chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2060763186076319GA31GENIChomozygous63345352
2060771266077127CT31GENIChomozygous63345353
2060773696077370CA29GENICpossibly homozygous63345355
2060774096077410GA30GENICpossibly homozygous63345357
2060790726079073TG15GENIChomozygous63345360
2060792016079202AG31GENIChomozygous63345361
2060792486079249AT22GENIChomozygous63345363
2060804636080464CT43GENIChomozygous63345366
2060814666081467AG28GENIChomozygous63345367
2060816886081689CT34GENIChomozygous63345369
2060825046082505AG70GENIChomozygous63345370
2060843246084325TC28GENIChomozygous63345372
2060858496085850CT40GENIChomozygous63345374
2060858676085868TC45GENIChomozygous63345375
2060869626086963GA65GENIChomozygous63345377
2060877056087706CT52GENIChomozygous63345378
2060885136088514GA37GENIChomozygous63345380
2060890316089032CT26GENICpossibly homozygous63345382
2060890776089078AG30GENICheterozygous84963995