| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208254063-208254292 | Common:1; Rare:43 | ||||
| chr2:208255032-208255255 | Common:2; Rare:59 | ||||
| chr2:208266119-208266293 | Common:6; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002473-210002659 | Common:5; Rare:60 | ||||
| chr2:210476659-210476845 | Rare:61 | ||||
| chr2:210477568-210477690 | Rare:39 | ||||
| chr2:212539117-212539394 | Common:7; Rare:52 | ||||
| chr2:213284238-213284528 | Rare:100 | ||||
| chr2:215311879-215312139 | Common:8; Rare:100 | ||||
| chr2:215435962-215436253 | Common:2; Rare:90 | ||||
| chr2:216081748-216081906 | Common:1; Rare:53 | ||||
| chr2:216412664-216412781 | Rare:13 | ||||
| chr2:216498732-216498894 | Common:6; Rare:70 | ||||
| chr2:216695515-216695584 | Rare:13 | ||||
| chr2:217434181-217434341 | Rare:32 |