| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:4882207-4882299 | Common:1; Rare:15 | ||||
| chr7:4882490-4882526 | Rare:7 | ||||
| chr7:5045817-5045931 | Common:3; Rare:55 | ||||
| chr7:5190056-5190260 | Common:1; Rare:89 | ||||
| chr7:5423757-5424058 | Common:3; Rare:77 | ||||
| chr7:5425417-5425765 | Rare:100 | ||||
| chr7:5513746-5513862 | Common:1; Rare:54 | ||||
| chr7:5529718-5530032 | Common:1; Rare:144 | ||||
| chr7:5530522-5530887 | Common:1; Rare:136; Clinvar (benign):4 | ||||
| chr7:5592651-5592839 | Common:1; Rare:65 | ||||
| chr7:5593397-5593617 | Common:1; Rare:68 | ||||
| chr7:5603293-5603549 | Common:2; Rare:92 | ||||
| chr7:5898646-5898820 | Common:4; Rare:34 | ||||
| chr7:6009021-6009413 | Common:4; Rare:167; Clinvar:10; Clinvar (benign):15 | ||||
| chr7:6009484-6009525 | Common:1; Rare:24 |