10529 |
| rs2119242 | snp | C/T | 0.240478 | 0.249819 | intron-variant | NEBL | GRCh38.p7 | 10:21055844 | CGGATCATTTCTTTT[C/T]ATTCTCACGCGGGAG | 10529 |
| rs2119243 | snp | A/G | 0.496905 | 0.0392151 | intron-variant | NEBL | GRCh38.p7 | 10:21055818 | GGGAGCCCCCTGAAC[A/G]CCCTCATCGGCATGG | 10529 |
| rs2148885 | snp | A/G | 0.256897 | 0.249905 | intron-variant | NEBL | GRCh38.p7 | 10:21084164 | CTGCAGTCCAGAGAG[A/G]TGGGAGTGGCTTTGA | 10529 |
| rs2153446 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | NEBL | GRCh38.p7 | 10:20962335 | TCAACTTCAGAAGGC[A/C]AACATATGGATACAA | 10529 |
| rs2165286 | snp | C/T | 0.463126 | 0.13068 | intron-variant | NEBL | GRCh38.p7 | 10:21056454 | CAAAACCTTTTCCTA[C/T]TGCTTTTAAAGTTCC | 10529 |
| rs2165287 | snp | C/T | 0.463234 | 0.130503 | intron-variant | NEBL | GRCh38.p7 | 10:21038366 | cctgccaggggctgg[C/T]agtaaaggggagaga | 10529 |
| rs2211200 | snp | C/G | 0.497445 | 0.0356514 | intron-variant | NEBL | GRCh38.p7 | 10:20952964 | gaaaagaaaaaacaa[C/G]aaaTTAGCTCATGAT | 10529 |
| rs2274361 | snp | A/T | 0.383053 | 0.211653 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20850754 | GGAGTTGTATAAAGC[A/T]TCTTGTCAAATGGCT | 10529 |
| rs2279311 | snp | C/T | 0.490119 | 0.0695896 | upstream-variant-2KB, nc-transcript-variant | NEBL, NEBL-AS1 | GRCh38.p7 | 10:21174904 | TGATTAATAAATGAA[C/T]ATGGCTCGTTTTGTT | 10529 |
| rs2281881 | snp | A/C | 0.383246 | 0.211531 | intron-variant | NEBL | GRCh38.p7 | 10:20840952 | AATGAGAAAATATTA[A/C]TAGGAAGGAATGAAT | 10529 |
| rs2281882 | snp | A/C | 0.383632 | 0.211288 | intron-variant | NEBL | GRCh38.p7 | 10:20841271 | AGGAGTGATGTAGCC[A/C]AAGGTTTTTTTTAAA | 10529 |
| rs2281883 | snp | A/G | 0.061077 | 0.163732 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20858215 | CCACAAGGCAACTAC[A/G]GTTGCCGCTAGATGA | 10529 |
| rs2296606 | snp | A/C | 0.203182 | 0.245577 | intron-variant | NEBL | GRCh38.p7 | 10:20787171 | AAATGGGAAGACCAG[A/C]TAAGGAGGAACGTAT | 10529 |
| rs2296607 | snp | C/T | 0.419616 | 0.183658 | intron-variant | NEBL | GRCh38.p7 | 10:20787378 | CCCATCCCAAACCCT[C/T]AGAGTGATGTTATGC | 10529 |
| rs2296608 | snp | A/T | 0.0482946 | 0.147699 | intron-variant | NEBL | GRCh38.p7 | 10:20787571 | CTATTGCAGATGCTC[A/T]GTTAAAAACATAAAC | 10529 |
| rs2296609 | snp | C/T | 0.43598 | 0.167067 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20868563 | ATTATCTCTGTTTAT[C/T]CTTGCAATTAAAGAT | 10529 |
| rs2296610 | snp | G/T | 0.0351764 | 0.12787 | intron-variant, missense, nc-transcript-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20868692 | TTAGAAGCTTCCACG[G/T]CATGTTCAAAATCTG | 10529 |
| rs2296611 | snp | A/G | 0.0908922 | 0.192833 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20869280 | GGTATTAACTAAAGC[A/G]GGCACCTTAGAGAAG | 10529 |
| rs2296612 | snp | A/G | 0.472429 | 0.114129 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20785415 | AAGTTTCAAACACAC[A/G]CTACATTTAAGGGAC | 10529 |
| rs2296613 | snp | C/T | 0.414245 | 0.188477 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20785526 | ATTAGCAGCACCAGG[C/T]GTCCAGACACAAAGA | 10529 |
| rs2296614 | snp | C/T | 0.143675 | 0.226263 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20785795 | CATTCCTGTTCTCCC[C/T]GTTCTCTGCACTGTG | 10529 |
| rs2574765 | snp | C/G/T | 0 | 0 | | | GRCh38.p7 | 10:20876169 | AACTTTTTCTCTCTT[C/G/T]TGAATAGTATCAGAA | 10529 |
| rs2574766 | snp | A/G | | | | | GRCh38.p7 | 10:20896482 | AAATAAATATtatat[A/G]catatatatatatat | 10529 |
| rs2574767 | snp | C/T | 0 | 0 | | | GRCh38.p7 | 10:20792299 | ATAAAGAGTCTAGGA[C/T]ACAATGCAATTATTG | 10529 |
| rs2574768 | snp | C/G | | | | | GRCh38.p7 | 10:20797865 | cagcaactcaggagg[C/G]tgagatgggagaatt | 10529 |
| rs2574769 | snp | A/G | 0 | 0 | | | GRCh38.p7 | 10:20885121 | TTTCATTAGAACCCA[A/G]AATGTCATTAAATTT | 10529 |
| rs2574771 | snp | C/G | 0.121369 | 0.214369 | | | GRCh38.p7 | 10:20807768 | TTCCCCCTCCTTGCT[C/G]TACTAAAATATAACT | 10529 |
| rs2581617 | snp | C/G | 0.300926 | 0.244758 | | | GRCh38.p7 | 10:21095223 | TGCCCTGAAAGCTGA[C/G]CCTCACAAAAGTTCC | 10529 |
| rs2613970 | snp | C/T | 0.029116 | 0.117091 | | | GRCh38.p7 | 10:21119637 | GTTAGTAGCAAGCAT[C/T]ATGACAATTAAGTCA | 10529 |
| rs2613971 | snp | A/G | 0.498871 | 0.0237351 | | | GRCh38.p7 | 10:21095711 | GGACATCTCAGTGGC[A/G]TCTGTCTCCTAGTCA | 10529 |
| rs2697027 | snp | C/G | 0.0968851 | 0.197625 | intron-variant | NEBL | GRCh38.p7 | 10:20787356 | CCTTAAAGTTAGCCT[C/G]GAAATACCCATCCCA | 10529 |
| rs2697028 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | NEBL | GRCh38.p7 | 10:20812388 | GTGGCACATGTATAC[A/G]TATGTAACAAACCTG | 10529 |
| rs2697029 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20797273 | GCAGAGGATATTCTA[A/G]AAATATGTATTGGAT | 10529 |
| rs2697030 | snp | A/C | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860920 | CTCAAAATATTTACC[A/C]AATGCTGTATTCCCA | 10529 |
| rs2697031 | snp | A/T | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860824 | TATGCATGCCTAAAA[A/T]ATTTGATGAGAGTCA | 10529 |
| rs2765835 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20838002 | ctggtcaccaaacag[C/T]tctgatagaaatgta | 10529 |
| rs2765836 | snp | G/T | | | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20857064 | gaacttctgacctca[G/T]gtgatccacccgcct | 10529 |
| rs2765838 | snp | C/T | 0.406986 | 0.194565 | intron-variant | NEBL | GRCh38.p7 | 10:20896501 | ATATATATATATATA[C/T]ATATATATATATATA | 10529 |
| rs2765844 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | NEBL | GRCh38.p7 | 10:20786155 | CACTAAATACGACAG[C/G]TAGCCCATCAAAAAG | 10529 |
| rs2765845 | snp | G/T | 0.0763149 | 0.179815 | intron-variant | NEBL | GRCh38.p7 | 10:20820308 | CATTGTTTGTGGTCA[G/T]CTTTCCCAACAATTC | 10529 |
| rs2768664 | snp | C/G | 0.465473 | 0.126772 | intron-variant | NEBL | GRCh38.p7 | 10:21159438 | CCTTCTTTTGCTCTC[C/G]TGAACTTCAACATAA | 10529 |
| rs2986672 | snp | C/T | 0.463234 | 0.130503 | intron-variant | NEBL | GRCh38.p7 | 10:21038365 | gtctctcccctttac[C/T]gccagcccctggcag | 10529 |
| rs2986673 | snp | C/T | 0.484632 | 0.086302 | intron-variant | NEBL | GRCh38.p7 | 10:21043321 | AAACAGCCGTCAACA[C/T]TGACGAATTTAGAAG | 10529 |
| rs3057115 | in-del | -/TT | 0.3744 | 0.216852 | intron-variant | NEBL | GRCh38.p7 | 10:20795125 | GAATTCAGAAAAGTG[-/TT]TAAGAGTACTATGGC | 10529 |
| rs3085048 | in-del | -/GT | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20868340 | tgtgtgtgtgtgtgt[-/GT]AGGTTAAAACACAAT | 10529 |
| rs3215820 | in-del | -/A | 0.123452 | 0.215605 | intron-variant | NEBL | GRCh38.p7 | 10:20787587 | GTTAAAAACATAAAC[-/A]AAAATTTTTCATACT | 10529 |
| rs3758599 | snp | C/T | 0.499693 | 0.0123764 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20898158 | TTAACCTTGGTTTTA[C/T]GTAACCAAGGACATA | 10529 |
| rs3758601 | snp | C/T | 0.489142 | 0.0728777 | intron-variant | NEBL | GRCh38.p7 | 10:20808840 | AAACGATGGTTAAGT[C/T]ATTCATGTAGTTGAT | 10529 |
| rs3781484 | snp | C/T | 0.126909 | 0.217598 | intron-variant | NEBL | GRCh38.p7 | 10:20816762 | ACTTGTGGCCTGCTC[C/T]GATTCCCTGTTGTTG | 10529 |
| rs3781485 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NEBL | GRCh38.p7 | 10:20798609 | TAAACTGTAAAGTGA[C/T]ATGCATGTAAAGGAG | 10529 |
| rs3781486 | snp | A/G | 0.391024 | 0.206427 | intron-variant | NEBL | GRCh38.p7 | 10:20798556 | GGATGGTTGAACATT[A/G]GCAAATGAAATGAAA | 10529 |
| rs3781487 | snp | C/G | 0.493107 | 0.0583 | intron-variant | NEBL | GRCh38.p7 | 10:20797603 | TGGGCCCTCTGAGAC[C/G]CAGACAATCATTCAC | 10529 |
| rs3781488 | snp | A/G | 0.417521 | 0.185571 | intron-variant | NEBL | GRCh38.p7 | 10:20797575 | CACATTTACTTTCTC[A/G]TATTTCTGTATCTTG | 10529 |
| rs3781489 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | NEBL | GRCh38.p7 | 10:20792985 | TAAACTTTGTGGACT[C/T]AACTCCCACTTATGT | 10529 |
| rs3781490 | snp | C/T | 0.436408 | 0.16659 | intron-variant | NEBL | GRCh38.p7 | 10:20792914 | AAACTCTCAGTGACA[C/T]GTGTAAAAGCAATTT | 10529 |
| rs3791197 | snp | C/T | 0.220544 | 0.248259 | intron-variant | NEBL | GRCh38.p7 | 10:20830012 | GTTTAATGCATTGAC[C/T]TAGGATTTTAGTTAA | 10529 |
| rs3791198 | snp | C/T | 0.41275 | 0.189769 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20856192 | CCACCTAAATGAAGA[C/T]CTAAACTTTATATAT | 10529 |
| rs3791199 | snp | A/G | 0.174932 | 0.238463 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20857337 | TAAGTTTTGCCTATA[A/G]ATTTCTAAGTCTAGG | 10529 |
| rs3791200 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20857451 | AAGCAGATATTCAAT[A/G]AATTATGATTAATTT | 10529 |
| rs3791201 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20857673 | CTGCAGGACTGACCA[C/T]GTGGGCAGTGCACCC | 10529 |
| rs3791202 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | NEBL | GRCh38.p7 | 10:20885743 | TCGTTATTGCTTAAT[G/T]GTTGCTTGTCACATA | 10529 |
| rs3791203 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | NEBL | GRCh38.p7 | 10:20890752 | TGCCGGGGGAAGACC[C/T]GGGTGGATATTTGAG | 10529 |
| rs3791204 | snp | C/T | 0.474363 | 0.110278 | intron-variant | NEBL | GRCh38.p7 | 10:20891067 | AGGATGTGAATAATA[C/T]TGATGTTATACACTA | 10529 |
| rs3802729 | snp | C/T | 0.159951 | 0.233219 | intron-variant | NEBL | GRCh38.p7 | 10:20913431 | CACTTTAATGGAATG[C/T]TTCATTAAAAGTACT | 10529 |
| rs3802730 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NEBL | GRCh38.p7 | 10:20913715 | attttattatattaa[C/T]aGATTTCCCAGTATT | 10529 |
| rs3824817 | snp | A/G | 0.178144 | 0.239451 | intron-variant | NEBL | GRCh38.p7 | 10:20833518 | ACTCTCAGGCTGAGA[A/G]TCTTAGTCAATAAAA | 10529 |
| rs3828160 | snp | C/T | 0.157972 | 0.232445 | intron-variant | NEBL | GRCh38.p7 | 10:20829654 | CCAGGCTTCATTACA[C/T]CCTCGTAAGTATCCC | 10529 |
| rs3831100 | in-del | -/G | 0.383077 | 0.211638 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20852512 | TACGGGTTGCTGGCA[-/G]GGAGGGTAGGTACCG | 10529 |
| rs3837357 | in-del | -/GGTA | 0.3742 | 0.216966 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20865240 | AATAATTTTACTTTA[-/GGTA]TTCAAAATAGTTTTC | 10529 |
| rs3845188 | snp | G/T | 0.440195 | 0.162252 | intron-variant | NEBL | GRCh38.p7 | 10:21094654 | CCAACAAAAATCCAG[G/T]CTGGAGTGGATTAGG | 10529 |
| rs3847373 | snp | C/T | 0.498589 | 0.02652 | intron-variant | NEBL | GRCh38.p7 | 10:20791609 | CTGGGAATTTGAGAC[C/T]AGGTTGGGCAATGTA | 10529 |
| rs3847374 | snp | G/T | 0.49907 | 0.0215454 | intron-variant | NEBL | GRCh38.p7 | 10:20791637 | GAGTCTGAGACAAGA[G/T]AATTGCTTGAGACTG | 10529 |
| rs3858197 | snp | C/G | 0.369754 | 0.219451 | intron-variant | NEBL | GRCh38.p7 | 10:20806854 | TCTCTGGTACATTGC[C/G]TTTGGGAGAGACATC | 10529 |
| rs3858198 | snp | C/T | 0.499902 | 0.00698814 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20877725 | ataatataattaggg[C/T]ggagcaaacagcttc | 10529 |
| rs3858199 | snp | C/T | 0.449599 | 0.150533 | intron-variant | NEBL | GRCh38.p7 | 10:21002701 | TAGCGCTTCCCCCTT[C/T]GCTCGCTCTCTTTCG | 10529 |
| rs3858200 | snp | C/T | 0.276534 | 0.248588 | intron-variant | NEBL | GRCh38.p7 | 10:21013920 | CCATTTTCCCCATTT[C/T]TTAATCCTAGGGGAC | 10529 |
| rs3858201 | snp | A/G | 0.470908 | 0.117046 | intron-variant | NEBL | GRCh38.p7 | 10:21026223 | accagaaatgtctcc[A/G]gacgttgcctattgc | 10529 |
| rs3858202 | snp | G/T | 0.499382 | 0.017561 | intron-variant | NEBL | GRCh38.p7 | 10:21026624 | GTTTGAGTGTAAATG[G/T]GACAGTGGTTAGGTA | 10529 |
| rs3858203 | snp | A/C | 0.470618 | 0.117591 | intron-variant | NEBL | GRCh38.p7 | 10:21029528 | ATCAAGCACAGGATA[A/C]AGACAGGGACGATCG | 10529 |
| rs3858204 | snp | A/G | 0.077417 | 0.180873 | intron-variant | NEBL | GRCh38.p7 | 10:21037810 | AAAAACACTCCCCTA[A/G]TGAAGAGTAGAAAGA | 10529 |
| rs3864840 | in-del | -/TCAC | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21098220 | cacacacattctcac[-/TCAC]acgtgcacacatacg | 10529 |
| rs3864841 | snp | C/G | 0.47666 | 0.105476 | intron-variant | NEBL | GRCh38.p7 | 10:21110884 | ATTAAAGTAACACTG[C/G]caactttgaaaatgt | 10529 |
| rs3864842 | snp | A/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21169066 | atatatatatatatt[A/T]ttttttttttttttt | 10529 |
| rs3885710 | snp | C/T | 0.315516 | 0.241263 | intron-variant | NEBL | GRCh38.p7 | 10:20998942 | GATGGCGGATCCTGT[C/T]TTGTTGGCGGCCCCC | 10529 |
| rs3897497 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20875456 | acatccactttcaaa[A/C]tctcatatgcatttc | 10529 |
| rs3900782 | snp | A/G | 0.322483 | 0.239262 | intron-variant | NEBL | GRCh38.p7 | 10:20998806 | TAAGGGACTTCATTG[A/G]GGCTAGTTGTGAATT | 10529 |
