chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2036937043693705AC22GENIChomozygous130025861
2036938193693820C29GENICpossibly homozygous140482842
2036938243693825CT29GENICpossibly homozygous130025862
2036940003694001AG29GENIChomozygous130025864
2036942093694210GC57GENIChomozygous130025866
2036943723694373CG58GENIChomozygous130025867
2036945093694510AG73GENIChomozygous130025868
2036947973694798TC80GENICpossibly homozygous130025870
2036948783694879AG74GENICpossibly homozygous130025871
2036957783695779CT49GENIChomozygous130025872
2036960673696068CT53GENIChomozygous130025873
2036961233696124CG64GENIChomozygous130025874
2036961763696177CT59GENIChomozygous130025875
2036961813696182TC61GENIChomozygous130025876