Variant report

Variant	rs2946632
Chromosome Location	chr3:21833212-21833213
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10513650	0.83[ASN][1000 genomes]
rs13062400	0.95[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs17009557	0.80[CHB][hapmap]
rs17009592	0.87[ASN][1000 genomes]
rs17009597	0.93[ASN][1000 genomes]
rs17009600	0.87[ASN][1000 genomes]
rs36108312	0.85[ASN][1000 genomes]
rs71310283	0.88[ASN][1000 genomes]
rs71310284	0.85[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	chr3:21826000-21833400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr3:21826600-21838200	Weak transcription	Right Atrium	heart
6	chr3:21832400-21834200	Enhancers	Adipose Nuclei	Adipose
7	chr3:21832800-21833800	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:21832800-21836600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr3:21833000-21836200	Weak transcription	Fetal Brain Male	brain
10	chr3:21833200-21833600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr3:21833200-21834400	Enhancers	Fetal Muscle Leg	muscle
12	chr3:21833200-21835000	Weak transcription	Fetal Lung	lung
13	chr3:21833200-21836600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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

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