| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:43358684-43359006 | Common:7; Rare:102 | ||||
| chr1:43367918-43368216 | Rare:77 | ||||
| chr1:43389741-43389940 | Common:3; Rare:90 | ||||
| chr1:44674421-44674701 | Common:3; Rare:79 | ||||
| chr1:44775473-44775614 | Common:1; Rare:58 | ||||
| chr1:44775848-44776140 | Common:2; Rare:108 | ||||
| chr1:44808403-44808581 | Common:1; Rare:44 | ||||
| chr1:45339938-45340223 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45500040-45500389 | Common:1; Rare:97; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr1:45521693-45522074 | Common:1; Rare:136 | ||||
| chr1:45687036-45687353 | Common:2; Rare:84 | ||||
| chr1:45688049-45688243 | Common:1; Rare:54 | ||||
| chr1:46198316-46198491 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):3 | ||||
| chr1:46303146-46303303 | Common:1; Rare:56 | ||||
| chr1:46303308-46303752 | Common:2; Rare:121 |