Variant report

Variant	rs7635817
Chromosome Location	chr3:70558764-70558765
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs72948808	1.00[AMR][1000 genomes]
rs72948811	1.00[AMR][1000 genomes]
rs72948812	1.00[AMR][1000 genomes]
rs72951046	1.00[AMR][1000 genomes]
rs72951058	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951060	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72951062	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72953103	0.87[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	nsv999046	chr3:70549472-70576944	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70558200-70558800	Enhancers	HUES64 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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