| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:28659049-28659355 | Common:2; Rare:160; Clinvar (pathogenic):2 | ||||
| chr13:29428130-29428825 | Common:7; Rare:241 | ||||
| chr13:29595559-29596045 | Common:5; Rare:256 | ||||
| chr13:30306840-30307310 | Common:12; Rare:232 | ||||
| chr13:30307330-30307910 | Common:8; Rare:228 | ||||
| chr13:30464673-30464816 | Common:1; Rare:49 | ||||
| chr13:30465878-30466101 | Rare:126 | ||||
| chr13:30616976-30617112 | Rare:47 | ||||
| chr13:30617503-30618063 | Common:2; Rare:304 | ||||
| chr13:31161702-31162690 | Common:8; Rare:613 | ||||
| chr13:31199894-31200056 | Common:1; Rare:64 | ||||
| chr13:31200340-31200790 | Common:2; Rare:212 | ||||
| chr13:32031255-32031425 | Common:1; Rare:48 | ||||
| chr13:32031430-32031860 | Common:2; Rare:148 | ||||
| chr13:32315384-32315568 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):3 |