chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116928822116928823AC10GENIChomozygous938500598
7116930571116930572TC21GENIChomozygous938500599
7116930950116930951TC16GENIChomozygous938500600
7116931640116931641TC23GENIChomozygous938500601
7116932522116932523GA22GENIChomozygous938500602
7116932532116932533GA25GENIChomozygous938500603
7116933057116933058AT22GENIChomozygous938500604
7116933972116933973AG13GENIChomozygous938500605
7116934411116934412GA26GENIChomozygous938500606
7116935780116935781GT11GENIChomozygous938500607
7116937285116937286GT17GENIChomozygous938500608
7116939739116939740TG28GENIChomozygous938500609
7116941317116941318TC21GENIChomozygous938500610
7116941522116941523AG32GENIChomozygous938500611
7116941528116941529TA31GENIChomozygous938500612
7116941529116941530CA32GENIChomozygous938500613
7116941720116941721CA17GENIChomozygous938500614
7116941721116941722TG17GENIChomozygous938500615