chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124069585940695860GA6GENIChomozygous115328579
124069586340695864CT6GENIChomozygous115328581
124069613340696134CA13GENIChomozygous115328583
124069615140696152GA14GENICpossibly homozygous115328585
124069621640696217TC17GENIChomozygous115328587
124069664840696649AT18GENIChomozygous115328589
124069688440696885AT25GENIChomozygous115328591
124069702040697021AC21GENICpossibly homozygous115328593
124069744640697447TC17GENIChomozygous115328595
124069746740697468CT17GENIChomozygous115328597
124069752440697525CA16GENIChomozygous115383945
124069805540698056GA4GENIChomozygous115328599
124069956440699565CA12GENIChomozygous115328601
124069961840699619TC17GENIChomozygous115328603
124070027840700279GT10GENIChomozygous115328605
124070065240700653CG21GENIChomozygous115383947
124070131740701318CA13GENIChomozygous115328607
124070156340701564GA18GENIChomozygous115328609
124070532540705326AG14GENIChomozygous115328611
124070656440706565TG11GENIChomozygous115383949
124070686040706861TG6GENIChomozygous115383951
124070728940707290CT10GENIChomozygous115494878
124070747640707477CT11GENIChomozygous115383953