| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32039738-32039919 | Rare:59 | ||||
| chr2:32063354-32063702 | Common:1; Rare:122; Clinvar:1 | ||||
| chr2:32165659-32165918 | Common:1; Rare:104 | ||||
| chr2:32277765-32277921 | Common:1; Rare:34 | ||||
| chr2:32356940-32356987 | Common:1; Rare:19 | ||||
| chr2:32627920-32628131 | Rare:62 | ||||
| chr2:33599222-33599453 | Common:1; Rare:85 | ||||
| chr2:37084267-37084565 | Common:4; Rare:113 | ||||
| chr2:37156924-37157115 | Common:1; Rare:62 | ||||
| chr2:37231499-37231757 | Common:6; Rare:145; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37925232-37925312 | Rare:31 | ||||
| chr2:38377224-38377443 | Common:2; Rare:101 | ||||
| chr2:38602894-38603180 | Common:4; Rare:113 | ||||
| chr2:38665837-38666131 | Common:3; Rare:75 | ||||
| chr2:38751266-38751662 | Common:6; Rare:207 |