Variant report

Variant	rs73043698
Chromosome Location	chr2:187943000-187943001
allele	A/G
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:11)

rs_ID	r²[population]
rs61358508	1.00[AFR][1000 genomes]
rs73038842	1.00[AFR][1000 genomes]
rs73038877	1.00[AFR][1000 genomes]
rs73043702	0.83[AFR][1000 genomes]
rs73044736	1.00[AFR][1000 genomes]
rs73045626	0.83[AFR][1000 genomes]
rs73046605	1.00[AFR][1000 genomes]
rs73046623	1.00[AFR][1000 genomes]
rs73049417	1.00[AFR][1000 genomes]
rs73049422	1.00[AFR][1000 genomes]
rs73049450	1.00[AFR][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	nsv949700	chr2:187713412-188361211	Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv875553	chr2:187856937-188067355	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv875554	chr2:187873808-187964942	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv834486	chr2:187876328-188032965	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv431857	chr2:187930023-188098798	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187940600-187943000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr2:187942800-187943600	Enhancers	NHDF-Ad	bronchial
3	chr2:187942800-187945200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr2:187943000-187943600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:187943000-187943600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr2:187943000-187943800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr2:187943000-187944000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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