chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3148635946148635947CG17GENIChomozygous111770471
3148636848148636849CT30GENIChomozygous111770473
3148636983148636984CT24GENIChomozygous111770475
3148637180148637181CA28GENIChomozygous111770477
3148637446148637447CG24GENIChomozygous111770479
3148638772148638773AG34GENIChomozygous111770481
3148639978148639979TC8GENIChomozygous119652213
3148639989148639990GT7GENIChomozygous119652214
3148639991148639992CA6GENIChomozygous119652215
3148643590148643591AT13GENIChomozygous119652216
3148643615148643616AT12GENIChomozygous119652217
3148646892148646893CT20GENIChomozygous111770487
3148647207148647208GA31GENIChomozygous111770489
3148648300148648301CT14GENIChomozygous111770491
3148650625148650626AG24GENIChomozygous111770493
3148652439148652440GC21GENIChomozygous111770495
3148655196148655197GA29GENIChomozygous111770497
3148661316148661317CT23GENIChomozygous111770500
3148661317148661318AG22GENIChomozygous111770502
3148661590148661591TC18GENIChomozygous111770504
3148662601148662602GA15GENIChomozygous111770506
3148662727148662728AG20GENIChomozygous111770508
3148663503148663504TG33GENIChomozygous111770510
3148665842148665843TA22GENIChomozygous111770526
3148667102148667103GA23GENIChomozygous111770528
3148670009148670010AC24GENIChomozygous111770530
3148671306148671307GC20GENIChomozygous111770532
3148677304148677305AT22GENIChomozygous111770534
3148680007148680008TA27GENIChomozygous111770538
3148681328148681329GA9GENIChomozygous111770540
3148682943148682944GT17GENIChomozygous111770542
3148684105148684106CT20GENIChomozygous111770548
3148689759148689760AG17GENIChomozygous111770552