| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51982505-51982611 | Rare:10 | ||||
| chr3:52482530-52482675 | Rare:24 | ||||
| chr3:53080151-53080242 | Common:1; Rare:14 | ||||
| chr3:53185611-53186027 | Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:53228289-53228533 | Common:2; Rare:66 | ||||
| chr3:53787629-53787637 | |||||
| chr3:53799937-53800257 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr3:53819012-53819349 | Common:3; Rare:67 | ||||
| chr3:58142585-58142728 | Rare:42; Clinvar:2 | ||||
| chr3:58249614-58249780 | Rare:24 | ||||
| chr3:58536124-58536280 | Rare:19 | ||||
| chr3:61560342-61560647 | Rare:77 | ||||
| chr3:61637443-61637669 | Rare:58 | ||||
| chr3:64005657-64005871 | Rare:34 | ||||
| chr3:65897052-65897295 | Common:1; Rare:42 |