Variant report

Variant	rs4352685
Chromosome Location	chr6:16038640-16038641
allele	C/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:14)

rs_ID	r²[population]
rs1267720	1.00[AMR][1000 genomes]
rs1342745	1.00[AMR][1000 genomes]
rs1891520	1.00[AMR][1000 genomes]
rs2327946	1.00[AMR][1000 genomes]
rs4502936	1.00[AMR][1000 genomes]
rs6459444	1.00[AMR][1000 genomes]
rs6921913	1.00[AMR][1000 genomes]
rs6925676	1.00[AMR][1000 genomes]
rs6931835	1.00[AMR][1000 genomes]
rs7453386	1.00[AMR][1000 genomes]
rs7749125	1.00[AMR][1000 genomes]
rs7771374	1.00[AMR][1000 genomes]
rs808367	1.00[AMR][1000 genomes]
rs9464855	1.00[AMR][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	nsv462642	chr6:16019115-16056026	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv601007	chr6:16019115-16056026	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 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	chr6:16037600-16038800	Weak transcription	K562	blood

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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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