| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:752311-752677 | Common:1; Rare:117 | ||||
| chr12:752930-753173 | Common:2; Rare:58; Clinvar (benign):2 | ||||
| chr12:949116-950060 | Common:9; Rare:237 | ||||
| chr12:950136-950282 | Common:1; Rare:35 | ||||
| chr12:990102-990418 | Common:3; Rare:68 | ||||
| chr12:991066-991363 | Common:5; Rare:125 | ||||
| chr12:1530209-1530428 | Common:1; Rare:65 | ||||
| chr12:1593345-1593583 | Common:2; Rare:57 | ||||
| chr12:1594175-1594395 | Common:1; Rare:60 | ||||
| chr12:1594495-1595021 | Common:4; Rare:161 | ||||
| chr12:1690768-1691125 | Common:4; Rare:126 | ||||
| chr12:1691424-1691525 | Rare:28 | ||||
| chr12:1796259-1796445 | Rare:57 | ||||
| chr12:1796864-1797038 | Common:1; Rare:39 | ||||
| chr12:1797290-1797459 | Common:1; Rare:62 |