| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:167826818-167827181 | Common:2; Rare:180 | ||||
| chr6:169702000-169702182 | Common:3; Rare:88 | ||||
| chr6:169751554-169751645 | Rare:36; Clinvar (benign):1 | ||||
| chr6:170554221-170554416 | Common:1; Rare:64 | ||||
| chr7:727236-727294 | Rare:19; Clinvar:1 | ||||
| chr7:1055292-1055393 | Rare:45 | ||||
| chr7:1537256-1537483 | Rare:75 | ||||
| chr7:1538212-1538336 | Rare:46 | ||||
| chr7:1570012-1570142 | Common:1; Rare:41 | ||||
| chr7:2242152-2242250 | Common:2; Rare:64 | ||||
| chr7:2403278-2403628 | Common:1; Rare:138 | ||||
| chr7:4775478-4775652 | Common:6; Rare:74; Clinvar:1 | ||||
| chr7:5513768-5513876 | Common:1; Rare:42 | ||||
| chr7:5592676-5592818 | Common:1; Rare:50 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 |