| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120250101-120250378 | Common:2; Rare:42 | ||||
| chr12:120437881-120438233 | Common:2; Rare:136; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446353-120446504 | Common:2; Rare:71 | ||||
| chr12:120469597-120469916 | Common:3; Rare:113 | ||||
| chr12:120495841-120496550 | Common:8; Rare:232 | ||||
| chr12:120529094-120529247 | Common:2; Rare:55 | ||||
| chr12:120581341-120581569 | Common:1; Rare:79 | ||||
| chr12:120687366-120687536 | Rare:43 | ||||
| chr12:120710134-120710474 | Common:4; Rare:82 | ||||
| chr12:120725700-120725882 | Common:2; Rare:57; Clinvar:1 | ||||
| chr12:120903469-120903658 | Rare:36 | ||||
| chr12:121210035-121210167 | Common:2; Rare:46 | ||||
| chr12:121399907-121400171 | Common:3; Rare:101 | ||||
| chr12:121537572-121537701 | Common:1; Rare:23 | ||||
| chr12:121580227-121580511 | Rare:79 |