| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44435154-44435463 | Common:3; Rare:91 | ||||
| chr13:44436587-44436789 | Common:2; Rare:52 | ||||
| chr13:44573267-44573451 | Common:1; Rare:66 | ||||
| chr13:44576174-44576404 | Common:2; Rare:68 | ||||
| chr13:44577109-44577252 | Rare:32 | ||||
| chr13:44577268-44577669 | Common:3; Rare:142 | ||||
| chr13:44989412-44989736 | Rare:128 | ||||
| chr13:45120383-45120631 | Common:2; Rare:83 | ||||
| chr13:45341037-45341617 | Common:4; Rare:259 | ||||
| chr13:45418299-45418578 | Rare:82 | ||||
| chr13:45464822-45465033 | Rare:59 | ||||
| chr13:46052434-46052870 | Common:2; Rare:119 | ||||
| chr13:46387178-46387398 | Rare:60 | ||||
| chr13:46553165-46553193 | Common:1; Rare:9 | ||||
| chr13:48001229-48001417 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):6 |