| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169232662-169232989 | Common:1; Rare:94 | ||||
| chr6:169250733-169250940 | Common:1; Rare:41 | ||||
| chr7:5603420-5603571 | Common:2; Rare:58 | ||||
| chr7:15685889-15686287 | Common:1; Rare:168 | ||||
| chr7:26193252-26193672 | Rare:147; Clinvar (benign):1 | ||||
| chr7:27192261-27192312 | Rare:8 | ||||
| chr7:32728590-32728879 | Common:10; Rare:98 | ||||
| chr7:44019101-44019389 | Common:2; Rare:106 | ||||
| chr7:44107915-44108103 | Common:2; Rare:62; Clinvar (pathogenic):1 | ||||
| chr7:44467646-44467881 | Common:3; Rare:44 | ||||
| chr7:44986577-44986734 | Common:3; Rare:78 | ||||
| chr7:45768893-45769141 | Common:3; Rare:71 | ||||
| chr7:55689466-55689703 | Rare:39 | ||||
| chr7:65081226-65081397 | Common:2; Rare:59 | ||||
| chr7:65750431-65750470 | Common:2; Rare:7 |