Variant report

Variant	rs559580
Chromosome Location	chr10:44752078-44752079
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:44749530..44752176-chr10:44753699..44756216,2	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1159931	0.81[JPT][hapmap]
rs1632484	0.92[EUR][1000 genomes]
rs1657345	0.86[EUR][1000 genomes]
rs1746047	0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1746048	0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1746049	0.92[EUR][1000 genomes]
rs1746050	0.92[EUR][1000 genomes]
rs1746052	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2209065	0.81[JPT][hapmap]
rs2576354	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2576355	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2760670	0.95[ASN][1000 genomes]
rs2781543	0.83[ASN][1000 genomes]
rs473501	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs474281	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs479596	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs487465	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs492152	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs494207	0.95[ASN][1000 genomes]
rs498810	0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs501120	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs504799	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs510785	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs513391	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs518594	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs522293	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs534079	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs535176	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs535949	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541483	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs546659	0.95[ASN][1000 genomes]
rs554565	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs559469	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs573141	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs579058	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs583489	0.95[ASN][1000 genomes]
rs587375	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs604674	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs605414	0.93[ASN][1000 genomes]
rs605445	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs607363	1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs607592	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs607609	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs607760	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs617035	0.94[ASN][1000 genomes]
rs617542	0.95[ASN][1000 genomes]
rs620356	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs620828	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs622472	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs622956	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs634963	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs635612	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs646890	0.95[ASN][1000 genomes]
rs649192	0.95[ASN][1000 genomes]
rs665855	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670056	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs671765	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs683297	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs684196	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs684521	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs684666	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs687175	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs694425	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7082209	0.80[CHD][hapmap];0.95[JPT][hapmap]
rs800330	0.95[JPT][hapmap]
rs915083	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv1038511	chr10:44596885-44870030	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv508579	chr10:44709770-44799256	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44749000-44757600	Enhancers	HepG2	liver
2	chr10:44749400-44752200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr10:44749400-44753600	Weak transcription	Fetal Intestine Small	intestine
4	chr10:44749400-44754400	Weak transcription	Placenta	Placenta
5	chr10:44749400-44754600	Weak transcription	Pancreas	Pancrea
6	chr10:44749400-44756200	Weak transcription	Lung	lung
7	chr10:44749600-44753600	Weak transcription	Fetal Intestine Large	intestine
8	chr10:44749600-44756400	Weak transcription	Stomach Smooth Muscle	stomach
9	chr10:44749800-44756800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr10:44750000-44754400	Weak transcription	Liver	Liver
11	chr10:44750200-44756000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links