chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85378086553780882TGGCTCGTCCTTCACCT-----------------25GENIChomozygous701112301
85378107053781071CT24GENIChomozygous550710178
85378121053781211AG20GENIChomozygous550710179
85378128753781288GGA15GENICheterozygous701112303
85378128753781288GGAA15GENICheterozygous701112304
85378128753781288GGAAA15GENICheterozygous701112305
85378133353781334AG28GENICpossibly homozygous550710180
85378146653781467AG36GENIChomozygous550710181
85378180553781806AG15GENIChomozygous550710182
85378193153781932TTTA11GENICheterozygous701112306
85378193153781932TTTTA11GENICheterozygous701112307
85378200853782013GTTTG-----9GENIChomozygous701112309
85378241353782414CT30GENIChomozygous550710183
85378260753782608TC17GENIChomozygous550710184
85378277053782771GA17GENIChomozygous550710185
85378331953783320AG27GENIChomozygous550710186
85378340253783403T-17GENIChomozygous701112310
85378373853783739GT19GENIChomozygous550710187
85378379353783794TC25GENIChomozygous550710188
85378391753783918T-22GENIChomozygous701112311
85378391953783926TGCGTGT-------22GENIChomozygous701112312
85378404853784049TC27GENIChomozygous550710189
85378438353784384A-16GENIChomozygous701112313
85378550753785508TTTTTTTC4GENIChomozygous701112314