| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:46925506-46925565 | Common:1; Rare:15 | ||||
| chr3:46987831-46988022 | Common:1; Rare:66 | ||||
| chr3:47003021-47003199 | Rare:52 | ||||
| chr3:47164798-47164840 | Common:2; Rare:11 | ||||
| chr3:47406259-47406400 | Rare:47; Clinvar (benign):1 | ||||
| chr3:47636104-47636423 | Rare:67 | ||||
| chr3:49111280-49111525 | Common:1; Rare:62 | ||||
| chr3:49131407-49131713 | Common:1; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49278416-49278497 | Rare:23 | ||||
| chr3:49716204-49716437 | Common:3; Rare:69 | ||||
| chr3:50258127-50258647 | Common:1; Rare:95 | ||||
| chr3:50368954-50368982 | Rare:5 | ||||
| chr3:50372336-50372606 | Common:1; Rare:63 | ||||
| chr3:50378282-50378547 | Rare:47; Clinvar (benign):2 | ||||
| chr3:50441912-50442108 | Rare:46 |