| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189580769-189580925 | Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189763180-189763289 | Rare:21 | ||||
| chr2:189783555-189783586 | Rare:3 | ||||
| chr2:189783929-189784160 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784268-189784593 | Common:5; Rare:113; Clinvar:8; Clinvar (benign):4 | ||||
| chr2:190343852-190344088 | Common:1; Rare:50 | ||||
| chr2:190646428-190646752 | Common:1; Rare:55 | ||||
| chr2:190648683-190648935 | Common:1; Rare:89 | ||||
| chr2:190880614-190880897 | Common:4; Rare:96 | ||||
| chr2:190881059-190881456 | Common:2; Rare:162 | ||||
| chr2:191013958-191014265 | Rare:91; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191041768-191041858 | Common:1; Rare:13 | ||||
| chr2:191245231-191245619 | Common:4; Rare:121 | ||||
| chr2:191246155-191246278 | Rare:40 | ||||
| chr2:191678564-191678603 | Rare:20 |