| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084269-37084561 | Common:4; Rare:110 | ||||
| chr2:37231551-37231712 | Common:4; Rare:93; Clinvar (benign):3 | ||||
| chr2:37324743-37324922 | Common:1; Rare:76 | ||||
| chr2:37671606-37671782 | Common:2; Rare:82 | ||||
| chr2:38076149-38076291 | Rare:38 | ||||
| chr2:38602895-38603193 | Common:4; Rare:117 | ||||
| chr2:38751339-38751616 | Common:3; Rare:128 | ||||
| chr2:38875886-38876055 | Common:1; Rare:63 | ||||
| chr2:39437087-39437447 | Common:4; Rare:127 | ||||
| chr2:42169214-42169399 | Common:1; Rare:108 | ||||
| chr2:43595978-43596205 | Common:1; Rare:79 | ||||
| chr2:44361751-44362005 | Common:1; Rare:77 | ||||
| chr2:46616982-46617262 | Common:7; Rare:122 | ||||
| chr2:46915722-46915895 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176436-47176864 | Common:4; Rare:189; Clinvar (benign):5 |