Variant report

Variant	rs11023555
Chromosome Location	chr11:15398966-15398967
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11023518	0.84[EUR][1000 genomes]
rs11023523	0.83[EUR][1000 genomes]
rs11023525	0.83[EUR][1000 genomes]
rs11023537	0.87[EUR][1000 genomes]
rs11023542	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11023543	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11023547	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11023568	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12363177	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12577240	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12800836	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35824480	0.87[EUR][1000 genomes]
rs4604863	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67068849	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67732927	0.88[EUR][1000 genomes]
rs67828350	0.87[EUR][1000 genomes]
rs72861982	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72861992	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9645645	0.88[EUR][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	esv2830370	chr11:15142247-15444094	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	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	chr11:15397200-15399400	Weak transcription	Liver	Liver

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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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