chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------17GENIChomozygous703227963
85378107053781071CT23GENIChomozygous554095116
85378121053781211AG26GENIChomozygous554095117
85378128753781288GGA14GENICheterozygous703227965
85378128753781288GGAA14GENICheterozygous703227966
85378128753781288GGAAA14GENICpossibly homozygous703227967
85378133353781334AG16GENIChomozygous554095118
85378146653781467AG22GENIChomozygous554095119
85378180553781806AG19GENIChomozygous554095120
85378193153781932TTTTA5GENICheterozygous703227969
85378193153781932TTTTTA5GENICheterozygous703227970
85378200853782013GTTTG-----7GENIChomozygous703227971
85378241353782414CT27GENIChomozygous554095121
85378260753782608TC19GENIChomozygous554095122
85378277053782771GA12GENIChomozygous554095123
85378331953783320AG14GENIChomozygous554095124
85378340253783403T-5GENIChomozygous703227972
85378373853783739GT17GENIChomozygous554095125
85378379353783794TC22GENIChomozygous554095126
85378391753783918T-9GENIChomozygous703227973
85378391953783926TGCGTGT-------10GENIChomozygous703227974
85378404853784049TC27GENIChomozygous554095127
85378550553785506T-4GENIChomozygous703227975
85378552153785522CCTTTT6GENIChomozygous703227977