Variant report

Variant	rs73650632
Chromosome Location	chr9:13762875-13762876
allele	A/C
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:24)

rs_ID	r²[population]
rs10961223	1.00[AFR][1000 genomes]
rs12002489	1.00[EUR][1000 genomes]
rs12005535	1.00[EUR][1000 genomes]
rs16930920	1.00[EUR][1000 genomes]
rs528841	1.00[EUR][1000 genomes]
rs55716496	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56145825	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56166354	1.00[EUR][1000 genomes]
rs56874646	1.00[AFR][1000 genomes]
rs57153569	1.00[EUR][1000 genomes]
rs591153	1.00[EUR][1000 genomes]
rs59355338	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59592609	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs598697	1.00[EUR][1000 genomes]
rs666487	1.00[EUR][1000 genomes]
rs7025657	1.00[EUR][1000 genomes]
rs73416910	1.00[EUR][1000 genomes]
rs73647698	1.00[AFR][1000 genomes]
rs73647702	1.00[AFR][1000 genomes]
rs73648007	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650630	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650634	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73650635	1.00[AFR][1000 genomes]
rs73650637	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892590	chr9:13689066-13777299	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1022001	chr9:13717736-13983738	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13758200-13787200	Weak transcription	Aorta	Aorta
2	chr9:13760000-13764600	Weak transcription	Fetal Muscle Leg	muscle
3	chr9:13762400-13763600	Enhancers	HSMMtube	muscle

Quick Search:

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

what's new

Quick links