chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7130326882130326883TC27GENIChomozygous115889870
7130327011130327012GA26GENIChomozygous115889872
7130327075130327076TG26GENIChomozygous115889874
7130327114130327115CT17GENIChomozygous115889876
7130327215130327216GT17GENIChomozygous115889878
7130327491130327492CA32GENIChomozygous116229502
7130328212130328213AT30GENIChomozygous115889880
7130329032130329033AG23GENIChomozygous115889886
7130329086130329087GT27GENIChomozygous115889888
7130329211130329212CT21GENIChomozygous115889890
7130329777130329778TC20GENIChomozygous115889892
7130331137130331138CT15GENIChomozygous116229504
7130332450130332451CG22GENIChomozygous115889896
7130334810130334811AC28GENIChomozygous116229507
7130332574130332575TC23GENIChomozygous115889898
7130333443130333444GA35GENIChomozygous116229506
7130333907130333908AC22GENIChomozygous115889908
7130334040130334041AT26GENIChomozygous115889910
7130335681130335682TC31GENIChomozygous115889916
7130335964130335965CG26GENIChomozygous116229508
7130337061130337062CT26GENIChomozygous115889922
7130337191130337192GA24GENIChomozygous115889926
7130338993130338994AG19GENIChomozygous116229510
7130339084130339085AT19GENIChomozygous115889944
7130339276130339277TC29GENIChomozygous115889946
7130339540130339541CA31GENIChomozygous116229511
7130339584130339585TC29GENIChomozygous115889948
7130340212130340213AG38GENIChomozygous115889950
7130340460130340461CG32GENIChomozygous116229512
7130340810130340811GT48GENIChomozygous115889954
7130342109130342110TG40GENIChomozygous115889956
7130342575130342576AG30GENIChomozygous115889958
7130342698130342699GA26GENIChomozygous116229513
7130343603130343604AG24GENIChomozygous116229514