| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6200005-6200426 | Common:3; Rare:117 | ||||
| chr12:6200595-6200764 | Common:2; Rare:38 | ||||
| chr12:6383988-6384250 | Common:1; Rare:57 | ||||
| chr12:6493107-6493386 | Common:7; Rare:87 | ||||
| chr12:6493746-6494126 | Common:2; Rare:112 | ||||
| chr12:6568249-6568384 | Rare:52 | ||||
| chr12:6689420-6689748 | Common:2; Rare:88 | ||||
| chr12:6723981-6724296 | Rare:79 | ||||
| chr12:6851902-6852182 | Rare:73 | ||||
| chr12:6873279-6873532 | Common:2; Rare:74 | ||||
| chr12:6943938-6944161 | Common:5; Rare:225; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944208-6944592 | Common:2; Rare:170; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:6970586-6970977 | Common:4; Rare:122; Clinvar (benign):1 | ||||
| chr12:6983394-6983456 | Rare:7 | ||||
| chr12:7018420-7018584 | Common:1; Rare:48 |