chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14107767881107767882GA12GENIChomozygous113618066
14107767883107767884TC12GENIChomozygous113539508
14107769187107769188GA22GENIChomozygous113618068
14107770521107770522CT21GENIChomozygous113618069
14107772898107772899GA10GENIChomozygous113618070
14107773426107773427CT6GENIChomozygous113618071
14107773435107773436TC8GENIChomozygous113618072
14107775101107775102GA16GENIChomozygous113618073
14107775567107775568TA5GENIChomozygous125925631
14107775571107775572GA6GENIChomozygous125925632
14107775574107775575CA6GENIChomozygous125925633
14107778137107778138GA28GENIChomozygous113694966
14107778330107778331GA12GENIChomozygous113618075
14107778440107778441GT4GENIChomozygous126044392