| rs3900922 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NEBL | GRCh38.p7 | 10:20998599 | AGTATGAGATGTAGA[C/T]GTAGCATTTTTATGG | 10529 |
| rs3906798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NEBL | GRCh38.p7 | 10:21020257 | ACAATGGGTGTGAAA[A/G]TGTTGTTTTGTAGCA | 10529 |
| rs3909022 | snp | C/T | 0.38555 | 0.210062 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20848972 | TGCTTACAAAATTCC[C/T]GAGAGTTTTTTTGTC | 10529 |
| rs3915911 | snp | C/T | 0.414576 | 0.188188 | intron-variant, downstream-variant-500B | NEBL | GRCh38.p7 | 10:20813478 | AGATAGTTGTGTAAC[C/T]GTAAATTATACTAGA | 10529 |
| rs3933259 | snp | A/T | 0.132751 | 0.2208 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20876791 | TGTCTCTCATAAGAC[A/T]GATGAGAACTAATAA | 10529 |
| rs3951498 | snp | A/C | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21082527 | TTTGAAGTGTTCCCC[A/C]CCCCCCCTaaaaaaa | 10529 |
| rs3951499 | snp | A/C | | | intron-variant | NEBL | GRCh38.p7 | 10:21082530 | GAAGTGTTCCCCCCC[A/C]CCCCTaaaaaaaaaa | 10529 |
| rs3990287 | in-del | -/CACAC/CACACACA/CACACACACACA/CACACACACACACA/CACACACACACACACA | | | intron-variant | NEBL | GRCh38.p7 | 10:20814640 | acacacacacacaca[lengthTooLong]NNNNNNNANTGGTTA | 10529 |
| rs4025860 | in-del | -/CA | | | intron-variant | NEBL | GRCh38.p7 | 10:21169255 | cacaataaaaaGTGA[-/CA]GGGGAAGACGAAGAG | 10529 |
| rs4025861 | snp | C/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21169257 | caataaaaaGTGACA[C/G]GGGAAGACGAAGAGT | 10529 |
| rs4025864 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21020104 | GGAACAAAACAAATC[C/T]TCTAGAAGTTACCTG | 10529 |
| rs4025865 | in-del | -/GA | | | intron-variant | NEBL | GRCh38.p7 | 10:21029941 | TCGTGCAGCTCCAGA[-/GA]TGATTTCTCTCGGGA | 10529 |
| rs4025866 | in-del | -/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21029988 | TGATAGACGTCCCCC[-/G]TCCCCCTCAAAGACC | 10529 |
| rs4025867 | in-del | -/AATA | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21037827 | AAGAGTAGAAAGATA[-/AATA]GACAAAATGAGAGAA | 10529 |
| rs4025868 | snp | C/G | 0.494976 | 0.0498674 | intron-variant | NEBL | GRCh38.p7 | 10:21056078 | GAGCAACTAGTACTT[C/G]CTGAGCTCTGACACA | 10529 |
| rs4025869 | snp | C/G | 0.463126 | 0.13068 | intron-variant | NEBL | GRCh38.p7 | 10:21056423 | CTGCAAAAAAAGATA[C/G]ACTGACTGTCCTCCC | 10529 |
| rs4025870 | snp | A/G | 0.375 | 0.216506 | intron-variant | NEBL | GRCh38.p7 | 10:21057589 | gggtctggctctgtc[A/G]cccaggctggagtgc | 10529 |
| rs4025871 | snp | C/G | 0.221737 | 0.248397 | intron-variant | NEBL | GRCh38.p7 | 10:21062764 | TGAGATCAACCCTCT[C/G]AGTTCTGCACCAGTC | 10529 |
| rs4025873 | snp | A/C | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21082533 | GTGTTCCCCACCACC[A/C]CTaaaaaaaaaaaaa | 10529 |
| rs4025874 | snp | A/G | 0.490618 | 0.0678448 | intron-variant | NEBL | GRCh38.p7 | 10:21083741 | TCCCAGCTACTTAGG[A/G]GGCTGAGGCAAGAGG | 10529 |
| rs4025883 | in-del | -/ATA | | | intron-variant | NEBL | GRCh38.p7 | 10:21092625 | ataataataataata[-/ATA]ATGGCTCACCACCAG | 10529 |
| rs4025884 | in-del | -/TT/TTTTTTTTT/TTTTTTTTTTT | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21093165 | TTTTTTTTTTTTTTT[-/TT/TTTTTTTTT/TTTTTTTTTTT]NNNNNNNNNNCCATT | 10529 |
| rs4025981 | snp | C/T | 0.121623 | 0.214521 | intron-variant, missense, nc-transcript-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20850460 | CAACAAATTCAAGCA[C/T]TGGCTTTCCCTTATT | 10529 |
| rs4111015 | snp | C/T | 0.497855 | 0.0326773 | intron-variant | NEBL | GRCh38.p7 | 10:20896070 | CCGTTAGAAAACAAA[C/T]GTGCAAAACATTCTG | 10529 |
| rs4111016 | snp | A/G | 0.497613 | 0.0344622 | intron-variant | NEBL | GRCh38.p7 | 10:20896123 | ACAGAAACAACCAGT[A/G]TTGTGCTCATCTCTC | 10529 |
| rs4142113 | snp | A/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20896672 | GGTTCTCAAATGGAA[A/T]aaatactgcaattca | 10529 |
| rs4261191 | snp | A/G | 0.498652 | 0.0259235 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20848891 | TATTCAGTAAACCAT[A/G]GTAATATCTGAGTGC | 10529 |
| rs4275522 | snp | A/T | 0.485596 | 0.0836329 | intron-variant | NEBL | GRCh38.p7 | 10:21120268 | TATCCCCAGCTACTC[A/T]GGAGGCTGAGATAGA | 10529 |
| rs4291572 | snp | A/C | 0.443464 | 0.15834 | intron-variant | NEBL | GRCh38.p7 | 10:21166596 | CTGCCATGTGCCAGA[A/C]ACCAGGCTACGGCCT | 10529 |
| rs4300308 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NEBL | GRCh38.p7 | 10:20938811 | agcctcagtagccga[C/T]gcgatcaactggaag | 10529 |
| rs4304658 | snp | C/T | 0.496905 | 0.0392151 | intron-variant | NEBL | GRCh38.p7 | 10:20938962 | caaatctatgtctgc[C/T]tggtgtacctgaaag | 10529 |
| rs4304659 | snp | C/T | 0.441841 | 0.160303 | intron-variant | NEBL | GRCh38.p7 | 10:20938990 | aagtgatggggagaa[C/T]ggaaccaagttggaa | 10529 |
| rs4311962 | snp | C/T | 0.437965 | 0.164831 | intron-variant | NEBL | GRCh38.p7 | 10:20940011 | acaacccactgtcaa[C/T]attagacagatcaac | 10529 |
| rs4311963 | snp | C/T | 0.486984 | 0.079614 | intron-variant | NEBL | GRCh38.p7 | 10:20940039 | AACGAGACAGAAAGT[C/T]AACAAGGATACCCAG | 10529 |
| rs4367852 | snp | C/T | 0.121497 | 0.214863 | intron-variant | NEBL | GRCh38.p7 | 10:21122986 | GGGTCATAGAAGATA[C/T]TCAGTAAAATCATTT | 10529 |
| rs4406712 | snp | A/T | 0.361894 | 0.223562 | intron-variant | NEBL | GRCh38.p7 | 10:21109456 | gatactggcctgaaa[A/T]tttctttttttgttg | 10529 |
| rs4408230 | snp | A/G | 0.495891 | 0.0451408 | intron-variant, upstream-variant-2KB | NEBL, LOC102725112 | GRCh38.p7 | 10:20844657 | TGCAGAGAATAAAAT[A/G]AAAAGTGGACATGAG | 10529 |
| rs4448585 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | NEBL | GRCh38.p7 | 10:20938865 | caaatgaatgaaatg[A/C]agcaagaagagaagt | 10529 |
| rs4491126 | snp | A/C | 0.459118 | 0.137002 | intron-variant | NEBL | GRCh38.p7 | 10:20939999 | tgggagactttaaca[A/C]cccactgtcaatatt | 10529 |
| rs4504971 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NEBL | GRCh38.p7 | 10:20943637 | TTTATCACATAATCC[A/G]TATAGCATAGGAAGT | 10529 |
| rs4543885 | snp | A/C | 0.232943 | 0.249417 | intron-variant | NEBL | GRCh38.p7 | 10:20951603 | TCCCTTGACTTATGA[A/C]CCTCCAATAAGCTAA | 10529 |
| rs4556442 | snp | A/G | 0.393434 | 0.20476 | intron-variant | NEBL | GRCh38.p7 | 10:20836998 | atcagccgttcctct[A/G]tctctttccctctct | 10529 |
| rs4575164 | snp | C/T | 0.193028 | 0.243422 | intron-variant | NEBL | GRCh38.p7 | 10:20917550 | GGCCACACATTACTA[C/T]GCATCACGTACCTCA | 10529 |
| rs4603205 | snp | A/G | 0.372794 | 0.217765 | intron-variant | NEBL | GRCh38.p7 | 10:20951039 | CTTTAGGAAGCTGAG[A/G]TGGGAGGATGGCTTG | 10529 |
| rs4631770 | snp | C/T | 0.304188 | 0.244057 | intron-variant | NEBL | GRCh38.p7 | 10:21082066 | aacatagcacccctt[C/T]catgaaatccctgcc | 10529 |
| rs4747424 | snp | A/T | 0.497855 | 0.0326773 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20859266 | TACTTCACAGCATTT[A/T]CACAAGGGATAAAAA | 10529 |
| rs4747425 | snp | G/T | 0.125874 | 0.217008 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20861279 | ACCTCCCAGGTTCAC[G/T]CCATTCTCCTGCCTC | 10529 |
| rs4747426 | snp | A/G | 0.485799 | 0.0830599 | intron-variant | NEBL | GRCh38.p7 | 10:20931284 | TAAAAAAAAATCTTT[A/G]GCACATCTTTAAACT | 10529 |
| rs4747427 | snp | A/G | 0.485799 | 0.0830599 | intron-variant | NEBL | GRCh38.p7 | 10:20931285 | AAAAAAAAATCTTTG[A/G]CACATCTTTAAACTG | 10529 |
| rs4747428 | snp | A/C | 0.491936 | 0.0629843 | intron-variant | NEBL | GRCh38.p7 | 10:20931392 | ACCAGTATATAAATA[A/C]GTTTATAAATTAAGA | 10529 |
| rs4747429 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21017837 | TTTTTTTTTTTTTTT[C/T]CCCCAAAATAGAGTC | 10529 |
| rs4747430 | snp | A/G | 0.463018 | 0.130857 | intron-variant | NEBL | GRCh38.p7 | 10:21055365 | AATCGGCTAATTCAC[A/G]CACCCCAAAGGAAAT | 10529 |
| rs4747431 | snp | A/G | 0.468047 | 0.122292 | intron-variant | NEBL | GRCh38.p7 | 10:21061224 | ATATAGAGAGATGTG[A/G]CATTATATATTGTGA | 10529 |
| rs4747432 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21065106 | TTCTTCTTGATAGCA[C/T]TGCAAAAAAAGATTC | 10529 |
| rs4747433 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21153087 | AAATGTGCAATGACC[A/G]TGAAAATAGGTAATA | 10529 |
| rs4748722 | snp | C/T | 0.48498 | 0.0853497 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20784592 | TTTTCCAAAAGAAGA[C/T]ACCAGATCATCTCTG | 10529 |
| rs4748724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NEBL | GRCh38.p7 | 10:20789919 | tatatgtatatatat[A/G]tgtgtgtgtatatgt | 10529 |
| rs4748725 | snp | A/G | 0.125874 | 0.217008 | intron-variant | NEBL | GRCh38.p7 | 10:20799211 | CCCAGGCTGGAGTGC[A/G]GTGGCGCAATCTTGG | 10529 |
| rs4748726 | snp | A/T | 0.125874 | 0.217008 | intron-variant | NEBL | GRCh38.p7 | 10:20799261 | CCCGGGTTCAAGTGA[A/T]TCTCCTGCCTCAGCA | 10529 |
| rs4748727 | snp | A/T | 0.494547 | 0.0519303 | intron-variant | NEBL | GRCh38.p7 | 10:20815765 | ATGAATCAATTCAAC[A/T]AAGAGACTTATTTAT | 10529 |
| rs4748728 | snp | A/T | 0.113844 | 0.20967 | intron-variant, missense, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20823208 | AAGAAATATGATCAC[A/T]TTGCTGATGTTCTTC | 10529 |
| rs4748729 | snp | A/C | 0.499982 | 0.00299515 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20859655 | ACAACACAGTCGATT[A/C]TAAAAAAAACAAGAA | 10529 |
| rs4748733 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | NEBL | GRCh38.p7 | 10:20911520 | CATTTATAAAACCTA[C/T]TACCATACACATCAA | 10529 |
| rs4748734 | snp | G/T | 0.480461 | 0.0968913 | intron-variant | NEBL | GRCh38.p7 | 10:20921609 | ACTTCCTGAATCTCG[G/T]GGCACCTCACTATCC | 10529 |
| rs4748735 | snp | A/T | 0.479014 | 0.100263 | intron-variant | NEBL | GRCh38.p7 | 10:20921916 | AAATAAGTACATATA[A/T]AAATATGTGTGAACA | 10529 |
| rs4748736 | snp | A/G | 0.419776 | 0.18351 | intron-variant | NEBL | GRCh38.p7 | 10:20923345 | GTACTGGGATCATAG[A/G]CATGAAACACCACAC | 10529 |
| rs4748737 | snp | C/T | 0.48692 | 0.0798058 | intron-variant | NEBL | GRCh38.p7 | 10:20930050 | CCATCTAGGTGCTGA[C/T]GACTCTCACATTTAT | 10529 |
| rs4748738 | snp | C/T | 0.485596 | 0.0836329 | intron-variant | NEBL | GRCh38.p7 | 10:20930477 | GCCAAGGTAGTCTTT[C/T]TGAAAATGCAAATTA | 10529 |
| rs4748739 | snp | G/T | 0.485324 | 0.0843964 | intron-variant | NEBL | GRCh38.p7 | 10:20931562 | CTTTTGCGCCATGGC[G/T]GTGGCCTGGAAAAAG | 10529 |
| rs4748740 | snp | A/C | 0.48666 | 0.0805725 | intron-variant | NEBL | GRCh38.p7 | 10:20931769 | TCTTCCCCACCCCAG[A/C]CCCATATTCTATCAT | 10529 |
| rs4748741 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | NEBL | GRCh38.p7 | 10:20970215 | GGATAAGCTGTAAGA[A/T]GTGCTCAGCACTCCT | 10529 |
| rs4748743 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | NEBL | GRCh38.p7 | 10:21023237 | TAATTTGAAAATTTT[A/G]CATATGGATTTTAAC | 10529 |
| rs4748745 | snp | A/C | 0.461813 | 0.132798 | intron-variant | NEBL | GRCh38.p7 | 10:21055534 | TTTAAGGTTACCATT[A/C]TGCATGTAACCACAT | 10529 |
| rs4748746 | snp | A/C | 0.478354 | 0.101757 | intron-variant | NEBL | GRCh38.p7 | 10:21060151 | GAAGAGGTGCTTCTA[A/C]ATGACAGAAGTTATA | 10529 |
| rs4748747 | snp | A/C | 0.491629 | 0.0641526 | intron-variant | NEBL | GRCh38.p7 | 10:21064919 | CAGGAAAAAAAAAAT[A/C]TTTAAGAATGAGATA | 10529 |
| rs4748749 | snp | C/T | 0.357664 | 0.225629 | intron-variant | NEBL | GRCh38.p7 | 10:21112836 | CACCCAGTCTTACAG[C/T]TGAAGTGTGGTTCAG | 10529 |
| rs4748751 | snp | G/T | 0.187502 | 0.243305 | intron-variant | NEBL | GRCh38.p7 | 10:21152222 | GATGGATTCTCTTTC[G/T]TGCTCATCTGTCTGG | 10529 |
| rs4748752 | snp | A/G | 0.207864 | 0.246424 | intron-variant | NEBL | GRCh38.p7 | 10:21165381 | TCCCTTGGAATTCAG[A/G]CTTAATGAACCCTAG | 10529 |
| rs4748753 | snp | C/G | 0.48178 | 0.0936921 | intron-variant | NEBL | GRCh38.p7 | 10:21167190 | GTGAACACAGGCAGA[C/G]CGAAAGTAAACACAA | 10529 |
| rs4748754 | snp | C/G | 0.489318 | 0.0722982 | intron-variant | NEBL | GRCh38.p7 | 10:21167392 | GTAGGCAGGTCAGAG[C/G]AAATGTTCAGCCCAA | 10529 |
| rs4950457 | snp | C/G/T | 0.375 | 0.216506 | intron-variant | NEBL | GRCh38.p7 | 10:20939667 | CTGAATACAGCACAC[C/G/T]GATGGGTCTTGACTC | 10529 |
| rs4994006 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20814617 | ACACACATACACACA[C/T]ACACACACACACACA | 10529 |
| rs5783753 | in-del | -/AC | 0.483995 | 0.0880135 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20855522 | AAGAAAACAAAACAA[-/AC]AACAAAAAAAAAACG | 10529 |
