chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74693577846935780TG58GENIChomozygous141913095
74693590646935907TC56GENIChomozygous138084669
74693974646939747TA69GENIChomozygous138084671
74694031546940316CT61GENIChomozygous138084672
74694192546941926GA44GENIChomozygous138084673
74694245246942453TC54GENIChomozygous138084674
74694283746942857AACATTCACGTTTCCAACTC66GENIChomozygous141913096
74694407746944078GA61GENIChomozygous138084676
74694470446944705AG62GENIChomozygous138084677
74694642346946423A47GENIChomozygous141913097
74695050546950506CT56GENIChomozygous138084678
74695052446950525TC58GENIChomozygous138084679
74695116446951168CTTA47GENIChomozygous141913098
74695208946952090TG48GENIChomozygous138084681
74695286446952865AT56GENIChomozygous141963855
74693938346939384GA45GENIChomozygous141963852
74694586846945869CT61GENIChomozygous141963853
74694981346949814AG61GENIChomozygous141963854
74695352546953526AG59GENIChomozygous141963856
74695414946954150AG45GENIChomozygous138084682
74695520946955210TG70GENIChomozygous138084685
74695671646956718GT44GENIChomozygous137952101
74695710746957109TG38GENICpossibly homozygous141913099
74695710846957109GT38GENICheterozygous154445837
74695710846957109G38GENICpossibly homozygous403614098
74695772146957722GA49GENIChomozygous141963858
74695762346957624TC55GENIChomozygous141963857