Variant report

Variant	rs10012565
Chromosome Location	chr4:26550517-26550518
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10028865	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10470786	1.00[MEX][hapmap]
rs10805265	1.00[MEX][hapmap]
rs11937874	1.00[MEX][hapmap]
rs166353	1.00[MEX][hapmap]
rs34803519	1.00[AMR][1000 genomes]
rs4285073	1.00[MEX][hapmap]
rs4583745	1.00[MEX][hapmap]
rs4594713	1.00[MEX][hapmap]
rs73247935	0.82[AFR][1000 genomes]
rs7667400	1.00[MEX][hapmap]
rs7672066	1.00[MEX][hapmap]
rs7674362	1.00[MEX][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762417	chr4:26491768-26576800	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26550400-26551200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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