| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32407988-32408102 | Rare:33 | ||||
| chr13:32426193-32426367 | Rare:49 | ||||
| chr13:32426400-32426936 | Common:4; Rare:212 | ||||
| chr13:32427105-32427307 | Common:2; Rare:48 | ||||
| chr13:32432769-32433274 | Rare:175 | ||||
| chr13:32443058-32443644 | Common:2; Rare:202; Clinvar (pathogenic):1 | ||||
| chr13:32443643-32444227 | Common:2; Rare:214 | ||||
| chr13:32472209-32472457 | Common:1; Rare:42 | ||||
| chr13:32587358-32587591 | Common:2; Rare:55 | ||||
| chr13:32737250-32737670 | Rare:183 | ||||
| chr13:32791848-32791969 | Rare:18 | ||||
| chr13:32811481-32811691 | Common:1; Rare:45 | ||||
| chr13:32829300-32829880 | Common:1; Rare:111 | ||||
| chr13:32905120-32905470 | Common:2; Rare:114 | ||||
| chr13:32969655-32970055 | Rare:127 |