| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108222594-108222972 | Rare:123; Clinvar:3 | ||||
| chr11:111766357-111766415 | Rare:33 | ||||
| chr11:112073995-112074349 | Common:1; Rare:72 | ||||
| chr11:112086704-112086928 | Rare:99; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:113875480-113875762 | Common:4; Rare:100 | ||||
| chr11:114400451-114400753 | Common:2; Rare:121 | ||||
| chr11:114439308-114439535 | Common:1; Rare:72 | ||||
| chr11:115504390-115504652 | Common:1; Rare:75 | ||||
| chr11:116772971-116773103 | Rare:45 | ||||
| chr11:117144183-117144361 | Common:2; Rare:90 | ||||
| chr11:117199029-117199411 | Common:6; Rare:121 | ||||
| chr11:118359451-118359653 | Common:3; Rare:89 | ||||
| chr11:118401329-118401661 | Rare:108 | ||||
| chr11:118790911-118791255 | Rare:98 | ||||
| chr11:118997980-118998152 | Common:4; Rare:46 |