| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138348415-138348758 | Common:2; Rare:90 | ||||
| chr3:138594198-138594445 | Rare:71 | ||||
| chr3:139389588-139389878 | Common:2; Rare:89 | ||||
| chr3:139539573-139539777 | Common:1; Rare:69 | ||||
| chr3:140941582-140941911 | Common:2; Rare:117 | ||||
| chr3:141231679-141231894 | Common:1; Rare:75 | ||||
| chr3:141368237-141368540 | Rare:63 | ||||
| chr3:141876491-141876656 | Common:1; Rare:61 | ||||
| chr3:142447979-142448107 | Common:1; Rare:43 | ||||
| chr3:142596328-142596449 | Common:1; Rare:34 | ||||
| chr3:142964003-142964067 | Common:2; Rare:18 | ||||
| chr3:143001472-143001630 | Common:2; Rare:57 | ||||
| chr3:146160986-146161260 | Common:1; Rare:92; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:149377600-149377813 | Common:1; Rare:50 | ||||
| chr3:149657883-149658056 | Common:1; Rare:31 |