| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:106194237-106194549 | Common:6; Rare:133 | ||||
| chr2:108534204-108534477 | Common:7; Rare:113 | ||||
| chr2:108621188-108621270 | Rare:7 | ||||
| chr2:108654818-108655037 | Rare:50 | ||||
| chr2:108719414-108719594 | Common:2; Rare:75; Clinvar (benign):2 | ||||
| chr2:109613811-109614008 | Common:2; Rare:69 | ||||
| chr2:111884165-111884255 | Rare:23 | ||||
| chr2:112275404-112275622 | Common:1; Rare:68 | ||||
| chr2:112584253-112584639 | Common:2; Rare:109 | ||||
| chr2:112645688-112645947 | Common:1; Rare:94 | ||||
| chr2:112764594-112764859 | Common:2; Rare:87; Clinvar (pathogenic):1 | ||||
| chr2:113117654-113118349 | Common:9; Rare:158; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:113437567-113437892 | Common:4; Rare:111 | ||||
| chr2:113627047-113627446 | Common:5; Rare:100 | ||||
| chr2:113756546-113756742 | Common:1; Rare:58 |