Variant report

Variant	rs16890419
Chromosome Location	chr6:159904910-159904911
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11964102	0.96[ASN][1000 genomes]
rs12333204	0.95[ASN][1000 genomes]
rs12530069	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13215914	0.95[ASN][1000 genomes]
rs16890423	0.96[ASN][1000 genomes]
rs2123165	0.96[ASN][1000 genomes]
rs2341625	0.93[ASN][1000 genomes]
rs2341626	0.93[ASN][1000 genomes]
rs2341627	0.95[ASN][1000 genomes]
rs2341628	0.95[ASN][1000 genomes]
rs4431465	0.95[ASN][1000 genomes]
rs4479966	0.91[ASN][1000 genomes]
rs4554341	0.95[ASN][1000 genomes]
rs4634488	0.93[ASN][1000 genomes]
rs4708830	0.95[ASN][1000 genomes]
rs4708833	0.95[ASN][1000 genomes]
rs4708834	0.95[ASN][1000 genomes]
rs4709332	0.95[ASN][1000 genomes]
rs4709333	0.95[ASN][1000 genomes]
rs4709338	0.95[ASN][1000 genomes]
rs4709339	0.96[ASN][1000 genomes]
rs4709341	0.94[ASN][1000 genomes]
rs57541589	0.93[ASN][1000 genomes]
rs62438468	0.96[ASN][1000 genomes]
rs6913852	0.93[ASN][1000 genomes]
rs6914036	0.95[ASN][1000 genomes]
rs6941120	0.90[ASN][1000 genomes]
rs720692	0.96[ASN][1000 genomes]
rs7738744	0.93[ASN][1000 genomes]
rs7740788	0.95[ASN][1000 genomes]
rs7748399	0.95[ASN][1000 genomes]
rs7748779	0.96[ASN][1000 genomes]
rs9295102	0.96[ASN][1000 genomes]
rs9456407	0.86[ASN][1000 genomes]
rs9456412	0.96[ASN][1000 genomes]
rs9456415	0.96[ASN][1000 genomes]
rs9457648	0.80[ASN][1000 genomes]
rs9457651	0.95[ASN][1000 genomes]
rs9457653	0.96[ASN][1000 genomes]
rs9457655	0.96[ASN][1000 genomes]
rs9457656	0.96[ASN][1000 genomes]
rs9457657	0.96[ASN][1000 genomes]
rs9457658	0.92[ASN][1000 genomes]
rs9457664	0.94[ASN][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	nsv1030483	chr6:159475679-159910480	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv538490	chr6:159475679-159910480	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	esv2763604	chr6:159509373-159942955	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1019191	chr6:159555100-160043247	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:159904000-159905600	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:159904400-159908000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:159904800-159916800	Weak transcription	Aorta	Aorta

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

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