| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118790877-118791368 | Common:2; Rare:165 | ||||
| chr11:118791569-118791955 | Common:2; Rare:99 | ||||
| chr11:118883592-118883985 | Common:4; Rare:88 | ||||
| chr11:118924934-118925002 | Rare:10 | ||||
| chr11:118925892-118926544 | Common:9; Rare:137 | ||||
| chr11:118997919-118998237 | Common:4; Rare:112 | ||||
| chr11:119018250-119018599 | Common:8; Rare:134 | ||||
| chr11:119018616-119018875 | Common:5; Rare:98 | ||||
| chr11:119030429-119030507 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr11:119030709-119030979 | Common:3; Rare:73; Clinvar (benign):3 | ||||
| chr11:119056469-119056748 | Common:2; Rare:86 | ||||
| chr11:119057033-119057660 | Common:5; Rare:208 | ||||
| chr11:119067545-119067912 | Common:4; Rare:114 | ||||
| chr11:119084766-119085286 | Common:5; Rare:173; Clinvar (benign):5 | ||||
| chr11:119094914-119094999 | Rare:33 |