| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:140941633-140941911 | Common:2; Rare:107 | ||||
| chr3:141367861-141367997 | Rare:21 | ||||
| chr3:141368207-141368706 | Rare:102 | ||||
| chr3:141368712-141368955 | Common:2; Rare:52 | ||||
| chr3:141402226-141402415 | Common:2; Rare:53 | ||||
| chr3:141486856-141487084 | Common:1; Rare:74 | ||||
| chr3:142225538-142225673 | Common:1; Rare:42 | ||||
| chr3:142447964-142448137 | Common:1; Rare:62 | ||||
| chr3:142578699-142578966 | Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142596282-142596449 | Common:1; Rare:44 | ||||
| chr3:143001393-143001638 | Common:3; Rare:90 | ||||
| chr3:146160318-146160501 | Rare:33 | ||||
| chr3:146160949-146161302 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146163649-146163931 | Rare:47 | ||||
| chr3:146544520-146544952 | Common:4; Rare:105 |