| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:239401641-239401739 | Rare:45 | ||||
| chr2:240025246-240025455 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136243-240136382 | Rare:55 | ||||
| chr2:240465982-240466090 | Common:5; Rare:42 | ||||
| chr2:240560760-240560901 | Common:2; Rare:65 | ||||
| chr2:240561046-240561326 | Common:4; Rare:125 | ||||
| chr2:241102269-241102395 | Common:2; Rare:44 | ||||
| chr2:241149450-241149564 | Common:1; Rare:33 | ||||
| chr2:241230757-241231093 | Common:1; Rare:91 | ||||
| chr2:241236747-241237048 | Common:7; Rare:82 | ||||
| chr2:241237255-241237471 | Common:1; Rare:41 | ||||
| chr2:241239983-241240323 | Common:1; Rare:88 | ||||
| chr2:241249839-241250140 | Common:3; Rare:72 | ||||
| chr2:241271929-241271997 | Rare:15 | ||||
| chr2:241272778-241272987 | Rare:76 |