| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:148698380-148698572 | Common:3; Rare:59 | ||||
| chr7:148698631-148699026 | Common:2; Rare:133 | ||||
| chr7:148884133-148884504 | Common:2; Rare:172; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:149028321-149028733 | Common:7; Rare:164 | ||||
| chr7:149028754-149028969 | Rare:62 | ||||
| chr7:149090638-149090907 | Rare:77 | ||||
| chr7:149126211-149126486 | Common:7; Rare:95 | ||||
| chr7:149147048-149147171 | Rare:17 | ||||
| chr7:149147231-149147723 | Common:5; Rare:113 | ||||
| chr7:149239509-149239721 | Common:2; Rare:56 | ||||
| chr7:149261934-149262236 | Common:2; Rare:100 | ||||
| chr7:149460586-149460704 | Rare:17 | ||||
| chr7:149460833-149461052 | Common:1; Rare:43 | ||||
| chr7:149461056-149461081 | Rare:2 | ||||
| chr7:149497652-149497894 | Common:2; Rare:72 |