chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116504135116504136CA32GENIChomozygous116669511
8116504170116504172GG18GENIChomozygous132669870
8116504637116504637T44GENICheterozygous130568494
8116504680116504681TC55GENIChomozygous116669517
8116507184116507185GC46GENIChomozygous116669527
8116507503116507504CT42GENIChomozygous116669529
8116507959116507960GA55GENIChomozygous116669533
8116508127116508128TC65GENIChomozygous116669539
8116509777116509777T47GENICpossibly homozygous132669871
8116513068116513070GG15GENIChomozygous128635026
8116508533116508534CT56GENIChomozygous116988104
8116513983116513984TC53GENIChomozygous116988106
8116514226116514227AG44GENIChomozygous116669543
8116517942116517943TC68GENIChomozygous116886563
8116521963116521964TC62GENIChomozygous116669557
8116523522116523523GA53GENICpossibly homozygous116988107
8116523749116523750CT33GENIChomozygous116669561
8116524740116524741TA37GENIChomozygous116669563
8116526869116526870A55GENIChomozygous128635032
8116528281116528282GC43GENIChomozygous116669569
8116529295116529296A58GENIChomozygous132669872
8116529663116529664CG52GENIChomozygous117059070
8116529671116529672CG54GENIChomozygous116988109
8116531025116531028CTA48GENIChomozygous132669873
8116517926116517927T62GENICheterozygous130770185