| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37925400-37925790 | Common:5; Rare:236 | ||||
| chr2:38376389-38377056 | Common:3; Rare:286 | ||||
| chr2:38377182-38377550 | Common:6; Rare:291 | ||||
| chr2:38602624-38603180 | Common:8; Rare:381 | ||||
| chr2:38665775-38666181 | Common:6; Rare:200 | ||||
| chr2:38681051-38681600 | Common:5; Rare:226 | ||||
| chr2:38751216-38751645 | Common:10; Rare:358 | ||||
| chr2:38875634-38876049 | Common:6; Rare:211 | ||||
| chr2:39120260-39120730 | Common:2; Rare:296; Clinvar:4; Clinvar (benign):16 | ||||
| chr2:39120631-39121456 | Common:7; Rare:423 | ||||
| chr2:39124167-39124620 | Common:2; Rare:277 | ||||
| chr2:39436830-39437040 | Common:4; Rare:90 | ||||
| chr2:39437051-39437486 | Common:8; Rare:297 | ||||
| chr2:39779184-39779359 | Common:4; Rare:66 | ||||
| chr2:42047734-42048084 | Common:8; Rare:205 |