| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107743582-107743802 | Common:3; Rare:84 | ||||
| chr7:107744053-107744171 | Rare:37 | ||||
| chr7:108002855-108003078 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr7:108526099-108526457 | Common:5; Rare:111 | ||||
| chr7:108569550-108570013 | Common:3; Rare:169 | ||||
| chr7:112206306-112206789 | Common:2; Rare:165 | ||||
| chr7:112450207-112450518 | Common:6; Rare:98 | ||||
| chr7:116210379-116210686 | Common:4; Rare:76 | ||||
| chr7:116499508-116499823 | Common:3; Rare:110 | ||||
| chr7:117872211-117872379 | Common:2; Rare:37 | ||||
| chr7:118183947-118184199 | Common:2; Rare:96 | ||||
| chr7:118214525-118214653 | Common:2; Rare:41 | ||||
| chr7:120950498-120950819 | Common:3; Rare:102 | ||||
| chr7:121396224-121396520 | Common:1; Rare:97 | ||||
| chr7:122144217-122144440 | Common:1; Rare:47 |