| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:17540443-17540739 | Common:1; Rare:70 | ||||
| chr2:17753671-17754159 | Common:4; Rare:153; Clinvar (benign):1 | ||||
| chr2:18560181-18560585 | Common:1; Rare:154 | ||||
| chr2:18560635-18560819 | Rare:55 | ||||
| chr2:19901642-19901726 | Rare:41 | ||||
| chr2:19901901-19902037 | Common:1; Rare:38 | ||||
| chr2:19990079-19990211 | Rare:34 | ||||
| chr2:20051469-20051832 | Common:1; Rare:110 | ||||
| chr2:20350828-20351039 | Common:1; Rare:88 | ||||
| chr2:20446851-20447081 | Common:3; Rare:94 | ||||
| chr2:20651054-20651242 | Rare:55 | ||||
| chr2:20823055-20823186 | Common:1; Rare:48 | ||||
| chr2:21123835-21124006 | Common:1; Rare:56 | ||||
| chr2:23927067-23927325 | Common:3; Rare:90 | ||||
| chr2:23940363-23940545 | Common:3; Rare:65 |