| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188974264-188974571 | Rare:76; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007886-189008141 | Rare:82; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):15 | ||||
| chr2:189179497-189179604 | Rare:30; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:189179606-189179875 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:189441067-189441526 | Common:2; Rare:151 | ||||
| chr2:189763186-189763250 | Rare:8 | ||||
| chr2:189783921-189784150 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784264-189784582 | Common:4; Rare:111; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190319719-190319792 | Common:1; Rare:39; Clinvar (benign):2 | ||||
| chr2:190343886-190344071 | Common:1; Rare:37 | ||||
| chr2:190534707-190534803 | Rare:27 | ||||
| chr2:190648697-190648928 | Common:1; Rare:83 | ||||
| chr2:190649468-190649604 | Common:1; Rare:39 | ||||
| chr2:190880631-190880898 | Common:4; Rare:90 | ||||
| chr2:190880958-190881466 | Common:2; Rare:200 |