chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118743511387435114CG13GENIChomozygous51030158
118743516987435195TGTGTGGGATGGGATAGTCCAAGTAG--------------------------3GENIChomozygous51192363
118743533587435336AG6GENIChomozygous51171061
118743534187435342GGCA6GENIChomozygous51192364
118743561287435617GTGTG-----1GENIChomozygous51192365
118743561887435643GGTGGAACAGCCCTATCTATAGTAG-------------------------3GENIChomozygous51171062
118743565787435658CT6GENIChomozygous51030171
118743566087435661TC9GENIChomozygous51030172
118743568387435684CG20GENIChomozygous51030173
118743587987435880CG19GENIChomozygous51030174
118743601087436011CT30GENIChomozygous51030175
118743605587436056TC33GENIChomozygous51030176
118743660387436604GA28GENIChomozygous51030177
118743751687437517TC18GENIChomozygous51030178
118743752287437523GGATAAATAAATAAATAA7GENIChomozygous51192366
118743824087438241CT17GENIChomozygous51030181
118743854687438547GA26GENIChomozygous51030182
118744084087440864CTCTGACTGTGAGTGATAGCATTC------------------------3GENIChomozygous51192368
118744113787441138GA23GENIChomozygous51030186
118744204387442044CG24GENIChomozygous51030187
118744223587442236GA21GENIChomozygous51030188
118744240387442404A-21GENIChomozygous51030189
118744271487442719TAATC-----23GENIChomozygous51030190
118744292787442928GGTA12GENIChomozygous51171063
118744293687442942TGTGTT------16GENIChomozygous51030191
118744296187442962GGTGTT22GENIChomozygous51171064
118744303987443065TGTGTGTGTGTGTGTGCGTGCGTGCA--------------------------17GENIChomozygous51030193
118744321987443220TC16GENIChomozygous51030194
118744322087443221TC16GENIChomozygous51030195
118744437187444372TC28GENIChomozygous51030196