| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235866842-235867178 | Common:3; Rare:104 | ||||
| chr1:236065005-236065333 | Common:2; Rare:124; Clinvar (pathogenic):1 | ||||
| chr1:236281920-236282249 | Common:6; Rare:99 | ||||
| chr1:236523560-236524054 | Common:6; Rare:112 | ||||
| chr1:236604459-236604626 | Common:4; Rare:52 | ||||
| chr1:236795086-236795453 | Common:5; Rare:153; Clinvar:3 | ||||
| chr1:240612114-240612292 | Rare:36 | ||||
| chr1:241519649-241519904 | Common:2; Rare:86; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):4 | ||||
| chr1:241639810-241639911 | Common:1; Rare:29 | ||||
| chr1:241848078-241848270 | Common:2; Rare:37 | ||||
| chr1:243255040-243255360 | Common:1; Rare:73 | ||||
| chr1:243255741-243256135 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:244451813-244452032 | Rare:67 | ||||
| chr1:244835123-244835333 | Rare:84 | ||||
| chr1:244835583-244835736 | Common:1; Rare:67; Clinvar (benign):4 |