| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101245053-101245135 | Common:1; Rare:29 | ||||
| chr7:101321733-101321860 | Common:2; Rare:44 | ||||
| chr7:102464840-102465013 | Common:1; Rare:70 | ||||
| chr7:103347351-103347697 | Common:3; Rare:84 | ||||
| chr7:104207973-104208153 | Common:4; Rare:78 | ||||
| chr7:105014065-105014274 | Common:2; Rare:83 | ||||
| chr7:105532078-105532227 | Rare:41 | ||||
| chr7:105876481-105876818 | Common:6; Rare:99 | ||||
| chr7:106112208-106112487 | Common:3; Rare:92 | ||||
| chr7:107563867-107564021 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:107580147-107580284 | Common:2; Rare:54 | ||||
| chr7:107744070-107744173 | Rare:33 | ||||
| chr7:108526099-108526455 | Common:5; Rare:111 | ||||
| chr7:108569615-108569931 | Common:1; Rare:101 | ||||
| chr7:112206392-112206751 | Common:1; Rare:129 |