| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143829039-143829138 | Rare:37 | ||||
| chr8:143829299-143829518 | Rare:84 | ||||
| chr8:143943913-143944125 | Rare:82 | ||||
| chr8:143950866-143951166 | Common:3; Rare:81 | ||||
| chr8:143953784-143953981 | Common:3; Rare:61 | ||||
| chr8:143986398-143986509 | Rare:22 | ||||
| chr8:143989951-143990198 | Common:1; Rare:84 | ||||
| chr8:143991532-143991804 | Rare:98 | ||||
| chr8:144060674-144060841 | Rare:50 | ||||
| chr8:144078474-144078740 | Common:1; Rare:82 | ||||
| chr8:144082473-144082701 | Common:2; Rare:72 | ||||
| chr8:144083751-144083973 | Rare:75; Clinvar (pathogenic):1 | ||||
| chr8:144095828-144096247 | Common:2; Rare:166; Clinvar (benign):3 | ||||
| chr8:144103601-144103881 | Common:2; Rare:97 | ||||
| chr8:144104130-144104542 | Common:4; Rare:144 |