| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44606459-44606646 | Common:1; Rare:62 | ||||
| chr7:44606779-44607078 | Common:2; Rare:96 | ||||
| chr7:44796388-44796790 | Common:3; Rare:155 | ||||
| chr7:44999985-45000261 | Common:1; Rare:65 | ||||
| chr7:45111665-45111799 | Common:1; Rare:50 | ||||
| chr7:50450322-50450453 | Common:1; Rare:54 | ||||
| chr7:55018910-55019117 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:55365983-55366073 | Rare:33 | ||||
| chr7:55572328-55572669 | Common:2; Rare:122 | ||||
| chr7:56051416-56051894 | Common:1; Rare:181; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064163-56064329 | Common:2; Rare:101 | ||||
| chr7:64882442-64882629 | Common:2; Rare:46 | ||||
| chr7:65982155-65982353 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114740-66114901 | Common:1; Rare:72 | ||||
| chr7:66115194-66115354 | Rare:35 |