chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121843219121843220AG20GENICpossibly homozygous631642465
8121843359121843360CT14GENIChomozygous631642466
8121843428121843429CT21GENICpossibly homozygous631642467
8121843478121843479AG20GENICpossibly homozygous631642468
8121843825121843826GA11GENICheterozygous631642469
8121844425121844426AC22GENICpossibly homozygous631642470
8121844635121844636TC7GENICheterozygous631642471
8121845798121845799GC26GENICpossibly homozygous631642472
8121846799121846800TA12GENICheterozygous631642473
8121846878121846879CT18GENICpossibly homozygous631642474
8121848181121848182CT12GENIChomozygous631642475
8121848295121848296AC14GENICheterozygous631642476