chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185122708051227081AG65GENIChomozygous46449707
185122733951227340TC76GENICpossibly homozygous46449708
185122798951227990CCTTG51GENIChomozygous46449709
185122949651229497AG29GENICheterozygous46449710
185122987351229874CCTTTATTTATTTA22GENIChomozygous46449711
185123018151230182GA59GENIChomozygous46449712
185123072851230729AG28GENICheterozygous46449713
185123182451231825AG56GENIChomozygous46449714
185123333751233338GC77GENIChomozygous46449715
185123368851233689A-3GENIChomozygous46602965
185123504451235045AG62GENIChomozygous46449716
185123666751236668CA77GENIChomozygous46449717