Variant report

Variant	rs9305758
Chromosome Location	chr21:17363400-17363401
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs56803200	1.00[EUR][1000 genomes]
rs60780925	1.00[EUR][1000 genomes]
rs9284475	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9305759	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][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	nsv1064664	chr21:17336936-17405756	Enhancers Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3376626	chr21:17363331-17365429	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17359000-17363600	Weak transcription	Fetal Kidney	kidney
2	chr21:17361000-17363400	Weak transcription	HUVEC	blood vessel
3	chr21:17363400-17365200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr21:17363400-17365600	Enhancers	Muscle Satellite Cultured Cells	--
5	chr21:17363400-17365600	Enhancers	HUVEC	blood vessel

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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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