| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94436500-94436694 | Rare:45 | ||||
| chr8:94436769-94437116 | Rare:74 | ||||
| chr8:94475048-94475252 | Common:3; Rare:55 | ||||
| chr8:94553431-94553777 | Common:3; Rare:124 | ||||
| chr8:94719741-94720129 | Common:4; Rare:113 | ||||
| chr8:94823126-94823389 | Common:2; Rare:92 | ||||
| chr8:94895194-94895336 | Rare:47 | ||||
| chr8:94895651-94895818 | Common:1; Rare:50 | ||||
| chr8:94949364-94949553 | Common:1; Rare:56 | ||||
| chr8:95024912-95025199 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95100476-95100836 | Common:2; Rare:57 | ||||
| chr8:95133581-95133991 | Common:3; Rare:128 | ||||
| chr8:95268723-95268857 | Common:8; Rare:31 | ||||
| chr8:95269185-95269339 | Common:6; Rare:61; Clinvar:1 | ||||
| chr8:96235496-96235652 | Common:1; Rare:85; Clinvar (benign):3 |