| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228146600-228146931 | Common:3; Rare:72 | ||||
| chr1:228212952-228213218 | Rare:61 | ||||
| chr1:228457854-228458130 | Common:1; Rare:100 | ||||
| chr1:228735301-228735528 | Common:1; Rare:68 | ||||
| chr1:229271003-229271301 | Rare:99 | ||||
| chr1:229508291-229508445 | Common:1; Rare:59 | ||||
| chr1:229625912-229626284 | Rare:122 | ||||
| chr1:230978697-230979138 | Common:3; Rare:165 | ||||
| chr1:231241110-231241362 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337823-231338311 | Common:4; Rare:151 | ||||
| chr1:231420204-231420452 | Rare:61 | ||||
| chr1:231528508-231528745 | Common:2; Rare:83 | ||||
| chr1:232950494-232950669 | Common:2; Rare:60 | ||||
| chr1:234373311-234373576 | Common:1; Rare:126; Clinvar (benign):4 | ||||
| chr1:234373625-234373775 | Rare:59; Clinvar (benign):3 |