| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188293001-188293102 | Rare:17 | ||||
| chr2:188974268-188974575 | Rare:76; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007462-189008161 | Common:2; Rare:184; Clinvar:8; Clinvar (benign):10; Clinvar (pathogenic):24 | ||||
| chr2:189441072-189441511 | Common:2; Rare:138 | ||||
| chr2:189763171-189763461 | Common:4; Rare:50 | ||||
| chr2:189783896-189784142 | Common:5; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784238-189784582 | Common:4; Rare:118; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190319717-190319958 | Common:5; Rare:89; Clinvar (benign):5 | ||||
| chr2:190343868-190344073 | Common:1; Rare:43 | ||||
| chr2:190534699-190534779 | Common:1; Rare:20 | ||||
| chr2:190648677-190648944 | Common:1; Rare:93 | ||||
| chr2:190880635-190880904 | Common:4; Rare:93 | ||||
| chr2:191245119-191245619 | Common:4; Rare:153 | ||||
| chr2:191246163-191246283 | Rare:37 | ||||
| chr2:191677858-191678188 | Common:4; Rare:94 |