Variant report

Variant	rs4943489
Chromosome Location	chr13:37903302-37903303
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs2038732	1.00[EUR][1000 genomes]
rs2038733	1.00[EUR][1000 genomes]
rs2038734	1.00[EUR][1000 genomes]
rs2093820	0.88[EUR][1000 genomes]
rs34265500	0.97[EUR][1000 genomes]
rs34783637	1.00[EUR][1000 genomes]
rs35019156	1.00[EUR][1000 genomes]
rs35789130	1.00[EUR][1000 genomes]
rs36053111	1.00[EUR][1000 genomes]
rs3858863	1.00[EUR][1000 genomes]
rs3940155	0.88[EUR][1000 genomes]
rs73181009	1.00[EUR][1000 genomes]
rs73181010	1.00[EUR][1000 genomes]
rs73181011	1.00[EUR][1000 genomes]
rs73181013	0.83[EUR][1000 genomes]
rs73181014	1.00[EUR][1000 genomes]
rs73181015	1.00[EUR][1000 genomes]
rs73181017	1.00[EUR][1000 genomes]
rs73181022	1.00[EUR][1000 genomes]
rs9532034	1.00[EUR][1000 genomes]
rs9532035	1.00[EUR][1000 genomes]
rs9532036	0.98[EUR][1000 genomes]
rs9547794	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9547795	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9547796	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9547801	0.88[EUR][1000 genomes]
rs9547803	1.00[EUR][1000 genomes]
rs9547804	1.00[EUR][1000 genomes]
rs9547805	1.00[EUR][1000 genomes]
rs9547806	1.00[EUR][1000 genomes]
rs9547807	1.00[EUR][1000 genomes]
rs9547809	1.00[EUR][1000 genomes]
rs9547810	1.00[EUR][1000 genomes]
rs9547811	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv899994	chr13:37816086-38087145	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1038850	chr13:37820489-38209571	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv34109	chr13:37843819-38276391	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37901200-37903600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links