| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124252-183124460 | Common:4; Rare:71 | ||||
| chr2:186485976-186486364 | Common:3; Rare:112 | ||||
| chr2:186589872-186590094 | Rare:67 | ||||
| chr2:186590193-186590456 | Rare:90 | ||||
| chr2:186849336-186849568 | Common:3; Rare:37 | ||||
| chr2:187554228-187554514 | Rare:61 | ||||
| chr2:188291672-188292054 | Common:4; Rare:105 | ||||
| chr2:188292603-188292855 | Common:1; Rare:56 | ||||
| chr2:189441086-189441529 | Common:2; Rare:142 | ||||
| chr2:189580714-189581103 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784133 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784275-189784537 | Common:4; Rare:94; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190180729-190181066 | Rare:104 | ||||
| chr2:190319745-190319942 | Common:5; Rare:68; Clinvar (benign):5 | ||||
| chr2:190343961-190344038 | Rare:15 |