| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:231528521-231528798 | Common:2; Rare:100 | ||||
| chr1:232950507-232950678 | Common:1; Rare:58 | ||||
| chr1:233613462-233613656 | Common:1; Rare:48 | ||||
| chr1:233613918-233614190 | Common:5; Rare:81 | ||||
| chr1:234373342-234373554 | Common:1; Rare:107; Clinvar (benign):3 | ||||
| chr1:234373610-234373768 | Rare:68; Clinvar (benign):3 | ||||
| chr1:234608080-234608312 | Common:1; Rare:75 | ||||
| chr1:235128703-235129025 | Rare:133 | ||||
| chr1:235328463-235328584 | Common:1; Rare:36 | ||||
| chr1:235650751-235651033 | Common:1; Rare:39 | ||||
| chr1:235866858-235867177 | Common:3; Rare:102 | ||||
| chr1:236064991-236065367 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
| chr1:236281936-236282258 | Common:6; Rare:95 | ||||
| chr1:236523200-236523454 | Common:2; Rare:48 | ||||
| chr1:236523616-236524060 | Common:5; Rare:106 |