| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6534431-6534860 | Common:8; Rare:183 | ||||
| chr12:6568249-6568425 | Rare:67 | ||||
| chr12:6689412-6689735 | Common:2; Rare:86 | ||||
| chr12:6723848-6724158 | Common:1; Rare:60 | ||||
| chr12:6753066-6753180 | Common:4; Rare:42 | ||||
| chr12:6851890-6852195 | Rare:79 | ||||
| chr12:6867406-6867680 | Common:2; Rare:131; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873334-6873664 | Common:3; Rare:93 | ||||
| chr12:6914267-6914657 | Common:1; Rare:93 | ||||
| chr12:6943938-6944172 | Common:5; Rare:235; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970426-6971001 | Common:4; Rare:184; Clinvar (benign):1 | ||||
| chr12:7018420-7018840 | Common:2; Rare:123 | ||||
| chr12:7130240-7130418 | Common:5; Rare:47 | ||||
| chr12:7789231-7789443 | Common:2; Rare:43 | ||||
| chr12:7862953-7863017 | Rare:20 |