| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178478515-178478677 | Common:1; Rare:54 | ||||
| chr2:179264502-179264861 | Common:4; Rare:133 | ||||
| chr2:180980245-180980545 | Common:1; Rare:94 | ||||
| chr2:180980830-180980967 | Rare:30 | ||||
| chr2:186485983-186486360 | Common:3; Rare:108 | ||||
| chr2:186589894-186590034 | Rare:40 | ||||
| chr2:186590072-186590448 | Rare:126 | ||||
| chr2:187448137-187448375 | Rare:37 | ||||
| chr2:187554254-187554547 | Rare:59 | ||||
| chr2:188292679-188292854 | Common:1; Rare:42 | ||||
| chr2:189441072-189441529 | Common:2; Rare:150 | ||||
| chr2:189783956-189784142 | Common:4; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784281-189784512 | Common:3; Rare:76; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190343559-190343816 | Common:2; Rare:72 | ||||
| chr2:190343868-190343960 | Rare:18 |