Variant report

Variant	rs4636065
Chromosome Location	chr6:110372029-110372030
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1381689	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56138638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60115070	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60542605	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6942351	1.00[AMR][1000 genomes]
rs73765638	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73765640	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73765642	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73765645	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73765647	1.00[AFR][1000 genomes]
rs73765661	0.94[AFR][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	nsv1017642	chr6:110252276-110386453	Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv538417	chr6:110252276-110386453	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr6:110371600-110374600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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