TABLE 3.

Some databases that may be used for driver identification.

Tools	Functional annotation	Link	References
LincSNP 2.0	Store and annotate disease-associated SNVs in human lncRNAs and their transcription factor binding sites (TFBSs)	http://bioinfo.hrbmu.edu.cn/LincSNP	Ning et al., 2017
lncRNASNP2	Comprehensive information of SNVs and mutations in lncRNAs, as well as their impacts on lncRNA structure and function	http://bioinfo.life.hust.edu.cn/lncRNASNP2	Miao et al., 2018
LncVar	A database of genetic variation associated with long non-coding genes in six species	http://bioinfo.ibp.ac.cn/LncVar	Chen et al., 2017
The 1000 Genomes Project	The largest public catalog of human variation and genotype data	http://www.internationalgenome.org/	Genomes Project et al., 2015
dbSNP	A public-domain archive for a broad collection of simple genetic polymorphisms	https://www.ncbi.nlm.nih.gov/snp
GWAS Catalog	A catalog that has provided data from published genome-wide association studies	www.ebi.ac.uk/gwas/	MacArthur et al., 2017
GWAS4D	A web server that systematically evaluates GWAS signals and identifies context-specific regulatory variants	http://mulinlab.tmu.edu.cn/gwas4d	Huang et al., 2018

SNVs, single-nucleotide variants; lncRNAs, long non-coding RNAs; GWAS, genome-wide association study.