chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4185058736185058737AT16GENIChomozygous655948037
4185058836185058837CCA12GENICpossibly homozygous760591512
4185059168185059169AC23GENICpossibly homozygous655948038
4185059565185059566CT29GENICpossibly homozygous655948039
4185060079185060080TC26GENIChomozygous655948040
4185061023185061024AG27GENIChomozygous655948041
4185061177185061201CACACACACACACACACACACACG------------------------36GENICpossibly homozygous760591513
4185061541185061548GCGCAAG-------20GENIChomozygous760591514
4185061608185061609GA11GENIChomozygous655948042
4185061624185061625AAAAAAAAAC11GENIChomozygous760591515
4185061821185061822GA16GENIChomozygous655948043
4185062022185062023T-14GENIChomozygous760591516
4185062231185062232CT29GENIChomozygous655948044
4185062253185062254CA33GENIChomozygous655948045