chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116504135116504136CA38GENIChomozygous116669511
8116504680116504681TC52GENIChomozygous116669517
8116506076116506077AG68GENICpossibly homozygous116886557
8116506258116506259TC47GENIChomozygous116886559
8116507184116507185GC75GENIChomozygous116669527
8116507503116507504CT84GENIChomozygous116669529
8116507959116507960GA54GENIChomozygous116669533
8116508127116508128TC67GENIChomozygous116669539
8116508722116508723GA65GENICheterozygous116886561
8116511287116511288TC28GENIChomozygous116669541
8116514226116514227AG68GENIChomozygous116669543
8116517942116517943TC53GENICheterozygous116886563
8116521963116521964TC66GENIChomozygous116669557
8116523749116523750CT21GENIChomozygous116669561
8116524740116524741TA51GENIChomozygous116669563
8116528281116528282GC45GENICpossibly homozygous116669569