| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62841797-62842082 | Common:6; Rare:121 | ||||
| chr11:62855874-62856161 | Rare:109 | ||||
| chr11:62881489-62881815 | Common:4; Rare:72 | ||||
| chr11:63681367-63681697 | Common:2; Rare:133 | ||||
| chr11:64226098-64226338 | Common:3; Rare:68 | ||||
| chr11:64240891-64241180 | Rare:79 | ||||
| chr11:64241311-64241703 | Rare:90 | ||||
| chr11:64247428-64247591 | Common:1; Rare:41 | ||||
| chr11:64284560-64284800 | Rare:98 | ||||
| chr11:64317458-64317668 | Common:3; Rare:75 | ||||
| chr11:64318047-64318368 | Common:1; Rare:143 | ||||
| chr11:64359063-64359171 | Rare:25 | ||||
| chr11:64643319-64643407 | Common:1; Rare:12 | ||||
| chr11:64643500-64643792 | Common:2; Rare:66 | ||||
| chr11:64810495-64810750 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 |