chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171053957610539577AG29GENIChomozygous809691344
171054242110542422AG48GENIChomozygous809691345
171054274510542746TC35GENIChomozygous809691346
171054305810543059TC61GENIChomozygous809691347
171054340610543407CT58GENIChomozygous809691348
171054360310543604AG42GENIChomozygous809691349
171054376810543769CG23GENICpossibly homozygous809691350
171054455010544551TC46GENICpossibly homozygous809691351
171054506710545068AG45GENIChomozygous809691352
171054586110545862CT38GENIChomozygous809691353
171054592610545927TG44GENICheterozygous809691354
171054682510546826AG62GENIChomozygous809691355
171054696010546961TC51GENIChomozygous809691356
171054748810547489GA43GENIChomozygous809691357