| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44978965-44979220 | Rare:50 | ||||
| chr7:44999576-44999777 | Common:4; Rare:72 | ||||
| chr7:44999886-45000322 | Common:1; Rare:106; Clinvar (benign):1 | ||||
| chr7:45027531-45027723 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr7:45111655-45111861 | Common:2; Rare:78 | ||||
| chr7:47979523-47979756 | Rare:86 | ||||
| chr7:48089019-48089286 | Common:3; Rare:70 | ||||
| chr7:56051557-56051833 | Rare:111; Clinvar:2 | ||||
| chr7:56064251-56064309 | Rare:40 | ||||
| chr7:56106455-56106691 | Common:5; Rare:68 | ||||
| chr7:65006625-65006866 | Common:2; Rare:74 | ||||
| chr7:66681965-66682188 | Common:5; Rare:96 | ||||
| chr7:66996557-66996872 | Common:2; Rare:73 | ||||
| chr7:73308786-73308865 | Rare:38 | ||||
| chr7:73578562-73578854 | Common:14; Rare:91 |