Variant report

Variant	rs10130096
Chromosome Location	chr14:67987653-67987654
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10143518	0.82[AMR][1000 genomes]
rs10873204	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11158676	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11158678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11621977	0.81[AMR][1000 genomes]
rs12878981	0.83[CEU][hapmap]
rs12887115	0.88[CEU][hapmap];0.81[AMR][1000 genomes]
rs1555397	0.87[CEU][hapmap]
rs4899206	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4902477	0.92[CEU][hapmap];0.81[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7155830	0.83[CEU][hapmap]
rs7155911	0.88[CEU][hapmap];0.84[JPT][hapmap];0.87[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7156144	0.88[CEU][hapmap];0.84[JPT][hapmap];0.81[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7161368	0.83[CEU][hapmap]
rs8011307	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8019974	0.83[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456331	chr14:67732861-68103780	Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv564961	chr14:67732861-68103780	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	nsv470651	chr14:67732861-68113293	Active TSS Strong transcription Flanking Active TSS Weak transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv902066	chr14:67873128-68103780	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 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	chr14:67982600-67999000	Weak transcription	Right Atrium	heart
2	chr14:67984000-67988600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr14:67984000-67988800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:67984000-67988800	Weak transcription	Brain Hippocampus Middle	brain
5	chr14:67984000-67989000	Weak transcription	Brain Angular Gyrus	brain
6	chr14:67984000-67989000	Weak transcription	Brain Anterior Caudate	brain
7	chr14:67984200-67988800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr14:67984400-67988800	Weak transcription	Brain Substantia Nigra	brain
9	chr14:67984400-67989000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr14:67987000-67989200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr14:67987400-67987800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr14:67987400-67988000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
13	chr14:67987600-67987800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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