| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12004258-12004388 | Common:2; Rare:39 | ||||
| chr3:12158902-12159021 | Rare:35 | ||||
| chr3:12288809-12289075 | Common:1; Rare:56 | ||||
| chr3:12484365-12484560 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664047-12664315 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:12759237-12759419 | Common:1; Rare:45 | ||||
| chr3:13073351-13073582 | Common:6; Rare:67 | ||||
| chr3:13420131-13420433 | Common:1; Rare:91 | ||||
| chr3:13480040-13480331 | Common:2; Rare:67 | ||||
| chr3:14124738-14125179 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178545-14178873 | Common:2; Rare:170; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402453-14402781 | Common:4; Rare:70 | ||||
| chr3:14402786-14402810 | Common:3; Rare:5 | ||||
| chr3:14432284-14432528 | Common:1; Rare:43 | ||||
| chr3:14651453-14651824 | Rare:110 |