| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99088704-99088888 | Common:6; Rare:80 | ||||
| chr4:99563989-99564127 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894357-99894625 | Common:3; Rare:91 | ||||
| chr4:99949735-99949964 | Common:3; Rare:85 | ||||
| chr4:99950228-99950542 | Rare:77 | ||||
| chr4:101346835-101347109 | Common:2; Rare:66 | ||||
| chr4:101347581-101347835 | Common:4; Rare:78 | ||||
| chr4:102760916-102761076 | Rare:55; Clinvar:1 | ||||
| chr4:102825531-102825771 | Common:3; Rare:66 | ||||
| chr4:102825772-102825783 | Rare:5 | ||||
| chr4:102826657-102826980 | Common:1; Rare:87 | ||||
| chr4:102827063-102827301 | Common:3; Rare:90 | ||||
| chr4:102827439-102827884 | Common:4; Rare:148 | ||||
| chr4:102827913-102827971 | Rare:20 | ||||
| chr4:102827985-102828142 | Rare:55 |