chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176416778176416779AC31GENICpossibly homozygous934738983
3176417058176417059CT27GENIChomozygous934738984
3176417847176417848TA20GENIChomozygous934738985
3176420655176420656AT19GENIChomozygous934738986
3176421058176421059CT30GENIChomozygous934738987
3176423063176423064TC31GENIChomozygous934738988
3176423384176423385GA34GENIChomozygous934738989
3176423703176423704AG39GENIChomozygous934738990
3176424176176424177GA35GENIChomozygous934738991
3176426813176426814AG24GENIChomozygous934738992
3176430018176430019CG13GENIChomozygous934738993
3176430050176430051AC17GENIChomozygous934738994
3176430869176430870CA13GENIChomozygous934738995
3176431217176431218TC4GENIChomozygous934738996