Variant report

Variant	rs9651675
Chromosome Location	chr11:106699744-106699745
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:15)

rs_ID	r²[population]
rs10160762	0.90[EUR][1000 genomes]
rs10789547	0.91[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10890604	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10890611	0.85[EUR][1000 genomes]
rs11211932	0.80[ASN][1000 genomes]
rs12274602	0.85[EUR][1000 genomes]
rs12285359	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1487889	0.92[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1487891	0.89[EUR][1000 genomes]
rs1487892	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4754169	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7924555	0.84[EUR][1000 genomes]
rs7926569	0.88[ASN][1000 genomes]
rs7937534	0.84[EUR][1000 genomes]
rs923327	0.98[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	nsv556230	chr11:106676942-106704250	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 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	chr11:106689600-106699800	Weak transcription	Fetal Heart	heart

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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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