Variant report

Variant	rs11042800
Chromosome Location	chr11:10450588-10450589
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11042799	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11042806	1.00[AMR][1000 genomes]
rs11042807	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11042810	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11042813	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11042850	1.00[CEU][hapmap]
rs11518196	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12360830	1.00[AMR][1000 genomes]
rs12363993	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12789993	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12802491	1.00[AMR][1000 genomes]
rs12803441	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34423417	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34827892	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34972496	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35027484	1.00[AMR][1000 genomes]
rs35526717	1.00[AMR][1000 genomes]
rs35548473	1.00[AMR][1000 genomes]
rs61890321	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61890324	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61891364	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430319	chr11:10027543-10711224	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10448600-10460000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:10449400-10456000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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