| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190881142-190881387 | Common:2; Rare:94 | ||||
| chr2:191014121-191014415 | Common:3; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191263172-191263362 | Rare:33 | ||||
| chr2:191677831-191678218 | Common:4; Rare:110 | ||||
| chr2:197434973-197435180 | Rare:70 | ||||
| chr2:197453210-197453563 | Rare:123 | ||||
| chr2:197499820-197500175 | Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500219-197500430 | Common:1; Rare:86 | ||||
| chr2:200811250-200811596 | Common:1; Rare:108 | ||||
| chr2:200889112-200889439 | Common:3; Rare:105 | ||||
| chr2:200963619-200963807 | Common:1; Rare:43 | ||||
| chr2:201071598-201072012 | Rare:88 | ||||
| chr2:201116143-201116454 | Rare:56 | ||||
| chr2:201117344-201117571 | Rare:26 | ||||
| chr2:201118570-201118807 | Rare:41 |