| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88306873-88307089 | Rare:47 | ||||
| chr7:90154353-90154514 | Rare:41 | ||||
| chr7:90211633-90211890 | Common:3; Rare:78 | ||||
| chr7:90245083-90245243 | Rare:52 | ||||
| chr7:90334901-90335188 | Common:2; Rare:49 | ||||
| chr7:90346556-90346765 | Common:4; Rare:91 | ||||
| chr7:90383532-90383700 | Rare:36 | ||||
| chr7:90403361-90403530 | Rare:46 | ||||
| chr7:90595880-90596097 | Common:6; Rare:81 | ||||
| chr7:90596218-90596443 | Rare:73 | ||||
| chr7:91880655-91880834 | Common:2; Rare:49 | ||||
| chr7:91940403-91940662 | Common:1; Rare:52 | ||||
| chr7:91940808-91941039 | Common:4; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134364-92134605 | Rare:76 | ||||
| chr7:92134734-92134908 | Common:3; Rare:47 |