| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102596785-102597162 | Common:2; Rare:151; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102773761-102773828 | Rare:30 | ||||
| chr13:102798998-102799352 | Rare:72 | ||||
| chr13:102845554-102845876 | Common:7; Rare:85; Clinvar (benign):3 | ||||
| chr13:106568088-106568261 | Rare:54 | ||||
| chr13:108215502-108215695 | Common:1; Rare:50 | ||||
| chr13:108218286-108218512 | Common:1; Rare:83 | ||||
| chr13:110307010-110307522 | Common:6; Rare:159; Clinvar:3; Clinvar (benign):9 | ||||
| chr13:110561664-110561889 | Common:5; Rare:81 | ||||
| chr13:110615406-110615666 | Common:2; Rare:90 | ||||
| chr13:110712978-110713266 | Common:2; Rare:130 | ||||
| chr13:110713487-110713659 | Common:2; Rare:73 | ||||
| chr13:111153575-111153714 | Common:2; Rare:64 | ||||
| chr13:112968386-112968476 | Rare:34 | ||||
| chr13:113208614-113208766 | Rare:92 |