| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:180980280-180980545 | Common:1; Rare:86 | ||||
| chr2:182716197-182716412 | Rare:72 | ||||
| chr2:183124252-183124460 | Common:4; Rare:71 | ||||
| chr2:186485951-186486455 | Common:3; Rare:143 | ||||
| chr2:186505486-186505761 | Rare:66 | ||||
| chr2:186589937-186590041 | Rare:27 | ||||
| chr2:186590101-186590355 | Rare:77 | ||||
| chr2:187554237-187554497 | Rare:54 | ||||
| chr2:188291827-188292020 | Common:3; Rare:65 | ||||
| chr2:188292692-188292861 | Common:1; Rare:42 | ||||
| chr2:188293001-188293064 | Rare:7 | ||||
| chr2:189441065-189441511 | Common:2; Rare:142 | ||||
| chr2:189783956-189784117 | Common:3; Rare:57; Clinvar (benign):1 | ||||
| chr2:189784281-189784547 | Common:4; Rare:97; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343072-190343237 | Common:1; Rare:25 |