| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162073986-162074025 | Rare:14 | ||||
| chr2:162074519-162074746 | Common:1; Rare:44 | ||||
| chr2:162318631-162318763 | Rare:24 | ||||
| chr2:165794117-165794197 | Rare:19; Clinvar:3 | ||||
| chr2:165794697-165794874 | Common:1; Rare:30 | ||||
| chr2:169584282-169584636 | Common:1; Rare:134 | ||||
| chr2:169584702-169584851 | Rare:43 | ||||
| chr2:169694333-169694571 | Common:5; Rare:83 | ||||
| chr2:169798647-169798968 | Rare:80 | ||||
| chr2:171433955-171434356 | Common:2; Rare:108 | ||||
| chr2:171434723-171434827 | Rare:28 | ||||
| chr2:171687401-171687828 | Common:1; Rare:92 | ||||
| chr2:171999837-171999981 | Common:1; Rare:59 | ||||
| chr2:172427325-172427705 | Common:9; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172487982-172488177 | Common:1; Rare:58; Clinvar:1 |