| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14652012-14652152 | Common:2; Rare:31 | ||||
| chr3:14946983-14947153 | Common:1; Rare:62 | ||||
| chr3:14947326-14947627 | Common:3; Rare:135 | ||||
| chr3:14947904-14948237 | Rare:151 | ||||
| chr3:14948350-14948673 | Common:2; Rare:102 | ||||
| chr3:15050514-15050658 | Common:2; Rare:32 | ||||
| chr3:15065190-15065448 | Common:5; Rare:96 | ||||
| chr3:15099059-15099368 | Common:2; Rare:83 | ||||
| chr3:15205940-15206315 | Common:1; Rare:135 | ||||
| chr3:15332510-15332648 | Common:2; Rare:40 | ||||
| chr3:15427417-15427696 | Common:1; Rare:90 | ||||
| chr3:15601506-15601806 | Common:4; Rare:125; Clinvar:1 | ||||
| chr3:15601850-15602064 | Common:1; Rare:107; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:15797905-15797971 | Rare:15 | ||||
| chr3:15797977-15798026 | Rare:10 |