Variant report

Variant	rs59859836
Chromosome Location	chr4:102942058-102942059
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1352173	1.00[AMR][1000 genomes]
rs1486573	1.00[AMR][1000 genomes]
rs16996753	1.00[AMR][1000 genomes]
rs17031752	1.00[AMR][1000 genomes]
rs17031772	1.00[AMR][1000 genomes]
rs17031808	1.00[AMR][1000 genomes]
rs17031827	1.00[AMR][1000 genomes]
rs17031842	1.00[AMR][1000 genomes]
rs17031852	1.00[AMR][1000 genomes]
rs17031854	1.00[AMR][1000 genomes]
rs17031862	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs17031870	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs17031876	1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2276333	1.00[AMR][1000 genomes]
rs2276334	1.00[AMR][1000 genomes]
rs41347351	1.00[AMR][1000 genomes]
rs41516147	1.00[AMR][1000 genomes]
rs55952681	1.00[AMR][1000 genomes]
rs56757011	1.00[AMR][1000 genomes]
rs56803425	1.00[AMR][1000 genomes]
rs57545925	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs58588907	1.00[AMR][1000 genomes]
rs58630066	1.00[AMR][1000 genomes]
rs58846155	1.00[AMR][1000 genomes]
rs59656969	1.00[AMR][1000 genomes]
rs59893832	1.00[AMR][1000 genomes]
rs60180803	1.00[AMR][1000 genomes]
rs61067451	1.00[AMR][1000 genomes]
rs61546925	1.00[AMR][1000 genomes]
rs72929954	1.00[AFR][1000 genomes]
rs72929956	1.00[AFR][1000 genomes]
rs72929959	1.00[AFR][1000 genomes]
rs72929964	1.00[AFR][1000 genomes]
rs72929967	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs72931986	1.00[AFR][1000 genomes]
rs72931993	0.85[AFR][1000 genomes]
rs72931994	1.00[AFR][1000 genomes]
rs72931995	1.00[AFR][1000 genomes]
rs72931999	1.00[AFR][1000 genomes]
rs72932000	1.00[AFR][1000 genomes]
rs72933903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs73834511	1.00[AMR][1000 genomes]
rs73834519	1.00[AMR][1000 genomes]
rs73834525	1.00[AMR][1000 genomes]
rs73834537	1.00[AMR][1000 genomes]
rs73834541	1.00[AMR][1000 genomes]
rs73834547	1.00[AMR][1000 genomes]
rs73834549	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869164	chr4:102483189-103213842	Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv2757945	chr4:102662699-103008940	Genic enhancers Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2759269	chr4:102662699-103008940	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1011180	chr4:102685236-102985945	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv537202	chr4:102685236-102985945	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv879682	chr4:102859835-103088491	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv461596	chr4:102935902-103008712	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv594955	chr4:102935902-103008712	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr4:102938400-102953600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:102938600-102946400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:102939800-102942800	Weak transcription	Primary B cells from peripheral blood	blood
4	chr4:102940000-102942600	Weak transcription	Primary B cells from cord blood	blood

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