| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6341375-6341530 | Common:2; Rare:38 | ||||
| chr12:6341628-6341756 | Common:1; Rare:43; Clinvar:1 | ||||
| chr12:6341897-6342194 | Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:6363337-6363708 | Common:4; Rare:147; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6363710-6364025 | Common:2; Rare:90 | ||||
| chr12:6364111-6364353 | Rare:51 | ||||
| chr12:6375371-6375747 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):6 | ||||
| chr12:6376141-6376492 | Common:3; Rare:72 | ||||
| chr12:6376728-6377055 | Rare:57 | ||||
| chr12:6377090-6377135 | Rare:6 | ||||
| chr12:6383750-6384260 | Common:4; Rare:111 | ||||
| chr12:6384661-6384799 | Common:2; Rare:25 | ||||
| chr12:6451436-6451708 | Common:1; Rare:64 | ||||
| chr12:6451749-6451861 | Rare:17 | ||||
| chr12:6452001-6452137 | Common:1; Rare:30 |