| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:36598225-36598484 | Common:1; Rare:50 | ||||
| chr11:43358813-43359096 | Rare:117 | ||||
| chr11:43680559-43680825 | Rare:82 | ||||
| chr11:43880706-43880915 | Common:2; Rare:58 | ||||
| chr11:44066204-44066569 | Common:3; Rare:85 | ||||
| chr11:44565275-44565714 | Common:3; Rare:111 | ||||
| chr11:45286181-45286437 | Rare:78 | ||||
| chr11:45804993-45805175 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45847210-45847487 | Common:2; Rare:111 | ||||
| chr11:46119777-46120002 | Common:2; Rare:60 | ||||
| chr11:46120944-46121025 | Rare:8 | ||||
| chr11:46121048-46121283 | Common:2; Rare:41 | ||||
| chr11:46277898-46278211 | Rare:83 | ||||
| chr11:46361466-46361626 | Rare:32 | ||||
| chr11:46371340-46371511 | Rare:52 |