| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14947351-14947591 | Common:3; Rare:112 | ||||
| chr3:15065230-15065409 | Common:5; Rare:65 | ||||
| chr3:15099128-15099303 | Rare:44 | ||||
| chr3:15206049-15206278 | Rare:88 | ||||
| chr3:15427471-15427629 | Common:1; Rare:57 | ||||
| chr3:15601515-15601801 | Common:4; Rare:121; Clinvar:1 | ||||
| chr3:15601859-15602030 | Common:1; Rare:86; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:16264872-16265239 | Common:2; Rare:122 | ||||
| chr3:17742539-17742956 | Common:4; Rare:152 | ||||
| chr3:19946974-19947222 | Common:4; Rare:89 | ||||
| chr3:20186139-20186365 | Common:3; Rare:66 | ||||
| chr3:23202938-23203220 | Common:1; Rare:95 | ||||
| chr3:23805840-23806069 | Common:1; Rare:47 | ||||
| chr3:23916878-23917224 | Rare:132 | ||||
| chr3:25783388-25783627 | Common:2; Rare:79; Clinvar (benign):3 |