| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92785005-92785463 | Common:17; Rare:348 | ||||
| chr1:92831872-92832170 | Common:1; Rare:133; Clinvar:7; Clinvar (benign):7 | ||||
| chr1:92832271-92833872 | Common:9; Rare:671; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:92961336-92961684 | Common:2; Rare:226 | ||||
| chr1:93079013-93079356 | Common:10; Rare:357 | ||||
| chr1:93079580-93080114 | Common:2; Rare:159 | ||||
| chr1:93179866-93179999 | Common:1; Rare:34 | ||||
| chr1:93180272-93180784 | Common:6; Rare:580 | ||||
| chr1:93181094-93181255 | Common:1; Rare:25 | ||||
| chr1:93345629-93346009 | Common:13; Rare:331 | ||||
| chr1:93447930-93448237 | Common:6; Rare:250 | ||||
| chr1:93585030-93585400 | Common:6; Rare:94 | ||||
| chr1:93614337-93615048 | Common:2; Rare:307 | ||||
| chr1:93680750-93681105 | Common:2; Rare:149 | ||||
| chr1:93681625-93681948 | Common:6; Rare:216 |