| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12288934-12289075 | Rare:29 | ||||
| chr3:12484389-12484529 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12663958-12664300 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:12796592-12796718 | Common:3; Rare:43 | ||||
| chr3:12841493-12841895 | Common:1; Rare:130 | ||||
| chr3:13480018-13480339 | Common:2; Rare:80 | ||||
| chr3:14124685-14125196 | Common:4; Rare:154; Clinvar:8; Clinvar (benign):2 | ||||
| chr3:14178564-14178866 | Common:2; Rare:158; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402722 | Rare:65 | ||||
| chr3:14651474-14651828 | Rare:107 | ||||
| chr3:14947236-14947569 | Common:4; Rare:153 | ||||
| chr3:14948419-14948637 | Common:2; Rare:62 | ||||
| chr3:15065204-15065369 | Common:2; Rare:70 | ||||
| chr3:15206121-15206329 | Common:1; Rare:79 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 |