Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:118294565..118296440-chr7:118304514..118306764,2	K562	blood:
2	chr7:118289392..118292258-chr7:118304193..118306771,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11509197	0.84[EUR][1000 genomes]
rs11761992	0.88[EUR][1000 genomes]
rs11762065	0.86[EUR][1000 genomes]
rs11763035	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11767676	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs11771057	0.84[EUR][1000 genomes]
rs1996945	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs2030649	0.84[EUR][1000 genomes]
rs2049368	0.84[EUR][1000 genomes]
rs2063370	0.84[EUR][1000 genomes]
rs2175297	0.84[EUR][1000 genomes]
rs2175298	0.84[EUR][1000 genomes]
rs2175299	0.84[EUR][1000 genomes]
rs4730879	0.84[EUR][1000 genomes]
rs4730884	0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4730885	0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs55698509	0.84[EUR][1000 genomes]
rs56141723	0.84[EUR][1000 genomes]
rs57668449	0.84[EUR][1000 genomes]
rs58071836	0.84[EUR][1000 genomes]
rs58152297	0.84[EUR][1000 genomes]
rs62467289	0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs62467290	0.90[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs62470082	0.84[EUR][1000 genomes]
rs62470083	0.84[EUR][1000 genomes]
rs62470084	0.83[EUR][1000 genomes]
rs62470086	0.84[EUR][1000 genomes]
rs62470087	0.84[EUR][1000 genomes]
rs6949669	0.84[EUR][1000 genomes]
rs778876	0.83[EUR][1000 genomes]
rs7796854	0.88[EUR][1000 genomes]
rs960884	0.84[EUR][1000 genomes]
rs960886	0.84[EUR][1000 genomes]
rs9641606	0.84[EUR][1000 genomes]
rs9641607	0.83[EUR][1000 genomes]
rs9641609	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889093	chr7:117977091-118709754	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv831109	chr7:118300593-118501778	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	1 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	chr7:118304200-118304800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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