chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------25GENIChomozygous733589589
85378107053781071CT28GENIChomozygous607371626
85378121053781211AG37GENIChomozygous607371627
85378128753781288GGA21GENICheterozygous733589591
85378128753781288GGAA21GENICheterozygous733589592
85378128753781288GGAAA21GENICheterozygous733589593
85378133353781334AG23GENIChomozygous607371628
85378146653781467AG25GENIChomozygous607371629
85378180553781806AG22GENIChomozygous607371630
85378193153781932TTTA13GENICheterozygous733589594
85378193153781932TTTTA13GENICheterozygous733589595
85378200853782013GTTTG-----24GENIChomozygous733589597
85378241353782414CT28GENIChomozygous607371631
85378260753782608TC25GENIChomozygous607371632
85378277053782771GA18GENIChomozygous607371633
85378331953783320AG24GENIChomozygous607371634
85378340253783403T-16GENICpossibly homozygous733589598
85378373853783739GT22GENIChomozygous607371635
85378379353783794TC18GENIChomozygous607371636
85378391753783918T-17GENIChomozygous733589599
85378391953783926TGCGTGT-------21GENIChomozygous733589600
85378404853784049TC25GENIChomozygous607371637
85378438353784384A-15GENIChomozygous733589601
85378550753785508TTTTTTTC10GENIChomozygous733589602