Variant report

Variant	rs73275179
Chromosome Location	chr10:45631420-45631421
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs17157448	1.00[AMR][1000 genomes]
rs58720456	1.00[AMR][1000 genomes]
rs59116619	1.00[AMR][1000 genomes]
rs60354481	1.00[AMR][1000 genomes]
rs7072240	1.00[AMR][1000 genomes]
rs7091078	1.00[AMR][1000 genomes]
rs73275136	1.00[AMR][1000 genomes]
rs73275149	1.00[AMR][1000 genomes]
rs73275181	1.00[AFR][1000 genomes]
rs73275183	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73277360	1.00[AMR][1000 genomes]
rs73277362	1.00[AMR][1000 genomes]
rs73287567	1.00[AMR][1000 genomes]
rs73287569	1.00[AMR][1000 genomes]
rs73287573	1.00[AMR][1000 genomes]
rs73287578	1.00[AMR][1000 genomes]
rs73287579	1.00[AMR][1000 genomes]
rs73287582	1.00[AMR][1000 genomes]
rs73287584	1.00[AMR][1000 genomes]
rs73287589	1.00[AMR][1000 genomes]
rs73287599	1.00[AMR][1000 genomes]
rs73287601	1.00[AMR][1000 genomes]
rs73289603	1.00[AMR][1000 genomes]
rs73289605	1.00[AMR][1000 genomes]
rs73289609	1.00[AMR][1000 genomes]
rs73289610	1.00[AMR][1000 genomes]
rs73289682	1.00[AMR][1000 genomes]
rs73289688	1.00[AMR][1000 genomes]
rs73289692	1.00[AMR][1000 genomes]
rs73289694	1.00[AMR][1000 genomes]
rs73289697	1.00[AMR][1000 genomes]
rs73291604	1.00[AMR][1000 genomes]
rs73291615	1.00[AMR][1000 genomes]
rs73291688	1.00[AMR][1000 genomes]
rs73291689	1.00[AMR][1000 genomes]
rs7902733	1.00[AMR][1000 genomes]
rs7906497	1.00[AMR][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	nsv831848	chr10:45490176-45667670	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
2	esv2750897	chr10:45550145-45820136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
3	nsv947903	chr10:45598715-45657182	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr10:45630600-45632000	Enhancers	Fetal Kidney	kidney
2	chr10:45631000-45631600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr10:45631000-45631800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr10:45631000-45632000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:45631000-45632200	Enhancers	HUVEC	blood vessel

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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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