| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7088608-7088969 | Common:1; Rare:109; Clinvar (pathogenic):2 | ||||
| chr12:7089297-7089731 | Common:3; Rare:140 | ||||
| chr12:7555889-7556066 | Common:1; Rare:31 | ||||
| chr12:8242933-8243223 | Common:8; Rare:84 | ||||
| chr12:9065054-9065186 | Rare:14 | ||||
| chr12:9072652-9073162 | Rare:109 | ||||
| chr12:9074558-9074967 | Rare:98 | ||||
| chr12:9240343-9240406 | Common:1; Rare:9 | ||||
| chr12:9283890-9284034 | Common:4; Rare:8 | ||||
| chr12:9438212-9438359 | Rare:13 | ||||
| chr12:9448192-9448310 | Common:1; Rare:61 | ||||
| chr12:9647951-9648179 | Common:4; Rare:77 | ||||
| chr12:10947297-10947538 | Rare:44 | ||||
| chr12:12472030-12472073 | Common:1; Rare:14 | ||||
| chr12:12558478-12558511 | Rare:2 |