| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173517951-173518251 | Rare:76 | ||||
| chr4:173519092-173519253 | Common:6; Rare:49 | ||||
| chr4:173525501-173525677 | Common:1; Rare:37 | ||||
| chr4:184537513-184537661 | Common:3; Rare:37 | ||||
| chr4:185408309-185408525 | Common:1; Rare:45; Clinvar (pathogenic):1 | ||||
| chr4:185642978-185643357 | Common:1; Rare:71 | ||||
| chr4:185734908-185735106 | Common:2; Rare:31 | ||||
| chr5:784688-784873 | Common:5; Rare:58 | ||||
| chr5:1633909-1634083 | Common:2; Rare:64 | ||||
| chr5:8457590-8457751 | Common:2; Rare:46 | ||||
| chr5:14186247-14186444 | Common:2; Rare:41 | ||||
| chr5:34918231-34918381 | Common:1; Rare:30 | ||||
| chr5:42837765-42837882 | Rare:32 | ||||
| chr5:42993259-42993532 | Common:6; Rare:62 | ||||
| chr5:43041725-43041770 | Rare:6 |