| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526864-122527262 | Common:4; Rare:136 | ||||
| chr12:122975151-122975254 | Common:1; Rare:33 | ||||
| chr12:122980568-122980735 | Common:1; Rare:54 | ||||
| chr12:123105457-123105640 | Common:1; Rare:33 | ||||
| chr12:123233093-123233486 | Common:2; Rare:128; Clinvar:1 | ||||
| chr12:123364808-123364948 | Common:1; Rare:54 | ||||
| chr12:123584317-123584616 | Common:6; Rare:103 | ||||
| chr12:123602023-123602128 | Common:3; Rare:33 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972550-123972899 | Common:6; Rare:119 | ||||
| chr12:123972968-123973314 | Common:2; Rare:111 | ||||
| chr12:132687334-132687713 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132710751-132710850 | Common:2; Rare:42 | ||||
| chr12:132887553-132887845 | Rare:85 | ||||
| chr12:132956254-132956426 | Common:1; Rare:38 |