| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202265639-202265822 | Rare:71 | ||||
| chr2:202911606-202911999 | Common:1; Rare:83 | ||||
| chr2:202912119-202912293 | Common:2; Rare:59 | ||||
| chr2:203014655-203014925 | Common:1; Rare:82 | ||||
| chr2:203238779-203239030 | Common:1; Rare:89 | ||||
| chr2:203239226-203239307 | Rare:27 | ||||
| chr2:203328047-203328499 | Common:2; Rare:160 | ||||
| chr2:205682353-205682557 | Rare:36 | ||||
| chr2:206159346-206159989 | Common:4; Rare:187; Clinvar (benign):1 | ||||
| chr2:206274921-206275065 | Common:1; Rare:50 | ||||
| chr2:206765278-206765668 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529701-207530025 | Common:3; Rare:105 | ||||
| chr2:207625193-207625598 | Common:1; Rare:112 | ||||
| chr2:208025503-208025650 | Common:1; Rare:39 | ||||
| chr2:208255024-208255234 | Common:2; Rare:55 |