| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79406219-79406339 | Common:3; Rare:38 | ||||
| chr13:79481014-79481378 | Common:2; Rare:143 | ||||
| chr13:83882259-83882453 | Rare:41; Clinvar:1 | ||||
| chr13:91398533-91398808 | Common:3; Rare:104 | ||||
| chr13:93226516-93226866 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr13:93226921-93227075 | Rare:27; Clinvar:1 | ||||
| chr13:94596139-94596325 | Common:2; Rare:61 | ||||
| chr13:94601623-94601954 | Common:3; Rare:106 | ||||
| chr13:95676828-95677232 | Common:3; Rare:156 | ||||
| chr13:96053353-96053496 | Common:2; Rare:55 | ||||
| chr13:97222194-97222402 | Rare:35 | ||||
| chr13:97434614-97434692 | Rare:11 | ||||
| chr13:99200668-99200911 | Common:6; Rare:116 | ||||
| chr13:99307364-99307420 | Rare:8 | ||||
| chr13:99606497-99606722 | Common:5; Rare:75 |