Variant report

Variant	rs6952618
Chromosome Location	chr7:27727799-27727800
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs56024856	1.00[AMR][1000 genomes]
rs57384233	1.00[AMR][1000 genomes]
rs58785596	1.00[AMR][1000 genomes]
rs6966984	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs73684029	1.00[AMR][1000 genomes]
rs73684034	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73684036	1.00[AMR][1000 genomes]
rs73684038	1.00[AMR][1000 genomes]
rs73684041	1.00[AMR][1000 genomes]
rs73684042	1.00[AMR][1000 genomes]
rs73684046	1.00[AMR][1000 genomes]
rs73684051	1.00[AMR][1000 genomes]
rs73684059	1.00[AMR][1000 genomes]
rs73684064	1.00[AMR][1000 genomes]
rs7789929	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949025	chr7:27578167-28075172	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27726200-27733000	Weak transcription	HepG2	liver
2	chr7:27726200-27733200	Weak transcription	Osteobl	bone
3	chr7:27726400-27728200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:27726400-27728400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:27727600-27727800	Enhancers	NHDF-Ad	bronchial
6	chr7:27727600-27729400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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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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