| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8914109-8914276 | Rare:32 | ||||
| chr12:8914280-8914835 | Common:7; Rare:159 | ||||
| chr12:8915167-8915226 | Rare:13 | ||||
| chr12:8949589-8950128 | Common:4; Rare:124 | ||||
| chr12:10212237-10212526 | Rare:80 | ||||
| chr12:10213215-10213484 | Rare:65 | ||||
| chr12:10613528-10613732 | Common:1; Rare:80 | ||||
| chr12:11171150-11171243 | Rare:36 | ||||
| chr12:11171565-11171790 | Common:6; Rare:74 | ||||
| chr12:12266725-12267399 | Common:9; Rare:270 | ||||
| chr12:12356981-12357204 | Common:4; Rare:111 | ||||
| chr12:12611763-12612055 | Common:2; Rare:84 | ||||
| chr12:12684432-12684920 | Common:3; Rare:60 | ||||
| chr12:12696683-12696744 | Rare:28 | ||||
| chr12:12717628-12717831 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 |