chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3129615999129616000TTA5GENIChomozygous57670328
3129616001129616002GC4GENIChomozygous58560477
3129616055129616056CT7GENIChomozygous57670332
3129616381129616382AAC10GENIChomozygous57670334
3129616483129616484TG3GENIChomozygous57670336
3129617020129617021GA17GENIChomozygous57670338
3129618023129618024GT6GENIChomozygous57670340
3129618102129618103CT10GENIChomozygous57670342
3129618158129618159AG9GENIChomozygous57670344
3129618162129618163GT12GENIChomozygous57670345
3129618729129618730AG19GENIChomozygous57670347
3129618844129618845CT20GENIChomozygous57670349
3129619524129619525TG19GENIChomozygous57670351
3129620017129620018GA13GENIChomozygous57670353
3129620051129620052TC11GENIChomozygous57670354
3129620204129620205GT23GENIChomozygous57670356
3129620321129620322AG21GENIChomozygous57670358
3129620365129620366GA19GENIChomozygous57670360
3129621132129621133GGTGCTTGCTAGGC2GENIChomozygous58672094
3129621137129621138GGCGCTCT4GENIChomozygous58623711
3129621141129621142GA3GENIChomozygous58623712
3129621144129621145GGA2GENIChomozygous58623713
3129621147129621148TTAAATCC3GENIChomozygous58623714
3129621149129621151GG--4GENIChomozygous58623715
3129621746129621747AAC10GENICpossibly homozygous57670364
3129621911129621912GGA10GENIChomozygous57670366
3129622560129622561TC23GENIChomozygous57670368
3129623103129623104A-4GENIChomozygous57670370
3129623578129623594TGTGTGTGTGTGTGTG----------------5GENICheterozygous57670372
3129624322129624323A-13GENIChomozygous57670374
3129624658129624659TC34GENIChomozygous57670376
3129624958129624959TC20GENIChomozygous57670378
3129625480129625481GA14GENIChomozygous57670380
3129625689129625690AC21GENIChomozygous57670382
3129625724129625725GGT10GENIChomozygous58695701
3129625733129625734AT10GENIChomozygous57670386
3129626553129626554GA23GENIChomozygous57670388
3129626979129626980CT27GENIChomozygous57670390