| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:207053109-207053340 | Common:1; Rare:63 | ||||
| chr1:207321653-207321819 | Rare:42 | ||||
| chr1:207322063-207322564 | Common:1; Rare:144; Clinvar:1 | ||||
| chr1:207496047-207496294 | Rare:53 | ||||
| chr1:207751854-207752458 | Common:2; Rare:188; Clinvar:1 | ||||
| chr1:207911004-207911403 | Common:1; Rare:101 | ||||
| chr1:208243761-208244050 | Common:1; Rare:62 | ||||
| chr1:208244193-208244532 | Common:2; Rare:90 | ||||
| chr1:209651365-209651423 | Common:1; Rare:3 | ||||
| chr1:209652369-209652615 | Common:3; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209675264-209675555 | Common:2; Rare:76 | ||||
| chr1:209756155-209756204 | Common:1; Rare:9 | ||||
| chr1:209784523-209784674 | Rare:46 | ||||
| chr1:209806050-209806269 | Common:4; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827869-209828076 | Common:1; Rare:58 |