Variant report

Variant	rs57715813
Chromosome Location	chr11:59934473-59934474
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11821697	1.00[AMR][1000 genomes]
rs11828298	1.00[AMR][1000 genomes]
rs34296021	1.00[AMR][1000 genomes]
rs7104106	1.00[AMR][1000 genomes]
rs7114016	1.00[AMR][1000 genomes]
rs73483239	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73483247	1.00[AFR][1000 genomes]
rs73487292	1.00[AMR][1000 genomes]
rs73489246	1.00[AMR][1000 genomes]
rs7935575	1.00[AMR][1000 genomes]
rs7939001	1.00[AMR][1000 genomes]
rs7946886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832173	chr11:59788884-59940560	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv468579	chr11:59814287-59975400	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv555150	chr11:59814287-59975400	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv33843	chr11:59908131-59945334	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv832174	chr11:59909267-60073908	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:59931800-59935600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr11:59932400-59935200	Enhancers	HUVEC	blood vessel
3	chr11:59933000-59934800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr11:59933000-59935800	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr11:59933400-59935400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr11:59933800-59936200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:59933800-59936200	Weak transcription	HMEC	breast
8	chr11:59934400-59934600	Enhancers	Primary B cells from cord blood	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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