chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118743511387435114CG13GENIChomozygous51030158
118743516987435195TGTGTGGGATGGGATAGTCCAAGTAG--------------------------14GENIChomozygous51192363
118743533587435336AG1GENIChomozygous51171061
118743534187435342GGCA1GENIChomozygous51192364
118743561287435617GTGTG-----3GENIChomozygous51192365
118743561887435643GGTGGAACAGCCCTATCTATAGTAG-------------------------8GENIChomozygous51171062
118743565787435658CT7GENIChomozygous51030171
118743566087435661TC7GENIChomozygous51030172
118743568387435684CG13GENIChomozygous51030173
118743587987435880CG22GENIChomozygous51030174
118743601087436011CT25GENIChomozygous51030175
118743605587436056TC17GENIChomozygous51030176
118743660387436604GA16GENIChomozygous51030177
118743751687437517TC7GENIChomozygous51030178
118743752287437523GGATAAATAAATAAATAA1GENIChomozygous51192366
118743824087438241CT11GENIChomozygous51030181
118743854687438547GA9GENIChomozygous51030182
118744084087440864CTCTGACTGTGAGTGATAGCATTC------------------------3GENIChomozygous51192368
118744113787441138GA19GENIChomozygous51030186
118744204387442044CG35GENICpossibly homozygous51030187
118744223587442236GA20GENIChomozygous51030188
118744240387442404A-16GENICpossibly homozygous51030189
118744271487442719TAATC-----18GENIChomozygous51030190
118744292787442928GGTA6GENIChomozygous51171063
118744293687442942TGTGTT------9GENIChomozygous51030191
118744296187442962GGTGTT13GENIChomozygous51171064
118744303987443065TGTGTGTGTGTGTGTGCGTGCGTGCA--------------------------15GENIChomozygous51030193
118744321987443220TC5GENIChomozygous51030194
118744322087443221TC5GENIChomozygous51030195
118744437187444372TC26GENIChomozygous51030196