| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32585175-32585621 | Common:3; Rare:133 | ||||
| chr5:32585966-32586119 | Common:1; Rare:55 | ||||
| chr5:32586202-32586492 | Common:4; Rare:69 | ||||
| chr5:33440600-33441079 | Common:6; Rare:128 | ||||
| chr5:34008027-34008251 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656229-34656554 | Common:2; Rare:87 | ||||
| chr5:34839074-34839240 | Rare:57 | ||||
| chr5:34839274-34839404 | Common:2; Rare:40 | ||||
| chr5:34915453-34915751 | Common:1; Rare:77 | ||||
| chr5:34929259-34929351 | Common:1; Rare:19 | ||||
| chr5:34929457-34929536 | Rare:21 | ||||
| chr5:34929665-34929890 | Rare:78 | ||||
| chr5:35617752-35617951 | Common:1; Rare:41 | ||||
| chr5:36151794-36152207 | Rare:112 | ||||
| chr5:36241504-36241959 | Common:6; Rare:159; Clinvar:1; Clinvar (benign):6 |