| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:2314344-2314627 | Common:5; Rare:109 | ||||
| chr7:2354041-2354127 | Rare:42 | ||||
| chr7:2403282-2403628 | Common:1; Rare:136 | ||||
| chr7:2555485-2555839 | Common:5; Rare:97 | ||||
| chr7:2558877-2559132 | Common:2; Rare:109 | ||||
| chr7:2652571-2652830 | Common:1; Rare:64 | ||||
| chr7:4775462-4775691 | Common:6; Rare:111; Clinvar:1 | ||||
| chr7:4804054-4804201 | Rare:41 | ||||
| chr7:5190126-5190244 | Rare:43 | ||||
| chr7:5513742-5513897 | Common:1; Rare:69 | ||||
| chr7:6009006-6009355 | Common:4; Rare:154; Clinvar:13; Clinvar (benign):17; Clinvar (pathogenic):2 | ||||
| chr7:6059033-6059313 | Common:5; Rare:105 | ||||
| chr7:6104626-6105002 | Common:5; Rare:135 | ||||
| chr7:6272547-6272737 | Rare:90 | ||||
| chr7:6348760-6348850 | Common:3; Rare:32 |