chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4180961389180961390GT35GENICpossibly homozygous113566951
4180961709180961710CT40GENIChomozygous113566952
4180961893180961894GA44GENICpossibly homozygous113566953
4180962287180962288AG24GENIChomozygous113566954
4180962324180962325AC29GENICpossibly homozygous113566955
4180962776180962777CA52GENICpossibly homozygous113566956
4180963040180963041GT59GENICheterozygous113566957
4180963092180963093TC60GENIChomozygous113566958
4180963671180963672AG51GENIChomozygous113566959
4180963847180963848AG57GENIChomozygous113566960
4180964777180964778CT21GENICheterozygous113566961
4180965306180965307TC44GENIChomozygous113566962
4180965914180965915GA41GENIChomozygous113566963
4180966050180966051CT32GENICpossibly homozygous113566964
4180966884180966885GA49GENIChomozygous113566965
4180967390180967391CT66GENIChomozygous113566966
4180967435180967436GT56GENIChomozygous113566967
4180967722180967723AG49GENIChomozygous113566968
4180967923180967924GC59GENIChomozygous113566969
4180967996180967997CT66GENICheterozygous112975955
4180968032180968033AG56GENICheterozygous112975960
4180968045180968046AT65GENICheterozygous112975961
4180968059180968060GA60GENICheterozygous112975962
4180968060180968061TA59GENICheterozygous112975963
4180968082180968083CT52GENICheterozygous112975964
4180968087180968088CT50GENICheterozygous112975965
4180968104180968105TC48GENICheterozygous113069076