Variant report

Variant	rs12782465
Chromosome Location	chr10:38085396-38085397
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11498322	1.00[EUR][1000 genomes]
rs12252533	1.00[EUR][1000 genomes]
rs12252678	1.00[EUR][1000 genomes]
rs12260004	1.00[EUR][1000 genomes]
rs12775243	1.00[EUR][1000 genomes]
rs28800635	1.00[EUR][1000 genomes]
rs34289403	1.00[EUR][1000 genomes]
rs34905591	1.00[EUR][1000 genomes]
rs71489400	1.00[EUR][1000 genomes]

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	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised 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	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS 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	40 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	chr10:38081200-38092000	Weak transcription	Ovary	ovary
2	chr10:38081200-38092200	Weak transcription	Pancreas	Pancrea
3	chr10:38081200-38097200	Weak transcription	Aorta	Aorta
4	chr10:38082600-38086400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:38083200-38086000	ZNF genes & repeats	Liver	Liver
6	chr10:38084000-38090600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr10:38084400-38092200	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr10:38085000-38088800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
9	chr10:38085200-38085400	ZNF genes & repeats	Left Ventricle	heart

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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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