| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:35694544-35694742 | Common:1; Rare:42 | ||||
| chr7:35694873-35695251 | Common:4; Rare:107 | ||||
| chr7:35800938-35801255 | Common:2; Rare:133 | ||||
| chr7:36724374-36724578 | Common:2; Rare:46 | ||||
| chr7:37342753-37342854 | Rare:17 | ||||
| chr7:37353630-37353884 | Common:3; Rare:44 | ||||
| chr7:37448822-37448963 | Rare:37 | ||||
| chr7:37448966-37449360 | Common:2; Rare:94 | ||||
| chr7:38178030-38178396 | Common:3; Rare:106 | ||||
| chr7:39566314-39566421 | Common:1; Rare:51 | ||||
| chr7:39623360-39623738 | Rare:128 | ||||
| chr7:39949928-39950299 | Common:1; Rare:119 | ||||
| chr7:39951595-39951842 | Rare:97; Clinvar (benign):1 | ||||
| chr7:40134556-40134762 | Rare:67 | ||||
| chr7:42932160-42932407 | Rare:101 |