chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2260127057260127058GT21GENIChomozygous990340881
2260127111260127112AT19GENIChomozygous990340882
2260128274260128275TC23GENIChomozygous990340883
2260128357260128358TC18GENIChomozygous990340884
2260131866260131867GA17GENIChomozygous990340885
2260135510260135511CG23GENIChomozygous990340886
2260137402260137403GA18GENIChomozygous990340887
2260137508260137509CT9GENIChomozygous990340888
2260138046260138047CT12GENIChomozygous990340889
2260138715260138716TC22GENIChomozygous990340890
2260139296260139297CT30GENIChomozygous990340891
2260139380260139381CA18GENIChomozygous990340892
2260139641260139642CT22GENIChomozygous990340893
2260139696260139697CT26GENIChomozygous990340894
2260139720260139721CT27GENIChomozygous990340895
2260139736260139737CT26GENIChomozygous990340896
2260140132260140133CT22GENIChomozygous990340897
2260140522260140523CT21GENIChomozygous990340898
2260140616260140617AC19GENIChomozygous990340899
2260140786260140787TA21GENIChomozygous990340900
2260140894260140895GA26GENIChomozygous990340901
2260141640260141641CA19GENIChomozygous990340902
2260141667260141668AC20GENIChomozygous990340903
2260141695260141696AG17GENIChomozygous990340904
2260141847260141848CT27GENIChomozygous990340905
2260142353260142354AG25GENIChomozygous990340906
2260143626260143627TC19GENIChomozygous990340907
2260143713260143714GC11GENIChomozygous990340908
2260143776260143777CT17GENIChomozygous990340909
2260144105260144106CT20GENIChomozygous990340910
2260144503260144504CT19GENIChomozygous990340911
2260144668260144669CA16GENIChomozygous990340912
2260145646260145647AG16GENIChomozygous990340913
2260146587260146588GA10GENIChomozygous990340914
2260147293260147294AT17GENIChomozygous990340915
2260148042260148043AG17GENIChomozygous990340916
2260148540260148541AG9GENIChomozygous990340917