| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39255557-39255906 | Common:3; Rare:55 | ||||
| chr3:39295142-39295530 | Common:2; Rare:61 | ||||
| chr3:39296145-39296491 | Common:2; Rare:52 | ||||
| chr3:39327942-39328105 | Common:1; Rare:29 | ||||
| chr3:39346867-39347053 | Rare:31 | ||||
| chr3:39361360-39361487 | Common:1; Rare:25 | ||||
| chr3:39361639-39361876 | Common:1; Rare:57 | ||||
| chr3:39378200-39378502 | Common:1; Rare:47 | ||||
| chr3:39384200-39384490 | Common:7; Rare:77 | ||||
| chr3:39388896-39389197 | Common:1; Rare:42 | ||||
| chr3:39411657-39411844 | Common:1; Rare:49; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:39750856-39751015 | Common:1; Rare:23 | ||||
| chr3:39754607-39754797 | Common:1; Rare:39 | ||||
| chr3:39755215-39755479 | Common:2; Rare:55 | ||||
| chr3:40187961-40188333 | Common:1; Rare:71 |