| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197696988-197697243 | Common:1; Rare:62 | ||||
| chr3:197850990-197851007 | |||||
| chr3:197899948-197900058 | Rare:24 | ||||
| chr3:198030585-198030729 | Rare:24 | ||||
| chr3:198038392-198038825 | Common:1; Rare:83 | ||||
| chr3:198157304-198157502 | Common:2; Rare:41 | ||||
| chr4:125539-125714 | Common:4; Rare:29 | ||||
| chr4:588472-588612 | Rare:20 | ||||
| chr4:679725-680003 | Common:2; Rare:85 | ||||
| chr4:774080-774347 | Common:1; Rare:72 | ||||
| chr4:781770-781992 | Rare:90 | ||||
| chr4:868621-868830 | Common:1; Rare:74 | ||||
| chr4:1799454-1799776 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):5 | ||||
| chr4:1815719-1816067 | Common:1; Rare:96 | ||||
| chr4:2363436-2363545 | Common:1; Rare:23 |