Variant report

Variant	rs11991573
Chromosome Location	chr8:54582515-54582516
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11988292	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11988352	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13262179	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13281270	0.84[ASN][1000 genomes]
rs28432290	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28485002	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28537471	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28585586	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28600939	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28699488	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28733973	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35389837	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35503029	0.92[ASN][1000 genomes]
rs35881966	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35981696	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36094567	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55732477	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56711910	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57265244	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs58186810	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61191446	0.92[ASN][1000 genomes]
rs6473882	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6473883	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6473884	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6980711	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6993279	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6994201	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7007030	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7014660	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7018412	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73682530	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73682531	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7464872	0.91[ASN][1000 genomes]
rs7814647	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758159	chr8:54474589-54737473	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2759616	chr8:54474589-54737473	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1830188	chr8:54520350-54601462	Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
4	nsv890919	chr8:54521248-54607336	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
5	nsv1020081	chr8:54528266-54592073	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
6	nsv611381	chr8:54528760-54589344	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1030947	chr8:54535233-54592073	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a
8	nsv890920	chr8:54559770-54626539	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	esv3333483	chr8:54581899-54585297	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
10	esv3333052	chr8:54582299-54585397	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	n/a
11	esv3348951	chr8:54582299-54585397	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:54571400-54583600	Weak transcription	Pancreas	Pancrea
2	chr8:54577800-54583600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr8:54580000-54583400	Weak transcription	Fetal Brain Male	brain
4	chr8:54581200-54584600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr8:54581400-54584800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr8:54582000-54583000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr8:54582000-54583400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr8:54582400-54583000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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