| rs5783754 | in-del | -/TG | | | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20868311 | TACTAAGTTAAAAAC[-/TG]TGTGTGTGTGTGTGT | 10529 |
| rs5783755 | in-del | -/A | | | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20868835 | ACATTGACATTAGCC[-/A]AAAAAAAAAAAAATA | 10529 |
| rs5783756 | in-del | -/T | 0.499996 | 0.00139776 | intron-variant | NEBL | GRCh38.p7 | 10:20910829 | TGTTTTTCGTTTTTG[-/T]TTTTTTTTTTTTGGC | 10529 |
| rs5783758 | in-del | -/GG | 0.355525 | 0.226637 | intron-variant | NEBL | GRCh38.p7 | 10:20981599 | TGGATAACATGACTT[-/GG]GGGACTGGCTAATCA | 10529 |
| rs5783759 | in-del | -/CTCT | | | intron-variant | NEBL | GRCh38.p7 | 10:20988606 | CATCAAATTGTCTCT[-/CTCT]ATTGGGTCACTGCCA | 10529 |
| rs5783760 | in-del | -/A | | | intron-variant | NEBL | GRCh38.p7 | 10:21024069 | GAAAAAAAAAAAAAA[-/A]CATTGAAAAGCTTCT | 10529 |
| rs5783761 | in-del | -/C | 0.287346 | 0.247195 | intron-variant | NEBL | GRCh38.p7 | 10:21026333 | CAGTACACTGTACAG[-/C]CCCCTCCCTGACAGA | 10529 |
| rs5783762 | in-del | -/A | 0.463343 | 0.130326 | intron-variant | NEBL | GRCh38.p7 | 10:21037443 | GAACAAATTGCAAAG[-/A]AAAAAAATGGGAATC | 10529 |
| rs5783763 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21037824 | AATGAAGAGTAGAAA[A/G]ATAGACAAAATGAGA | 10529 |
| rs5783764 | in-del | -/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21057558 | TTTTTTTTTTTTTTT[-/T]GAGACGGGGTCTGGC | 10529 |
| rs5783768 | in-del | -/TT | | | intron-variant | NEBL | GRCh38.p7 | 10:21093151 | TTTAGCAACAAGTCT[-/TT]TTTTTTTTTTTTTTC | 10529 |
| rs6415963 | snp | C/T | 0.424814 | 0.178718 | intron-variant | NEBL | GRCh38.p7 | 10:20951414 | AAGAAAGAAATGCAA[C/T]TTTTATGACATAATC | 10529 |
| rs6482151 | snp | C/T | 0.463126 | 0.13068 | intron-variant | NEBL | GRCh38.p7 | 10:20888865 | ATCTGCACGGGAGAA[C/T]GGAACATAGCTAAGA | 10529 |
| rs6482152 | snp | C/T | 0.499776 | 0.0105807 | intron-variant | NEBL | GRCh38.p7 | 10:20903605 | gcaatggcaaggata[C/T]ggaaccagactcact | 10529 |
| rs6482153 | snp | A/G | 0.327445 | 0.237702 | intron-variant | NEBL | GRCh38.p7 | 10:20932615 | ATTTTTAAGAAAAGA[A/G]TAAGTATTCTTGCTG | 10529 |
| rs6482154 | snp | C/T | 0.297636 | 0.24542 | intron-variant | NEBL | GRCh38.p7 | 10:20936187 | CAAATCTTTTACTCA[C/T]ATTCTAAGAGCTAAT | 10529 |
| rs6482156 | snp | G/T | 0.452842 | 0.146134 | intron-variant | NEBL | GRCh38.p7 | 10:20951957 | TATTCTCACCTCTCT[G/T]CCCTCCTTTTTATTC | 10529 |
| rs6482157 | snp | G/T | 0.396 | 0.202938 | intron-variant | NEBL | GRCh38.p7 | 10:20952133 | GGAAATGAAAAGTTT[G/T]AAAGGTTCAATTAAG | 10529 |
| rs6482158 | snp | A/G | 0.46754 | 0.123192 | intron-variant | NEBL | GRCh38.p7 | 10:21012989 | GGTCGAAAACCTAGC[A/G]GTGCACAAAAATCAA | 10529 |
| rs6482159 | snp | C/T | 0.467132 | 0.12391 | intron-variant | NEBL | GRCh38.p7 | 10:21075574 | ATCCTTCCAGAAGCA[C/T]GATGCAGTTGCCCAA | 10529 |
| rs6482160 | snp | G/T | 0.489434 | 0.0719116 | intron-variant | NEBL | GRCh38.p7 | 10:21103478 | ttggcctcccaaagt[G/T]ctgggattacaggca | 10529 |
| rs6482163 | snp | A/C | 0.353154 | 0.227726 | intron-variant | NEBL | GRCh38.p7 | 10:21163203 | AGTCTGCTAGAAACC[A/C]AGTTTTTTTTCCTAT | 10529 |
| rs6482164 | snp | A/G | 0.376989 | 0.215346 | intron-variant | NEBL | GRCh38.p7 | 10:21169381 | CTGGTAGCAGTATAC[A/G]TAAGAAAATCAATTT | 10529 |
| rs7067794 | snp | C/T | 0.030665 | 0.119967 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21134726 | TAATATTAGCAGATG[C/T]GCAATATAATTAGAT | 10529 |
| rs7068183 | snp | A/T | 0.214541 | 0.247473 | intron-variant | NEBL | GRCh38.p7 | 10:21112947 | AAACTCTTAAGTGTA[A/T]CTGGAAAGTGATCTG | 10529 |
| rs7068289 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | NEBL | GRCh38.p7 | 10:20790908 | GTAAGATGTCAGGTT[A/C]ATTTGGCAACAAACA | 10529 |
| rs7068608 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | NEBL | GRCh38.p7 | 10:20903762 | aagtgaagtaactca[A/G]gaatgaaaaaccaaa | 10529 |
| rs7070831 | snp | G/T | 0.480931 | 0.0957637 | intron-variant | NEBL | GRCh38.p7 | 10:20794506 | GCAAATCTATTTATT[G/T]TGGTGAAATATACAT | 10529 |
| rs7070978 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20867318 | GTCTTTTCATTTGTT[C/T]GGGACTTATTTTATG | 10529 |
| rs7071065 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NEBL | GRCh38.p7 | 10:21168235 | AATGCCCTCAGGTAG[C/T]GATTAAAATGAGAAA | 10529 |
| rs7071220 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | NEBL | GRCh38.p7 | 10:20912729 | CCCCTGGTTAAAACG[C/T]TGTGACTTGAGATTT | 10529 |
| rs7071726 | snp | G/T | 0.0391387 | 0.134304 | intron-variant | NEBL | GRCh38.p7 | 10:20797578 | GATACAGAAATACGA[G/T]AAAGTAAATGTGAAT | 10529 |
| rs7072918 | snp | A/G | 0.232651 | 0.249397 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20870795 | GCATGTTAGACACAA[A/G]CCAAAGTATGGTAAG | 10529 |
| rs7073109 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | NEBL | GRCh38.p7 | 10:21086181 | AAAGAGTTCGACTCC[A/G]TGTTGTTATCATTTA | 10529 |
| rs7073813 | snp | A/C | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21055858 | TGAAAAGAAATGATC[A/C]GGAATGACTCCAAGT | 10529 |
| rs7073838 | snp | C/T | 0.46703 | 0.124089 | intron-variant | NEBL | GRCh38.p7 | 10:21013273 | TGAAACGTAATCTCT[C/T]ATCATTTACGTTGCC | 10529 |
| rs7073874 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | NEBL | GRCh38.p7 | 10:20925466 | TTCACCTTCTCTCTC[C/T]TGACTGGTTCTACTC | 10529 |
| rs7074610 | snp | C/G | 0.304688 | 0.243945 | intron-variant | NEBL | GRCh38.p7 | 10:21081324 | CACAGGATGACAAAG[C/G]CTTTCATGGGAAGCA | 10529 |
| rs7074795 | snp | C/T | 0.179425 | 0.239831 | intron-variant | NEBL | GRCh38.p7 | 10:21151651 | GGTCCCCACCGTCCC[C/T]AGGCCCCTTCCTCCT | 10529 |
| rs7074881 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | NEBL | GRCh38.p7 | 10:21080778 | TATATACCCTCCCAA[C/T]AGTGCTAATTCTGGC | 10529 |
| rs7074923 | snp | C/G | 0.481242 | 0.0950111 | intron-variant | NEBL | GRCh38.p7 | 10:21080841 | TTTTTAAAATGTGAT[C/G]TGGTTTTTTTGTTTG | 10529 |
| rs7076273 | snp | A/G | 0.084728 | 0.187577 | intron-variant | NEBL | GRCh38.p7 | 10:21164321 | TTCTAAGCCCTCGAG[A/G]ACAAGGGTGTCATGC | 10529 |
| rs7076759 | snp | A/C | 0.18134 | 0.240387 | intron-variant | NEBL | GRCh38.p7 | 10:20789307 | TAAAAATTAAATTCT[A/C]ATTCATTGTTACACC | 10529 |
| rs7077698 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NEBL | GRCh38.p7 | 10:21029326 | TATGATGTGACAGAA[A/G]AGTCAATTAAGGAAT | 10529 |
| rs7077775 | snp | G/T | 0.462472 | 0.13174 | intron-variant | NEBL | GRCh38.p7 | 10:21057042 | AGGTAGAAAAGTCAA[G/T]TTTACTCCATTAAAT | 10529 |
| rs7077975 | snp | A/G | 0.165853 | 0.235413 | intron-variant | NEBL | GRCh38.p7 | 10:21124546 | GGTCACTTTTAACAA[A/G]TTAAGCAGAACCCAC | 10529 |
| rs7078108 | snp | A/C | 0.046775 | 0.145601 | intron-variant | NEBL | GRCh38.p7 | 10:21028850 | AACAGTTGGGAGAAA[A/C]AATTCAATAATCATA | 10529 |
| rs7078477 | snp | C/G | 0.462144 | 0.132269 | intron-variant | NEBL | GRCh38.p7 | 10:21057463 | TGTGTGTCACTAGAG[C/G]TAAAGGTTACTACAA | 10529 |
| rs7078595 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NEBL | GRCh38.p7 | 10:20889075 | CATTAGCAGAAATAA[C/T]CCCAAGGACATCCAG | 10529 |
| rs7079238 | snp | C/T | 0.462472 | 0.13174 | intron-variant | NEBL | GRCh38.p7 | 10:21057268 | CCGGGAAGGGTTGCT[C/T]TTTGACTTTTGGCGG | 10529 |
| rs7079324 | snp | C/G | 0.400934 | 0.199296 | intron-variant | NEBL | GRCh38.p7 | 10:21017183 | TGTTACCTAAATAGA[C/G]ATAATAATAAACACC | 10529 |
| rs7079443 | snp | C/T | 0.118933 | 0.212888 | intron-variant | NEBL | GRCh38.p7 | 10:20999657 | TTCTATATCCAGGAT[C/T]TATATACCCAGGGTT | 10529 |
| rs7079790 | snp | A/G | 0.466515 | 0.124985 | intron-variant | NEBL | GRCh38.p7 | 10:21008034 | CCATTCATAACAAAA[A/G]AGAAAAGACACTTCA | 10529 |
| rs7079923 | snp | C/T | 0.460027 | 0.135605 | intron-variant | NEBL | GRCh38.p7 | 10:21089749 | GAATCTTCTCCCTTT[C/T]CTCCCTCCTTCCCCT | 10529 |
| rs7080172 | snp | A/C | 0.16028 | 0.233346 | intron-variant | NEBL | GRCh38.p7 | 10:20832640 | AACTATAGCCAATTA[A/C]ATTTGCTTTAAAACA | 10529 |
| rs7081012 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20789915 | tagatatatgtatat[A/G]tatatgtgtgtgtat | 10529 |
| rs7081531 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | NEBL | GRCh38.p7 | 10:21026134 | GTGAACAACTCAGAC[A/G]TATAAAGCTAAGATC | 10529 |
| rs7082232 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NEBL | GRCh38.p7 | 10:21064990 | GTAACTGGTTTTAGG[A/G]AAGGTGTGTTGGAAT | 10529 |
| rs7082326 | snp | C/T | 0.277067 | 0.24853 | intron-variant | NEBL | GRCh38.p7 | 10:20952385 | gaggttgccatgagc[C/T]gaaattgtaccactg | 10529 |
| rs7082397 | snp | C/T | 0.489608 | 0.0713316 | intron-variant | NEBL | GRCh38.p7 | 10:20894680 | agcactttgggaggc[C/T]gaggcgggcagatca | 10529 |
| rs7082620 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEBL | GRCh38.p7 | 10:21165595 | TCTAAATGCCAGGCT[C/T]Atctacggccatacc | 10529 |
| rs7083341 | snp | G/T | 0.286825 | 0.247273 | intron-variant | NEBL | GRCh38.p7 | 10:20929764 | GTGGGGAGGGTGGGA[G/T]GGGATGACAGATGAA | 10529 |
| rs7083342 | snp | A/G | 0.283684 | 0.24772 | intron-variant | NEBL | GRCh38.p7 | 10:20929765 | TGGGGAGGGTGGGAG[A/G]GGATGACAGATGAAA | 10529 |
| rs7083378 | snp | A/G | 0.180702 | 0.240204 | intron-variant | NEBL | GRCh38.p7 | 10:21118710 | AATCTCAGTGAAACA[A/G]AGTCAGTTTTCTTTT | 10529 |
| rs7083474 | snp | C/G | 0.214843 | 0.247516 | intron-variant | NEBL | GRCh38.p7 | 10:21112802 | CCAGTGATTTCCCTT[C/G]GGGGCTTTGAAATTA | 10529 |
| rs7084365 | snp | A/G | 0.498832 | 0.0241331 | intron-variant | NEBL | GRCh38.p7 | 10:21171228 | TAATCCCAACTACTC[A/G]GGAGGCTGAGGCAGA | 10529 |
| rs7084909 | snp | C/T | 0.304937 | 0.243889 | intron-variant | NEBL | GRCh38.p7 | 10:20930231 | ccactcactcattta[C/T]tagaaacaaaattct | 10529 |
| rs7085478 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | NEBL | GRCh38.p7 | 10:21101041 | AACTTTAGAGACACA[A/G]GGGAGGTTATTTCCT | 10529 |
| rs7085509 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21127610 | ttatcaggcctgttg[A/G]tctatgagtttatat | 10529 |
| rs7086221 | snp | C/T | 0.396909 | 0.202282 | intron-variant | NEBL | GRCh38.p7 | 10:20925748 | AGAAGCTATCAAGAG[C/T]ACACAATTTGGAGTA | 10529 |
| rs7087041 | snp | A/C | 0.440746 | 0.161604 | intron-variant | NEBL | GRCh38.p7 | 10:21101369 | GGTCAAGTAACAGCT[A/C]TGGCTAAAACAATCC | 10529 |
| rs7087832 | snp | C/G | 0.180702 | 0.240204 | intron-variant | NEBL | GRCh38.p7 | 10:21118764 | GAGTCTTAATAAAGC[C/G]ACTGATTAAGTTTCT | 10529 |
| rs7087917 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | NEBL | GRCh38.p7 | 10:21031735 | TCTTTCTTTCCCACC[A/G]GGAGCCCAAGTTGTA | 10529 |
| rs7088409 | snp | C/T | 0.470908 | 0.117046 | intron-variant | NEBL | GRCh38.p7 | 10:21074101 | aaaTACCTACTATAG[C/T]TATCATTTTGCTTTT | 10529 |
| rs7089148 | snp | C/T | 0.470327 | 0.118136 | intron-variant | NEBL | GRCh38.p7 | 10:21074637 | tgcacaccaccaagc[C/T]cggctaatttttttg | 10529 |
| rs7089564 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NEBL | GRCh38.p7 | 10:20790911 | AGATGTCAGGTTCAT[C/T]TGGCAACAAACAAGG | 10529 |
| rs7090013 | snp | A/G | 0.385359 | 0.210185 | intron-variant | NEBL | GRCh38.p7 | 10:21155971 | TTGCCACCGCTCAAA[A/G]GCAATATTGGGAACA | 10529 |
| rs7091275 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | NEBL | GRCh38.p7 | 10:21007619 | TGTGGTTATTTATTA[A/G]TAACCATTAAATTAA | 10529 |
| rs7092686 | snp | A/T | 0.0535932 | 0.154675 | intron-variant | NEBL | GRCh38.p7 | 10:21074814 | ttgttgttgttgttg[A/T]tgttgttgagacagg | 10529 |
| rs7092710 | snp | C/T | 0.0770498 | 0.180522 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20861820 | GCTCTCCCAAGTAAA[C/T]GTTACAGACACCCCT | 10529 |
| rs7093356 | snp | A/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21081398 | caggagggttgatca[A/T]ataagtaaacacata | 10529 |
| rs7093475 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | NEBL | GRCh38.p7 | 10:21155935 | CCCCAAGAGGTGGAG[C/T]TGGCCCCCACCTACT | 10529 |
| rs7095974 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NEBL | GRCh38.p7 | 10:21086931 | GAAAGATCTCCCTGC[A/G]CCCCAACACCAATCC | 10529 |
| rs7096446 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20789921 | tatgtatatatatat[A/G]tgtgtgtatatgtgt | 10529 |
| rs7096447 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20789923 | tgtatatatatatgt[A/G]tgtgtatatgtgtat | 10529 |
| rs7096480 | snp | C/T | 0.264358 | 0.249587 | intron-variant | NEBL | GRCh38.p7 | 10:21073183 | CTTCATTCATCAggg[C/T]gcagtagttcacatc | 10529 |
