Variant report

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

rs_ID	r²[population]
rs10461438	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10461639	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10487616	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10940577	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11740778	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11744848	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12516650	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12659683	0.88[CEU][hapmap]
rs13169816	0.84[ASN][1000 genomes]
rs13175128	0.85[AMR][1000 genomes]
rs13181681	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1968422	0.88[CEU][hapmap]
rs34194290	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs34275130	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34645667	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34962616	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs35497805	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35602156	0.89[AMR][1000 genomes]
rs35694981	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4323195	0.81[CEU][hapmap]
rs56029970	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs66639127	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs68023515	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72751331	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525330	chr5:56931673-57320343	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2756302	chr5:56978143-57180143	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv830310	chr5:56989346-57176006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2763454	chr5:57006531-57161140	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57118000-57122600	Enhancers	HMEC	breast
2	chr5:57118600-57122400	Enhancers	HSMM	muscle
3	chr5:57118600-57122600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:57118600-57122600	Enhancers	NHEK	skin
5	chr5:57120600-57123000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:57121400-57132800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:57121600-57124000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr5:57121600-57128800	Weak transcription	NHLF	lung
9	chr5:57121800-57129000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr5:57122000-57124200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr5:57122000-57128000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:57122200-57122600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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