| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28870262-28870437 | Rare:66 | ||||
| chr2:30146600-30147061 | Common:5; Rare:151 | ||||
| chr2:30447165-30447283 | Common:2; Rare:34 | ||||
| chr2:32039732-32039854 | Rare:36 | ||||
| chr2:32165732-32165898 | Common:1; Rare:63 | ||||
| chr2:32627952-32628119 | Rare:52 | ||||
| chr2:33134427-33134645 | Common:2; Rare:42 | ||||
| chr2:33599242-33599580 | Common:1; Rare:117 | ||||
| chr2:37084269-37084561 | Common:4; Rare:110 | ||||
| chr2:37231542-37231726 | Common:4; Rare:108; Clinvar (benign):4 | ||||
| chr2:37324731-37324950 | Common:1; Rare:93 | ||||
| chr2:37671501-37671782 | Common:2; Rare:113 | ||||
| chr2:38076138-38076301 | Rare:40 | ||||
| chr2:38751348-38751587 | Common:3; Rare:104 | ||||
| chr2:38875877-38876055 | Common:2; Rare:67 |