| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39026149-39026402 | Common:1; Rare:59 | ||||
| chr1:39738748-39739016 | Common:3; Rare:72 | ||||
| chr1:39883441-39883586 | Common:1; Rare:58; Clinvar (pathogenic):1 | ||||
| chr1:39954963-39955205 | Common:1; Rare:65 | ||||
| chr1:40039869-40040088 | Common:2; Rare:49 | ||||
| chr1:40040433-40040819 | Common:3; Rare:120 | ||||
| chr1:40097214-40097336 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr1:40161247-40161399 | Rare:39 | ||||
| chr1:40257845-40258332 | Common:4; Rare:137; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr1:40317276-40317452 | Common:1; Rare:39 | ||||
| chr1:40374566-40374639 | Common:12; Rare:17 | ||||
| chr1:40449907-40450174 | Common:4; Rare:101 | ||||
| chr1:40477167-40477368 | Common:3; Rare:60 | ||||
| chr1:40508615-40508824 | Common:6; Rare:66 | ||||
| chr1:40531487-40531721 | Common:1; Rare:64 |