chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141613295141613296CT57GENIChomozygous120676551
1141616134141616135CT63GENIChomozygous120676553
1141622465141622466AC58GENIChomozygous120676555
1141636052141636053CT42GENICpossibly homozygous120676557
1141636971141636972GA61GENIChomozygous120676559
1141639623141639623G6GENIChomozygous127438976
1141639624141639624TCAGT6GENIChomozygous127438977
1141639626141639626TAGAGCGCTTGCCTAGC6GENIChomozygous127438978
1141639629141639629CA3GENIChomozygous127438979
1141646156141646156C8GENIChomozygous131577781
1141646165141646166G11GENIChomozygous131577782
1141646177141646178T8GENIChomozygous131577783
1141646185141646187TC7GENIChomozygous131577784
1141646190141646191CG7GENIChomozygous131594343
1141646200141646202GC3GENIChomozygous131577785
1141646209141646210TA2GENIChomozygous131594344
1141646211141646212G2GENIChomozygous131577786
1141646218141646219G2GENIChomozygous131577787
1141654294141654295CA41GENIChomozygous108261404
1141654621141654622CT47GENIChomozygous120676561
1141640566141640567GA12GENIChomozygous133805447
1141647415141647416GA24GENIChomozygous133805448