chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117605048117605049AC43GENIChomozygous115847689
7117605199117605200AG45GENIChomozygous115847691
7117605314117605315CT39GENIChomozygous115847693
7117605350117605351GA41GENIChomozygous115847695
7117607063117607064GA48GENIChomozygous115847697
7117607217117607218AG42GENIChomozygous115847699
7117607304117607305CT43GENIChomozygous115847701
7117607433117607434AT42GENIChomozygous115847703
7117607742117607743CT37GENIChomozygous115847705
7117607800117607801GT34GENIChomozygous115847707
7117608005117608007AA49GENICpossibly homozygous128510635
7117608106117608107CT49GENIChomozygous115847709
7117608165117608166CG37GENIChomozygous115847711
7117608170117608171AG34GENIChomozygous115847713