| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177552759-177553068 | Common:4; Rare:94 | ||||
| chr2:178072745-178072855 | Rare:32 | ||||
| chr2:178451090-178451378 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:179264502-179264857 | Common:4; Rare:131 | ||||
| chr2:180980258-180980545 | Common:1; Rare:90 | ||||
| chr2:180980801-180980963 | Rare:41 | ||||
| chr2:182426577-182427094 | Common:1; Rare:109 | ||||
| chr2:183037995-183038141 | Rare:44 | ||||
| chr2:186485962-186486348 | Common:3; Rare:106 | ||||
| chr2:186589974-186590034 | Rare:12 | ||||
| chr2:186590229-186590465 | Rare:81 | ||||
| chr2:188292616-188292861 | Common:1; Rare:57 | ||||
| chr2:188974307-188974564 | Rare:63; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441086-189441511 | Common:2; Rare:130 | ||||
| chr2:189783966-189784125 | Common:3; Rare:60; Clinvar (benign):1 |