| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:39949455-39949830 | Common:6; Rare:142 | ||||
| chr7:40134581-40135023 | Rare:138; Clinvar:1 | ||||
| chr7:41700568-41700675 | Rare:15 | ||||
| chr7:41703060-41703389 | Common:1; Rare:52 | ||||
| chr7:42932140-42932424 | Rare:117 | ||||
| chr7:43583382-43583446 | Rare:19 | ||||
| chr7:43926362-43926457 | Rare:34 | ||||
| chr7:44044473-44044757 | Common:4; Rare:87 | ||||
| chr7:44490568-44490925 | Common:1; Rare:122 | ||||
| chr7:44573866-44574062 | Common:3; Rare:61 | ||||
| chr7:44748343-44748588 | Common:2; Rare:61 | ||||
| chr7:44796384-44796692 | Common:2; Rare:112 | ||||
| chr7:44999551-44999768 | Common:4; Rare:74 | ||||
| chr7:44999969-45000358 | Common:1; Rare:91; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:47582036-47582233 | Common:1; Rare:65 |