Variant report

Variant	rs7134824
Chromosome Location	chr12:62369598-62369599
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2582333	1.00[CEU][hapmap]
rs2701154	1.00[CEU][hapmap]
rs349873	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs349875	0.92[ASN][1000 genomes]
rs349881	0.86[AFR][1000 genomes]
rs349883	1.00[CEU][hapmap];0.92[ASN][1000 genomes]
rs349884	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs349885	0.92[ASN][1000 genomes]
rs349887	1.00[CEU][hapmap]
rs349888	1.00[CEU][hapmap]
rs851903	1.00[CEU][hapmap]
rs851905	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs851908	1.00[CEU][hapmap]
rs851909	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs851910	1.00[CEU][hapmap];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs851911	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs851914	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs969173	1.00[CEU][hapmap]

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	nsv1039741	chr12:62046850-62491052	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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