chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121057491910574920AT13GENICheterozygous881073520
121057514010575141AC15GENIChomozygous881073519
121057530010575301AG4GENICheterozygous881073518
121057726110577262CA11GENIChomozygous881073517
121057776410577765CA8GENIChomozygous881073516
121057816310578164TC25GENIChomozygous881073515
121057931610579317TG14GENIChomozygous881073514
121058054210580543AG12GENIChomozygous881073513
121058068010580681AG6GENIChomozygous881073512
121058252410582525AG20GENIChomozygous881073511
121058277010582771GA19GENIChomozygous881073510