Variant report

Variant	rs16912405
Chromosome Location	chr11:24314047-24314048
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11027753	0.84[ASN][1000 genomes]
rs11027786	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11027791	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11027795	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12269768	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12270316	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12273122	0.86[ASN][1000 genomes]
rs12274916	0.88[ASN][1000 genomes]
rs12275366	0.88[ASN][1000 genomes]
rs12294118	0.88[ASN][1000 genomes]
rs12788438	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1443047	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16912302	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16912350	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16912383	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16912409	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1806939	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28439532	0.89[ASN][1000 genomes]
rs28666941	0.89[ASN][1000 genomes]
rs55735854	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs56300401	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59509035	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60149726	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7107738	0.81[ASN][1000 genomes]
rs7110982	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7119181	0.91[ASN][1000 genomes]
rs7128158	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7942689	0.86[ASN][1000 genomes]
rs894530	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv553775	chr11:24001975-24323572	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	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
3	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
4	nsv467753	chr11:24190138-24335921	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv553783	chr11:24190138-24335921	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv897083	chr11:24210635-24346093	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv897086	chr11:24261507-24356464	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv1804412	chr11:24285000-24324926	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv1806348	chr11:24285000-24324926	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv1811560	chr11:24285000-24324926	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:24309800-24315400	Weak transcription	Dnd41	blood
2	chr11:24310800-24316800	Weak transcription	Pancreatic Islets	Pancreatic Islet

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