Variant report

Variant	rs4933765
Chromosome Location	chr10:83067537-83067538
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10882901	0.86[ASN][1000 genomes]
rs10882902	0.86[ASN][1000 genomes]
rs11189147	0.86[ASN][1000 genomes]
rs11189347	0.81[ASN][1000 genomes]
rs12412550	0.86[ASN][1000 genomes]
rs265454	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61853861	0.86[ASN][1000 genomes]

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	esv3449683	chr10:82972143-83304804	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3421917	chr10:82972163-83304774	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv870428	chr10:83035110-83306265	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:83067000-83067600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:83067200-83067600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:83067200-83067600	Enhancers	HMEC	breast

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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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