| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:121396265-121396586 | Common:1; Rare:111 | ||||
| chr7:121873002-121873237 | Common:3; Rare:77 | ||||
| chr7:122144229-122144437 | Common:1; Rare:41 | ||||
| chr7:123534573-123534794 | Common:4; Rare:47 | ||||
| chr7:123557751-123557980 | Common:1; Rare:60 | ||||
| chr7:123748848-123749305 | Common:3; Rare:161 | ||||
| chr7:124929791-124929961 | Common:3; Rare:57 | ||||
| chr7:124929970-124930005 | Rare:9 | ||||
| chr7:127585584-127585693 | Rare:33 | ||||
| chr7:127588305-127588496 | Rare:81 | ||||
| chr7:127588987-127589133 | Rare:45 | ||||
| chr7:127651957-127652256 | Common:1; Rare:91 | ||||
| chr7:128361623-128361791 | Common:1; Rare:50 | ||||
| chr7:128405862-128406129 | Common:2; Rare:92 | ||||
| chr7:128409924-128410076 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 |