| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:45111631-45111806 | Common:1; Rare:70 | ||||
| chr7:48088917-48089291 | Common:6; Rare:105 | ||||
| chr7:50450329-50450453 | Rare:51 | ||||
| chr7:50561036-50561214 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:50565312-50565536 | Rare:46 | ||||
| chr7:51316596-51317011 | Common:6; Rare:137 | ||||
| chr7:55365894-55366073 | Rare:74 | ||||
| chr7:56051429-56051866 | Common:1; Rare:168; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064185-56064332 | Common:2; Rare:92 | ||||
| chr7:56106402-56106715 | Common:9; Rare:108 | ||||
| chr7:66075787-66076074 | Rare:70; Clinvar (benign):2 | ||||
| chr7:66114773-66114992 | Common:1; Rare:97 | ||||
| chr7:66682024-66682192 | Common:6; Rare:80 | ||||
| chr7:66921052-66921268 | Rare:63 | ||||
| chr7:66996531-66996941 | Common:3; Rare:101 |