chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221711780221711781GA6GENIChomozygous109368567
1221712040221712041CG17GENICpossibly homozygous109368568
1221715642221715643AG16GENIChomozygous108545115
1221715973221715974AG19GENIChomozygous108545117
1221716116221716117AG8GENIChomozygous108545119
1221716804221716805CT10GENIChomozygous109368570
1221716836221716837AG9GENIChomozygous108545123
1221721048221721049GA12GENIChomozygous109368572
1221722402221722403AG11GENIChomozygous108545131
1221722581221722582GA21GENIChomozygous109368574
1221724705221724706TG18GENIChomozygous108545141
1221726009221726010AG22GENIChomozygous108545143