Variant report

Variant	rs11027285
Chromosome Location	chr11:23548673-23548674
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10430917	0.85[EUR][1000 genomes]
rs10430918	0.85[EUR][1000 genomes]
rs10767079	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10767081	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10834123	0.80[EUR][1000 genomes]
rs10834124	0.86[EUR][1000 genomes]
rs10834125	0.92[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs10834126	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10834130	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11027281	0.83[ASN][1000 genomes]
rs11027284	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11027310	0.88[ASN][1000 genomes]
rs12224604	0.91[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes]
rs1350951	0.85[EUR][1000 genomes]
rs1462542	0.85[EUR][1000 genomes]
rs1462562	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1564096	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1564097	0.91[ASN][1000 genomes]
rs2126509	0.85[EUR][1000 genomes]
rs34766222	0.81[EUR][1000 genomes]
rs4244499	0.83[EUR][1000 genomes]
rs4244500	0.84[EUR][1000 genomes]
rs4244501	0.84[EUR][1000 genomes]
rs4267070	0.85[EUR][1000 genomes]
rs4923111	0.92[CEU][hapmap];1.00[JPT][hapmap]
rs6483959	0.92[ASN][1000 genomes]
rs7121472	0.85[EUR][1000 genomes]
rs7483970	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7931400	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7931521	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7946303	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9943664	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832087	chr11:23404474-23569183	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1051066	chr11:23459759-23550295	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv1810883	chr11:23547384-23554704	Enhancers Weak transcription	n/a	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	chr11:23548600-23549200	Enhancers	HUES48 Cell Line	embryonic stem cell

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