chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113156116931561170TC63GENIChomozygous115811940
113156221331562214CG28GENICpossibly homozygous118141549
113156228131562282CA41GENIChomozygous115811944
113156321331563214TC58GENIChomozygous115811946
113156334531563346CT47GENIChomozygous115811948
113156420931564210CT44GENIChomozygous116109620
113156439431564395CG26GENIChomozygous118141550
113156458531564586TG37GENIChomozygous116096717
113156485531564856TA36GENIChomozygous115811954
113156529931565300GT52GENIChomozygous115811956
113156583531565836CT52GENICpossibly homozygous116129285
113156638831566389TG57GENIChomozygous115811968
113156647431566475TC81GENIChomozygous115811970
113156836231568363CT52GENIChomozygous115811972
113156930031569301AG83GENIChomozygous115811974
113157002531570026GA49GENICpossibly homozygous118141554
113157174131571742TC47GENIChomozygous115811978
113157268531572686GA65GENIChomozygous115811980
113157601431576015CA54GENIChomozygous115811984
113157656031576561CT46GENIChomozygous115811986
113157772131577722GA49GENIChomozygous115811988
113157808631578087AT63GENIChomozygous115811990
113157809931578100TA69GENIChomozygous115811992
113157810031578101AG68GENICpossibly homozygous115811994
113157813731578138CT74GENIChomozygous115811996
113158090931580910TC58GENICpossibly homozygous115960345
113158117831581179AG65GENIChomozygous115811998
113158139831581399TC52GENIChomozygous115812000
113158176331581764GA54GENIChomozygous115812002
113158227231582273TC52GENIChomozygous115812004
113158234031582341TG44GENIChomozygous115812006
113156599231565993CT54GENIChomozygous116035365
113158096631580967GA47GENICheterozygous118179917