chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
374243677424368AG19GENIChomozygous111440577
374276487427649CT15GENIChomozygous111440578
374316097431610TC23GENIChomozygous111440580
374341097434110AG23GENIChomozygous111440581
374372247437225CT26GENIChomozygous111440582
374374297437430GT25GENIChomozygous111440583
374387527438753AG15GENIChomozygous111440584
374411947441195TC20GENIChomozygous111440585
374441597444160AC10GENIChomozygous111440586
374445227444523TC12GENIChomozygous111440587
374452577445258CA19GENIChomozygous111440588
374464317446432AG22GENIChomozygous111440589
374484397448440GA29GENIChomozygous111440591
374494597449460AG24GENIChomozygous111440592
374498907449891AG22GENIChomozygous111440593
374529157452916AT37GENIChomozygous111440594
374543947454395AG24GENIChomozygous111440596
374544487454449TG14GENIChomozygous111440597
374547317454732GA18GENIChomozygous111440598
374584937458494AG17GENIChomozygous111440599
374588327458833CG12GENIChomozygous111440600
374600527460053GT16GENIChomozygous111440601
374619407461941AG18GENIChomozygous111440602
374647047464705CG12GENIChomozygous111440604
374691407469141CT26GENIChomozygous111440605
374699737469974CA18GENIChomozygous111440606
374703267470327GT15GENIChomozygous111440607
374705907470591GA13GENIChomozygous111440608
374759047475905CT12GENIChomozygous111440611
374763697476370TG10GENIChomozygous111440612
374763707476371TA11GENIChomozygous111440613
374775397477540GA12GENIChomozygous111440614
374780567478057CA31GENIChomozygous111440615
374794807479481TG21GENIChomozygous111440616
374797247479725TA23GENIChomozygous111440617
374799277479928AG24GENIChomozygous111440618
374813607481361TC21GENIChomozygous111440619
374826117482612TC15GENIChomozygous111440620
374826817482682GA26GENIChomozygous111440621
374827007482701AT29GENIChomozygous111440622
374862947486295GT20GENIChomozygous111440623
374870057487006AG16GENIChomozygous111440624
374877037487704GA10GENIChomozygous111440625