| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:94601550-94601932 | Common:4; Rare:118 | ||||
| chr13:95301417-95301539 | Rare:33 | ||||
| chr13:95552627-95552748 | Rare:46 | ||||
| chr13:95676930-95677205 | Common:3; Rare:97 | ||||
| chr13:96053344-96053594 | Common:2; Rare:107 | ||||
| chr13:97222214-97222451 | Rare:41 | ||||
| chr13:98576210-98576293 | Common:1; Rare:23 | ||||
| chr13:98977954-98978179 | Common:2; Rare:45 | ||||
| chr13:99200668-99200894 | Common:6; Rare:104 | ||||
| chr13:99606523-99606698 | Common:5; Rare:51 | ||||
| chr13:100088894-100089123 | Rare:82; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674774-100675156 | Common:4; Rare:159 | ||||
| chr13:102596785-102597057 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr13:102773716-102773842 | Rare:59 | ||||
| chr13:102798945-102799124 | Common:1; Rare:39 |