| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:63852859-63853135 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
| chr14:63853422-63853648 | Common:1; Rare:62 | ||||
| chr14:64213215-64213292 | Common:1; Rare:16 | ||||
| chr14:64338369-64339099 | Common:7; Rare:195 | ||||
| chr14:64387753-64388449 | Common:3; Rare:215 | ||||
| chr14:64465291-64465596 | Common:1; Rare:81 | ||||
| chr14:64503403-64503558 | Rare:28 | ||||
| chr14:64503565-64503873 | Common:2; Rare:100 | ||||
| chr14:64503902-64503985 | Rare:42 | ||||
| chr14:64504183-64504475 | Common:3; Rare:96 | ||||
| chr14:64504516-64504849 | Rare:100 | ||||
| chr14:64504976-64505107 | Common:2; Rare:49 | ||||
| chr14:64505156-64505400 | Common:1; Rare:68 | ||||
| chr14:64539912-64539989 | Common:1; Rare:17 | ||||
| chr14:64540039-64540111 | Common:1; Rare:15 |