Variant report

Variant	rs4460168
Chromosome Location	chr5:116681499-116681500
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:116680619..116683137-chr5:116684782..116686469,2	MCF-7	breast:
2	chr5:116680122..116681946-chr5:116688874..116691608,2	MCF-7	breast:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10036986	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10039799	0.98[ASN][1000 genomes]
rs10039823	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs10061651	0.94[ASN][1000 genomes]
rs10069843	0.98[ASN][1000 genomes]
rs10073605	0.82[ASN][1000 genomes]
rs11749394	0.98[ASN][1000 genomes]
rs13159487	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs13172380	0.91[ASN][1000 genomes]
rs13187413	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs34173130	0.98[ASN][1000 genomes]
rs34205076	0.98[ASN][1000 genomes]
rs34227028	0.80[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs34411893	0.88[ASN][1000 genomes]
rs34729533	0.95[ASN][1000 genomes]
rs34937570	0.98[ASN][1000 genomes]
rs35130393	0.83[ASN][1000 genomes]
rs35533033	0.80[ASN][1000 genomes]
rs35844713	0.88[ASN][1000 genomes]
rs36110927	0.82[ASN][1000 genomes]
rs4259204	0.98[ASN][1000 genomes]
rs4443456	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4448037	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4457117	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4458619	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4464733	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4464734	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4469226	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4481380	0.95[ASN][1000 genomes]
rs4498285	0.92[ASN][1000 genomes]
rs4547957	0.95[ASN][1000 genomes]
rs4552663	0.98[ASN][1000 genomes]
rs4563664	0.97[ASN][1000 genomes]
rs4566827	0.97[ASN][1000 genomes]
rs4568397	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs4593300	0.98[ASN][1000 genomes]
rs4623185	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs4629633	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs5011797	0.95[ASN][1000 genomes]
rs61332533	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs62380367	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6595039	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs6595040	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs6595041	0.92[ASN][1000 genomes]
rs6860005	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6869527	0.95[ASN][1000 genomes]
rs6870045	0.92[ASN][1000 genomes]
rs6870063	0.92[ASN][1000 genomes]
rs6879112	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6888983	0.92[ASN][1000 genomes]
rs71593206	0.98[ASN][1000 genomes]
rs7447809	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs7708255	0.94[ASN][1000 genomes]
rs7712311	0.98[ASN][1000 genomes]
rs7712524	0.98[ASN][1000 genomes]
rs7716581	0.91[ASN][1000 genomes]
rs7733520	0.83[AMR][1000 genomes]
rs7733545	0.89[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	nsv882755	chr5:116647725-116748877	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 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	chr5:116680200-116683000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:116680200-116683000	Weak transcription	HUES64 Cell Line	embryonic stem cell

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