| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118401369-118401717 | Rare:121 | ||||
| chr11:118572290-118572471 | Common:3; Rare:62 | ||||
| chr11:118630906-118631334 | Common:2; Rare:75 | ||||
| chr11:118790894-118791316 | Rare:144 | ||||
| chr11:118997980-118998200 | Common:4; Rare:68 | ||||
| chr11:119018280-119018479 | Common:7; Rare:81 | ||||
| chr11:119018626-119018795 | Common:5; Rare:71 | ||||
| chr11:119057073-119057481 | Common:3; Rare:160 | ||||
| chr11:119067624-119067838 | Common:3; Rare:70 | ||||
| chr11:119084796-119084939 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr11:119121297-119121636 | Common:1; Rare:76 | ||||
| chr11:119195838-119196111 | Rare:60 | ||||
| chr11:119206180-119206403 | Common:5; Rare:98; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317097-119317247 | Rare:53 | ||||
| chr11:119334283-119334555 | Rare:73 |