chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X118451633118451634CG14GENICheterozygous119948212
X118451657118451658GA17GENICheterozygous119948213
X118451659118451660GT18GENICheterozygous119948214
X118451720118451721TG23GENICheterozygous119948217
X118451724118451725GT24GENICheterozygous119948219
X118451728118451729GA24GENICheterozygous129826022
X118451732118451733TG24GENICheterozygous129826023
X118451814118451815TA18GENICheterozygous129826024
X118451846118451847CT20GENICheterozygous119948220
X118481842118481843CT12GENICheterozygous130615967
X118481850118481851AT14GENICheterozygous130615968
X118481862118481863AG13GENICheterozygous130615969
X118481957118481958CT7GENICheterozygous130615971
X118482218118482219GA12GENICheterozygous130615975
X118482256118482257GT12GENICheterozygous130202431
X118482270118482271AG12GENICheterozygous130615976
X118482300118482301CT13GENICheterozygous130615977
X118494433118494434T2GENIChomozygous129783271
X118494448118494450TC2GENIChomozygous129783272
X118494454118494454T2GENIChomozygous129783273
X118494455118494455A2GENIChomozygous129783274
X118494464118494464G2GENIChomozygous129783275
X118494472118494473AG1GENIChomozygous120721638
X118494473118494474CA1GENIChomozygous120721639