| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1028267-1028522 | Common:2; Rare:98 | ||||
| chr7:1087964-1088124 | Common:1; Rare:36 | ||||
| chr7:1138198-1138461 | Common:2; Rare:82 | ||||
| chr7:1537324-1537451 | Rare:41 | ||||
| chr7:1570018-1570146 | Common:1; Rare:43 | ||||
| chr7:2242171-2242268 | Common:2; Rare:57 | ||||
| chr7:2354036-2354093 | Rare:29 | ||||
| chr7:2403339-2403622 | Common:1; Rare:115 | ||||
| chr7:2558882-2559113 | Common:1; Rare:105 | ||||
| chr7:4775369-4775691 | Common:7; Rare:150; Clinvar:1 | ||||
| chr7:5423771-5424022 | Common:2; Rare:62 | ||||
| chr7:5425342-5425774 | Rare:123 | ||||
| chr7:5513746-5513865 | Common:1; Rare:54 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6447940-6448066 | Common:1; Rare:42 |