Variant report

Variant	rs10519898
Chromosome Location	chr15:34267473-34267474
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10519889	1.00[MEX][hapmap]
rs58368948	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58547397	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58922383	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60044628	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6495303	1.00[MEX][hapmap]
rs7177269	1.00[MEX][hapmap]
rs73383745	0.80[AFR][1000 genomes]
rs73383757	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73383760	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74007643	0.80[AFR][1000 genomes]
rs8026540	1.00[MEX][hapmap]
rs8041225	0.89[YRI][hapmap]
rs9972474	0.94[YRI][hapmap];0.80[AFR][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	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv456789	chr15:34034421-34426618	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv568920	chr15:34034421-34426618	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv471235	chr15:34035529-34421951	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv1044844	chr15:34065524-34296829	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv456790	chr15:34264018-34281733	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv568923	chr15:34264018-34281733	Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34236800-34277200	Weak transcription	Left Ventricle	heart
2	chr15:34238000-34282400	Weak transcription	Ovary	ovary
3	chr15:34261200-34277200	Weak transcription	Brain Anterior Caudate	brain
4	chr15:34263800-34277200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr15:34264400-34277000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:34264600-34269200	Weak transcription	Brain Angular Gyrus	brain
7	chr15:34264800-34269200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr15:34264800-34281200	Weak transcription	GM12878-XiMat	blood
9	chr15:34265200-34299600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:34265400-34294200	Weak transcription	Fetal Stomach	stomach
11	chr15:34265400-34311800	Weak transcription	Liver	Liver
12	chr15:34265600-34272800	Weak transcription	Brain Substantia Nigra	brain
13	chr15:34267200-34269600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr15:34267400-34268000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr15:34267400-34268200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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

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