| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228082439-228082774 | Common:4; Rare:130 | ||||
| chr1:228103045-228103512 | Common:2; Rare:185 | ||||
| chr1:228109216-228109520 | Rare:97 | ||||
| chr1:228139837-228139962 | Common:1; Rare:30 | ||||
| chr1:228140072-228140372 | Common:3; Rare:107 | ||||
| chr1:228165430-228165836 | Rare:120; Clinvar (benign):2 | ||||
| chr1:228165920-228166134 | Common:2; Rare:120; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr1:228213616-228213866 | Common:2; Rare:75 | ||||
| chr1:228407013-228407202 | Common:1; Rare:23 | ||||
| chr1:228457321-228457646 | Common:2; Rare:115 | ||||
| chr1:228457769-228458142 | Common:2; Rare:173 | ||||
| chr1:228487025-228487427 | Common:4; Rare:118 | ||||
| chr1:228735274-228735495 | Common:1; Rare:66 | ||||
| chr1:229271001-229271208 | Rare:80 | ||||
| chr1:229342463-229342684 | Rare:83 |