| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44044572-44044752 | Common:2; Rare:53 | ||||
| chr7:44104592-44104822 | Common:2; Rare:76 | ||||
| chr7:44573881-44574092 | Common:3; Rare:71 | ||||
| chr7:44581795-44581856 | Rare:28 | ||||
| chr7:44582122-44582532 | Common:1; Rare:158 | ||||
| chr7:44606440-44606653 | Common:1; Rare:69 | ||||
| chr7:44606773-44607103 | Common:2; Rare:106 | ||||
| chr7:44748318-44748592 | Common:2; Rare:67 | ||||
| chr7:44796375-44796784 | Common:3; Rare:159 | ||||
| chr7:44978988-44979189 | Rare:34 | ||||
| chr7:44999986-45000285 | Common:1; Rare:68 | ||||
| chr7:45111665-45111806 | Common:1; Rare:53 | ||||
| chr7:48088859-48089278 | Common:6; Rare:106 | ||||
| chr7:50450311-50450476 | Common:1; Rare:79 | ||||
| chr7:55018976-55019253 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):2 |