chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199555566199555567TA28GENIChomozygous108501059
1199556330199556331CT24GENIChomozygous108501061
1199556716199556717TC24GENIChomozygous108501063
1199557409199557410AC35GENIChomozygous108501065
1199557450199557451CA39GENIChomozygous108501067
1199557704199557705AG37GENIChomozygous108501069
1199557918199557919TC33GENIChomozygous108501071
1199557993199557994CA26GENIChomozygous108501073
1199558171199558172AG31GENIChomozygous108501077
1199558392199558393GA44GENIChomozygous108501079
1199558425199558426TC42GENIChomozygous108501081
1199558484199558485GA33GENIChomozygous108501083
1199559274199559275GA42GENIChomozygous108501085
1199559696199559697TC34GENIChomozygous108501087
1199560025199560026CT31GENIChomozygous108501089
1199561029199561030CT33GENIChomozygous108501091
1199561138199561139GA37GENIChomozygous108501093
1199563299199563300CT30GENIChomozygous108501095
1199566312199566313AG38GENIChomozygous108501097
1199566476199566477AG40GENIChomozygous108501099
1199566724199566725AG27GENIChomozygous108501101
1199567746199567747CT39GENIChomozygous108501103
1199567763199567764AG39GENIChomozygous108501105
1199568301199568302AG31GENIChomozygous108501108
1199569298199569299CA23GENIChomozygous108501110
1199570052199570053CA33GENIChomozygous108501112
1199571553199571554CG19GENIChomozygous108501114
1199571689199571690CA36GENIChomozygous108501116
1199571841199571842GA27GENIChomozygous108501118
1199572386199572387TC32GENIChomozygous120475413
1199573524199573525GA34GENIChomozygous108501130