| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:163349121-163349277 | Common:1; Rare:26 | ||||
| chr2:164690493-164690698 | Rare:40 | ||||
| chr2:164826711-164826796 | Common:1; Rare:16 | ||||
| chr2:164974361-164974661 | Common:4; Rare:51 | ||||
| chr2:164980787-164981012 | Rare:35 | ||||
| chr2:164981697-164981796 | Common:1; Rare:18 | ||||
| chr2:165357958-165358002 | Rare:5 | ||||
| chr2:165373289-165373359 | Rare:10; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:165406453-165406561 | Common:1; Rare:18 | ||||
| chr2:165408304-165408473 | Common:1; Rare:43 | ||||
| chr2:165451895-165451917 | Common:1; Rare:4 | ||||
| chr2:165452463-165452589 | Common:1; Rare:20 | ||||
| chr2:165452590-165452702 | Common:2; Rare:19 | ||||
| chr2:165453269-165453429 | Common:1; Rare:19 | ||||
| chr2:165462405-165462576 | Rare:26 |