Variant report

Variant	rs4304326
Chromosome Location	chr8:34503172-34503173
allele	C/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:19)

rs_ID	r²[population]
rs10503965	0.81[ASN][1000 genomes]
rs12114700	0.86[AFR][1000 genomes]
rs12543513	0.81[ASN][1000 genomes]
rs12543518	0.81[ASN][1000 genomes]
rs12543568	0.81[ASN][1000 genomes]
rs12545278	0.83[ASN][1000 genomes]
rs12546023	0.81[ASN][1000 genomes]
rs12547489	0.83[ASN][1000 genomes]
rs16882701	0.81[ASN][1000 genomes]
rs35008961	0.81[ASN][1000 genomes]
rs4237089	0.83[ASN][1000 genomes]
rs4263763	0.80[ASN][1000 genomes]
rs4342589	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4463416	0.83[ASN][1000 genomes]
rs59950658	0.81[ASN][1000 genomes]
rs6468257	0.90[CHB][hapmap]
rs6468266	0.81[ASN][1000 genomes]
rs7844647	0.83[ASN][1000 genomes]
rs953271	0.83[ASN][1000 genomes]

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	nsv831283	chr8:34501243-34662634	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr8:34501200-34503200	Weak transcription	H1 Derived Neuronal Progenitor 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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