| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:676957-677214 | Common:2; Rare:77 | ||||
| chr2:677341-677557 | Common:1; Rare:93 | ||||
| chr2:1262664-1262838 | Common:17; Rare:59 | ||||
| chr2:1676461-1676603 | Rare:28 | ||||
| chr2:1842818-1842986 | Common:6; Rare:75 | ||||
| chr2:3377774-3378016 | Common:1; Rare:73 | ||||
| chr2:3379594-3379814 | Common:2; Rare:87 | ||||
| chr2:3389526-3389731 | Rare:63 | ||||
| chr2:3448617-3448820 | Common:5; Rare:58 | ||||
| chr2:3459655-3459951 | Common:3; Rare:70 | ||||
| chr2:3519478-3519660 | Common:2; Rare:57 | ||||
| chr2:3558230-3558495 | Common:5; Rare:117 | ||||
| chr2:3575080-3575358 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:3594938-3595163 | Rare:81 | ||||
| chr2:3605237-3605681 | Common:8; Rare:74 |