| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37925185-37925410 | Common:3; Rare:97 | ||||
| chr2:37925433-37925543 | Rare:45 | ||||
| chr2:38076085-38076301 | Rare:57 | ||||
| chr2:38602578-38603196 | Common:5; Rare:232 | ||||
| chr2:38751272-38751574 | Common:4; Rare:157 | ||||
| chr2:38875886-38876080 | Common:1; Rare:71 | ||||
| chr2:39120986-39121086 | Common:1; Rare:35 | ||||
| chr2:39437078-39437464 | Common:4; Rare:138 | ||||
| chr2:42169160-42169520 | Common:1; Rare:167 | ||||
| chr2:42792538-42792813 | Common:3; Rare:77 | ||||
| chr2:43226559-43226869 | Common:3; Rare:129 | ||||
| chr2:43595947-43596205 | Common:1; Rare:93 | ||||
| chr2:43995982-43996289 | Common:4; Rare:129; Clinvar (benign):1 | ||||
| chr2:44361437-44362018 | Common:4; Rare:193 | ||||
| chr2:46297216-46297493 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):1 |