| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:183635666-183636100 | Common:4; Rare:124 | ||||
| chr1:183805022-183805268 | Rare:70 | ||||
| chr1:184051615-184051768 | Common:3; Rare:58 | ||||
| chr1:185045262-185045638 | Common:2; Rare:128 | ||||
| chr1:185156929-185157303 | Common:1; Rare:101 | ||||
| chr1:185157446-185157534 | Common:1; Rare:34 | ||||
| chr1:185307078-185307261 | Rare:36 | ||||
| chr1:185316963-185317147 | Common:1; Rare:41 | ||||
| chr1:185317149-185317567 | Common:2; Rare:120 | ||||
| chr1:186375070-186375899 | Common:1; Rare:235 | ||||
| chr1:190475810-190475903 | Common:2; Rare:23 | ||||
| chr1:193059321-193059426 | Rare:37 | ||||
| chr1:193059434-193059737 | Common:1; Rare:151 | ||||
| chr1:193105431-193105522 | Common:2; Rare:36 | ||||
| chr1:193121747-193122203 | Common:2; Rare:164; Clinvar:5; Clinvar (benign):4 |