chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------15GENIChomozygous737696476
85378107053781071CT29GENIChomozygous614497677
85378121053781211AG17GENIChomozygous614497678
85378128753781288GGAA11GENICheterozygous737696479
85378128753781288GGAAA11GENICpossibly homozygous737696480
85378133353781334AG30GENIChomozygous614497679
85378146653781467AG41GENIChomozygous614497680
85378180553781806AG25GENIChomozygous614497681
85378193153781932TTTTA9GENICheterozygous737696482
85378193153781932TTTTTA9GENICheterozygous737696483
85378200853782013GTTTG-----17GENIChomozygous737696484
85378241353782414CT30GENIChomozygous614497682
85378260753782608TC31GENIChomozygous614497683
85378277053782771GA30GENIChomozygous614497684
85378331953783320AG24GENIChomozygous614497685
85378353253783533GGT27GENIChomozygous737696485
85378373853783739GT30GENIChomozygous614497686
85378379353783794TC23GENIChomozygous614497687
85378391753783918T-6GENIChomozygous737696486
85378391953783926TGCGTGT-------10GENIChomozygous737696487
85378404853784049TC31GENIChomozygous614497688
85378461253784613TC21GENIChomozygous614497689
85378550553785506T-17GENIChomozygous737696488
85378552153785522CCTTTCTT19GENIChomozygous737696491