| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32165745-32165901 | Common:1; Rare:59 | ||||
| chr2:32627931-32628035 | Rare:32 | ||||
| chr2:32628037-32628119 | Rare:25 | ||||
| chr2:33599210-33599445 | Common:1; Rare:89 | ||||
| chr2:37084269-37084561 | Common:4; Rare:110 | ||||
| chr2:37231537-37231722 | Common:4; Rare:107; Clinvar (benign):3 | ||||
| chr2:37344666-37344731 | Common:1; Rare:25 | ||||
| chr2:38075550-38075653 | Common:1; Rare:26 | ||||
| chr2:38076102-38076245 | Rare:31 | ||||
| chr2:38751320-38751592 | Common:4; Rare:131 | ||||
| chr2:38875886-38876082 | Common:1; Rare:72 | ||||
| chr2:39437271-39437453 | Common:2; Rare:63 | ||||
| chr2:40512472-40512727 | Common:3; Rare:46 | ||||
| chr2:42169151-42169492 | Common:1; Rare:159 | ||||
| chr2:42792520-42792757 | Common:2; Rare:72 |