| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31617936-31618021 | Common:2; Rare:24; Clinvar (benign):1 | ||||
| chr3:31621331-31621478 | Common:1; Rare:26 | ||||
| chr3:31628066-31628246 | Common:1; Rare:42 | ||||
| chr3:31646740-31646796 | Rare:11 | ||||
| chr3:31646962-31647068 | Common:1; Rare:19 | ||||
| chr3:31647122-31647385 | Common:4; Rare:53 | ||||
| chr3:31656759-31656830 | Rare:8 | ||||
| chr3:31670946-31671017 | Rare:24 | ||||
| chr3:31747372-31747484 | Common:1; Rare:12 | ||||
| chr3:31772776-31772997 | Rare:42 | ||||
| chr3:31882388-31882681 | Common:3; Rare:53 | ||||
| chr3:31914772-31914927 | Rare:27 | ||||
| chr3:31936715-31936759 | Rare:6 | ||||
| chr3:31938295-31938376 | Rare:13 | ||||
| chr3:31963209-31963515 | Common:1; Rare:53 |