| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171687989-171688026 | Rare:6 | ||||
| chr2:171999798-171999972 | Common:1; Rare:71 | ||||
| chr2:174395619-174395795 | Common:2; Rare:57 | ||||
| chr2:174486998-174487385 | Common:2; Rare:94 | ||||
| chr2:175181624-175181830 | Common:4; Rare:73 | ||||
| chr2:176002241-176002417 | Common:2; Rare:74 | ||||
| chr2:176188497-176188678 | Common:1; Rare:71 | ||||
| chr2:176188937-176189105 | Common:2; Rare:55 | ||||
| chr2:176269375-176269500 | Common:1; Rare:51 | ||||
| chr2:177212416-177212821 | Common:4; Rare:164 | ||||
| chr2:177264539-177264881 | Common:2; Rare:98 | ||||
| chr2:177392651-177393070 | Common:3; Rare:144; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:178451098-178451297 | Common:4; Rare:62; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:178478522-178478759 | Common:1; Rare:74 | ||||
| chr2:179264524-179264856 | Common:4; Rare:125 |