| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237966736-237967083 | Common:4; Rare:110 | ||||
| chr2:239401009-239401269 | Common:3; Rare:74 | ||||
| chr2:239401641-239401771 | Rare:66 | ||||
| chr2:240025297-240025455 | Rare:64; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:240136271-240136445 | Common:1; Rare:79 | ||||
| chr2:241102279-241102360 | Common:2; Rare:31 | ||||
| chr2:241149450-241149629 | Common:2; Rare:54 | ||||
| chr2:241272794-241272930 | Rare:56 | ||||
| chr2:241315150-241315296 | Common:1; Rare:53 | ||||
| chr2:241315655-241315981 | Common:5; Rare:128 | ||||
| chr2:241508539-241508872 | Common:2; Rare:104 | ||||
| chr2:241637506-241637717 | Common:1; Rare:117 | ||||
| chr20:325207-325576 | Rare:109 | ||||
| chr20:347048-347155 | Rare:31 | ||||
| chr20:380995-381278 | Common:6; Rare:79 |