| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:93232194-93232396 | Common:2; Rare:38 | ||||
| chr7:93921775-93922177 | Common:5; Rare:101 | ||||
| chr7:94394532-94394847 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:94425755-94426050 | Rare:91; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:94656059-94656387 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
| chr7:95396363-95396472 | Common:2; Rare:43 | ||||
| chr7:95596155-95596749 | Common:7; Rare:152 | ||||
| chr7:95596868-95596953 | Common:3; Rare:9 | ||||
| chr7:96321993-96322088 | Rare:59; Clinvar:3 | ||||
| chr7:97117472-97117759 | Common:2; Rare:123 | ||||
| chr7:98252136-98252372 | Common:1; Rare:54 | ||||
| chr7:98282098-98282431 | Common:2; Rare:118 | ||||
| chr7:98617106-98617285 | Rare:65 | ||||
| chr7:99325795-99325968 | Common:1; Rare:70 | ||||
| chr7:99408534-99408710 | Common:2; Rare:51 |