| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44582104-44582525 | Common:1; Rare:162 | ||||
| chr7:44606428-44606635 | Common:1; Rare:71 | ||||
| chr7:44606799-44607141 | Common:3; Rare:104 | ||||
| chr7:44748309-44748591 | Common:2; Rare:68 | ||||
| chr7:44796384-44796780 | Common:3; Rare:155 | ||||
| chr7:44848227-44848493 | Common:2; Rare:67 | ||||
| chr7:44999553-44999743 | Common:4; Rare:67 | ||||
| chr7:45111638-45111825 | Common:1; Rare:77 | ||||
| chr7:47979500-47979784 | Common:1; Rare:107 | ||||
| chr7:48089006-48089228 | Common:2; Rare:45 | ||||
| chr7:50450291-50450476 | Common:1; Rare:85 | ||||
| chr7:50561030-50561262 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:54541860-54542004 | Rare:27 | ||||
| chr7:54542149-54542518 | Common:2; Rare:97 | ||||
| chr7:54546519-54546687 | Common:7; Rare:80 |