| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33599212-33599445 | Common:1; Rare:89 | ||||
| chr2:37084269-37084566 | Common:4; Rare:113 | ||||
| chr2:37231502-37231714 | Common:5; Rare:115; Clinvar (benign):3 | ||||
| chr2:37925278-37925538 | Common:3; Rare:111 | ||||
| chr2:38076137-38076291 | Rare:39 | ||||
| chr2:38875897-38876047 | Common:1; Rare:52 | ||||
| chr2:39437078-39437464 | Common:4; Rare:138 | ||||
| chr2:42169182-42169492 | Common:1; Rare:150 | ||||
| chr2:42317300-42317510 | Common:1; Rare:46 | ||||
| chr2:42792456-42792781 | Common:2; Rare:108 | ||||
| chr2:43595931-43596158 | Common:1; Rare:76 | ||||
| chr2:43838761-43839045 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:43839220-43839340 | Rare:26 | ||||
| chr2:44361479-44362010 | Common:4; Rare:166 | ||||
| chr2:46616972-46617275 | Common:7; Rare:131 |