| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:39691381-39691568 | Common:4; Rare:37 | ||||
| chr1:39738691-39738962 | Common:2; Rare:71 | ||||
| chr1:39771227-39771386 | Common:3; Rare:44 | ||||
| chr1:39883394-39883564 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
| chr1:40040108-40040307 | Common:2; Rare:39 | ||||
| chr1:40040444-40040812 | Common:3; Rare:114 | ||||
| chr1:40097214-40097281 | Rare:32; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr1:40161214-40161409 | Common:1; Rare:51 | ||||
| chr1:40257903-40258332 | Common:4; Rare:125; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr1:40373560-40373795 | Common:1; Rare:56 | ||||
| chr1:40449983-40450174 | Common:3; Rare:75 | ||||
| chr1:40488721-40489058 | Common:3; Rare:46 | ||||
| chr1:40508626-40508821 | Common:6; Rare:61 | ||||
| chr1:40531502-40531682 | Rare:45 | ||||
| chr1:40691495-40691864 | Common:3; Rare:166 |