| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:148698556-148698965 | Common:3; Rare:147 | ||||
| chr7:149028402-149028969 | Common:7; Rare:204 | ||||
| chr7:149126261-149126408 | Common:6; Rare:46 | ||||
| chr7:150379084-150379327 | Common:1; Rare:78 | ||||
| chr7:151059505-151059716 | Common:1; Rare:63 | ||||
| chr7:151080782-151080955 | Rare:51 | ||||
| chr7:151227166-151227435 | Common:1; Rare:71 | ||||
| chr7:152025569-152025775 | Rare:83 | ||||
| chr7:152676099-152676295 | Common:2; Rare:82; Clinvar (benign):6 | ||||
| chr7:155644349-155644737 | Common:2; Rare:133 | ||||
| chr7:157336778-157337108 | Common:3; Rare:157; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158856433-158856625 | Common:5; Rare:66 | ||||
| chr8:232176-232436 | Common:3; Rare:104 | ||||
| chr8:1755616-1755783 | Common:3; Rare:55 | ||||
| chr8:6406527-6406673 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):1 |