chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1133047058133047059CT15GENIChomozygous141250447
1133047098133047099CT21GENIChomozygous141250448
1133047893133047894AG23GENIChomozygous135670894
1133047949133047950GA25GENIChomozygous135670895
1133049221133049222TC29GENIChomozygous141250449
1133049874133049875GA28GENIChomozygous141250450
1133051418133051419GC30GENIChomozygous135670901
1133051881133051882GA20GENIChomozygous141250451
1133052672133052673CG12GENICpossibly homozygous141250452
1133053578133053579AG19GENIChomozygous135670903
1133054653133054654AC22GENIChomozygous135670904
1133055644133055645GC9GENIChomozygous141250453
1133055926133055927AG14GENIChomozygous135670906
1133056028133056029CT25GENIChomozygous141250454
1133056401133056402CT17GENIChomozygous141250455
1133056566133056567CA17GENIChomozygous141250456
1133056781133056782CT22GENIChomozygous135670908
1133057378133057379CT27GENIChomozygous135670911
1133058794133058795GA17GENIChomozygous141250457
1133059057133059058TC20GENIChomozygous141250458
1133059267133059268CT14GENIChomozygous141250459
1133059715133059716GT18GENIChomozygous141250460
1133059806133059807GA22GENIChomozygous141250461
1133060828133060829TA21GENIChomozygous141250462
1133061072133061073AG16GENIChomozygous141250463
1133061607133061608TC22GENIChomozygous135670914
1133061961133061962CA11GENIChomozygous141250464
1133061966133061967AC11GENICheterozygous402963903
1133055707133055708GA13GENIChomozygous153796839
1133062175133062176CA14GENIChomozygous135670916
1133062429133062429A18GENIChomozygous141169278
1133057742133057743A5GENIChomozygous141169275
1133058716133058724CAAGATGC19GENIChomozygous141169276
1133061966133061967A11GENIChomozygous141169277
1133062627133062628TG19GENIChomozygous135670917
1133063055133063056TC20GENIChomozygous135670918
1133063616133063617AG23GENIChomozygous135670919
1133064043133064044A20GENIChomozygous141169279
1133064044133064045AG20GENIChomozygous141250465