| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144291368-144291621 | Common:1; Rare:77 | ||||
| chr8:144409286-144409485 | Common:1; Rare:66 | ||||
| chr8:144428503-144428679 | Common:2; Rare:67 | ||||
| chr8:144465435-144465487 | Common:2; Rare:21 | ||||
| chr8:144508983-144509082 | Rare:27 | ||||
| chr8:144517675-144518009 | Common:1; Rare:114; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144529044-144529318 | Common:4; Rare:91 | ||||
| chr8:144787282-144787429 | Common:2; Rare:53 | ||||
| chr8:144792345-144792583 | Common:3; Rare:95 | ||||
| chr8:144827190-144827592 | Common:2; Rare:115 | ||||
| chr8:144901414-144901755 | Common:1; Rare:96 | ||||
| chr8:145052182-145052497 | Common:10; Rare:84 | ||||
| chr9:214692-214870 | Common:4; Rare:100; Clinvar (benign):1 | ||||
| chr9:272827-273071 | Common:3; Rare:66 | ||||
| chr9:2015111-2015369 | Common:2; Rare:69 |