chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162029897020298971CT11GENIChomozygous47992667
162029914220299143TG8GENICpossibly homozygous47327076
162029941720299418CT11GENIChomozygous47992668
162029964720299648CA17GENIChomozygous47327078
162030078320300784AG11GENICpossibly homozygous47327080
162030237020302371AG20GENICpossibly homozygous47327084
162030504020305041AT8GENIChomozygous47327088
162030875420308755TTG13GENICheterozygous47327092
162030936320309364CT1GENIChomozygous47992669
162030942220309423TC10GENIChomozygous47327098
162031036320310364G-5GENICheterozygous47327104
162031152220311523CT19GENIChomozygous47327108
162031177820311779CG7GENICheterozygous47992670
162031353020313531GT23GENIChomozygous47327112
162031490620315027GGTCTCGCTTGTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGTGCTAAATCCCCAGCCCC-------------------------------------------------------------------------------------------------------------------------7GENICheterozygous47904380
162031554720315548CT25GENICpossibly homozygous47740366
162031601420316015CT15GENICpossibly homozygous47740368
162031622620316227TTC1GENIChomozygous47740370
162031631920316320TC7GENIChomozygous47327121
162031659920316600GA7GENICheterozygous47740372
162031714020317141AG4GENIChomozygous47327125
162031719420317195TA6GENICheterozygous47740376