| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77820950-77821152 | Common:1; Rare:57 | ||||
| chr11:88337714-88337843 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:94973552-94973843 | Rare:72 | ||||
| chr11:108222636-108222933 | Rare:87; Clinvar:2 | ||||
| chr11:111913145-111913300 | Rare:44 | ||||
| chr11:112086730-112086893 | Rare:65 | ||||
| chr11:114296266-114296566 | Rare:56 | ||||
| chr11:117200008-117200211 | Common:5; Rare:42 | ||||
| chr11:118790900-118791248 | Rare:99 | ||||
| chr11:119018383-119018792 | Common:9; Rare:147 | ||||
| chr11:124673731-124673935 | Common:4; Rare:54 | ||||
| chr11:125887522-125887730 | Common:2; Rare:60 | ||||
| chr11:126211644-126211806 | Rare:75 | ||||
| chr11:126268818-126269171 | Common:1; Rare:130; Clinvar:1 | ||||
| chr11:134253336-134253568 | Common:2; Rare:69; Clinvar (benign):1 |