Variant report

Variant	rs13426434
Chromosome Location	chr2:182304181-182304182
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10153755	0.94[AFR][1000 genomes]
rs10153780	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005870	chr2:181968637-182921439	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv536063	chr2:181968637-182921439	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv1002647	chr2:182078521-182392273	Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv536064	chr2:182078521-182392273	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
5	nsv834476	chr2:182179249-182360259	Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182301600-182306600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr2:182301800-182306200	Enhancers	Primary hematopoietic stem cells	blood
3	chr2:182301800-182306800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:182302400-182305400	Enhancers	Thymus	Thymus
5	chr2:182302800-182304200	Enhancers	Primary T cells from cord blood	blood
6	chr2:182302800-182304200	Enhancers	GM12878-XiMat	blood
7	chr2:182303000-182304600	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr2:182303600-182305800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr2:182303600-182308800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr2:182303600-182308800	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr2:182303800-182309400	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr2:182304000-182304400	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr2:182304000-182305000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:182304000-182305200	Weak transcription	HSMMtube	muscle
15	chr2:182304000-182305600	Enhancers	Dnd41	blood
16	chr2:182304000-182307800	Enhancers	Fetal Thymus	thymus
17	chr2:182304000-182308800	Weak transcription	Primary B cells from peripheral blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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