| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12755653-12755742 | Rare:20 | ||||
| chr3:12758081-12758138 | Rare:9 | ||||
| chr3:12838888-12838930 | Common:1; Rare:12 | ||||
| chr3:13580233-13580523 | Common:2; Rare:78 | ||||
| chr3:13820319-13820550 | Common:2; Rare:40 | ||||
| chr3:13832631-13832654 | Rare:2 | ||||
| chr3:13836229-13836318 | Common:1; Rare:22 | ||||
| chr3:13840589-13840696 | Common:3; Rare:20 | ||||
| chr3:13841001-13841027 | Rare:4 | ||||
| chr3:13851679-13851700 | Common:1; Rare:2 | ||||
| chr3:14125716-14125748 | Rare:4 | ||||
| chr3:14138254-14138500 | Common:1; Rare:69 | ||||
| chr3:14138981-14139298 | Common:4; Rare:87; Clinvar:6; Clinvar (benign):7 | ||||
| chr3:14942887-14943504 | Common:6; Rare:145 | ||||
| chr3:14944002-14944100 | Common:1; Rare:26 |