chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185058736185058737AT21GENIChomozygous648346557
4185058836185058837CCA9GENICheterozygous756089087
4185059168185059169AC28GENIChomozygous648346558
4185059565185059566CT28GENIChomozygous648346559
4185060079185060080TC27GENIChomozygous648346560
4185061023185061024AG10GENIChomozygous648346561
4185061177185061201CACACACACACACACACACACACG------------------------12GENICpossibly homozygous756089088
4185061541185061548GCGCAAG-------9GENIChomozygous756089089
4185061608185061609GA9GENIChomozygous648346562
4185061624185061625AAAAAAAAAC10GENIChomozygous756089090
4185061821185061822GA14GENIChomozygous648346563
4185062022185062023T-16GENIChomozygous756089091
4185062231185062232CT9GENIChomozygous648346564
4185062253185062254CA10GENIChomozygous648346565