| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217609947-217610790 | Common:5; Rare:490 | ||||
| chr2:217653180-217653660 | Common:1; Rare:93 | ||||
| chr2:217656116-217656800 | Common:8; Rare:278 | ||||
| chr2:217672470-217672870 | Common:7; Rare:161 | ||||
| chr2:217681908-217682063 | Rare:15 | ||||
| chr2:217685160-217685570 | Common:1; Rare:192 | ||||
| chr2:217686073-217686748 | Common:18; Rare:198 | ||||
| chr2:217707040-217707507 | Common:7; Rare:144 | ||||
| chr2:217707430-217707740 | Rare:53 | ||||
| chr2:218010214-218010980 | Common:10; Rare:259 | ||||
| chr2:218294910-218295530 | Common:1; Rare:208 | ||||
| chr2:218310810-218311712 | Common:6; Rare:198 | ||||
| chr2:218313470-218313830 | Rare:80 | ||||
| chr2:218323902-218324235 | Common:10; Rare:160 | ||||
| chr2:218367559-218368301 | Common:8; Rare:291 |