| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37084269-37084563 | Common:4; Rare:111 | ||||
| chr2:37156906-37157173 | Common:4; Rare:86 | ||||
| chr2:37189719-37189724 | Rare:1 | ||||
| chr2:37196226-37196669 | Common:4; Rare:137 | ||||
| chr2:37231404-37231776 | Common:6; Rare:190; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:37324695-37324950 | Common:1; Rare:100 | ||||
| chr2:37344486-37344850 | Common:2; Rare:126 | ||||
| chr2:37671625-37671752 | Common:1; Rare:58 | ||||
| chr2:37925154-37925390 | Common:2; Rare:96 | ||||
| chr2:38076138-38076295 | Rare:39 | ||||
| chr2:38602886-38603180 | Common:4; Rare:115 | ||||
| chr2:38750849-38750928 | Common:1; Rare:29 | ||||
| chr2:38751233-38751607 | Common:5; Rare:193 | ||||
| chr2:38875868-38876059 | Common:2; Rare:69 | ||||
| chr2:39120998-39121143 | Rare:53 |