Variant report

Variant	rs73686537
Chromosome Location	chr8:64641127-64641128
allele	A/C
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:15)

rs_ID	r²[population]
rs10957295	0.94[ASN][1000 genomes]
rs11779429	0.96[EUR][1000 genomes]
rs12675689	0.94[ASN][1000 genomes]
rs12678656	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12682101	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1520921	0.83[ASN][1000 genomes]
rs16930598	1.00[EUR][1000 genomes]
rs16930623	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17288060	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2355593	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28685087	0.83[ASN][1000 genomes]
rs3862073	0.91[EUR][1000 genomes]
rs6472122	0.83[ASN][1000 genomes]
rs7465464	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7832628	0.81[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	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr8:64640800-64653000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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