chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2053988465398847CT25GENICpossibly homozygous45731719
2054010135401014TC27GENICpossibly homozygous45386585
2054011195401120AG18GENIChomozygous45731721
2054012895401290AG36GENICpossibly homozygous45386589
2054015145401515TC18GENICpossibly homozygous45386591
2054016775401691TCTGCCACATGTAG--------------1GENIChomozygous45731722
2054019205401927ATGCTAT-------1GENIChomozygous45731723
2054022515402252GT12GENICheterozygous45731725
2054033895403390AG15GENIChomozygous45386613
2054034915403492CT15GENIChomozygous45731726