| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188974295-188974573 | Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441065-189441504 | Common:2; Rare:135 | ||||
| chr2:189580741-189580938 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783916-189784123 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chr2:189784260-189784537 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190180723-190181046 | Rare:97 | ||||
| chr2:190343880-190343949 | Rare:10 | ||||
| chr2:190534640-190534949 | Common:3; Rare:100 | ||||
| chr2:190648725-190648913 | Rare:69 | ||||
| chr2:190880614-190880859 | Common:4; Rare:83 | ||||
| chr2:191014089-191014353 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191246152-191246314 | Common:1; Rare:47 | ||||
| chr2:191677846-191678174 | Common:4; Rare:94 | ||||
| chr2:191847034-191847376 | Rare:58 | ||||
| chr2:192194913-192195025 | Rare:20 |