chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------16GENIChomozygous739773401
85378107053781071CT26GENIChomozygous622267605
85378121053781211AG18GENIChomozygous622267606
85378128753781288GGAA14GENICheterozygous739773404
85378128753781288GGAAA14GENICpossibly homozygous739773405
85378133353781334AG22GENIChomozygous622267607
85378146653781467AG25GENIChomozygous622267608
85378180553781806AG16GENIChomozygous622267609
85378193153781932TTTA10GENICheterozygous739773406
85378193153781932TTTTA10GENICheterozygous739773407
85378200853782013GTTTG-----14GENIChomozygous739773409
85378241353782414CT36GENIChomozygous622267610
85378260753782608TC29GENIChomozygous622267611
85378268153782682GGGTGT5GENICheterozygous739773410
85378277053782771GA17GENIChomozygous622267612
85378331953783320AG23GENIChomozygous622267613
85378340253783403T-11GENIChomozygous739773411
85378373853783739GT19GENIChomozygous622267614
85378379353783794TC20GENIChomozygous622267615
85378391753783918T-17GENIChomozygous739773412
85378391953783926TGCGTGT-------18GENIChomozygous739773413
85378404853784049TC35GENIChomozygous622267616
85378550553785506T-3GENIChomozygous739773414
85378552153785522CCTTTT3GENIChomozygous739773416