| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3519461-3519660 | Common:2; Rare:62 | ||||
| chr2:3558220-3558658 | Common:6; Rare:166 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423198-9423721 | Rare:150 | ||||
| chr2:9474433-9474630 | Common:7; Rare:73 | ||||
| chr2:9555664-9555966 | Common:2; Rare:101 | ||||
| chr2:9630944-9631346 | Common:3; Rare:128 | ||||
| chr2:9843250-9843539 | Common:6; Rare:86 | ||||
| chr2:10689934-10690004 | Common:2; Rare:22 | ||||
| chr2:10812678-10812986 | Common:3; Rare:117 | ||||
| chr2:11466126-11466206 | Common:1; Rare:25 | ||||
| chr2:11746389-11746671 | Common:2; Rare:80; Clinvar:4 | ||||
| chr2:12716604-12717005 | Common:4; Rare:128 | ||||
| chr2:17753699-17754168 | Common:4; Rare:146; Clinvar (benign):1 | ||||
| chr2:19358612-19358758 | Rare:32 |