| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46380841-46381164 | Common:1; Rare:76 | ||||
| chr11:46593997-46594155 | Common:2; Rare:32 | ||||
| chr11:46617136-46617600 | Common:5; Rare:131 | ||||
| chr11:46700549-46700830 | Common:1; Rare:72 | ||||
| chr11:46700976-46701077 | Common:1; Rare:35 | ||||
| chr11:46846211-46846421 | Common:1; Rare:60 | ||||
| chr11:47168281-47168343 | Rare:16 | ||||
| chr11:47172375-47172401 | Rare:7 | ||||
| chr11:47176837-47177138 | Common:1; Rare:126 | ||||
| chr11:47185309-47185471 | Common:2; Rare:41 | ||||
| chr11:47186356-47186567 | Rare:58 | ||||
| chr11:47214328-47214485 | Common:1; Rare:17 | ||||
| chr11:47214784-47215125 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47245307-47245543 | Common:1; Rare:72; Clinvar (benign):1 | ||||
| chr11:47248769-47248955 | Rare:77 |