| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14124728-14125191 | Common:4; Rare:132; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:14178559-14178873 | Common:2; Rare:164; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651423-14651818 | Common:1; Rare:116 | ||||
| chr3:14947223-14947585 | Common:4; Rare:162 | ||||
| chr3:14948030-14948208 | Rare:78 | ||||
| chr3:15206064-15206322 | Common:1; Rare:101 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601512-15601801 | Common:4; Rare:122; Clinvar:1 | ||||
| chr3:15797900-15798033 | Rare:26 | ||||
| chr3:16264881-16265243 | Common:2; Rare:119 | ||||
| chr3:16513481-16513775 | Common:4; Rare:76 | ||||
| chr3:17742591-17742952 | Common:4; Rare:127 | ||||
| chr3:19946970-19947457 | Common:7; Rare:180 | ||||
| chr3:20186182-20186415 | Common:2; Rare:75 | ||||
| chr3:23916872-23917208 | Rare:132 |