chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124688028946880290TC47GENIChomozygous115511796
124688345246883453GC46GENIChomozygous115342657
124688365146883652TC29GENIChomozygous115397205
124688375446883755TC21GENIChomozygous118272518
124688461746884618GA44GENIChomozygous115511797
124688522946885230GA36GENICheterozygous118272521
124688523446885235CT40GENICheterozygous118272522
124688650146886502TG70GENIChomozygous118366249
124688756646887567CT41GENIChomozygous115511798
124688777246887773AG46GENIChomozygous118366250
124688778046887781AG42GENIChomozygous118366251
124688866946888670GC8GENIChomozygous118272523
124688867546888676CT8GENIChomozygous118272524
124688870546888706AG13GENIChomozygous118272525
124688908046889081GT60GENIChomozygous115397211
124688911646889117GA58GENIChomozygous115397213
124688929246889293TC42GENIChomozygous115342671
124688960246889603AG57GENIChomozygous115480594
124688967746889678GA47GENIChomozygous115342673