| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139389582-139389828 | Common:1; Rare:77 | ||||
| chr3:143001426-143001626 | Common:3; Rare:73 | ||||
| chr3:146161039-146161098 | Rare:26; Clinvar:3 | ||||
| chr3:150603178-150603299 | Common:1; Rare:37 | ||||
| chr3:155079824-155080358 | Common:2; Rare:124 | ||||
| chr3:156674374-156674618 | Common:3; Rare:66 | ||||
| chr3:157160130-157160319 | Rare:78 | ||||
| chr3:160399177-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399514-160399651 | Rare:28 | ||||
| chr3:160565414-160565811 | Common:2; Rare:144 | ||||
| chr3:169773331-169773418 | Rare:25 | ||||
| chr3:172039494-172039709 | Common:2; Rare:73 | ||||
| chr3:179604632-179604818 | Common:1; Rare:55 | ||||
| chr3:184181694-184181947 | Rare:55 | ||||
| chr3:184248892-184249214 | Common:3; Rare:118; Clinvar:5; Clinvar (benign):1 |