Variant report

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

rs_ID	r²[population]
rs11101510	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11101538	1.00[ASN][1000 genomes]
rs11101540	1.00[ASN][1000 genomes]
rs11101541	1.00[ASN][1000 genomes]
rs11101546	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11101547	0.83[AFR][1000 genomes]
rs12241547	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12242384	1.00[YRI][hapmap]
rs12242587	1.00[YRI][hapmap]
rs12249664	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12251201	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12253134	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12255123	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12257888	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12260981	1.00[ASN][1000 genomes]
rs12263861	1.00[ASN][1000 genomes]
rs12265642	1.00[YRI][hapmap]
rs12265786	1.00[ASN][1000 genomes]
rs12267445	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12267721	1.00[ASN][1000 genomes]
rs17011252	1.00[ASN][1000 genomes]
rs2127587	1.00[ASN][1000 genomes]
rs57495630	1.00[ASN][1000 genomes]
rs73312014	1.00[ASN][1000 genomes]
rs73312016	1.00[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831865	chr10:49994254-50164239	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50054400-50081600	Weak transcription	Spleen	Spleen
2	chr10:50072200-50087800	Weak transcription	Gastric	stomach
3	chr10:50072800-50126200	Strong transcription	Primary B cells from peripheral blood	blood
4	chr10:50074200-50107000	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr10:50074400-50078200	Strong transcription	GM12878-XiMat	blood
6	chr10:50074600-50093200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr10:50074600-50129600	Strong transcription	Primary B cells from cord blood	blood
8	chr10:50074800-50077800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:50074800-50079000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:50075200-50077800	Strong transcription	Primary hematopoietic stem cells	blood
11	chr10:50075200-50093600	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr10:50075400-50126000	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr10:50075600-50079400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr10:50076600-50092000	Weak transcription	Primary T cells from cord blood	blood

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