| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6378479-6378694 | Rare:91 | ||||
| chr5:6633040-6633335 | Common:7; Rare:87; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9546073-9546357 | Common:7; Rare:67 | ||||
| chr5:10249874-10250167 | Common:16; Rare:140 | ||||
| chr5:10353597-10353905 | Common:3; Rare:111 | ||||
| chr5:16465732-16465895 | Rare:30 | ||||
| chr5:31532052-31532352 | Common:3; Rare:87 | ||||
| chr5:32174267-32174416 | Common:1; Rare:53 | ||||
| chr5:32710538-32710731 | Common:1; Rare:42 | ||||
| chr5:33440631-33441100 | Common:7; Rare:132 | ||||
| chr5:34656124-34656473 | Common:3; Rare:92 | ||||
| chr5:34915461-34915741 | Common:1; Rare:68 | ||||
| chr5:35230332-35230425 | Common:1; Rare:19 | ||||
| chr5:35617677-35617989 | Common:1; Rare:73 |