| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700312-46700380 | Rare:10 | ||||
| chr11:46700479-46700907 | Common:1; Rare:101 | ||||
| chr11:46700963-46701133 | Common:1; Rare:70 | ||||
| chr11:46701629-46701658 | Rare:10 | ||||
| chr11:46826721-46826991 | Rare:84 | ||||
| chr11:46845770-46846099 | Common:1; Rare:68 | ||||
| chr11:46846137-46846660 | Common:1; Rare:140 | ||||
| chr11:46918301-46918341 | Rare:10; Clinvar:1 | ||||
| chr11:46918494-46918673 | Common:2; Rare:41; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:46936586-46937020 | Common:2; Rare:111 | ||||
| chr11:47176418-47176637 | Rare:63 | ||||
| chr11:47176775-47177168 | Common:1; Rare:168 | ||||
| chr11:47177316-47177504 | Rare:26 | ||||
| chr11:47185667-47185794 | Rare:27 | ||||
| chr11:47186137-47186281 | Rare:36 |