| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160755944-160756254 | Common:1; Rare:81 | ||||
| chr3:161105032-161105388 | Common:4; Rare:105 | ||||
| chr3:167734823-167735209 | Common:3; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735586-167735752 | Rare:41 | ||||
| chr3:168094789-168095108 | Common:2; Rare:70 | ||||
| chr3:169773341-169773415 | Rare:21 | ||||
| chr3:170222296-170222545 | Common:2; Rare:78 | ||||
| chr3:172711011-172711160 | Rare:73 | ||||
| chr3:172711175-172711264 | Rare:14 | ||||
| chr3:179347595-179347804 | Common:1; Rare:55 | ||||
| chr3:179604626-179604939 | Common:3; Rare:120 | ||||
| chr3:180602111-180602242 | Common:1; Rare:46 | ||||
| chr3:180957692-180957923 | Rare:39 | ||||
| chr3:180989620-180989793 | Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099442-183099742 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):5 |