| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106285539-106285616 | Rare:21 | ||||
| chr7:106661150-106661200 | Common:1; Rare:9 | ||||
| chr7:107168705-107169034 | Rare:110 | ||||
| chr7:107169717-107169818 | Rare:34 | ||||
| chr7:107563818-107564047 | Common:2; Rare:129; Clinvar:3; Clinvar (benign):6 | ||||
| chr7:107564330-107564603 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:107580071-107580530 | Common:4; Rare:143 | ||||
| chr7:107743569-107743819 | Common:3; Rare:97 | ||||
| chr7:107743976-107744205 | Common:1; Rare:74 | ||||
| chr7:107929562-107929707 | Rare:35; Clinvar:1 | ||||
| chr7:108176776-108176910 | Common:1; Rare:30 | ||||
| chr7:108526032-108526411 | Common:5; Rare:115 | ||||
| chr7:108569419-108570100 | Common:5; Rare:229 | ||||
| chr7:111090741-111091454 | Common:1; Rare:138 | ||||
| chr7:111392944-111393015 | Rare:21 |