| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183038022-183038058 | Rare:11 | ||||
| chr2:183038320-183038621 | Common:4; Rare:96 | ||||
| chr2:186486117-186486443 | Common:3; Rare:108 | ||||
| chr2:186589919-186590094 | Rare:53 | ||||
| chr2:187554263-187554548 | Rare:56 | ||||
| chr2:188292512-188292869 | Common:2; Rare:82 | ||||
| chr2:188293005-188293064 | Rare:7 | ||||
| chr2:188974263-188974568 | Rare:77; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:188991483-188991722 | Rare:64; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr2:189441075-189441507 | Common:2; Rare:131 | ||||
| chr2:189783956-189784140 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784264-189784564 | Common:4; Rare:107; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190343883-190343955 | Rare:12 | ||||
| chr2:190534742-190535016 | Common:3; Rare:87 | ||||
| chr2:190648707-190648923 | Common:1; Rare:80 |