| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45339927-45340212 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:45340381-45340566 | Common:1; Rare:47; Clinvar:1 | ||||
| chr1:45500046-45500385 | Common:1; Rare:94; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr1:45521800-45522089 | Common:1; Rare:108 | ||||
| chr1:45550721-45551097 | Common:3; Rare:91 | ||||
| chr1:45583801-45584125 | Common:1; Rare:114 | ||||
| chr1:45687059-45687357 | Common:1; Rare:77 | ||||
| chr1:45688091-45688243 | Common:1; Rare:48 | ||||
| chr1:46198399-46198525 | Common:1; Rare:50; Clinvar:1 | ||||
| chr1:46303138-46303776 | Common:3; Rare:190 | ||||
| chr1:46604186-46604442 | Common:1; Rare:69 | ||||
| chr1:47314093-47314430 | Common:3; Rare:70; Clinvar:1 | ||||
| chr1:47333773-47334005 | Common:2; Rare:76 | ||||
| chr1:51878677-51878961 | Common:1; Rare:84 | ||||
| chr1:52055101-52055272 | Common:1; Rare:47 |