| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27442215-27442410 | Common:1; Rare:64 | ||||
| chr2:27582797-27583101 | Rare:103 | ||||
| chr2:27628981-27629090 | Common:1; Rare:58 | ||||
| chr2:27663395-27663926 | Rare:169 | ||||
| chr2:27771607-27771766 | Common:1; Rare:59 | ||||
| chr2:27890446-27890746 | Rare:73 | ||||
| chr2:28751689-28752124 | Common:2; Rare:190 | ||||
| chr2:28870254-28870463 | Rare:85 | ||||
| chr2:30447149-30447283 | Common:2; Rare:45 | ||||
| chr2:32039457-32039908 | Rare:132 | ||||
| chr2:32165752-32165903 | Common:1; Rare:58 | ||||
| chr2:32277766-32277948 | Common:1; Rare:45 | ||||
| chr2:32627957-32628125 | Rare:54 | ||||
| chr2:37084276-37084544 | Common:3; Rare:96 | ||||
| chr2:37231551-37231703 | Common:4; Rare:86; Clinvar (benign):3 |