| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39105179-39105920 | Common:10; Rare:324 | ||||
| chr1:39204151-39205137 | Common:4; Rare:374 | ||||
| chr1:39268164-39268564 | Rare:83 | ||||
| chr1:39408521-39409179 | Common:14; Rare:445 | ||||
| chr1:39491359-39491699 | Common:15; Rare:310 | ||||
| chr1:39576490-39576670 | Rare:72 | ||||
| chr1:39576739-39576889 | Rare:64 | ||||
| chr1:39639540-39640001 | Common:1; Rare:332 | ||||
| chr1:39691362-39691606 | Common:5; Rare:49 | ||||
| chr1:39738594-39739021 | Common:10; Rare:226 | ||||
| chr1:39788763-39789320 | Common:14; Rare:376 | ||||
| chr1:39883438-39883642 | Common:1; Rare:165; Clinvar (pathogenic):2 | ||||
| chr1:39901821-39902150 | Common:18; Rare:254 | ||||
| chr1:39954892-39955208 | Common:3; Rare:194 | ||||
| chr1:40039722-40040156 | Common:6; Rare:220 |