| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10248243-10248620 | Common:10; Rare:224 | ||||
| chr3:10321035-10321247 | Common:2; Rare:90 | ||||
| chr3:11136720-11137340 | Rare:207 | ||||
| chr3:11137310-11137707 | Common:1; Rare:129 | ||||
| chr3:11154304-11154557 | Common:7; Rare:92 | ||||
| chr3:11225821-11226039 | Rare:64 | ||||
| chr3:11272190-11272467 | Common:4; Rare:72 | ||||
| chr3:11643800-11644016 | Common:2; Rare:63 | ||||
| chr3:11719430-11719810 | Common:2; Rare:217 | ||||
| chr3:11846777-11847027 | Common:3; Rare:117 | ||||
| chr3:12287500-12288090 | Common:17; Rare:168 | ||||
| chr3:12288890-12289092 | Common:3; Rare:77 | ||||
| chr3:12484325-12484618 | Common:10; Rare:163; Clinvar:6; Clinvar (benign):4 | ||||
| chr3:12556832-12557164 | Common:10; Rare:185 | ||||
| chr3:12664064-12664360 | Common:4; Rare:168; Clinvar:2; Clinvar (benign):7 |