| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606440-44606653 | Common:1; Rare:69 | ||||
| chr7:44796410-44796784 | Common:3; Rare:146 | ||||
| chr7:44999733-44999751 | Rare:4 | ||||
| chr7:47979507-47979765 | Common:1; Rare:100 | ||||
| chr7:50450329-50450453 | Rare:51 | ||||
| chr7:51316637-51316960 | Common:4; Rare:105 | ||||
| chr7:55572328-55572617 | Common:1; Rare:108 | ||||
| chr7:56051420-56051985 | Common:1; Rare:200; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:65006679-65006806 | Common:1; Rare:32 | ||||
| chr7:66114753-66114904 | Common:1; Rare:71 | ||||
| chr7:66115194-66115353 | Rare:35 | ||||
| chr7:66682036-66682141 | Common:4; Rare:47 | ||||
| chr7:66996569-66996872 | Common:2; Rare:65 | ||||
| chr7:73303973-73304266 | Rare:93 | ||||
| chr7:73557566-73557769 | Common:2; Rare:68 |