| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144078512-144078722 | Common:1; Rare:64 | ||||
| chr8:144082503-144082657 | Common:2; Rare:54 | ||||
| chr8:144413552-144413729 | Common:1; Rare:51; Clinvar:1 | ||||
| chr8:144428487-144428638 | Common:2; Rare:55 | ||||
| chr8:144500914-144501178 | Rare:131 | ||||
| chr8:144755429-144755716 | Common:1; Rare:104 | ||||
| chr8:144792335-144792576 | Common:3; Rare:93 | ||||
| chr8:144827235-144827592 | Common:2; Rare:90 | ||||
| chr8:144950817-144950922 | Common:2; Rare:38 | ||||
| chr8:145052220-145052497 | Common:10; Rare:81 | ||||
| chr9:504574-504730 | Common:1; Rare:79 | ||||
| chr9:2015060-2015387 | Common:3; Rare:96 | ||||
| chr9:2158158-2158499 | Common:1; Rare:71 | ||||
| chr9:2181339-2181676 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr9:2844045-2844353 | Common:5; Rare:118 |