| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76726408-76726916 | Common:5; Rare:192 | ||||
| chr17:76727149-76727275 | Common:1; Rare:43 | ||||
| chr17:76736456-76736645 | Rare:125 | ||||
| chr17:76737109-76737776 | Common:6; Rare:268 | ||||
| chr17:76737820-76738164 | Common:4; Rare:99 | ||||
| chr17:77086444-77086710 | Common:3; Rare:50 | ||||
| chr17:77088500-77088867 | Common:3; Rare:98 | ||||
| chr17:77089381-77089412 | Rare:11 | ||||
| chr17:77140219-77140392 | Rare:44 | ||||
| chr17:77140398-77140659 | Common:3; Rare:80 | ||||
| chr17:77140791-77141115 | Rare:105 | ||||
| chr17:77141606-77141711 | Rare:19 | ||||
| chr17:77281137-77281512 | Common:6; Rare:154 | ||||
| chr17:77319389-77319620 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77322071-77322279 | Rare:41 |