| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89111371-89111629 | Common:3; Rare:94 | ||||
| chr4:99088706-99088857 | Common:5; Rare:62 | ||||
| chr4:99894357-99894608 | Common:2; Rare:89 | ||||
| chr4:99950229-99950532 | Rare:71 | ||||
| chr4:101347517-101347812 | Common:5; Rare:92 | ||||
| chr4:102827492-102827603 | Rare:39 | ||||
| chr4:102827985-102828299 | Common:3; Rare:106 | ||||
| chr4:102868844-102869041 | Common:2; Rare:65 | ||||
| chr4:105552297-105552682 | Rare:56 | ||||
| chr4:105708654-105708874 | Common:3; Rare:73 | ||||
| chr4:106316179-106316597 | Common:5; Rare:135 | ||||
| chr4:107824447-107824735 | Common:1; Rare:60 | ||||
| chr4:107989690-107989910 | Common:5; Rare:104; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:112636880-112637197 | Common:1; Rare:87 | ||||
| chr4:118685339-118685415 | Common:1; Rare:25 |