chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159932269159932270AT28GENIChomozygous114358660
5159933947159933948CA23GENIChomozygous114358662
5159934252159934253CT18GENIChomozygous114160444
5159935564159935565TG28GENIChomozygous114160445
5159936882159936883TC33GENIChomozygous114073604
5159937100159937101AG14GENIChomozygous114160446
5159937645159937646TC40GENIChomozygous114073605
5159938097159938098CA44GENICheterozygous114160447
5159938314159938315TC14GENIChomozygous114073607
5159938591159938592TC28GENIChomozygous114073608
5159939161159939162GA25GENIChomozygous114160451
5159939327159939328CT27GENIChomozygous114358664
5159939921159939922CT28GENIChomozygous114073609
5159940114159940115AG23GENIChomozygous114073610
5159940919159940920AC39GENIChomozygous114073614
5159942951159942952TG20GENICheterozygous114358666
5159942980159942981TC27GENICheterozygous114358668
5159945939159945940CA29GENIChomozygous114073621
5159945943159945944TA29GENIChomozygous114073622
5159945948159945949GA26GENIChomozygous114073623
5159945949159945950CT26GENIChomozygous114073624
5159945953159945954CT27GENIChomozygous114073625
5159945991159945992CT33GENIChomozygous114073626
5159946459159946460GA33GENIChomozygous114358670