| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617087-30617137 | Rare:11 | ||||
| chr13:30617235-30617398 | Rare:33 | ||||
| chr13:30617484-30618039 | Common:1; Rare:181 | ||||
| chr13:32031571-32031786 | Common:1; Rare:62 | ||||
| chr13:32254089-32254385 | Common:3; Rare:68 | ||||
| chr13:33016018-33016087 | Common:1; Rare:16 | ||||
| chr13:33205939-33206191 | Rare:50 | ||||
| chr13:33285660-33285834 | Rare:37 | ||||
| chr13:33818013-33818171 | Common:1; Rare:64 | ||||
| chr13:34942171-34942298 | Common:3; Rare:39 | ||||
| chr13:35476662-35476819 | Common:1; Rare:24 | ||||
| chr13:36131364-36131548 | Rare:51 | ||||
| chr13:36345542-36345657 | Common:1; Rare:23 | ||||
| chr13:36346238-36346490 | Common:3; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36346622-36346796 | Common:4; Rare:49 |