| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:4775375-4775652 | Common:7; Rare:122; Clinvar:1 | ||||
| chr7:6009021-6009376 | Common:4; Rare:150; Clinvar:9; Clinvar (benign):15 | ||||
| chr7:6104626-6105003 | Common:5; Rare:135 | ||||
| chr7:6272556-6272774 | Common:1; Rare:104 | ||||
| chr7:6447940-6448028 | Rare:34 | ||||
| chr7:6706953-6707098 | Rare:54 | ||||
| chr7:7182344-7182705 | Common:4; Rare:135 | ||||
| chr7:7566979-7567033 | Rare:19 | ||||
| chr7:12687475-12687652 | Common:5; Rare:41 | ||||
| chr7:16645790-16646140 | Common:2; Rare:105 | ||||
| chr7:17298444-17298660 | Common:3; Rare:55 | ||||
| chr7:17940398-17940571 | Common:1; Rare:88 | ||||
| chr7:20330702-20330737 | Rare:12 | ||||
| chr7:20330755-20330918 | Rare:46 | ||||
| chr7:20331733-20331775 | Common:1; Rare:13 |