chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176416778176416779AC22GENIChomozygous798099409
3176417058176417059CT29GENIChomozygous798099410
3176417847176417848TA24GENIChomozygous798099411
3176417978176417979GA23GENICpossibly homozygous798099412
3176420334176420335CT39GENICheterozygous798099413
3176420655176420656AT27GENIChomozygous798099414
3176421058176421059CT30GENIChomozygous798099415
3176423063176423064TC30GENIChomozygous798099416
3176423384176423385GA23GENIChomozygous798099417
3176423703176423704AG18GENIChomozygous798099418
3176424176176424177GA32GENIChomozygous798099419
3176426813176426814AG39GENIChomozygous798099420
3176430018176430019CG31GENIChomozygous798099421
3176430050176430051AC26GENIChomozygous798099422
3176430869176430870CA50GENIChomozygous798099423
3176431217176431218TC42GENIChomozygous798099424