chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225017049225017050TC14GENIChomozygous108556368
1225017237225017238AC19GENIChomozygous108556369
1225017786225017787TC14GENIChomozygous108556370
1225018222225018223GC6GENIChomozygous108556371
1225018407225018408GA10GENIChomozygous108556372
1225018880225018881GT20GENIChomozygous108556373
1225019768225019769CT9GENIChomozygous108556374
1225020601225020602GA14GENIChomozygous108556375
1225020653225020654GT17GENIChomozygous108556376
1225021558225021559CT22GENIChomozygous108556377
1225022030225022031GA11GENIChomozygous108556378
1225023550225023551AG16GENIChomozygous108556379
1225023815225023816GA14GENIChomozygous108556380
1225024091225024092TC24GENIChomozygous108556381
1225024602225024603GA11GENIChomozygous108556382
1225024832225024833AG16GENIChomozygous108556383
1225025522225025523AG5GENIChomozygous108556384
1225026357225026358AG11GENIChomozygous108556385
1225026661225026662CT10GENIChomozygous108556387