Variant report

Variant	rs11901445
Chromosome Location	chr2:191018607-191018608
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11688590	0.83[JPT][hapmap]
rs11690677	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13382543	0.88[CHD][hapmap];0.83[JPT][hapmap];0.80[ASN][1000 genomes]
rs13416537	0.91[ASN][1000 genomes]
rs13429506	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs58808199	1.00[ASN][1000 genomes]
rs6710331	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs72911367	0.83[ASN][1000 genomes]
rs72913453	0.96[ASN][1000 genomes]
rs72913465	0.95[ASN][1000 genomes]
rs72913476	0.80[ASN][1000 genomes]
rs785223	0.82[CHD][hapmap];0.80[MEX][hapmap]
rs785225	0.81[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	esv3439178	chr2:190877215-191124499	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr2:191015400-191023400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr2:191018600-191020200	Enhancers	Primary neutrophils fromperipheralblood	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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