Variant report

Variant	rs7932759
Chromosome Location	chr11:47922715-47922716
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10769307	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10838790	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11039473	0.81[EUR][1000 genomes]
rs11039480	0.81[EUR][1000 genomes]
rs12270546	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12273589	0.83[ASN][1000 genomes]
rs1227997	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1227999	0.81[EUR][1000 genomes]
rs1228000	0.81[EUR][1000 genomes]
rs1228004	0.81[EUR][1000 genomes]
rs1228008	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1228018	0.86[EUR][1000 genomes]
rs1228019	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1228020	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1228021	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1228022	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1228023	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12290628	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12294218	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12295364	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1681604	0.81[EUR][1000 genomes]
rs1681627	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1681631	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1681637	0.81[EUR][1000 genomes]
rs1729281	0.81[EUR][1000 genomes]
rs1729294	0.82[EUR][1000 genomes]
rs1729297	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2626567	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2697810	0.81[EUR][1000 genomes]
rs2930188	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2930189	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2930195	0.81[EUR][1000 genomes]
rs2950888	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4752883	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4752886	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6485797	0.90[EUR][1000 genomes]
rs7113640	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7116080	0.83[ASN][1000 genomes]
rs7117644	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7119280	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7928153	0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7941441	0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052397	chr11:47675470-48594256	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	97 gene(s)	inside rSNPs	diseases
2	nsv530620	chr11:47765455-48664555	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
3	nsv1036992	chr11:47794621-48666024	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv1049835	chr11:47837089-47928822	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv541036	chr11:47837089-47928822	Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv897326	chr11:47891334-48035474	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1036451	chr11:47902321-48616646	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
8	nsv541037	chr11:47902321-48616646	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv1047490	chr11:47916708-48388686	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:47919200-47924000	Enhancers	Primary B cells from cord blood	blood
2	chr11:47919600-47923800	Enhancers	Primary B cells from peripheral blood	blood
3	chr11:47920600-47927000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:47921200-47923000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:47922200-47923000	Enhancers	GM12878-XiMat	blood
6	chr11:47922200-47927400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr11:47922200-47930000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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