| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26764138-26764564 | Common:8; Rare:319 | ||||
| chr2:26785713-26786184 | Rare:225 | ||||
| chr2:26970325-26970708 | Rare:200 | ||||
| chr2:27032765-27033036 | Rare:228 | ||||
| chr2:27050596-27051067 | Common:5; Rare:240 | ||||
| chr2:27051488-27051737 | Rare:193 | ||||
| chr2:27071310-27071573 | Common:1; Rare:131 | ||||
| chr2:27071488-27071924 | Common:3; Rare:294 | ||||
| chr2:27083940-27084206 | Rare:97 | ||||
| chr2:27086438-27086837 | Common:16; Rare:320; Clinvar (benign):7 | ||||
| chr2:27087000-27087270 | Common:1; Rare:94; Clinvar:5 | ||||
| chr2:27118731-27119158 | Common:1; Rare:137 | ||||
| chr2:27123590-27123930 | Common:4; Rare:123 | ||||
| chr2:27134539-27134792 | Common:2; Rare:301 | ||||
| chr2:27211492-27212194 | Common:8; Rare:389 |