| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206085604-206085991 | Common:2; Rare:96 | ||||
| chr2:206085993-206086160 | Common:1; Rare:31 | ||||
| chr2:206086269-206086306 | Rare:4 | ||||
| chr2:206159342-206159924 | Common:4; Rare:156; Clinvar (benign):1 | ||||
| chr2:206765267-206765663 | Common:3; Rare:113; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165789-207166144 | Rare:71 | ||||
| chr2:207529698-207530128 | Common:3; Rare:123 | ||||
| chr2:207625212-207625602 | Common:1; Rare:107 | ||||
| chr2:208254399-208254467 | Rare:14 | ||||
| chr2:208255024-208255238 | Common:2; Rare:57 | ||||
| chr2:208266031-208266408 | Common:9; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:208359515-208359721 | Common:1; Rare:48 | ||||
| chr2:210477527-210477695 | Rare:50 | ||||
| chr2:213151591-213151889 | Rare:127 | ||||
| chr2:213284200-213284481 | Rare:90 |