chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95277892152778922A-4GENICheterozygous745752425
95278047052780471T-11GENIChomozygous745752426
95278049652780497CT10GENICpossibly homozygous631719017
95278050652780507GGT5GENIChomozygous745752427
95278094052780941AG2GENIChomozygous631719018
95278104852781049AC3GENIChomozygous631719019
95278107352781074TC1GENIChomozygous631719020
95278214952782150TC17GENICpossibly homozygous631719021
95278282852782829CT27GENIChomozygous631719022
95278360252783603TC22GENIChomozygous631719023
95278409952784100AG12GENICheterozygous631719024