| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524756-89524891 | Common:1; Rare:25 | ||||
| chr12:89525377-89525599 | Common:1; Rare:51 | ||||
| chr12:89525975-89526062 | Rare:36 | ||||
| chr12:92145806-92146205 | Common:4; Rare:133 | ||||
| chr12:92929257-92929517 | Rare:81 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441876-93442166 | Common:2; Rare:91 | ||||
| chr12:93570826-93571075 | Rare:65 | ||||
| chr12:93571719-93571900 | Common:6; Rare:69 | ||||
| chr12:93677211-93677458 | Common:2; Rare:58 | ||||
| chr12:94459783-94460047 | Common:3; Rare:75 | ||||
| chr12:95003593-95003827 | Common:3; Rare:96; Clinvar (benign):6 | ||||
| chr12:95217384-95217769 | Common:4; Rare:105 | ||||
| chr12:95474039-95474210 | Common:2; Rare:81 | ||||
| chr12:95858822-95859075 | Common:3; Rare:74 |