| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106660905-106661052 | Rare:61 | ||||
| chr7:107563861-107564021 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107579906-107580331 | Common:4; Rare:133 | ||||
| chr7:107744084-107744193 | Rare:38 | ||||
| chr7:107929601-107929779 | Common:1; Rare:34 | ||||
| chr7:108526039-108526416 | Common:5; Rare:118 | ||||
| chr7:108569565-108570019 | Common:3; Rare:164 | ||||
| chr7:111091069-111091165 | Rare:14 | ||||
| chr7:112206418-112206740 | Common:1; Rare:115 | ||||
| chr7:116499505-116499809 | Common:3; Rare:108 | ||||
| chr7:116525406-116525720 | Common:2; Rare:71 | ||||
| chr7:117323045-117323338 | Rare:63 | ||||
| chr7:118183952-118184202 | Common:2; Rare:96 | ||||
| chr7:122144204-122144426 | Common:1; Rare:48 | ||||
| chr7:123748934-123749226 | Common:3; Rare:102 |