| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855551-3855766 | Common:2; Rare:45 | ||||
| chr11:3855872-3856352 | Common:1; Rare:124; Clinvar:1 | ||||
| chr11:4094558-4094712 | Common:1; Rare:42 | ||||
| chr11:4094735-4094909 | Common:1; Rare:52 | ||||
| chr11:4393651-4393814 | Rare:41 | ||||
| chr11:4608125-4608380 | Common:1; Rare:78 | ||||
| chr11:4643805-4644001 | Common:3; Rare:31 | ||||
| chr11:5226924-5227213 | Common:2; Rare:107; Clinvar:32; Clinvar (benign):4; Clinvar (pathogenic):38 | ||||
| chr11:5596604-5596736 | Common:3; Rare:48 | ||||
| chr11:5624882-5625040 | Rare:28 | ||||
| chr11:5689672-5689891 | Common:1; Rare:46 | ||||
| chr11:6234592-6234871 | Common:2; Rare:90 | ||||
| chr11:6320160-6320246 | Common:1; Rare:32 | ||||
| chr11:6390313-6390616 | Common:2; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:6419382-6419439 | Rare:19 |