| rs7097035 | snp | C/T | 0.286303 | 0.24735 | intron-variant | NEBL | GRCh38.p7 | 10:21081491 | ttggtgggaactcat[C/T]tttaatagtacctat | 10529 |
| rs7097419 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20789868 | Ttatatatatatata[C/T]atacacatacacaca | 10529 |
| rs7097421 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20789872 | atatatatatacata[C/T]acatacacacacaca | 10529 |
| rs7097427 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20789882 | acatacacatacaca[C/T]acacatatatatatg | 10529 |
| rs7097882 | snp | A/G | 0.275197 | 0.248727 | intron-variant | NEBL | GRCh38.p7 | 10:20996670 | ACTAGTTCTCAGGGG[A/G]CTAGACTGTAATGTG | 10529 |
| rs7098153 | snp | C/T | 0.131038 | 0.219882 | intron-variant | NEBL | GRCh38.p7 | 10:21149037 | aagaacctgaaagga[C/T]gggactggctgggtt | 10529 |
| rs7098616 | snp | C/T | 0.330947 | 0.236533 | intron-variant | NEBL | GRCh38.p7 | 10:20936314 | TTACTCTATTTCCTA[C/T]GGTAAAAGGGGCAAT | 10529 |
| rs7098864 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NEBL | GRCh38.p7 | 10:20951806 | CTACTCACTGTGGCT[A/G]TGTCCCAAAAGGTAT | 10529 |
| rs7099416 | snp | C/T | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20865939 | GTAGATTACCACTGT[C/T]ACAGCCCAGCTGGCT | 10529 |
| rs7099461 | snp | A/C | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20873147 | TACCATCCATCAGAG[A/C]TCAGGAAGAATAAAA | 10529 |
| rs7100279 | snp | A/T | 0.41833 | 0.184838 | intron-variant | NEBL | GRCh38.p7 | 10:20939443 | aaggaagcacgaaac[A/T]tggaaaggaacaact | 10529 |
| rs7100818 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | NEBL | GRCh38.p7 | 10:20949452 | catgtatcccagaac[G/T]taaagtaaaaaataa | 10529 |
| rs7101127 | snp | A/T | 0.0298908 | 0.118541 | intron-variant | NEBL | GRCh38.p7 | 10:20787372 | GAAATACCCATCCCA[A/T]ACCCTCAGAGTGATG | 10529 |
| rs7342117 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | NEBL | GRCh38.p7 | 10:21087169 | CTGGAGAACAGGGAA[A/C]GTTACTGTCTCCTCC | 10529 |
| rs7392777 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20940683 | acaaaattgatagac[C/T]gctagcaagactaat | 10529 |
| rs7392984 | snp | G/T | 0.115788 | 0.21092 | intron-variant | NEBL | GRCh38.p7 | 10:20941040 | cattccttctgaaac[G/T]attccaatcaataga | 10529 |
| rs7393489 | snp | C/T | 0.427119 | 0.176434 | intron-variant | NEBL | GRCh38.p7 | 10:20940639 | tcaaaaatcaatgaa[C/T]acaaggagctggttt | 10529 |
| rs7476367 | snp | A/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21020733 | CATCTTGAAATGTCG[A/T]CTCCCCGGGTTTACA | 10529 |
| rs7478163 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NEBL | GRCh38.p7 | 10:20943429 | ggaacatcacacacc[A/G]cggcctgtggtgggt | 10529 |
| rs7893606 | snp | C/T | 0.360842 | 0.224085 | intron-variant | NEBL | GRCh38.p7 | 10:20987447 | ctcatttcttcacct[C/T]tctttgtgctttctc | 10529 |
| rs7893616 | snp | C/T | 0.362523 | 0.223246 | intron-variant | NEBL | GRCh38.p7 | 10:20987474 | tctcagtgacctcaa[C/T]gtcacttatgcaatg | 10529 |
| rs7894485 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NEBL | GRCh38.p7 | 10:20791438 | agatggggtctcact[C/T]tgtcacccaggctgt | 10529 |
| rs7894881 | snp | A/C | 0.0640965 | 0.167152 | intron-variant | NEBL | GRCh38.p7 | 10:20997450 | AGCCGCAAACCACAC[A/C]AAATAAACGCACAGT | 10529 |
| rs7895448 | snp | A/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20911981 | AAATAAGTTTTCGTG[A/T]CATCGCAAATGGGGA | 10529 |
| rs7895807 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20912252 | GCTCACAGACGTGGC[C/T]TGCAAGAAAAGCAAG | 10529 |
| rs7895973 | snp | C/T | 0.40157 | 0.198813 | intron-variant | NEBL | GRCh38.p7 | 10:20912444 | TGACTGAATGAGACC[C/T]TGTCTTTAAAAACAA | 10529 |
| rs7896023 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20940085 | ctgcaccaagcggac[C/T]taatagacatctaca | 10529 |
| rs7896084 | snp | C/G | 0.38286 | 0.211774 | intron-variant, upstream-variant-2KB | NEBL, LOC102725112 | GRCh38.p7 | 10:20844437 | TTTATACTTAGGGAA[C/G]ACTTTCCCTTAATAT | 10529 |
| rs7896089 | snp | A/G | 0.200182 | 0.244986 | intron-variant | NEBL | GRCh38.p7 | 10:20976425 | ccatactaggtacat[A/G]cccaaaagaacataa | 10529 |
| rs7896127 | snp | C/T | 0.114387 | 0.210022 | intron-variant | NEBL | GRCh38.p7 | 10:20824656 | CCAACCTCATGCAGA[C/T]ACAGAACTATGCATT | 10529 |
| rs7896773 | snp | A/G | 0.402982 | 0.197728 | intron-variant | NEBL | GRCh38.p7 | 10:21010530 | AAGCACTGGGATTAC[A/G]GGCATGAGCCACCAC | 10529 |
| rs7897164 | snp | A/T | 0.496245 | 0.0431677 | intron-variant | NEBL | GRCh38.p7 | 10:20839880 | TATCCTTTTATTAAG[A/T]GGGTTCATTGCATGG | 10529 |
| rs7897830 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | NEBL | GRCh38.p7 | 10:21083520 | TGCACTGCAGTCACT[C/T]AGCTAAGATCATCAG | 10529 |
| rs7898090 | snp | G/T | 0.400325 | 0.199756 | intron-variant | NEBL | GRCh38.p7 | 10:20998338 | GCTAACCTAAGAAAG[G/T]TATGGGGAAGATTAA | 10529 |
| rs7898342 | snp | A/G | 0.48155 | 0.0942576 | intron-variant | NEBL | GRCh38.p7 | 10:21028575 | TGAGAGGGCATATGA[A/G]AATTAAAGTATTCTA | 10529 |
| rs7898940 | snp | A/C | 0.499703 | 0.0121769 | intron-variant | NEBL | GRCh38.p7 | 10:20901637 | AAAAATGAATTCAAC[A/C]TTTCTTATTATAAAA | 10529 |
| rs7899344 | snp | G/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20953528 | ttttttttttttttt[G/T]GTAGGCTCTTGGATT | 10529 |
| rs7899379 | snp | C/T | 0.0991586 | 0.199366 | intron-variant | NEBL | GRCh38.p7 | 10:21159315 | GTATGGCACACATCG[C/T]TTATCTTAGAGTTTC | 10529 |
| rs7899845 | snp | C/T | 0.375399 | 0.216275 | intron-variant | NEBL | GRCh38.p7 | 10:20976664 | ctaagcaaattaatg[C/T]agaaacagaaaacca | 10529 |
| rs7900317 | snp | C/T | 0.206029 | 0.246103 | intron-variant | NEBL | GRCh38.p7 | 10:21111160 | tatcatgaaaatgac[C/T]atatttcccaaggta | 10529 |
| rs7901012 | snp | C/T | 0.478437 | 0.10157 | intron-variant | NEBL | GRCh38.p7 | 10:21059429 | ATTTCCTTAGATATG[C/T]TCAGAGAAACTAGGG | 10529 |
| rs7901323 | snp | C/T | 0.355311 | 0.226737 | intron-variant | NEBL | GRCh38.p7 | 10:20980764 | TCTCTTCCTGGCTGC[C/T]TTTGTTAACAAAAGT | 10529 |
| rs7901714 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | NEBL | GRCh38.p7 | 10:20950991 | ATATTCCTTTGTggc[C/T]tggtatggtggctca | 10529 |
| rs7902325 | snp | A/C | 0.313814 | 0.241719 | intron-variant | NEBL | GRCh38.p7 | 10:20931897 | AAAGAAATAATAAAG[A/C]AATCAAACATTTCTT | 10529 |
| rs7902401 | snp | C/T | 0.275197 | 0.248727 | intron-variant | NEBL | GRCh38.p7 | 10:20951526 | ATCATAAAATTTTCT[C/T]TAATTGTATAAACTT | 10529 |
| rs7904437 | snp | A/G | 0.105569 | 0.204058 | intron-variant | NEBL | GRCh38.p7 | 10:21052519 | AAAGTCAGTGGAACA[A/G]GGGACTCACCCCTGC | 10529 |
| rs7904906 | snp | A/G | 0.441841 | 0.160303 | intron-variant | NEBL | GRCh38.p7 | 10:21015704 | GTTTGTAGAAACAGG[A/G]GTCTCCCTATGGCGC | 10529 |
| rs7904982 | snp | A/T | 0.0678174 | 0.1712 | intron-variant | NEBL | GRCh38.p7 | 10:21073506 | cttgtaatccgagct[A/T]ctcaggaggccaaga | 10529 |
| rs7905899 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NEBL | GRCh38.p7 | 10:20935800 | TAGCTCATTTGTGAA[A/C]TAATAATCTAAGAAG | 10529 |
| rs7906223 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20911923 | TTATCATAGCATTCA[A/G]TCTGTTGCAAAAATT | 10529 |
| rs7906317 | snp | A/C | | | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20855529 | acaaaacaaaacaaa[A/C]aaaaaacgaaggaaa | 10529 |
| rs7906482 | snp | G/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20912144 | TAAAAACATGAAAAT[G/T]ACTTTTAAAAATAAA | 10529 |
| rs7906562 | snp | A/C | 0.402982 | 0.197728 | intron-variant | NEBL | GRCh38.p7 | 10:20996475 | TCCTAGGTCTACTGG[A/C]TCGATGCCTTATCAC | 10529 |
| rs7906855 | snp | A/C | 0.150333 | 0.229274 | intron-variant | NEBL | GRCh38.p7 | 10:20902850 | CAGCTTGACTCCCAC[A/C]GAGTGTCCCTTTCCT | 10529 |
| rs7906875 | snp | A/G | 0.150333 | 0.229274 | intron-variant | NEBL | GRCh38.p7 | 10:20902905 | GAATAATTGTGAAAG[A/G]CTTTGAAATGGGCAC | 10529 |
| rs7907121 | snp | A/G | 0.499885 | 0.00758699 | intron-variant | NEBL | GRCh38.p7 | 10:20903055 | ATAGAAATGCAAATT[A/G]Tagtagcccccagac | 10529 |
| rs7907553 | snp | A/C/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20912168 | AAATAAACTAGATAA[A/C/G]CAACACAACTATTTT | 10529 |
| rs7907567 | snp | A/C | 0.318896 | 0.240319 | intron-variant | NEBL | GRCh38.p7 | 10:20903433 | gaatgtaaatgagta[A/C]aacctctacgggaga | 10529 |
| rs7907683 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20912246 | AGGAATGCTCACAGA[C/T]GTGGCTTGCAAGAAA | 10529 |
| rs7907748 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20939951 | aagtccttagagacc[C/T]agaaagagaattaga | 10529 |
| rs7908443 | snp | A/C | 0.0785177 | 0.181917 | intron-variant | NEBL | GRCh38.p7 | 10:21000674 | GTTAAATACTTACTG[A/C]AAACAGAAATAAGGC | 10529 |
| rs7908709 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | NEBL | GRCh38.p7 | 10:21008948 | atttattatatatgt[A/C]tatAAAAAACCCATA | 10529 |
| rs7909462 | snp | C/T | 0.45946 | 0.136478 | intron-variant | NEBL | GRCh38.p7 | 10:21121312 | TTGATCACTTTAATG[C/T]CACGGTCATGCCAAT | 10529 |
| rs7909970 | snp | A/G | 0.499987 | 0.00259581 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20878787 | ACACAGCCTTCTCCC[A/G]TAAGTACACAGTATT | 10529 |
| rs7910035 | snp | C/G | 0.0821764 | 0.185298 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20864778 | AAACTAAACTTGCTG[C/G]CCAAATTTCTGTTAT | 10529 |
| rs7910227 | snp | A/G | 0.214541 | 0.247473 | intron-variant | NEBL | GRCh38.p7 | 10:20953453 | ctgtcgctttacgct[A/G]cccaacctgcaatat | 10529 |
| rs7910371 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | NEBL | GRCh38.p7 | 10:20791258 | TGTCTCTTCTACTGT[A/G]CAATAAAGTACTTCC | 10529 |
| rs7910863 | snp | C/T | 0.0926964 | 0.194308 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21144061 | GATTACTGACAATAG[C/T]TATGTTCTCTGGTCT | 10529 |
| rs7910946 | snp | A/T | 0.150333 | 0.229274 | intron-variant | NEBL | GRCh38.p7 | 10:20903460 | gagacaatatgaagc[A/T]tttttaaagaactaa | 10529 |
| rs7911223 | snp | C/G/T | 0.0236746 | 0.106192 | intron-variant | NEBL | GRCh38.p7 | 10:21159313 | GGGTATGGCACACAT[C/G/T]GTTTATCTTAGAGTT | 10529 |
| rs7911561 | snp | C/G | 0.47802 | 0.102502 | intron-variant | NEBL | GRCh38.p7 | 10:21059169 | CCCCTCACTTGTTCA[C/G]CCTAAGCACCCTGCA | 10529 |
| rs7911673 | snp | A/G | 0.371177 | 0.218669 | intron-variant | NEBL | GRCh38.p7 | 10:20904189 | tcagaaaggaaaacc[A/G]tagataagggagcat | 10529 |
| rs7913123 | snp | C/T | 0.489201 | 0.0726845 | intron-variant | NEBL | GRCh38.p7 | 10:20790825 | TCACTGAGAATTTGG[C/T]TGAAAGATAGCTATT | 10529 |
| rs7913231 | snp | A/G | 0.256897 | 0.249905 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20783672 | TCACAAAAGAAAATG[A/G]CCTGCCTGGGTGAAA | 10529 |
| rs7913928 | snp | A/G | 0.132751 | 0.2208 | intron-variant | NEBL | GRCh38.p7 | 10:20980451 | AAAGAAAAGTAGAGA[A/G]GAAAGAAAAATAAAC | 10529 |
| rs7913981 | snp | A/G | 0.492727 | 0.0598633 | intron-variant | NEBL | GRCh38.p7 | 10:20827726 | GTACATATACACCAC[A/G]GAATACCATGCAGTC | 10529 |
| rs7914197 | snp | A/C | 0.356811 | 0.226034 | intron-variant | NEBL | GRCh38.p7 | 10:20980658 | TCAAGACCAGTGTGA[A/C]GGCAAAGATCCACAT | 10529 |
| rs7914249 | snp | G/T | 0.365024 | 0.221967 | intron-variant | NEBL | GRCh38.p7 | 10:20997432 | AGGTACCCCCATCCC[G/T]ACAGCCGCAAACCAC | 10529 |
| rs7915193 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20822596 | gactatctaatatag[A/G]ctatatataaactaa | 10529 |
| rs7915328 | snp | C/T | 0.401747 | 0.198678 | intron-variant | NEBL | GRCh38.p7 | 10:20992236 | tgaacattttttatg[C/T]tttatgactatctag | 10529 |
| rs7915437 | snp | C/T | 0.116488 | 0.211364 | intron-variant | NEBL | GRCh38.p7 | 10:20992281 | cattcctaagtttca[C/T]caattttccacattt | 10529 |
| rs7915465 | snp | C/T | 0.0755793 | 0.179102 | intron-variant, upstream-variant-2KB | NEBL, LOC102725112 | GRCh38.p7 | 10:20844253 | TTAATCTCAAATTTA[C/T]TTCACTGGTCTAAGA | 10529 |
| rs7915827 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21160367 | TTCCTGACTCCCAGC[C/T]AATTAAACCTGACAT | 10529 |
| rs7916412 | snp | G/T | 0.487049 | 0.0794222 | intron-variant | NEBL | GRCh38.p7 | 10:20826977 | AGGATGCCCACATTC[G/T]CTTCCAAGAAAATGT | 10529 |
| rs7916457 | snp | A/G | 0.340559 | 0.233022 | intron-variant | NEBL | GRCh38.p7 | 10:21111158 | aatatcatgaaaatg[A/G]ccatatttcccaagg | 10529 |
| rs7917486 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20784537 | TCTTTTGATTAACCC[A/G]TTTTGGTGGCTAGAT | 10529 |
