| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1570012-1570142 | Common:1; Rare:41 | ||||
| chr7:2242168-2242268 | Common:2; Rare:60 | ||||
| chr7:2354047-2354137 | Rare:41 | ||||
| chr7:2403278-2403635 | Common:1; Rare:140 | ||||
| chr7:2555489-2555836 | Common:5; Rare:92 | ||||
| chr7:2558917-2559113 | Common:1; Rare:84 | ||||
| chr7:4775521-4775701 | Common:4; Rare:87; Clinvar:1 | ||||
| chr7:5045597-5045898 | Common:3; Rare:124 | ||||
| chr7:5190134-5190260 | Rare:53 | ||||
| chr7:5423776-5424058 | Common:3; Rare:70 | ||||
| chr7:5513742-5513886 | Common:1; Rare:63 | ||||
| chr7:5529774-5530077 | Common:1; Rare:139 | ||||
| chr7:6009021-6009376 | Common:4; Rare:150; Clinvar:9; Clinvar (benign):15 | ||||
| chr7:6026749-6027116 | Common:3; Rare:99 | ||||
| chr7:6104622-6104930 | Common:5; Rare:116 |