| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:48088866-48089238 | Common:4; Rare:90 | ||||
| chr7:55572328-55572635 | Common:1; Rare:112 | ||||
| chr7:56051405-56051845 | Common:1; Rare:166; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106404-56106735 | Common:9; Rare:113 | ||||
| chr7:66114791-66114898 | Common:1; Rare:52 | ||||
| chr7:66115238-66115357 | Rare:25 | ||||
| chr7:66996569-66996865 | Common:2; Rare:60 | ||||
| chr7:73683416-73683622 | Common:3; Rare:82 | ||||
| chr7:73738768-73739004 | Common:1; Rare:73 | ||||
| chr7:74174131-74174405 | Common:1; Rare:146 | ||||
| chr7:74254346-74254528 | Rare:84 | ||||
| chr7:75878857-75879088 | Common:12; Rare:87 | ||||
| chr7:75914944-75915173 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994528-75994772 | Common:4; Rare:129 | ||||
| chr7:76047943-76048194 | Common:2; Rare:86 |