chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120457525120457526AT15GENIChomozygous138197327
7120458607120458608GA15GENIChomozygous138197328
7120460309120460310CA19GENIChomozygous138197329
7120462169120462170TA16GENIChomozygous138197330
7120462426120462427GA13GENIChomozygous138197331
7120462689120462690CG20GENIChomozygous138197332
7120461244120461244CACCACCACCACCACCAT2GENIChomozygous147848363
7120463120120463121TC14GENIChomozygous403224316
7120463120120463121T14GENICheterozygous403224317
7120463346120463347AG12GENIChomozygous138197333
7120463607120463608AG15GENIChomozygous138197334
7120464604120464605CA15GENIChomozygous138197335
7120465190120465191CA26GENIChomozygous138197336
7120466061120466062GA19GENIChomozygous138197337
7120466243120466244CT13GENIChomozygous138197338
7120466674120466674CT21GENIChomozygous137977943
7120464368120464368T23GENIChomozygous137977941
7120465713120465714T17GENIChomozygous137977942
7120466917120466918CT14GENIChomozygous138197339
7120467539120467540GA21GENIChomozygous138197340
7120467549120467550AG21GENIChomozygous138197341
7120469440120469441TC14GENIChomozygous138197342
7120471101120471102TC11GENIChomozygous138197343
7120474095120474095TCTTATAACTTTTTTTTTTTTTTTTG4GENIChomozygous147436044
7120475382120475383AG17GENIChomozygous138197344
7120478276120478277AT15GENIChomozygous138197345
7120478278120478279GC15GENIChomozygous138197346
7120478280120478283AGA15GENIChomozygous137977944
7120478336120478337AG16GENIChomozygous138197347
7120478944120478945AG13GENIChomozygous138197348
7120478987120478988CT9GENIChomozygous138197349
7120479636120479637GA15GENIChomozygous138197350
7120480982120480982AATA8GENIChomozygous137977945
7120481623120481624GA22GENIChomozygous138197352
7120482093120482094TC23GENIChomozygous138197353
7120482588120482589TA13GENIChomozygous138197354
7120473799120473800AC19GENIChomozygous144809986