| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41061144-41061645 | Common:4; Rare:170 | ||||
| chr13:41132787-41132978 | Rare:51 | ||||
| chr13:41194530-41194771 | Common:2; Rare:59 | ||||
| chr13:41457315-41457552 | Common:2; Rare:68 | ||||
| chr13:43879467-43879594 | Rare:35 | ||||
| chr13:43879700-43879880 | Common:18; Rare:57 | ||||
| chr13:44435159-44435452 | Common:3; Rare:85 | ||||
| chr13:44436712-44437028 | Common:3; Rare:90 | ||||
| chr13:44989443-44989641 | Rare:79 | ||||
| chr13:45120220-45120577 | Common:2; Rare:90 | ||||
| chr13:45340710-45341623 | Common:7; Rare:395 | ||||
| chr13:46052553-46052819 | Common:2; Rare:67 | ||||
| chr13:46387235-46387376 | Rare:38 | ||||
| chr13:46553056-46553396 | Common:4; Rare:101 | ||||
| chr13:48001265-48001397 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):2 |