| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95308432-95308501 | Rare:8 | ||||
| chr12:95310220-95310427 | Rare:37 | ||||
| chr12:95654276-95654458 | Common:1; Rare:36 | ||||
| chr12:96427332-96427583 | Common:3; Rare:54 | ||||
| chr12:96955175-96955459 | Common:1; Rare:45 | ||||
| chr12:100210192-100210337 | Rare:30 | ||||
| chr12:100296319-100296383 | Rare:11 | ||||
| chr12:101379281-101379424 | Rare:26 | ||||
| chr12:101720062-101720178 | Rare:28 | ||||
| chr12:101780564-101780873 | Common:2; Rare:66; Clinvar (pathogenic):1 | ||||
| chr12:102025716-102025995 | Rare:47 | ||||
| chr12:103493252-103493564 | Common:1; Rare:50 | ||||
| chr12:103766734-103766777 | Rare:11 | ||||
| chr12:103787284-103787461 | Rare:32 | ||||
| chr12:103830457-103830600 | Common:2; Rare:25 |