Variant report

Variant	rs61994010
Chromosome Location	chr14:79387442-79387443
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs58186092	1.00[EUR][1000 genomes]
rs61994011	1.00[EUR][1000 genomes]
rs61994012	1.00[EUR][1000 genomes]
rs61994013	1.00[EUR][1000 genomes]
rs61994014	1.00[EUR][1000 genomes]
rs61994016	1.00[EUR][1000 genomes]
rs61994058	1.00[EUR][1000 genomes]
rs61994059	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61995260	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs61995261	1.00[EUR][1000 genomes]
rs61995262	1.00[EUR][1000 genomes]
rs61995263	1.00[EUR][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	nsv832838	chr14:79306627-79445382	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv1048274	chr14:79323592-79417906	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79387000-79390400	Enhancers	HUVEC	blood vessel

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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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