chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116946414116946415GA19GENICpossibly homozygous53306063
8116946637116946638CG8GENICheterozygous53306064
8116948364116948365GT19GENICpossibly homozygous53291594
8116948396116948397CT14GENIChomozygous52829112
8116949515116949516TC19GENICheterozygous52829114
8116949850116949851GA20GENICpossibly homozygous53306065
8116955484116955485AG10GENICpossibly homozygous52829120
8116956461116956462TG17GENICpossibly homozygous52829121
8116956977116956978CT15GENICheterozygous53222448
8116948524116948656GGAAGCTTCTTAAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAGAACCAAAAAAAAAAAAAAAAAAAAGTACCTA------------------------------------------------------------------------------------------------------------------------------------4GENIChomozygous53368046