| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37231559-37231722 | Common:4; Rare:93; Clinvar (benign):3 | ||||
| chr2:37324713-37324950 | Common:1; Rare:96 | ||||
| chr2:37344675-37344745 | Common:1; Rare:29 | ||||
| chr2:37925254-37925402 | Common:3; Rare:63 | ||||
| chr2:38076147-38076291 | Rare:38 | ||||
| chr2:38602867-38603187 | Common:4; Rare:129 | ||||
| chr2:38875886-38876064 | Common:1; Rare:65 | ||||
| chr2:39437078-39437469 | Common:4; Rare:141 | ||||
| chr2:42169168-42169468 | Common:1; Rare:143 | ||||
| chr2:42792530-42792766 | Common:2; Rare:69 | ||||
| chr2:43226545-43226865 | Common:3; Rare:135 | ||||
| chr2:43595941-43596191 | Common:1; Rare:86 | ||||
| chr2:43838265-43838408 | Rare:28 | ||||
| chr2:43838728-43839015 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:43839173-43839321 | Rare:30 |