Variant report

Variant	rs10092680
Chromosome Location	chr8:99444653-99444654
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10111589	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12681956	1.00[CEU][hapmap]
rs13274127	1.00[GIH][hapmap]
rs16897028	1.00[CHB][hapmap]
rs17372001	1.00[CHB][hapmap]
rs28784957	0.82[ASW][hapmap]
rs35696573	1.00[CHD][hapmap];1.00[JPT][hapmap]
rs7831149	1.00[CHD][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	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1034492	chr8:99436341-99456516	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99440400-99449600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:99440800-99449400	Weak transcription	NHDF-Ad	bronchial
3	chr8:99441400-99451600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr8:99441400-99451800	Weak transcription	Brain Anterior Caudate	brain
5	chr8:99441400-99458000	Weak transcription	Ovary	ovary
6	chr8:99441400-99472600	Weak transcription	Pancreas	Pancrea
7	chr8:99442000-99451600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr8:99442400-99446200	Weak transcription	Brain Angular Gyrus	brain
9	chr8:99443600-99449400	Weak transcription	Brain Inferior Temporal Lobe	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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