Variant report

Variant	rs7476345
Chromosome Location	chr10:26376550-26376551
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:15)

rs_ID	r²[population]
rs11015010	1.00[EUR][1000 genomes]
rs12253114	1.00[EUR][1000 genomes]
rs16926523	1.00[EUR][1000 genomes]
rs16926634	1.00[EUR][1000 genomes]
rs57059254	1.00[EUR][1000 genomes]
rs61322866	1.00[EUR][1000 genomes]
rs7068224	1.00[EUR][1000 genomes]
rs7090388	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs7897279	1.00[EUR][1000 genomes]
rs7922748	1.00[EUR][1000 genomes]
rs8190585	1.00[EUR][1000 genomes]
rs8190593	1.00[EUR][1000 genomes]
rs8190689	1.00[EUR][1000 genomes]
rs8190714	1.00[EUR][1000 genomes]
rs8190720	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1792417	chr10:26263695-26395038	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26373400-26390400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr10:26374600-26376600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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Input of quick search could be:

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

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