| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:234373606-234373775 | Rare:71; Clinvar (benign):3 | ||||
| chr1:234608080-234608333 | Common:1; Rare:84 | ||||
| chr1:235328142-235328526 | Common:3; Rare:112 | ||||
| chr1:235866847-235867142 | Common:3; Rare:87 | ||||
| chr1:236064987-236065342 | Common:2; Rare:131; Clinvar (pathogenic):1 | ||||
| chr1:236281936-236282193 | Common:5; Rare:71 | ||||
| chr1:236523845-236524060 | Common:2; Rare:57 | ||||
| chr1:236524550-236524608 | Common:1; Rare:11 | ||||
| chr1:236604476-236604628 | Common:4; Rare:44 | ||||
| chr1:236795088-236795453 | Common:5; Rare:153; Clinvar:3 | ||||
| chr1:241519661-241519977 | Common:2; Rare:102; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr1:241848123-241848219 | Rare:19 | ||||
| chr1:241998597-241998849 | Rare:74 | ||||
| chr1:243255045-243255497 | Common:1; Rare:104 | ||||
| chr1:243255752-243256157 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):1 |