Variant report

Variant	rs16849012
Chromosome Location	chr2:213513153-213513154
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11890705	1.00[EUR][1000 genomes]
rs11890828	1.00[EUR][1000 genomes]
rs11900459	1.00[EUR][1000 genomes]
rs16848963	1.00[EUR][1000 genomes]
rs16849014	1.00[EUR][1000 genomes]
rs56872909	1.00[EUR][1000 genomes]
rs57284153	1.00[EUR][1000 genomes]
rs59672960	1.00[EUR][1000 genomes]
rs60939515	1.00[EUR][1000 genomes]
rs7558191	1.00[EUR][1000 genomes]
rs7601573	1.00[EUR][1000 genomes]
rs7608382	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	nsv948878	chr2:213345197-213534298	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213510800-213513600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:213512200-213513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:213512400-213522200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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