chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120457525120457526AT23GENIChomozygous138197327
7120458023120458024GA19GENIChomozygous147554912
7120460230120460231CT18GENIChomozygous147554913
7120460309120460310CA20GENIChomozygous138197329
7120461225120461226C6GENICheterozygous403896320
7120461225120461226CT6GENIChomozygous403896321
7120462689120462690CG27GENIChomozygous138197332
7120465190120465191CA26GENIChomozygous138197336
7120462698120462699CG22GENIChomozygous147554914
7120463346120463347AG12GENIChomozygous138197333
7120464368120464368T19GENIChomozygous137977941
7120465313120465313TT16GENIChomozygous147551290
7120466674120466674CT18GENIChomozygous137977943
7120466786120466792GTTCCT23GENIChomozygous147551291
7120466834120466835GA24GENIChomozygous147554915
7120467502120467503CT20GENIChomozygous147554916
7120467539120467540GA23GENIChomozygous138197340
7120467549120467550AG23GENIChomozygous138197341
7120469440120469441TC22GENIChomozygous138197342
7120469917120469918CT17GENIChomozygous147554917
7120470040120470041CG24GENIChomozygous146201995
7120471101120471102TC14GENIChomozygous138197343
7120471464120471465CT7GENIChomozygous146201997
7120475382120475383AG27GENIChomozygous138197344
7120477356120477358AT16GENIChomozygous147551292
7120478336120478337AG18GENIChomozygous138197347
7120478944120478945AG14GENIChomozygous138197348
7120478987120478988CT16GENIChomozygous138197349
7120479636120479637GA10GENIChomozygous138197350
7120480639120480640TC9GENIChomozygous138197351
7120481623120481624GA25GENIChomozygous138197352
7120482093120482094TC16GENIChomozygous138197353
7120482588120482589TA16GENIChomozygous138197354