| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124736-14125179 | Common:4; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178559-14178873 | Common:2; Rare:164; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651828 | Rare:103 | ||||
| chr3:14947377-14947549 | Common:3; Rare:82 | ||||
| chr3:15099128-15099293 | Rare:40 | ||||
| chr3:15427471-15427629 | Common:1; Rare:57 | ||||
| chr3:15601512-15601804 | Common:4; Rare:123; Clinvar:1 | ||||
| chr3:15859787-15860114 | Common:4; Rare:103 | ||||
| chr3:16264907-16265243 | Common:2; Rare:104 | ||||
| chr3:19946996-19947415 | Common:4; Rare:157 | ||||
| chr3:20186176-20186355 | Common:1; Rare:52 | ||||
| chr3:21751086-21751386 | Common:2; Rare:94 | ||||
| chr3:23202975-23203200 | Rare:74 | ||||
| chr3:23805812-23806053 | Common:1; Rare:50 | ||||
| chr3:23916887-23917214 | Rare:126 |