| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116830417-116830891 | Common:4; Rare:164; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:116837128-116837248 | Rare:30 | ||||
| chr11:116837510-116837884 | Common:3; Rare:65 | ||||
| chr11:117178998-117179338 | Common:1; Rare:104 | ||||
| chr11:117182587-117182767 | Common:1; Rare:65 | ||||
| chr11:117187378-117187696 | Rare:94 | ||||
| chr11:117199088-117199403 | Common:5; Rare:97 | ||||
| chr11:117200993-117201127 | Common:1; Rare:33 | ||||
| chr11:117203097-117203360 | Common:4; Rare:91 | ||||
| chr11:117232025-117232177 | Rare:39 | ||||
| chr11:117232483-117232758 | Common:2; Rare:88 | ||||
| chr11:117316257-117316405 | Common:1; Rare:31 | ||||
| chr11:117986290-117986445 | Common:3; Rare:59; Clinvar:2 | ||||
| chr11:118076816-118077128 | Common:4; Rare:76 | ||||
| chr11:118264284-118264591 | Common:1; Rare:50 |