| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144291373-144291668 | Common:1; Rare:97 | ||||
| chr8:144359416-144359744 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr8:144373779-144374080 | Common:3; Rare:97 | ||||
| chr8:144413548-144413719 | Rare:51; Clinvar:1 | ||||
| chr8:144477880-144478102 | Common:4; Rare:83 | ||||
| chr8:144517699-144518014 | Common:1; Rare:107; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144792264-144792562 | Common:3; Rare:102 | ||||
| chr8:144901373-144901671 | Common:1; Rare:85 | ||||
| chr8:144950860-144950919 | Common:2; Rare:20 | ||||
| chr8:145052193-145052494 | Common:10; Rare:83 | ||||
| chr9:2015071-2015398 | Common:3; Rare:95 | ||||
| chr9:2158435-2158493 | Rare:17 | ||||
| chr9:2844024-2844367 | Common:6; Rare:138 | ||||
| chr9:3525968-3526106 | Common:1; Rare:60 | ||||
| chr9:3526381-3526516 | Common:4; Rare:70 |