| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124713-14125185 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178471-14178873 | Common:3; Rare:193; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402343-14402659 | Common:1; Rare:86 | ||||
| chr3:14651486-14651854 | Rare:114 | ||||
| chr3:14947164-14947585 | Common:5; Rare:176 | ||||
| chr3:14948065-14948197 | Rare:62 | ||||
| chr3:14948347-14948718 | Common:2; Rare:123 | ||||
| chr3:14948836-14948930 | Common:2; Rare:31 | ||||
| chr3:15065181-15065389 | Common:2; Rare:79 | ||||
| chr3:15098777-15098900 | Rare:15 | ||||
| chr3:15099115-15099309 | Rare:48 | ||||
| chr3:15206046-15206359 | Common:1; Rare:115 | ||||
| chr3:15332398-15332586 | Common:3; Rare:62 | ||||
| chr3:15427402-15427834 | Common:2; Rare:138 | ||||
| chr3:15601495-15601810 | Common:4; Rare:133; Clinvar:2 |