| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6201169-6201522 | Common:7; Rare:191 | ||||
| chr12:6232251-6232746 | Common:6; Rare:157 | ||||
| chr12:6310561-6310751 | Common:8; Rare:96 | ||||
| chr12:6312390-6313052 | Common:9; Rare:167 | ||||
| chr12:6341886-6342166 | Rare:95; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:6363339-6363541 | Common:3; Rare:147; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6363760-6364629 | Common:6; Rare:395 | ||||
| chr12:6374920-6375350 | Common:6; Rare:133 | ||||
| chr12:6375353-6375770 | Common:7; Rare:206; Clinvar:3; Clinvar (benign):14 | ||||
| chr12:6383875-6384279 | Common:10; Rare:236 | ||||
| chr12:6384712-6385149 | Common:7; Rare:229 | ||||
| chr12:6451454-6452296 | Common:13; Rare:333 | ||||
| chr12:6470555-6471226 | Common:20; Rare:412 | ||||
| chr12:6493069-6493486 | Common:21; Rare:254 | ||||
| chr12:6493460-6493690 | Common:11; Rare:95 |