| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:9265445-9265586 | Common:5; Rare:35 | ||||
| chr5:9265806-9265876 | Common:1; Rare:15 | ||||
| chr5:9545964-9546344 | Common:10; Rare:93 | ||||
| chr5:10249738-10250445 | Common:19; Rare:329; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10250451-10250786 | Common:2; Rare:111 | ||||
| chr5:10353560-10353952 | Common:4; Rare:152 | ||||
| chr5:10441802-10441923 | Rare:36 | ||||
| chr5:14664551-14664914 | Common:4; Rare:153 | ||||
| chr5:16465310-16465401 | Rare:29 | ||||
| chr5:16465559-16465913 | Rare:94 | ||||
| chr5:16616979-16617269 | Common:2; Rare:79; Clinvar (benign):5 | ||||
| chr5:16742226-16742346 | Rare:21 | ||||
| chr5:16935995-16936521 | Common:4; Rare:157 | ||||
| chr5:31532026-31532395 | Common:4; Rare:106 | ||||
| chr5:31537936-31538323 | Common:2; Rare:76 |