| rs7917492 | snp | C/T | 0.356811 | 0.226034 | intron-variant | NEBL | GRCh38.p7 | 10:20980583 | ACCACCAGTAACCAG[C/T]GGCCTTACACTTGGT | 10529 |
| rs7917604 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | NEBL | GRCh38.p7 | 10:20950772 | TACACAACAAAAATA[A/T]ATATTTCAATCACTT | 10529 |
| rs7918175 | snp | C/T | 0.119978 | 0.213528 | intron-variant | NEBL | GRCh38.p7 | 10:20998007 | GAGCCAAAAAATAAA[C/T]TAAATACAATAAAAG | 10529 |
| rs7918237 | snp | A/C | 0.489608 | 0.0713316 | intron-variant | NEBL | GRCh38.p7 | 10:21069213 | TATTTTCGAGTTTGC[A/C]TGGAACCCACTTTGC | 10529 |
| rs7918562 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NEBL | GRCh38.p7 | 10:21055392 | AAATAGGTCTGGAGG[C/T]AGAGGGTCTGTGGCA | 10529 |
| rs7918689 | snp | C/T | 0.481703 | 0.0938806 | intron-variant | NEBL | GRCh38.p7 | 10:21028522 | GTCTACTATATAGGA[C/T]TTTTTTAAAGACAAA | 10529 |
| rs7920067 | snp | C/T | 0.455502 | 0.142369 | intron-variant | NEBL | GRCh38.p7 | 10:21015717 | GGAGTCTCCCTATGG[C/T]GCCCAGACTGATGTC | 10529 |
| rs7920103 | snp | G/T | 0.482683 | 0.0914256 | intron-variant | NEBL | GRCh38.p7 | 10:20915363 | gcacccactaactca[G/T]catctagcattaggt | 10529 |
| rs7920119 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | NEBL | GRCh38.p7 | 10:21043415 | TCTATGCACAATAAA[A/C]AGGATAATTAGCTCT | 10529 |
| rs7920722 | snp | C/G | 0.0360663 | 0.129354 | intron-variant | NEBL | GRCh38.p7 | 10:20936256 | ccattttacagatgt[C/G]gaaacttagacataa | 10529 |
| rs7920752 | snp | C/T | 0.499913 | 0.00658888 | intron-variant | NEBL | GRCh38.p7 | 10:20915208 | CTTCACCAACAAATA[C/T]TTGTTAGACATTTAT | 10529 |
| rs7921219 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | NEBL | GRCh38.p7 | 10:21164114 | TGAGCATGGAAGAAA[A/T]CAATAATAATCATTT | 10529 |
| rs7921413 | snp | A/C | 0.295088 | 0.245901 | intron-variant | NEBL | GRCh38.p7 | 10:20936057 | GAAATACTGCTGCTA[A/C]TTCTACAAATTCAAA | 10529 |
| rs7922552 | snp | C/G | 0.143622 | 0.226238 | intron-variant | NEBL | GRCh38.p7 | 10:20896095 | ATTCTGATCATTTTG[C/G]TTATTATCAACAACA | 10529 |
| rs7922734 | snp | C/G | 0.318896 | 0.240319 | intron-variant | NEBL | GRCh38.p7 | 10:20903459 | ggagacaatatgaag[C/G]ttttttaaagaacta | 10529 |
| rs7923995 | snp | C/T | 0.0901694 | 0.192235 | intron-variant | NEBL | GRCh38.p7 | 10:20891156 | TGGTAGAACTAGATA[C/T]AGATTAAGTGAAGTT | 10529 |
| rs7924089 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NEBL | GRCh38.p7 | 10:21009201 | ATTGAGGCTCTATGA[C/T]TGCCTAATTAAAAAT | 10529 |
| rs8181308 | snp | C/T | 0.179744 | 0.239925 | intron-variant | NEBL | GRCh38.p7 | 10:21151054 | ACTGAAAGGCAGAGA[C/T]GGGAAGGATGAAATG | 10529 |
| rs8181457 | snp | A/C | 0.18325 | 0.240924 | intron-variant | NEBL | GRCh38.p7 | 10:21149535 | acctcaagtgatccg[A/C]ctctcttggcttccc | 10529 |
| rs9299775 | snp | C/T | 0.476227 | 0.106402 | intron-variant | NEBL | GRCh38.p7 | 10:21061318 | TTATGTGATATGTAA[C/T]ATATTACATATTATG | 10529 |
| rs9633625 | snp | C/T | 0.464096 | 0.129085 | intron-variant | NEBL | GRCh38.p7 | 10:21077849 | TCAGGCACAGCAGAA[C/T]TGATAGACCTTTCAA | 10529 |
| rs9651369 | snp | A/T | 0.115788 | 0.21092 | intron-variant | NEBL | GRCh38.p7 | 10:20979700 | AACACAGtttttttt[A/T]attcatttatgtgtt | 10529 |
| rs9663304 | snp | C/T | 0.127599 | 0.217986 | intron-variant | NEBL | GRCh38.p7 | 10:21072246 | ctatcttagtctcct[C/T]atagccctcccttct | 10529 |
| rs9664022 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | NEBL | GRCh38.p7 | 10:21072804 | gagaccagcatggcc[A/G]acatgataaaactcc | 10529 |
| rs9665295 | snp | A/C | 0.157642 | 0.232314 | intron-variant | NEBL | GRCh38.p7 | 10:21067663 | ACCTCTCAGCTTAAT[A/C]TGAGAGAGAACACCT | 10529 |
| rs9665716 | snp | A/C | 0.166832 | 0.235761 | intron-variant | NEBL | GRCh38.p7 | 10:21061119 | aactggtgtcctcat[A/C]aaaaggggagCATGT | 10529 |
| rs9702521 | snp | C/T | 0.418169 | 0.184985 | intron-variant | NEBL | GRCh38.p7 | 10:20941546 | GGATGCCCTCTCTCA[C/T]CACTCCTATTCAACA | 10529 |
| rs9731385 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | NEBL | GRCh38.p7 | 10:21061768 | CAGCCTCACAGAGTG[C/G]ATAAGGACTGAGCCA | 10529 |
| rs9732008 | snp | C/T | 0.406814 | 0.194704 | intron-variant | NEBL | GRCh38.p7 | 10:20942651 | ATCAGAGTGAACAGG[C/T]GACCTACAGAATGGG | 10529 |
| rs9732969 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | NEBL | GRCh38.p7 | 10:21149440 | ggactacaggtgcct[A/G]ccaccacacccagat | 10529 |
| rs9888042 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | NEBL | GRCh38.p7 | 10:21102682 | atgagtactattgca[C/T]tgtatgagtataaca | 10529 |
| rs9888068 | snp | C/G | 0.269809 | 0.249214 | intron-variant | NEBL | GRCh38.p7 | 10:21102736 | aattctggattgttt[C/G]tagtttagagctatc | 10529 |
| rs9971347 | snp | C/T | 0.426813 | 0.17674 | intron-variant | NEBL | GRCh38.p7 | 10:21063751 | ATTTTCAAAATGTGG[C/T]CCCAGCTACTTGGGA | 10529 |
| rs10047294 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | NEBL | GRCh38.p7 | 10:20945858 | aaaaacaaaccaaca[A/C]acttggactccagtc | 10529 |
| rs10047342 | snp | G/T | 0.138207 | 0.223612 | intron-variant | NEBL | GRCh38.p7 | 10:20944103 | TAACTTGtatttaaa[G/T]atagttaaatatagg | 10529 |
| rs10082441 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | NEBL | GRCh38.p7 | 10:20935482 | AGAACATGCTCCCCT[C/T]GGTAGTGAGCCTTAA | 10529 |
| rs10082506 | snp | A/G | 0.0475351 | 0.146656 | intron-variant | NEBL | GRCh38.p7 | 10:20933108 | AACCTAGATTCTCTC[A/G]ATGTGTTTGCCATTC | 10529 |
| rs10128348 | snp | A/G | 0.495818 | 0.0455352 | intron-variant | NEBL | GRCh38.p7 | 10:20834673 | GCCCCCACCTAACCA[A/G]CCTTGAGATAAGTGA | 10529 |
| rs10128495 | snp | G/T | 0.495999 | 0.0445491 | intron-variant | NEBL | GRCh38.p7 | 10:20834896 | GTGATGTGATACCCA[G/T]CCTGTCACAGAATTT | 10529 |
| rs10159777 | snp | A/C/T | 0.0229036 | 0.104597 | intron-variant | NEBL | GRCh38.p7 | 10:20915919 | TATCCAGGTATTCAA[A/C/T]GAACATTCTATTTAA | 10529 |
| rs10159961 | snp | A/C | 0.469445 | 0.119766 | intron-variant | NEBL | GRCh38.p7 | 10:20916079 | AATAATCTTTTATTT[A/C]CTAGATGAGAAGTAA | 10529 |
| rs10159995 | snp | C/T | 0.484841 | 0.0857308 | intron-variant | NEBL | GRCh38.p7 | 10:20915776 | GTATATACCCAGTAA[C/T]GGGATGGCTGGGTCA | 10529 |
| rs10160126 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20850599 | ACTAGTCATCTTGTT[A/G]TCTAAAATCATATTA | 10529 |
| rs10218859 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | NEBL | GRCh38.p7 | 10:20800502 | ATACCAGAAGAGGAA[A/C]TGCTGAGTTGTATGG | 10529 |
| rs10218906 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NEBL | GRCh38.p7 | 10:20798827 | ACTGAATCTTGGCAC[A/G]TCGATGAAAGACACA | 10529 |
| rs10491054 | snp | A/G | 0.116838 | 0.211584 | intron-variant | NEBL | GRCh38.p7 | 10:20797539 | ATATAAAACTGACTC[A/G]ATGTGTCCCCAACAT | 10529 |
| rs10491055 | snp | A/G | 0.127599 | 0.217986 | intron-variant | NEBL | GRCh38.p7 | 10:20811126 | ATTATGGAAATTTCA[A/G]TGGAAAACAGTTCTT | 10529 |
| rs10491056 | snp | A/G | 0.475493 | 0.107948 | intron-variant | NEBL | GRCh38.p7 | 10:20831187 | TGAGCATCTTCATTC[A/G]TGACCAACCTGGCTA | 10529 |
| rs10508634 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NEBL | GRCh38.p7 | 10:20924346 | CTATCTGCTTTGTAT[C/T]CACACCTTAAGTTAC | 10529 |
| rs10508635 | snp | A/C | 0.428937 | 0.17459 | intron-variant | NEBL | GRCh38.p7 | 10:20927439 | AAATGGTGATCATCA[A/C]TGATAGTAAATAAGA | 10529 |
| rs10508636 | snp | G/T | 0.307671 | 0.243257 | intron-variant | NEBL | GRCh38.p7 | 10:20983348 | TGCAAAAGTATGTGC[G/T]AAACTTCAACGCAAA | 10529 |
| rs10508637 | snp | C/T | 0.38821 | 0.208322 | intron-variant | NEBL | GRCh38.p7 | 10:20984509 | CTCATCAGGTTTTGA[C/T]AATGAGATGTCTCTC | 10529 |
| rs10532070 | in-del | -/AA | 0.453911 | 0.144639 | intron-variant | NEBL | GRCh38.p7 | 10:20902407 | CAAAGACACTGTCTC[-/AA]AAAAAAAAAAATTTA | 10529 |
| rs10539676 | in-del | -/TTTTT | 0.0138799 | 0.0821421 | intron-variant | NEBL | GRCh38.p7 | 10:21003004 | TTTTCATTATGTGGC[-/TTTTT]TTTTTTTTTTTTTTT | 10529 |
| rs10540045 | snp | A/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21169069 | AAAAAAAAAAAAAAA[A/T]ATATATATATATATA | 10529 |
| rs10541564 | in-del | -/GTGTGT | | | intron-variant | NEBL | GRCh38.p7 | 10:21096523 | TGTGTGTGTGTGTGT[-/GTGTGT]TTTGAGACAGGGTCT | 10529 |
| rs10554894 | in-del | -/AT | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20789887 | CACATACACACACAC[-/AT]ATATATATGTATAGA | 10529 |
| rs10594967 | in-del | -/A | | | intron-variant | NEBL | GRCh38.p7 | 10:21073637 | AAAAAAAAAAAAAAA[-/A]GTCTTTATTTCAATC | 10529 |
| rs10595673 | in-del | -/CAAAAAA | | | intron-variant | NEBL | GRCh38.p7 | 10:21054051 | ACAAAAAACAAAAAA[-/CAAAAAA]GAAGTATGCCTAAAA | 10529 |
| rs10626391 | in-del | -/AA | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21048468 | AAAAAAAAAAAAAAA[-/AA]CCTAAGTAACAGAAG | 10529 |
| rs10631047 | in-del | -/AG | 0.361684 | 0.223667 | intron-variant | NEBL | GRCh38.p7 | 10:20828765 | GAGAGAGAGAGAGAG[-/AG]GTGGAGAGACAGAGA | 10529 |
| rs10715435 | in-del | -/A | 0.358847 | 0.225061 | intron-variant | NEBL | GRCh38.p7 | 10:20980391 | AAGAACCAGAAAAAG[-/A]AAAAAAAATATATTT | 10529 |
| rs10715595 | in-del | -/A | 0.196149 | 0.244131 | intron-variant | NEBL | GRCh38.p7 | 10:20951476 | CATAGTTGCATACTT[-/A]AAAAAAAAAAGACAT | 10529 |
| rs10734036 | snp | C/T | 0.493925 | 0.054776 | intron-variant | NEBL | GRCh38.p7 | 10:20801226 | TTTATTTTTTATTTT[C/T]TTTTGAGGCAGGGTC | 10529 |
| rs10734037 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | NEBL | GRCh38.p7 | 10:21175785 | ATTAGAAATGTATGA[C/G]GAGGGGAAAAAAAGT | 10529 |
| rs10740985 | snp | C/T | 0.49753 | 0.0350569 | intron-variant | NEBL | GRCh38.p7 | 10:20799810 | GGAGTGTATTTTCTT[C/T]TTCTTAAATAAAGCT | 10529 |
| rs10740986 | snp | C/T | 0.493432 | 0.0569306 | intron-variant | NEBL | GRCh38.p7 | 10:20825591 | AGAATCACTTGAATC[C/T]GGGAGGCAGTTGCGG | 10529 |
| rs10740987 | snp | A/G | 0.3744 | 0.216852 | intron-variant | NEBL | GRCh38.p7 | 10:20905611 | TTGGGTGGGGACACA[A/G]AGCCAAACCATGTCA | 10529 |
| rs10740988 | snp | C/T | 0.464523 | 0.128375 | intron-variant | NEBL | GRCh38.p7 | 10:20906130 | TAAGGGAAATTCATT[C/T]GTATTATGTAGACCC | 10529 |
| rs10764285 | snp | C/T | 0.454784 | 0.1434 | intron-variant | NEBL | GRCh38.p7 | 10:20820130 | TAACAAAATCCTGTA[C/T]CTGAACTTTAGTGAT | 10529 |
| rs10764286 | snp | C/T | 0.499784 | 0.0103811 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20856897 | TGGAGCACATTGGTG[C/T]CATCTCAGCTCACAG | 10529 |
| rs10764287 | snp | A/T | 0.499982 | 0.00299515 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20884462 | TCATAGATCTCTAAA[A/T]TAAAGTTTACTGGCC | 10529 |
| rs10764288 | snp | C/T | 0.495095 | 0.0492773 | intron-variant, downstream-variant-500B | NEBL, LOC102725112 | GRCh38.p7 | 10:20885343 | GTTATGACAGTTACA[C/T]AAATCTTTGAAGTAG | 10529 |
| rs10764289 | snp | C/G | 0.499767 | 0.0107802 | intron-variant | NEBL | GRCh38.p7 | 10:20905821 | ACCCTTCAGCCTCCA[C/G]GATGTCAGGGGAGAG | 10529 |
| rs10764290 | snp | A/G | 0.39527 | 0.203462 | intron-variant | NEBL | GRCh38.p7 | 10:20907210 | TAAGCAAGCAATAAA[A/G]TCTACAACCTGATTT | 10529 |
| rs10764291 | snp | C/G | 0.152001 | 0.229992 | intron-variant | NEBL | GRCh38.p7 | 10:20918619 | ACTTTGGGAGGCCGA[C/G]GGGGGCAGATCAAGG | 10529 |
| rs10764292 | snp | C/T | 0.388021 | 0.208447 | intron-variant | NEBL | GRCh38.p7 | 10:20920265 | AATGACATATGCATT[C/T]ACTTTTTAACCCATC | 10529 |
| rs10764293 | snp | C/G | 0.420096 | 0.183214 | intron-variant | NEBL | GRCh38.p7 | 10:20927733 | ACAGCCTGTGGCAGC[C/G]AGACAGCCAGGGTTC | 10529 |
| rs10764294 | snp | C/T | 0.446641 | 0.154377 | intron-variant | NEBL | GRCh38.p7 | 10:20934974 | AAATAAACTGGCATG[C/T]TGTGCAATAGTGAAG | 10529 |
| rs10764295 | snp | C/T | 0.373598 | 0.21731 | intron-variant | NEBL | GRCh38.p7 | 10:20942728 | AATCTACAATGAACT[C/T]AAACAATGTACAAGA | 10529 |
| rs10764300 | snp | C/T | 0.275999 | 0.248644 | intron-variant | NEBL | GRCh38.p7 | 10:21016709 | ATAAAATATTAATAG[C/T]CAATTTTCCACCAAA | 10529 |
| rs10764301 | snp | C/G | 0.461037 | 0.134028 | intron-variant | NEBL | GRCh38.p7 | 10:21023394 | TCTTCTGCCATTTAC[C/G]TTTAATTTAAAATTC | 10529 |
| rs10764302 | snp | A/G | 0.398894 | 0.200825 | intron-variant | NEBL | GRCh38.p7 | 10:21026006 | ACCTCTGTGTCTCAC[A/G]ACCTTCATCTATATA | 10529 |
| rs10764305 | snp | C/T | 0.230896 | 0.249269 | intron-variant | NEBL | GRCh38.p7 | 10:21111282 | AAAGAGCCCACAGAG[C/T]CAAGATAATCCTAAG | 10529 |
