chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------10GENIChomozygous52634727
85378107053781071CT13GENIChomozygous52634729
85378121053781211AG17GENIChomozygous52634731
85378128753781288GGAA10GENICheterozygous52634733
85378128753781288GGAAA10GENICheterozygous52976474
85378133353781334AG11GENIChomozygous52634737
85378146653781467AG12GENIChomozygous52634739
85378180553781806AG21GENIChomozygous52634741
85378193153781932TTTTA10GENIChomozygous52634743
85378200853782013GTTTG-----11GENIChomozygous52634748
85378241353782414CT22GENIChomozygous52634752
85378260753782608TC36GENIChomozygous52976475
85378268153782682GGGTGT2GENIChomozygous53460597
85378277053782771GA14GENIChomozygous52634754
85378331953783320AG16GENIChomozygous52634756
85378340253783403T-9GENICpossibly homozygous52976476
85378373853783739GT28GENIChomozygous52634758
85378379353783794TC22GENIChomozygous52634760
85378391753783918T-17GENIChomozygous52976477
85378391953783926TGCGTGT-------18GENIChomozygous52634762
85378404853784049TC30GENIChomozygous52976479
85378550553785506T-3GENIChomozygous52634782
85378552153785522CCTTTT2GENIChomozygous52976481