chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123946875123946876CCTCTGTCTGTCTGTCTG16GENIChomozygous710350875
7123946972123946973CG23GENIChomozygous567893469
7123946973123946974CT23GENIChomozygous567893470
7123948908123948909GA18GENIChomozygous567893471
7123949878123949879GA21GENIChomozygous567893472
7123952086123952087TTAAAAA2GENIChomozygous710350876
7123953709123953710GC12GENIChomozygous567893473
7123954115123954119CACT----18GENIChomozygous710350877
7123954444123954447GGA---20GENIChomozygous710350878
7123954569123954570GA27GENIChomozygous567893474
7123954775123954776AG16GENIChomozygous567893475
7123955564123955565A-19GENIChomozygous710350879
7123957238123957239AT26GENIChomozygous567893476
7123957699123957701TT--15GENIChomozygous710350880
7123957708123957709TC16GENIChomozygous567893477
7123958179123958180AG17GENIChomozygous567893478
7123958273123958274GGGTTT11GENIChomozygous710350882
7123958336123958337CT5GENIChomozygous567893479
7123958418123958419TC17GENIChomozygous567893480
7123958498123958499T-9GENICpossibly homozygous710350884
7123958712123958713TTTGTTTTG12GENIChomozygous710350885
7123962584123962585GA11GENIChomozygous567893481
7123963081123963082AC18GENIChomozygous567893482
7123963136123963137GT13GENIChomozygous567893483
7123965178123965179GA22GENIChomozygous567893484
7123965574123965575GA16GENIChomozygous567422145
7123966714123966715AG24GENIChomozygous567893485
7123966828123966829GA18GENIChomozygous567893486
7123966948123966949TC14GENIChomozygous567893487
7123967255123967256CT10GENIChomozygous567893488
7123968071123968072TC21GENIChomozygous567422146
7123969622123969623TC20GENIChomozygous567893489
7123969693123969694CT11GENIChomozygous567893490
7123969895123969896CA16GENIChomozygous567893491
7123970186123970187GT18GENIChomozygous567893492
7123970264123970265AAT16GENIChomozygous710350886
7123971180123971181T-8GENIChomozygous710350887
7123971210123971211T-4GENIChomozygous710350888
7123971671123971672CT18GENIChomozygous567893493
7123972384123972385CT15GENIChomozygous567893494