Variant report

Variant	rs11929056
Chromosome Location	chr3:179819486-179819487
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10513775	1.00[EUR][1000 genomes]
rs11916351	1.00[EUR][1000 genomes]
rs11919129	1.00[EUR][1000 genomes]
rs11922852	1.00[EUR][1000 genomes]
rs11923122	1.00[EUR][1000 genomes]
rs11924444	0.97[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13320900	1.00[EUR][1000 genomes]
rs13324315	1.00[EUR][1000 genomes]
rs13327114	1.00[EUR][1000 genomes]
rs13327183	1.00[EUR][1000 genomes]
rs1543266	1.00[EUR][1000 genomes]
rs16831253	1.00[EUR][1000 genomes]
rs16831270	1.00[EUR][1000 genomes]
rs28373443	1.00[EUR][1000 genomes]
rs28377416	1.00[EUR][1000 genomes]
rs28545820	1.00[EUR][1000 genomes]
rs28623139	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28701054	1.00[EUR][1000 genomes]
rs28726303	1.00[EUR][1000 genomes]
rs28736488	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28758960	1.00[EUR][1000 genomes]
rs2879655	1.00[EUR][1000 genomes]
rs4499599	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs4621328	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs56406807	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs57727445	1.00[EUR][1000 genomes]
rs58213740	1.00[AMR][1000 genomes]
rs60008753	1.00[EUR][1000 genomes]
rs6765080	1.00[EUR][1000 genomes]
rs6765906	1.00[EUR][1000 genomes]
rs6776289	1.00[EUR][1000 genomes]
rs6777029	1.00[EUR][1000 genomes]
rs6779403	1.00[EUR][1000 genomes]
rs6787700	1.00[EUR][1000 genomes]
rs6795109	1.00[EUR][1000 genomes]
rs6797862	1.00[EUR][1000 genomes]
rs6804532	1.00[EUR][1000 genomes]
rs6809894	1.00[EUR][1000 genomes]
rs73055498	1.00[EUR][1000 genomes]
rs73885453	1.00[EUR][1000 genomes]
rs73885465	1.00[EUR][1000 genomes]
rs73885473	1.00[EUR][1000 genomes]
rs7612350	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7614651	1.00[EUR][1000 genomes]
rs7628443	1.00[EUR][1000 genomes]
rs7635460	1.00[EUR][1000 genomes]
rs7646970	1.00[EUR][1000 genomes]
rs9290693	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9290694	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9290698	1.00[EUR][1000 genomes]
rs9815044	1.00[EUR][1000 genomes]
rs9818567	1.00[EUR][1000 genomes]
rs9819315	1.00[EUR][1000 genomes]
rs9825264	1.00[EUR][1000 genomes]
rs9826576	1.00[EUR][1000 genomes]
rs9827331	1.00[EUR][1000 genomes]
rs9828833	1.00[EUR][1000 genomes]
rs9830454	1.00[EUR][1000 genomes]
rs9830623	1.00[EUR][1000 genomes]
rs9832076	1.00[EUR][1000 genomes]
rs9836941	1.00[EUR][1000 genomes]
rs9841268	1.00[EUR][1000 genomes]
rs9841642	1.00[EUR][1000 genomes]
rs9841905	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9842405	1.00[EUR][1000 genomes]
rs9844266	1.00[EUR][1000 genomes]
rs9844627	1.00[EUR][1000 genomes]
rs9844929	1.00[EUR][1000 genomes]
rs9845131	1.00[EUR][1000 genomes]
rs9846836	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9849568	1.00[EUR][1000 genomes]
rs9852228	1.00[EUR][1000 genomes]
rs9856995	0.90[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9858982	1.00[EUR][1000 genomes]
rs9859460	1.00[EUR][1000 genomes]
rs9861136	1.00[EUR][1000 genomes]
rs9862085	1.00[EUR][1000 genomes]
rs9863397	1.00[EUR][1000 genomes]
rs9863949	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9871675	1.00[EUR][1000 genomes]
rs9872191	1.00[EUR][1000 genomes]
rs9872323	1.00[EUR][1000 genomes]
rs9872365	1.00[EUR][1000 genomes]
rs9873559	1.00[EUR][1000 genomes]
rs9877145	1.00[EUR][1000 genomes]
rs9884094	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1000756	chr3:179672703-179827373	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1012880	chr3:179772283-179835563	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1012271	chr3:179806875-180234871	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr3:179810600-179843600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:179819000-179820200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links