chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2060763186076319GA32GENIChomozygous63345352
2060771266077127CT18GENIChomozygous63345353
2060773696077370CA11GENIChomozygous63345355
2060774096077410GA15GENIChomozygous63345357
2060790726079073TG12GENIChomozygous63345360
2060792016079202AG21GENIChomozygous63345361
2060792486079249AT15GENIChomozygous63345363
2060804636080464CT31GENIChomozygous63345366
2060814666081467AG22GENIChomozygous63345367
2060816886081689CT20GENIChomozygous63345369
2060825046082505AG19GENIChomozygous63345370
2060843246084325TC23GENIChomozygous63345372
2060858496085850CT19GENIChomozygous63345374
2060858676085868TC16GENIChomozygous63345375
2060869626086963GA28GENIChomozygous63345377
2060877056087706CT28GENIChomozygous63345378
2060885136088514GA16GENIChomozygous63345380
2060890316089032CT14GENICpossibly homozygous63345382
2060890776089078AG23GENICheterozygous84963995