| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855555-3855677 | Common:2; Rare:27 | ||||
| chr11:4094588-4094877 | Common:2; Rare:79 | ||||
| chr11:4393641-4393787 | Common:1; Rare:35 | ||||
| chr11:5624893-5625029 | Rare:22 | ||||
| chr11:5689689-5689886 | Common:1; Rare:43 | ||||
| chr11:6319751-6319877 | Rare:27 | ||||
| chr11:6320481-6320578 | Common:2; Rare:32 | ||||
| chr11:6390249-6390502 | Common:2; Rare:73 | ||||
| chr11:6481292-6481562 | Common:5; Rare:125 | ||||
| chr11:6603542-6603869 | Common:4; Rare:95; Clinvar (benign):3 | ||||
| chr11:8682644-8682820 | Common:2; Rare:77 | ||||
| chr11:8964348-8964518 | Common:4; Rare:65 | ||||
| chr11:8964932-8965044 | Common:2; Rare:26 | ||||
| chr11:9384572-9384702 | Common:1; Rare:53 | ||||
| chr11:9460627-9461048 | Common:4; Rare:109 |