| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:43946561-43946983 | Rare:113 | ||||
| chr1:43974796-43975068 | Common:3; Rare:74 | ||||
| chr1:44213370-44213498 | Common:1; Rare:26 | ||||
| chr1:44355276-44355373 | Rare:21 | ||||
| chr1:44632402-44632469 | Common:3; Rare:35 | ||||
| chr1:44674411-44674749 | Common:3; Rare:90 | ||||
| chr1:44739658-44739927 | Common:2; Rare:103 | ||||
| chr1:44775430-44775599 | Common:1; Rare:67 | ||||
| chr1:44775783-44776149 | Common:2; Rare:134 | ||||
| chr1:44986512-44986778 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr1:45011921-45012269 | Common:5; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45339946-45340047 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr1:45340109-45340243 | Rare:58; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45340346-45340470 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:45500044-45500365 | Common:1; Rare:78; Clinvar:4; Clinvar (pathogenic):3 |