chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171436708714367088CT23GENICpossibly homozygous111170800
171436808514368086TC16GENIChomozygous110966188
171436859114368592AG12GENIChomozygous111170802
171437171714371718AC30GENICheterozygous111496019
171437179614371797CT22GENICheterozygous111496021
171437221914372220CG14GENIChomozygous111496023
171437231714372318AC17GENIChomozygous111170804
171437242814372429CG19GENIChomozygous110966190
171437266714372668TC23GENIChomozygous110966192
171437292914372930TC16GENIChomozygous110966194
171437309614373097TG13GENIChomozygous111496025
171437347214373473TC15GENIChomozygous111170806