| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117199017-117199411 | Common:6; Rare:126 | ||||
| chr11:117200008-117200197 | Common:4; Rare:41 | ||||
| chr11:117203004-117203484 | Common:5; Rare:164 | ||||
| chr11:117203558-117203882 | Common:2; Rare:89 | ||||
| chr11:117232025-117232177 | Rare:39 | ||||
| chr11:117232520-117232725 | Common:2; Rare:70 | ||||
| chr11:117314769-117315011 | Common:4; Rare:47 | ||||
| chr11:117876593-117876853 | Common:1; Rare:69 | ||||
| chr11:117986254-117986618 | Common:6; Rare:135; Clinvar:6; Clinvar (benign):2 | ||||
| chr11:117986776-117987101 | Common:1; Rare:68 | ||||
| chr11:117987103-117987140 | Rare:2 | ||||
| chr11:117987173-117987474 | Common:1; Rare:64 | ||||
| chr11:117989600-117989758 | Rare:36 | ||||
| chr11:117989760-117990180 | Common:1; Rare:63 | ||||
| chr11:118212880-118213054 | Common:1; Rare:33 |