chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121893134618931347CT16INTERGENICpossibly homozygous795333100
121893184618931847CT49GENIChomozygous795333101
121893185818931859GA48GENIChomozygous795333102
121893194818931949TC35GENIChomozygous795333103
121893227218932273AG56GENIChomozygous795333104
121893231318932314GA57GENIChomozygous795333105
121893313218933133TC35GENIChomozygous795333106
121893456818934569AG23GENICheterozygous795333107
121893470318934704TC19GENIChomozygous795333108
121893489718934898CT48GENIChomozygous795333109
121893571918935720AT45GENICpossibly homozygous795333110
121893620418936205AT177GENICheterozygous795333111
121893620618936207CT180GENICheterozygous795333112
121893622818936229TC247GENICheterozygous795333113
121893623718936238AC245GENICheterozygous795333114
121893624918936250CT101GENICheterozygous795333115
121893625618936257AC148GENICheterozygous795333116
121893628318936284TC91GENICheterozygous795333117
121893632118936322TC49GENIChomozygous795333118
121893695118936952CT40GENICpossibly homozygous795333119
121893712318937124TC201GENICheterozygous795333120
121893759418937595GA42GENIChomozygous795333121
121893802618938027GT29GENICheterozygous795333122