| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:65056160-65056473 | Common:2; Rare:109 | ||||
| chr2:65227591-65227863 | Rare:73 | ||||
| chr2:68062964-68063119 | Common:2; Rare:51 | ||||
| chr2:68157478-68157931 | Common:2; Rare:235 | ||||
| chr2:68467267-68467599 | Common:1; Rare:81 | ||||
| chr2:69387190-69387406 | Rare:60; Clinvar:2 | ||||
| chr2:69437418-69437581 | Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:69643643-69643826 | Rare:70 | ||||
| chr2:69829524-69829729 | Rare:84 | ||||
| chr2:69893813-69893998 | Rare:41 | ||||
| chr2:70086938-70087118 | Rare:88 | ||||
| chr2:70087427-70087723 | Rare:114 | ||||
| chr2:70248482-70248766 | Common:4; Rare:119 | ||||
| chr2:70257902-70258158 | Common:1; Rare:78 | ||||
| chr2:70293667-70293844 | Common:2; Rare:58 |