| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118252111-118252211 | Rare:45 | ||||
| chr11:118252254-118252389 | Rare:48 | ||||
| chr11:118344264-118344444 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:118359386-118359667 | Common:3; Rare:110 | ||||
| chr11:118401329-118401704 | Rare:127 | ||||
| chr11:118572300-118572482 | Common:3; Rare:66 | ||||
| chr11:118610278-118610424 | Rare:17 | ||||
| chr11:118790894-118791324 | Common:1; Rare:146 | ||||
| chr11:118883808-118883983 | Common:1; Rare:48 | ||||
| chr11:118997973-118998211 | Common:4; Rare:75 | ||||
| chr11:119018280-119018462 | Common:6; Rare:75 | ||||
| chr11:119018620-119018808 | Common:5; Rare:76 | ||||
| chr11:119057074-119057481 | Common:3; Rare:159 | ||||
| chr11:119067624-119067840 | Common:3; Rare:71 | ||||
| chr11:119084801-119084963 | Rare:49 |