| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118572290-118572471 | Common:3; Rare:62 | ||||
| chr11:118790904-118791255 | Rare:100 | ||||
| chr11:118997994-118998155 | Common:4; Rare:41 | ||||
| chr11:119018292-119018462 | Common:6; Rare:69 | ||||
| chr11:119018626-119018795 | Common:5; Rare:71 | ||||
| chr11:119057074-119057438 | Common:3; Rare:141 | ||||
| chr11:119067630-119067821 | Common:3; Rare:65 | ||||
| chr11:119084808-119084921 | Rare:35 | ||||
| chr11:119334303-119334555 | Rare:69 | ||||
| chr11:124673715-124673929 | Common:4; Rare:65 | ||||
| chr11:124953989-124954213 | Common:4; Rare:60 | ||||
| chr11:125592520-125592918 | Common:6; Rare:130 | ||||
| chr11:125625809-125625993 | Common:3; Rare:71 | ||||
| chr11:125887513-125887731 | Common:2; Rare:62 | ||||
| chr11:126268802-126269207 | Common:2; Rare:159; Clinvar:2; Clinvar (benign):4 |