| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144787279-144787374 | Rare:30 | ||||
| chr8:144792304-144792576 | Common:3; Rare:103 | ||||
| chr8:144798802-144798924 | Common:1; Rare:34 | ||||
| chr8:144827235-144827605 | Common:2; Rare:95 | ||||
| chr8:144901400-144901600 | Common:1; Rare:59 | ||||
| chr8:144950805-144950890 | Common:1; Rare:27 | ||||
| chr8:145052139-145052504 | Common:11; Rare:94 | ||||
| chr9:178946-179274 | Common:6; Rare:63 | ||||
| chr9:214711-214869 | Common:3; Rare:87; Clinvar (benign):1 | ||||
| chr9:2015054-2015398 | Common:3; Rare:102 | ||||
| chr9:2017476-2017700 | Rare:67 | ||||
| chr9:2844047-2844314 | Common:5; Rare:101 | ||||
| chr9:3525788-3526072 | Common:1; Rare:94 | ||||
| chr9:4662275-4662323 | Common:1; Rare:15 | ||||
| chr9:4666388-4666477 | Common:1; Rare:22 |