| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:127585584-127585653 | Rare:23 | ||||
| chr7:127588188-127588489 | Rare:110 | ||||
| chr7:127651826-127652235 | Common:3; Rare:121 | ||||
| chr7:128409908-128410044 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455729-128455965 | Common:2; Rare:126 | ||||
| chr7:128476645-128476822 | Common:1; Rare:66 | ||||
| chr7:128739091-128739427 | Common:3; Rare:99 | ||||
| chr7:128830140-128830460 | Common:4; Rare:85 | ||||
| chr7:128830573-128830804 | Common:1; Rare:81; Clinvar:6; Clinvar (benign):5 | ||||
| chr7:128841250-128841466 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr7:129054884-129055231 | Common:2; Rare:66 | ||||
| chr7:129434248-129434479 | Common:1; Rare:85 | ||||
| chr7:129611616-129611817 | Common:1; Rare:61 | ||||
| chr7:129951527-129951725 | Common:1; Rare:35 | ||||
| chr7:129952503-129952771 | Common:5; Rare:79 |