Variant report

Variant	rs62348126
Chromosome Location	chr5:15969138-15969139
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10037390	1.00[EUR][1000 genomes]
rs10041092	1.00[EUR][1000 genomes]
rs10475070	1.00[EUR][1000 genomes]
rs13357073	1.00[EUR][1000 genomes]
rs1354183	1.00[EUR][1000 genomes]
rs16867861	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16867864	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16867867	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs17525353	1.00[EUR][1000 genomes]
rs1875547	0.93[EUR][1000 genomes]
rs1875548	1.00[EUR][1000 genomes]
rs59174236	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59606669	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs62348127	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs62348128	1.00[EUR][1000 genomes]
rs62348129	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs62348130	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs62348131	1.00[EUR][1000 genomes]
rs62348154	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs62348155	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs62348156	1.00[EUR][1000 genomes]
rs62348157	0.87[EUR][1000 genomes]
rs62348158	1.00[EUR][1000 genomes]
rs62348504	0.93[EUR][1000 genomes]
rs62348505	0.93[EUR][1000 genomes]
rs62348508	0.87[EUR][1000 genomes]
rs62349962	0.93[EUR][1000 genomes]
rs73040691	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73040701	1.00[EUR][1000 genomes]
rs7709814	1.00[EUR][1000 genomes]
rs993537	0.87[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	nsv830216	chr5:15860662-16060420	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv427712	chr5:15883439-16055856	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15967000-15969200	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