chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------10GENIChomozygous710403980
85378107053781071CT13GENIChomozygous567248064
85378121053781211AG17GENIChomozygous567248065
85378128753781288GGAA10GENICheterozygous710403983
85378128753781288GGAAA10GENICheterozygous710403984
85378133353781334AG11GENIChomozygous567248066
85378146653781467AG12GENIChomozygous567248067
85378180553781806AG21GENIChomozygous567248068
85378193153781932TTTTA10GENIChomozygous710403986
85378200853782013GTTTG-----11GENIChomozygous710403988
85378241353782414CT22GENIChomozygous567248069
85378260753782608TC36GENIChomozygous567248070
85378268153782682GGGTGT2GENIChomozygous710403989
85378277053782771GA14GENIChomozygous567248071
85378331953783320AG16GENIChomozygous567248072
85378340253783403T-9GENICpossibly homozygous710403990
85378373853783739GT28GENIChomozygous567248073
85378379353783794TC22GENIChomozygous567248074
85378391753783918T-17GENIChomozygous710403991
85378391953783926TGCGTGT-------18GENIChomozygous710403992
85378404853784049TC30GENIChomozygous567248075
85378550553785506T-3GENIChomozygous710403993
85378552153785522CCTTTT2GENIChomozygous710403995