| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:824339-824672 | Common:2; Rare:135; Clinvar:5; Clinvar (benign):4 | ||||
| chr11:1231929-1232023 | Rare:28 | ||||
| chr11:2336028-2336130 | Rare:20 | ||||
| chr11:2377990-2378074 | Common:2; Rare:26 | ||||
| chr11:2699991-2700214 | Common:1; Rare:84 | ||||
| chr11:3477000-3477170 | Common:2; Rare:52 | ||||
| chr11:3512011-3512260 | Common:2; Rare:53 | ||||
| chr11:5666033-5666332 | Common:1; Rare:77 | ||||
| chr11:6488657-6488803 | Rare:33 | ||||
| chr11:6605862-6605992 | Common:2; Rare:29 | ||||
| chr11:7698173-7698275 | Rare:15 | ||||
| chr11:7905908-7906061 | Common:2; Rare:36 | ||||
| chr11:8696567-8696800 | Rare:60 | ||||
| chr11:9747663-9747909 | Common:1; Rare:45 | ||||
| chr11:9758160-9758336 | Rare:50 |