chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125213182125213183CA17GENIChomozygous878912919
1125213926125213927CT15GENIChomozygous878912920
1125214231125214232TC15GENIChomozygous878912921
1125214871125214872AG19GENIChomozygous878912922
1125214953125214954CT24GENIChomozygous878912923
1125215239125215240GA13GENIChomozygous878912924
1125215546125215547TA3GENICheterozygous878912925
1125217485125217486GA13GENIChomozygous878912926
1125218976125218977TC15GENIChomozygous878912927
1125221356125221357CT25GENIChomozygous878912928
1125224111125224112CT20GENIChomozygous878912929
1125224239125224240CA20GENIChomozygous878912930
1125224413125224414AG20GENIChomozygous878912931
1125226171125226172TC13GENIChomozygous878912932
1125226820125226821GA17GENIChomozygous878912933
1125226862125226863GA20GENIChomozygous878912934
1125226934125226935GA14GENIChomozygous878912935
1125226967125226968CT16GENIChomozygous878912936
1125227524125227525CA12GENIChomozygous878912937
1125227655125227656GA15GENIChomozygous878912938
1125228013125228014TC12GENIChomozygous878912939
1125228026125228027AC10GENICheterozygous878912940
1125228141125228142GT21GENIChomozygous878912941
1125228215125228216CT19GENIChomozygous878912942
1125228275125228276CG16GENIChomozygous878912943
1125228284125228285TA15GENIChomozygous878912944
1125228363125228364TC25GENIChomozygous878912945
1125228434125228435TC15GENIChomozygous878912946
1125228819125228820CT17GENIChomozygous878912947