chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118743511387435114CG6GENICheterozygous51030158
118743533587435336AG2GENICheterozygous51171061
118743561887435643GGTGGAACAGCCCTATCTATAGTAG-------------------------1GENIChomozygous51171062
118743565787435658CT2GENIChomozygous51030171
118743566087435661TC2GENIChomozygous51030172
118743568387435684CG10GENIChomozygous51030173
118743587987435880CG28GENICpossibly homozygous51030174
118743601087436011CT9GENIChomozygous51030175
118743605587436056TC18GENICpossibly homozygous51030176
118743660387436604GA18GENICpossibly homozygous51030177
118743751687437517TC8GENIChomozygous51030178
118743824087438241CT27GENICpossibly homozygous51030181
118743854687438547GA26GENICpossibly homozygous51030182
118744113787441138GA26GENICpossibly homozygous51030186
118744204387442044CG15GENIChomozygous51030187
118744223587442236GA18GENICheterozygous51030188
118744240387442404A-2GENIChomozygous51030189
118744271487442719TAATC-----4GENIChomozygous51030190
118744292787442928GGTA2GENICheterozygous51171063
118744293687442942TGTGTT------2GENICheterozygous51030191
118744296187442962GGTGTT3GENICheterozygous51171064
118744303987443065TGTGTGTGTGTGTGTGCGTGCGTGCA--------------------------5GENICheterozygous51030193
118744321987443220TC15GENICheterozygous51030194
118744322087443221TC15GENICheterozygous51030195
118744437187444372TC20GENIChomozygous51030196