chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155171000151710002CG11GENIChomozygous48307585
155171063151710632TG13GENIChomozygous48307586
155171089551710896TC27GENIChomozygous48307587
155171103151711032AG20GENIChomozygous48307588
155171156851711569AAGGGTTTGAGGATCTCTCCCCCATCCCATCTAGCTACCTTCTATAGGGGTGACCTTTTAAATCTACGCCCACCCT14GENIChomozygous49052874
155171189451711895AAT17GENIChomozygous48307589
155171255751712558CCT20GENICpossibly homozygous48307590