chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137694300276943003TTG11GENICheterozygous50101902
137694300376943004G-11GENICheterozygous49824295
137696564576965646AAC15GENICheterozygous49824356
137696564776965649GG--17GENICheterozygous49824357
137695217776952178AAAG12GENICheterozygous50523958
137698380576983806AG18GENIChomozygous49824451
137698340176983402TTAC14GENICheterozygous51007970
137699657176996572TTG22GENIChomozygous49824469
137701324277013243G-36GENIChomozygous49824494
137701325777013258G-40GENIChomozygous49824495
137701335477013355CCTCTCACTGGTAGCCTGCACTACACAGATCTGCCGTTCTCCAAGAGTCTTTCTGTTTTTGCTCCCTCCCCTATTCCTGGT23GENIChomozygous50523971
137703252077032522AC--15GENICheterozygous49824554
137705427177054272GGT25GENIChomozygous49824632
137705761077057612AC--13GENICheterozygous50523980
137706125777061258TG24GENICpossibly homozygous50364348
137706160777061608TTC11GENIChomozygous49824648
137706180977061810GA14GENIChomozygous50364350
137706289577062896AATGTGTG13GENICpossibly homozygous49824650
137706306577063066AG12GENIChomozygous50102278
137706330877063309T-6GENIChomozygous50364352
137706404777064048CA7GENIChomozygous50364354
137706454977064550CT5GENIChomozygous50364356
137706787777067878CT17GENIChomozygous50102280
137707201077072012TA--6GENIChomozygous50102284
137707232577072326AAATATAT4GENICheterozygous50523981
137707307577073076TC8GENIChomozygous50102286
137707330777073308GA4GENIChomozygous50364358
137707433677074337CT10GENIChomozygous50102290
137707435377074354CT10GENIChomozygous50102292
137707441177074412A-15GENICpossibly homozygous50102294