| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31509575-31509806 | Common:1; Rare:76 | ||||
| chr11:33257133-33257466 | Common:3; Rare:106 | ||||
| chr11:33257608-33257762 | Rare:36 | ||||
| chr11:33257764-33257885 | Common:1; Rare:29 | ||||
| chr11:33258010-33258626 | Common:4; Rare:210 | ||||
| chr11:33722635-33722778 | Common:2; Rare:29 | ||||
| chr11:33774457-33774670 | Common:2; Rare:79 | ||||
| chr11:34052138-34052624 | Common:4; Rare:219 | ||||
| chr11:34438784-34439038 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr11:34916263-34916657 | Common:11; Rare:155; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139369 | Common:1; Rare:116 | ||||
| chr11:35943942-35944119 | Common:2; Rare:61 | ||||
| chr11:36510224-36510377 | Rare:47 | ||||
| chr11:43358834-43358983 | Rare:73 | ||||
| chr11:44066125-44066569 | Common:5; Rare:106 |