| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:93700441-93700630 | Common:1; Rare:79 | ||||
| chr8:93740907-93741202 | Common:1; Rare:92 | ||||
| chr8:93754730-93755057 | Common:1; Rare:123; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr8:93916625-93917073 | Common:5; Rare:162; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:94261956-94262424 | Common:1; Rare:106 | ||||
| chr8:94475048-94475225 | Common:3; Rare:47 | ||||
| chr8:94553428-94553738 | Common:3; Rare:112 | ||||
| chr8:94719756-94719983 | Common:1; Rare:69 | ||||
| chr8:94895178-94895292 | Rare:39 | ||||
| chr8:94949313-94949632 | Common:3; Rare:92 | ||||
| chr8:96235503-96235652 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr8:96261571-96261937 | Common:6; Rare:121 | ||||
| chr8:96493571-96493989 | Common:1; Rare:119 | ||||
| chr8:97644078-97644439 | Common:5; Rare:98 | ||||
| chr8:97644654-97644880 | Common:1; Rare:77 |