| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177218774-177219034 | Rare:63 | ||||
| chr2:177263400-177263736 | Common:2; Rare:78 | ||||
| chr2:177264546-177264865 | Common:2; Rare:92 | ||||
| chr2:177392634-177393085 | Common:3; Rare:149; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:178072759-178072854 | Rare:28 | ||||
| chr2:178451071-178451382 | Common:6; Rare:89; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478314-178478715 | Common:1; Rare:127 | ||||
| chr2:180980266-180980545 | Common:1; Rare:87 | ||||
| chr2:180980863-180981266 | Rare:104 | ||||
| chr2:181891656-181892294 | Common:6; Rare:249 | ||||
| chr2:182715935-182716480 | Common:3; Rare:179 | ||||
| chr2:183038380-183038805 | Common:4; Rare:115 | ||||
| chr2:186486087-186486445 | Common:3; Rare:116 | ||||
| chr2:186589921-186590056 | Rare:41 | ||||
| chr2:188292716-188292895 | Common:1; Rare:44 |