| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:24160562-24160759 | Rare:57 | ||||
| chr13:24512739-24512870 | Common:3; Rare:38 | ||||
| chr13:24922801-24923131 | Common:2; Rare:115; Clinvar:1 | ||||
| chr13:25301485-25301706 | Common:1; Rare:83 | ||||
| chr13:26221791-26221983 | Rare:57 | ||||
| chr13:27251245-27251616 | Common:5; Rare:112 | ||||
| chr13:27450137-27450212 | Common:2; Rare:21 | ||||
| chr13:28658951-28659187 | Rare:104; Clinvar (pathogenic):1 | ||||
| chr13:30306813-30307197 | Common:7; Rare:102 | ||||
| chr13:30465824-30466119 | Common:1; Rare:91 | ||||
| chr13:33285719-33285884 | Rare:38 | ||||
| chr13:37000756-37000805 | Rare:23 | ||||
| chr13:37059585-37059727 | Common:1; Rare:49 | ||||
| chr13:39603128-39603464 | Common:2; Rare:116 | ||||
| chr13:39655629-39655750 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 |