chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------12GENIChomozygous756583664
85378107053781071CT19GENIChomozygous649171851
85378121053781211AG12GENIChomozygous649171852
85378128753781288GGAA14GENICheterozygous756583667
85378128753781288GGAAA14GENICpossibly homozygous756583668
85378133353781334AG15GENIChomozygous649171853
85378146653781467AG21GENIChomozygous649171854
85378180553781806AG16GENIChomozygous649171855
85378193153781932TTTTA12GENICheterozygous756583670
85378193153781932TTTTTA12GENICheterozygous756583671
85378200853782013GTTTG-----28GENIChomozygous756583672
85378241353782414CT23GENIChomozygous649171856
85378260753782608TC25GENIChomozygous649171857
85378277053782771GA25GENIChomozygous649171858
85378331953783320AG21GENIChomozygous649171859
85378353253783533GGT25GENIChomozygous756583673
85378373853783739GT24GENIChomozygous649171860
85378379353783794TC24GENIChomozygous649171861
85378391753783918T-15GENIChomozygous756583674
85378391953783926TGCGTGT-------15GENIChomozygous756583675
85378404853784049TC23GENIChomozygous649171862
85378461253784613TC25GENIChomozygous649171863
85378550553785506T-16GENIChomozygous756583676
85378552153785522CCTTTT17GENICheterozygous756583678
85378552153785522CCTTTCTT17GENICpossibly homozygous756583679