| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:169702600-169702817 | Rare:94 | ||||
| chr6:169751526-169751649 | Rare:47; Clinvar (benign):2 | ||||
| chr6:170306540-170306820 | Common:2; Rare:90 | ||||
| chr6:170554197-170554457 | Common:2; Rare:80 | ||||
| chr7:727242-727308 | Rare:21; Clinvar:1 | ||||
| chr7:975513-975660 | Common:1; Rare:62 | ||||
| chr7:1138194-1138475 | Common:2; Rare:85 | ||||
| chr7:1537185-1537500 | Rare:105 | ||||
| chr7:1570012-1570146 | Common:1; Rare:43 | ||||
| chr7:2242171-2242256 | Common:2; Rare:51 | ||||
| chr7:2249134-2249325 | Common:3; Rare:39 | ||||
| chr7:4775510-4775728 | Common:4; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:5513742-5513855 | Common:1; Rare:54 | ||||
| chr7:5592694-5593017 | Common:2; Rare:126 | ||||
| chr7:5593022-5593146 | Rare:30 |