| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:34941973-34942493 | Common:3; Rare:138 | ||||
| chr13:36346294-36346518 | Common:3; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36432313-36432496 | Common:2; Rare:57 | ||||
| chr13:36819055-36819294 | Common:1; Rare:101; Clinvar:3 | ||||
| chr13:36999194-36999488 | Rare:117 | ||||
| chr13:36999919-37000111 | Common:1; Rare:51 | ||||
| chr13:37000211-37000416 | Common:2; Rare:38 | ||||
| chr13:37000418-37000946 | Common:4; Rare:180; Clinvar (pathogenic):1 | ||||
| chr13:37059397-37059877 | Common:3; Rare:161 | ||||
| chr13:38349450-38349964 | Common:5; Rare:171; Clinvar (pathogenic):1 | ||||
| chr13:38350205-38350332 | Rare:50 | ||||
| chr13:39037569-39037689 | Common:1; Rare:39 | ||||
| chr13:39037929-39038572 | Common:1; Rare:162 | ||||
| chr13:39038639-39038860 | Common:1; Rare:50 | ||||
| chr13:39603128-39603341 | Common:2; Rare:74 |