chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------16GENIChomozygous754290663
85378107053781071CT17GENIChomozygous645365890
85378121053781211AG13GENIChomozygous645365891
85378128753781288GGAA20GENICheterozygous754290666
85378128753781288GGAAA20GENICpossibly homozygous754290667
85378133353781334AG24GENIChomozygous645365892
85378146653781467AG16GENIChomozygous645365893
85378180553781806AG24GENIChomozygous645365894
85378193153781932TTTTA13GENICheterozygous754290669
85378193153781932TTTTTA13GENICheterozygous754290670
85378200853782013GTTTG-----19GENIChomozygous754290671
85378241353782414CT25GENIChomozygous645365895
85378260753782608TC22GENIChomozygous645365896
85378277053782771GA14GENIChomozygous645365897
85378331953783320AG10GENIChomozygous645365898
85378353253783533GGT20GENIChomozygous754290672
85378373853783739GT32GENIChomozygous645365899
85378379353783794TC21GENIChomozygous645365900
85378391753783918T-25GENIChomozygous754290673
85378391953783926TGCGTGT-------25GENIChomozygous754290674
85378404853784049TC30GENIChomozygous645365901
85378461253784613TC28GENIChomozygous645365902
85378550553785506T-10GENIChomozygous754290675
85378552153785522CCTTTCTT12GENIChomozygous754290678