Variant report

Variant	rs10212456
Chromosome Location	chr3:21837191-21837192
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10212289	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11716091	0.86[AFR][1000 genomes]
rs17009541	1.00[AMR][1000 genomes]
rs28546711	1.00[AMR][1000 genomes]
rs3849549	1.00[AMR][1000 genomes]
rs9831481	0.81[AFR][1000 genomes]
rs9831973	0.83[AFR][1000 genomes]
rs9833224	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9851416	1.00[AMR][1000 genomes]
rs9871254	1.00[AMR][1000 genomes]
rs9878994	1.00[AMR][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:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21826600-21838200	Weak transcription	Right Atrium	heart
2	chr3:21833800-21837200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr3:21835000-21837800	Enhancers	Fetal Lung	lung
4	chr3:21835600-21837800	Enhancers	Fetal Muscle Leg	muscle
5	chr3:21836000-21837800	Enhancers	Aorta	Aorta
6	chr3:21836000-21837800	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr3:21836200-21837600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr3:21836600-21837200	Enhancers	Fetal Stomach	stomach
9	chr3:21836600-21837600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:21836600-21837800	Enhancers	Fetal Heart	heart
11	chr3:21836600-21837800	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr3:21836800-21837200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle

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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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