| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114648251-114648286 | Common:2; Rare:8 | ||||
| chr11:114650277-114650969 | Common:8; Rare:186 | ||||
| chr11:114651303-114651568 | Common:4; Rare:107 | ||||
| chr11:114651570-114651865 | Common:3; Rare:48 | ||||
| chr11:114668993-114669222 | Rare:43 | ||||
| chr11:117210888-117211138 | Common:2; Rare:53 | ||||
| chr11:117217214-117217368 | Common:2; Rare:29 | ||||
| chr11:117658938-117659068 | Common:1; Rare:21 | ||||
| chr11:118106782-118107057 | Common:4; Rare:44 | ||||
| chr11:118406821-118406993 | Common:2; Rare:51 | ||||
| chr11:118647766-118647929 | Rare:35 | ||||
| chr11:119007520-119007832 | Rare:57 | ||||
| chr11:119028286-119028522 | Common:3; Rare:59; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:119094708-119094834 | Common:1; Rare:38 | ||||
| chr11:119189235-119189521 | Common:1; Rare:57 |