| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138115594-138115721 | Common:3; Rare:30 | ||||
| chr3:138187243-138187569 | Rare:93 | ||||
| chr3:138594198-138594502 | Rare:99 | ||||
| chr3:138609029-138609087 | Rare:20 | ||||
| chr3:139389552-139389875 | Common:2; Rare:105 | ||||
| chr3:139539483-139539792 | Common:3; Rare:101 | ||||
| chr3:141231616-141231888 | Common:2; Rare:94 | ||||
| chr3:141368193-141368761 | Rare:115 | ||||
| chr3:141386765-141386990 | Rare:35 | ||||
| chr3:141402085-141402415 | Common:2; Rare:81 | ||||
| chr3:141738024-141738351 | Common:2; Rare:137 | ||||
| chr3:142225560-142225678 | Rare:38 | ||||
| chr3:142447968-142448174 | Common:1; Rare:81 | ||||
| chr3:142578702-142578925 | Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:143001472-143001640 | Common:2; Rare:60 |