| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37859550-37859834 | Common:7; Rare:183 | ||||
| chr1:37946210-37946580 | Common:5; Rare:152 | ||||
| chr1:37989969-37990324 | Common:2; Rare:203 | ||||
| chr1:37999500-37999960 | Common:11; Rare:168 | ||||
| chr1:38005443-38005785 | Common:2; Rare:181 | ||||
| chr1:38012496-38012826 | Common:1; Rare:180 | ||||
| chr1:38046760-38047110 | Common:1; Rare:94 | ||||
| chr1:38859698-38860033 | Rare:248 | ||||
| chr1:38873266-38873593 | Common:7; Rare:205 | ||||
| chr1:38991001-38991361 | Common:10; Rare:244 | ||||
| chr1:39026231-39026408 | Common:2; Rare:91 | ||||
| chr1:39105017-39105612 | Common:12; Rare:277 | ||||
| chr1:39215097-39215283 | Rare:56 | ||||
| chr1:39408787-39409122 | Common:5; Rare:115 | ||||
| chr1:39883421-39883595 | Common:2; Rare:132; Clinvar (pathogenic):2 |