| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32627954-32628125 | Rare:55 | ||||
| chr2:33134339-33134655 | Common:3; Rare:67 | ||||
| chr2:33599202-33599442 | Common:1; Rare:90 | ||||
| chr2:37084275-37084566 | Common:3; Rare:111 | ||||
| chr2:37196416-37196669 | Common:3; Rare:85 | ||||
| chr2:37212382-37212468 | Rare:24 | ||||
| chr2:37231491-37231726 | Common:5; Rare:128; Clinvar (benign):4 | ||||
| chr2:37324698-37324911 | Common:1; Rare:82 | ||||
| chr2:37344574-37344756 | Common:1; Rare:68 | ||||
| chr2:37671614-37671745 | Common:1; Rare:63 | ||||
| chr2:38076143-38076288 | Rare:37 | ||||
| chr2:38602871-38603187 | Common:4; Rare:128 | ||||
| chr2:38751324-38751646 | Common:5; Rare:158 | ||||
| chr2:38875858-38876055 | Common:2; Rare:72 | ||||
| chr2:39121001-39121184 | Common:1; Rare:69 |