| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182144450-182144734 | Common:3; Rare:92 | ||||
| chr4:182917319-182917547 | Common:4; Rare:79 | ||||
| chr4:183659096-183659411 | Common:1; Rare:104 | ||||
| chr4:184474529-184474690 | Rare:40 | ||||
| chr4:184649396-184649796 | Common:5; Rare:130 | ||||
| chr4:185143148-185143274 | Common:1; Rare:39; Clinvar (benign):2 | ||||
| chr4:185203906-185204097 | Rare:64 | ||||
| chr4:185396581-185396850 | Rare:86 | ||||
| chr4:185425880-185426289 | Common:4; Rare:123 | ||||
| chr4:186723769-186723950 | Common:5; Rare:72 | ||||
| chr4:189940634-189940983 | Common:10; Rare:127 | ||||
| chr5:218134-218369 | Common:3; Rare:97; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443095-443251 | Common:5; Rare:68 | ||||
| chr5:612191-612359 | Rare:68 | ||||
| chr5:892535-892929 | Common:5; Rare:120 |