| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190319740-190319960 | Common:5; Rare:79; Clinvar (benign):5 | ||||
| chr2:190344001-190344020 | Rare:3 | ||||
| chr2:190534350-190534877 | Common:9; Rare:161 | ||||
| chr2:190648697-190648902 | Common:1; Rare:78 | ||||
| chr2:190880644-190880897 | Common:4; Rare:88 | ||||
| chr2:191014133-191014357 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245251-191245599 | Common:2; Rare:110 | ||||
| chr2:191677840-191678147 | Common:4; Rare:87 | ||||
| chr2:191678560-191678841 | Common:1; Rare:104 | ||||
| chr2:191847066-191847365 | Rare:51 | ||||
| chr2:192194913-192195053 | Rare:26 | ||||
| chr2:195656837-195657267 | Common:2; Rare:121 | ||||
| chr2:196171508-196171883 | Common:1; Rare:120 | ||||
| chr2:196639473-196639660 | Rare:46 | ||||
| chr2:197434981-197435198 | Rare:71 |