| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9575464-9575541 | Common:1; Rare:9 | ||||
| chr11:9663893-9664194 | Common:4; Rare:99 | ||||
| chr11:10294028-10294303 | Common:1; Rare:88; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr11:10304900-10305089 | Common:1; Rare:44 | ||||
| chr11:10541131-10541309 | Common:1; Rare:68 | ||||
| chr11:10568568-10568907 | Common:1; Rare:60 | ||||
| chr11:10751130-10751302 | Rare:51 | ||||
| chr11:10808709-10808990 | Common:1; Rare:102 | ||||
| chr11:10858023-10858260 | Common:2; Rare:76 | ||||
| chr11:11841938-11842118 | Common:1; Rare:46 | ||||
| chr11:12377459-12377726 | Rare:103 | ||||
| chr11:12473815-12473963 | Rare:46 | ||||
| chr11:13463159-13463340 | Common:1; Rare:65 | ||||
| chr11:14520298-14520449 | Rare:51 | ||||
| chr11:14643630-14643830 | Common:1; Rare:77 |