| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:6625033-6625252 | Rare:174 | ||||
| chr1:6701748-6702002 | Rare:205 | ||||
| chr1:6784468-6784825 | Common:1; Rare:113 | ||||
| chr1:6784901-6785750 | Common:12; Rare:874 | ||||
| chr1:7771096-7771369 | Common:12; Rare:295 | ||||
| chr1:7783740-7784443 | Common:10; Rare:439 | ||||
| chr1:7954020-7954430 | Common:7; Rare:296 | ||||
| chr1:7961354-7961792 | Common:12; Rare:399; Clinvar:9; Clinvar (benign):9 | ||||
| chr1:8026200-8026539 | Common:9; Rare:389 | ||||
| chr1:8422813-8423514 | Common:3; Rare:296 | ||||
| chr1:8423630-8424050 | Common:4; Rare:289 | ||||
| chr1:8703004-8703986 | Common:5; Rare:403 | ||||
| chr1:8816664-8817064 | Rare:151 | ||||
| chr1:8817500-8817931 | Common:14; Rare:346 | ||||
| chr1:8877802-8878202 | Common:6; Rare:204 |