| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9944039-9944340 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr3:10308218-10308318 | Rare:19 | ||||
| chr3:11184473-11184604 | Common:1; Rare:19 | ||||
| chr3:11198675-11198758 | Common:1; Rare:16 | ||||
| chr3:11482695-11482742 | Rare:5 | ||||
| chr3:12584557-12584737 | Rare:65; Clinvar:5; Clinvar (benign):3 | ||||
| chr3:15042136-15042447 | Common:3; Rare:50 | ||||
| chr3:15714402-15714615 | Common:8; Rare:47 | ||||
| chr3:15746965-15747127 | Common:1; Rare:19 | ||||
| chr3:15747251-15747589 | Common:2; Rare:54 | ||||
| chr3:15794398-15794529 | Rare:34 | ||||
| chr3:15971960-15972198 | Common:2; Rare:29 | ||||
| chr3:15972238-15972269 | Rare:4 | ||||
| chr3:16060412-16060656 | Common:5; Rare:37 | ||||
| chr3:17363341-17363532 | Rare:41 |