| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:80340859-80341127 | Common:1; Rare:82 | ||||
| chr13:80341317-80341478 | Rare:48 | ||||
| chr13:87672401-87672589 | Common:1; Rare:49 | ||||
| chr13:93226820-93227107 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:93227167-93227539 | Common:1; Rare:96; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:94596106-94596325 | Common:2; Rare:80 | ||||
| chr13:94601592-94601961 | Common:3; Rare:117 | ||||
| chr13:95301353-95301543 | Common:1; Rare:57 | ||||
| chr13:95552893-95552958 | Rare:24; Clinvar (pathogenic):1 | ||||
| chr13:95676778-95677281 | Common:5; Rare:192 | ||||
| chr13:96053269-96053608 | Common:3; Rare:145 | ||||
| chr13:96994325-96994412 | Common:1; Rare:24 | ||||
| chr13:97222190-97222472 | Rare:48 | ||||
| chr13:97433925-97434158 | Common:1; Rare:86 | ||||
| chr13:97992938-97993120 | Common:1; Rare:49 |