chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------18GENIChomozygous716663489
85378107053781071CT15GENIChomozygous577064206
85378121053781211AG20GENIChomozygous577064207
85378128753781288GGAA11GENICheterozygous716663492
85378128753781288GGAAA11GENICpossibly homozygous716663493
85378133353781334AG16GENIChomozygous577064208
85378146653781467AG14GENIChomozygous577064209
85378180553781806AG16GENIChomozygous577064210
85378193153781932TTTA13GENICheterozygous716663494
85378193153781932TTTTA13GENICheterozygous716663495
85378200853782013GTTTG-----16GENIChomozygous716663497
85378241353782414CT23GENIChomozygous577064211
85378260753782608TC22GENIChomozygous577064212
85378268153782682GGGTGT1GENIChomozygous716663498
85378277053782771GA10GENIChomozygous577064213
85378331953783320AG17GENIChomozygous577064214
85378340253783403T-20GENIChomozygous716663499
85378373853783739GT21GENIChomozygous577064215
85378379353783794TC34GENIChomozygous577064216
85378391753783918T-9GENIChomozygous716663500
85378391953783926TGCGTGT-------9GENIChomozygous716663501
85378404853784049TC23GENIChomozygous577064217
85378550553785506T-9GENIChomozygous716663502
85378552153785522CCTTTT7GENIChomozygous716663504