chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----21GENIChomozygous760470392
3154514259154514260CT22GENIChomozygous655740945
3154514276154514277TG27GENIChomozygous655740946
3154514414154514415AAGTCT26GENIChomozygous760470394
3154515300154515301GA19GENIChomozygous655740947
3154515475154515476GA20GENIChomozygous655740948
3154515627154515628GA20GENIChomozygous655740949
3154515681154515682TA22GENIChomozygous655740950
3154515884154515885AG22GENIChomozygous655740951
3154516260154516261TC23GENIChomozygous655740952
3154516490154516491AT30GENIChomozygous655740953
3154516884154516885AG29GENIChomozygous655740954
3154516887154516888GA33GENIChomozygous655740955
3154517156154517157AG25GENIChomozygous655740956
3154517166154517167TG25GENIChomozygous655740957
3154517351154517352G-23GENIChomozygous760470395
3154517632154517633G-27GENIChomozygous760470396
3154517898154517899TC29GENIChomozygous655740958
3154518068154518069GA32GENIChomozygous655740959
3154518158154518159TTA29GENIChomozygous760470397
3154519184154519185CCCA9GENIChomozygous760470399
3154519630154519636TCCCTC------8GENIChomozygous760470400
3154519872154519873AC19GENIChomozygous655740960
3154519897154519899TT--18GENIChomozygous760470401
3154519985154519986AG27GENIChomozygous655740961
3154520058154520059TC28GENICpossibly homozygous655740962
3154521686154521687CT30GENICpossibly homozygous655740963
3154521914154521915TTAA15GENICheterozygous760470404
3154521915154521916A-15GENICpossibly homozygous760470403
3154522134154522135AG19GENIChomozygous655740964