| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164840548-164840756 | Common:1; Rare:39 | ||||
| chr2:164841137-164841364 | Rare:63 | ||||
| chr2:164841739-164841933 | Common:1; Rare:53 | ||||
| chr2:164842052-164842244 | Common:1; Rare:47 | ||||
| chr2:164955478-164955614 | Rare:29 | ||||
| chr2:165794052-165794344 | Common:2; Rare:72; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794680-165794795 | Common:1; Rare:17 | ||||
| chr2:168456172-168456463 | Rare:105 | ||||
| chr2:169584558-169584630 | Rare:14 | ||||
| chr2:169584744-169584816 | Rare:18 | ||||
| chr2:169694343-169694579 | Common:5; Rare:80 | ||||
| chr2:171160302-171160634 | Common:1; Rare:114 | ||||
| chr2:171433110-171433470 | Common:1; Rare:62 | ||||
| chr2:171433933-171434248 | Common:3; Rare:81 | ||||
| chr2:171434674-171434774 | Rare:28 |