| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:205682356-205682597 | Rare:42 | ||||
| chr2:206085771-206085981 | Common:1; Rare:60 | ||||
| chr2:206086141-206086283 | Rare:15 | ||||
| chr2:206159345-206159989 | Common:4; Rare:188; Clinvar (benign):1 | ||||
| chr2:206274520-206274774 | Common:1; Rare:75 | ||||
| chr2:206274857-206274878 | Rare:4 | ||||
| chr2:206274906-206275073 | Common:1; Rare:56 | ||||
| chr2:206765276-206765670 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):5 | ||||
| chr2:207166184-207166387 | Common:3; Rare:89 | ||||
| chr2:207166822-207167102 | Common:4; Rare:114 | ||||
| chr2:207529768-207530119 | Common:3; Rare:95 | ||||
| chr2:207624957-207625150 | Common:1; Rare:47 | ||||
| chr2:207625221-207625521 | Common:1; Rare:83 | ||||
| chr2:207625926-207626105 | Common:2; Rare:44 | ||||
| chr2:208025466-208025624 | Common:1; Rare:41 |