| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:93788049-93788135 | Common:1; Rare:14 | ||||
| chr6:147156987-147157098 | Common:1; Rare:24 | ||||
| chr7:1124023-1124069 | Common:1; Rare:10 | ||||
| chr7:6165399-6165608 | Common:1; Rare:73 | ||||
| chr7:38335574-38335860 | Common:2; Rare:63 | ||||
| chr7:44983900-44983908 | Common:1; Rare:2 | ||||
| chr7:64500502-64500670 | Common:1; Rare:23 | ||||
| chr7:65750918-65751083 | Common:2; Rare:65 | ||||
| chr7:66493554-66493727 | Common:2; Rare:68 | ||||
| chr7:66654425-66654586 | Common:1; Rare:65 | ||||
| chr7:73005926-73006143 | Rare:13 | ||||
| chr7:94410274-94410477 | Rare:45; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:94423066-94423366 | Common:5; Rare:58; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr7:97972029-97972177 | Common:1; Rare:32 | ||||
| chr7:100335859-100336136 | Common:1; Rare:91 |