chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113156116931561170TC16GENIChomozygous115811940
113156321331563214TC27GENIChomozygous115811946
113156334531563346CT41GENIChomozygous115811948
113156458531564586TG19GENIChomozygous116096717
113156463731564638GC32GENIChomozygous116096719
113156484131564842GC24GENIChomozygous115811950
113156484331564844AG26GENIChomozygous115811952
113156485531564856TA27GENIChomozygous115811954
113156529931565300GT22GENIChomozygous115811956
113156572531565726CA31GENIChomozygous115811962
113156572631565727AC32GENIChomozygous115811964
113156602231566023CA15GENICheterozygous115811966
113156638831566389TG24GENIChomozygous115811968
113156647431566475TC23GENIChomozygous115811970
113156836231568363CT19GENIChomozygous115811972
113156930031569301AG37GENIChomozygous115811974
113157174131571742TC27GENIChomozygous115811978
113157268531572686GA24GENIChomozygous115811980
113157601431576015CA19GENIChomozygous115811984
113156599231565993CT19GENIChomozygous116035365
113157656031576561CT29GENIChomozygous115811986
113157772131577722GA25GENIChomozygous115811988
113157808631578087AT23GENIChomozygous115811990
113157809931578100TA24GENIChomozygous115811992
113157810031578101AG23GENIChomozygous115811994
113157813731578138CT32GENIChomozygous115811996
113158117831581179AG34GENIChomozygous115811998
113158139831581399TC40GENIChomozygous115812000
113158176331581764GA27GENIChomozygous115812002
113158227231582273TC24GENIChomozygous115812004
113158234031582341TG19GENIChomozygous115812006
113158090931580910TC24GENIChomozygous115960345