The total number of records retrieved from this search are 25. Click on ID to see further detail.

CancerEnD_ID	Cancer Type	Enhancer Start	Enhancer Stop	Mutation	Reference Allele	Mutated Allele	Cosmic	Copy Number Change	Survival	Gene Name	Gene Start	Gene End	Source
CancerEnD_140852	SKCM	15513029	15513231	Confirmed somatic variant	A	G	COSN20383280	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140853	SKCM	16062752	16063225	Confirmed somatic variant	G	T	COSN6382878	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140854	SKCM	16062752	16063225	Confirmed somatic variant	G	A	COSN6382877	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140858	SKCM	16100753	16101130	Confirmed somatic variant	C	A	COSN23476829	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140859	SKCM	16103638	16104031	Confirmed somatic variant	G	A	COSN29034074	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140860	SKCM	16103638	16104031	Confirmed somatic variant	C	T	COSN28216104	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140861	SKCM	16103638	16104031	Confirmed somatic variant	C	T	COSN22573368	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140862	SKCM	16139034	16139449	Confirmed somatic variant	G	C	COSN4887434	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140863	SKCM	16139034	16139449	Confirmed somatic variant	A	C	COSN15035606	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140866	SKCM	16159777	16160100	Confirmed somatic variant	A	NA	COSN27579756	NA	No	CCDC171	15553086	16061663	TCGA+COSMIC
CancerEnD_140867	SKCM	17520540	17520838	Confirmed somatic variant	A	C	COSN21931969	NA	No	SH3GL2	17579082	17797129	TCGA+COSMIC
CancerEnD_140871	SKCM	211500	211823	Confirmed somatic variant	T	A	COSN23372279	NA	No	FOXD4	116231	118204	TCGA+COSMIC
CancerEnD_140872	SKCM	211500	211823	Confirmed somatic variant	C	G	COSN14689570	NA	No	FOXD4	116231	118204	TCGA+COSMIC
CancerEnD_140874	SKCM	5269155	5269233	Confirmed somatic variant	A	NA	COSN27410985	NA	No	INSL4	5231419	5235304	TCGA+COSMIC
CancerEnD_140876	SKCM	5269155	5269233	Confirmed somatic variant	A	NA	COSN29039428	NA	No	INSL4	5231419	5235304	TCGA+COSMIC
CancerEnD_140877	SKCM	6384866	6385180	Confirmed somatic variant	G	A	COSN16415732	NA	No	TPD52L3	6328375	6331900	TCGA+COSMIC
CancerEnD_140878	SKCM	969561	969923	Confirmed somatic variant	NA	C	COSN28362756	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140879	SKCM	969561	969923	Confirmed somatic variant	A	C	COSN5245790	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140880	SKCM	969561	969923	Confirmed somatic variant	C	A	COSN7578324	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140881	SKCM	969561	969923	Confirmed somatic variant	C	T	COSN16085909	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140882	SKCM	969561	969923	Confirmed somatic variant	C	T	COSN14861024	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140883	SKCM	972038	972418	Confirmed somatic variant	C	T	COSN17006014	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140884	SKCM	972038	972418	Confirmed somatic variant	G	A	COSN25774511	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140885	SKCM	972038	972418	Confirmed somatic variant	G	A	COSN6400088	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC
CancerEnD_140886	SKCM	972038	972418	Confirmed somatic variant	C	T	COSN25658857	NA	No	DMRT2	1049858	1057552	TCGA+COSMIC