Variant report

Variant	rs11676369
Chromosome Location	chr2:11878495-11878496
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10185333	0.98[ASN][1000 genomes]
rs10191952	0.95[ASN][1000 genomes]
rs10191977	0.95[ASN][1000 genomes]
rs4669778	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs62113306	0.82[ASN][1000 genomes]
rs6731096	0.82[ASN][1000 genomes]
rs72773975	0.93[ASN][1000 genomes]
rs893349	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][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	nsv1010506	chr2:11430965-12057286	Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS 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 miRNA target site	88 gene(s)	inside rSNPs	diseases
2	nsv535585	chr2:11430965-12057286	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
4	nsv580973	chr2:11864946-11898931	Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv580974	chr2:11867841-11898931	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11874800-11878800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr2:11875000-11878800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:11875200-11883000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr2:11876000-11878600	Weak transcription	Colonic Mucosa	Colon
5	chr2:11876000-11878600	Weak transcription	Hela-S3	cervix
6	chr2:11876200-11878600	Weak transcription	Liver	Liver
7	chr2:11876800-11878600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:11877000-11882800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:11877000-11883400	Weak transcription	Right Atrium	heart
10	chr2:11877200-11878600	Weak transcription	Psoas Muscle	Psoas
11	chr2:11878400-11878600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:11878400-11879200	Enhancers	Right Ventricle	heart
13	chr2:11878400-11879400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:11878400-11879600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:11878400-11880000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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