Regulator ID	target symbol	target name	hgnc_id	ensembl_gene_id	uniprot ID	Entrez_id	type	type_class	cell_line	cell_id	species	cell_disease	ICD_disease	method	PMID	GSE	log2FoldChange	perturbation	direction	pvalue
REG00025	TCEB3C	elongin A3, pseudogene	HGNC:24617	ENSG00000288631	.	162699	Unknown	Other	Hela	CVCL_0030	Homo sapiens	Cervical cancer	2C77: Cervix uteri cancer	RIP-seq	28106072	GSE86214	Inf	.	.	.
REG00025	C5orf64	Chromosome 5 putative open reading frame 64	HGNC:26744	ENSG00000178722	CE064_HUMAN	285668	Unknown	Other	HEK293T	CVCL_0063	Homo sapiens	Normal	.	iCLIP-seq	27602518	GSE78030	.	.	.	.
REG00025	C1orf220	Chromosome 1 putative open reading frame 220	HGNC:33805	ENSG00000213057	CA220_HUMAN	400798	Unknown	Other	Hela	CVCL_0030	Homo sapiens	Cervical cancer	2C77: Cervix uteri cancer	RIP-seq	28106072	GSE86214	2.60E+00	.	.	.