Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:95516614-95516756 | Common:2; Rare:30 | ||||
chr14:96039068-96039456 | Common:2; Rare:95 | ||||
chr14:98973098-98973308 | Common:1; Rare:44 | ||||
chr14:100127934-100127966 | Rare:8 | ||||
chr14:100129367-100129588 | Common:1; Rare:51 | ||||
chr14:100130725-100130915 | Common:3; Rare:38 | ||||
chr14:100297230-100297530 | Common:5; Rare:64 | ||||
chr14:100303013-100303048 | Common:1; Rare:10 | ||||
chr14:100825911-100826160 | Rare:49 | ||||
chr14:101731299-101731441 | Common:3; Rare:40 | ||||
chr14:101948045-101948369 | Common:2; Rare:96 | ||||
chr14:101994522-101994849 | Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr14:102153347-102153376 | Rare:3 | ||||
chr14:102927355-102927592 | Rare:50 | ||||
chr14:103680984-103681303 | Common:4; Rare:70 |