| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48183567-48183670 | Common:1; Rare:28 | ||||
| chr12:48184046-48184125 | Common:2; Rare:26 | ||||
| chr12:48350790-48351073 | Common:5; Rare:106 | ||||
| chr12:48716679-48716996 | Common:4; Rare:96 | ||||
| chr12:48815480-48815637 | Common:1; Rare:33 | ||||
| chr12:48818571-48818821 | Common:1; Rare:86 | ||||
| chr12:48852086-48852371 | Common:2; Rare:85 | ||||
| chr12:48903835-48904153 | Common:8; Rare:78 | ||||
| chr12:48957367-48957592 | Common:2; Rare:59 | ||||
| chr12:49018736-49018928 | Common:1; Rare:78 | ||||
| chr12:49110654-49110753 | Rare:18 | ||||
| chr12:49131301-49131606 | Common:2; Rare:124 | ||||
| chr12:49188455-49188583 | Common:1; Rare:19 | ||||
| chr12:49188975-49189308 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265082 | Common:4; Rare:104 |