| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:20331704-20331870 | Common:2; Rare:58 | ||||
| chr7:20786884-20787204 | Common:1; Rare:93 | ||||
| chr7:21427827-21428111 | Common:2; Rare:105 | ||||
| chr7:21542892-21543088 | Common:1; Rare:67 | ||||
| chr7:21543311-21543377 | Common:3; Rare:27; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:22822675-22822958 | Common:3; Rare:108 | ||||
| chr7:23013940-23013975 | Rare:9 | ||||
| chr7:23105625-23106305 | Common:5; Rare:246; Clinvar:5; Clinvar (benign):3 | ||||
| chr7:23106524-23106663 | Common:1; Rare:20 | ||||
| chr7:23181840-23182262 | Common:5; Rare:178 | ||||
| chr7:23299197-23299406 | Common:2; Rare:112 | ||||
| chr7:23307806-23307918 | Rare:40 | ||||
| chr7:23467891-23468132 | Common:3; Rare:62 | ||||
| chr7:23470163-23470640 | Common:2; Rare:133 | ||||
| chr7:23531113-23531390 | Rare:55 |