| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144798821-144798922 | Common:1; Rare:27 | ||||
| chr8:144827262-144827596 | Common:1; Rare:86 | ||||
| chr8:144853008-144853151 | Rare:52 | ||||
| chr8:144901400-144901702 | Common:1; Rare:87 | ||||
| chr8:145052153-145052497 | Common:11; Rare:87 | ||||
| chr9:214701-214906 | Common:4; Rare:113; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215081-215237 | Common:2; Rare:86 | ||||
| chr9:706904-707224 | Common:4; Rare:108 | ||||
| chr9:2015060-2015392 | Common:3; Rare:96 | ||||
| chr9:2017633-2017739 | Rare:30 | ||||
| chr9:2844045-2844357 | Common:5; Rare:123 | ||||
| chr9:3525968-3526119 | Common:1; Rare:72 | ||||
| chr9:3526409-3526545 | Common:4; Rare:72 | ||||
| chr9:4662283-4662323 | Common:1; Rare:13 | ||||
| chr9:4666388-4666483 | Common:1; Rare:24 |