| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171433973-171434234 | Common:2; Rare:66 | ||||
| chr2:171687653-171687881 | Rare:66 | ||||
| chr2:171999831-171999972 | Common:1; Rare:58 | ||||
| chr2:173075135-173075573 | Common:5; Rare:73 | ||||
| chr2:173075607-173075994 | Common:4; Rare:114 | ||||
| chr2:173965251-173965510 | Common:1; Rare:88 | ||||
| chr2:174395629-174395800 | Common:1; Rare:57 | ||||
| chr2:174486998-174487381 | Common:2; Rare:91 | ||||
| chr2:176002195-176002414 | Common:4; Rare:91 | ||||
| chr2:176129635-176129730 | Rare:55 | ||||
| chr2:176188538-176188668 | Common:1; Rare:50 | ||||
| chr2:177212614-177212802 | Common:1; Rare:82 | ||||
| chr2:177263427-177263687 | Common:1; Rare:63 | ||||
| chr2:177264601-177264764 | Common:2; Rare:52 | ||||
| chr2:177392651-177392813 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 |