| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:12718177-12718244 | Common:1; Rare:13 | ||||
| chr2:14632420-14632728 | Common:1; Rare:104 | ||||
| chr2:15561300-15561412 | Rare:46 | ||||
| chr2:15940346-15940743 | Common:2; Rare:99 | ||||
| chr2:17540476-17540839 | Common:2; Rare:79 | ||||
| chr2:17753721-17754168 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr2:18560693-18560801 | Rare:28 | ||||
| chr2:19901628-19902051 | Common:2; Rare:175 | ||||
| chr2:19990079-19990231 | Rare:40 | ||||
| chr2:20051545-20051831 | Common:1; Rare:77 | ||||
| chr2:20350605-20351050 | Common:1; Rare:152 | ||||
| chr2:20352212-20352385 | Common:2; Rare:36 | ||||
| chr2:20446849-20447075 | Common:3; Rare:92 | ||||
| chr2:20651061-20651224 | Rare:44 | ||||
| chr2:20823055-20823186 | Common:1; Rare:48 |