| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:8435300-8435770 | Common:12; Rare:237 | ||||
| chr6:10404210-10404545 | Common:3; Rare:195; Clinvar (pathogenic):2 | ||||
| chr6:10410770-10411170 | Common:7; Rare:115 | ||||
| chr6:10412007-10412327 | Common:2; Rare:166 | ||||
| chr6:10412329-10412635 | Common:6; Rare:115 | ||||
| chr6:10414600-10414969 | Common:6; Rare:131 | ||||
| chr6:10414981-10415423 | Common:3; Rare:242 | ||||
| chr6:10417105-10417540 | Common:2; Rare:205 | ||||
| chr6:10418955-10419188 | Rare:82 | ||||
| chr6:10419516-10419752 | Common:2; Rare:78 | ||||
| chr6:10419950-10420099 | Rare:27 | ||||
| chr6:10520920-10521800 | Common:10; Rare:313 | ||||
| chr6:10528194-10528547 | Common:2; Rare:61 | ||||
| chr6:10694547-10694986 | Common:13; Rare:243 | ||||
| chr6:10722767-10723228 | Common:12; Rare:302 |