Variant report

Variant	rs73753928
Chromosome Location	chr5:15994965-15994966
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:15993011..15995112-chr5:15996938..15999410,2	MCF-7	breast:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs55704539	1.00[AMR][1000 genomes]
rs55762424	1.00[AMR][1000 genomes]
rs55792048	1.00[AMR][1000 genomes]
rs55842606	1.00[AMR][1000 genomes]
rs55900820	1.00[AMR][1000 genomes]
rs56804352	1.00[AMR][1000 genomes]
rs56917287	1.00[AMR][1000 genomes]
rs57018497	1.00[AMR][1000 genomes]
rs57456523	1.00[AMR][1000 genomes]
rs57789337	1.00[AMR][1000 genomes]
rs58172920	1.00[AMR][1000 genomes]
rs58451844	1.00[AMR][1000 genomes]
rs58539280	1.00[AMR][1000 genomes]
rs58700467	1.00[AMR][1000 genomes]
rs59015531	1.00[AMR][1000 genomes]
rs60910436	1.00[AMR][1000 genomes]
rs60964517	1.00[AMR][1000 genomes]
rs61489070	1.00[AMR][1000 genomes]
rs61619084	1.00[AMR][1000 genomes]
rs6861989	1.00[AMR][1000 genomes]
rs6888839	1.00[AMR][1000 genomes]
rs73752328	1.00[AMR][1000 genomes]
rs73752329	1.00[AMR][1000 genomes]
rs73752334	1.00[AMR][1000 genomes]
rs73752337	1.00[AMR][1000 genomes]
rs73752342	1.00[AMR][1000 genomes]
rs73752345	1.00[AMR][1000 genomes]
rs73752347	1.00[AMR][1000 genomes]
rs73752348	1.00[AMR][1000 genomes]
rs73752349	1.00[AMR][1000 genomes]
rs73752350	1.00[AMR][1000 genomes]
rs73752351	1.00[AMR][1000 genomes]
rs73752352	1.00[AMR][1000 genomes]
rs73752353	1.00[AMR][1000 genomes]
rs73752354	1.00[AMR][1000 genomes]
rs73752355	1.00[AMR][1000 genomes]
rs73752356	1.00[AMR][1000 genomes]
rs73752357	1.00[AMR][1000 genomes]
rs73752358	1.00[AMR][1000 genomes]
rs73752359	1.00[AMR][1000 genomes]
rs73752360	1.00[AMR][1000 genomes]
rs73752361	1.00[AMR][1000 genomes]
rs73752362	1.00[AMR][1000 genomes]
rs73752365	1.00[AMR][1000 genomes]
rs73752368	1.00[AMR][1000 genomes]
rs73752369	1.00[AMR][1000 genomes]
rs73752370	1.00[AMR][1000 genomes]
rs73752371	1.00[AMR][1000 genomes]
rs73752372	1.00[AMR][1000 genomes]
rs73752373	1.00[AMR][1000 genomes]
rs73752374	1.00[AMR][1000 genomes]
rs73752375	1.00[AMR][1000 genomes]
rs73752378	1.00[AMR][1000 genomes]
rs73752379	1.00[AMR][1000 genomes]
rs73752380	1.00[AMR][1000 genomes]
rs73752381	1.00[AMR][1000 genomes]
rs73752382	1.00[AMR][1000 genomes]
rs73752383	1.00[AMR][1000 genomes]
rs73752384	1.00[AMR][1000 genomes]
rs73752385	1.00[AMR][1000 genomes]
rs73752390	1.00[AMR][1000 genomes]
rs73752397	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73752399	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7710993	1.00[AMR][1000 genomes]
rs7730859	1.00[AMR][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:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15992800-15995800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr5:15992800-15996000	Enhancers	Fetal Heart	heart
3	chr5:15993400-15995400	Weak transcription	Liver	Liver
4	chr5:15993600-15995600	Enhancers	HUVEC	blood vessel
5	chr5:15994200-15995200	Weak transcription	NH-A	brain
6	chr5:15994400-15995400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:15994400-15995400	Weak transcription	NHEK	skin
8	chr5:15994800-15995400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links