Variant report

Variant	rs7706560
Chromosome Location	chr5:59579719-59579720
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs13165296	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13168619	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13172481	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34038162	0.92[EUR][1000 genomes]
rs35335033	0.81[EUR][1000 genomes]
rs35644384	0.92[EUR][1000 genomes]
rs35914313	0.92[EUR][1000 genomes]
rs4502776	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4699954	0.85[EUR][1000 genomes]
rs56341652	0.92[EUR][1000 genomes]
rs6860626	0.92[EUR][1000 genomes]
rs6861084	0.92[EUR][1000 genomes]
rs6862735	0.92[EUR][1000 genomes]
rs6869495	0.81[EUR][1000 genomes]
rs71630006	0.92[EUR][1000 genomes]
rs7733705	0.92[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	nsv1025856	chr5:59188419-59928852	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv830316	chr5:59480269-59689829	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59559600-59584800	Weak transcription	Primary B cells from cord blood	blood
2	chr5:59567400-59581600	Weak transcription	Fetal Brain Male	brain
3	chr5:59575400-59580800	Weak transcription	Aorta	Aorta
4	chr5:59577800-59581400	Weak transcription	HepG2	liver
5	chr5:59578600-59581600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:59579400-59579800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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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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