Variant report

Variant	rs62434461
Chromosome Location	chr7:11588154-11588155
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10229585	0.92[ASN][1000 genomes]
rs10240390	0.86[EUR][1000 genomes]
rs10241518	1.00[ASN][1000 genomes]
rs10265301	0.92[ASN][1000 genomes]
rs10271276	1.00[ASN][1000 genomes]
rs10273150	0.92[ASN][1000 genomes]
rs10280808	0.92[ASN][1000 genomes]
rs10280951	0.92[ASN][1000 genomes]
rs10486150	0.81[ASN][1000 genomes]
rs12334075	0.92[ASN][1000 genomes]
rs13438231	0.86[EUR][1000 genomes]
rs1557878	0.89[ASN][1000 genomes]
rs17164717	0.86[EUR][1000 genomes]
rs17164840	0.92[ASN][1000 genomes]
rs17164850	0.81[ASN][1000 genomes]
rs1989990	0.92[ASN][1000 genomes]
rs1989991	0.92[ASN][1000 genomes]
rs2214589	0.92[ASN][1000 genomes]
rs5027108	1.00[ASN][1000 genomes]
rs62432827	0.95[EUR][1000 genomes]
rs62432828	0.95[EUR][1000 genomes]
rs62432829	0.95[EUR][1000 genomes]
rs62432831	1.00[EUR][1000 genomes]
rs62432834	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62432836	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62432838	1.00[ASN][1000 genomes]
rs62432854	1.00[ASN][1000 genomes]
rs62432855	1.00[ASN][1000 genomes]
rs62432856	1.00[ASN][1000 genomes]
rs62432859	0.90[EUR][1000 genomes]
rs62434462	0.92[ASN][1000 genomes]
rs62434463	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62434464	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62434466	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62434471	0.92[ASN][1000 genomes]
rs62434474	0.92[ASN][1000 genomes]
rs62434493	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62434494	0.90[EUR][1000 genomes]
rs62434495	0.90[EUR][1000 genomes]
rs62434496	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62434497	0.92[ASN][1000 genomes]
rs62434501	0.92[ASN][1000 genomes]
rs62434503	0.92[ASN][1000 genomes]
rs62434504	0.92[ASN][1000 genomes]
rs62434505	0.92[ASN][1000 genomes]
rs62434506	0.92[ASN][1000 genomes]
rs62434507	0.92[ASN][1000 genomes]
rs62434523	0.92[ASN][1000 genomes]
rs62434525	0.92[ASN][1000 genomes]
rs62434526	0.92[ASN][1000 genomes]
rs6945973	0.92[ASN][1000 genomes]
rs6957991	0.92[ASN][1000 genomes]
rs7455869	1.00[ASN][1000 genomes]
rs7458209	1.00[ASN][1000 genomes]
rs7781076	0.92[ASN][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	nsv1028326	chr7:11221209-11754436	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv538733	chr7:11221209-11754436	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1023665	chr7:11457493-11773517	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv887606	chr7:11473561-11771288	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	nsv1028614	chr7:11511684-11596934	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv464366	chr7:11522525-11602899	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv606200	chr7:11522525-11602899	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv1793156	chr7:11584813-11595992	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region	1 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	chr7:11570400-11592000	Weak transcription	Fetal Brain Male	brain
2	chr7:11577400-11615200	Weak transcription	Placenta	Placenta
3	chr7:11582800-11595000	Weak transcription	Fetal Kidney	kidney
4	chr7:11582800-11598600	Weak transcription	Fetal Lung	lung
5	chr7:11586000-11590400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:11586200-11592200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr7:11587400-11588400	Enhancers	HUVEC	blood vessel

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