chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5140889027140889028CG8GENIChomozygous114031128
5140889822140889823GA26GENIChomozygous114031129
5140890257140890258AG20GENIChomozygous114031130
5140891222140891223AG14GENIChomozygous114031132
5140891391140891392CT21GENIChomozygous114031133
5140895798140895799CT22GENIChomozygous114031134
5140901941140901942AC16GENIChomozygous114031135
5140906242140906243GA18GENIChomozygous114031136
5140906504140906505TC26GENIChomozygous114031137
5140908025140908026GA39GENIChomozygous114031138
5140908075140908076GA39GENIChomozygous114031139
5140908117140908118AG28GENIChomozygous114031140
5140908873140908874AT20GENIChomozygous114031141
5140908881140908882AG15GENIChomozygous114031142
5140908907140908908GA16GENIChomozygous114031143