Variant report

Variant	rs58324836
Chromosome Location	chr1:56414883-56414884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11206696	0.99[ASN][1000 genomes]
rs11206701	0.96[ASN][1000 genomes]
rs12021564	0.94[ASN][1000 genomes]
rs12026559	1.00[ASN][1000 genomes]
rs12036133	1.00[ASN][1000 genomes]
rs12037326	1.00[ASN][1000 genomes]
rs12037328	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12037782	1.00[ASN][1000 genomes]
rs12040812	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12047844	1.00[ASN][1000 genomes]
rs2404389	0.99[ASN][1000 genomes]
rs2404390	1.00[ASN][1000 genomes]
rs56902790	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57468354	0.96[ASN][1000 genomes]
rs58323289	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6588595	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72906401	0.97[AFR][1000 genomes]
rs7531302	0.81[EUR][1000 genomes];1.00[ASN][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	nsv870513	chr1:56407227-56493106	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv528440	chr1:56412081-56420193	Enhancers ZNF genes & repeats Weak transcription	TF binding region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56402000-56416800	Weak transcription	Aorta	Aorta
2	chr1:56404600-56416200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:56410600-56418600	Weak transcription	H1 BMP4 Derived Trophoblast 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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