| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233419172-233419363 | Common:1; Rare:36 | ||||
| chr2:237085726-237085934 | Common:2; Rare:60 | ||||
| chr2:238060745-238061052 | Common:4; Rare:96 | ||||
| chr2:238426877-238427064 | Common:1; Rare:67 | ||||
| chr2:240025227-240025477 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560766-240560835 | Rare:29 | ||||
| chr2:240561018-240561310 | Common:4; Rare:134 | ||||
| chr2:240586224-240586385 | Common:1; Rare:52 | ||||
| chr2:240625220-240625510 | Rare:61 | ||||
| chr2:241102272-241102539 | Common:2; Rare:78 | ||||
| chr2:241127727-241127959 | Rare:52 | ||||
| chr2:241149422-241149680 | Common:4; Rare:89 | ||||
| chr2:241272829-241273017 | Rare:67 | ||||
| chr2:241315153-241315390 | Common:4; Rare:78 | ||||
| chr2:241315664-241315994 | Common:4; Rare:127 |