| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:84966651-84966703 | Rare:13 | ||||
| chr4:86594055-86594332 | Rare:88 | ||||
| chr4:86934824-86935054 | Common:2; Rare:88 | ||||
| chr4:86936177-86936353 | Rare:38 | ||||
| chr4:88523738-88523864 | Common:2; Rare:36 | ||||
| chr4:89111393-89111583 | Common:2; Rare:72 | ||||
| chr4:94451828-94451987 | Common:3; Rare:50 | ||||
| chr4:95548911-95549350 | Common:3; Rare:92 | ||||
| chr4:98929101-98929378 | Common:3; Rare:70 | ||||
| chr4:98995515-98995744 | Common:5; Rare:77 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563933-99564127 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894344-99894600 | Common:2; Rare:93 | ||||
| chr4:99950266-99950527 | Rare:54 | ||||
| chr4:101347552-101347816 | Common:4; Rare:80 |