| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:50450329-50450453 | Rare:51 | ||||
| chr7:55366305-55366330 | Rare:7 | ||||
| chr7:55964295-55964672 | Common:1; Rare:113 | ||||
| chr7:56051416-56051884 | Common:1; Rare:177; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064203-56064318 | Common:1; Rare:74 | ||||
| chr7:64562970-64563229 | Common:4; Rare:78 | ||||
| chr7:66115194-66115353 | Rare:35 | ||||
| chr7:66681987-66682147 | Common:4; Rare:72 | ||||
| chr7:66996557-66996924 | Common:2; Rare:88 | ||||
| chr7:73557574-73557741 | Common:2; Rare:59 | ||||
| chr7:73683412-73683807 | Common:4; Rare:174 | ||||
| chr7:73738786-73739024 | Common:1; Rare:69 | ||||
| chr7:74254385-74254520 | Rare:61 | ||||
| chr7:74453929-74454133 | Rare:55 | ||||
| chr7:75486240-75486452 | Common:2; Rare:80 |