| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207625306-207625403 | Common:1; Rare:33 | ||||
| chr2:208025503-208025635 | Rare:31 | ||||
| chr2:208254238-208254482 | Rare:62 | ||||
| chr2:208255005-208255238 | Common:2; Rare:61 | ||||
| chr2:208266023-208266302 | Common:9; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:215311859-215312139 | Common:8; Rare:106 | ||||
| chr2:215436060-215436234 | Common:2; Rare:62 | ||||
| chr2:216081781-216081911 | Common:1; Rare:44 | ||||
| chr2:216412694-216412775 | Rare:10 | ||||
| chr2:216498753-216498898 | Common:4; Rare:65 | ||||
| chr2:218217076-218217246 | Common:1; Rare:60 | ||||
| chr2:218270104-218270559 | Common:5; Rare:141; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:218568301-218568598 | Common:2; Rare:82 | ||||
| chr2:218568804-218568942 | Common:1; Rare:43 | ||||
| chr2:218659600-218659755 | Rare:40 |