| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119018280-119018511 | Common:7; Rare:96 | ||||
| chr11:119018626-119018808 | Common:5; Rare:75 | ||||
| chr11:119057068-119057446 | Common:3; Rare:147 | ||||
| chr11:119067615-119067816 | Common:3; Rare:62 | ||||
| chr11:119317124-119317246 | Rare:44 | ||||
| chr11:121292615-121292916 | Rare:92; Clinvar:3 | ||||
| chr11:123062109-123062339 | Rare:91 | ||||
| chr11:123062440-123062663 | Common:2; Rare:102 | ||||
| chr11:123741609-123741799 | Common:2; Rare:57 | ||||
| chr11:124673716-124673929 | Common:4; Rare:64 | ||||
| chr11:125625871-125626003 | Rare:44 | ||||
| chr11:125887387-125887727 | Common:3; Rare:106 | ||||
| chr11:126211634-126211809 | Rare:79 | ||||
| chr11:126268814-126269198 | Common:1; Rare:148; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126303961-126304081 | Rare:67 |