chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74693341446933415CT9GENIChomozygous138084667
74693420946934210CT25GENIChomozygous138084668
74693590646935907TC14GENIChomozygous138084669
74693859946938600GA15GENIChomozygous138084670
74693974646939747TA15GENIChomozygous138084671
74694031546940316CT21GENIChomozygous138084672
74694192546941926GA25GENICpossibly homozygous138084673
74694245246942453TC22GENIChomozygous138084674
74694370546943706CA23GENIChomozygous138084675
74694407746944078GA23GENIChomozygous138084676
74694470446944705AG30GENIChomozygous138084677
74693600346936003G11GENIChomozygous137952097
74694191646941920TTTC25GENICpossibly homozygous137952098
74694514746945151TGTT19GENIChomozygous137952099
74695023146950231T21GENIChomozygous137952100
74695050546950506CT13GENIChomozygous138084678
74695052446950525TC13GENIChomozygous138084679
74695205746952058CT16GENIChomozygous138084680
74695512746955128CT17GENIChomozygous138084684
74695208946952090TG20GENIChomozygous138084681
74695414946954150AG20GENIChomozygous138084682
74695449146954492GA22GENIChomozygous138084683
74695520946955210TG22GENIChomozygous138084685
74695636146956362AG15GENIChomozygous138084686
74695671646956718GT26GENIChomozygous137952101
74695710146957101T11GENIChomozygous137952102