| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132686780-132687128 | Rare:100 | ||||
| chr12:132687225-132687703 | Common:5; Rare:173; Clinvar:15; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr12:132687941-132688071 | Rare:28 | ||||
| chr12:132710515-132710923 | Common:5; Rare:144 | ||||
| chr12:132711426-132711489 | Rare:9 | ||||
| chr12:132761209-132761372 | Common:3; Rare:48 | ||||
| chr12:132761704-132762340 | Common:5; Rare:223 | ||||
| chr12:132828338-132828554 | Common:1; Rare:62 | ||||
| chr12:132828775-132828910 | Common:1; Rare:59 | ||||
| chr12:132829004-132829279 | Rare:114 | ||||
| chr12:132887317-132887342 | Rare:10 | ||||
| chr12:132887480-132888042 | Common:2; Rare:164 | ||||
| chr12:132888080-132888134 | Common:1; Rare:10 | ||||
| chr12:132908439-132908767 | Common:3; Rare:79 | ||||
| chr12:132908889-132908998 | Common:2; Rare:28 |