| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9423594-9423801 | Rare:60 | ||||
| chr2:9474498-9474642 | Common:6; Rare:70 | ||||
| chr2:9555630-9555977 | Common:2; Rare:115 | ||||
| chr2:9843250-9843539 | Common:6; Rare:86 | ||||
| chr2:10043318-10043658 | Common:4; Rare:138; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:10689910-10690029 | Common:2; Rare:40 | ||||
| chr2:11465810-11465981 | Rare:62 | ||||
| chr2:11746369-11746671 | Common:2; Rare:85; Clinvar:4 | ||||
| chr2:12716754-12717069 | Common:1; Rare:89 | ||||
| chr2:17753711-17753918 | Common:2; Rare:73 | ||||
| chr2:18560236-18560383 | Common:1; Rare:53 | ||||
| chr2:18560643-18560801 | Rare:46 | ||||
| chr2:19358476-19358683 | Common:1; Rare:55 | ||||
| chr2:19901937-19902037 | Common:1; Rare:31 | ||||
| chr2:19990046-19990229 | Rare:51 |