| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124252-183124452 | Common:4; Rare:67 | ||||
| chr2:186486118-186486344 | Common:3; Rare:73 | ||||
| chr2:188292692-188292863 | Common:1; Rare:42 | ||||
| chr2:189783966-189784133 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784276-189784512 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190880619-190880859 | Common:4; Rare:81 | ||||
| chr2:191014090-191014340 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678184 | Common:4; Rare:94 | ||||
| chr2:191678750-191678986 | Common:1; Rare:72 | ||||
| chr2:195657042-195657270 | Common:1; Rare:61 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197499788-197500192 | Common:1; Rare:141; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500195-197500431 | Common:1; Rare:99 | ||||
| chr2:200510058-200510263 | Common:1; Rare:58 | ||||
| chr2:200811279-200811596 | Common:1; Rare:96 |