Variant report

Variant	rs9808431
Chromosome Location	chr2:32565753-32565754
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10176897	1.00[AMR][1000 genomes]
rs10177302	1.00[AMR][1000 genomes]
rs10192406	1.00[AMR][1000 genomes]
rs10194703	1.00[AMR][1000 genomes]
rs13401451	1.00[AMR][1000 genomes]
rs13406947	1.00[AMR][1000 genomes]
rs28453677	1.00[AMR][1000 genomes]
rs28509390	1.00[AMR][1000 genomes]
rs28594218	1.00[AMR][1000 genomes]
rs2886813	1.00[AMR][1000 genomes]
rs4952213	1.00[AMR][1000 genomes]
rs56237513	1.00[AMR][1000 genomes]
rs57496465	1.00[AMR][1000 genomes]
rs73922708	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949102	chr2:32030307-33011548	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv817386	chr2:32332893-32724794	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1001038	chr2:32333378-32657112	Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv1009359	chr2:32333378-32725117	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
5	nsv535613	chr2:32333378-32725117	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	esv2422335	chr2:32412330-33200581	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
7	nsv533153	chr2:32514528-33249136	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats 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 miRNA target site	54 gene(s)	inside rSNPs	diseases
8	esv2751888	chr2:32539236-33331549	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
9	nsv516173	chr2:32541438-33329957	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:32528800-32566200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:32536000-32581400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr2:32536200-32566000	Weak transcription	Thymus	Thymus
4	chr2:32536400-32565800	Weak transcription	Left Ventricle	heart
5	chr2:32536400-32567400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr2:32536600-32566400	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr2:32536800-32566400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr2:32546400-32567800	Weak transcription	Adipose Nuclei	Adipose
9	chr2:32547200-32567400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr2:32547200-32570600	Weak transcription	Fetal Stomach	stomach
11	chr2:32547200-32581200	Weak transcription	Primary B cells from cord blood	blood
12	chr2:32547400-32566400	Weak transcription	Primary T cells from cord blood	blood
13	chr2:32550000-32581200	Weak transcription	Stomach Smooth Muscle	stomach
14	chr2:32557600-32569200	Weak transcription	Fetal Intestine Small	intestine
15	chr2:32560200-32573800	Weak transcription	HSMM	muscle
16	chr2:32560600-32568800	Weak transcription	Placenta	Placenta

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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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