| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:1570015-1570146 | Common:1; Rare:43 | ||||
| chr7:2242160-2242270 | Common:2; Rare:66 | ||||
| chr7:2354047-2354114 | Rare:35 | ||||
| chr7:2403278-2403622 | Common:1; Rare:135 | ||||
| chr7:2555485-2555838 | Common:5; Rare:96 | ||||
| chr7:2558870-2559155 | Common:2; Rare:118 | ||||
| chr7:4775401-4775684 | Common:7; Rare:135; Clinvar:1 | ||||
| chr7:5425497-5425767 | Rare:75 | ||||
| chr7:5513707-5513886 | Common:1; Rare:75 | ||||
| chr7:6009018-6009350 | Common:4; Rare:144; Clinvar:9; Clinvar (benign):15 | ||||
| chr7:6059033-6059331 | Common:5; Rare:113 | ||||
| chr7:6104626-6104946 | Common:5; Rare:122 | ||||
| chr7:6272563-6272759 | Common:1; Rare:92 | ||||
| chr7:6374364-6374762 | Common:3; Rare:142 | ||||
| chr7:6447891-6448071 | Common:1; Rare:71 |