| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133080728-133080943 | Rare:68 | ||||
| chr12:133130380-133130652 | Common:6; Rare:97 | ||||
| chr13:19782923-19783082 | Common:2; Rare:58 | ||||
| chr13:21140418-21140622 | Rare:100 | ||||
| chr13:21176484-21176704 | Common:2; Rare:97 | ||||
| chr13:23579236-23579383 | Common:3; Rare:44 | ||||
| chr13:24512739-24512839 | Common:3; Rare:30 | ||||
| chr13:25301398-25301692 | Common:1; Rare:104 | ||||
| chr13:26221814-26222043 | Common:1; Rare:75 | ||||
| chr13:27251258-27251599 | Common:3; Rare:100 | ||||
| chr13:28138019-28138200 | Common:1; Rare:51 | ||||
| chr13:28659076-28659178 | Rare:46; Clinvar (pathogenic):1 | ||||
| chr13:30617552-30618000 | Common:1; Rare:146 | ||||
| chr13:32031027-32031328 | Common:2; Rare:68 | ||||
| chr13:32538737-32539123 | Common:1; Rare:96 |