| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:186589775-186590408 | Rare:194 | ||||
| chr2:186693895-186694108 | Rare:87 | ||||
| chr2:187448223-187448413 | Rare:30 | ||||
| chr2:189440905-189441200 | Common:2; Rare:82 | ||||
| chr2:189441335-189441785 | Common:3; Rare:161 | ||||
| chr2:189661343-189661603 | Common:4; Rare:84 | ||||
| chr2:189674475-189674859 | Common:2; Rare:85 | ||||
| chr2:189762442-189762915 | Rare:145 | ||||
| chr2:189763155-189763377 | Common:2; Rare:44 | ||||
| chr2:189783526-189783582 | Rare:11 | ||||
| chr2:189783907-189784204 | Common:5; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784214-189784604 | Common:5; Rare:128; Clinvar:8; Clinvar (benign):4 | ||||
| chr2:189784677-189784804 | Common:2; Rare:42 | ||||
| chr2:190180223-190180593 | Common:3; Rare:83 | ||||
| chr2:190180735-190180917 | Rare:54 |