| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202377523-202378000 | Rare:280; Clinvar (pathogenic):1 | ||||
| chr2:202634537-202635100 | Common:17; Rare:377 | ||||
| chr2:202635816-202636110 | Common:10; Rare:153 | ||||
| chr2:202871456-202871777 | Common:3; Rare:161 | ||||
| chr2:202871920-202872390 | Rare:76 | ||||
| chr2:202911850-202912296 | Common:3; Rare:206 | ||||
| chr2:203014390-203014968 | Common:2; Rare:258 | ||||
| chr2:203238746-203239076 | Common:5; Rare:263 | ||||
| chr2:203239125-203239471 | Rare:267 | ||||
| chr2:203328134-203328614 | Common:6; Rare:359 | ||||
| chr2:203328690-203329250 | Common:5; Rare:269 | ||||
| chr2:203535060-203535664 | Common:11; Rare:512 | ||||
| chr2:203535735-203535861 | Common:1; Rare:28 | ||||
| chr2:204545144-204545754 | Common:6; Rare:301 | ||||
| chr2:204545988-204546380 | Rare:165 |