| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166342443-166342653 | Common:5; Rare:88 | ||||
| chr6:166999074-166999424 | Common:1; Rare:118 | ||||
| chr6:169253819-169254095 | Rare:48 | ||||
| chr6:169702027-169702188 | Common:3; Rare:81 | ||||
| chr6:169702403-169702678 | Common:2; Rare:133 | ||||
| chr6:169751520-169751644 | Rare:45; Clinvar (benign):1 | ||||
| chr7:727249-727281 | Rare:10; Clinvar:1 | ||||
| chr7:727283-727326 | Rare:11 | ||||
| chr7:727572-727890 | Common:1; Rare:58 | ||||
| chr7:1138196-1138504 | Common:2; Rare:89 | ||||
| chr7:1448436-1448622 | Rare:55 | ||||
| chr7:1570018-1570142 | Common:1; Rare:41 | ||||
| chr7:2242171-2242290 | Common:2; Rare:66 | ||||
| chr7:2354041-2354114 | Rare:36 | ||||
| chr7:2403304-2403600 | Common:1; Rare:113 |