chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3160324825160324826TC30GENIChomozygous57763231
3160324864160324865AG22GENIChomozygous57763232
3160327256160327257GC10GENIChomozygous57763233
3160327957160327961TTTT----17GENICheterozygous57763234
3160327968160327969TG19GENICheterozygous57763236
3160327968160327969TTG16GENICheterozygous57763237
3160327972160327974TT--20GENIChomozygous57763238
3160327973160327974TTG19GENICpossibly homozygous57763239
3160327998160328000TT--13GENICpossibly homozygous58241047
3160328007160328008TTG17GENIChomozygous58241048
3160328016160328017GGT17GENICpossibly homozygous57763242
3160328820160328821AG31GENIChomozygous57763243
3160329081160329082CCAA2GENIChomozygous57763245
3160328018160328019TTG19GENIChomozygous58399364
3160332734160332735CT22GENIChomozygous58399365
3160333192160333193CT30GENIChomozygous58399366
3160333373160333374CT26GENIChomozygous58399367
3160334539160334540AC14GENIChomozygous57763247
3160334822160334823TC40GENIChomozygous57763248
3160335082160335083CT22GENIChomozygous58399368
3160335594160335595AG43GENIChomozygous57763250
3160339068160339074ACACAC------8GENICheterozygous58241078
3160339070160339074ACAC----8GENICheterozygous57763252
3160339144160339145CT20GENICheterozygous57763253
3160340033160340034CT31GENICpossibly homozygous57763254
3160340104160340107AAA---3GENIChomozygous58399369
3160340381160340382CA28GENIChomozygous57763255
3160340878160340879CA17GENIChomozygous58399370
3160341067160341068TC22GENIChomozygous58399372
3160341921160341922CA21GENICpossibly homozygous58399373