| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53267750-53267830 | Rare:16 | ||||
| chr12:53268069-53268368 | Common:3; Rare:75 | ||||
| chr12:53295368-53295622 | Common:2; Rare:85 | ||||
| chr12:53299585-53299821 | Common:3; Rare:128 | ||||
| chr12:53299909-53299944 | Rare:14 | ||||
| chr12:53300339-53300455 | Common:1; Rare:20 | ||||
| chr12:53321171-53321642 | Common:3; Rare:152; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr12:53324825-53325057 | Common:1; Rare:59 | ||||
| chr12:53325063-53325357 | Common:1; Rare:49 | ||||
| chr12:53344875-53344958 | Rare:19 | ||||
| chr12:53344967-53345076 | Rare:19 | ||||
| chr12:53380111-53380217 | Rare:47 | ||||
| chr12:53380290-53380422 | Rare:40 | ||||
| chr12:53380558-53380737 | Rare:59 | ||||
| chr12:53441189-53441793 | Common:2; Rare:154 |