| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124450682-124450826 | Common:4; Rare:44 | ||||
| chr8:124474516-124474714 | Common:1; Rare:74 | ||||
| chr8:124474953-124475121 | Rare:57 | ||||
| chr8:124539025-124539291 | Common:2; Rare:129; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728401-124728767 | Common:5; Rare:111 | ||||
| chr8:125091725-125091914 | Common:2; Rare:66; Clinvar (benign):3 | ||||
| chr8:126557695-126557915 | Rare:55 | ||||
| chr8:126558258-126558638 | Common:2; Rare:129 | ||||
| chr8:127735836-127736076 | Rare:53 | ||||
| chr8:127736109-127736294 | Common:3; Rare:40 | ||||
| chr8:132675317-132675647 | Common:2; Rare:110; Clinvar:1 | ||||
| chr8:133297194-133297431 | Common:3; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:133489634-133489851 | Common:2; Rare:42 | ||||
| chr8:133571817-133572251 | Rare:113 | ||||
| chr8:134713017-134713239 | Common:1; Rare:77 |