| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89524748-89524853 | Common:1; Rare:20 | ||||
| chr12:89525301-89525621 | Common:1; Rare:69 | ||||
| chr12:89525885-89525971 | Common:1; Rare:33 | ||||
| chr12:89525987-89526127 | Rare:50 | ||||
| chr12:89708792-89709085 | Common:1; Rare:113 | ||||
| chr12:92145396-92145655 | Common:2; Rare:109 | ||||
| chr12:92145810-92146215 | Common:4; Rare:135 | ||||
| chr12:92929102-92929512 | Common:2; Rare:124 | ||||
| chr12:93377728-93377934 | Rare:57 | ||||
| chr12:93378493-93378657 | Rare:48 | ||||
| chr12:93441880-93442173 | Common:2; Rare:94 | ||||
| chr12:93570826-93571085 | Rare:67 | ||||
| chr12:93571734-93571912 | Common:7; Rare:67 | ||||
| chr12:94459833-94460047 | Common:2; Rare:63 | ||||
| chr12:95003593-95003829 | Common:3; Rare:98; Clinvar (benign):6 |