chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
317747091774710TC25GENIChomozygous111428403
318065921806593CT24GENIChomozygous111428404
318124421812443GT36GENIChomozygous111428405
318336641833665AT7GENIChomozygous111428406
318346691834670GC30GENICheterozygous111428407
318349251834926CT11GENICheterozygous112222224
318475591847560TC26GENIChomozygous111428409
318528111852812TG35GENIChomozygous111428410
318716771871678AG9GENIChomozygous111428412
318763471876348GC28GENIChomozygous111428413
318849891884990AT25GENIChomozygous111428415
318850961885097CT48GENIChomozygous111428416
318997631899764AT19GENIChomozygous111428418
318999731899974CT28GENIChomozygous111428419
319006571900658GC26GENIChomozygous111428420
319009921900993GA9GENIChomozygous111428421
319013371901338GA11GENIChomozygous111428422
319020831902084GA14GENIChomozygous111428423
319031481903149AG38GENIChomozygous111428424
319050211905022GA15GENIChomozygous111428425
319061091906110TG47GENICheterozygous111428427
319061261906127GT43GENICheterozygous111428428
319076351907636CG17GENIChomozygous111428429
319083651908366GT11GENIChomozygous111428430
319109311910932AG39GENIChomozygous111428431
319113681911369CT38GENIChomozygous111428432
319130921913093GA28GENIChomozygous111428433
319159661915967CT41GENIChomozygous111428434
319176951917696AG12GENICheterozygous111428435
319198461919847TC33GENIChomozygous111428440
319211641921165AT3GENIChomozygous111428441
319213941921395GA25GENIChomozygous111428442
319234911923492TC21GENIChomozygous111428443