| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36345549-36345657 | Common:1; Rare:21 | ||||
| chr13:36346086-36346239 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chr13:36346243-36346478 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:36346622-36347047 | Common:4; Rare:110 | ||||
| chr13:37059585-37059751 | Common:1; Rare:55 | ||||
| chr13:38350249-38350569 | Common:2; Rare:84 | ||||
| chr13:39038086-39038433 | Common:1; Rare:87 | ||||
| chr13:41060156-41060533 | Common:3; Rare:132 | ||||
| chr13:41060873-41061068 | Common:16; Rare:113 | ||||
| chr13:41061141-41061285 | Common:1; Rare:54 | ||||
| chr13:41061355-41061645 | Common:2; Rare:89 | ||||
| chr13:41061730-41061839 | Common:1; Rare:37 | ||||
| chr13:41132731-41132968 | Rare:63 | ||||
| chr13:42271760-42272041 | Common:2; Rare:81 | ||||
| chr13:43023537-43023633 | Common:1; Rare:38 |