chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
23071130430711305AG24GENIChomozygous110501590
23071227330712274TG13GENIChomozygous110501592
23071521030715211GA19GENIChomozygous110501594
23071586630715867CT14GENIChomozygous110501596
23071861330718614AG25GENIChomozygous110501598
23071911330719114GA30GENIChomozygous110501600
23071950730719508AC15GENIChomozygous110501602
23071960930719610TC28GENIChomozygous110501604
23072054330720544AG22GENIChomozygous110501606
23072209330722094GA21GENIChomozygous110501608
23072209430722095CG21GENIChomozygous110501610
23072211330722114TC24GENIChomozygous110501612
23072384630723847GA30GENIChomozygous110501614
23072422530724226GT21GENIChomozygous110501616
23072425130724252CT23GENIChomozygous110501618
23072438130724382CG12GENIChomozygous110501620
23072441030724411CT13GENIChomozygous110501622
23072740630727407AG18GENIChomozygous110501632
23072783730727838CT28GENIChomozygous110501634
23072962230729623GA14GENIChomozygous110501636
23073063930730640AG27GENIChomozygous110501638
23073071630730717GA22GENIChomozygous110501640
23073090730730908GA25GENIChomozygous110501642
23073109430731095AG23GENIChomozygous110501644
23073285130732852CT24GENIChomozygous110501648
23073316130733162TG24GENIChomozygous110501654
23073361830733619AG22GENIChomozygous110501656
23073390930733910GA17GENIChomozygous110501658
23073472430734725GC25GENIChomozygous110501660