Variant report

Variant	rs11971942
Chromosome Location	chr7:65656035-65656036
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10081219	1.00[EUR][1000 genomes]
rs10232498	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10234562	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10236404	1.00[EUR][1000 genomes]
rs10246941	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10247708	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10256705	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10266831	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10272408	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11979489	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12112556	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28447397	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28460479	1.00[AMR][1000 genomes]
rs28566023	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55983755	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73699720	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73699756	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	esv2761079	chr7:65092426-65689733	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	nsv1021186	chr7:65492601-65663438	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv1026559	chr7:65617368-66370805	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65652400-65656200	Enhancers	Liver	Liver
2	chr7:65652800-65660600	Weak transcription	Spleen	Spleen
3	chr7:65654800-65656200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:65655800-65657800	Weak transcription	HepG2	liver

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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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