| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:15686549-15686811 | Common:3; Rare:78 | ||||
| chr7:16645721-16646229 | Common:5; Rare:180 | ||||
| chr7:17298500-17298672 | Common:2; Rare:46 | ||||
| chr7:17940412-17940542 | Common:1; Rare:77 | ||||
| chr7:21427839-21428170 | Common:1; Rare:117 | ||||
| chr7:22822676-22822901 | Common:2; Rare:94 | ||||
| chr7:23105682-23105890 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23181932-23182096 | Rare:71 | ||||
| chr7:24757420-24757539 | Common:1; Rare:36 | ||||
| chr7:25125207-25125633 | Rare:176; Clinvar:3 | ||||
| chr7:26200573-26201008 | Common:2; Rare:211 | ||||
| chr7:26201187-26201290 | Rare:47 | ||||
| chr7:26201323-26201555 | Rare:82 | ||||
| chr7:26201574-26201800 | Common:2; Rare:121 | ||||
| chr7:27095986-27096198 | Rare:62 |