| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49131302-49131615 | Common:2; Rare:124 | ||||
| chr12:49188482-49188607 | Common:2; Rare:18 | ||||
| chr12:49188991-49189150 | Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265179 | Common:5; Rare:161 | ||||
| chr12:49322980-49323302 | Common:3; Rare:73 | ||||
| chr12:49366650-49366872 | Common:2; Rare:59 | ||||
| chr12:49367214-49367583 | Common:1; Rare:99 | ||||
| chr12:49568104-49568237 | Common:2; Rare:43 | ||||
| chr12:49741326-49741616 | Rare:86 | ||||
| chr12:49828387-49828526 | Common:1; Rare:54 | ||||
| chr12:50085287-50085453 | Common:1; Rare:42 | ||||
| chr12:50103861-50104051 | Rare:47 | ||||
| chr12:50167263-50167558 | Common:2; Rare:90 | ||||
| chr12:50283452-50283656 | Common:1; Rare:64 | ||||
| chr12:50505231-50505557 | Common:3; Rare:73 |