| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:75435029-75435379 | Common:4; Rare:122 | ||||
| chr3:75641092-75641304 | Rare:37 | ||||
| chr3:80770396-80770579 | Common:1; Rare:9 | ||||
| chr3:81761420-81761590 | Common:5; Rare:67; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:98808107-98808349 | Rare:45 | ||||
| chr3:101676254-101676500 | Common:2; Rare:83 | ||||
| chr3:107240586-107240764 | Rare:75 | ||||
| chr3:123335221-123335425 | Common:1; Rare:43 | ||||
| chr3:126301206-126301406 | Common:5; Rare:41 | ||||
| chr3:131361588-131361916 | Common:3; Rare:99 | ||||
| chr3:139352581-139352692 | Rare:32; Clinvar (benign):2 | ||||
| chr3:150408860-150409021 | Rare:46 | ||||
| chr3:152403836-152403974 | Common:3; Rare:28 | ||||
| chr3:167864613-167864849 | Rare:47 | ||||
| chr3:183447462-183447709 | Common:1; Rare:59 |