| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:102736821-102736974 | Common:1; Rare:74 | ||||
| chr2:105037884-105038169 | Common:4; Rare:104 | ||||
| chr2:105337213-105337606 | Common:5; Rare:139 | ||||
| chr2:106194206-106194554 | Common:6; Rare:150 | ||||
| chr2:108449086-108449277 | Rare:81 | ||||
| chr2:108533900-108533970 | Rare:24 | ||||
| chr2:108534190-108534534 | Common:8; Rare:138 | ||||
| chr2:108719345-108719598 | Common:3; Rare:116; Clinvar (benign):2 | ||||
| chr2:108786571-108786841 | Common:6; Rare:128 | ||||
| chr2:109613578-109614067 | Common:5; Rare:156 | ||||
| chr2:109614155-109614370 | Common:2; Rare:73 | ||||
| chr2:110115701-110115923 | Common:2; Rare:63 | ||||
| chr2:110115933-110116060 | Common:2; Rare:24 | ||||
| chr2:110204941-110205064 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:110677997-110678212 | Rare:68 |