| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45847217-45847487 | Common:2; Rare:108 | ||||
| chr11:46277342-46277709 | Rare:72 | ||||
| chr11:46381016-46381320 | Common:4; Rare:72 | ||||
| chr11:46594005-46594225 | Common:1; Rare:40 | ||||
| chr11:46617218-46617600 | Common:5; Rare:105 | ||||
| chr11:46700555-46700842 | Common:1; Rare:74 | ||||
| chr11:46846211-46846421 | Common:1; Rare:60 | ||||
| chr11:47176813-47177138 | Common:1; Rare:140 | ||||
| chr11:47214837-47215127 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47234208-47234470 | Common:2; Rare:49 | ||||
| chr11:47269514-47269723 | Common:1; Rare:71 | ||||
| chr11:47270012-47270184 | Common:1; Rare:59 | ||||
| chr11:47426390-47426642 | Common:1; Rare:66 | ||||
| chr11:47565493-47565640 | Common:3; Rare:28 | ||||
| chr11:47578959-47579097 | Rare:70; Clinvar:2; Clinvar (pathogenic):1 |