| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617233-30618046 | Common:1; Rare:246 | ||||
| chr13:30735377-30735623 | Common:2; Rare:53 | ||||
| chr13:31162349-31162454 | Common:1; Rare:27 | ||||
| chr13:32031564-32031648 | Rare:17 | ||||
| chr13:32586227-32586593 | Common:2; Rare:113 | ||||
| chr13:33285650-33285954 | Common:2; Rare:72 | ||||
| chr13:33818013-33818204 | Common:1; Rare:84 | ||||
| chr13:36345538-36345671 | Common:1; Rare:25 | ||||
| chr13:36346249-36346460 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346622-36346796 | Common:4; Rare:49 | ||||
| chr13:36673847-36674088 | Common:1; Rare:78 | ||||
| chr13:37059587-37059726 | Common:1; Rare:48 | ||||
| chr13:37869759-37869914 | Common:1; Rare:34 | ||||
| chr13:37869971-37870279 | Common:2; Rare:66 | ||||
| chr13:38349787-38349916 | Common:1; Rare:62 |