Variant report

Variant	rs11229466
Chromosome Location	chr11:58213440-58213441
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10160409	1.00[YRI][hapmap]
rs11229437	1.00[YRI][hapmap]
rs11229507	1.00[YRI][hapmap]
rs11229508	1.00[YRI][hapmap]
rs11229520	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11229523	1.00[YRI][hapmap]
rs11229525	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11229539	1.00[YRI][hapmap];1.00[AFR][1000 genomes]
rs11229546	1.00[YRI][hapmap]
rs11229547	1.00[YRI][hapmap]
rs11229570	1.00[AFR][1000 genomes]
rs11229571	1.00[AFR][1000 genomes]
rs12271331	0.89[AFR][1000 genomes]
rs12272722	1.00[AFR][1000 genomes]
rs12276093	1.00[YRI][hapmap]
rs12278099	0.90[AFR][1000 genomes]
rs12281441	1.00[AFR][1000 genomes]
rs12282241	0.89[AFR][1000 genomes]
rs12282490	1.00[YRI][hapmap]
rs12282535	1.00[YRI][hapmap]
rs12282976	1.00[YRI][hapmap]
rs12285076	1.00[AFR][1000 genomes]
rs12286542	1.00[AFR][1000 genomes]
rs12293904	0.89[AFR][1000 genomes]
rs12295771	1.00[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv517849	chr11:58129053-58264181	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
3	nsv1042491	chr11:58134936-58263639	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 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	chr11:58211800-58214000	ZNF genes & repeats	Adipose Nuclei	Adipose
2	chr11:58212200-58213800	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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