| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39383500-39383750 | Common:1; Rare:63; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:39406464-39406752 | Common:7; Rare:121 | ||||
| chr3:40309409-40309754 | Common:8; Rare:107 | ||||
| chr3:40457131-40457376 | Common:4; Rare:105 | ||||
| chr3:40476860-40477270 | Common:2; Rare:92 | ||||
| chr3:40505853-40506144 | Rare:72 | ||||
| chr3:40524737-40525004 | Common:2; Rare:76 | ||||
| chr3:41199092-41199577 | Common:1; Rare:186 | ||||
| chr3:41961511-41961688 | Rare:46 | ||||
| chr3:41961984-41962380 | Common:7; Rare:99 | ||||
| chr3:41962428-41962612 | Common:4; Rare:44 | ||||
| chr3:42013419-42013663 | Common:5; Rare:60 | ||||
| chr3:42581240-42581640 | Common:1; Rare:102 | ||||
| chr3:42581900-42582213 | Common:3; Rare:90 | ||||
| chr3:42590632-42590927 | Common:3; Rare:87 |