Variant report

Variant	rs2668796
Chromosome Location	chr9:100483138-100483139
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:100477106..100478683-chr9:100480479..100483251,2	MCF-7	breast:
2	chr9:100458306..100461038-chr9:100482799..100485082,2	MCF-7	breast:
3	chr9:100480674..100483581-chr9:100484932..100487285,2	K562	blood:
4	chr9:100476626..100478474-chr9:100481765..100484991,3	MCF-7	breast:
5	chr9:100481943..100484213-chr9:100684517..100686414,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136936	Chromatin interaction
ENSG00000136932	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs2244833	0.98[EUR][1000 genomes]
rs2668794	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2668795	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2668797	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2668799	0.98[EUR][1000 genomes]
rs2668802	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2668803	0.98[EUR][1000 genomes]
rs2668804	0.99[EUR][1000 genomes]
rs2668805	0.98[EUR][1000 genomes]
rs2805768	0.95[EUR][1000 genomes]
rs2805769	0.95[EUR][1000 genomes]
rs2805770	0.95[EUR][1000 genomes]
rs2805771	0.97[EUR][1000 genomes]
rs2805773	0.98[EUR][1000 genomes]
rs2805778	0.99[EUR][1000 genomes]
rs2805780	0.99[EUR][1000 genomes]
rs2805781	0.99[EUR][1000 genomes]
rs2805782	0.98[EUR][1000 genomes]
rs2805784	0.99[EUR][1000 genomes]
rs2805789	0.99[EUR][1000 genomes]
rs2805790	0.99[EUR][1000 genomes]
rs2805794	0.99[EUR][1000 genomes]
rs2805795	0.88[EUR][1000 genomes]
rs2805796	0.99[EUR][1000 genomes]
rs2805797	0.99[EUR][1000 genomes]
rs2805798	0.99[EUR][1000 genomes]
rs2805799	0.99[EUR][1000 genomes]
rs2805800	0.99[EUR][1000 genomes]
rs2805809	0.99[EUR][1000 genomes]
rs2805811	0.98[EUR][1000 genomes]
rs2805812	0.98[EUR][1000 genomes]
rs2805813	0.98[EUR][1000 genomes]
rs2805814	0.98[EUR][1000 genomes]
rs2805815	0.98[EUR][1000 genomes]
rs2805816	0.99[EUR][1000 genomes]
rs2805817	0.99[EUR][1000 genomes]
rs2805818	0.98[EUR][1000 genomes]
rs2805820	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2805822	0.98[EUR][1000 genomes]
rs2808681	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2808682	1.00[EUR][1000 genomes]
rs2808684	1.00[EUR][1000 genomes]
rs2808688	0.98[EUR][1000 genomes]
rs2808693	0.98[EUR][1000 genomes]
rs2808695	0.98[EUR][1000 genomes]
rs2808696	0.98[EUR][1000 genomes]
rs2808697	0.98[EUR][1000 genomes]
rs2808698	0.98[EUR][1000 genomes]
rs2808699	0.95[EUR][1000 genomes]
rs2808700	0.95[EUR][1000 genomes]
rs2808702	0.95[EUR][1000 genomes]
rs62560521	0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7864297	0.90[EUR][1000 genomes]
rs7874554	0.99[EUR][1000 genomes]
rs7875449	0.99[EUR][1000 genomes]
rs7875482	0.99[EUR][1000 genomes]
rs953198	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv893610	chr9:100324086-100496160	Active TSS Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1043753	chr9:100458109-100599265	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv614934	chr9:100482976-100550253	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100483000-100483400	Weak transcription	HSMMtube	muscle

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