| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:207052978-207053300 | Common:1; Rare:83 | ||||
| chr1:207321482-207321819 | Common:1; Rare:87 | ||||
| chr1:207751920-207752284 | Common:2; Rare:115; Clinvar:1 | ||||
| chr1:207911013-207911347 | Common:1; Rare:84 | ||||
| chr1:208244255-208244512 | Common:1; Rare:79 | ||||
| chr1:209675217-209675267 | Common:1; Rare:9 | ||||
| chr1:209675268-209675346 | Rare:24 | ||||
| chr1:209675396-209675917 | Common:3; Rare:141 | ||||
| chr1:209686014-209686283 | Rare:47 | ||||
| chr1:209704633-209704978 | Rare:74 | ||||
| chr1:209768441-209768612 | Rare:25 | ||||
| chr1:209784523-209784722 | Common:1; Rare:67 | ||||
| chr1:209806121-209806274 | Common:4; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827866-209828076 | Common:1; Rare:59 | ||||
| chr1:209937864-209938267 | Common:4; Rare:134; Clinvar (pathogenic):1 |