| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138608827-138609127 | Common:1; Rare:74 | ||||
| chr3:138834848-138835190 | Rare:107 | ||||
| chr3:139343933-139344051 | Rare:40; Clinvar (benign):2 | ||||
| chr3:139344389-139344559 | Rare:28 | ||||
| chr3:139389574-139389957 | Common:2; Rare:118 | ||||
| chr3:139539632-139539873 | Common:2; Rare:58 | ||||
| chr3:139934989-139935196 | Common:1; Rare:53 | ||||
| chr3:140941641-140941904 | Common:2; Rare:100 | ||||
| chr3:140942628-140942777 | Common:1; Rare:38 | ||||
| chr3:141051204-141051410 | Rare:59 | ||||
| chr3:141076756-141077156 | Common:8; Rare:127 | ||||
| chr3:141231596-141231914 | Common:2; Rare:107 | ||||
| chr3:141368220-141368524 | Rare:63 | ||||
| chr3:141386668-141387096 | Common:5; Rare:157 | ||||
| chr3:141402348-141402620 | Common:2; Rare:75 |