| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44213324-44213535 | Common:1; Rare:44 | ||||
| chr1:44674413-44674769 | Common:3; Rare:95 | ||||
| chr1:44739667-44739900 | Common:1; Rare:91 | ||||
| chr1:44775440-44775620 | Common:1; Rare:72 | ||||
| chr1:44775667-44775885 | Common:2; Rare:72 | ||||
| chr1:44776488-44776750 | Rare:86 | ||||
| chr1:44777700-44777941 | Common:1; Rare:73 | ||||
| chr1:44800168-44800393 | Common:1; Rare:51 | ||||
| chr1:44986501-44986791 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:45014738-45014979 | Rare:75; Clinvar (pathogenic):3 | ||||
| chr1:45339962-45340250 | Rare:104; Clinvar:9; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr1:45340386-45340579 | Common:1; Rare:47; Clinvar:1 | ||||
| chr1:45500046-45500358 | Common:1; Rare:76; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521814-45522064 | Common:1; Rare:96 | ||||
| chr1:45550550-45551123 | Common:4; Rare:132 |