| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88580409-88580556 | Common:2; Rare:53 | ||||
| chr12:89352464-89352655 | Rare:52 | ||||
| chr12:89524708-89524853 | Common:1; Rare:28 | ||||
| chr12:89525283-89525645 | Common:1; Rare:81 | ||||
| chr12:89526022-89526094 | Rare:22 | ||||
| chr12:89708779-89709071 | Common:1; Rare:111 | ||||
| chr12:92145810-92146211 | Common:4; Rare:134 | ||||
| chr12:93377728-93377929 | Rare:54 | ||||
| chr12:93441884-93442173 | Common:2; Rare:93 | ||||
| chr12:93571709-93571912 | Common:7; Rare:79 | ||||
| chr12:93677312-93677390 | Rare:16 | ||||
| chr12:94459822-94460041 | Common:2; Rare:62 | ||||
| chr12:95003615-95003829 | Common:3; Rare:87; Clinvar (benign):5 | ||||
| chr12:95073406-95073644 | Common:2; Rare:83 | ||||
| chr12:95217441-95217843 | Common:3; Rare:107 |