| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:88337695-88337882 | Common:3; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:93741481-93741683 | Common:5; Rare:75 | ||||
| chr11:95089733-95089901 | Common:3; Rare:70 | ||||
| chr11:95924075-95924135 | Rare:22 | ||||
| chr11:96389863-96390043 | Common:1; Rare:72 | ||||
| chr11:106077335-106077713 | Common:2; Rare:115 | ||||
| chr11:112074010-112074343 | Common:1; Rare:67 | ||||
| chr11:112086709-112086893 | Rare:78 | ||||
| chr11:114400456-114400747 | Common:2; Rare:117 | ||||
| chr11:114439455-114439649 | Common:2; Rare:77 | ||||
| chr11:117144205-117144371 | Common:2; Rare:86 | ||||
| chr11:117200007-117200201 | Common:5; Rare:43 | ||||
| chr11:118790981-118791288 | Rare:102 | ||||
| chr11:119018335-119018795 | Common:11; Rare:165 | ||||
| chr11:119057042-119057481 | Common:3; Rare:165 |