| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177552755-177553068 | Common:4; Rare:96 | ||||
| chr2:177618684-177618837 | Common:1; Rare:55 | ||||
| chr2:178072757-178072850 | Rare:29 | ||||
| chr2:178450685-178450907 | Common:1; Rare:83 | ||||
| chr2:178451090-178451363 | Common:6; Rare:82; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478492-178478644 | Common:1; Rare:46 | ||||
| chr2:178807205-178807551 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:179049846-179050318 | Common:2; Rare:109 | ||||
| chr2:180980828-180980963 | Rare:31 | ||||
| chr2:180983893-180984052 | Rare:48 | ||||
| chr2:181891623-181892116 | Common:4; Rare:206 | ||||
| chr2:181954203-181954492 | Rare:63 | ||||
| chr2:182030634-182030795 | Common:2; Rare:33 | ||||
| chr2:182715887-182716461 | Common:3; Rare:187 | ||||
| chr2:182866550-182866765 | Common:1; Rare:51 |