| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:229625950-229626269 | Rare:105 | ||||
| chr1:230714090-230714324 | Common:3; Rare:47; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:231241089-231241238 | Rare:77; Clinvar:2 | ||||
| chr1:231337831-231338056 | Common:2; Rare:81 | ||||
| chr1:231528522-231528738 | Common:2; Rare:76 | ||||
| chr1:232950458-232950658 | Common:3; Rare:74 | ||||
| chr1:234373342-234373775 | Common:1; Rare:198; Clinvar (benign):7 | ||||
| chr1:235128749-235129070 | Common:1; Rare:133 | ||||
| chr1:235328245-235328579 | Common:1; Rare:84 | ||||
| chr1:235866852-235867177 | Common:3; Rare:102 | ||||
| chr1:236064991-236065342 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
| chr1:236281943-236282258 | Common:6; Rare:93 | ||||
| chr1:236523860-236524034 | Common:2; Rare:46 | ||||
| chr1:236604466-236604626 | Common:4; Rare:48 | ||||
| chr1:236795056-236795453 | Common:6; Rare:161; Clinvar:3 |