Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42773371-42773478 | Rare:32 | ||||
chr17:42798654-42798767 | Rare:36 | ||||
chr17:42833346-42833475 | Rare:48 | ||||
chr17:42851075-42851262 | Rare:47 | ||||
chr17:42964408-42964539 | Rare:63 | ||||
chr17:42980500-42980571 | Common:1; Rare:26 | ||||
chr17:42998278-42998522 | Common:4; Rare:74 | ||||
chr17:43022318-43022489 | Rare:49 | ||||
chr17:43025111-43025273 | Rare:34 | ||||
chr17:43125318-43125714 | Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
chr17:43170243-43170718 | Common:3; Rare:99 | ||||
chr17:43170962-43171274 | Common:1; Rare:107 | ||||
chr17:43211750-43211903 | Common:1; Rare:34 | ||||
chr17:43398878-43399007 | Common:1; Rare:39 | ||||
chr17:43483661-43484098 | Rare:130 |