chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
72453571524535716CT13GENIChomozygous115619022
72458721524587216TC8GENIChomozygous126515338
72459155324591554AG35GENIChomozygous115619079
72459383024593831AG23GENIChomozygous115619082
72459571824595719CA17GENIChomozygous115619083
72459718724597188GA24GENIChomozygous115619084
72459954324599544GA28GENIChomozygous115619085
72460074624600747AG15GENIChomozygous115619086
72460267524602676AC17GENIChomozygous115619088
72460651124606512GA21GENIChomozygous115619089
72461072324610724GT26GENICpossibly homozygous126515340
72461173124611732AG4GENICheterozygous116124937
72461218524612186GA15GENIChomozygous115619091
72461273124612732GA18GENIChomozygous115619092
72461289024612891TC12GENIChomozygous115619093
72461628524616286GA25GENIChomozygous115619094
72461980024619801GC29GENIChomozygous115619095
72462233924622340TC18GENIChomozygous126515344
72462238324622384TG12GENIChomozygous126515346
72462807524628076GA25GENIChomozygous115619097
72463258424632585CT11GENIChomozygous115619099
72462848424628485CT19GENIChomozygous115619098
72463182524631826AG9GENIChomozygous116324251
72457403024574031AG8GENIChomozygous126595626
72461134524611346TA5GENICheterozygous126595627
72462478824624789CT6GENICheterozygous126595628
72463294224632943CA13GENIChomozygous115619100