| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88811579-88811626 | Rare:8 | ||||
| chr7:88898586-88898886 | Common:3; Rare:39 | ||||
| chr7:91263279-91263569 | Common:1; Rare:53 | ||||
| chr7:91265503-91265612 | Rare:30 | ||||
| chr7:91266874-91267189 | Common:2; Rare:67 | ||||
| chr7:91267656-91267949 | Rare:47 | ||||
| chr7:91267951-91268180 | Rare:44 | ||||
| chr7:94396794-94397009 | Rare:36 | ||||
| chr7:94404553-94404903 | Rare:87; Clinvar:7; Clinvar (pathogenic):1 | ||||
| chr7:94409318-94409819 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr7:94410239-94410526 | Rare:62; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr7:94420407-94420658 | Rare:67; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr7:95544985-95545230 | Common:5; Rare:44 | ||||
| chr7:95550310-95550449 | Common:2; Rare:23 | ||||
| chr7:95552174-95552192 | Common:1; Rare:12 |