| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202634795-202635015 | Common:4; Rare:84 | ||||
| chr2:202870765-202870837 | Common:2; Rare:12 | ||||
| chr2:202911908-202912300 | Common:2; Rare:107 | ||||
| chr2:203014552-203014959 | Common:1; Rare:133 | ||||
| chr2:203238775-203239050 | Common:2; Rare:98 | ||||
| chr2:206085771-206085975 | Common:1; Rare:58 | ||||
| chr2:206086268-206086303 | Rare:4 | ||||
| chr2:206159370-206159989 | Common:4; Rare:185; Clinvar (benign):1 | ||||
| chr2:206765276-206765654 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529779-207530111 | Common:3; Rare:92 | ||||
| chr2:207625227-207625403 | Common:1; Rare:50 | ||||
| chr2:208025475-208025586 | Common:1; Rare:30 | ||||
| chr2:208255019-208255234 | Common:2; Rare:56 | ||||
| chr2:208266019-208266263 | Common:8; Rare:83; Clinvar (benign):1 | ||||
| chr2:209424155-209424241 | Common:2; Rare:21 |