| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105522172-105522344 | Common:4; Rare:106 | ||||
| chr7:105532054-105532267 | Common:6; Rare:109 | ||||
| chr7:105876425-105876840 | Common:12; Rare:217 | ||||
| chr7:106112200-106112518 | Common:6; Rare:207 | ||||
| chr7:106284516-106284673 | Common:1; Rare:47 | ||||
| chr7:106284885-106285276 | Common:4; Rare:301 | ||||
| chr7:106660999-106661279 | Common:2; Rare:71 | ||||
| chr7:107168122-107169053 | Common:3; Rare:373 | ||||
| chr7:107169580-107170085 | Common:8; Rare:244 | ||||
| chr7:107563803-107564062 | Common:4; Rare:200; Clinvar:4; Clinvar (benign):8 | ||||
| chr7:107564280-107564740 | Common:5; Rare:169; Clinvar:6; Clinvar (benign):2 | ||||
| chr7:107579740-107580020 | Rare:102 | ||||
| chr7:107580106-107580307 | Common:4; Rare:126 | ||||
| chr7:107580350-107580770 | Common:5; Rare:180 | ||||
| chr7:107743510-107743860 | Common:8; Rare:201 |