| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:29115358-29115658 | Common:1; Rare:79 | ||||
| chr2:30146595-30147023 | Common:5; Rare:135 | ||||
| chr2:30447191-30447314 | Rare:34 | ||||
| chr2:31233956-31234000 | Rare:12 | ||||
| chr2:32010962-32011106 | Rare:42 | ||||
| chr2:32039732-32039851 | Rare:35 | ||||
| chr2:32165745-32165893 | Common:1; Rare:51 | ||||
| chr2:32627948-32628139 | Rare:62 | ||||
| chr2:33476634-33476688 | Rare:10 | ||||
| chr2:33599217-33599434 | Common:1; Rare:84 | ||||
| chr2:37084272-37084561 | Common:3; Rare:108 | ||||
| chr2:37231533-37231719 | Common:4; Rare:107; Clinvar (benign):3 | ||||
| chr2:37671437-37671736 | Common:1; Rare:105 | ||||
| chr2:37672164-37672213 | Common:2; Rare:19 | ||||
| chr2:37672519-37672627 | Common:3; Rare:35 |