Variant report

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

rs_ID	r²[population]
rs10866614	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs10866615	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11134476	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11134477	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11134478	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs11134479	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs11738159	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs12517071	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1363204	1.00[YRI][hapmap]
rs1421980	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1421981	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs1421985	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs1421988	0.83[CHB][hapmap];1.00[JPT][hapmap]
rs1592800	1.00[YRI][hapmap]
rs17526010	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2193981	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2909798	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs7378687	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7379874	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7380412	1.00[YRI][hapmap]

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	nsv462511	chr5:167275087-167324809	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
2	nsv600254	chr5:167275087-167324809	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
3	nsv830546	chr5:167303135-167456271	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167266600-167326200	Weak transcription	HMEC	breast
2	chr5:167285600-167325600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:167298000-167311000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr5:167299200-167310600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:167300000-167311000	Weak transcription	Fetal Lung	lung
6	chr5:167300200-167308600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr5:167300800-167310600	Strong transcription	NHEK	skin
8	chr5:167301800-167306000	Weak transcription	HSMM	muscle
9	chr5:167302000-167308400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr5:167303600-167308600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr5:167303800-167305800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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