| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166342488-166342653 | Common:4; Rare:69 | ||||
| chr6:166956544-166956769 | Common:5; Rare:77; Clinvar:3 | ||||
| chr6:166999028-166999415 | Common:1; Rare:132 | ||||
| chr6:169701960-169702384 | Common:5; Rare:175 | ||||
| chr6:169702534-169702687 | Rare:77 | ||||
| chr6:169751526-169751651 | Rare:48; Clinvar (benign):2 | ||||
| chr6:170554195-170554440 | Common:1; Rare:76 | ||||
| chr7:519243-519287 | Rare:9 | ||||
| chr7:727213-727314 | Rare:35; Clinvar:2 | ||||
| chr7:1044461-1044654 | Common:3; Rare:84 | ||||
| chr7:1159973-1159976 | |||||
| chr7:1537256-1537483 | Rare:75 | ||||
| chr7:1555432-1555650 | Rare:80 | ||||
| chr7:1570018-1570146 | Common:1; Rare:43 | ||||
| chr7:2242166-2242261 | Common:2; Rare:58 |