| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:25125228-25125720 | Common:1; Rare:186; Clinvar:3 | ||||
| chr7:26196555-26196903 | Common:2; Rare:137; Clinvar (benign):1 | ||||
| chr7:26197079-26197735 | Common:3; Rare:246; Clinvar (benign):2 | ||||
| chr7:26200566-26201080 | Common:2; Rare:240 | ||||
| chr7:26201383-26201550 | Rare:59 | ||||
| chr7:26201558-26201824 | Common:2; Rare:141 | ||||
| chr7:26864376-26864396 | Common:1; Rare:4 | ||||
| chr7:26864421-26864659 | Common:1; Rare:65 | ||||
| chr7:27096020-27096136 | Rare:35 | ||||
| chr7:28180511-28180692 | Common:1; Rare:61 | ||||
| chr7:30026682-30026825 | Rare:33 | ||||
| chr7:30504762-30505049 | Common:1; Rare:95 | ||||
| chr7:30594709-30595134 | Common:7; Rare:188; Clinvar:11; Clinvar (benign):15 | ||||
| chr7:32490378-32490520 | Common:1; Rare:39 | ||||
| chr7:32495256-32495564 | Rare:77 |