chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170145407170145408AG43GENIChomozygous108374816
1170145613170145614TC19GENIChomozygous108374818
1170145989170145990CA28GENIChomozygous108374820
1170146620170146621AG20GENIChomozygous108374822
1170147462170147463GA29GENIChomozygous108374824
1170147476170147477AG27GENIChomozygous108374826
1170147647170147648AG45GENIChomozygous108374828
1170147708170147709CA38GENIChomozygous108374830
1170147783170147784CT39GENIChomozygous108374832
1170147899170147900CT51GENIChomozygous108374834
1170147968170147969CA63GENIChomozygous108374836
1170148074170148075CA80GENICpossibly homozygous108374839
1170148302170148303GA32GENIChomozygous108374841
1170148360170148361AG35GENIChomozygous108374843
1170148460170148461AG23GENIChomozygous108374845