Variant report

Variant	rs6892039
Chromosome Location	chr5:151884268-151884269
allele	A/C
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]
rs10055345	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10057671	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10061448	1.00[AMR][1000 genomes]
rs10477018	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11949836	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13355915	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13358768	1.00[AMR][1000 genomes]
rs34397381	1.00[AMR][1000 genomes]
rs6892353	1.00[AMR][1000 genomes]
rs9324727	0.81[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	nsv1023828	chr5:151522149-151956217	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr5:151879200-151884800	Weak transcription	H9 Cell Line	embryonic stem cell

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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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