Variant report

Variant	rs507809
Chromosome Location	chr6:54293766-54293767
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1648216	1.00[CEU][hapmap]
rs171488	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs171490	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs183108	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs183109	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs190274	0.81[EUR][1000 genomes]
rs190275	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs243742	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs243747	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs243750	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs243767	0.81[EUR][1000 genomes]
rs243797	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs243803	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs573110	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs669917	0.87[EUR][1000 genomes]
rs9767142	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]

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	nsv1067663	chr6:53796341-54449718	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529158	chr6:53796341-54449718	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv528901	chr6:54290333-54337130	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54291200-54293800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:54291600-54296200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:54291800-54294600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr6:54292000-54297000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:54292200-54295600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:54293000-54294200	Weak transcription	NHDF-Ad	bronchial
7	chr6:54293000-54296200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:54293400-54293800	Enhancers	Fetal Kidney	kidney
9	chr6:54293400-54294400	Enhancers	GM12878-XiMat	blood
10	chr6:54293600-54296000	Weak transcription	Osteobl	bone

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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