| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190534696-190534853 | Common:1; Rare:53 | ||||
| chr2:190648860-190649122 | Common:2; Rare:78 | ||||
| chr2:190880621-190880834 | Common:3; Rare:67 | ||||
| chr2:190974920-190975218 | Rare:60; Clinvar (benign):1 | ||||
| chr2:191014139-191014353 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245300-191245588 | Common:1; Rare:94 | ||||
| chr2:191677846-191678201 | Common:4; Rare:100 | ||||
| chr2:191678560-191678698 | Rare:51 | ||||
| chr2:191847241-191847440 | Rare:33 | ||||
| chr2:196068825-196068915 | Common:1; Rare:22 | ||||
| chr2:197434970-197435181 | Rare:71 | ||||
| chr2:197453201-197453563 | Rare:128 | ||||
| chr2:197499791-197500436 | Common:2; Rare:245; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515955-197516087 | Rare:56 | ||||
| chr2:199851141-199851265 | Rare:45 |