| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46367265-46367567 | Common:2; Rare:63 | ||||
| chr12:46372636-46373022 | Common:1; Rare:151 | ||||
| chr12:47705955-47706124 | Rare:72 | ||||
| chr12:48105828-48106200 | Common:2; Rare:115 | ||||
| chr12:48350790-48350953 | Rare:62 | ||||
| chr12:48815497-48815642 | Common:1; Rare:29 | ||||
| chr12:48904064-48904159 | Common:1; Rare:20 | ||||
| chr12:48957314-48957568 | Common:2; Rare:71 | ||||
| chr12:49018738-49018937 | Common:1; Rare:83 | ||||
| chr12:49131305-49131614 | Common:2; Rare:124 | ||||
| chr12:49187040-49187335 | Rare:49 | ||||
| chr12:49188485-49188586 | Common:1; Rare:15 | ||||
| chr12:49188975-49189353 | Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322960-49323319 | Common:3; Rare:89 | ||||
| chr12:49367212-49367586 | Common:1; Rare:100 |