Variant report

Variant	rs9446390
Chromosome Location	chr6:72134860-72134861
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10080965	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10155717	1.00[AMR][1000 genomes]
rs16881197	0.88[AFR][1000 genomes]
rs59106567	0.88[AFR][1000 genomes]
rs73520627	0.91[AFR][1000 genomes]
rs769352	0.85[AFR][1000 genomes]
rs9446382	0.83[AFR][1000 genomes]
rs9446388	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455453	0.90[AFR][1000 genomes]
rs9455466	0.82[AFR][1000 genomes];1.00[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	nsv830684	chr6:72094842-72282684	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	488 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	chr6:72131200-72139400	Weak transcription	H9 Derived Neuron 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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