| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:101063772-101064030 | Common:3; Rare:56 | ||||
| chr8:101254585-101254764 | Common:1; Rare:34 | ||||
| chr8:118027097-118027167 | Rare:7 | ||||
| chr8:119209616-119209725 | Rare:13 | ||||
| chr8:124555853-124555985 | Common:10; Rare:56 | ||||
| chr8:124559734-124559983 | Common:1; Rare:50 | ||||
| chr8:124848533-124848782 | Rare:42 | ||||
| chr8:127670899-127671014 | Rare:23 | ||||
| chr8:127737428-127737794 | Common:2; Rare:90 | ||||
| chr8:127739763-127739931 | Common:1; Rare:24 | ||||
| chr8:127794276-127794542 | Rare:68 | ||||
| chr8:133248650-133248775 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:133256759-133257267 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:133258359-133258658 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:133279012-133279269 | Common:2; Rare:57 |