Variant report

Variant	rs56268007
Chromosome Location	chr15:29847986-29847987
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs11073082	0.81[ASN][1000 genomes]
rs11631257	0.82[ASN][1000 genomes]
rs11631497	0.82[ASN][1000 genomes]
rs11632460	0.82[ASN][1000 genomes]
rs11634036	0.82[ASN][1000 genomes]
rs11634681	0.80[ASN][1000 genomes]
rs11636674	0.82[ASN][1000 genomes]
rs11636716	0.82[ASN][1000 genomes]
rs11636798	0.82[ASN][1000 genomes]
rs11638080	0.82[ASN][1000 genomes]
rs11638211	0.82[ASN][1000 genomes]
rs12913565	0.81[ASN][1000 genomes]
rs12917374	0.82[ASN][1000 genomes]
rs34390915	0.81[ASN][1000 genomes]
rs36004058	0.82[ASN][1000 genomes]
rs56086218	0.82[ASN][1000 genomes]
rs56236273	0.89[EUR][1000 genomes]
rs56306531	0.89[EUR][1000 genomes]
rs58484246	0.85[EUR][1000 genomes]
rs59800030	0.84[EUR][1000 genomes]
rs66870189	0.83[ASN][1000 genomes]
rs66912732	0.80[ASN][1000 genomes]
rs66919218	0.82[ASN][1000 genomes]
rs67149073	0.82[ASN][1000 genomes]
rs67542351	0.82[ASN][1000 genomes]
rs67695074	0.82[ASN][1000 genomes]
rs7162050	0.82[ASN][1000 genomes]
rs7162759	0.82[ASN][1000 genomes]
rs7162953	0.81[ASN][1000 genomes]
rs7163749	0.82[ASN][1000 genomes]
rs7164745	0.82[ASN][1000 genomes]
rs7166001	0.82[ASN][1000 genomes]
rs7166045	0.82[ASN][1000 genomes]
rs7167974	0.81[ASN][1000 genomes]
rs7169924	0.82[ASN][1000 genomes]
rs7169938	0.82[ASN][1000 genomes]
rs7170313	0.82[ASN][1000 genomes]
rs7170395	0.80[ASN][1000 genomes]
rs7170926	0.81[ASN][1000 genomes]
rs7172391	0.82[ASN][1000 genomes]
rs7174101	0.82[ASN][1000 genomes]
rs7177210	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7178072	0.82[ASN][1000 genomes]
rs7179489	0.81[ASN][1000 genomes]
rs7180209	0.81[ASN][1000 genomes]
rs7181288	0.81[ASN][1000 genomes]
rs7182730	0.82[ASN][1000 genomes]
rs7182850	0.82[ASN][1000 genomes]
rs7183007	0.82[ASN][1000 genomes]
rs7494798	0.81[ASN][1000 genomes]
rs7495240	0.82[ASN][1000 genomes]
rs7495317	0.82[ASN][1000 genomes]
rs7495389	0.82[ASN][1000 genomes]
rs7497385	0.81[ASN][1000 genomes]
rs7497443	0.82[ASN][1000 genomes]
rs8024352	0.82[ASN][1000 genomes]
rs8025341	0.82[ASN][1000 genomes]
rs8029633	0.82[ASN][1000 genomes]
rs8031657	0.82[ASN][1000 genomes]
rs8032779	0.82[ASN][1000 genomes]
rs8039813	0.82[ASN][1000 genomes]
rs8040300	0.82[ASN][1000 genomes]
rs8041925	0.80[ASN][1000 genomes]
rs9806691	0.82[ASN][1000 genomes]
rs982914	0.82[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	nsv456736	chr15:29327352-30208654	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv568675	chr15:29327352-30208654	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv903747	chr15:29361126-30008977	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv3364436	chr15:29459739-29853229	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv995038	chr15:29744279-30366124	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
6	nsv832943	chr15:29788334-29924284	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv456737	chr15:29812777-29875999	Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv568680	chr15:29812777-29875999	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv456738	chr15:29812777-29889806	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1038495	chr15:29825859-30351687	Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
11	nsv542293	chr15:29825859-30351687	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:29842000-29849000	Weak transcription	Pancreas	Pancrea
2	chr15:29843400-29848400	Weak transcription	Fetal Lung	lung
3	chr15:29846400-29849200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr15:29847000-29848400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr15:29847400-29848000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:29847800-29848200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr15:29847800-29848200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr15:29847800-29848200	Enhancers	Lung	lung
9	chr15:29847800-29848600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived

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