Variant report

Variant	rs7635184
Chromosome Location	chr3:56226041-56226042
allele	A/G
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]
rs11719222	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1452220	0.87[ASN][1000 genomes]
rs4974124	0.86[ASN][1000 genomes]
rs4974182	0.87[ASN][1000 genomes]
rs755322	0.82[ASN][1000 genomes]
rs7626886	0.87[ASN][1000 genomes]
rs9810491	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9830173	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9867216	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9873480	0.82[EUR][1000 genomes];0.92[ASN][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	nsv1009709	chr3:56000827-56294945	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:56225400-56227000	Enhancers	HSMMtube	muscle

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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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