Variant report

Variant	rs1884740
Chromosome Location	chr6:87644452-87644453
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1013019	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10498959	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12663746	1.00[ASN][1000 genomes]
rs1408447	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1535228	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16877863	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16877883	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16877984	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16877987	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16877991	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17545444	0.91[ASN][1000 genomes]
rs2145050	0.83[ASN][1000 genomes]
rs3763231	1.00[ASN][1000 genomes]
rs4371828	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55859404	1.00[ASN][1000 genomes]
rs55982849	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56152175	0.91[ASN][1000 genomes]
rs56364606	0.91[ASN][1000 genomes]
rs62439115	1.00[ASN][1000 genomes]
rs62439116	1.00[ASN][1000 genomes]
rs62439143	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439144	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62439145	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439146	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62439147	0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62440765	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62440766	1.00[ASN][1000 genomes]
rs62440767	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62440790	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62440822	1.00[ASN][1000 genomes]
rs6940008	0.90[JPT][hapmap];0.88[YRI][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73751775	1.00[ASN][1000 genomes]
rs73751802	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9444442	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9444447	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9450536	1.00[ASN][1000 genomes]
rs9450544	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9450568	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9450569	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9450573	0.81[ASN][1000 genomes]
rs9450587	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018878	chr6:86778852-87691755	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1031639	chr6:86815397-87721507	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1024751	chr6:87433199-87908721	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	esv1811101	chr6:87456503-87645214	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2758066	chr6:87456503-87645214	Enhancers Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2759452	chr6:87456503-87645214	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	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	chr6:87643800-87644600	Enhancers	Primary B cells from peripheral blood	blood
2	chr6:87644400-87644600	Enhancers	GM12878-XiMat	blood

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