| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99086367-99086835 | Common:8; Rare:304 | ||||
| chr13:99200535-99200959 | Common:21; Rare:457 | ||||
| chr13:99501187-99501574 | Common:1; Rare:119 | ||||
| chr13:99606482-99606723 | Common:11; Rare:149 | ||||
| chr13:99971050-99971570 | Common:15; Rare:296 | ||||
| chr13:99980911-99981449 | Rare:286 | ||||
| chr13:99981497-99981934 | Common:3; Rare:393 | ||||
| chr13:99982238-99983237 | Common:2; Rare:333; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr13:100088803-100089166 | Rare:353; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr13:100588377-100588526 | Rare:39 | ||||
| chr13:100588587-100588937 | Common:9; Rare:169 | ||||
| chr13:100674689-100675176 | Common:11; Rare:434 | ||||
| chr13:102596749-102597198 | Common:4; Rare:421; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:102773663-102773969 | Common:2; Rare:279 | ||||
| chr13:102798893-102799211 | Common:3; Rare:165 |