| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94895194-94895362 | Rare:53 | ||||
| chr8:94895651-94895802 | Rare:46 | ||||
| chr8:94896600-94896704 | Common:2; Rare:25 | ||||
| chr8:94949330-94949574 | Common:2; Rare:73 | ||||
| chr8:95024917-95025205 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr8:95133616-95133964 | Common:3; Rare:111 | ||||
| chr8:95268680-95268846 | Common:9; Rare:38 | ||||
| chr8:95269195-95269328 | Common:6; Rare:53; Clinvar:1 | ||||
| chr8:95269395-95269704 | Common:5; Rare:116 | ||||
| chr8:96235510-96235703 | Common:1; Rare:103; Clinvar (benign):2 | ||||
| chr8:96261544-96261997 | Common:6; Rare:152 | ||||
| chr8:96493748-96494171 | Common:4; Rare:118 | ||||
| chr8:96645082-96645381 | Common:2; Rare:79 | ||||
| chr8:97277299-97277596 | Common:3; Rare:112 | ||||
| chr8:97277863-97278028 | Common:1; Rare:55 |