Variant report

Variant	rs2045763
Chromosome Location	chr2:184132034-184132035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs17707407	0.86[EUR][1000 genomes]
rs17707482	0.86[EUR][1000 genomes]
rs17707626	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17707992	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17708224	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17758271	0.86[EUR][1000 genomes]
rs17758295	0.86[EUR][1000 genomes]
rs17758560	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17758692	0.88[EUR][1000 genomes]
rs17758722	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17758734	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17758764	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17758808	0.88[EUR][1000 genomes]
rs2045761	0.94[AFR][1000 genomes]
rs2045762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56724347	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs58870754	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7601755	0.86[EUR][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	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv875485	chr2:183827018-184195265	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1010799	chr2:183855680-184244721	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv536072	chr2:183855680-184244721	Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv583951	chr2:184121475-184142975	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
6	nsv1014807	chr2:184123737-184181052	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv961917	chr2:184125770-184132151	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184128600-184132400	Weak transcription	Spleen	Spleen
2	chr2:184131600-184132600	Enhancers	Primary B cells from peripheral blood	blood
3	chr2:184131800-184147600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:184132000-184132600	Enhancers	GM12878-XiMat	blood

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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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