| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74890520-74890812 | Common:3; Rare:93 | ||||
| chr7:75359036-75359235 | Rare:3 | ||||
| chr7:82410567-82410820 | Common:3; Rare:59 | ||||
| chr7:91267624-91267777 | Rare:27 | ||||
| chr7:97972259-97972377 | Rare:29 | ||||
| chr7:100335881-100336146 | Common:1; Rare:86 | ||||
| chr7:105013586-105013644 | Rare:20 | ||||
| chr7:112995585-112995769 | Common:2; Rare:26 | ||||
| chr7:113118548-113118666 | Common:1; Rare:39 | ||||
| chr7:128843226-128843463 | Common:1; Rare:75; Clinvar:9; Clinvar (benign):3 | ||||
| chr7:128848582-128849203 | Common:3; Rare:184; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr7:128850932-128851360 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:128853471-128853835 | Common:1; Rare:102; Clinvar:5; Clinvar (benign):8 | ||||
| chr7:128856814-128857335 | Rare:138; Clinvar:15; Clinvar (benign):6 | ||||
| chr7:128858005-128858498 | Common:2; Rare:125; Clinvar:10; Clinvar (benign):14 |