Variant report

Variant	rs9550429
Chromosome Location	chr13:29565916-29565917
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs17072532	1.00[ASN][1000 genomes]
rs28681163	1.00[ASN][1000 genomes]
rs3886729	1.00[ASN][1000 genomes]
rs3895287	1.00[ASN][1000 genomes]
rs4002260	1.00[ASN][1000 genomes]
rs4417411	1.00[ASN][1000 genomes]
rs56027878	1.00[ASN][1000 genomes]
rs74045516	1.00[ASN][1000 genomes]
rs9314926	1.00[ASN][1000 genomes]
rs9550430	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29564200-29566200	Weak transcription	Aorta	Aorta
2	chr13:29565000-29566800	Enhancers	Fetal Heart	heart
3	chr13:29565800-29566600	Enhancers	Liver	Liver

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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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