| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7389394-7389475 | Rare:17 | ||||
| chr6:7389740-7389851 | Common:1; Rare:35 | ||||
| chr6:7910780-7910910 | Rare:44 | ||||
| chr6:8064365-8064570 | Common:3; Rare:57 | ||||
| chr6:8435488-8435585 | Rare:43 | ||||
| chr6:10747617-10747806 | Common:2; Rare:71 | ||||
| chr6:10838510-10838655 | Common:3; Rare:42; Clinvar:3 | ||||
| chr6:11382243-11382554 | Common:3; Rare:73 | ||||
| chr6:12008625-12008826 | Common:1; Rare:49 | ||||
| chr6:13272589-13272761 | Rare:49 | ||||
| chr6:13328483-13328621 | Common:5; Rare:61 | ||||
| chr6:13615149-13615466 | Common:3; Rare:134 | ||||
| chr6:14117375-14118017 | Common:5; Rare:235 | ||||
| chr6:15533041-15533395 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:17705839-17706192 | Common:2; Rare:95 |