Variant report

Variant	rs73289967
Chromosome Location	chr7:16131930-16131931
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10452774	1.00[AFR][1000 genomes]
rs57367584	1.00[AFR][1000 genomes]
rs58468591	1.00[AFR][1000 genomes]
rs59899265	0.83[AFR][1000 genomes]
rs73289907	0.91[AFR][1000 genomes]
rs73289925	0.91[AFR][1000 genomes]
rs73289946	0.91[AFR][1000 genomes]
rs73289947	0.91[AFR][1000 genomes]
rs73289949	0.91[AFR][1000 genomes]
rs73289954	1.00[AFR][1000 genomes]
rs73289968	0.91[AFR][1000 genomes]
rs73291411	1.00[AFR][1000 genomes]
rs73291476	0.81[AFR][1000 genomes]
rs73291836	0.91[AFR][1000 genomes]
rs73291837	0.91[AFR][1000 genomes]
rs73291846	0.91[AFR][1000 genomes]
rs73291853	1.00[AFR][1000 genomes]
rs73291855	1.00[AFR][1000 genomes]
rs73291856	1.00[AFR][1000 genomes]
rs73291859	1.00[AFR][1000 genomes]
rs73291880	1.00[AFR][1000 genomes]
rs73291882	1.00[AFR][1000 genomes]
rs73291891	1.00[AFR][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	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv949309	chr7:15986709-16236162	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv949555	chr7:16078412-16279290	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16122200-16133000	Weak transcription	Psoas Muscle	Psoas
2	chr7:16122400-16135400	Weak transcription	Left Ventricle	heart
3	chr7:16131000-16132400	Enhancers	HUVEC	blood vessel
4	chr7:16131200-16132000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr7:16131200-16133000	Enhancers	Fetal Lung	lung
6	chr7:16131400-16132000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:16131400-16132000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:16131400-16132000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:16131400-16132000	Active TSS	Right Atrium	heart
10	chr7:16131600-16135400	Weak transcription	Fetal Stomach	stomach
11	chr7:16131800-16138000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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