| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149549585-149549684 | Rare:19 | ||||
| chr5:150119562-150119840 | Common:1; Rare:56 | ||||
| chr5:150121030-150121322 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:150488708-150488854 | Common:2; Rare:33 | ||||
| chr5:150778660-150778882 | Common:1; Rare:85 | ||||
| chr5:151108178-151108548 | Rare:82 | ||||
| chr5:151270373-151270513 | Rare:26 | ||||
| chr5:151668863-151669018 | Rare:18 | ||||
| chr5:151670543-151670829 | Common:1; Rare:47 | ||||
| chr5:151678396-151678437 | Rare:10 | ||||
| chr5:151678788-151679116 | Common:2; Rare:58 | ||||
| chr5:151680462-151680541 | Common:1; Rare:15 | ||||
| chr5:151683049-151683364 | Common:2; Rare:59 | ||||
| chr5:151684079-151684254 | Common:2; Rare:26 | ||||
| chr5:151685855-151685957 | Common:1; Rare:26 |