| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102464844-102465014 | Common:1; Rare:69 | ||||
| chr7:102748706-102749022 | Common:2; Rare:71 | ||||
| chr7:103297310-103297496 | Common:2; Rare:70 | ||||
| chr7:103344697-103344869 | Common:1; Rare:56 | ||||
| chr7:104207945-104208146 | Common:4; Rare:100 | ||||
| chr7:105013579-105013715 | Common:1; Rare:46 | ||||
| chr7:105014055-105014261 | Common:2; Rare:86 | ||||
| chr7:105532078-105532225 | Rare:41 | ||||
| chr7:105876484-105876829 | Common:6; Rare:101 | ||||
| chr7:106112208-106112485 | Common:3; Rare:91 | ||||
| chr7:106112547-106112596 | Rare:25 | ||||
| chr7:106284973-106285263 | Common:2; Rare:109 | ||||
| chr7:107563879-107564043 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):5 | ||||
| chr7:107580147-107580285 | Common:2; Rare:54 | ||||
| chr7:107744023-107744177 | Rare:48 |