Variant report

Variant	rs73405745
Chromosome Location	chr6:35103661-35103662
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs35847323	1.00[EUR][1000 genomes]
rs61403214	1.00[EUR][1000 genomes]
rs73405707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73405753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73405762	1.00[AMR][1000 genomes]
rs73405763	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73405773	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73405794	1.00[AMR][1000 genomes]
rs73405800	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	esv3441631	chr6:35103524-35106522	Enhancers Weak transcription	Chromatin interactive region	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	chr6:35103600-35104200	Enhancers	GM12878-XiMat	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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