chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
557102065710207GA33GENICpossibly homozygous113631963
557103375710338GA31GENIChomozygous113631964
557104325710433GA32GENIChomozygous114166943
557106945710695AG25GENIChomozygous113631965
557111015711102TG23GENIChomozygous113631966
557114625711463GT36GENIChomozygous113631968
557116105711611AC42GENIChomozygous113631969
557116915711692CT45GENICpossibly homozygous113631970
557125475712548GA40GENIChomozygous113631971
557126035712604CT41GENIChomozygous113631972
557126725712673GA39GENIChomozygous113631973
557134905713491GA35GENIChomozygous113631974
557136605713661AG49GENIChomozygous113631975
557138865713887AT36GENICpossibly homozygous113631976
557143565714357AT33GENICpossibly homozygous113631977
557151415715142GA47GENIChomozygous113631978
557157565715757GA34GENIChomozygous113631979
557158715715872CT25GENICheterozygous113631980
557160725716073CT22GENIChomozygous113631981
557163595716360GT23GENIChomozygous114385761
557165115716512CA31GENIChomozygous113631982
557167525716753AG27GENIChomozygous113631983
557184075718408AG37GENIChomozygous113631984
557220215722022AT14GENIChomozygous113631985
557290835729084GC18GENIChomozygous113631986
557294985729499GA23GENIChomozygous113631987
557296495729650TC42GENIChomozygous113631988
557300675730068TC43GENIChomozygous113631989
557302475730248AG29GENIChomozygous113631990
557191345719135TG3GENIChomozygous114106438