chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141099486141099487TG23GENIChomozygous109327447
1141099701141099702GA30GENIChomozygous109327448
1141101245141101246AC17GENIChomozygous108260086
1141101421141101422GA19GENIChomozygous109327449
1141102193141102194CA12GENIChomozygous108260088
1141102413141102414AC10GENIChomozygous108260090
1141102901141102902CT23GENIChomozygous109327450
1141103600141103601AG19GENIChomozygous109327451
1141104542141104543AG20GENIChomozygous108260098
1141106043141106044CT26GENIChomozygous109327452
1141106076141106077TA29GENIChomozygous109327453
1141107668141107669GT10GENIChomozygous109327458
1141107707141107708TC12GENIChomozygous109327459
1141107758141107759AG21GENIChomozygous109327460
1141108119141108120CT13GENIChomozygous108260106
1141108415141108416GA22GENIChomozygous109327461
1141108916141108917GA22GENIChomozygous109327462
1141110129141110130CT29GENIChomozygous109327463
1141110595141110596CG20GENIChomozygous109327464
1141111118141111119CT16GENIChomozygous109327465