chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7114819561114819562TC18GENIChomozygous115835542
7114819710114819711AG14GENIChomozygous115835544
7114822415114822416TC5GENIChomozygous115835548
7114824800114824801CT10GENIChomozygous115835560
7114831751114831752AG17GENIChomozygous115835566
7114831862114831863TC11GENIChomozygous115835568
7114833291114833292AG18GENIChomozygous115835570
7114833401114833402AG11GENIChomozygous115835572
7114833547114833548GA13GENIChomozygous115835574
7114833725114833726GA21GENIChomozygous115835576
7114834759114834760CT12GENIChomozygous115835578
7114835019114835020TC4GENIChomozygous115835580
7114836863114836864GA13GENIChomozygous115835582
7114837653114837654TC11GENIChomozygous115835584
7114837823114837824CT20GENIChomozygous115835586
7114839050114839051TC9GENIChomozygous115835590
7114839065114839066TC17GENIChomozygous115835592
7114839118114839119GA11GENIChomozygous115835594
7114839510114839511CT5GENIChomozygous115835596
7114839640114839641TC4GENIChomozygous115835600
7114840116114840117AC10GENIChomozygous115835602
7114844051114844052GA13GENIChomozygous115835606
7114855437114855438GA11GENIChomozygous115835610
7114855479114855480CT17GENIChomozygous115835612
7114858027114858028GA22GENIChomozygous115835614
7114861045114861046TC13GENIChomozygous115835616
7114862036114862037AG12GENIChomozygous115835620
7114870973114870974CT10GENIChomozygous115835628
7114876892114876893TC23GENIChomozygous115835632