| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39182204-39182548 | Rare:74; Clinvar:2 | ||||
| chr4:39366319-39366431 | Rare:35 | ||||
| chr4:39458857-39459122 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527337-39527780 | Common:4; Rare:119 | ||||
| chr4:39527944-39528029 | Rare:20 | ||||
| chr4:39638805-39639149 | Common:1; Rare:122 | ||||
| chr4:39697936-39698203 | Common:2; Rare:116 | ||||
| chr4:40056673-40056950 | Common:4; Rare:92 | ||||
| chr4:41216696-41216781 | Common:2; Rare:14 | ||||
| chr4:41256721-41257020 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:41935000-41935256 | Common:3; Rare:73 | ||||
| chr4:41990402-41990573 | Common:1; Rare:63 | ||||
| chr4:44678369-44678731 | Common:1; Rare:137 | ||||
| chr4:44726537-44726635 | Rare:40 | ||||
| chr4:47463629-47463790 | Common:2; Rare:56 |