| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:43946622-43946987 | Rare:100 | ||||
| chr1:43974861-43975061 | Common:3; Rare:61 | ||||
| chr1:44213255-44213527 | Common:3; Rare:56 | ||||
| chr1:44355265-44355470 | Common:1; Rare:46 | ||||
| chr1:44674425-44674724 | Common:3; Rare:76 | ||||
| chr1:44739667-44739931 | Common:2; Rare:104 | ||||
| chr1:44775324-44775622 | Common:2; Rare:112 | ||||
| chr1:44775824-44776165 | Common:2; Rare:123 | ||||
| chr1:44808184-44808550 | Common:2; Rare:77 | ||||
| chr1:44986532-44986799 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr1:45012108-45012284 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45012693-45012820 | Common:1; Rare:25 | ||||
| chr1:45326759-45326939 | Rare:46 | ||||
| chr1:45339927-45340047 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr1:45340109-45340247 | Rare:60; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 |