| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114447530-114447601 | Rare:4 | ||||
| chr11:116784272-116784415 | Common:1; Rare:36 | ||||
| chr11:116996525-116996728 | Common:1; Rare:35 | ||||
| chr11:117058214-117058282 | Rare:9 | ||||
| chr11:117097431-117097485 | Rare:12 | ||||
| chr11:117097493-117097507 | Rare:5 | ||||
| chr11:117097630-117097705 | Common:1; Rare:17 | ||||
| chr11:117147324-117147604 | Common:1; Rare:54 | ||||
| chr11:117211711-117211777 | Rare:5 | ||||
| chr11:117212121-117212186 | Common:1; Rare:16 | ||||
| chr11:117272630-117272696 | Rare:6 | ||||
| chr11:117293204-117293401 | Rare:40 | ||||
| chr11:117379653-117379783 | Common:1; Rare:27 | ||||
| chr11:117390651-117390819 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:117390841-117391142 | Common:1; Rare:101; Clinvar (benign):1 |