| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:151828383-151828665 | Common:3; Rare:85 | ||||
| chr2:151973918-151974049 | Rare:26 | ||||
| chr2:152097545-152098343 | Common:2; Rare:169; Clinvar:1 | ||||
| chr2:152098460-152098920 | Common:2; Rare:122; Clinvar (benign):1 | ||||
| chr2:152175332-152175577 | Rare:74 | ||||
| chr2:152175751-152176167 | Common:2; Rare:105 | ||||
| chr2:152334979-152335208 | Common:1; Rare:76 | ||||
| chr2:152717369-152717695 | Common:3; Rare:180 | ||||
| chr2:152718413-152718646 | Common:2; Rare:88 | ||||
| chr2:152719030-152719360 | Common:3; Rare:107 | ||||
| chr2:153478746-153479032 | Common:1; Rare:70 | ||||
| chr2:153871622-153871934 | Common:1; Rare:71 | ||||
| chr2:154697737-154698137 | Rare:152 | ||||
| chr2:156332066-156332466 | Rare:105 | ||||
| chr2:156341561-156342012 | Rare:146 |