Variant report

Variant	rs73289925
Chromosome Location	chr7:16091361-16091362
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:22)

rs_ID	r²[population]
rs10452774	0.91[AFR][1000 genomes]
rs11975695	1.00[ASN][1000 genomes]
rs57367584	0.91[AFR][1000 genomes]
rs58468591	0.91[AFR][1000 genomes]
rs73289907	1.00[AFR][1000 genomes]
rs73289946	0.82[AFR][1000 genomes]
rs73289947	0.82[AFR][1000 genomes]
rs73289949	0.82[AFR][1000 genomes]
rs73289954	0.91[AFR][1000 genomes]
rs73289967	0.91[AFR][1000 genomes]
rs73289968	0.82[AFR][1000 genomes]
rs73291411	0.91[AFR][1000 genomes]
rs73291836	0.82[AFR][1000 genomes]
rs73291837	0.82[AFR][1000 genomes]
rs73291846	0.82[AFR][1000 genomes]
rs73291853	0.91[AFR][1000 genomes]
rs73291855	0.91[AFR][1000 genomes]
rs73291856	0.91[AFR][1000 genomes]
rs73291859	0.91[AFR][1000 genomes]
rs73291880	0.91[AFR][1000 genomes]
rs73291882	0.91[AFR][1000 genomes]
rs73291891	0.91[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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	nsv517991	chr7:16042596-16104327	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16084600-16091400	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:16086400-16100200	Weak transcription	NHDF-Ad	bronchial
3	chr7:16090600-16092800	Enhancers	Fetal Lung	lung
4	chr7:16090800-16092200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr7:16091000-16092000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:16091000-16092200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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