Variant report

Variant	rs11986637
Chromosome Location	chr8:62217006-62217007
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10504323	0.80[EUR][1000 genomes]
rs10504324	0.81[EUR][1000 genomes]
rs11783318	0.81[EUR][1000 genomes]
rs11985051	0.80[EUR][1000 genomes]
rs11985918	0.84[EUR][1000 genomes]
rs17187457	0.82[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs17766175	0.80[EUR][1000 genomes]
rs73684471	0.81[EUR][1000 genomes]
rs73684477	0.81[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs7845823	0.81[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:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62211800-62220400	Weak transcription	GM12878-XiMat	blood
2	chr8:62213400-62217400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr8:62215200-62223800	Weak transcription	Fetal Brain Female	brain
4	chr8:62216200-62217600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:62216400-62217600	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:62216600-62217200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr8:62216800-62217200	Enhancers	Fetal Muscle Leg	muscle
8	chr8:62216800-62217600	Enhancers	Brain Angular Gyrus	brain
9	chr8:62216800-62217600	Enhancers	Brain Cingulate Gyrus	brain
10	chr8:62216800-62221400	Weak transcription	Brain Germinal Matrix	brain
11	chr8:62217000-62217200	Enhancers	Fetal Brain Male	brain
12	chr8:62217000-62217400	Enhancers	Brain Anterior Caudate	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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