Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:124270665..124272540-chr7:124297946..124299539,2	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11770045	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11972367	0.83[EUR][1000 genomes]
rs11975826	0.84[EUR][1000 genomes]
rs11977373	0.83[EUR][1000 genomes]
rs1357795	0.83[EUR][1000 genomes]
rs1404412	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1524762	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1917355	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1917360	0.83[EUR][1000 genomes]
rs1917363	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1917365	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1917366	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2030722	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28710176	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28729091	0.84[EUR][1000 genomes]
rs28830928	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2896356	0.84[EUR][1000 genomes]
rs56134204	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6972148	0.83[EUR][1000 genomes]
rs73221450	0.83[EUR][1000 genomes]
rs73221460	0.83[EUR][1000 genomes]
rs73221461	0.83[EUR][1000 genomes]
rs884805	0.83[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	nsv429809	chr7:123937674-124835925	Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	49 gene(s)	inside rSNPs	diseases
2	nsv831118	chr7:124172267-124347527	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3330349	chr7:124249050-124277678	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3331383	chr7:124249050-124281444	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:124270000-124271400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:124270600-124271600	Enhancers	Fetal Brain Female	brain

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