| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44044627-44044733 | Common:1; Rare:29 | ||||
| chr7:44200847-44201067 | Common:2; Rare:75 | ||||
| chr7:44490589-44490753 | Common:1; Rare:65 | ||||
| chr7:44573866-44574053 | Common:3; Rare:58 | ||||
| chr7:44582164-44582497 | Common:1; Rare:130 | ||||
| chr7:44606812-44607055 | Common:2; Rare:70 | ||||
| chr7:44796389-44796775 | Common:3; Rare:152 | ||||
| chr7:45111672-45111799 | Common:1; Rare:48 | ||||
| chr7:48089064-48089265 | Common:2; Rare:52 | ||||
| chr7:50450322-50450440 | Common:1; Rare:47 | ||||
| chr7:55951780-55951931 | Rare:46 | ||||
| chr7:56051434-56051840 | Common:1; Rare:156; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114773-66114886 | Common:1; Rare:60 | ||||
| chr7:73683419-73683622 | Common:3; Rare:81 | ||||
| chr7:73738798-73739076 | Common:1; Rare:85 |