| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127628955-127629227 | Common:1; Rare:91 | ||||
| chr3:127672785-127673008 | Common:2; Rare:109 | ||||
| chr3:127822445-127822638 | Rare:42 | ||||
| chr3:127823129-127823331 | Common:3; Rare:45 | ||||
| chr3:128052202-128052539 | Common:2; Rare:115 | ||||
| chr3:128123760-128123944 | Rare:51 | ||||
| chr3:128153365-128153509 | Rare:45 | ||||
| chr3:128493195-128493357 | Rare:51 | ||||
| chr3:128726131-128726233 | Common:1; Rare:36; Clinvar:3 | ||||
| chr3:128879385-128879704 | Common:5; Rare:153; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160991-129161134 | Rare:58 | ||||
| chr3:129183762-129184084 | Common:2; Rare:109 | ||||
| chr3:129249503-129249737 | Common:3; Rare:64 | ||||
| chr3:129278761-129278905 | Common:4; Rare:46 | ||||
| chr3:129316251-129316391 | Common:1; Rare:51 |