| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:170928920-170929335 | Common:4; Rare:125 | ||||
| chr2:171160302-171160589 | Rare:104 | ||||
| chr2:171433917-171434277 | Common:3; Rare:94 | ||||
| chr2:171434692-171434721 | Rare:5 | ||||
| chr2:171434729-171434755 | Rare:6 | ||||
| chr2:171522291-171522525 | Common:3; Rare:54 | ||||
| chr2:171687928-171688008 | Common:1; Rare:16 | ||||
| chr2:171894210-171894393 | Rare:78; Clinvar:1 | ||||
| chr2:171999831-171999972 | Common:1; Rare:58 | ||||
| chr2:172427357-172427963 | Common:10; Rare:185; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:172556495-172556818 | Common:1; Rare:80 | ||||
| chr2:173964054-173964349 | Rare:131 | ||||
| chr2:173965281-173965509 | Common:1; Rare:80 | ||||
| chr2:174248456-174248744 | Common:1; Rare:87 | ||||
| chr2:174395618-174395887 | Common:2; Rare:86 |