| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99088689-99088916 | Common:7; Rare:111 | ||||
| chr4:99321309-99321727 | Common:4; Rare:92 | ||||
| chr4:99563668-99563874 | Rare:65 | ||||
| chr4:99563969-99564173 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99946557-99946786 | Rare:83 | ||||
| chr4:99950266-99950485 | Rare:42 | ||||
| chr4:101347517-101347807 | Common:5; Rare:89 | ||||
| chr4:102827112-102827425 | Common:1; Rare:116 | ||||
| chr4:102827442-102827625 | Rare:64 | ||||
| chr4:102827670-102827836 | Common:3; Rare:48 | ||||
| chr4:102827837-102828135 | Rare:96 | ||||
| chr4:102868836-102869059 | Common:2; Rare:76 | ||||
| chr4:103076286-103076388 | Rare:30 | ||||
| chr4:105708641-105708816 | Rare:55 | ||||
| chr4:105895334-105895535 | Rare:58 |