| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:168890331-168890565 | Common:2; Rare:60 | ||||
| chr2:169362466-169362758 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169479354-169479788 | Common:5; Rare:150; Clinvar (benign):2 | ||||
| chr2:169573758-169574022 | Common:2; Rare:75 | ||||
| chr2:169584237-169584652 | Common:1; Rare:149 | ||||
| chr2:169584713-169584838 | Rare:37 | ||||
| chr2:169585026-169585113 | Common:1; Rare:14 | ||||
| chr2:169694294-169694638 | Common:7; Rare:123 | ||||
| chr2:169694677-169694836 | Common:2; Rare:53 | ||||
| chr2:169733524-169733693 | Common:2; Rare:35 | ||||
| chr2:169733770-169734012 | Common:2; Rare:69 | ||||
| chr2:169734186-169734310 | Rare:30 | ||||
| chr2:169734313-169734477 | Common:1; Rare:53 | ||||
| chr2:169798711-169799016 | Common:1; Rare:80 | ||||
| chr2:169799018-169799139 | Common:1; Rare:37 |