chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145688324145688325TG48GENICpossibly homozygous112871372
4145688560145688561GA47GENIChomozygous112871373
4145691519145691520TC44GENIChomozygous112871374
4145692307145692308AG30GENICpossibly homozygous112871375
4145693646145693647CT44GENIChomozygous112871376
4145697005145697006TC64GENIChomozygous112871377
4145697239145697240TC40GENIChomozygous112871378
4145698268145698269AT37GENIChomozygous112871379
4145698409145698410GA41GENIChomozygous112871380
4145698560145698561TC33GENICpossibly homozygous112871381