| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177618688-177618784 | Common:1; Rare:42 | ||||
| chr2:178451083-178451297 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478515-178478659 | Common:1; Rare:45 | ||||
| chr2:180980873-180981218 | Rare:87 | ||||
| chr2:182522518-182522636 | Common:2; Rare:20 | ||||
| chr2:182522637-182522836 | Common:1; Rare:39 | ||||
| chr2:183124252-183124452 | Common:4; Rare:67 | ||||
| chr2:186485994-186486344 | Common:3; Rare:97 | ||||
| chr2:186590072-186590335 | Rare:79 | ||||
| chr2:188291596-188292088 | Common:7; Rare:140 | ||||
| chr2:188974360-188974555 | Rare:58; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189580762-189580962 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783956-189784053 | Common:2; Rare:30 | ||||
| chr2:189784281-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190534696-190534919 | Common:1; Rare:71 |