| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124673710-124673936 | Common:4; Rare:68 | ||||
| chr11:124800415-124800466 | Rare:20 | ||||
| chr11:124935937-124936081 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:124936113-124936142 | Rare:5 | ||||
| chr11:124936298-124936517 | Rare:35 | ||||
| chr11:124953989-124954203 | Common:4; Rare:59 | ||||
| chr11:125164544-125164762 | Rare:40 | ||||
| chr11:125481534-125481742 | Common:1; Rare:37 | ||||
| chr11:125495388-125495595 | Common:4; Rare:73 | ||||
| chr11:125496019-125496123 | Common:2; Rare:16 | ||||
| chr11:125496130-125496355 | Rare:58 | ||||
| chr11:125592506-125592930 | Common:6; Rare:137 | ||||
| chr11:125625871-125626012 | Rare:47 | ||||
| chr11:125887480-125887727 | Common:2; Rare:78 | ||||
| chr11:125903188-125903273 | Rare:22 |