| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:57853419-57853446 | Rare:7 | ||||
| chr19:58088749-58088930 | Rare:45 | ||||
| chr19:58349549-58349717 | Common:3; Rare:33 | ||||
| chr2:271588-271915 | Common:3; Rare:63 | ||||
| chr2:10301319-10301394 | Rare:10 | ||||
| chr2:10365432-10365676 | Rare:51 | ||||
| chr2:10426704-10426731 | Rare:8 | ||||
| chr2:11374750-11374753 | |||||
| chr2:20447687-20448040 | Rare:107 | ||||
| chr2:20448114-20448216 | Rare:27 | ||||
| chr2:20448362-20448625 | Common:1; Rare:71 | ||||
| chr2:21029639-21030024 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):10 | ||||
| chr2:24077730-24077961 | Common:1; Rare:38 | ||||
| chr2:26191740-26191743 | |||||
| chr2:26221029-26221144 | Common:1; Rare:17 |