| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:228140131-228140379 | Common:2; Rare:92 | ||||
| chr1:228165472-228165575 | Rare:29 | ||||
| chr1:228416592-228416736 | Common:1; Rare:29 | ||||
| chr1:228425046-228425517 | Common:9; Rare:262 | ||||
| chr1:228457837-228458113 | Common:1; Rare:105 | ||||
| chr1:228735230-228735504 | Common:1; Rare:78 | ||||
| chr1:229270981-229271315 | Rare:109 | ||||
| chr1:229508215-229508513 | Common:1; Rare:118 | ||||
| chr1:229625902-229626293 | Rare:136 | ||||
| chr1:230642289-230642594 | Common:1; Rare:111 | ||||
| chr1:230978745-230979153 | Common:2; Rare:159 | ||||
| chr1:231241094-231241362 | Common:2; Rare:130; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:231337819-231338073 | Common:3; Rare:90 | ||||
| chr1:231338221-231338586 | Common:1; Rare:108 | ||||
| chr1:231528294-231528826 | Common:4; Rare:145 |