| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34008015-34008237 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34839082-34839219 | Rare:47 | ||||
| chr5:34915279-34915293 | Rare:2 | ||||
| chr5:34915472-34915755 | Common:1; Rare:75 | ||||
| chr5:34929690-34929890 | Rare:70 | ||||
| chr5:35230473-35230495 | Rare:4 | ||||
| chr5:35617711-35617989 | Common:1; Rare:66 | ||||
| chr5:35938552-35938818 | Common:1; Rare:53 | ||||
| chr5:36151812-36152195 | Rare:109 | ||||
| chr5:36301875-36302138 | Common:2; Rare:38 | ||||
| chr5:36606450-36606644 | Rare:35 | ||||
| chr5:36606851-36606929 | Rare:9 | ||||
| chr5:36876607-36876915 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37249266-37249531 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371040-37371189 | Rare:55 |