Variant report

Variant	rs10767187
Chromosome Location	chr11:24430111-24430112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10500977	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10834345	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11027913	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11027918	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11027922	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs11027923	0.86[ASN][1000 genomes]
rs11529206	0.84[ASN][1000 genomes]
rs11529783	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12226856	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12805416	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1343880	0.83[ASN][1000 genomes]
rs16912582	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1878442	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2403940	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2403941	0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs35644420	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4344487	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6484051	0.85[ASN][1000 genomes]
rs7110772	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7113480	0.83[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7933633	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055026	chr11:24151133-24737122	Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1037744	chr11:24174588-24737122	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1042325	chr11:24399097-24432782	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv467755	chr11:24407381-24527958	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv553791	chr11:24407381-24527958	Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv897088	chr11:24419481-24543475	Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region	2 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	chr11:24429000-24430800	Enhancers	Fetal Heart	heart

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