| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186589937-186590076 | Rare:42 | ||||
| chr2:186590241-186590523 | Rare:99 | ||||
| chr2:187554228-187554514 | Rare:61 | ||||
| chr2:188291392-188291626 | Common:3; Rare:59 | ||||
| chr2:188291664-188292217 | Common:5; Rare:147 | ||||
| chr2:188292669-188292877 | Common:1; Rare:50 | ||||
| chr2:188292955-188293075 | Rare:15 | ||||
| chr2:188974092-188974304 | Rare:45 | ||||
| chr2:188974320-188974568 | Rare:63; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007497-189008142 | Common:1; Rare:173; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):24 | ||||
| chr2:189441094-189441523 | Common:2; Rare:135 | ||||
| chr2:189580732-189580938 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783947-189784125 | Common:4; Rare:67; Clinvar (benign):1 | ||||
| chr2:189784260-189784547 | Common:4; Rare:104; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190180656-190181081 | Rare:124 |