| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:106568002-106568261 | Rare:71 | ||||
| chr13:108218287-108218520 | Common:1; Rare:88 | ||||
| chr13:110305499-110305816 | Common:1; Rare:52 | ||||
| chr13:110306954-110307544 | Common:7; Rare:179; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110307625-110308146 | Common:4; Rare:172 | ||||
| chr13:110561672-110561893 | Common:5; Rare:78 | ||||
| chr13:110615401-110615656 | Common:2; Rare:91 | ||||
| chr13:110713018-110713261 | Common:2; Rare:105 | ||||
| chr13:110713487-110713670 | Common:2; Rare:78 | ||||
| chr13:113001557-113001801 | Common:1; Rare:50 | ||||
| chr13:113208620-113208751 | Rare:78 | ||||
| chr13:113759069-113759281 | Common:1; Rare:59 | ||||
| chr13:114281310-114281699 | Common:5; Rare:168 | ||||
| chr13:114281837-114282073 | Common:5; Rare:107 | ||||
| chr13:114282155-114282430 | Common:4; Rare:76 |