| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93766526-93766591 | Rare:9 | ||||
| chr11:94512390-94512513 | Common:1; Rare:29 | ||||
| chr11:102398722-102399162 | Common:4; Rare:134 | ||||
| chr11:108147030-108147306 | Common:4; Rare:60; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:111778220-111778533 | Common:1; Rare:60 | ||||
| chr11:111794128-111794332 | Common:1; Rare:30 | ||||
| chr11:114058772-114058893 | Common:4; Rare:25 | ||||
| chr11:114061933-114062211 | Common:6; Rare:57 | ||||
| chr11:114153257-114153504 | Common:1; Rare:40 | ||||
| chr11:114171264-114171343 | Rare:15 | ||||
| chr11:114176341-114176350 | Rare:2 | ||||
| chr11:114302324-114302432 | Rare:15 | ||||
| chr11:114308518-114308726 | Common:1; Rare:26 | ||||
| chr11:116813986-116814217 | Common:3; Rare:39 | ||||
| chr11:116831477-116831641 | Common:2; Rare:24 |