chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123948713123948714GA12GENIChomozygous625400264
7123951427123951428TG28GENIChomozygous625400265
7123951722123951723CT1GENIChomozygous625400266
7123952873123952874GA13GENIChomozygous625400267
7123954115123954119CACT----6GENICheterozygous740798975
7123954444123954447GGA---1GENIChomozygous740798976
7123954775123954776AG12GENIChomozygous625400268
7123957238123957239AT22GENICpossibly homozygous625400269
7123957389123957390CT15GENICpossibly homozygous625400270
7123958179123958180AG11GENIChomozygous625400271
7123958418123958419TC5GENICheterozygous625400272
7123958712123958713TTTGTTTTG1GENIChomozygous740798977
7123958869123958871CT--5GENIChomozygous740798978
7123959628123959629CA2GENICheterozygous625400273
7123963136123963137GT21GENICpossibly homozygous625400274
7123963294123963295AT29GENICpossibly homozygous625400275
7123965962123965963CT15GENIChomozygous625400276
7123966166123966167GA24GENICpossibly homozygous625400277
7123966714123966715AG18GENICheterozygous625400278
7123968071123968072TC16GENIChomozygous625400279
7123968092123968093GA11GENIChomozygous625400280
7123968614123968615CT8GENIChomozygous625400281
7123968675123968676GA11GENIChomozygous625400282
7123969622123969623TC13GENIChomozygous625400283
7123969895123969896CA11GENICpossibly homozygous625400284
7123972384123972385CT18GENICpossibly homozygous625400285
7123972491123972492AG4GENIChomozygous625400286
7123972517123972518TC8GENIChomozygous625400287
7123972571123972572CT2GENIChomozygous625400288