| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33039912-33040034 | Rare:37 | ||||
| chr11:33161406-33161563 | Common:4; Rare:40 | ||||
| chr11:33257157-33257432 | Common:3; Rare:96 | ||||
| chr11:33257591-33257737 | Rare:36 | ||||
| chr11:33257806-33257870 | Common:1; Rare:16 | ||||
| chr11:33258158-33258387 | Rare:88 | ||||
| chr11:33258454-33258599 | Rare:52 | ||||
| chr11:33701163-33701272 | Rare:13 | ||||
| chr11:34052125-34052510 | Common:4; Rare:172 | ||||
| chr11:34105515-34105717 | Common:2; Rare:69 | ||||
| chr11:34620889-34621183 | Common:3; Rare:57 | ||||
| chr11:34624158-34624290 | Common:1; Rare:27 | ||||
| chr11:34632535-34632577 | Rare:9 | ||||
| chr11:34916292-34916661 | Common:10; Rare:149; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139017-35139201 | Common:1; Rare:36 |