| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108475594-108475838 | Common:2; Rare:67 | ||||
| chr2:108533890-108534003 | Common:1; Rare:35 | ||||
| chr2:108534114-108534583 | Common:8; Rare:176 | ||||
| chr2:108719377-108719566 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr2:109613823-109613996 | Common:1; Rare:60 | ||||
| chr2:109614153-109614397 | Common:2; Rare:82 | ||||
| chr2:110115689-110115914 | Common:2; Rare:63 | ||||
| chr2:110678021-110678235 | Rare:64 | ||||
| chr2:111883952-111884255 | Common:1; Rare:72 | ||||
| chr2:111898303-111898614 | Common:2; Rare:67 | ||||
| chr2:112055445-112055589 | Common:2; Rare:38 | ||||
| chr2:112275394-112275648 | Common:1; Rare:87 | ||||
| chr2:112542122-112542540 | Common:2; Rare:136 | ||||
| chr2:112584385-112584643 | Common:1; Rare:72 | ||||
| chr2:112645665-112645954 | Common:2; Rare:104 |