Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:41511986..41516214-chr5:41517012..41519107,3	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11746987	0.81[CEU][hapmap];0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13174932	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs191162	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs318022	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs318040	0.91[EUR][1000 genomes]
rs318042	0.80[CEU][hapmap];0.91[EUR][1000 genomes]
rs318043	0.90[EUR][1000 genomes]
rs318044	0.85[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs318045	0.89[CEU][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs318046	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs318047	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs318050	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs318051	0.81[AMR][1000 genomes]
rs318081	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs318084	0.85[CEU][hapmap]
rs318086	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs318087	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs35350798	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3907521	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913721	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4245981	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4315963	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4346812	0.89[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4957155	0.85[CEU][hapmap];0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv969281	chr5:41509672-41514269	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:41511600-41513000	Enhancers	Fetal Heart	heart
2	chr5:41511800-41513200	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr5:41511800-41513200	Weak transcription	Left Ventricle	heart
4	chr5:41511800-41521800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:41511800-41521800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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