chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151519051151519052GC41GENICheterozygous134126494
3151519404151519405TC56GENIChomozygous112041862
3151519994151519995GC55GENIChomozygous111777676
3151522593151522594A44GENIChomozygous127943658
3151527834151527836CC50GENICpossibly homozygous127943659
3151528785151528786AG58GENIChomozygous111777692
3151530256151530257CT49GENIChomozygous111777694
3151531761151531762TC70GENIChomozygous111777696
3151535190151535191AG65GENIChomozygous111777698
3151541015151541016AG54GENIChomozygous111777700
3151543171151543172AG67GENIChomozygous111777702