chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126196656126196657GA15GENIChomozygous113996640
5126198484126198485GT9GENIChomozygous113996642
5126198694126198695AG18GENIChomozygous113996644
5126200159126200160AG5GENICheterozygous126260257
5126206686126206687AT11GENIChomozygous113996652
5126208062126208063CT22GENIChomozygous113996654
5126208247126208248GT13GENIChomozygous113996656
5126208411126208412GA15GENIChomozygous113996658
5126208590126208591TA14GENIChomozygous113996660
5126209139126209140GA29GENIChomozygous113996662
5126209608126209609AG5GENIChomozygous113996664
5126209611126209612GA6GENIChomozygous113996666
5126209708126209709GA6GENIChomozygous113996670
5126209715126209716GC5GENIChomozygous113996672
5126209768126209769CA16GENIChomozygous113996674
5126210065126210066TA20GENIChomozygous113996675
5126210514126210515AG21GENIChomozygous113996677
5126210631126210632TA25GENIChomozygous113996679
5126210873126210874TC16GENIChomozygous113996681
5126211601126211602CA10GENIChomozygous113996683
5126212657126212658CT9GENIChomozygous113996685
5126215100126215101GA8GENIChomozygous113996689
5126216747126216748CT14GENIChomozygous113996691
5126218232126218233CT20GENIChomozygous113996693
5126219108126219109AC14GENIChomozygous113996695
5126219778126219779TC14GENIChomozygous113996697
5126220266126220267CT27GENIChomozygous113996699
5126220467126220468AC39GENIChomozygous113996701