| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28751696-28752134 | Common:2; Rare:186 | ||||
| chr2:28870238-28870429 | Rare:83 | ||||
| chr2:30447069-30447314 | Common:4; Rare:84 | ||||
| chr2:31234004-31234160 | Rare:40 | ||||
| chr2:32011006-32011119 | Rare:34 | ||||
| chr2:32039425-32039580 | Rare:44 | ||||
| chr2:32039693-32039913 | Rare:66 | ||||
| chr2:32165623-32165903 | Common:1; Rare:110 | ||||
| chr2:32277701-32277955 | Common:1; Rare:57 | ||||
| chr2:32627906-32628133 | Rare:64 | ||||
| chr2:33599210-33599469 | Common:1; Rare:97 | ||||
| chr2:37084276-37084550 | Common:3; Rare:101 | ||||
| chr2:37197053-37197253 | Rare:46 | ||||
| chr2:37231451-37231743 | Common:5; Rare:153; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37324828-37325144 | Common:1; Rare:87 |