chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3151513746151513747CT18GENIChomozygous119998398
3151519994151519995GC25GENIChomozygous111777676
3151522593151522594A19GENICpossibly homozygous127943658
3151527834151527836CC23GENIChomozygous127943659
3151528785151528786AG18GENIChomozygous111777692
3151530256151530257CT24GENIChomozygous111777694
3151531761151531762TC20GENIChomozygous111777696
3151535190151535191AG19GENIChomozygous111777698
3151541015151541016AG22GENIChomozygous111777700
3151543171151543172AG20GENIChomozygous111777702
3151519404151519405TC21GENIChomozygous112041862