| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32277723-32277999 | Common:2; Rare:66 | ||||
| chr2:32627996-32628177 | Rare:62 | ||||
| chr2:33476547-33476691 | Common:2; Rare:24 | ||||
| chr2:33599210-33599432 | Common:1; Rare:86 | ||||
| chr2:37084269-37084563 | Common:4; Rare:111 | ||||
| chr2:37212382-37212628 | Rare:55 | ||||
| chr2:37231421-37231722 | Common:5; Rare:153; Clinvar (benign):3 | ||||
| chr2:37324713-37324929 | Common:1; Rare:85 | ||||
| chr2:37671482-37671791 | Common:3; Rare:114 | ||||
| chr2:37925433-37925538 | Rare:42 | ||||
| chr2:38076138-38076282 | Rare:35 | ||||
| chr2:38602895-38603196 | Common:4; Rare:117 | ||||
| chr2:38666100-38666146 | Rare:21 | ||||
| chr2:38751313-38751616 | Common:4; Rare:153 | ||||
| chr2:38875897-38876059 | Common:1; Rare:57 |