chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167472417974724180TC60GENICpossibly homozygous112079456
167472418674724187AT64GENICpossibly homozygous112079458
167472563774725638CT38GENIChomozygous112079460
167472679474726795TC13GENICheterozygous119222709
167472680074726801AC13GENICheterozygous119222710
167472933274729333TC58GENIChomozygous111861647
167473142774731428CT22GENIChomozygous119129695
167473142874731429GA22GENIChomozygous119129697
167473151674731517TC44GENIChomozygous111861651
167473202674732027CT28GENICpossibly homozygous112079462
167473202774732028AG29GENICpossibly homozygous111861652
167473206674732067AG37GENIChomozygous112079464
167473211774732118AG36GENIChomozygous111861653
167473224374732244AG48GENIChomozygous112032774
167473277774732778TC55GENIChomozygous111861659
167473393174733932GA21GENICheterozygous119222711
167473450174734502GT37GENIChomozygous112079466
167473484674734847GT16GENIChomozygous119129704
167473484974734850AG14GENIChomozygous119129706
167473582874735829TC43GENICpossibly homozygous111861665
167473925774739258CT36GENIChomozygous111861673
167472992374729924TC36GENICpossibly homozygous119210787
167473392574733926GA21GENICheterozygous112252790
167473403974734040GA17GENIChomozygous112212834
167474089474740895GT46GENIChomozygous111861680
167474287974742880GC40GENICpossibly homozygous112079468
167474353774743538AG20GENIChomozygous111861682
167474365374743654GA24GENIChomozygous111861683
167474100174741002TG18GENICheterozygous112132615