chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152473554624735547CT16GENICpossibly homozygous48479689
152473591624735917TC16GENIChomozygous48479691
152473633924736340CT10GENICpossibly homozygous48479693
152473692224736923TC7GENIChomozygous48479695
152474483724744838AG13GENICpossibly homozygous48479709
152474616824746169AG15GENIChomozygous48479713
152474627324746274TG18GENIChomozygous48479715
152474778924747790TC2GENIChomozygous48479717
152474779824747799CG6GENIChomozygous48479719
152474803424748036TT--1GENIChomozygous48570958
152474862924748630GC16GENIChomozygous48479725
152474890624748907GA13GENIChomozygous48479727
152474903724749038TA1GENIChomozygous49359013
152474903924749040TA1GENIChomozygous49359014