| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:155590340-155590686 | Common:3; Rare:75 | ||||
| chr7:155803680-155804150 | Common:3; Rare:105; Clinvar (benign):2 | ||||
| chr7:155804718-155804907 | Rare:41 | ||||
| chr7:155804944-155805344 | Common:4; Rare:171 | ||||
| chr7:155811040-155811440 | Common:3; Rare:116 | ||||
| chr7:155813015-155813415 | Common:7; Rare:128 | ||||
| chr7:155824040-155824700 | Common:7; Rare:122 | ||||
| chr7:155944958-155945261 | Common:5; Rare:52 | ||||
| chr7:156295574-156295974 | Common:2; Rare:137 | ||||
| chr7:156383615-156384295 | Common:5; Rare:152 | ||||
| chr7:156516370-156516790 | Common:4; Rare:73 | ||||
| chr7:156614457-156615245 | Common:4; Rare:241 | ||||
| chr7:157089219-157089746 | Common:11; Rare:246 | ||||
| chr7:157432531-157432931 | Common:11; Rare:136 | ||||
| chr7:157463994-157464394 | Common:5; Rare:105 |