| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105037884-105038117 | Common:3; Rare:84 | ||||
| chr2:105337448-105337606 | Common:2; Rare:78 | ||||
| chr2:106194237-106194554 | Common:6; Rare:135 | ||||
| chr2:108449108-108449277 | Rare:68 | ||||
| chr2:108533900-108533970 | Rare:24 | ||||
| chr2:108534164-108534529 | Common:8; Rare:148 | ||||
| chr2:108588130-108588472 | Common:2; Rare:59 | ||||
| chr2:108654702-108655055 | Rare:69 | ||||
| chr2:108719404-108719625 | Common:2; Rare:90; Clinvar (benign):2 | ||||
| chr2:108719813-108719993 | Common:1; Rare:61 | ||||
| chr2:109613798-109613997 | Common:2; Rare:69 | ||||
| chr2:110115796-110115930 | Common:2; Rare:34 | ||||
| chr2:110204913-110205125 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:111122436-111122723 | Common:3; Rare:123 | ||||
| chr2:111884170-111884255 | Rare:19 |