| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:234951803-234952109 | Common:1; Rare:79 | ||||
| chr2:234981377-234981697 | Common:3; Rare:52 | ||||
| chr2:237085819-237085983 | Common:1; Rare:68 | ||||
| chr2:237486296-237486471 | Rare:36 | ||||
| chr2:237487132-237487354 | Common:3; Rare:58 | ||||
| chr2:237518001-237518254 | Common:4; Rare:47 | ||||
| chr2:238060707-238061158 | Common:6; Rare:142 | ||||
| chr2:238426886-238427081 | Common:1; Rare:70 | ||||
| chr2:240025225-240025482 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560354-240560678 | Common:2; Rare:98 | ||||
| chr2:240560753-240560882 | Common:1; Rare:58 | ||||
| chr2:240560946-240561337 | Common:4; Rare:194 | ||||
| chr2:240586607-240586760 | Common:2; Rare:41 | ||||
| chr2:241102263-241102380 | Common:2; Rare:45 | ||||
| chr2:241149422-241149686 | Common:4; Rare:92 |