| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40679674-40679960 | Common:2; Rare:69 | ||||
| chr5:40755865-40756066 | Rare:52 | ||||
| chr5:40798165-40798435 | Common:1; Rare:104 | ||||
| chr5:40835183-40835326 | Common:2; Rare:61 | ||||
| chr5:43067331-43067459 | Rare:16 | ||||
| chr5:43120761-43120944 | Common:3; Rare:79 | ||||
| chr5:43313410-43313657 | Common:3; Rare:66 | ||||
| chr5:43556835-43557192 | Common:4; Rare:114 | ||||
| chr5:43603087-43603250 | Rare:41 | ||||
| chr5:44808713-44808974 | Common:2; Rare:87 | ||||
| chr5:50667361-50667414 | Common:1; Rare:16 | ||||
| chr5:50667757-50667918 | Common:1; Rare:51 | ||||
| chr5:53109739-53109885 | Common:1; Rare:68; Clinvar:2 | ||||
| chr5:53560615-53560671 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:54310522-54310714 | Rare:62 |