| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106285539-106285592 | Rare:14 | ||||
| chr7:107168738-107169021 | Rare:98 | ||||
| chr7:107563848-107564037 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580126-107580459 | Common:3; Rare:119 | ||||
| chr7:107743588-107743861 | Common:4; Rare:106 | ||||
| chr7:107744002-107744171 | Common:1; Rare:52 | ||||
| chr7:108526071-108526377 | Common:3; Rare:99 | ||||
| chr7:108569592-108569981 | Common:1; Rare:141 | ||||
| chr7:112206343-112206765 | Common:2; Rare:142 | ||||
| chr7:112939705-112940014 | Common:4; Rare:113 | ||||
| chr7:116210417-116210676 | Common:3; Rare:62 | ||||
| chr7:116499521-116499851 | Common:3; Rare:116 | ||||
| chr7:116672274-116672449 | Common:1; Rare:44; Clinvar:2 | ||||
| chr7:116953184-116953492 | Common:3; Rare:64 | ||||
| chr7:117427467-117427658 | Common:1; Rare:88 |