| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562361-108562675 | Common:9; Rare:126; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109477259-109477643 | Common:3; Rare:101 | ||||
| chr12:109573470-109573813 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880381-109880676 | Common:1; Rare:89 | ||||
| chr12:110346074-110346276 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr12:110468843-110468907 | Rare:23 | ||||
| chr12:110496024-110496351 | Common:2; Rare:61 | ||||
| chr12:110501559-110501626 | Common:1; Rare:21 | ||||
| chr12:110502047-110502283 | Common:1; Rare:80 | ||||
| chr12:111685822-111686094 | Rare:103 | ||||
| chr12:111841875-111842224 | Common:3; Rare:94 | ||||
| chr12:112013129-112013460 | Common:1; Rare:114 | ||||
| chr12:113185384-113185769 | Common:10; Rare:151 | ||||
| chr12:114684173-114684350 | Rare:43 | ||||
| chr12:118061041-118061407 | Common:3; Rare:85 |