| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:54115446-54115481 | Rare:10 | ||||
| chr2:54115510-54115689 | Rare:64 | ||||
| chr2:54115876-54115977 | Common:2; Rare:41 | ||||
| chr2:54557899-54557930 | Rare:7 | ||||
| chr2:54558152-54558446 | Common:2; Rare:94 | ||||
| chr2:54723337-54723681 | Common:2; Rare:111 | ||||
| chr2:55050495-55050784 | Common:3; Rare:88 | ||||
| chr2:55232249-55232872 | Common:5; Rare:198 | ||||
| chr2:55269176-55269310 | Common:2; Rare:37 | ||||
| chr2:55419834-55420205 | Common:6; Rare:144 | ||||
| chr2:55519404-55519731 | Common:1; Rare:93 | ||||
| chr2:55618847-55619139 | Common:1; Rare:67 | ||||
| chr2:55693821-55693947 | Rare:45; Clinvar (benign):2 | ||||
| chr2:58046622-58046644 | Rare:6 | ||||
| chr2:58046664-58046875 | Common:2; Rare:67 |