| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372714-46372954 | Rare:105 | ||||
| chr12:47705962-47706124 | Rare:69 | ||||
| chr12:47758849-47759030 | Common:1; Rare:38 | ||||
| chr12:48106038-48106062 | Rare:8 | ||||
| chr12:48106064-48106139 | Common:1; Rare:27 | ||||
| chr12:48716679-48717003 | Common:4; Rare:97 | ||||
| chr12:48852086-48852409 | Common:2; Rare:90 | ||||
| chr12:48957367-48957669 | Common:4; Rare:83 | ||||
| chr12:49018733-49018928 | Common:1; Rare:78 | ||||
| chr12:49069958-49070144 | Common:2; Rare:48 | ||||
| chr12:49131301-49131592 | Rare:118 | ||||
| chr12:49188482-49188636 | Common:2; Rare:21 | ||||
| chr12:49188981-49189296 | Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264744-49265183 | Common:5; Rare:163 | ||||
| chr12:49322980-49323323 | Common:3; Rare:79 |