| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086716-112086910 | Rare:82; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:112226314-112226438 | Rare:59 | ||||
| chr11:113314430-113314594 | Rare:59 | ||||
| chr11:113875497-113875775 | Common:4; Rare:103 | ||||
| chr11:114296314-114296556 | Rare:48 | ||||
| chr11:114400444-114400766 | Common:2; Rare:125 | ||||
| chr11:117144203-117144385 | Common:2; Rare:90 | ||||
| chr11:117199277-117199415 | Common:1; Rare:38 | ||||
| chr11:117232542-117232720 | Common:2; Rare:61 | ||||
| chr11:118401329-118401672 | Rare:114 | ||||
| chr11:118610173-118610440 | Rare:37 | ||||
| chr11:118790894-118791065 | Rare:38 | ||||
| chr11:118791102-118791264 | Rare:54 | ||||
| chr11:118997977-118998193 | Common:4; Rare:68 | ||||
| chr11:119018280-119018844 | Common:13; Rare:215 |