Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs158414	0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs158416	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs158420	0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286745	1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286754	1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286758	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286782	0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286784	0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286787	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286789	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286792	1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs286795	1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs289231	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs289233	1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs56159704	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs57486712	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73778620	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73778623	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73778625	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73778642	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882682	chr5:107213361-107458336	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv534281	chr5:107357579-107674981	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1029650	chr5:107370079-107435314	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107388400-107510800	Weak transcription	Primary B cells from cord blood	blood
2	chr5:107396800-107409400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:107400200-107414600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:107403800-107429800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:107404000-107410200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr5:107404600-107407000	Enhancers	Dnd41	blood
7	chr5:107405600-107406800	Weak transcription	Primary T cells from cord blood	blood
8	chr5:107405600-107406800	Weak transcription	Fetal Kidney	kidney

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