| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:190318542-190318962 | Common:3; Rare:66 | ||||
| chr3:190321151-190321256 | Common:1; Rare:21 | ||||
| chr3:190321736-190321858 | Common:1; Rare:15 | ||||
| chr3:190323262-190323586 | Common:1; Rare:76 | ||||
| chr3:195657873-195658144 | Common:13; Rare:45 | ||||
| chr3:195908123-195908248 | Common:2; Rare:39 | ||||
| chr3:195990216-195990414 | Rare:23 | ||||
| chr3:197477781-197478025 | Common:1; Rare:43 | ||||
| chr3:197627826-197628019 | Common:6; Rare:74 | ||||
| chr3:197850988-197851179 | Rare:35 | ||||
| chr4:679743-680005 | Common:2; Rare:85 | ||||
| chr4:760770-760924 | Common:1; Rare:49 | ||||
| chr4:761140-761413 | Common:4; Rare:87 | ||||
| chr4:1805356-1805919 | Common:1; Rare:250; Clinvar:13; Clinvar (benign):10; Clinvar (pathogenic):7 | ||||
| chr4:1806047-1806326 | Common:2; Rare:100; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 |