| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:182715887-182716357 | Common:3; Rare:158 | ||||
| chr2:183124252-183124460 | Common:4; Rare:71 | ||||
| chr2:186486037-186486360 | Common:3; Rare:95 | ||||
| chr2:186590161-186590443 | Rare:93 | ||||
| chr2:187448081-187448398 | Rare:51 | ||||
| chr2:187554312-187554531 | Rare:44 | ||||
| chr2:188291580-188291939 | Common:4; Rare:101 | ||||
| chr2:188292706-188292869 | Common:1; Rare:40 | ||||
| chr2:189441131-189441495 | Common:2; Rare:104 | ||||
| chr2:189783956-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr2:189784275-189784547 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343957-190344019 | Rare:11 | ||||
| chr2:190880623-190880848 | Common:4; Rare:71 | ||||
| chr2:191013625-191013720 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:191014133-191014366 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):2 |