| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9810207-9810289 | Rare:38 | ||||
| chr3:9843907-9844172 | Common:4; Rare:119 | ||||
| chr3:9890474-9890684 | Common:2; Rare:84 | ||||
| chr3:9917033-9917186 | Common:1; Rare:30 | ||||
| chr3:9933523-9933899 | Common:3; Rare:150; Clinvar:3 | ||||
| chr3:9934014-9934087 | Rare:18 | ||||
| chr3:10011076-10011454 | Common:2; Rare:103 | ||||
| chr3:10026299-10026482 | Rare:60 | ||||
| chr3:10115508-10115722 | Common:4; Rare:78 | ||||
| chr3:10141672-10141870 | Common:1; Rare:91; Clinvar:15; Clinvar (benign):18 | ||||
| chr3:11272233-11272427 | Common:1; Rare:43 | ||||
| chr3:11643759-11644008 | Common:2; Rare:64 | ||||
| chr3:11719427-11719577 | Rare:47 | ||||
| chr3:11720713-11720867 | Rare:26 | ||||
| chr3:11846827-11846982 | Common:1; Rare:49 |