| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37925181-37925325 | Rare:56 | ||||
| chr2:37925338-37925727 | Common:6; Rare:161 | ||||
| chr2:38076132-38076291 | Rare:40 | ||||
| chr2:38376325-38376407 | Rare:22 | ||||
| chr2:38376743-38377000 | Common:1; Rare:99 | ||||
| chr2:38377203-38377535 | Common:3; Rare:141 | ||||
| chr2:38602695-38602776 | Rare:22 | ||||
| chr2:38602778-38603266 | Common:5; Rare:198 | ||||
| chr2:38665792-38666163 | Common:3; Rare:99 | ||||
| chr2:38751266-38751651 | Common:6; Rare:203 | ||||
| chr2:38778051-38778260 | Common:1; Rare:54 | ||||
| chr2:38875839-38876049 | Common:2; Rare:72 | ||||
| chr2:39120355-39120497 | Rare:67; Clinvar:2; Clinvar (benign):6 | ||||
| chr2:39120860-39121362 | Common:4; Rare:173 | ||||
| chr2:39124170-39124658 | Common:1; Rare:151 |