chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120466504120466505AG20GENIChomozygous115856354
7120467151120467152CA12GENIChomozygous115856356
7120467180120467181CT13GENIChomozygous115856358
7120467263120467264GA13GENIChomozygous115856360
7120467320120467321TG14GENIChomozygous115856362
7120467481120467482GA7GENIChomozygous115856364
7120467575120467576AG18GENIChomozygous115856366
7120469163120469164AG9GENIChomozygous115856372
7120469269120469270TG17GENICheterozygous115856374
7120470340120470341TC16GENIChomozygous115856376
7120471831120471832AC7GENIChomozygous115856378
7120472298120472299GA18GENIChomozygous115856382
7120472418120472419AG13GENIChomozygous115856384
7120473806120473807TC9GENIChomozygous115856386
7120474188120474189AT16GENIChomozygous115856388
7120474894120474895GA21GENIChomozygous115856390
7120476105120476106GA11GENIChomozygous115856392
7120476189120476190AC9GENIChomozygous115856394
7120476332120476333CT13GENIChomozygous115856396
7120477760120477761AC14GENIChomozygous115856398
7120478633120478634GA15GENIChomozygous115856400
7120479174120479175AG8GENIChomozygous115856404
7120479942120479943TG8GENIChomozygous115856408
7120479954120479955TC9GENIChomozygous115856410
7120480956120480957CT9GENIChomozygous115856412
7120481542120481543TC17GENIChomozygous115856414
7120481702120481703TC14GENIChomozygous115856416
7120482377120482378AG15GENIChomozygous115856418
7120482754120482755TC8GENIChomozygous115856420
7120482884120482885GT16GENIChomozygous115856422
7120483751120483752CA11GENIChomozygous115856426
7120484324120484325AG7GENIChomozygous115856428