chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101158821911588220GA55GENIChomozygous138725257
101158837811588379TC60GENIChomozygous138725258
101158954611589547GT60GENICpossibly homozygous138725259
101158981411589815AG73GENIChomozygous138725260
101159126511591266AG55GENIChomozygous138725261
101159139211591393CT46GENIChomozygous138725262
101159398711593988GA47GENIChomozygous138725263
101159540311595404GA53GENIChomozygous138725264
101159680811596809CA56GENIChomozygous138725265
101159717111597172CT56GENIChomozygous138725266
101159819011598191AT58GENIChomozygous138725267
101159951811599519CT51GENICheterozygous138725274
101160272911602730GA49GENIChomozygous138725275
101160360711603608TC65GENIChomozygous138725276
101160372511603726AT67GENIChomozygous138725277
101160390411603905AG54GENIChomozygous138725278
101160404511604046GA70GENIChomozygous138725279
101160476311604764AG56GENIChomozygous138725280
101160504111605042AG46GENIChomozygous138725281
101161110311611104CT49GENIChomozygous138725282
101161212611612127CT50GENIChomozygous138725283
101161240311612404TC72GENIChomozygous138725284
101161240911612410AG67GENIChomozygous138725285
101161367811613679CT72GENIChomozygous138725286
101161396911613970AC68GENIChomozygous138725287
101160173811601739T61GENICpossibly homozygous138668872
101159544611595448GT42GENIChomozygous138668869
101159569311595693AGAC49GENIChomozygous138668870
101159943511599502TGGGGGGCCGAGTCAGCCGTTATGTTCCAAAAAGGTAGCTAAGAAACTTGCCCCCGGGCTGAACCCT56GENICheterozygous138668871
101160304511603045T33GENICpossibly homozygous138668873
101161657311616585GGTAGAAAAATA40GENIChomozygous138668874
101159957911599580AG49GENICheterozygous140903965
101161848911618490AG79GENIChomozygous142213593
101159949011599491G51GENICheterozygous403732384
101159949011599491GA51GENICheterozygous403732385
101161855811618559CT76GENIChomozygous142213594