| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:74134279-74134553 | Common:3; Rare:100 | ||||
| chr13:75549475-75549837 | Common:8; Rare:90 | ||||
| chr13:75760400-75760704 | Common:1; Rare:62 | ||||
| chr13:77918800-77918908 | Common:1; Rare:24 | ||||
| chr13:79405802-79405911 | Rare:39 | ||||
| chr13:79406203-79406332 | Common:4; Rare:39 | ||||
| chr13:93227176-93227374 | Rare:44; Clinvar:3 | ||||
| chr13:94601592-94601892 | Common:3; Rare:81 | ||||
| chr13:95552523-95552748 | Common:2; Rare:72 | ||||
| chr13:95676911-95677182 | Common:3; Rare:96 | ||||
| chr13:96053335-96053545 | Common:2; Rare:96 | ||||
| chr13:99200668-99200911 | Common:6; Rare:116 | ||||
| chr13:100088955-100089139 | Rare:69; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674814-100675156 | Common:4; Rare:143 | ||||
| chr13:102596794-102597039 | Common:1; Rare:115 |