| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32174267-32174421 | Common:1; Rare:55 | ||||
| chr5:32233858-32234153 | Common:1; Rare:60 | ||||
| chr5:33440600-33440788 | Common:1; Rare:45 | ||||
| chr5:33440802-33441129 | Common:5; Rare:96 | ||||
| chr5:33441175-33441445 | Common:1; Rare:66 | ||||
| chr5:33461009-33461296 | Common:4; Rare:82 | ||||
| chr5:33984237-33984794 | Common:1; Rare:191; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr5:34007997-34008351 | Common:2; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656153-34656449 | Common:3; Rare:73 | ||||
| chr5:34839270-34839410 | Common:2; Rare:41 | ||||
| chr5:34915212-34915355 | Rare:38 | ||||
| chr5:34915436-34915921 | Common:2; Rare:143 | ||||
| chr5:35230322-35230610 | Common:1; Rare:54 | ||||
| chr5:35617682-35617930 | Common:1; Rare:49 | ||||
| chr5:36151874-36152180 | Rare:95 |