chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7115318660115318661TC16GENIChomozygous138187279
7115318780115318781GA17GENIChomozygous142008920
7115318930115318931GT26GENIChomozygous138187280
7115320471115320472GT21GENIChomozygous138187286
7115322297115322298CT10GENIChomozygous142008921
7115324090115324091GC26GENIChomozygous142008922
7115325829115325830GC21GENIChomozygous142008923
7115325838115325839AG20GENIChomozygous138187290
7115325844115325845AG21GENIChomozygous138187291
7115322400115322401A24GENIChomozygous141922837
7115322208115322208GGAG10GENIChomozygous137975862
7115322404115322405AG24GENICheterozygous154480457
7115322402115322405ATA24GENIChomozygous141922838
7115325840115325840G20GENIChomozygous141922839
7115322404115322405A24GENIChomozygous403223172
7115327455115327456AG25GENIChomozygous138187293
7115327775115327776CT15GENIChomozygous142008924
7115328247115328248CT24GENIChomozygous142008925
7115328512115328513TC23GENIChomozygous138187294
7115329725115329725C9GENIChomozygous137975864
7115332157115332158GA23GENIChomozygous142008926
7115333388115333389GA14GENIChomozygous142008927
7115333602115333603GA18GENIChomozygous142008928
7115335224115335225TC19GENIChomozygous138187313
7115335997115335998AT15GENIChomozygous142008929
7115336080115336080GT7GENICpossibly homozygous141922840
7115336655115336655TG14GENIChomozygous137975868
7115337589115337590GC21GENIChomozygous138187318
7115337615115337616TA20GENIChomozygous142008930
7115339385115339386TC16GENIChomozygous138187324
7115341191115341192TG25GENIChomozygous138187326