Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs588674	1.00[EUR][1000 genomes]
rs590058	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs619595	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs634198	0.93[AFR][1000 genomes]
rs682746	1.00[EUR][1000 genomes]
rs6910647	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6941591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9320461	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481346	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481349	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481350	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9481351	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488162	1.00[EUR][1000 genomes]
rs9488166	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488170	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488175	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488179	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488180	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488182	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488183	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9488186	0.91[AMR][1000 genomes];1.00[EUR][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	nsv916294	chr6:113518489-113904305	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv830778	chr6:113662011-113729804	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1034256	chr6:113703567-113793790	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1021815	chr6:113703567-113799956	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:113718200-113727400	Weak transcription	Left Ventricle	heart
2	chr6:113725200-113727800	Enhancers	Fetal Stomach	stomach
3	chr6:113726000-113727800	Enhancers	Stomach Mucosa	stomach
4	chr6:113726200-113727400	Weak transcription	Esophagus	oesophagus
5	chr6:113726200-113728200	Enhancers	NHDF-Ad	bronchial
6	chr6:113726200-113736800	Weak transcription	Colon Smooth Muscle	Colon
7	chr6:113726400-113727600	Enhancers	Adipose Nuclei	Adipose
8	chr6:113726400-113728000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:113726800-113727200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:113726800-113727200	Weak transcription	Fetal Kidney	kidney
11	chr6:113726800-113727400	Enhancers	Fetal Lung	lung
12	chr6:113726800-113727600	Enhancers	Ovary	ovary
13	chr6:113726800-113728200	Enhancers	NHLF	lung

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