| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88306794-88307002 | Rare:46 | ||||
| chr7:88307007-88307108 | Rare:25 | ||||
| chr7:90211628-90211934 | Common:4; Rare:95 | ||||
| chr7:90245083-90245243 | Rare:52 | ||||
| chr7:90346589-90346757 | Common:4; Rare:72 | ||||
| chr7:90403380-90403530 | Rare:44 | ||||
| chr7:91880668-91880812 | Common:1; Rare:40 | ||||
| chr7:91940755-91941041 | Common:4; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:91941050-91941145 | Rare:31; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:92134409-92134612 | Rare:63 | ||||
| chr7:92134702-92134890 | Common:3; Rare:56 | ||||
| chr7:92245648-92245994 | Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528364-92528900 | Common:5; Rare:168; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92833902-92834074 | Rare:43 | ||||
| chr7:92836527-92836620 | Rare:21 |