| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27662695-27663149 | Common:14; Rare:304 | ||||
| chr7:27740022-27740248 | Common:11; Rare:131 | ||||
| chr7:29146304-29147050 | Common:17; Rare:436 | ||||
| chr7:29193860-29194545 | Rare:182 | ||||
| chr7:29194664-29194911 | Common:2; Rare:103 | ||||
| chr7:29483223-29483801 | Common:11; Rare:227 | ||||
| chr7:29563645-29563946 | Common:3; Rare:134 | ||||
| chr7:29564230-29564430 | Common:1; Rare:78 | ||||
| chr7:29564610-29565250 | Common:2; Rare:224 | ||||
| chr7:29989713-29989924 | Rare:169 | ||||
| chr7:30026520-30026994 | Common:1; Rare:202; Clinvar (benign):1 | ||||
| chr7:30028215-30028465 | Common:2; Rare:159 | ||||
| chr7:30284250-30284800 | Common:12; Rare:431 | ||||
| chr7:30478670-30479060 | Common:8; Rare:191; Clinvar:2 | ||||
| chr7:30504744-30505068 | Common:2; Rare:202 |