| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:68157419-68158001 | Common:3; Rare:293 | ||||
| chr2:68158253-68158320 | Rare:9 | ||||
| chr2:68251171-68251624 | Common:2; Rare:124 | ||||
| chr2:68252398-68252992 | Common:4; Rare:194 | ||||
| chr2:68253027-68253105 | Common:1; Rare:33 | ||||
| chr2:68365112-68365396 | Common:2; Rare:52 | ||||
| chr2:68365463-68365528 | Rare:11 | ||||
| chr2:68387714-68387918 | Common:3; Rare:42 | ||||
| chr2:68467167-68467725 | Common:2; Rare:150 | ||||
| chr2:68467818-68467909 | Common:1; Rare:24 | ||||
| chr2:68734727-68734838 | Common:2; Rare:22 | ||||
| chr2:68774736-68774910 | Common:1; Rare:32 | ||||
| chr2:69387125-69387546 | Common:2; Rare:118; Clinvar:2 | ||||
| chr2:69436841-69437213 | Common:1; Rare:92 | ||||
| chr2:69437281-69437728 | Common:2; Rare:203; Clinvar:7; Clinvar (benign):6 |