Variant report

Variant	rs9651372
Chromosome Location	chr10:23051222-23051223
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10508649	1.00[CEU][hapmap]
rs10508653	0.83[ASN][1000 genomes]
rs11013123	1.00[ASN][1000 genomes]
rs11013124	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11013125	0.83[ASN][1000 genomes]
rs12240894	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12248702	0.83[ASN][1000 genomes]
rs12256270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12266336	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12266776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12267858	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16922574	1.00[CEU][hapmap]
rs16922601	1.00[CEU][hapmap]
rs16922612	1.00[CEU][hapmap]
rs16922619	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs16922629	1.00[CEU][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16922641	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16922673	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16922694	0.83[ASN][1000 genomes]
rs16922697	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2032026	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2032027	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs55855627	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56310787	1.00[ASN][1000 genomes]
rs58587913	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58854363	0.83[EUR][1000 genomes]
rs59134467	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59278361	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59760845	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61295423	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61587496	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7078735	1.00[CEU][hapmap]
rs74121608	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74121610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74121611	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74121869	0.83[EUR][1000 genomes]
rs74121889	0.83[EUR][1000 genomes]
rs74121891	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74121893	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74121894	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74121897	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74125205	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74125206	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7914338	1.00[CEU][hapmap]
rs9651370	0.91[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	nsv831809	chr10:22918101-23069676	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv550210	chr10:23012096-23064702	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv550211	chr10:23020350-23079385	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv550212	chr10:23030282-23086690	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv894960	chr10:23049139-23113841	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv894961	chr10:23049139-23128475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv466833	chr10:23050683-23110797	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv894962	chr10:23050683-23113841	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv894963	chr10:23050683-23121820	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv894964	chr10:23050683-23128475	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	esv3401743	chr10:23051084-23051636	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23049000-23051800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr10:23050000-23051600	Enhancers	Brain Angular Gyrus	brain
3	chr10:23050000-23051600	Enhancers	Brain Substantia Nigra	brain
4	chr10:23050000-23052400	Enhancers	Brain Hippocampus Middle	brain
5	chr10:23050200-23051400	Enhancers	Brain Anterior Caudate	brain
6	chr10:23050200-23051800	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr10:23050400-23051400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr10:23050800-23051400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr10:23051200-23053200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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