Variant report

Variant	rs11033560
Chromosome Location	chr11:36357813-36357814
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11033549	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11033553	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033554	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033564	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11033565	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1160014	0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1160015	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12099418	0.94[ASN][1000 genomes]
rs12363040	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12364237	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1466038	0.84[ASN][1000 genomes]
rs56985814	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58248666	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73443133	0.91[EUR][1000 genomes]
rs73443135	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73443138	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7931498	0.94[ASN][1000 genomes]
rs7931590	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv467791	chr11:36108497-36999385	Flanking Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	nsv554003	chr11:36108497-36999385	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:36353400-36361000	Weak transcription	Brain Cingulate Gyrus	brain
2	chr11:36355400-36358000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr11:36356200-36361200	Weak transcription	Brain Anterior Caudate	brain
4	chr11:36356600-36361200	Weak transcription	Brain Substantia Nigra	brain

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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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