Variant report

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10484756	0.81[AMR][1000 genomes]
rs17053217	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054080	0.81[AMR][1000 genomes]
rs17054134	0.81[AMR][1000 genomes]
rs17054160	0.93[AMR][1000 genomes]
rs17054190	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054191	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054195	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17054204	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1970592	0.81[AMR][1000 genomes]
rs1999559	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2153990	0.81[AMR][1000 genomes]
rs56721799	0.83[EUR][1000 genomes]
rs62439182	0.88[EUR][1000 genomes]
rs62439186	0.88[EUR][1000 genomes]
rs6569472	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6917816	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6918236	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6918438	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6930721	0.81[AMR][1000 genomes]
rs6934463	0.82[AMR][1000 genomes]
rs6941470	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7738754	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026498	chr6:126812609-127397240	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1024206	chr6:126873187-127475713	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv538438	chr6:126873187-127475713	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1020322	chr6:127087551-127331285	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv604640	chr6:127227094-127298394	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:127235000-127240400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr6:127235400-127240800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:127236000-127240600	Weak transcription	Fetal Lung	lung
4	chr6:127236000-127241800	Enhancers	HUVEC	blood vessel
5	chr6:127236200-127240400	Weak transcription	NHDF-Ad	bronchial
6	chr6:127236200-127240600	Weak transcription	Fetal Stomach	stomach
7	chr6:127236400-127237200	Enhancers	H9 Cell Line	embryonic stem cell
8	chr6:127236600-127237000	Enhancers	HUES6 Cell Line	embryonic stem cell

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