Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:82319110..82321365-chr15:82323956..82326070,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11855070	0.84[ASN][1000 genomes]
rs12902481	0.91[CEU][hapmap];0.80[EUR][1000 genomes]
rs12902907	0.83[CEU][hapmap]
rs2089009	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs28513741	0.80[ASN][1000 genomes]
rs28565868	0.80[ASN][1000 genomes]
rs28661931	0.85[ASN][1000 genomes]
rs2867552	1.00[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs34590775	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4325512	0.83[CEU][hapmap]
rs4778960	0.82[ASN][1000 genomes]
rs4778972	0.87[CHD][hapmap]
rs55732978	0.92[ASN][1000 genomes]
rs57570430	0.84[ASN][1000 genomes]
rs67548148	0.81[EUR][1000 genomes]
rs7162281	0.92[ASN][1000 genomes]
rs7171545	0.81[ASN][1000 genomes]
rs7171792	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73439249	0.98[ASN][1000 genomes]
rs73439254	0.99[ASN][1000 genomes]
rs8031443	0.81[CEU][hapmap]
rs8041457	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[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	nsv833067	chr15:82234980-82450485	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	esv2422504	chr15:82293064-82426400	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:82308200-82331600	Weak transcription	Fetal Brain Female	brain
2	chr15:82324000-82333200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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