| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228109204-228109522 | Rare:99 | ||||
| chr1:228139778-228140398 | Common:4; Rare:185 | ||||
| chr1:228140492-228140624 | Common:1; Rare:28 | ||||
| chr1:228165375-228165866 | Rare:150; Clinvar (benign):2 | ||||
| chr1:228165906-228166209 | Common:2; Rare:154; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
| chr1:228406197-228406211 | Rare:3 | ||||
| chr1:228406713-228407260 | Common:6; Rare:122 | ||||
| chr1:228457530-228457698 | Rare:69 | ||||
| chr1:228457719-228458194 | Common:2; Rare:234 | ||||
| chr1:228486670-228486937 | Common:6; Rare:68 | ||||
| chr1:228487007-228487469 | Common:5; Rare:137 | ||||
| chr1:228735108-228735174 | Rare:18 | ||||
| chr1:228735231-228735541 | Common:1; Rare:84 | ||||
| chr1:229271011-229271219 | Rare:79 | ||||
| chr1:229342287-229342334 | Rare:13 |