chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118743511387435114CG12GENIChomozygous51030158
118743516987435195TGTGTGGGATGGGATAGTCCAAGTAG--------------------------2GENICheterozygous51192363
118743533587435336AG5GENIChomozygous51171061
118743534187435342GGCA5GENIChomozygous51192364
118743561287435617GTGTG-----3GENIChomozygous51192365
118743561887435643GGTGGAACAGCCCTATCTATAGTAG-------------------------5GENIChomozygous51171062
118743565787435658CT2GENIChomozygous51030171
118743566087435661TC2GENIChomozygous51030172
118743568387435684CG13GENIChomozygous51030173
118743587987435880CG25GENICpossibly homozygous51030174
118743601087436011CT19GENIChomozygous51030175
118743605587436056TC25GENICpossibly homozygous51030176
118743660387436604GA21GENIChomozygous51030177
118743751687437517TC8GENIChomozygous51030178
118743752287437523GGATAAATAAATAAATAAATAA3GENIChomozygous51597823
118743824087438241CT28GENIChomozygous51030181
118743854687438547GA28GENIChomozygous51030182
118744084087440864CTCTGACTGTGAGTGATAGCATTC------------------------2GENIChomozygous51192368
118744113787441138GA30GENIChomozygous51030186
118744204387442044CG27GENIChomozygous51030187
118744223587442236GA17GENIChomozygous51030188
118744240387442404A-16GENIChomozygous51030189
118744271487442719TAATC-----23GENIChomozygous51030190
118744292787442928GGTA14GENICpossibly homozygous51171063
118744293687442942TGTGTT------18GENICpossibly homozygous51030191
118744296187442962GGTGTT16GENIChomozygous51171064
118744303987443065TGTGTGTGTGTGTGTGCGTGCGTGCA--------------------------21GENICpossibly homozygous51030193
118744321987443220TC19GENIChomozygous51030194
118744322087443221TC20GENIChomozygous51030195
118744437187444372TC30GENICpossibly homozygous51030196