Variant report

Variant	rs6983011
Chromosome Location	chr8:64059053-64059054
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10957275	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10957276	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12056437	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12056441	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12056447	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12542182	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12542741	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12547669	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12549833	0.89[EUR][1000 genomes]
rs12550222	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12550793	0.97[EUR][1000 genomes]
rs12677153	1.00[CEU][hapmap];0.84[EUR][1000 genomes]
rs12678231	0.89[EUR][1000 genomes]
rs1975246	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2241753	1.00[CEU][hapmap];0.80[CHB][hapmap];0.85[EUR][1000 genomes]
rs34803356	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3857972	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3929126	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4601308	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4739053	0.97[EUR][1000 genomes]
rs4739066	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs4739068	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs61223024	0.82[EUR][1000 genomes]
rs7000495	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7000788	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7000927	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7001014	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7011111	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs73254967	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73254968	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73684686	0.87[EUR][1000 genomes]
rs73684689	0.89[EUR][1000 genomes]
rs9643383	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9643384	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9643556	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9643557	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9643558	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9643559	0.82[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	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv465701	chr8:63951237-64080486	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv611448	chr8:63951237-64080486	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv890965	chr8:64006201-64104092	Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64058400-64059600	Enhancers	Placenta	Placenta
2	chr8:64058800-64059200	Enhancers	Adipose Nuclei	Adipose
3	chr8:64058800-64060000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:64058800-64060000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr8:64058800-64060000	Enhancers	NHDF-Ad	bronchial
6	chr8:64058800-64060000	Enhancers	Osteobl	bone
7	chr8:64059000-64059200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:64059000-64059200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:64059000-64059200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:64059000-64059400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr8:64059000-64059400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr8:64059000-64059600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:64059000-64060000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:64059000-64060000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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