| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:677382-677552 | Rare:69 | ||||
| chr2:3519495-3519660 | Common:2; Rare:46 | ||||
| chr2:3558251-3558715 | Common:6; Rare:168 | ||||
| chr2:3575107-3575373 | Common:2; Rare:82; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423491-9423709 | Rare:70 | ||||
| chr2:9555730-9555992 | Common:2; Rare:86 | ||||
| chr2:15940331-15940557 | Rare:56 | ||||
| chr2:17540458-17540802 | Common:2; Rare:73 | ||||
| chr2:17753731-17754135 | Common:3; Rare:129 | ||||
| chr2:19901652-19901798 | Common:1; Rare:81 | ||||
| chr2:19990046-19990209 | Rare:45 | ||||
| chr2:20350831-20351039 | Common:1; Rare:87 | ||||
| chr2:20651070-20651242 | Rare:50 | ||||
| chr2:20823064-20823159 | Rare:36 | ||||
| chr2:23940385-23940514 | Common:3; Rare:48 |