| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139344472-139344573 | Rare:20 | ||||
| chr3:139389557-139389868 | Common:1; Rare:102 | ||||
| chr3:139539516-139539788 | Common:3; Rare:92 | ||||
| chr3:140941672-140941916 | Common:2; Rare:90 | ||||
| chr3:141231639-141231888 | Common:2; Rare:88 | ||||
| chr3:141368218-141368575 | Rare:77 | ||||
| chr3:141402267-141402431 | Common:2; Rare:48 | ||||
| chr3:141486869-141487119 | Common:3; Rare:93; Clinvar:1 | ||||
| chr3:141875989-141876286 | Rare:78 | ||||
| chr3:141876360-141876729 | Common:2; Rare:126 | ||||
| chr3:141877573-141877852 | Common:2; Rare:57 | ||||
| chr3:141922158-141922211 | Common:1; Rare:6 | ||||
| chr3:142225456-142225678 | Common:3; Rare:79 | ||||
| chr3:142447940-142448126 | Common:1; Rare:61 | ||||
| chr3:142578705-142578989 | Rare:107; Clinvar:1; Clinvar (benign):1 |