| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46470300-46470348 | Rare:10 | ||||
| chr12:46480968-46481141 | Rare:29 | ||||
| chr12:48789568-48789689 | Common:1; Rare:18 | ||||
| chr12:49052639-49052925 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:51955020-51955339 | Common:3; Rare:44 | ||||
| chr12:52147321-52147569 | Common:2; Rare:57 | ||||
| chr12:52896417-52896628 | Common:7; Rare:36 | ||||
| chr12:52900118-52900407 | Common:1; Rare:46 | ||||
| chr12:53038967-53039342 | Common:5; Rare:80 | ||||
| chr12:53052722-53052832 | Rare:17 | ||||
| chr12:53370842-53370991 | Rare:30 | ||||
| chr12:55833915-55833992 | Common:1; Rare:20 | ||||
| chr12:55980297-55980440 | Rare:29 | ||||
| chr12:56170151-56170470 | Common:3; Rare:86 | ||||
| chr12:56171269-56171803 | Common:2; Rare:113 |