| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107580196-107580304 | Rare:42 | ||||
| chr7:107744073-107744219 | Rare:57 | ||||
| chr7:108001593-108001896 | Common:3; Rare:111; Clinvar:1 | ||||
| chr7:108569524-108570019 | Common:3; Rare:178 | ||||
| chr7:111090953-111091135 | Rare:34 | ||||
| chr7:112206368-112206806 | Common:2; Rare:159 | ||||
| chr7:112790347-112790452 | Rare:28 | ||||
| chr7:114922371-114922538 | Common:1; Rare:57 | ||||
| chr7:116210224-116210725 | Common:4; Rare:128 | ||||
| chr7:116499419-116500217 | Common:5; Rare:236 | ||||
| chr7:116524900-116525250 | Common:5; Rare:110; Clinvar (benign):2 | ||||
| chr7:116525627-116525816 | Rare:37 | ||||
| chr7:116526240-116526694 | Common:3; Rare:119; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:116953388-116953573 | Rare:63 | ||||
| chr7:117323045-117323394 | Rare:73 |