| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124742-14125105 | Common:4; Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178870 | Common:2; Rare:155; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14651486-14651818 | Rare:98 | ||||
| chr3:14947377-14947551 | Common:3; Rare:84 | ||||
| chr3:15206069-15206278 | Rare:84 | ||||
| chr3:15427471-15427625 | Common:1; Rare:57 | ||||
| chr3:15601506-15601810 | Common:4; Rare:128; Clinvar:2 | ||||
| chr3:15859782-15860158 | Common:5; Rare:114 | ||||
| chr3:16264881-16265239 | Common:2; Rare:117 | ||||
| chr3:17742596-17742935 | Common:4; Rare:116 | ||||
| chr3:19946980-19947393 | Common:5; Rare:153 | ||||
| chr3:23202930-23203194 | Common:1; Rare:93 | ||||
| chr3:23916916-23917177 | Rare:96 | ||||
| chr3:23917648-23917990 | Common:2; Rare:90; Clinvar (benign):1 | ||||
| chr3:24495208-24495510 | Common:5; Rare:81 |