Variant report

Variant	rs2978563
Chromosome Location	chr8:62216873-62216874
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs28460733	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2919304	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2919307	0.96[CEU][hapmap];0.86[CHB][hapmap]
rs2919309	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2919316	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2919317	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2919318	0.80[EUR][1000 genomes]
rs2931287	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2931293	0.91[CEU][hapmap];0.81[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2931296	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2931297	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2978490	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2978516	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978518	0.96[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2978523	0.96[CEU][hapmap];0.86[CHB][hapmap]
rs2978526	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2978528	0.96[CEU][hapmap];0.86[CHB][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2978551	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2978557	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2978559	0.96[CEU][hapmap];0.86[CHB][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2978560	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2978561	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2978562	0.96[CEU][hapmap];0.86[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3864675	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3886396	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948922	chr8:61818964-62475097	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv831336	chr8:62188396-62364873	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1027742	chr8:62206883-62613533	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv539633	chr8:62206883-62613533	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv1021377	chr8:62214279-62596721	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv539634	chr8:62214279-62596721	ZNF genes & repeats Genic enhancers Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 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	chr8:62203400-62217000	Weak transcription	Brain Anterior Caudate	brain
2	chr8:62204600-62217000	Weak transcription	Fetal Brain Male	brain
3	chr8:62211800-62220400	Weak transcription	GM12878-XiMat	blood
4	chr8:62213400-62217400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr8:62215200-62223800	Weak transcription	Fetal Brain Female	brain
6	chr8:62216200-62217600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:62216400-62217600	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr8:62216600-62217200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:62216800-62217000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
10	chr8:62216800-62217200	Enhancers	Fetal Muscle Leg	muscle
11	chr8:62216800-62217600	Enhancers	Brain Angular Gyrus	brain
12	chr8:62216800-62217600	Enhancers	Brain Cingulate Gyrus	brain
13	chr8:62216800-62221400	Weak transcription	Brain Germinal Matrix	brain

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