| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144755426-144755684 | Common:1; Rare:95 | ||||
| chr8:144792335-144792562 | Common:3; Rare:85 | ||||
| chr8:144853008-144853352 | Common:2; Rare:102 | ||||
| chr8:145052145-145052497 | Common:11; Rare:89 | ||||
| chr9:214752-214868 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr9:215081-215215 | Common:2; Rare:76 | ||||
| chr9:470150-470320 | Common:14; Rare:67 | ||||
| chr9:2015027-2015387 | Common:3; Rare:107 | ||||
| chr9:2017492-2017718 | Rare:69 | ||||
| chr9:2844034-2844339 | Common:5; Rare:113 | ||||
| chr9:3525871-3526106 | Common:1; Rare:98 | ||||
| chr9:3526421-3526556 | Common:2; Rare:67 | ||||
| chr9:4662238-4662323 | Common:1; Rare:28 | ||||
| chr9:4666351-4666578 | Common:3; Rare:59 | ||||
| chr9:4679437-4679775 | Common:1; Rare:148 |