| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17352424-17352513 | Common:1; Rare:13 | ||||
| chr11:17352625-17353203 | Common:2; Rare:105 | ||||
| chr11:17353356-17353505 | Rare:43 | ||||
| chr11:17353601-17353852 | Common:5; Rare:74 | ||||
| chr11:17786979-17787145 | Rare:29 | ||||
| chr11:18012187-18012291 | Common:3; Rare:18 | ||||
| chr11:18310869-18310950 | Rare:26; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:18314142-18314289 | Common:1; Rare:35 | ||||
| chr11:18383694-18384064 | Common:2; Rare:68 | ||||
| chr11:18384152-18384193 | Rare:12 | ||||
| chr11:18384253-18384477 | Common:1; Rare:36 | ||||
| chr11:18384535-18384602 | Rare:6 | ||||
| chr11:18384726-18384807 | Rare:10 | ||||
| chr11:18395311-18395369 | Common:1; Rare:7 | ||||
| chr11:18633361-18633497 | Rare:24 |