chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2060763186076319GA40GENICpossibly homozygous63345352
2060771266077127CT22GENICpossibly homozygous63345353
2060773696077370CA14GENIChomozygous63345355
2060774096077410GA10GENIChomozygous63345357
2060792016079202AG17GENIChomozygous63345361
2060792486079249AT22GENIChomozygous63345363
2060804636080464CT29GENIChomozygous63345366
2060814666081467AG26GENIChomozygous63345367
2060816886081689CT24GENIChomozygous63345369
2060825046082505AG25GENIChomozygous63345370
2060843246084325TC21GENICpossibly homozygous63345372
2060858496085850CT25GENICpossibly homozygous63345374
2060858676085868TC29GENICpossibly homozygous63345375
2060869626086963GA39GENICpossibly homozygous63345377
2060877056087706CT19GENIChomozygous63345378
2060885136088514GA17GENICheterozygous63345380
2060890316089032CT17GENICheterozygous63345382
2060894056089406GA28GENICheterozygous63643716