Variant report

Variant	rs13298146
Chromosome Location	chr9:7412183-7412184
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10116696	0.87[ASN][1000 genomes]
rs10121497	0.83[ASN][1000 genomes]
rs10976292	0.85[ASN][1000 genomes]
rs11789935	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11791635	0.83[ASN][1000 genomes]
rs11793437	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12338203	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12344690	0.85[ASN][1000 genomes]
rs12344766	0.86[ASN][1000 genomes]
rs12682909	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12682938	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12683302	0.89[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12684895	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12685065	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12685373	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13284744	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13285065	0.84[ASN][1000 genomes]
rs13288442	0.87[ASN][1000 genomes]
rs13290242	0.83[ASN][1000 genomes]
rs13290290	0.83[ASN][1000 genomes]
rs13291981	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13292143	0.84[ASN][1000 genomes]
rs13293332	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13294039	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13294606	0.83[ASN][1000 genomes]
rs13297315	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13298225	0.83[ASN][1000 genomes]
rs13298703	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13299416	0.84[ASN][1000 genomes]
rs13300293	0.84[ASN][1000 genomes]
rs13300332	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13300962	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13301053	0.84[ASN][1000 genomes]
rs13301132	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13301399	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13302304	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1926400	0.83[ASN][1000 genomes]
rs1926409	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1926412	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1926413	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2148349	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2148351	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2148352	0.80[AMR][1000 genomes]
rs2148354	0.83[ASN][1000 genomes]
rs4119627	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4631517	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4742345	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4742346	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4742350	0.82[ASN][1000 genomes]
rs5016529	0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs66825775	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7035570	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs767642	0.84[ASN][1000 genomes]
rs767643	0.82[ASN][1000 genomes]
rs7848304	0.86[ASN][1000 genomes]
rs7851639	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7857046	0.84[ASN][1000 genomes]
rs7860733	0.85[ASN][1000 genomes]
rs7867077	0.84[ASN][1000 genomes]
rs7868920	0.85[ASN][1000 genomes]
rs7869063	0.85[ASN][1000 genomes]
rs7871280	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7872416	0.85[ASN][1000 genomes]
rs7875445	0.84[ASN][1000 genomes]
rs7875457	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv613259	chr9:7032776-7541338	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv1015874	chr9:7048807-7434890	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv539971	chr9:7048807-7434890	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	esv2758178	chr9:7175387-7482982	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2759662	chr9:7175387-7482982	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	esv34566	chr9:7291742-7781370	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv818681	chr9:7292836-7781365	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1019226	chr9:7299548-7415463	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv539975	chr9:7299548-7415463	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv613262	chr9:7336443-7417689	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1033077	chr9:7358832-7990735	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
12	nsv539977	chr9:7358832-7990735	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7408000-7431200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links