| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32712219-32712314 | Rare:22 | ||||
| chr5:33440593-33441112 | Common:7; Rare:144 | ||||
| chr5:34656159-34656497 | Common:3; Rare:83 | ||||
| chr5:34915218-34915355 | Rare:38 | ||||
| chr5:34915483-34915744 | Common:1; Rare:63 | ||||
| chr5:36151841-36152174 | Rare:95 | ||||
| chr5:36876655-36876859 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877064-36877155 | Rare:35; Clinvar:1 | ||||
| chr5:37249285-37249565 | Common:1; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:38845712-38846058 | Common:2; Rare:91 | ||||
| chr5:39074347-39074480 | Common:1; Rare:58 | ||||
| chr5:39425106-39425308 | Common:2; Rare:49 | ||||
| chr5:40798094-40798401 | Common:1; Rare:112 | ||||
| chr5:40835176-40835418 | Common:2; Rare:97 | ||||
| chr5:40909249-40909603 | Common:1; Rare:76 |