Variant report

Variant	rs4754869
Chromosome Location	chr11:102566396-102566397
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11225392	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12099177	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1276266	0.94[ASN][1000 genomes]
rs1276269	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs12785344	0.96[ASN][1000 genomes]
rs1296221	0.94[ASN][1000 genomes]
rs17093633	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17099334	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17099389	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17099411	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17099419	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17099436	0.89[AMR][1000 genomes]
rs17099451	1.00[CEU][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];0.89[AMR][1000 genomes]
rs17099452	1.00[CEU][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes]
rs1892885	0.81[EUR][1000 genomes]
rs1940052	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34433762	0.89[AMR][1000 genomes]
rs35308160	0.89[AMR][1000 genomes]
rs3740936	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3740938	1.00[CEU][hapmap];0.94[JPT][hapmap];0.81[MEX][hapmap];0.89[AMR][1000 genomes]
rs3758860	1.00[CEU][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes]
rs4376870	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4498962	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4564300	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754049	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754864	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4754866	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4754867	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4754870	1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4754871	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4754872	0.89[AMR][1000 genomes]
rs4754874	0.89[AMR][1000 genomes]
rs4754876	0.84[AMR][1000 genomes]
rs58406046	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60059188	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60964518	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72973542	0.85[EUR][1000 genomes]
rs72973547	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72973559	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72973562	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72973563	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72975539	0.89[AMR][1000 genomes]
rs72975567	0.84[AMR][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	nsv832252	chr11:102445479-102627879	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1037454	chr11:102487521-102601233	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv541156	chr11:102487521-102601233	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102565600-102566400	Enhancers	H9 Cell Line	embryonic stem cell
2	chr11:102565600-102566400	Enhancers	Colon Smooth Muscle	Colon
3	chr11:102565600-102568800	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr11:102566000-102566400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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