chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3147504996147504997TC18GENIChomozygous119997421
3147506297147506298CG24GENIChomozygous119997423
3147506343147506344GA23GENIChomozygous119997425
3147508769147508770CT23GENIChomozygous119997427
3147510312147510313GA31GENIChomozygous119997429
3147510620147510621TC29GENIChomozygous119997431
3147511256147511257CT14GENIChomozygous119997433
3147511512147511513AG22GENIChomozygous119997435
3147512289147512309CCTTCTTCCTTCCTTCCTTC9GENIChomozygous131329840
3147512338147512339TA17GENIChomozygous120102607
3147512369147512370GA20GENIChomozygous119997437
3147514452147514453AT25GENIChomozygous119997439
3147514816147514817TC17GENIChomozygous119997441
3147515392147515393CT14GENIChomozygous119997443
3147515663147515664CT15GENIChomozygous119997445
3147516362147516363TC18GENIChomozygous120102609
3147516810147516811TC22GENIChomozygous119997447
3147516941147516942CT23GENIChomozygous119997449
3147517435147517436CT21GENIChomozygous119997451
3147517450147517451GA22GENIChomozygous119997453