chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2224984741224984742GGT19GENIChomozygous59415485
2224986015224986016AG22GENIChomozygous59415486
2224987875224987876CT26GENIChomozygous59415488
2224988729224988730T-5GENIChomozygous59415489
2224991528224991529AG15GENIChomozygous59415491
2224991905224991906AATAT6GENIChomozygous59415495
2224993101224993102AATGTGTG12GENICpossibly homozygous60549987
2224993161224993162AATATG9GENIChomozygous59415496