Variant report

Variant	rs9963812
Chromosome Location	chr18:45016735-45016736
allele	C/G/T
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]
rs28638438	0.90[EUR][1000 genomes]
rs56207056	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57771146	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58556444	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs60530780	0.81[AMR][1000 genomes]
rs61263060	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62095734	0.81[AMR][1000 genomes]
rs62097082	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62097086	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs62097121	0.93[EUR][1000 genomes]
rs6507738	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6507751	0.90[ASN][1000 genomes]
rs8095582	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9956704	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9964645	0.81[AMR][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	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45012200-45017200	Weak transcription	Left Ventricle	heart
2	chr18:45014600-45017600	Weak transcription	Right Atrium	heart
3	chr18:45016600-45017800	Enhancers	hESC Derived CD56+ Mesoderm 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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