| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66114750-66114895 | Common:1; Rare:70 | ||||
| chr7:66682040-66682229 | Common:6; Rare:83 | ||||
| chr7:71131395-71131712 | Common:5; Rare:105 | ||||
| chr7:73683399-73683659 | Common:3; Rare:118 | ||||
| chr7:73738798-73739029 | Common:1; Rare:67 | ||||
| chr7:74027996-74028267 | Common:1; Rare:91; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:74046684-74047054 | Common:1; Rare:100; Clinvar:1 | ||||
| chr7:74051907-74052524 | Common:1; Rare:145; Clinvar:1; Clinvar (benign):6 | ||||
| chr7:74053097-74053375 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr7:74174092-74174386 | Common:1; Rare:146 | ||||
| chr7:74209729-74210032 | Common:1; Rare:71 | ||||
| chr7:74254366-74254620 | Rare:105 | ||||
| chr7:74657965-74658025 | Rare:12 | ||||
| chr7:75914925-75915168 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994493-75994792 | Common:5; Rare:147 |