| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45992049-45992148 | Common:1; Rare:19 | ||||
| chr12:46267839-46267986 | Common:1; Rare:27 | ||||
| chr12:46268479-46268797 | Common:2; Rare:74 | ||||
| chr12:46268804-46268823 | Rare:2 | ||||
| chr12:46372643-46372940 | Rare:125 | ||||
| chr12:47705960-47706124 | Rare:70 | ||||
| chr12:47758127-47758222 | Rare:14 | ||||
| chr12:47758819-47759027 | Common:2; Rare:39 | ||||
| chr12:48105825-48105943 | Rare:29 | ||||
| chr12:48105985-48106158 | Common:2; Rare:52 | ||||
| chr12:48119181-48119379 | Common:2; Rare:36; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48852086-48852394 | Common:2; Rare:86 | ||||
| chr12:48957367-48957647 | Common:4; Rare:77 | ||||
| chr12:49018741-49018935 | Common:1; Rare:79 | ||||
| chr12:49069974-49070160 | Common:2; Rare:44 |