| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5045779-5045860 | Common:2; Rare:41 | ||||
| chr7:5423819-5424058 | Common:3; Rare:59 | ||||
| chr7:5425425-5425774 | Rare:101 | ||||
| chr7:5513732-5513906 | Common:2; Rare:75 | ||||
| chr7:5530522-5530866 | Common:1; Rare:127; Clinvar (benign):4 | ||||
| chr7:5562709-5562924 | Rare:57 | ||||
| chr7:6008913-6009350 | Common:5; Rare:195; Clinvar:20; Clinvar (benign):24; Clinvar (pathogenic):3 | ||||
| chr7:6059033-6059324 | Common:5; Rare:110 | ||||
| chr7:6104617-6105009 | Common:5; Rare:138 | ||||
| chr7:6172747-6172838 | Rare:38 | ||||
| chr7:6272534-6272806 | Common:1; Rare:134 | ||||
| chr7:6447854-6448071 | Common:1; Rare:91 | ||||
| chr7:6483997-6484263 | Common:2; Rare:127 | ||||
| chr7:6577359-6577495 | Common:1; Rare:43 | ||||
| chr7:6706927-6707109 | Common:2; Rare:73 |