| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:75159518-75160012 | Common:1; Rare:101 | ||||
| chr11:75160052-75160113 | Rare:7 | ||||
| chr11:75241244-75241374 | Rare:32 | ||||
| chr11:75351462-75351534 | Common:1; Rare:17 | ||||
| chr11:75351571-75351933 | Common:3; Rare:101 | ||||
| chr11:75399359-75399670 | Common:5; Rare:118 | ||||
| chr11:75525760-75526202 | Common:2; Rare:133 | ||||
| chr11:75561948-75562363 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:75562662-75562922 | Common:1; Rare:59 | ||||
| chr11:75563232-75563450 | Rare:37 | ||||
| chr11:75668086-75668347 | Common:1; Rare:71 | ||||
| chr11:75668575-75668709 | Rare:28 | ||||
| chr11:75668905-75669005 | Rare:29 | ||||
| chr11:75768145-75768253 | Common:1; Rare:19 | ||||
| chr11:75768383-75768611 | Rare:67 |