| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179624286-179624565 | Common:2; Rare:56 | ||||
| chr5:179634301-179634567 | Common:1; Rare:7 | ||||
| chr5:179680999-179681140 | Common:1; Rare:21 | ||||
| chr5:179698463-179699243 | Common:4; Rare:271 | ||||
| chr5:179805264-179805429 | Common:1; Rare:39 | ||||
| chr5:179806298-179806448 | Rare:46 | ||||
| chr5:179806884-179807063 | Common:3; Rare:69 | ||||
| chr5:179820803-179821105 | Common:2; Rare:116; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:179858792-179859063 | Rare:144 | ||||
| chr5:179871470-179871638 | Common:1; Rare:41 | ||||
| chr5:179907775-179908021 | Common:2; Rare:114 | ||||
| chr5:180071640-180071896 | Common:2; Rare:108 | ||||
| chr5:180136771-180136978 | Common:4; Rare:52 | ||||
| chr5:180291909-180292197 | Common:2; Rare:105 | ||||
| chr5:180353313-180353512 | Common:5; Rare:88 |