| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186590101-186590491 | Rare:128 | ||||
| chr2:187554249-187554578 | Common:2; Rare:64 | ||||
| chr2:188291574-188292060 | Common:6; Rare:139 | ||||
| chr2:188292603-188292967 | Common:1; Rare:82 | ||||
| chr2:188974230-188974576 | Rare:88; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189003408-189003787 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:189007497-189007937 | Common:1; Rare:103; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):11 | ||||
| chr2:189441072-189441511 | Common:2; Rare:138 | ||||
| chr2:189580720-189580896 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189661279-189661608 | Common:6; Rare:108 | ||||
| chr2:189783931-189784125 | Common:4; Rare:69; Clinvar (benign):1 | ||||
| chr2:189784260-189784560 | Common:4; Rare:105; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190319719-190319950 | Common:5; Rare:83; Clinvar (benign):5 | ||||
| chr2:190343838-190344038 | Rare:43 | ||||
| chr2:190344086-190344174 | Common:2; Rare:25 |