| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341052-45341679 | Common:8; Rare:525 | ||||
| chr13:45418342-45418539 | Rare:58 | ||||
| chr13:45464683-45465024 | Common:1; Rare:139 | ||||
| chr13:46052690-46052859 | Common:4; Rare:78 | ||||
| chr13:46553024-46553419 | Common:6; Rare:171 | ||||
| chr13:46797094-46797330 | Common:5; Rare:135 | ||||
| chr13:48001255-48001422 | Common:2; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr13:48037569-48037769 | Rare:149 | ||||
| chr13:48095049-48095260 | Common:1; Rare:99 | ||||
| chr13:48233056-48233255 | Common:1; Rare:72 | ||||
| chr13:48303510-48303978 | Common:1; Rare:254; Clinvar:13; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:48532600-48532920 | Common:6; Rare:221 | ||||
| chr13:48533040-48533158 | Common:2; Rare:37 | ||||
| chr13:48975310-48975932 | Common:5; Rare:230 | ||||
| chr13:48976358-48976726 | Common:3; Rare:121 |