| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:168248046-168248225 | Rare:30 | ||||
| chr2:168455520-168455920 | Common:15; Rare:135 | ||||
| chr2:168456062-168456454 | Common:1; Rare:333 | ||||
| chr2:168456444-168456860 | Common:1; Rare:204 | ||||
| chr2:168890338-168890441 | Common:1; Rare:30 | ||||
| chr2:169479348-169479582 | Common:9; Rare:221; Clinvar (benign):3 | ||||
| chr2:169479610-169479830 | Common:2; Rare:121 | ||||
| chr2:169584290-169584632 | Common:1; Rare:206 | ||||
| chr2:169584558-169584843 | Rare:159 | ||||
| chr2:169584884-169585293 | Common:8; Rare:149 | ||||
| chr2:169694295-169694660 | Common:17; Rare:302 | ||||
| chr2:169733707-169734055 | Common:2; Rare:96 | ||||
| chr2:169734190-169734630 | Common:2; Rare:122 | ||||
| chr2:169798713-169799086 | Common:1; Rare:218 | ||||
| chr2:169824797-169825098 | Common:4; Rare:87 |