chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2217603943217603944GA19GENICpossibly homozygous59395552
2217604035217604036CT9GENIChomozygous59395553
2217604902217604903A-16GENIChomozygous59936377
2217605122217605123CT17GENICpossibly homozygous59936378
2217606793217606794AAC16GENIChomozygous59395565
2217607748217607749AT17GENIChomozygous59395568