Variant report

Variant	rs7325216
Chromosome Location	chr13:29609783-29609784
allele	C/T
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:15)

rs_ID	r²[population]
rs11840020	1.00[AMR][1000 genomes]
rs11841551	1.00[AMR][1000 genomes]
rs17072559	1.00[AMR][1000 genomes]
rs17072560	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17072573	1.00[AMR][1000 genomes]
rs17072578	1.00[AMR][1000 genomes]
rs58460051	1.00[AMR][1000 genomes]
rs60156590	1.00[AMR][1000 genomes]
rs6490341	1.00[AMR][1000 genomes]
rs6490342	1.00[AMR][1000 genomes]
rs7319939	1.00[AMR][1000 genomes]
rs7321572	1.00[AMR][1000 genomes]
rs73441370	1.00[AMR][1000 genomes]
rs73441387	1.00[AMR][1000 genomes]
rs9783547	0.91[AFR][1000 genomes];1.00[AMR][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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:29606200-29623600	Weak transcription	Aorta	Aorta
2	chr13:29609400-29613200	Weak transcription	Fetal Heart	heart

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