Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:32727633..32729387-chr14:32733655..32736313,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10483404	0.98[ASN][1000 genomes]
rs12586272	0.85[EUR][1000 genomes]
rs12586994	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12587340	1.00[EUR][1000 genomes]
rs12590485	0.88[ASN][1000 genomes]
rs17098551	0.87[EUR][1000 genomes]
rs17098631	1.00[CEU][hapmap];0.87[CHB][hapmap];0.85[JPT][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17098636	0.94[ASN][1000 genomes]
rs17098637	0.88[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs17098675	0.93[ASN][1000 genomes]
rs1885719	0.87[ASN][1000 genomes]
rs1951679	0.88[ASN][1000 genomes]
rs28583364	0.89[ASN][1000 genomes]
rs4145676	1.00[EUR][1000 genomes]
rs60778747	0.87[ASN][1000 genomes]
rs61022282	0.93[EUR][1000 genomes]
rs6571501	0.88[CHB][hapmap];0.80[JPT][hapmap];0.90[ASN][1000 genomes]
rs7142879	0.86[ASN][1000 genomes]
rs7146618	0.95[ASN][1000 genomes]
rs7149287	0.89[ASN][1000 genomes]
rs7150633	0.87[ASN][1000 genomes]
rs7161530	0.87[CHB][hapmap]
rs74043711	0.92[ASN][1000 genomes]
rs74043719	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8007042	0.81[ASN][1000 genomes]
rs9788513	1.00[EUR][1000 genomes];1.00[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	esv3527777	chr14:32669175-32761850	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3527778	chr14:32669175-32761850	Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32719000-32737600	Weak transcription	Left Ventricle	heart
2	chr14:32728200-32742400	Weak transcription	Right Ventricle	heart
3	chr14:32729600-32739000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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