| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:118214534-118214664 | Common:2; Rare:44 | ||||
| chr7:120273595-120273673 | Rare:26 | ||||
| chr7:120273682-120273720 | Rare:9 | ||||
| chr7:120950498-120950825 | Common:3; Rare:104 | ||||
| chr7:121396224-121396548 | Common:1; Rare:112 | ||||
| chr7:121872949-121873237 | Common:4; Rare:86 | ||||
| chr7:121873301-121873540 | Common:5; Rare:78 | ||||
| chr7:122144229-122144440 | Common:1; Rare:44 | ||||
| chr7:123534573-123534794 | Common:4; Rare:47 | ||||
| chr7:123557773-123558027 | Common:1; Rare:64 | ||||
| chr7:123748868-123749257 | Common:3; Rare:138 | ||||
| chr7:124929793-124929983 | Common:3; Rare:61 | ||||
| chr7:127585546-127585699 | Common:2; Rare:57 | ||||
| chr7:127651820-127652231 | Common:3; Rare:119 | ||||
| chr7:128409950-128410265 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 |