| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:6680269-6680382 | Common:3; Rare:21 | ||||
| chr3:6717423-6717710 | Common:5; Rare:65 | ||||
| chr3:7204686-7205089 | Common:4; Rare:79 | ||||
| chr3:8767846-8768023 | Common:1; Rare:47 | ||||
| chr3:9396239-9396430 | Common:1; Rare:84 | ||||
| chr3:9396455-9396873 | Common:2; Rare:169 | ||||
| chr3:9398867-9398892 | Rare:5 | ||||
| chr3:9780165-9780359 | Common:2; Rare:39 | ||||
| chr3:9897976-9898108 | Common:1; Rare:22 | ||||
| chr3:9932736-9933100 | Common:2; Rare:131; Clinvar (benign):1 | ||||
| chr3:9946415-9946604 | Common:1; Rare:72 | ||||
| chr3:9951287-9951543 | Common:1; Rare:41 | ||||
| chr3:10009093-10009274 | Common:4; Rare:49 | ||||
| chr3:10194293-10194478 | Common:2; Rare:24 | ||||
| chr3:10194915-10194975 | Rare:9 |