chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087252670872527G-13GENICheterozygous51689606
107087252670872527GGT13GENICheterozygous51689608
107087280470872805AG37GENIChomozygous51489542
107087283870872839CCT23GENIChomozygous51689610
107087387570873876AG56GENIChomozygous51489543
107087387870873879TC53GENIChomozygous51489544
107087439870874399CA50GENIChomozygous51689612
107087453870874539G-36GENIChomozygous51689614
107087497670874977AG60GENIChomozygous51489546
107087519170875192GGTTT5GENICheterozygous51489548
107087519170875192GGTT5GENICheterozygous51489549
107087529370875294CT35GENIChomozygous51689616
107087529570875296GA36GENIChomozygous51689618
107087540170875402AG48GENIChomozygous51489550
107087553670875538GT--27GENICheterozygous51489552
107087616670876167GA44GENIChomozygous51689620
107087630770876308AG44GENIChomozygous51489555
107087637770876378CCAGG45GENIChomozygous51489556
107087658870876589TA65GENIChomozygous51489557
107087679170876792AAG63GENIChomozygous51489558
107087721770877218AG42GENIChomozygous51689622
107087727970877280GA42GENIChomozygous51489559
107087770770877708AT57GENIChomozygous51689624
107087835670878357GGA28GENICpossibly homozygous51689626
107087928870879289AC55GENIChomozygous51689628
107088013870880140AA--4GENIChomozygous51489566
107088016170880162AG43GENIChomozygous51489567
107088079870880799GA62GENICpossibly homozygous51689630
107088349970883501AA--26GENIChomozygous51689632
107088358470883585AT16GENICheterozygous51489571
107088369570883696TG29GENIChomozygous51689634
107088531070885311TC46GENIChomozygous51689636
107088584370885850TTGTGTC-------35GENICheterozygous51489574
107088584370885844TTG40GENIChomozygous51489575
107088584470885845T-35GENICheterozygous51689638
107088258470882585GT40GENICheterozygous51911655