| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:30658714-30659044 | Common:3; Rare:44 | ||||
| chr3:32401941-32402030 | Rare:16 | ||||
| chr3:32457929-32458023 | Common:3; Rare:15 | ||||
| chr3:32465963-32466128 | Common:4; Rare:33 | ||||
| chr3:32484083-32484210 | Rare:28 | ||||
| chr3:32493309-32493470 | Common:2; Rare:30 | ||||
| chr3:37055128-37055227 | Rare:30 | ||||
| chr3:37058790-37059065 | Common:2; Rare:65 | ||||
| chr3:37063741-37063862 | Common:1; Rare:32 | ||||
| chr3:37093635-37093764 | Rare:23 | ||||
| chr3:37454032-37454306 | Common:1; Rare:38 | ||||
| chr3:37803720-37803928 | Common:2; Rare:58 | ||||
| chr3:39091424-39091682 | Common:2; Rare:30 | ||||
| chr3:39384263-39384335 | Common:3; Rare:20 | ||||
| chr3:39411642-39411960 | Common:1; Rare:83; Clinvar (benign):1; Clinvar (pathogenic):1 |