| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27663604-27663917 | Rare:112 | ||||
| chr2:28751731-28752127 | Common:1; Rare:165 | ||||
| chr2:28870254-28870425 | Rare:70 | ||||
| chr2:32039732-32039868 | Rare:40 | ||||
| chr2:32165752-32165898 | Common:1; Rare:54 | ||||
| chr2:32627954-32628125 | Rare:55 | ||||
| chr2:33599222-33599434 | Common:1; Rare:80 | ||||
| chr2:37084289-37084551 | Common:3; Rare:97 | ||||
| chr2:37231537-37231703 | Common:4; Rare:93; Clinvar (benign):3 | ||||
| chr2:37324724-37324950 | Common:1; Rare:93 | ||||
| chr2:38751339-38751645 | Common:4; Rare:143 | ||||
| chr2:38875892-38876055 | Common:1; Rare:60 | ||||
| chr2:39437283-39437464 | Common:2; Rare:63 | ||||
| chr2:42568424-42568739 | Common:4; Rare:82 | ||||
| chr2:44361782-44361977 | Common:1; Rare:60 |