| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48903832-48904168 | Common:8; Rare:85 | ||||
| chr12:48957310-48957568 | Common:2; Rare:72 | ||||
| chr12:49003507-49003778 | Common:2; Rare:72 | ||||
| chr12:49018736-49019029 | Common:1; Rare:111; Clinvar (benign):1 | ||||
| chr12:49110827-49111059 | Rare:56 | ||||
| chr12:49131296-49131621 | Common:2; Rare:126 | ||||
| chr12:49188991-49189326 | Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265179 | Common:4; Rare:154 | ||||
| chr12:49297528-49297666 | Common:3; Rare:50; Clinvar:3 | ||||
| chr12:49322985-49323347 | Common:5; Rare:82 | ||||
| chr12:49367152-49367596 | Common:1; Rare:120 | ||||
| chr12:49567850-49568240 | Common:2; Rare:106 | ||||
| chr12:49623250-49623582 | Common:1; Rare:94 | ||||
| chr12:49759160-49759260 | Rare:37 | ||||
| chr12:49828362-49828558 | Common:1; Rare:72 |