chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146095904360959044GGA17INTERGENIChomozygous48746258
146095923660959237TC22INTERGENIChomozygous49115585
146096042160960422CCT17INTERGENICpossibly homozygous49005932
146096154560961546TC30INTERGENIChomozygous48746282
146096334260963343GA30INTERGENIChomozygous48746298
146096442160964422AG29INTERGENIChomozygous48746306
146096521460965215AAT18INTERGENICheterozygous49115586
146096744660967447CT23INTERGENIChomozygous49115587
146096790660967907AG24INTERGENIChomozygous48746320
146096850260968503C-27INTERGENIChomozygous49115588
146096902460969025AT26INTERGENIChomozygous48746324
146096992060969921AG28INTERGENIChomozygous49115589