| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207625176-207625615 | Common:1; Rare:121 | ||||
| chr2:207625691-207625761 | Rare:15 | ||||
| chr2:207625801-207626032 | Common:2; Rare:51 | ||||
| chr2:207711319-207711646 | Common:1; Rare:96 | ||||
| chr2:208025475-208025610 | Common:1; Rare:34 | ||||
| chr2:208253884-208254481 | Common:1; Rare:125 | ||||
| chr2:208254941-208255255 | Common:2; Rare:78 | ||||
| chr2:208265995-208266302 | Common:9; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423696-209424149 | Common:2; Rare:125 | ||||
| chr2:210002432-210002664 | Common:6; Rare:83 | ||||
| chr2:210476647-210476862 | Rare:68 | ||||
| chr2:210477527-210477728 | Rare:58 | ||||
| chr2:210556494-210556857 | Common:4; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:213284238-213284495 | Rare:84 | ||||
| chr2:215311853-215312145 | Common:8; Rare:111 |