| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127651806-127652266 | Common:3; Rare:139 | ||||
| chr7:128343700-128344005 | Common:4; Rare:97 | ||||
| chr7:128409884-128410031 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455697-128455931 | Common:3; Rare:126 | ||||
| chr7:128476645-128476849 | Common:1; Rare:81 | ||||
| chr7:128672192-128672329 | Rare:26 | ||||
| chr7:128708946-128709106 | Common:1; Rare:28 | ||||
| chr7:128715261-128715413 | Common:2; Rare:27 | ||||
| chr7:128739185-128739425 | Common:1; Rare:63 | ||||
| chr7:128790723-128790819 | Common:1; Rare:20 | ||||
| chr7:129054521-129054576 | Rare:13 | ||||
| chr7:129054867-129055289 | Common:2; Rare:89 | ||||
| chr7:129434248-129434485 | Common:1; Rare:89 | ||||
| chr7:129502213-129502658 | Common:3; Rare:121 | ||||
| chr7:129611595-129611813 | Common:2; Rare:73 |