| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3575098-3575345 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:9423410-9423746 | Rare:104 | ||||
| chr2:9474498-9474642 | Common:6; Rare:70 | ||||
| chr2:9555621-9555925 | Common:2; Rare:99 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:9843397-9843541 | Common:5; Rare:41 | ||||
| chr2:10689910-10690004 | Common:2; Rare:33 | ||||
| chr2:10812697-10812984 | Common:3; Rare:112 | ||||
| chr2:11132771-11132830 | Rare:13 | ||||
| chr2:11466135-11466213 | Common:2; Rare:20 | ||||
| chr2:11746333-11746655 | Common:1; Rare:85; Clinvar:2 | ||||
| chr2:12716604-12717009 | Common:4; Rare:129 | ||||
| chr2:15561298-15561427 | Rare:51 | ||||
| chr2:15940343-15940564 | Rare:53 | ||||
| chr2:16665794-16665916 | Common:4; Rare:27 |