| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12841457-12841905 | Common:2; Rare:139 | ||||
| chr3:12967620-12967980 | Common:4; Rare:130 | ||||
| chr3:13420177-13420500 | Common:2; Rare:186 | ||||
| chr3:13480011-13480354 | Common:4; Rare:156 | ||||
| chr3:14124685-14125156 | Common:8; Rare:268; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14178558-14178868 | Common:4; Rare:306; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402415-14402744 | Common:3; Rare:134 | ||||
| chr3:14651397-14651813 | Common:1; Rare:218 | ||||
| chr3:14947050-14947350 | Common:3; Rare:112 | ||||
| chr3:14947381-14947753 | Common:7; Rare:262 | ||||
| chr3:14947978-14948220 | Rare:200 | ||||
| chr3:14948319-14948662 | Common:4; Rare:200 | ||||
| chr3:15065122-15065389 | Common:4; Rare:181 | ||||
| chr3:15098790-15099080 | Common:1; Rare:65 | ||||
| chr3:15099107-15099327 | Rare:101 |