| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8964366-8964570 | Common:4; Rare:69 | ||||
| chr11:8964919-8965039 | Common:2; Rare:30 | ||||
| chr11:9314519-9314862 | Common:5; Rare:109 | ||||
| chr11:9460650-9461057 | Common:4; Rare:106 | ||||
| chr11:9663893-9664266 | Common:4; Rare:124 | ||||
| chr11:10294067-10294309 | Common:1; Rare:83; Clinvar:5 | ||||
| chr11:10304866-10305229 | Common:1; Rare:80 | ||||
| chr11:10455137-10455275 | Common:2; Rare:24; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:10455921-10456067 | Rare:20 | ||||
| chr11:10541127-10541349 | Common:1; Rare:80 | ||||
| chr11:10568446-10568907 | Common:1; Rare:99 | ||||
| chr11:10751144-10751302 | Rare:48 | ||||
| chr11:10799064-10799418 | Common:3; Rare:131 | ||||
| chr11:10800691-10801096 | Common:1; Rare:118 | ||||
| chr11:10802263-10802652 | Common:2; Rare:110 |