chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
88189196181891962TC42GENIChomozygous506092264
88189237981892380AG36GENIChomozygous506092265
88189242981892430CT45GENICpossibly homozygous506092266
88189244081892441GA45GENICpossibly homozygous506092267
88189248581892486CT55GENIChomozygous506092268
88189248681892487CG52GENIChomozygous506092269
88189283281892833TC44GENIChomozygous506092270
88189287681892877AG40GENIChomozygous506092271
88189289581892896AC48GENIChomozygous506092272
88189302681893027GA42GENIChomozygous506092273
88189309981893100GA30GENICpossibly homozygous506092274
88189310581893106GGA31GENICheterozygous684232367
88189350781893508TTCCCTC12GENIChomozygous684232368
88189422781894228AG68GENIChomozygous506092275
88189431381894314CA67GENIChomozygous503406057
88189462481894626TT--9GENICheterozygous684232369
88189463781894638TG9GENICheterozygous506092276
88189468081894681GA6GENIChomozygous503406058
88189686981896870TC52GENIChomozygous506092277
88189747481897475CG39GENIChomozygous506092278
88189765181897652TC55GENIChomozygous506092279
88189767281897673TC62GENIChomozygous506092280
88189786281897863CT38GENICpossibly homozygous506092281