| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459820-94460043 | Common:2; Rare:63 | ||||
| chr12:95003665-95003808 | Common:3; Rare:54; Clinvar (benign):3 | ||||
| chr12:95217377-95217831 | Common:4; Rare:123 | ||||
| chr12:95474043-95474203 | Common:2; Rare:75 | ||||
| chr12:95548788-95548914 | Common:2; Rare:43 | ||||
| chr12:95943217-95943343 | Rare:20 | ||||
| chr12:96400559-96400707 | Rare:68 | ||||
| chr12:98515478-98515653 | Rare:54; Clinvar:1 | ||||
| chr12:98644703-98644843 | Common:3; Rare:47 | ||||
| chr12:98645060-98645296 | Common:2; Rare:63 | ||||
| chr12:100267060-100267461 | Common:3; Rare:159 | ||||
| chr12:101407678-101408079 | Common:3; Rare:97 | ||||
| chr12:101697558-101697685 | Common:2; Rare:37 | ||||
| chr12:101877415-101877769 | Common:4; Rare:92 | ||||
| chr12:102120060-102120261 | Rare:81 |