| rs10764307 | snp | A/G | 0.303438 | 0.244222 | intron-variant | NEBL | GRCh38.p7 | 10:21120828 | TACACACAACTCTGC[A/G]TCGGCTGCTATGAAG | 10529 |
| rs10764308 | snp | C/T | 0.371785 | 0.218331 | intron-variant | NEBL | GRCh38.p7 | 10:21167491 | ACTATTGCGTCGTTC[C/T]TTGGTGGCACCCCAG | 10529 |
| rs10828131 | snp | G/T | 0.44858 | 0.151875 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20780243 | TTTTATGTACTCAAT[G/T]TGTGCACTTTCTATT | 10529 |
| rs10828132 | snp | C/T | 0.49306 | 0.0584955 | intron-variant | NEBL | GRCh38.p7 | 10:20788671 | TCTCCACTTGAATTA[C/T]AGTATATTGCAAAGT | 10529 |
| rs10828133 | snp | C/T | 0.417034 | 0.18601 | intron-variant | NEBL | GRCh38.p7 | 10:20800105 | ATATCTGCTACTTTG[C/T]ATCATTTGAGTTACA | 10529 |
| rs10828134 | snp | A/G | 0.127599 | 0.217986 | intron-variant | NEBL | GRCh38.p7 | 10:20802802 | CCAAGTACTTCATTC[A/G]TAAAGTAAAACAGAC | 10529 |
| rs10828135 | snp | C/G | 0.3752 | 0.216391 | intron-variant | NEBL | GRCh38.p7 | 10:20808283 | CAAATCCATTGCTGC[C/G]ATAATAGTGAAGTAA | 10529 |
| rs10828136 | snp | C/T | 0.488965 | 0.0734569 | intron-variant | NEBL | GRCh38.p7 | 10:20812494 | CCTCACAACAGGCCC[C/T]GGTGTGTGATACAAG | 10529 |
| rs10828137 | snp | C/T | 0.408017 | 0.193729 | intron-variant | NEBL | GRCh38.p7 | 10:20819921 | AGTCACACTTTTTGT[C/T]GTTTTCCTTCAGATT | 10529 |
| rs10828138 | snp | A/C | 0.497387 | 0.0360476 | intron-variant | NEBL | GRCh38.p7 | 10:20822357 | TATCTATCTATCTAT[A/C]TATAGGTCTATCTAT | 10529 |
| rs10828139 | snp | A/C | 0.488726 | 0.0742286 | intron-variant | NEBL | GRCh38.p7 | 10:20826679 | CGGAATTATAGGAAC[A/C]AATTAAATAATCCAT | 10529 |
| rs10828140 | snp | C/T | 0.495782 | 0.0457324 | intron-variant | NEBL | GRCh38.p7 | 10:20834031 | AGTTTTGGCCTGTAA[C/T]GTTGAGATCCCATTA | 10529 |
| rs10828141 | snp | A/G | 0.495368 | 0.0478996 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20848817 | CACTGAATAAGACAC[A/G]AAAAATACAAGTAAT | 10529 |
| rs10828142 | snp | A/G | 0.497241 | 0.037038 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20849645 | GCAAGAAGACCCTTG[A/G]CAGATGTGAATCCTT | 10529 |
| rs10828144 | snp | C/T | 0.499732 | 0.0115784 | intron-variant | NEBL | GRCh38.p7 | 10:20902178 | GGAGACCGAGACAGG[C/T]GGATCATGAGGTCAG | 10529 |
| rs10828145 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | NEBL | GRCh38.p7 | 10:20904429 | GTCATGACTTTACCA[C/T]TTAAAAAATTCTTTA | 10529 |
| rs10828146 | snp | A/G | 0.499732 | 0.0115784 | intron-variant | NEBL | GRCh38.p7 | 10:20905339 | AATTTATAAATAAAA[A/G]AGGTTTAATTGACTC | 10529 |
| rs10828147 | snp | A/T | 0.499609 | 0.0139722 | intron-variant | NEBL | GRCh38.p7 | 10:20905626 | AAGCCAAACCATGTC[A/T]CCAATAAATGACCAG | 10529 |
| rs10828148 | snp | C/T | 0.484279 | 0.0872533 | intron-variant | NEBL | GRCh38.p7 | 10:20906783 | TTCACAAATGTTTCT[C/T]GTGTGCATTCTATGG | 10529 |
| rs10828149 | snp | C/T | 0.490997 | 0.0664859 | intron-variant | NEBL | GRCh38.p7 | 10:20909780 | AAACAATAATATATA[C/T]AAAAGAAATACAGAA | 10529 |
| rs10828150 | snp | A/G | 0.478437 | 0.10157 | intron-variant | NEBL | GRCh38.p7 | 10:20916702 | AGTGTGAGCCACCAC[A/G]CCTGGCTTGATTTAA | 10529 |
| rs10828151 | snp | A/C | 0.144296 | 0.226554 | intron-variant | NEBL | GRCh38.p7 | 10:20922826 | TTCAGAAACCAAGTC[A/C]ATTAAAGGGAAAGGG | 10529 |
| rs10828152 | snp | C/T | 0.484771 | 0.0859212 | intron-variant | NEBL | GRCh38.p7 | 10:20925368 | GGCTCCTAGGAATAC[C/T]CTGAAACAGCAAAAG | 10529 |
| rs10828153 | snp | C/G | 0.420255 | 0.183066 | intron-variant | NEBL | GRCh38.p7 | 10:20926968 | ACAGATGAGTGGGGA[C/G]GAAAAATCATTGAAC | 10529 |
| rs10828154 | snp | C/T | 0.320096 | 0.239972 | intron-variant | NEBL | GRCh38.p7 | 10:20927583 | ATACTCTGAGAGTCA[C/T]AATTTCAACTATGAG | 10529 |
| rs10828155 | snp | A/G | 0.486855 | 0.0799975 | intron-variant | NEBL | GRCh38.p7 | 10:20930999 | TTACTCCAGTCAATC[A/G]TGGAAAATCAGTACT | 10529 |
| rs10828156 | snp | A/G | 0.485799 | 0.0830599 | intron-variant | NEBL | GRCh38.p7 | 10:20931029 | TGTTTAGGCTTTCAG[A/G]AAAGACATCACAACT | 10529 |
| rs10828157 | snp | C/T | 0.301177 | 0.244706 | intron-variant | NEBL | GRCh38.p7 | 10:20935117 | CTCAAAGAACCACAG[C/T]CTACCTGGCTAGAAA | 10529 |
| rs10828158 | snp | G/T | 0.486266 | 0.0817214 | intron-variant | NEBL | GRCh38.p7 | 10:20938034 | CATAGCCAAACAAAA[G/T]GCAGCAGAATCCTCC | 10529 |
| rs10828160 | snp | G/T | 0.225597 | 0.248806 | intron-variant | NEBL | GRCh38.p7 | 10:20943031 | TGGAAGTCAGTGTGG[G/T]GATTCCTCAGGGATG | 10529 |
| rs10828161 | snp | A/G | 0.373598 | 0.21731 | intron-variant | NEBL | GRCh38.p7 | 10:20944355 | CACTGAGCCAAGATC[A/G]CGTGACTGCACTCCA | 10529 |
| rs10828162 | snp | A/G | 0.491525 | 0.0645418 | intron-variant | NEBL | GRCh38.p7 | 10:20954629 | GGGACTCCCTGCAAG[A/G]CCAGAGTCCCCTGCT | 10529 |
| rs10828163 | snp | C/G | 0.375996 | 0.215928 | intron-variant | NEBL | GRCh38.p7 | 10:20977898 | TAACTCAAGCCTAAC[C/G]TTCCTGCTCATCTCT | 10529 |
| rs10828164 | snp | A/G | 0.40733 | 0.194287 | intron-variant | NEBL | GRCh38.p7 | 10:20983095 | TGGTGAAAAATCCTG[A/G]ATTTCCAACTTGGAG | 10529 |
| rs10828167 | snp | C/G | 0.273049 | 0.248935 | intron-variant | NEBL | GRCh38.p7 | 10:20996202 | ACTACGATGTGATAC[C/G]CTTTCAAGGTTCTCC | 10529 |
| rs10828168 | snp | A/T | 0.31503 | 0.241394 | intron-variant | NEBL | GRCh38.p7 | 10:20998910 | CAAGGATGGAAGGTC[A/T]CACCGCAGCAAGTTC | 10529 |
| rs10828169 | snp | C/T | 0.301932 | 0.244547 | intron-variant | NEBL | GRCh38.p7 | 10:20999428 | ATGGCAAGACCCCAT[C/T]CCTACTAAAAATTTA | 10529 |
| rs10828170 | snp | C/G/T | 0.221141 | 0.248329 | intron-variant | NEBL | GRCh38.p7 | 10:21000922 | GGGCAGAGAAAAAGG[C/G/T]AAGAAGCCCAGATAG | 10529 |
| rs10828171 | snp | C/G | 0.221439 | 0.248363 | intron-variant | NEBL | GRCh38.p7 | 10:21001193 | CCAGGTCCAGCCAGC[C/G]GACAGACCGCCAGAG | 10529 |
| rs10828172 | snp | G/T | 0.221439 | 0.248363 | intron-variant | NEBL | GRCh38.p7 | 10:21001233 | TAACAGCACCTGGTT[G/T]TCACATTCCAGGTGA | 10529 |
| rs10828173 | snp | A/G | 0.453453 | 0.145282 | intron-variant | NEBL | GRCh38.p7 | 10:21005122 | CAAATACCAAATTGA[A/G]GACAGAAAGTTCAAT | 10529 |
| rs10828174 | snp | C/T | 0.396546 | 0.202545 | intron-variant | NEBL | GRCh38.p7 | 10:21009216 | CTGCCTAATTAAAAA[C/T]AGAATGGAATTCTTG | 10529 |
| rs10828175 | snp | G/T | 0.275197 | 0.248727 | intron-variant | NEBL | GRCh38.p7 | 10:21016142 | GATGTGTGATCAAAA[G/T]GGAACTAGTAACTAT | 10529 |
| rs10828176 | snp | G/T | 0.467946 | 0.122472 | intron-variant | NEBL | GRCh38.p7 | 10:21022319 | CTCTCCTGGTAAAAG[G/T]TTCTTTTCAGCATCC | 10529 |
| rs10828177 | snp | A/G | 0.104149 | 0.203046 | intron-variant | NEBL | GRCh38.p7 | 10:21028254 | aaaaaaaaaaaaaaa[A/G]aagaagaaGAAGAAG | 10529 |
| rs10828178 | snp | G/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21039088 | TTTTTTTTTTTTTTG[G/T]AAATTTGTTTAAGTC | 10529 |
| rs10828179 | snp | C/T | 0.478271 | 0.101943 | intron-variant | NEBL | GRCh38.p7 | 10:21059934 | GAAAATACTAGGTCA[C/T]ATTTTAAGGAAACTT | 10529 |
| rs10828180 | snp | A/G | 0.476918 | 0.104919 | intron-variant | NEBL | GRCh38.p7 | 10:21061269 | TGTGATATGTAACAT[A/G]TTACATATTATGTGA | 10529 |
| rs10828181 | snp | A/G | 0.375 | 0.216506 | intron-variant | NEBL | GRCh38.p7 | 10:21061295 | TGTGATATGTAACAT[A/G]TTACATATTATGTGA | 10529 |
| rs10828182 | snp | A/G | 0.474453 | 0.110094 | intron-variant | NEBL | GRCh38.p7 | 10:21061321 | TGTGATATGTAATAT[A/G]TTACATATTATGTGA | 10529 |
| rs10828183 | snp | C/T | 0.481932 | 0.0933148 | intron-variant | NEBL | GRCh38.p7 | 10:21064622 | TAAGTGTTGTTGGTG[C/T]TTTAAAAGTAACAGT | 10529 |
| rs10828184 | snp | A/T | 0.362732 | 0.22314 | intron-variant | NEBL | GRCh38.p7 | 10:21080075 | CTCAGAACATAAATC[A/T]TCACAGGTGAACTGT | 10529 |
| rs10828185 | snp | C/T | 0.473451 | 0.112115 | intron-variant | NEBL | GRCh38.p7 | 10:21084767 | GCCTTCTCCCTCCTG[C/T]TCCATTGCCAGCAAC | 10529 |
| rs10828186 | snp | A/C | 0.264084 | 0.249603 | intron-variant | NEBL | GRCh38.p7 | 10:21094587 | ACTCGGAGGCTGAAG[A/C]AAGGGAATCACTTGA | 10529 |
| rs10828187 | snp | C/T | 0.499653 | 0.0131743 | intron-variant | NEBL | GRCh38.p7 | 10:21099011 | GGTGGCACACACCTG[C/T]GGTCCTATCTACTCG | 10529 |
| rs10828188 | snp | A/C | 0.429538 | 0.173972 | intron-variant | NEBL | GRCh38.p7 | 10:21101384 | CTGGCTAAAACAATC[A/C]ACGCAGAAGTGATGG | 10529 |
| rs10828189 | snp | C/G | 0.368324 | 0.220226 | intron-variant | NEBL | GRCh38.p7 | 10:21104385 | TATATCTCCCCATTT[C/G]ACTAGGCCTTATTTA | 10529 |
| rs10828190 | snp | C/T | 0.267091 | 0.249415 | intron-variant | NEBL | GRCh38.p7 | 10:21116114 | CATACTCTTTTTTTT[C/T]CCTCTACATACTTGA | 10529 |
| rs10828191 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21120393 | AAAAAAAAAAAAATA[C/T]ATATATATATATATA | 10529 |
| rs10828192 | snp | A/G | 0.18134 | 0.240387 | intron-variant | NEBL | GRCh38.p7 | 10:21120636 | TCCCATCATCCTTCT[A/G]TATTTATTGGGGATT | 10529 |
| rs10828193 | snp | C/T | 0.482492 | 0.0919113 | intron-variant | NEBL | GRCh38.p7 | 10:21125227 | ATGCACACATGCATA[C/T]ACACACACACACACA | 10529 |
| rs10828194 | snp | A/C | 0.197703 | 0.244469 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21125372 | TGAAAGGGATGTTTC[A/C]GGTTTAAAAGTCTTC | 10529 |
| rs10828195 | snp | C/G | 0.193028 | 0.243422 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21129834 | TATAAGACAGAGAAA[C/G]GAAAGAACAAGGGCA | 10529 |
| rs10828196 | snp | A/C | 0.188631 | 0.242351 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21130342 | CAGTACCAGACAGAT[A/C]CAGCAGGCAGAAAAT | 10529 |
| rs10828197 | snp | C/T | 0.485731 | 0.0832509 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21137001 | CTTCCCTGACTGGCA[C/T]AGCATTTTCTTAATT | 10529 |
| rs10828198 | snp | C/T | 0.469544 | 0.119585 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21140999 | TGGTCCCATCAATAA[C/T]GGAAACCCTGAATCT | 10529 |
| rs10828199 | snp | A/G | 0.180383 | 0.240111 | intron-variant | NEBL | GRCh38.p7 | 10:21148587 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 10529 |
| rs10828200 | snp | C/T | 0.293294 | 0.246223 | intron-variant | NEBL | GRCh38.p7 | 10:21167415 | CAGCCCAAAAATATG[C/T]CTGTGAATAATGTTC | 10529 |
| rs10828201 | snp | C/T | 0.190205 | 0.242744 | intron-variant, upstream-variant-2KB | NEBL, NEBL-AS1 | GRCh38.p7 | 10:21172931 | AGCTATGTAAGTACC[C/T]CTACACCTGACCAGC | 10529 |
| rs11012336 | snp | A/G | 0.43088 | 0.172575 | downstream-variant-500B | NEBL | GRCh38.p7 | 10:20779766 | AAAAAAAAATCTAAG[A/G]TATTCATTTCCTCTG | 10529 |
| rs11012337 | snp | C/T | 0.488118 | 0.0761554 | downstream-variant-500B | NEBL | GRCh38.p7 | 10:20779945 | TTCATTTCATACTTA[C/T]GGAATATGAAAAACA | 10529 |
| rs11012338 | snp | A/G | 0.067446 | 0.170804 | utr-variant-3-prime, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20781464 | GCTCAGCAATTCATT[A/G]CATGGACACTGGAGA | 10529 |
| rs11012339 | snp | A/C | 0.428635 | 0.174898 | intron-variant | NEBL | GRCh38.p7 | 10:20788706 | AAAACATCATTAAAT[A/C]TCAAATACTTCAGAA | 10529 |
| rs11012340 | snp | A/G | 0.251859 | 0.249993 | intron-variant | NEBL | GRCh38.p7 | 10:20789493 | CAGTCCCAGCTTAGT[A/G]CCTGTTAAGTGCTGA | 10529 |
| rs11012341 | snp | A/G | 0.116838 | 0.211584 | intron-variant | NEBL | GRCh38.p7 | 10:20794844 | CAATTTGGGATGTTC[A/G]GTTTTTTTCCTTACA | 10529 |
| rs11012342 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | NEBL | GRCh38.p7 | 10:20795105 | TAATTTCAAAATAAC[A/C]ACTGTGAATTCAGAA | 10529 |
| rs11012346 | snp | A/G | 0.140919 | 0.224948 | intron-variant | NEBL | GRCh38.p7 | 10:20800764 | ATTAATCCCTCTAGC[A/G]GACCACTGAGAAGGT | 10529 |
| rs11012347 | snp | A/G | 0.127599 | 0.217986 | intron-variant | NEBL | GRCh38.p7 | 10:20802033 | CCCCATCACACTCCC[A/G]TATCCTTTTACGTTT | 10529 |
| rs11012348 | snp | A/G | 0.114036 | 0.209795 | intron-variant | NEBL | GRCh38.p7 | 10:20802893 | TTAGGGCACTTAGCT[A/G]AGGAAATGTAAAATA | 10529 |
| rs11012349 | snp | C/G | 0.375996 | 0.215928 | intron-variant | NEBL | GRCh38.p7 | 10:20803484 | ACCAAAAAATTTTAA[C/G]TACATTTTGTTTTTA | 10529 |
| rs11012351 | snp | G/T | 0.000115332 | 0.00759293 | intron-variant, missense, nc-transcript-variant | NEBL | GRCh38.p7 | 10:20819501 | TGGCCTTGTAGTTTT[G/T]CTCTTTATACTGGAG | 10529 |
| rs11012352 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NEBL | GRCh38.p7 | 10:20819607 | TAAATGTCACATGGC[C/T]ACAGAACATTCATTA | 10529 |
| rs11012353 | snp | A/T | 0.43768 | 0.165155 | intron-variant | NEBL | GRCh38.p7 | 10:20823182 | TACAATAAAATTTTT[A/T]AAAAATACTTAAGAA | 10529 |
