Variant report

Variant	rs4722547
Chromosome Location	chr7:25961082-25961083
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:25960299..25962459-chr7:25988241..25989933,2	K562	blood:

Variant related genes	Relation type
ENSG00000199085	Chromatin interaction
ENSG00000270933	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10258485	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10951118	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10951119	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10951120	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10951121	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11760762	1.00[ASN][1000 genomes]
rs11983649	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12700679	1.00[ASN][1000 genomes]
rs12700680	1.00[ASN][1000 genomes]
rs12700681	1.00[ASN][1000 genomes]
rs12700682	1.00[ASN][1000 genomes]
rs13226851	1.00[ASN][1000 genomes]
rs13231897	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17729097	1.00[ASN][1000 genomes]
rs1966841	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2391172	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2391175	1.00[ASN][1000 genomes]
rs2893222	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35336240	1.00[ASN][1000 genomes]
rs4000713	0.82[ASN][1000 genomes]
rs4236321	0.95[CEU][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4412274	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4422683	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4640955	0.88[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722543	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4722545	0.96[CEU][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722546	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722548	0.96[CEU][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4722550	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4722551	0.93[ASN][1000 genomes]
rs6461895	0.84[AFR][1000 genomes]
rs6461896	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6461897	0.82[AFR][1000 genomes]
rs66700050	1.00[ASN][1000 genomes]
rs67494041	1.00[ASN][1000 genomes]
rs67612070	0.87[AFR][1000 genomes]
rs6954557	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6977848	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs735316	1.00[ASN][1000 genomes]
rs7803374	0.93[EUR][1000 genomes]
rs7805035	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7810017	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7810027	0.82[AFR][1000 genomes]
rs997988	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs998357	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016813	chr7:25405859-26150509	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
2	nsv538803	chr7:25405859-26150509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	108 gene(s)	inside rSNPs	diseases
3	nsv830928	chr7:25820147-25965014	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	esv1792444	chr7:25902015-25964180	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	6 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	chr7:25961000-25964000	Enhancers	HMEC	breast

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