chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141614109141614110GA50GENIChomozygous109327679
1141614630141614631CA53GENIChomozygous109327682
1141614795141614796CT64GENIChomozygous109327683
1141614809141614810GA64GENIChomozygous109327684
1141614821141614822TC60GENIChomozygous108937013
1141615466141615467CT58GENICpossibly homozygous109327685
1141615671141615672CA61GENICpossibly homozygous109327686
1141616415141616416TA46GENIChomozygous109327687
1141616974141616975CT54GENIChomozygous108937023
1141618503141618504GA55GENIChomozygous109327688
1141619858141619859CA56GENIChomozygous132001963
1141621204141621205GA42GENIChomozygous109327689
1141622163141622164TA62GENIChomozygous109327690
1141622662141622663TC43GENIChomozygous108937038
1141622879141622880GA50GENICpossibly homozygous109327691
1141623775141623776GA57GENIChomozygous109327692
1141624426141624427TC30GENIChomozygous108937041
1141630931141630932CT45GENIChomozygous108261386
1141633222141633223AG29GENICpossibly homozygous109327693
1141639334141639335GA1GENIChomozygous108261390
1141639623141639623G11GENIChomozygous127438976
1141639624141639624TCAGT11GENIChomozygous127438977
1141639626141639626TAGAGCGCTTGCCTAGC10GENIChomozygous127438978
1141639629141639629CA8GENIChomozygous127438979
1141645663141645663GTGCTCCCA6GENICheterozygous132264613
1141646190141646191CG5GENIChomozygous131594343
1141646200141646202GC5GENIChomozygous131577785
1141646156141646156C9GENIChomozygous131577781
1141646165141646166G8GENIChomozygous131577782
1141646177141646178T5GENIChomozygous131577783
1141646185141646187TC5GENIChomozygous131577784
1141646209141646210TA5GENIChomozygous131594344
1141646211141646212G5GENIChomozygous131577786
1141646218141646219G4GENIChomozygous131577787
1141654294141654295CA42GENIChomozygous108261404