| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30735393-30735612 | Common:2; Rare:49 | ||||
| chr13:32031088-32031658 | Common:2; Rare:125 | ||||
| chr13:32031753-32031802 | Rare:21 | ||||
| chr13:32315433-32315559 | Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32428086-32428205 | Rare:27 | ||||
| chr13:33205939-33206162 | Rare:44 | ||||
| chr13:33285604-33286018 | Common:2; Rare:96 | ||||
| chr13:33818024-33818208 | Common:1; Rare:83 | ||||
| chr13:34942171-34942306 | Common:3; Rare:44 | ||||
| chr13:35476323-35476445 | Rare:24 | ||||
| chr13:35476645-35476809 | Common:1; Rare:25 | ||||
| chr13:35855582-35855762 | Common:1; Rare:38 | ||||
| chr13:36131357-36131499 | Rare:38 | ||||
| chr13:36297787-36297897 | Rare:38 | ||||
| chr13:36345533-36345871 | Common:2; Rare:76 |