| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:173965828-173965968 | Rare:50 | ||||
| chr2:174248454-174248744 | Common:1; Rare:87 | ||||
| chr2:174395596-174395887 | Common:2; Rare:94 | ||||
| chr2:174486994-174487409 | Common:2; Rare:103 | ||||
| chr2:175167907-175168257 | Common:1; Rare:91 | ||||
| chr2:175168303-175168511 | Common:1; Rare:47 | ||||
| chr2:175181572-175181775 | Common:4; Rare:74 | ||||
| chr2:176002198-176002445 | Common:5; Rare:95 | ||||
| chr2:177212416-177212825 | Common:4; Rare:164 | ||||
| chr2:177231896-177232138 | Common:2; Rare:60 | ||||
| chr2:177263405-177263687 | Common:1; Rare:65 | ||||
| chr2:177264569-177264916 | Common:2; Rare:97 | ||||
| chr2:177392651-177393076 | Common:3; Rare:145; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552748-177553068 | Common:4; Rare:97 | ||||
| chr2:177618704-177619012 | Common:7; Rare:82 |