| rs11012354 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | NEBL | GRCh38.p7 | 10:20826395 | CTAAAAACATTTGTC[G/T]ATAGTTTTGGTTTGC | 10529 |
| rs11012355 | snp | A/T | 0.0349115 | 0.127424 | intron-variant | NEBL | GRCh38.p7 | 10:20838661 | ACAGAGAAATCTTTC[A/T]TGAGAGGAAGAGGCA | 10529 |
| rs11012356 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NEBL | GRCh38.p7 | 10:20841802 | atctcttggttctgt[C/T]ttctctattggcttt | 10529 |
| rs11012357 | snp | A/C | 0.385741 | 0.209939 | intron-variant, upstream-variant-2KB | NEBL, LOC102725112 | GRCh38.p7 | 10:20843658 | ATTTTTCTTCCAAAA[A/C]GCCTTATGGCCAACT | 10529 |
| rs11012358 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20846501 | GATATAGCCACAAGG[A/G]GAGAAACAAAGGATG | 10529 |
| rs11012359 | snp | G/T | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20848300 | GTAATCTAGGGAAAT[G/T]TATTCCATTAAATGT | 10529 |
| rs11012360 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20852477 | GACGCACGGCAGTGA[A/G]CGGCGGGCCTCAGGA | 10529 |
| rs11012361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20853811 | gaatgagtttaagat[C/T]tagtattcaatgcca | 10529 |
| rs11012362 | snp | C/T | | | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20853876 | tacattttaaaataa[C/T]taagagtggaattga | 10529 |
| rs11012363 | snp | C/T | 0.029116 | 0.117091 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20854188 | TTAAGAAGCTAAAGA[C/T]AGCTGCTTATTAGAC | 10529 |
| rs11012364 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20860616 | ATGTCATACCCCCTT[C/T]AACTTACTGTAGCCA | 10529 |
| rs11012365 | snp | C/T | 0.029116 | 0.117091 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20864940 | TGAATACGATAGCTA[C/T]AATGTAAGTTAAAAA | 10529 |
| rs11012366 | snp | C/T | 0.0622301 | 0.165053 | intron-variant, nc-transcript-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20865365 | AAGTAAATACTGTTG[C/T]TGTCATCCCTATTTT | 10529 |
| rs11012367 | snp | A/C | 0.0341408 | 0.126114 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20869569 | CTGTTTCTGCATATA[A/C]CCAAATAATTAACAT | 10529 |
| rs11012369 | snp | A/G | 0 | 0 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20874235 | TTTTTTGTCAGCCTA[A/G]GTTTTTTAATTTGGA | 10529 |
| rs11012370 | snp | A/C | 0.0263992 | 0.111815 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20874653 | aattacatacacaac[A/C]gaatctcatttttca | 10529 |
| rs11012371 | snp | C/T | 0.48955 | 0.071525 | intron-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20876643 | TAATACACATTGAAT[C/T]GACTACCAATATGGT | 10529 |
| rs11012372 | snp | A/G | 0.0221141 | 0.102801 | intron-variant, nc-transcript-variant | NEBL, LOC102725112 | GRCh38.p7 | 10:20880091 | CAATAggccaggcac[A/G]gtggctcgtgcctgt | 10529 |
| rs11012373 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NEBL | GRCh38.p7 | 10:20889324 | GCTGGAAAATGAATA[C/T]AGCGTATTCCTCAGT | 10529 |
| rs11012375 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | NEBL | GRCh38.p7 | 10:20892604 | AGACAAAAAGGGCAA[A/T]ATTGATGACTTTATG | 10529 |
| rs11012376 | snp | A/G | 0.176219 | 0.238865 | intron-variant | NEBL | GRCh38.p7 | 10:20894637 | AAGCCAGAATAggcc[A/G]ggcatggtggctcac | 10529 |
| rs11012377 | snp | C/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20894749 | gaaaccccgtctcta[C/G]taaaaaaaaaaaaaa | 10529 |
| rs11012378 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20900154 | GGCAAAATCTCTGTA[A/G]CTGCTCATAGCTTTT | 10529 |
| rs11012379 | snp | A/C | 0.206947 | 0.246265 | intron-variant | NEBL | GRCh38.p7 | 10:20902526 | AGGAAGTGAAAAACA[A/C]GAAACTGGAAATAGT | 10529 |
| rs11012381 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NEBL | GRCh38.p7 | 10:20906953 | ttatattttttccta[C/T]taagtctttaaaatc | 10529 |
| rs11012382 | snp | C/T | 0.234692 | 0.249531 | intron-variant | NEBL | GRCh38.p7 | 10:20907218 | CAATAAAGTCTACAA[C/T]CTGATTTTAATTTCC | 10529 |
| rs11012383 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | NEBL | GRCh38.p7 | 10:20908067 | ACCTATACCAGGTAC[C/T]GAGAAAAGGTACCAA | 10529 |
| rs11012384 | snp | G/T | 0.487558 | 0.0778863 | intron-variant | NEBL | GRCh38.p7 | 10:20909451 | GCCTCTAAGATATTG[G/T]ACACACAAATGAAGC | 10529 |
| rs11012385 | snp | C/T | 0.499017 | 0.0221427 | intron-variant | NEBL | GRCh38.p7 | 10:20909696 | AGCTAATGAAGATAA[C/T]TTACAGAATAACTCA | 10529 |
| rs11012387 | snp | A/C | 0.122411 | 0.214991 | intron-variant | NEBL | GRCh38.p7 | 10:20915364 | cacccactaactcag[A/C]atctagcattaggta | 10529 |
| rs11012388 | snp | A/C | | | intron-variant | NEBL | GRCh38.p7 | 10:20915604 | cattttttatggctg[A/C]atagtattccatggt | 10529 |
| rs11012389 | snp | C/T | 0.485731 | 0.0832509 | intron-variant | NEBL | GRCh38.p7 | 10:20917411 | TCACTGATATACCCA[C/T]TGGCGTCACAACAGA | 10529 |
| rs11012390 | snp | C/T | 0.483636 | 0.0889627 | intron-variant | NEBL | GRCh38.p7 | 10:20917474 | GCTGAAAGTTGAGAC[C/T]GTTCAGGGGATGTCT | 10529 |
| rs11012391 | snp | A/G | 0.482234 | 0.0925596 | intron-variant | NEBL | GRCh38.p7 | 10:20918448 | CATTACTCATCAGTA[A/G]TAGTGAAATAATAAA | 10529 |
| rs11012392 | snp | G/T | 0.168135 | 0.236216 | intron-variant | NEBL | GRCh38.p7 | 10:20919253 | AATTATGCAACGTAC[G/T]GGTTGAGAACATAGG | 10529 |
| rs11012393 | snp | A/G | | | intron-variant | NEBL | GRCh38.p7 | 10:20920466 | TGTCAAAATGTATAA[A/G]GCAGATTTCTGCATA | 10529 |
| rs11012394 | snp | C/G | 0.152334 | 0.230133 | intron-variant | NEBL | GRCh38.p7 | 10:20923823 | TGTTCTCTATCAACA[C/G]AAGGCAGACCCTTGA | 10529 |
| rs11012399 | snp | A/G | 0.030278 | 0.119257 | intron-variant | NEBL | GRCh38.p7 | 10:20929855 | TTACACTAAAAGCCC[A/G]GACTTCACCACTGTG | 10529 |
| rs11012400 | snp | A/G | 0.208779 | 0.246578 | intron-variant | NEBL | GRCh38.p7 | 10:20932372 | GGAGTTAAACAATGA[A/G]AACACATGGATACAA | 10529 |
| rs11012401 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | NEBL | GRCh38.p7 | 10:20933461 | GAAGAAggccgggtg[C/T]ggtggctcataccta | 10529 |
| rs11012403 | snp | C/G | 0.244205 | 0.249933 | intron-variant | NEBL | GRCh38.p7 | 10:20937679 | AGGGGTCAGGGAATT[C/G]CCTTTCCTAGTCAAA | 10529 |
| rs11012404 | snp | A/T | 0.207559 | 0.246371 | intron-variant | NEBL | GRCh38.p7 | 10:20938026 | GGGCAGGGCATAGCC[A/T]AACAAAAGGCAGCAG | 10529 |
| rs11012405 | snp | A/G | 0.48666 | 0.0805725 | intron-variant | NEBL | GRCh38.p7 | 10:20939599 | ATATTAACCTTAAAC[A/G]TAAATGGGCTAAATG | 10529 |
| rs11012408 | snp | C/T | 0.45889 | 0.13735 | intron-variant | NEBL | GRCh38.p7 | 10:20941689 | TCTAGAAAACCCCAT[C/T]GTCTCAGCCCAAAAC | 10529 |
| rs11012409 | snp | A/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20946902 | GGTTTTTTTGAATCG[A/T]TAATAGCTACTTCTG | 10529 |
| rs11012410 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | NEBL | GRCh38.p7 | 10:20948008 | GTATAAATCTCATAA[C/T]GTTTTAAGAAAGTTG | 10529 |
| rs11012411 | snp | A/G | 0.0696718 | 0.173152 | intron-variant | NEBL | GRCh38.p7 | 10:20948317 | ATAAAGCCTAGGATC[A/G]GAATCCAATATGCTA | 10529 |
| rs11012412 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20952738 | ggcgaaaccccattt[C/T]tactaaaaatacaaa | 10529 |
| rs11012413 | snp | C/T | 0.305436 | 0.243776 | intron-variant | NEBL | GRCh38.p7 | 10:20953912 | TATTCTAGGCATAAC[C/T]GATCTTGCATTGAAG | 10529 |
| rs11012414 | snp | A/G | 0.305186 | 0.243833 | intron-variant | NEBL | GRCh38.p7 | 10:20954003 | GACTGAAAAGTGGAT[A/G]GGATGGCAAACTCTT | 10529 |
| rs11012415 | snp | A/G | 0.305934 | 0.243663 | intron-variant | NEBL | GRCh38.p7 | 10:20954275 | TCACACAAGGCCAGG[A/G]GATTCACTCATCAAA | 10529 |
| rs11012416 | snp | A/G | 0.171704 | 0.237423 | intron-variant | NEBL | GRCh38.p7 | 10:20954836 | AATGGTAGCCTCTGA[A/G]CCAGTGTGGATGGGG | 10529 |
| rs11012417 | snp | C/T | 0.153332 | 0.230554 | intron-variant | NEBL | GRCh38.p7 | 10:20955001 | TTATCCTAAAGGCAG[C/T]AGAGAGACTTAACAG | 10529 |
| rs11012418 | snp | A/G | 0.136166 | 0.22258 | intron-variant | NEBL | GRCh38.p7 | 10:20955120 | TATTCCCACACTCCT[A/G]TCAAGGGGTAGGGAG | 10529 |
| rs11012419 | snp | C/T | 0.291493 | 0.246533 | intron-variant, utr-variant-5-prime | NEBL | GRCh38.p7 | 10:20958026 | CCCTTGAATGTCTGG[C/T]GATGGTTGTGCTTTG | 10529 |
| rs11012420 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20961638 | CAGAAATGCACATCA[A/G]AGCCATCATGCTATT | 10529 |
| rs11012421 | snp | A/G | 0.143622 | 0.226238 | intron-variant, upstream-variant-2KB | NEBL | GRCh38.p7 | 10:20962010 | ACCACTCTGTGCTCA[A/G]TGGTGTCATCTGTAC | 10529 |
| rs11012422 | snp | A/G | 0.338523 | 0.233803 | intron-variant | NEBL | GRCh38.p7 | 10:20964964 | ATGTGTTGTACACAC[A/G]TATGACAAGGCTCCC | 10529 |
| rs11012423 | snp | G/T | 0.143959 | 0.226396 | intron-variant | NEBL | GRCh38.p7 | 10:20968754 | ATTTCATACATTTCT[G/T]ATACAATGAAATCCA | 10529 |
| rs11012424 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20971447 | ATAGAATTTTTTTTT[C/T]TTTTTTTTTTTATTA | 10529 |
| rs11012425 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20971448 | TAGAATTTTTTTTTC[C/T]TTTTTTTTTTATTAT | 10529 |
| rs11012426 | snp | A/G | 0.143284 | 0.226079 | intron-variant | NEBL | GRCh38.p7 | 10:20971536 | GTGCCATGCTGGTGC[A/G]CTGCACCCACTAACT | 10529 |
| rs11012427 | snp | A/G | 0.389903 | 0.207189 | intron-variant | NEBL | GRCh38.p7 | 10:20972505 | ATCCCAGCACTTTGG[A/G]AGGCCAAGGTGGGCG | 10529 |
| rs11012428 | snp | C/T | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20973552 | ATCGCTCCCAGACTA[C/T]CATTTTTTTACATAG | 10529 |
| rs11012429 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20974250 | ATCGCTTAGtttttt[C/T]tcttttttttttttt | 10529 |
| rs11012430 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20974252 | CGCTTAGtttttttt[C/T]ttttttttttttttt | 10529 |
| rs11012431 | snp | G/T | | | intron-variant | NEBL | GRCh38.p7 | 10:20974261 | ttttttctttttttt[G/T]ttttttcttttagac | 10529 |
| rs11012432 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | NEBL | GRCh38.p7 | 10:20974298 | tcactctgttgccca[A/C/G]actggaatgcagtgg | 10529 |
| rs11012433 | snp | A/G | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20974518 | CCTCACAAAGTGCCG[A/G]AACTATAAGCATGAG | 10529 |
| rs11012434 | snp | C/T | 0.155987 | 0.23165 | intron-variant | NEBL | GRCh38.p7 | 10:20977017 | TCTGTAATACACATA[C/T]GTGAAGAGATACTGG | 10529 |
| rs11012435 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20977416 | TGACAGGCACATAAC[C/T]TTATCAAATTTCTAG | 10529 |
| rs11012436 | snp | A/G | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20977665 | CAATCAAAAGACCCC[A/G]CACTGGGGTGAAAAA | 10529 |
| rs11012437 | snp | C/T | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20977905 | AGCCTAACGTTCCTG[C/T]TCATCTCTAGGATTT | 10529 |
| rs11012438 | snp | A/G | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20978010 | AATTAATCTTAAAAT[A/G]TGGTATGAAACACAC | 10529 |
| rs11012439 | snp | A/T | 0.149999 | 0.229128 | intron-variant | NEBL | GRCh38.p7 | 10:20978014 | AATCTTAAAATGTGG[A/T]ATGAAACACACATCC | 10529 |
| rs11012440 | snp | C/T | 0.375 | 0.216506 | intron-variant | NEBL | GRCh38.p7 | 10:20978144 | AGTCAGCTAGGCAAT[C/T]CCCCAGCTAAAAGAC | 10529 |
| rs11012441 | snp | A/T | 0.150667 | 0.229419 | intron-variant | NEBL | GRCh38.p7 | 10:20978603 | CTCTAATAAAAATTT[A/T]AAAAAATTAGCCAGG | 10529 |
| rs11012442 | snp | A/G | 0.264358 | 0.249587 | intron-variant | NEBL | GRCh38.p7 | 10:20978860 | GAGGAGTATGTCTCC[A/G]TATCTACCCCTAGAA | 10529 |
| rs11012443 | snp | C/T | 0.293037 | 0.246268 | intron-variant | NEBL | GRCh38.p7 | 10:20978913 | AATAGCACAGTGAAA[C/T]CTGCAATCTAAATGT | 10529 |
| rs11012444 | snp | A/G | 0.269809 | 0.249214 | intron-variant | NEBL | GRCh38.p7 | 10:20979588 | GAGTAGAATTGCATC[A/G]TGAAATGCTTATCCC | 10529 |
| rs11012445 | snp | A/G | 0.356597 | 0.226135 | intron-variant | NEBL | GRCh38.p7 | 10:20979683 | TTAAGCAAACATAAT[A/G]TAACACAGTTTTTTT | 10529 |
| rs11012446 | snp | A/G | 0.356811 | 0.226034 | intron-variant | NEBL | GRCh38.p7 | 10:20980781 | TTGTTAACAAAAGTG[A/G]GACTGATTTTCTTTG | 10529 |
| rs11012447 | snp | A/C | 0.356811 | 0.226034 | intron-variant | NEBL | GRCh38.p7 | 10:20981048 | TACCACCTCAGCCTC[A/C]CAAAGTGCAGTGATT | 10529 |
| rs11012448 | snp | A/T | 0.267908 | 0.249358 | intron-variant | NEBL | GRCh38.p7 | 10:20981070 | GCAGTGATTATAGGC[A/T]TAAGCCACTGTGCCC | 10529 |
| rs11012449 | snp | A/G | 0.355096 | 0.226837 | intron-variant | NEBL | GRCh38.p7 | 10:20981194 | AACTTGATGTGTCCT[A/G]AAGATAGAGAACACA | 10529 |
