Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:84751809..84754653-chr14:84755331..84758306,2	MCF-7	breast:

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

rs_ID	r²[population]
rs10129851	0.95[ASN][1000 genomes]
rs10132898	0.95[ASN][1000 genomes]
rs10134005	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10137608	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10145673	0.96[ASN][1000 genomes]
rs10150745	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17119896	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28399118	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28446157	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3935697	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4075208	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4277283	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4372623	0.96[ASN][1000 genomes]
rs7142508	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7143199	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7148565	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7154367	0.96[ASN][1000 genomes]
rs7157365	0.96[ASN][1000 genomes]
rs7157373	0.95[ASN][1000 genomes]
rs8005901	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8009583	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8012477	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8019836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][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	nsv902161	chr14:84699866-84769903	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv832845	chr14:84726378-84900199	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	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	chr14:84752400-84758800	Weak transcription	Adipose Nuclei	Adipose
2	chr14:84757200-84757400	Enhancers	HUES64 Cell Line	embryonic stem cell

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