chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115618485656184858AT--4GENICheterozygous51412535
115618505856185059GGA10GENICheterozygous51364878
115618682256186823C-16GENIChomozygous50786665
115618708256187084GT--15GENICheterozygous51196265
115619550256195503TTTGTGTGTGTG9GENICheterozygous51233561
115619550356195505TG--9GENICheterozygous51184774
115620751056207511CCTTTTTTT6GENICheterozygous51184778
115622895056228951TG13GENIChomozygous50786714
115624983156249832CCA5GENICheterozygous51184780
115625015456250155T-9GENICheterozygous50958631
115625146756251468AATAC13GENIChomozygous50786736
115626333456263335T-22GENICheterozygous51270844
115631113856311139CCT17GENIChomozygous50786781
115631602956316030T-13GENICheterozygous50958635
115631723056317231AG19GENIChomozygous50786790
115631723356317234TC19GENIChomozygous50881331
115631723456317235GT20GENICpossibly homozygous50786791
115631723856317239AT20GENICpossibly homozygous50958637
115632153456321535G-17GENICheterozygous51161969
115633082356330837ACACACACACACAC--------------5GENICheterozygous50786817
115633083556330837AC--5GENICheterozygous51184785
115623424956234250T-7GENICpossibly homozygous51213859
115628736056287361GGGAAA1GENIChomozygous51213860
115637376056373762GG--7GENICheterozygous51184787
115638479756384798GGA4GENICheterozygous51184789
115639547056395472CA--23GENICheterozygous51201918
115639620356396205CT--16GENICheterozygous51196269