| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100336320-100336395 | Common:2; Rare:29 | ||||
| chr7:100365535-100365577 | Rare:8 | ||||
| chr7:100365780-100366068 | Common:1; Rare:71 | ||||
| chr7:100430790-100430810 | Rare:3 | ||||
| chr7:100444961-100445012 | Rare:10 | ||||
| chr7:100450514-100450659 | Rare:28 | ||||
| chr7:100478157-100478554 | Common:6; Rare:75 | ||||
| chr7:100527612-100527742 | Rare:18 | ||||
| chr7:100545434-100545677 | Common:2; Rare:26 | ||||
| chr7:100545733-100546044 | Rare:61 | ||||
| chr7:100546673-100546843 | Rare:30 | ||||
| chr7:100626652-100626864 | Common:1; Rare:76; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100694202-100694549 | Common:5; Rare:102 | ||||
| chr7:100705366-100705453 | Rare:17 | ||||
| chr7:100803542-100803820 | Common:3; Rare:56 |