chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134722989647229897AG17GENIChomozygous142369426
134723119247231193CA23GENIChomozygous144930896
134723251347232514AG12GENIChomozygous142369428
134723340147233402TC20GENIChomozygous142369429
134723465447234655GA17GENIChomozygous144930897
134723522747235228CT10GENIChomozygous144930898
134723525247235253TC9GENIChomozygous144930899
134723541447235415CT13GENIChomozygous144930900
134723552147235521A7GENIChomozygous144925075
134723554747235548GA6GENIChomozygous144930901
134723570947235710AG13GENIChomozygous144930902
134723592347235924CT12GENIChomozygous144930906
134723571147235712GA12GENIChomozygous144930903
134723586547235866GA8GENIChomozygous144930904
134723586947235870GC8GENIChomozygous144930905
134723624747236248TC21GENIChomozygous144930907
134723638447236385CT10GENIChomozygous144930908
134723662747236629TG18GENICheterozygous142344117
134723690147236902TC13GENIChomozygous144930909
134723709447237098TTTG6GENIChomozygous144925076
134723722347237224TC16GENIChomozygous144930910
134723732047237320AAAC14GENIChomozygous144925077
134723735047237351C12GENIChomozygous144925078
134723768847237689CT22GENIChomozygous144930911
134723777047237771TG17GENIChomozygous144930912
134723785747237858GA17GENIChomozygous144930913
134723835147238352CT18GENIChomozygous144930914
134723846447238465GA17GENIChomozygous144930915
134723848447238485AG16GENIChomozygous144930916
134723849747238498CT14GENIChomozygous144930917
134723851947238520TG16GENIChomozygous144930918
134723857947238580AG16GENIChomozygous144930919
134723910247239103TA16GENIChomozygous144930920
134723953947239540CT16GENIChomozygous144930921
134724042447240425TC15GENIChomozygous142369430
134724055047240550T18GENICpossibly homozygous144925079
134724109447241095TC20GENIChomozygous142369432
134724122447241225AG22GENIChomozygous144930922
134723662847236629G18GENICheterozygous403338135
134723662847236629GT18GENICheterozygous403338134