Variant report

Variant	rs8181004
Chromosome Location	chr8:125300067-125300068
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11985656	0.80[CEU][hapmap]
rs13282297	0.81[EUR][1000 genomes]
rs4870895	0.84[EUR][1000 genomes]
rs6470236	0.87[CEU][hapmap];0.81[EUR][1000 genomes]
rs6997326	0.80[AFR][1000 genomes]
rs7016827	0.87[CEU][hapmap];0.83[EUR][1000 genomes]
rs7832694	0.83[AFR][1000 genomes]
rs9297692	0.81[CEU][hapmap]

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	esv2762769	chr8:125167256-125480574	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125295600-125306800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:125299600-125300400	Enhancers	NHDF-Ad	bronchial
3	chr8:125299800-125301600	Enhancers	K562	blood
4	chr8:125300000-125300600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:125300000-125300800	Weak transcription	Fetal Heart	heart

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

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