chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------3GENIChomozygous745698938
85378107053781071CT16GENICheterozygous631560624
85378121053781211AG5GENIChomozygous631560625
85378133353781334AG12GENICheterozygous631560626
85378146653781467AG18GENICpossibly homozygous631560627
85378180553781806AG11GENIChomozygous631560628
85378200853782013GTTTG-----6GENIChomozygous745698942
85378241353782414CT15GENICpossibly homozygous631560629
85378260753782608TC19GENIChomozygous631560630
85378277053782771GA7GENICpossibly homozygous631560631
85378331953783320AG7GENIChomozygous631560632
85378373853783739GT14GENIChomozygous631560633
85378379353783794TC10GENICpossibly homozygous631560634
85378404853784049TC7GENIChomozygous631560635