| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108507406-108507513 | Common:1; Rare:24 | ||||
| chr2:108586629-108586866 | Common:1; Rare:40 | ||||
| chr2:108593676-108594079 | Rare:72 | ||||
| chr2:108594237-108594448 | Common:1; Rare:40 | ||||
| chr2:108595057-108595396 | Rare:66 | ||||
| chr2:108637447-108637472 | |||||
| chr2:108637538-108637851 | Common:2; Rare:51 | ||||
| chr2:108661304-108661351 | Common:1; Rare:9 | ||||
| chr2:108661631-108661885 | Common:4; Rare:50 | ||||
| chr2:108667652-108667982 | Common:1; Rare:62 | ||||
| chr2:108683050-108683120 | Rare:10 | ||||
| chr2:108683497-108683527 | Rare:2 | ||||
| chr2:108782095-108782812 | Rare:180; Clinvar:2 | ||||
| chr2:108782826-108783110 | Rare:56; Clinvar (benign):3 | ||||
| chr2:108783169-108783653 | Common:2; Rare:100; Clinvar (benign):1 |