chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2198390075198390076GT41GENICheterozygous132950271
2198390075198390075G38GENICheterozygous132945883
2198390592198390593CT77GENICheterozygous110997299
2198390698198390700TT48GENIChomozygous132945884
2198396143198396144GA43GENIChomozygous110997301
2198390722198390723GT52GENIChomozygous110200387
2198393153198393154TA31GENICpossibly homozygous110200388
2198404528198404529CT45GENICpossibly homozygous110997303
2198406130198406131AG7GENICheterozygous127833629
2198406109198406110GA5GENICheterozygous127833628
2198406151198406160GAGATTGTG9GENICheterozygous127723602
2198406166198406167GT9GENICheterozygous127833631
2198406177198406178AG10GENICheterozygous127833632
2198406342198406343GA8GENICheterozygous127833635
2198411696198411697TC5GENIChomozygous110997305
2198411758198411759AG22GENIChomozygous110200395
2198412348198412349TA38GENIChomozygous110200397
2198413388198413389AG11GENIChomozygous110997307
2198414124198414147TTATTCTCCCAAAAAGTCATTTG27GENICheterozygous127723604
2198414152198414198TCGCAAAAGTGTCCCTTCTTCCTTTCTCTTTCCCATGTACTTTAGG24GENICheterozygous127723605
2198414203198414216GGACCCCAAATTC19GENICheterozygous127723606
2198414219198414221CC16GENICheterozygous127723607
2198414222198414230CCCACTTT16GENICheterozygous127723608
2198414233198414234T16GENICpossibly homozygous127723609
2198417060198417061AT18GENICpossibly homozygous110997309
2198417120198417120A3GENIChomozygous127723610
2198417300198417301AT14GENIChomozygous110997311
2198417882198417883GA38GENIChomozygous110200399
2198406756198406757AC23GENICheterozygous132285800