| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018651-49018943 | Common:2; Rare:124 | ||||
| chr12:49110647-49111045 | Rare:89 | ||||
| chr12:49130737-49130914 | Common:4; Rare:68 | ||||
| chr12:49131300-49131671 | Common:2; Rare:146 | ||||
| chr12:49187329-49187499 | Rare:33 | ||||
| chr12:49187737-49187930 | Rare:32 | ||||
| chr12:49188439-49188632 | Common:2; Rare:27 | ||||
| chr12:49188972-49189426 | Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322963-49323252 | Common:2; Rare:72 | ||||
| chr12:49337097-49337343 | Common:2; Rare:50 | ||||
| chr12:49367152-49367581 | Common:1; Rare:118 | ||||
| chr12:49568078-49568260 | Common:2; Rare:59 | ||||
| chr12:49741273-49741607 | Rare:94 | ||||
| chr12:49828359-49828600 | Common:1; Rare:91 | ||||
| chr12:49843086-49843203 | Common:1; Rare:45 |