chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116946414116946415GA25GENICpossibly homozygous53306063
8116946637116946638CG9GENICpossibly homozygous53306064
8116948364116948365GT14GENIChomozygous53291594
8116948396116948397CT14GENICpossibly homozygous52829112
8116949515116949516TC17GENICpossibly homozygous52829114
8116949850116949851GA18GENIChomozygous53306065
8116955484116955485AG7GENICpossibly homozygous52829120
8116956461116956462TG20GENIChomozygous52829121
8116956977116956978CT12GENIChomozygous53222448
8116948524116948656GGAAGCTTCTTAAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAGTACCTA------------------------------------------------------------------------------------------------------------------------------------4GENIChomozygous53368046