| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98657621-98657830 | Rare:40 | ||||
| chr4:98929020-98929408 | Common:3; Rare:108 | ||||
| chr4:98995463-98995774 | Common:6; Rare:112 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563586-99563805 | Common:2; Rare:66 | ||||
| chr4:99563969-99564127 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894344-99894625 | Common:3; Rare:96 | ||||
| chr4:99949727-99949964 | Common:3; Rare:87 | ||||
| chr4:99950203-99950542 | Common:1; Rare:92 | ||||
| chr4:101347581-101347840 | Common:4; Rare:78 | ||||
| chr4:102760882-102761076 | Rare:65; Clinvar:1 | ||||
| chr4:102826788-102827005 | Rare:65 | ||||
| chr4:102827120-102827258 | Rare:50 | ||||
| chr4:102827428-102827656 | Common:1; Rare:87 | ||||
| chr4:102827687-102827978 | Common:3; Rare:86 |