| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184825917-184826246 | Common:7; Rare:105 | ||||
| chr4:184826752-184826803 | Common:1; Rare:9 | ||||
| chr4:184826851-184827055 | Common:3; Rare:32 | ||||
| chr4:185143168-185143375 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185396581-185396843 | Rare:83 | ||||
| chr4:185425864-185426265 | Common:4; Rare:126 | ||||
| chr4:185535446-185535632 | Common:1; Rare:61; Clinvar (benign):2 | ||||
| chr4:185810828-185810945 | Common:1; Rare:25 | ||||
| chr4:185811665-185811834 | Common:1; Rare:34 | ||||
| chr4:185811836-185811925 | Rare:16 | ||||
| chr4:185813118-185813325 | Common:1; Rare:32 | ||||
| chr4:186266041-186266300 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:186723759-186723908 | Common:4; Rare:63 | ||||
| chr4:186726395-186726467 | Rare:14 | ||||
| chr4:186726566-186726939 | Common:4; Rare:116 |