| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161308328-161308597 | Common:2; Rare:67 | ||||
| chr2:162343862-162344227 | Common:1; Rare:124 | ||||
| chr2:162838493-162839163 | Common:1; Rare:149 | ||||
| chr2:163735982-163736113 | Rare:24 | ||||
| chr2:163736131-163736568 | Common:4; Rare:150 | ||||
| chr2:165469532-165469711 | Rare:30 | ||||
| chr2:165574135-165574337 | Rare:44 | ||||
| chr2:165953704-165954109 | Common:3; Rare:143; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:165954189-165954275 | Common:1; Rare:20 | ||||
| chr2:166375819-166376306 | Common:5; Rare:122; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168456651-168456826 | Rare:55 | ||||
| chr2:168890341-168890590 | Common:2; Rare:62 | ||||
| chr2:169479348-169479565 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584764-169584809 | Rare:14 |