chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------15GENIChomozygous52634727
85378107053781071CT29GENIChomozygous52634729
85378121053781211AG17GENIChomozygous52634731
85378128753781288GGAA11GENICheterozygous52634733
85378128753781288GGAAA11GENICpossibly homozygous52976474
85378133353781334AG30GENIChomozygous52634737
85378146653781467AG41GENIChomozygous52634739
85378180553781806AG25GENIChomozygous52634741
85378193153781932TTTTA9GENICheterozygous52634743
85378193153781932TTTTTA9GENICheterozygous53431314
85378200853782013GTTTG-----17GENIChomozygous52634748
85378241353782414CT30GENIChomozygous52634752
85378260753782608TC31GENIChomozygous52976475
85378277053782771GA30GENIChomozygous52634754
85378331953783320AG24GENIChomozygous52634756
85378353253783533GGT27GENIChomozygous53698073
85378373853783739GT30GENIChomozygous52634758
85378379353783794TC23GENIChomozygous52634760
85378391753783918T-6GENIChomozygous52976477
85378391953783926TGCGTGT-------10GENIChomozygous52634762
85378404853784049TC31GENIChomozygous52976479
85378461253784613TC21GENIChomozygous53698074
85378550553785506T-17GENIChomozygous52634782
85378552153785522CCTTTCTT19GENIChomozygous53698075