chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2224955828224955829A-8GENIChomozygous59415453
2224956843224956847TTTT----7GENIChomozygous59415454
2224957415224957416CCTT10GENIChomozygous59415456
2224958080224958081CT13GENIChomozygous59415461
2224958890224958891CT12GENIChomozygous59415462
2224958897224958898CT8GENIChomozygous59415463
2224959623224959624GGCACA9GENICheterozygous60827452
2224960452224960453TC17GENIChomozygous59415466
2224962375224962376GA16GENIChomozygous59415467
2224962936224962937TG9GENIChomozygous59415468
2224969020224969021AG7GENIChomozygous59415472
2224972904224972905CT12GENIChomozygous60166615
2224975339224975340AG11GENIChomozygous59415476
2224976399224976400TG17GENIChomozygous59415478
2224976562224976563TA18GENIChomozygous59415479
2224977718224977719AG27GENIChomozygous59415480
2224978449224978450TA21GENIChomozygous59415481
2224979629224979630GA13GENIChomozygous59415483