| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002257-176002406 | Common:2; Rare:58 | ||||
| chr2:176137160-176137451 | Common:1; Rare:38 | ||||
| chr2:176188538-176188678 | Common:1; Rare:55 | ||||
| chr2:177212434-177212820 | Common:4; Rare:155 | ||||
| chr2:177213197-177213288 | Rare:38 | ||||
| chr2:177216670-177217148 | Common:2; Rare:142 | ||||
| chr2:177263412-177263682 | Common:1; Rare:62 | ||||
| chr2:177264548-177264876 | Common:2; Rare:94 | ||||
| chr2:177392638-177392804 | Common:1; Rare:43; Clinvar:1 | ||||
| chr2:178072726-178072849 | Rare:35 | ||||
| chr2:178451067-178451427 | Common:6; Rare:107; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478538-178478686 | Common:1; Rare:48 | ||||
| chr2:181891619-181892275 | Common:6; Rare:266 | ||||
| chr2:182715915-182716480 | Common:3; Rare:185 | ||||
| chr2:182716860-182717070 | Common:1; Rare:40 |