| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6867379-6867619 | Common:2; Rare:122; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868001-6868161 | Common:4; Rare:64 | ||||
| chr12:6873295-6873534 | Common:1; Rare:71 | ||||
| chr12:6904587-6904903 | Common:1; Rare:68 | ||||
| chr12:6914434-6914659 | Common:2; Rare:61 | ||||
| chr12:6943531-6943817 | Common:4; Rare:116 | ||||
| chr12:6970602-6970969 | Common:4; Rare:114; Clinvar (benign):1 | ||||
| chr12:7018387-7018455 | Rare:22 | ||||
| chr12:7018468-7018577 | Common:1; Rare:30 | ||||
| chr12:7130161-7130432 | Common:5; Rare:67 | ||||
| chr12:7189556-7189733 | Rare:66; Clinvar:4 | ||||
| chr12:8032542-8032770 | Common:5; Rare:72 | ||||
| chr12:8227619-8227691 | Rare:22 | ||||
| chr12:8697830-8698124 | Common:2; Rare:101 | ||||
| chr12:8914359-8914795 | Common:6; Rare:128 |