| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39458837-39459103 | Common:3; Rare:148; Clinvar (benign):4 | ||||
| chr4:39527361-39527742 | Common:2; Rare:90 | ||||
| chr4:39638850-39639125 | Common:1; Rare:105 | ||||
| chr4:44678624-44678680 | Rare:27 | ||||
| chr4:52659254-52659527 | Common:1; Rare:85 | ||||
| chr4:56435534-56435776 | Common:3; Rare:80 | ||||
| chr4:56467555-56467642 | Rare:33 | ||||
| chr4:56977485-56977739 | Common:2; Rare:93 | ||||
| chr4:57110055-57110207 | Rare:51 | ||||
| chr4:67701125-67701404 | Common:4; Rare:127 | ||||
| chr4:73258787-73258937 | Rare:51 | ||||
| chr4:74158016-74158223 | Rare:101 | ||||
| chr4:75514276-75514492 | Rare:72 | ||||
| chr4:75724401-75724692 | Common:1; Rare:83 | ||||
| chr4:76148357-76148577 | Common:3; Rare:70 |