chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1114392258114392259AG13GENIChomozygous120872070
1114394540114394541TA24GENIChomozygous108188445
1114397453114397454GA8GENIChomozygous108188448
1114398549114398550GT9GENIChomozygous108188451
1114398812114398813GA10GENIChomozygous120872071
1114399222114399223CT15GENIChomozygous108188452
1114399595114399596GT5GENICheterozygous108737353
1114400744114400745CT24GENIChomozygous120872072
1114403633114403634CA6GENIChomozygous108188454
1114404017114404018CT13GENIChomozygous120872073
1114404336114404337GA11GENIChomozygous120872074
1114404455114404456GA16GENIChomozygous125486357
1114405303114405304TC12GENIChomozygous120872075
1114406173114406174TC22GENIChomozygous108188456
1114406842114406843GA15GENIChomozygous120872076
1114408292114408293AG16GENIChomozygous108188458
1114408372114408373TC19GENIChomozygous108188459
1114410204114410205TA22GENIChomozygous108188460
1114410262114410263TC21GENIChomozygous108188461
1114411798114411799GA10GENIChomozygous108188462
1114412657114412658AG15GENIChomozygous108188464
1114417638114417639TC6GENIChomozygous108188465