| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20332574-20332661 | Rare:16 | ||||
| chr14:20332813-20333099 | Rare:66 | ||||
| chr14:20333256-20333417 | Common:1; Rare:32 | ||||
| chr14:20343094-20343797 | Common:13; Rare:376 | ||||
| chr14:20412970-20413276 | Common:4; Rare:52 | ||||
| chr14:20413348-20413607 | Common:4; Rare:68 | ||||
| chr14:20454574-20454870 | Common:3; Rare:94 | ||||
| chr14:20455008-20455304 | Common:2; Rare:81 | ||||
| chr14:20455365-20455611 | Rare:59 | ||||
| chr14:20461003-20461213 | Common:1; Rare:65 | ||||
| chr14:20461330-20462047 | Common:5; Rare:198 | ||||
| chr14:20469127-20469529 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:20609409-20609683 | Common:5; Rare:77 | ||||
| chr14:20609857-20610135 | Common:3; Rare:77 | ||||
| chr14:20683544-20683673 | Common:1; Rare:34 |