| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88592267-88592506 | Common:1; Rare:70 | ||||
| chr4:98261153-98261493 | Common:1; Rare:107 | ||||
| chr4:98657610-98657794 | Rare:35 | ||||
| chr4:98658598-98658922 | Common:2; Rare:91 | ||||
| chr4:99088691-99088894 | Common:7; Rare:97 | ||||
| chr4:99564011-99564134 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894351-99894620 | Common:3; Rare:93 | ||||
| chr4:99950271-99950535 | Rare:56 | ||||
| chr4:101347422-101347771 | Common:3; Rare:100 | ||||
| chr4:102826784-102827188 | Common:4; Rare:139 | ||||
| chr4:102827484-102827647 | Common:1; Rare:59 | ||||
| chr4:102827730-102827857 | Common:1; Rare:34 | ||||
| chr4:102827985-102828142 | Rare:55 | ||||
| chr4:102868859-102869061 | Common:2; Rare:65 | ||||
| chr4:105708633-105708847 | Common:1; Rare:69 |