| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202912474-202912554 | Common:2; Rare:26 | ||||
| chr2:203014676-203014945 | Common:1; Rare:81 | ||||
| chr2:203238779-203239050 | Common:2; Rare:97 | ||||
| chr2:203239220-203239298 | Rare:26 | ||||
| chr2:205682356-205682594 | Rare:41 | ||||
| chr2:205682810-205683112 | Common:2; Rare:43 | ||||
| chr2:206085824-206085981 | Common:1; Rare:43 | ||||
| chr2:206086085-206086303 | Rare:28 | ||||
| chr2:206159346-206159989 | Common:4; Rare:187; Clinvar (benign):1 | ||||
| chr2:206274876-206275057 | Common:1; Rare:62 | ||||
| chr2:206765276-206765654 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165763-207165783 | Rare:4 | ||||
| chr2:207165928-207166094 | Rare:30 | ||||
| chr2:207167223-207167280 | Common:2; Rare:17 | ||||
| chr2:207529593-207530110 | Common:3; Rare:138 |