| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74370466-74370845 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:74377430-74377674 | Common:1; Rare:62 | ||||
| chr2:74425388-74425729 | Common:1; Rare:104 | ||||
| chr2:74428542-74428737 | Rare:52 | ||||
| chr2:78701620-78701759 | Common:2; Rare:56 | ||||
| chr2:84431634-84431862 | Rare:42 | ||||
| chr2:85317440-85317531 | Common:3; Rare:16 | ||||
| chr2:85340521-85340721 | Common:2; Rare:32 | ||||
| chr2:85394478-85394778 | Rare:46 | ||||
| chr2:85540635-85540870 | Common:4; Rare:67 | ||||
| chr2:86045285-86045583 | Common:3; Rare:57 | ||||
| chr2:86172831-86172996 | Common:4; Rare:23 | ||||
| chr2:87521271-87521466 | Common:1; Rare:39 | ||||
| chr2:87824888-87825126 | Rare:40 | ||||
| chr2:87825266-87825326 | Common:1; Rare:13 |