chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------15GENIChomozygous685941324
85378107053781071CT36GENIChomozygous508071363
85378121053781211AG49GENIChomozygous508071364
85378128753781288GGAA12GENICheterozygous685941325
85378128753781288GGAAA12GENICheterozygous685941326
85378133353781334AG31GENIChomozygous508071365
85378146653781467AG40GENIChomozygous508071366
85378180553781806AG58GENIChomozygous508071367
85378193153781932TTTTA26GENICheterozygous685941328
85378193153781932TTTA26GENICheterozygous685941329
85378200853782013GTTTG-----35GENIChomozygous685941330
85378201253782013G-43GENICpossibly homozygous685941331
85378241353782414CT40GENIChomozygous508071368
85378260753782608TC63GENIChomozygous508071369
85378277053782771GA37GENIChomozygous508071370
85378331953783320AG68GENIChomozygous508071371
85378340253783403T-39GENIChomozygous685941332
85378373853783739GT65GENICpossibly homozygous508071372
85378379353783794TC50GENIChomozygous508071373
85378391753783918T-25GENICheterozygous685941333
85378391953783926TGCGTGT-------23GENIChomozygous685941334
85378393753783938TC26GENICheterozygous508071374
85378404853784049TC43GENIChomozygous508071375
85378550553785506T-42GENIChomozygous685941335
85378550753785508TTTTTTTC39GENICpossibly homozygous685941336
85378552153785522CCTTTT29GENIChomozygous685941338