Variant report

Variant	rs56269360
Chromosome Location	chr3:21833636-21833637
allele	G/T
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:14)

rs_ID	r²[population]
rs12630540	0.85[ASN][1000 genomes]
rs12630569	0.85[ASN][1000 genomes]
rs12633290	0.90[ASN][1000 genomes]
rs12638755	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12639479	0.94[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs17621507	0.95[ASN][1000 genomes]
rs3849551	0.91[ASN][1000 genomes]
rs55794313	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62236196	0.85[ASN][1000 genomes]
rs62236197	0.85[ASN][1000 genomes]
rs73142803	0.95[AFR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73142809	0.91[AFR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73142818	0.82[AFR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73142832	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534005	chr3:21387588-22003293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1010460	chr3:21516810-21839871	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1007048	chr3:21666807-21865229	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv536516	chr3:21666807-21865229	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv2751992	chr3:21786893-22212357	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv948555	chr3:21786893-22212357	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv834632	chr3:21803941-21974082	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21820800-21835600	Weak transcription	Left Ventricle	heart
2	chr3:21823800-21833800	Weak transcription	Psoas Muscle	Psoas
3	chr3:21823800-21836000	Weak transcription	Aorta	Aorta
4	chr3:21826600-21838200	Weak transcription	Right Atrium	heart
5	chr3:21832400-21834200	Enhancers	Adipose Nuclei	Adipose
6	chr3:21832800-21833800	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr3:21832800-21836600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr3:21833000-21836200	Weak transcription	Fetal Brain Male	brain
9	chr3:21833200-21834400	Enhancers	Fetal Muscle Leg	muscle
10	chr3:21833200-21835000	Weak transcription	Fetal Lung	lung
11	chr3:21833200-21836600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:21833400-21834400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr3:21833600-21835800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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

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