| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32173810-32174034 | Rare:64 | ||||
| chr5:32174247-32174395 | Common:1; Rare:57 | ||||
| chr5:33440611-33441117 | Common:7; Rare:141 | ||||
| chr5:34656159-34656486 | Common:3; Rare:81 | ||||
| chr5:34839278-34839338 | Common:2; Rare:18 | ||||
| chr5:34915201-34915348 | Rare:42 | ||||
| chr5:34915461-34915755 | Common:1; Rare:78 | ||||
| chr5:34929678-34930012 | Common:1; Rare:104 | ||||
| chr5:36151794-36152146 | Rare:85 | ||||
| chr5:36242135-36242413 | Common:2; Rare:77 | ||||
| chr5:36876636-36876915 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877064-36877161 | Rare:36; Clinvar:1 | ||||
| chr5:37248906-37249072 | Common:3; Rare:29 | ||||
| chr5:37249285-37249433 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37379064-37379392 | Common:3; Rare:87 |