| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:28180474-28180673 | Common:1; Rare:62 | ||||
| chr7:29806260-29806571 | Common:2; Rare:78 | ||||
| chr7:29989722-29989898 | Rare:69 | ||||
| chr7:30026403-30026520 | Rare:38; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:30026638-30026735 | Rare:27 | ||||
| chr7:30284311-30284782 | Common:6; Rare:194 | ||||
| chr7:30478419-30478561 | Common:1; Rare:33 | ||||
| chr7:30478681-30478830 | Common:1; Rare:54 | ||||
| chr7:30504728-30505090 | Common:4; Rare:121 | ||||
| chr7:30594678-30595096 | Common:9; Rare:186; Clinvar:10; Clinvar (benign):18 | ||||
| chr7:30771299-30771562 | Common:1; Rare:88 | ||||
| chr7:31517129-31517364 | Common:3; Rare:47 | ||||
| chr7:31695881-31695999 | Common:2; Rare:19 | ||||
| chr7:32299368-32299525 | Common:1; Rare:22 | ||||
| chr7:32490287-32490468 | Common:1; Rare:59 |