Variant report

Variant	rs73092693
Chromosome Location	chr1:216188456-216188457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17025843	0.91[AFR][1000 genomes]
rs17025852	0.91[AFR][1000 genomes]
rs17025869	0.96[AFR][1000 genomes]
rs17025907	1.00[AMR][1000 genomes]
rs17025937	1.00[AMR][1000 genomes]
rs17025950	1.00[AMR][1000 genomes]
rs4509554	1.00[AFR][1000 genomes]
rs58401403	1.00[AFR][1000 genomes]
rs60180090	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73092501	0.81[AFR][1000 genomes]
rs73092675	0.96[AFR][1000 genomes]
rs73092683	0.85[AFR][1000 genomes]
rs73092689	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73092691	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73094509	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7538298	1.00[AMR][1000 genomes]
rs7542948	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006504	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv535288	chr1:215890460-216642124	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv428599	chr1:216086224-216267211	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv873172	chr1:216144827-216281673	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv873173	chr1:216151789-216204488	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv873174	chr1:216151789-216211989	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216187200-216188600	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr1:216187200-216188800	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr1:216187200-216188800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr1:216187800-216188800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:216187800-216188800	Enhancers	H9 Cell Line	embryonic stem cell
6	chr1:216187800-216188800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr1:216188200-216188800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr1:216188200-216188800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr1:216188200-216189200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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