| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210476686-210476845 | Rare:45 | ||||
| chr2:212538569-212538893 | Common:1; Rare:100 | ||||
| chr2:213284238-213284483 | Rare:79 | ||||
| chr2:215311910-215312114 | Common:6; Rare:86 | ||||
| chr2:216081771-216081939 | Common:1; Rare:59 | ||||
| chr2:216412272-216412512 | Common:1; Rare:53 | ||||
| chr2:216412709-216412775 | Rare:10 | ||||
| chr2:216498779-216498904 | Common:4; Rare:64 | ||||
| chr2:216694622-216694659 | Rare:11 | ||||
| chr2:218217057-218217212 | Common:1; Rare:54 | ||||
| chr2:218270082-218270532 | Common:5; Rare:141; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218292479-218292626 | Common:1; Rare:43 | ||||
| chr2:218568301-218568598 | Common:2; Rare:82 | ||||
| chr2:218659587-218659738 | Rare:34 | ||||
| chr2:218671967-218672300 | Common:2; Rare:84 |