| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:134295060-134295151 | Rare:31 | ||||
| chr7:134447981-134448490 | Common:3; Rare:149 | ||||
| chr7:134646545-134646854 | Common:8; Rare:92 | ||||
| chr7:134779274-134779748 | Rare:77 | ||||
| chr7:134891265-134891673 | Common:3; Rare:99 | ||||
| chr7:134965554-134965734 | Rare:33 | ||||
| chr7:135170431-135170849 | Common:3; Rare:147 | ||||
| chr7:135193644-135193715 | Rare:22 | ||||
| chr7:135510058-135510327 | Common:3; Rare:62 | ||||
| chr7:135619530-135619810 | Common:2; Rare:75 | ||||
| chr7:135662394-135662591 | Common:4; Rare:102 | ||||
| chr7:135977033-135977203 | Rare:50 | ||||
| chr7:136868428-136868939 | Common:2; Rare:103 | ||||
| chr7:136868957-136869411 | Common:3; Rare:89; Clinvar (benign):3 | ||||
| chr7:137343436-137343904 | Rare:135 |