| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33285662-33285944 | Common:1; Rare:65 | ||||
| chr13:33818045-33818189 | Rare:66 | ||||
| chr13:35476659-35476809 | Common:1; Rare:21 | ||||
| chr13:35855551-35855813 | Common:1; Rare:56 | ||||
| chr13:36131318-36131486 | Rare:38 | ||||
| chr13:36345542-36345657 | Common:1; Rare:23 | ||||
| chr13:36346249-36346466 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346627-36346787 | Common:4; Rare:45 | ||||
| chr13:36999254-36999465 | Rare:86 | ||||
| chr13:37000763-37000815 | Rare:27; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059758 | Common:1; Rare:57 | ||||
| chr13:38350229-38350474 | Common:1; Rare:72 | ||||
| chr13:39038087-39038567 | Common:1; Rare:117 | ||||
| chr13:39603086-39603306 | Common:1; Rare:76 | ||||
| chr13:40771138-40771424 | Common:3; Rare:86 |