| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174395629-174395795 | Common:1; Rare:55 | ||||
| chr2:174487061-174487329 | Common:1; Rare:58 | ||||
| chr2:176116587-176116824 | Common:2; Rare:56 | ||||
| chr2:176188520-176188668 | Common:1; Rare:53 | ||||
| chr2:176269376-176269500 | Common:1; Rare:50 | ||||
| chr2:177212435-177212821 | Common:4; Rare:154 | ||||
| chr2:177263419-177263603 | Rare:42 | ||||
| chr2:177264630-177264845 | Common:2; Rare:69 | ||||
| chr2:177392657-177392863 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:178072766-178072850 | Rare:25 | ||||
| chr2:178451090-178451353 | Common:6; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478538-178478659 | Common:1; Rare:35 | ||||
| chr2:179264517-179264857 | Common:4; Rare:128 | ||||
| chr2:181891645-181892021 | Common:4; Rare:152 | ||||
| chr2:182715935-182716339 | Common:3; Rare:139 |