| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:16665796-16666009 | Common:4; Rare:42 | ||||
| chr2:17518394-17518655 | Common:3; Rare:81 | ||||
| chr2:17538820-17539200 | Common:4; Rare:111 | ||||
| chr2:17540410-17540790 | Common:2; Rare:88 | ||||
| chr2:17753610-17754220 | Common:6; Rare:186; Clinvar (benign):1 | ||||
| chr2:17800237-17800560 | Common:6; Rare:58 | ||||
| chr2:18560028-18560285 | Common:1; Rare:74 | ||||
| chr2:18560381-18560873 | Rare:191 | ||||
| chr2:19358548-19358698 | Rare:50 | ||||
| chr2:19901586-19901814 | Common:2; Rare:113 | ||||
| chr2:19901933-19902241 | Common:4; Rare:91 | ||||
| chr2:19990045-19990267 | Rare:66 | ||||
| chr2:20012653-20012807 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr2:20051571-20051896 | Common:1; Rare:85 | ||||
| chr2:20052038-20052236 | Common:1; Rare:45 |