| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:209651359-209651581 | Common:4; Rare:31 | ||||
| chr1:209652330-209652654 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:209652753-209652847 | Rare:14 | ||||
| chr1:209652932-209653255 | Common:1; Rare:53 | ||||
| chr1:209784274-209784868 | Common:4; Rare:159 | ||||
| chr1:209805595-209805747 | Common:2; Rare:28 | ||||
| chr1:209805957-209806573 | Common:6; Rare:157; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:209827789-209828270 | Common:4; Rare:146 | ||||
| chr1:209828286-209828424 | Common:1; Rare:22 | ||||
| chr1:209937987-209938041 | Common:1; Rare:14 | ||||
| chr1:209938094-209938251 | Common:2; Rare:62 | ||||
| chr1:209938463-209938497 | Rare:10 | ||||
| chr1:210232559-210232894 | Common:2; Rare:72 | ||||
| chr1:210233011-210233277 | Common:3; Rare:78 | ||||
| chr1:210328715-210329087 | Common:1; Rare:125 |