| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:29595491-29595526 | Rare:12 | ||||
| chr13:29850081-29850404 | Common:2; Rare:104 | ||||
| chr13:30307404-30307490 | Common:1; Rare:37 | ||||
| chr13:30465760-30466029 | Common:1; Rare:92 | ||||
| chr13:30617294-30618039 | Common:1; Rare:231 | ||||
| chr13:32586234-32586582 | Common:2; Rare:104 | ||||
| chr13:33015987-33016082 | Common:1; Rare:26 | ||||
| chr13:33206022-33206146 | Rare:25 | ||||
| chr13:33818011-33818185 | Common:1; Rare:75 | ||||
| chr13:34942169-34942288 | Common:3; Rare:37 | ||||
| chr13:35476687-35476971 | Common:1; Rare:38 | ||||
| chr13:36297787-36297924 | Rare:50 | ||||
| chr13:36346282-36346454 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:37000764-37000802 | Rare:21 | ||||
| chr13:37059449-37059737 | Common:1; Rare:83 |