| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:160284775-160285026 | Rare:67 | ||||
| chr2:160407516-160407785 | Rare:76 | ||||
| chr2:160493334-160493599 | Common:1; Rare:85 | ||||
| chr2:160493798-160494044 | Common:1; Rare:58 | ||||
| chr2:161160861-161161131 | Common:1; Rare:58 | ||||
| chr2:161308388-161308590 | Common:2; Rare:47 | ||||
| chr2:162074007-162074244 | Common:1; Rare:59 | ||||
| chr2:162183120-162183453 | Common:1; Rare:69 | ||||
| chr2:162195028-162195288 | Common:2; Rare:54 | ||||
| chr2:162318650-162318794 | Rare:29 | ||||
| chr2:163735985-163736022 | Rare:6 | ||||
| chr2:164955523-164955647 | Rare:33 | ||||
| chr2:165953694-165954088 | Common:3; Rare:146; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:166375697-166375723 | Rare:5 | ||||
| chr2:166375891-166376094 | Common:4; Rare:61; Clinvar:1; Clinvar (benign):5 |