Variant report

Variant	rs10520004
Chromosome Location	chr4:150090591-150090592
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11721908	0.94[ASN][1000 genomes]
rs11725480	0.94[ASN][1000 genomes]
rs1438776	0.94[ASN][1000 genomes]
rs1438778	0.94[ASN][1000 genomes]
rs1438779	0.94[ASN][1000 genomes]
rs1438780	0.94[ASN][1000 genomes]
rs1438781	0.80[ASN][1000 genomes]
rs17025774	0.94[ASN][1000 genomes]
rs55888252	0.94[ASN][1000 genomes]
rs56216840	0.87[ASN][1000 genomes]
rs57512821	0.94[ASN][1000 genomes]
rs6825179	0.80[ASN][1000 genomes]
rs6842668	1.00[CHB][hapmap];0.93[CHD][hapmap];0.89[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880247	chr4:150057979-150159936	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1022438	chr4:150066349-150196711	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv595687	chr4:150070596-150178533	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr4:150083400-150092200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte 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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