| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:226982696-226983034 | Common:3; Rare:126; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr1:227735229-227735477 | Common:3; Rare:142 | ||||
| chr1:228103317-228103491 | Common:1; Rare:57 | ||||
| chr1:228139856-228140363 | Common:4; Rare:156 | ||||
| chr1:228207911-228208075 | Common:1; Rare:35 | ||||
| chr1:228457843-228458113 | Common:1; Rare:99 | ||||
| chr1:229271027-229271341 | Rare:104 | ||||
| chr1:229625964-229626284 | Rare:110 | ||||
| chr1:230978753-230979127 | Common:2; Rare:147 | ||||
| chr1:231241101-231241286 | Rare:102; Clinvar:3 | ||||
| chr1:231337830-231338056 | Common:2; Rare:82 | ||||
| chr1:231528540-231528750 | Common:2; Rare:77 | ||||
| chr1:234373361-234373554 | Common:1; Rare:102; Clinvar (benign):3 | ||||
| chr1:234373636-234373775 | Rare:53; Clinvar (benign):3 | ||||
| chr1:236065066-236065353 | Common:3; Rare:111; Clinvar (pathogenic):1 |