| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102798891-102799425 | Common:2; Rare:112 | ||||
| chr13:102799481-102799579 | Common:1; Rare:28 | ||||
| chr13:102800004-102800474 | Common:2; Rare:114 | ||||
| chr13:102800485-102800637 | Common:1; Rare:33 | ||||
| chr13:102800737-102800770 | Rare:12 | ||||
| chr13:102845638-102846232 | Common:11; Rare:153; Clinvar:4; Clinvar (benign):6 | ||||
| chr13:102846318-102846928 | Common:2; Rare:141; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr13:106534574-106534763 | Common:4; Rare:40 | ||||
| chr13:106534767-106534806 | Rare:15 | ||||
| chr13:106535044-106535256 | Common:2; Rare:64 | ||||
| chr13:106535466-106535961 | Common:4; Rare:182 | ||||
| chr13:106567182-106567352 | Common:1; Rare:41 | ||||
| chr13:106567589-106567753 | Rare:56 | ||||
| chr13:106567881-106568281 | Rare:109 | ||||
| chr13:108215307-108215744 | Common:5; Rare:85 |