| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36346301-36346526 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:37059596-37059754 | Common:1; Rare:52 | ||||
| chr13:37869765-37869884 | Common:1; Rare:28 | ||||
| chr13:38350249-38350363 | Rare:34 | ||||
| chr13:39603128-39603284 | Common:1; Rare:53 | ||||
| chr13:41019281-41019417 | Rare:19 | ||||
| chr13:41060933-41061020 | Common:9; Rare:48 | ||||
| chr13:41061395-41061579 | Common:2; Rare:49 | ||||
| chr13:41457289-41457551 | Common:2; Rare:76 | ||||
| chr13:43879467-43879648 | Common:1; Rare:47 | ||||
| chr13:43879707-43879913 | Common:18; Rare:61 | ||||
| chr13:44436783-44436999 | Common:2; Rare:66 | ||||
| chr13:44989432-44989607 | Rare:67 | ||||
| chr13:45120383-45120596 | Common:2; Rare:68 | ||||
| chr13:45341040-45341617 | Common:4; Rare:259 |