chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2264868555264868556CT8GENIChomozygous110442254
2264869362264869363CT4GENIChomozygous110442255
2264869866264869867GT19GENICpossibly homozygous110442256
2264870156264870157GA9GENIChomozygous111053882
2264873565264873566TG19GENIChomozygous110442257
2264873640264873641GA19GENIChomozygous110442258
2264874264264874265TC33GENIChomozygous110442260
2264874513264874514TC22GENIChomozygous110442262
2264875711264875712CT24GENIChomozygous111053884
2264877655264877656GA13GENICheterozygous110442264
2264879555264879556CT19GENIChomozygous111053886
2264880559264880560GA17GENIChomozygous110442266
2264881879264881880TG20GENIChomozygous110442268
2264885588264885589AG15GENIChomozygous110442271
2264885611264885612CT17GENIChomozygous110442272
2264891789264891790AG9GENIChomozygous110442274
2264892179264892180CA29GENIChomozygous110442275
2264892223264892224CT28GENICpossibly homozygous111053890
2264892399264892400GA18GENIChomozygous111053892
2264894301264894302AC12GENIChomozygous111053894