chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162027464920274650TA49GENIChomozygous47992647
162027469920274700G-43GENIChomozygous47740306
162027496620274967CG27GENIChomozygous47992648
162027551020275511TC37GENIChomozygous47992649
162027577920275780CT40GENIChomozygous47992650
162027584220275843GA46GENICpossibly homozygous47992651
162027631320276314CT24GENIChomozygous47992652
162027720620277207AG37GENICpossibly homozygous47740317
162027769720277698TC32GENIChomozygous47327032
162027925620279260GTGT----36GENICheterozygous47740330
162027925820279260GT--36GENICpossibly homozygous47327034
162028041720280418CT30GENIChomozygous47992653