| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138174877-138174960 | Common:1; Rare:17 | ||||
| chr3:138348349-138348747 | Common:2; Rare:106 | ||||
| chr3:138608971-138609113 | Common:1; Rare:43 | ||||
| chr3:138834830-138835031 | Rare:71 | ||||
| chr3:139389552-139389876 | Common:2; Rare:105 | ||||
| chr3:139539512-139539788 | Common:3; Rare:92 | ||||
| chr3:140941600-140941926 | Common:2; Rare:118 | ||||
| chr3:140942080-140942244 | Common:2; Rare:36 | ||||
| chr3:141231623-141231894 | Common:2; Rare:94 | ||||
| chr3:141368264-141368569 | Rare:66 | ||||
| chr3:141401995-141402437 | Common:2; Rare:109 | ||||
| chr3:141402940-141403035 | Common:2; Rare:25 | ||||
| chr3:142447957-142448130 | Common:1; Rare:59 | ||||
| chr3:142578701-142578950 | Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596282-142596459 | Common:1; Rare:47 |