| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:97976942-97977035 | Common:1; Rare:24 | ||||
| chr13:98142836-98142891 | Common:1; Rare:18 | ||||
| chr13:98142999-98143318 | Common:3; Rare:112 | ||||
| chr13:98576178-98576232 | Rare:17 | ||||
| chr13:98576989-98577295 | Common:2; Rare:111 | ||||
| chr13:98577560-98577750 | Rare:49 | ||||
| chr13:99086639-99086785 | Common:2; Rare:59 | ||||
| chr13:99200466-99200948 | Common:8; Rare:189 | ||||
| chr13:99201261-99201366 | Rare:30 | ||||
| chr13:99307357-99307479 | Rare:13 | ||||
| chr13:99501062-99501588 | Common:2; Rare:149 | ||||
| chr13:99606440-99606969 | Common:7; Rare:181 | ||||
| chr13:100088772-100089268 | Rare:185; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:100588379-100588466 | Rare:27 | ||||
| chr13:100588567-100588875 | Common:6; Rare:101 |