Variant report

Variant	rs536624
Chromosome Location	chr3:119326188-119326189
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:119318615..119321815-chr3:119324739..119327300,3	K562	blood:
2	chr3:119324918..119326771-chr3:119333086..119335282,2	K562	blood:

Variant related genes	Relation type
ENSG00000144837	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10433338	0.99[ASN][1000 genomes]
rs13443	0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1525838	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1534154	0.95[CHB][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1723969	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1797831	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1797832	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2049501	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2171025	0.90[CHB][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2248483	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2251566	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.97[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2272267	0.99[ASN][1000 genomes]
rs2272268	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2272269	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2272270	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2629399	0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2629400	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2629408	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2670293	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2670298	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2688637	0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2688638	0.94[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2688639	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2688646	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2688647	0.83[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2688648	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2692612	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2692613	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2692614	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2692615	0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2692621	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2692623	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs474926	0.99[ASN][1000 genomes]
rs485257	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs487124	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs528765	0.95[CHB][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs530389	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs530783	0.91[CHB][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs538136	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs551885	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs555525	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55670246	0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55801535	0.90[ASN][1000 genomes]
rs56197198	0.83[ASN][1000 genomes]
rs58020513	0.97[ASN][1000 genomes]
rs593968	0.95[CHB][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs666134	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6807201	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6807613	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72954966	0.83[EUR][1000 genomes];0.97[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	esv3487859	chr3:118570588-119419623	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	esv3487860	chr3:118570588-119419623	Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv829695	chr3:119178890-119367996	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	esv1831824	chr3:119263607-119402474	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv3963	chr3:119301064-119345904	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv591363	chr3:119316828-119345950	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119316200-119340600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:119317600-119327800	Weak transcription	Fetal Intestine Small	intestine
3	chr3:119318600-119344200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:119318800-119327800	Weak transcription	Liver	Liver
5	chr3:119320200-119327400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:119320200-119345000	Weak transcription	Right Ventricle	heart
7	chr3:119322000-119326400	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr3:119322200-119349200	Weak transcription	Gastric	stomach
9	chr3:119322400-119334600	Weak transcription	Brain Anterior Caudate	brain
10	chr3:119324000-119329000	Enhancers	Placenta	Placenta
11	chr3:119324200-119326200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:119324400-119331600	Weak transcription	HSMMtube	muscle
13	chr3:119325600-119326600	Enhancers	Spleen	Spleen

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