| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169799180-169799360 | Common:3; Rare:29 | ||||
| chr2:169799755-169799889 | Common:1; Rare:23 | ||||
| chr2:169824182-169824479 | Common:3; Rare:62 | ||||
| chr2:169824744-169825148 | Common:4; Rare:100 | ||||
| chr2:169827317-169827551 | Rare:69 | ||||
| chr2:169827896-169827952 | Rare:11 | ||||
| chr2:170715036-170715465 | Common:2; Rare:104 | ||||
| chr2:170715499-170715544 | Rare:21 | ||||
| chr2:170715717-170716029 | Common:1; Rare:78 | ||||
| chr2:170716131-170716249 | Common:1; Rare:35 | ||||
| chr2:170816749-170817040 | Common:2; Rare:58; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:170817370-170817499 | Rare:40 | ||||
| chr2:170928148-170928583 | Common:2; Rare:76 | ||||
| chr2:170928631-170928851 | Common:2; Rare:33 | ||||
| chr2:170928854-170929116 | Common:3; Rare:67 |