| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5423760-5424090 | Common:3; Rare:79 | ||||
| chr7:5425439-5425816 | Rare:111 | ||||
| chr7:5513741-5513942 | Common:2; Rare:88 | ||||
| chr7:5529589-5529989 | Common:3; Rare:360; Clinvar:2; Clinvar (benign):9 | ||||
| chr7:5530593-5530814 | Common:1; Rare:71 | ||||
| chr7:5562640-5563040 | Common:1; Rare:93 | ||||
| chr7:5592815-5593557 | Common:1; Rare:329 | ||||
| chr7:5594690-5595200 | Common:1; Rare:137 | ||||
| chr7:5781591-5781703 | Rare:54 | ||||
| chr7:6008979-6009353 | Common:4; Rare:170; Clinvar:20; Clinvar (benign):22; Clinvar (pathogenic):3 | ||||
| chr7:6059112-6059332 | Common:4; Rare:80 | ||||
| chr7:6104559-6104975 | Common:5; Rare:170 | ||||
| chr7:6272596-6272799 | Common:1; Rare:99 | ||||
| chr7:6348910-6349163 | Common:4; Rare:103 | ||||
| chr7:6374257-6374535 | Common:3; Rare:104 |