Variant report

Variant	rs35769500
Chromosome Location	chr13:29526531-29526532
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12869570	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17072399	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2146141	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs327132	0.94[EUR][1000 genomes]
rs34889317	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs589511	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs590512	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs604014	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs633914	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71433292	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71433293	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71433294	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71433295	0.88[AMR][1000 genomes];0.97[EUR][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	nsv533835	chr13:29141132-29962069	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv561390	chr13:29486244-29563080	Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv520663	chr13:29515875-29557614	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29520600-29531000	Weak transcription	Aorta	Aorta
2	chr13:29526200-29527800	Enhancers	Fetal Heart	heart

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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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