| rs11012450 | snp | A/G | 0.155656 | 0.231515 | intron-variant | NEBL | GRCh38.p7 | 10:20981934 | GCCAATGACAATTGG[A/G]GTTGAGATATCTGGC | 10529 |
| rs11012451 | snp | C/T | 0.355525 | 0.226637 | intron-variant | NEBL | GRCh38.p7 | 10:20981955 | GATATCTGGCATTTC[C/T]AACAAAAAGAATTCC | 10529 |
| rs11012452 | snp | A/G | 0.0722614 | 0.17581 | intron-variant | NEBL | GRCh38.p7 | 10:20982010 | TGTTAGCATTAAAAC[A/G]TATCTCAATGGGTTT | 10529 |
| rs11012453 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | NEBL | GRCh38.p7 | 10:20982157 | GAAAATCCTAAACAG[C/T]GGGTACTCAAAAATC | 10529 |
| rs11012454 | snp | A/G | 0.108048 | 0.20579 | intron-variant | NEBL | GRCh38.p7 | 10:20982467 | TAAAAGTACACTATA[A/G]TATCACTAAAATGGT | 10529 |
| rs11012455 | snp | A/C | 0.350109 | 0.229081 | intron-variant | NEBL | GRCh38.p7 | 10:20983015 | CTGGAAGCTGATCTT[A/C]TAGGATGGGTAGGGT | 10529 |
| rs11012456 | snp | C/T | 0.349233 | 0.229462 | intron-variant | NEBL | GRCh38.p7 | 10:20983058 | CTAACCCTTGGGAAC[C/T]GAAGAGGGGAGTATG | 10529 |
| rs11012457 | snp | A/G | 0.301429 | 0.244653 | intron-variant | NEBL | GRCh38.p7 | 10:20983515 | TCCGTAAGTATTCCA[A/G]TTTTATTTGGCAATA | 10529 |
| rs11012458 | snp | C/T | 0.221737 | 0.248397 | intron-variant | NEBL | GRCh38.p7 | 10:20983789 | TCCAGGAAAATGCTA[C/T]ACATGACATGTACAA | 10529 |
| rs11012459 | snp | A/G | 0.344147 | 0.231595 | intron-variant | NEBL | GRCh38.p7 | 10:20983963 | AGTAATGACCCTAAT[A/G]TATCTATTTTGCAAA | 10529 |
| rs11012460 | snp | A/C | 0.327445 | 0.237702 | intron-variant | NEBL | GRCh38.p7 | 10:20986027 | TTACAAGCATGGAGA[A/C]TGGACGCTGCTCTAC | 10529 |
| rs11012461 | snp | A/G | 0.28578 | 0.247426 | intron-variant | NEBL | GRCh38.p7 | 10:20986398 | ATTCAGCAACTCTTC[A/G]CTTCCCTTCAAAATT | 10529 |
| rs11012462 | snp | A/T | 0.322721 | 0.23919 | intron-variant | NEBL | GRCh38.p7 | 10:20986424 | AAATTCCCAAAGTAC[A/T]TTTCAATTAGATCCT | 10529 |
| rs11012463 | snp | A/G | 0.152667 | 0.230274 | intron-variant | NEBL | GRCh38.p7 | 10:20987723 | AAGGCTAACTTCTGC[A/G]TGGTGAGGAAGAACT | 10529 |
| rs11012464 | snp | A/T | 0.149665 | 0.228982 | intron-variant | NEBL | GRCh38.p7 | 10:20987854 | CAATCCTCTGACATC[A/T]CTAGGACTTCCACTG | 10529 |
| rs11012465 | snp | C/G | 0.246485 | 0.249975 | intron-variant | NEBL | GRCh38.p7 | 10:20989679 | agaacaaagcagaag[C/G]cccagcaatagaacc | 10529 |
| rs11012466 | snp | A/T | 0.152667 | 0.230274 | intron-variant | NEBL | GRCh38.p7 | 10:20994009 | TAAACCACAGCCACA[A/T]AAACAACTGCAGCCA | 10529 |
| rs11012467 | snp | A/G | 0.150667 | 0.229419 | intron-variant | NEBL | GRCh38.p7 | 10:20994691 | ATAACATAAACAGTC[A/G]ATTAACACATAGTTA | 10529 |
| rs11012468 | snp | A/G | 0.308661 | 0.24302 | intron-variant | NEBL | GRCh38.p7 | 10:20995046 | CAAACACCTCTCCCA[A/G]AAGCCAACCACAGAC | 10529 |
| rs11012469 | snp | G/T | 0.170408 | 0.236992 | intron-variant | NEBL | GRCh38.p7 | 10:20995510 | GTGTAATTATGAGGG[G/T]ATTTGCAGCAGCACC | 10529 |
| rs11012470 | snp | A/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:20997528 | aaCAGAACTCCTGAA[A/G]AATTTAGGATTCGGA | 10529 |
| rs11012471 | snp | A/G | 0.304188 | 0.244057 | intron-variant | NEBL | GRCh38.p7 | 10:20999161 | CAGAGGTGTGTGGGG[A/G]GAAAAAAAAAAAAAA | 10529 |
| rs11012472 | snp | A/G | 0.326741 | 0.23793 | intron-variant | NEBL | GRCh38.p7 | 10:20999162 | AGAGGTGTGTGGGGG[A/G]AAAAAAAAAAAAAAA | 10529 |
| rs11012473 | snp | C/T | 0.312348 | 0.242101 | intron-variant | NEBL | GRCh38.p7 | 10:21000548 | CCCAGGTAAATGAGT[C/T]AAGCAGGAGACCAGC | 10529 |
| rs11012474 | snp | A/C | 0.417521 | 0.185571 | intron-variant | NEBL | GRCh38.p7 | 10:21001506 | AGGGAAAGAAACCCC[A/C]AGGAACATCATGCCA | 10529 |
| rs11012475 | snp | A/G | 0.164546 | 0.234942 | intron-variant | NEBL | GRCh38.p7 | 10:21001567 | GGAGGTAACTAACAC[A/G]CAATCCACAGGTGAA | 10529 |
| rs11012476 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | NEBL | GRCh38.p7 | 10:21003994 | ATCAAATGTGTATCA[C/T]GGCTAAAAATTCTGG | 10529 |
| rs11012477 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | NEBL | GRCh38.p7 | 10:21004126 | AGCATCAGATTGTTG[A/T]TTTTTTTAAACCATT | 10529 |
| rs11012478 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | NEBL | GRCh38.p7 | 10:21005710 | ctgcacttcagcctg[A/G]gtgacagagcaagtg | 10529 |
| rs11012479 | snp | C/G | 0.275197 | 0.248727 | intron-variant | NEBL | GRCh38.p7 | 10:21005798 | TCTACCCACCCATAA[C/G]TATAATCTGATACAA | 10529 |
| rs11012480 | snp | C/G | 0.0387552 | 0.1337 | intron-variant | NEBL | GRCh38.p7 | 10:21007046 | AAGAGTCACTTTGGG[C/G]TTTCTTTCAAAGAAA | 10529 |
| rs11012481 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | NEBL | GRCh38.p7 | 10:21008261 | TAGTCCCCTCTTATC[C/T]CTAGTTTCACTTTAC | 10529 |
| rs11012482 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | NEBL | GRCh38.p7 | 10:21011106 | CAGAACATTTTTGTA[C/G]TAAAATCAGAGACTA | 10529 |
| rs11012483 | snp | C/T | 0.402454 | 0.198136 | intron-variant | NEBL | GRCh38.p7 | 10:21011273 | CCAATAAAATCAAAG[C/T]GTATACAACAGGTCA | 10529 |
| rs11012484 | snp | C/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21012101 | AACTTTCATCTCTGA[C/G]CCTGCAGTCAGCAGA | 10529 |
| rs11012485 | snp | C/T | 0.388398 | 0.208197 | intron-variant | NEBL | GRCh38.p7 | 10:21012701 | TTAAAACATCCTCCT[C/T]GATAGATAGACTATA | 10529 |
| rs11012486 | snp | C/T | 0.346147 | 0.230772 | intron-variant | NEBL | GRCh38.p7 | 10:21013052 | TGACATTTTTGTCTC[C/T]TACATCATTTTATCC | 10529 |
| rs11012487 | snp | C/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21013552 | GAAGCAGTGTTTGTG[C/T]TTAGAAGTCTGAAGT | 10529 |
| rs11012488 | snp | A/G | 0.180383 | 0.240111 | intron-variant | NEBL | GRCh38.p7 | 10:21017893 | CAGTGGCACGATCTC[A/G]GCTCACTGCAACCTC | 10529 |
| rs11012489 | snp | C/T | 0.467744 | 0.122832 | intron-variant | NEBL | GRCh38.p7 | 10:21018657 | GAGACTACAGGCAAC[C/T]GCAACCTCCCCTGTG | 10529 |
| rs11012490 | snp | A/C/T | 0.0520825 | 0.152737 | intron-variant | NEBL | GRCh38.p7 | 10:21019031 | gactccgtTCTCCCA[A/C/T]CCCTCCCCCCAGAAA | 10529 |
| rs11012491 | snp | A/G | 0.2768 | 0.248559 | intron-variant | NEBL | GRCh38.p7 | 10:21019482 | AAAGACAGCTTCTTT[A/G]AAAGAGAGCACCCCA | 10529 |
| rs11012492 | snp | C/G | 0.46703 | 0.124089 | intron-variant | NEBL | GRCh38.p7 | 10:21019739 | GACGGGGTGTTAGCC[C/G]CACACACACTGCAAC | 10529 |
| rs11012493 | snp | A/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21028237 | atctcaaacatctca[A/T]aaaaaaaaaaaaaaa | 10529 |
| rs11012495 | snp | C/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21044270 | ggcgtggtggtgggc[C/G]cctgtaatcccagca | 10529 |
| rs11012496 | snp | A/G | 0.417683 | 0.185425 | intron-variant | NEBL | GRCh38.p7 | 10:21045982 | TAAGTGCCCGTCGGC[A/G]GATGAATGGATAAAA | 10529 |
| rs11012498 | snp | A/G | 0.474992 | 0.108989 | intron-variant | NEBL | GRCh38.p7 | 10:21058543 | ACAATGACAGTGTAG[A/G]TAAAGTTTTGTAGTG | 10529 |
| rs11012499 | snp | A/G | 0.474992 | 0.108989 | intron-variant | NEBL | GRCh38.p7 | 10:21058603 | CAACATTATTTAATG[A/G]CATGTTTATCAAATG | 10529 |
| rs11012500 | snp | C/G | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21063358 | ATGATACTTAATGCT[C/G]TAAGTTCCCAATTAA | 10529 |
| rs11012501 | snp | C/T | 0.419776 | 0.18351 | intron-variant | NEBL | GRCh38.p7 | 10:21067117 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 10529 |
| rs11012502 | snp | A/G | 0.118584 | 0.212673 | intron-variant | NEBL | GRCh38.p7 | 10:21070097 | AATACTGTATCCACT[A/G]GTAGCTGCAGGGGGA | 10529 |
| rs11012503 | snp | A/G | 0.285519 | 0.247464 | intron-variant | NEBL | GRCh38.p7 | 10:21071771 | TTTGCAGTTCCAAAG[A/G]TCAGAGGTCCAAAAT | 10529 |
| rs11012504 | snp | G/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21071813 | TAGTGTTGGGCTTTT[G/T]GTTTTTGATTTTGTC | 10529 |
| rs11012505 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | NEBL | GRCh38.p7 | 10:21073616 | agcaagactctgtcg[C/T]caaaaaaaaaaaaaa | 10529 |
| rs11012506 | snp | A/C | 0.250732 | 0.249999 | intron-variant | NEBL | GRCh38.p7 | 10:21074362 | CTGCCATTGGCTTCT[A/C]TGGGATTCCTAGAAA | 10529 |
| rs11012508 | snp | G/T | 0.202959 | 0.245534 | intron-variant | NEBL | GRCh38.p7 | 10:21074527 | CTCTGTTGCCCAGGC[G/T]GGAGTGCAGTGGTGA | 10529 |
| rs11012509 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | NEBL | GRCh38.p7 | 10:21074947 | tagctggaactacag[A/G]catgtaccaccatgc | 10529 |
| rs11012510 | snp | A/G | 0.0456336 | 0.143994 | intron-variant | NEBL | GRCh38.p7 | 10:21076375 | GCTTGAACCTGAGAG[A/G]CAGAGGTTGCAGTGA | 10529 |
| rs11012512 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | NEBL | GRCh38.p7 | 10:21078207 | CATGAGTACAAAATA[A/G]ACTCTTTCTAATGAC | 10529 |
| rs11012513 | snp | C/T | 0.191461 | 0.24305 | intron-variant | NEBL | GRCh38.p7 | 10:21078567 | CACACAGCCCCCATC[C/T]CTCAGTTTTTATAAA | 10529 |
| rs11012514 | snp | A/T | 0.311859 | 0.242226 | intron-variant | NEBL | GRCh38.p7 | 10:21079513 | AGGACTGGAGCTTCA[A/T]CCTTTTCTCCAAGTT | 10529 |
| rs11012515 | snp | C/T | 0.128288 | 0.218372 | intron-variant | NEBL | GRCh38.p7 | 10:21080105 | TAAAGCATAGAGAGA[C/T]GGTTCTGGTGGCTGT | 10529 |
| rs11012516 | snp | A/G | 0.0766824 | 0.180169 | intron-variant | NEBL | GRCh38.p7 | 10:21080981 | tgcctcagcctccca[A/G]gtagctgggtctaca | 10529 |
| rs11012517 | snp | C/T | 0.206947 | 0.246265 | intron-variant | NEBL | GRCh38.p7 | 10:21086078 | ACCAGGAGAATCTGG[C/T]GTTGTATTGGTGTAC | 10529 |
| rs11012518 | snp | A/C | 0.186421 | 0.24178 | intron-variant | NEBL | GRCh38.p7 | 10:21089305 | AGCTGGATCCCAGGC[A/C]TGAAGCTCAAGGTAA | 10529 |
| rs11012519 | snp | A/G | 0.192401 | 0.243274 | intron-variant | NEBL | GRCh38.p7 | 10:21089483 | GGGGAGCAAGAGCAC[A/G]TAGCCAAAGAGGTGG | 10529 |
| rs11012520 | snp | A/G | 0.142272 | 0.225598 | intron-variant | NEBL | GRCh38.p7 | 10:21089640 | AAAGCCTGGGTAAGG[A/G]GGGCAGGACTGGAGG | 10529 |
| rs11012521 | snp | A/G | 0.229723 | 0.249176 | intron-variant | NEBL | GRCh38.p7 | 10:21089693 | GAATGGGAAGCGGGG[A/G]GGCAGAGGCATCCTT | 10529 |
| rs11012522 | snp | C/T | | | intron-variant | NEBL | GRCh38.p7 | 10:21092992 | CACAGTATATTTTCT[C/T]TGATGTGGGAACAGT | 10529 |
| rs11012523 | snp | C/T | 0.248471 | 0.249995 | intron-variant | NEBL | GRCh38.p7 | 10:21096555 | GTCTCAGTCTGTCAC[C/T]CATGCTGGAGAGCAG | 10529 |
| rs11012524 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | NEBL | GRCh38.p7 | 10:21100870 | AACTATTATCCATTA[A/G/T]ATGATGATAACAAAT | 10529 |
| rs11012525 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | NEBL | GRCh38.p7 | 10:21105546 | GCTGTATAGTATTCC[A/G]TGGTGCATATGTGCC | 10529 |
| rs11012526 | snp | C/T | 0.182296 | 0.240658 | intron-variant | NEBL | GRCh38.p7 | 10:21108983 | TTCCTATTGGAATAC[C/T]GTTTATTTCTTTCTC | 10529 |
| rs11012527 | snp | A/G | 0.182296 | 0.240658 | intron-variant | NEBL | GRCh38.p7 | 10:21109260 | TACTGAGAGAATCAT[A/G]TGGTTTTTGTCATTG | 10529 |
| rs11012528 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NEBL | GRCh38.p7 | 10:21109395 | GTGCTGCTGGATTCA[A/G]TTTGCCAGTATTTTA | 10529 |
| rs11012529 | snp | A/G | 0.26326 | 0.249648 | intron-variant | NEBL | GRCh38.p7 | 10:21114504 | CTATTTGTTCTACCA[A/G]TTATCAAGAGTAAGG | 10529 |
| rs11012530 | snp | A/G | 0.187685 | 0.242109 | intron-variant | NEBL | GRCh38.p7 | 10:21115601 | TGCATTGTTTCCAAC[A/G]AGGAGTTCGCTCAAT | 10529 |
| rs11012531 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NEBL | GRCh38.p7 | 10:21116745 | CACAATCATAGCTCA[A/G]TGCAACCTCAAACTC | 10529 |
| rs11012532 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | NEBL | GRCh38.p7 | 10:21118640 | AAAAAAAAAACTATT[A/G]TTTGTTAGATGTATT | 10529 |
| rs11012533 | snp | C/G | | | intron-variant | NEBL | GRCh38.p7 | 10:21119085 | TCTACTCCAAAAATA[C/G]TTAATTCTGGATGAT | 10529 |
| rs11012534 | snp | A/T | 0 | 0 | intron-variant | NEBL | GRCh38.p7 | 10:21120422 | TATATATATATATAT[A/T]TAAATTTGATCACTG | 10529 |
| rs11012535 | snp | A/G | 0.366885 | 0.220993 | intron-variant | NEBL | GRCh38.p7 | 10:21122810 | GGAAAAGGGAAATGA[A/G]AGAAAGAACAGCAGC | 10529 |
| rs11012536 | snp | C/T | 0.369958 | 0.21934 | intron-variant | NEBL | GRCh38.p7 | 10:21123882 | GCTTATGTTATTTAG[C/T]AAATTTTTCATGTAA | 10529 |
| rs11012537 | snp | A/G | 0.190205 | 0.242744 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21126655 | AGATTAAGAGTGTCA[A/G]AGAGACACACAAGCC | 10529 |
| rs11012538 | snp | A/G | 0.194902 | 0.243853 | intron-variant | C10orf113, NEBL | GRCh38.p7 | 10:21128153 | AAAGGAAACACAAAC[A/G]GTAAATTTTTTTAAT | 10529 |