Variant report

Variant	rs6492714
Chromosome Location	chr13:95207513-95207514
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	chr13:95201752..95203295-chr13:95205384..95208174,2	MCF-7	breast:

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs1408995	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17181801	0.84[ASN][1000 genomes]
rs17181808	0.84[ASN][1000 genomes]
rs1886787	0.81[ASN][1000 genomes]
rs1886789	0.81[ASN][1000 genomes]
rs1891099	0.89[ASN][1000 genomes]
rs1891100	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2389132	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2389133	0.81[ASN][1000 genomes]
rs2389134	0.82[ASN][1000 genomes]
rs2389135	0.86[ASN][1000 genomes]
rs2389137	0.83[ASN][1000 genomes]
rs2389138	0.83[ASN][1000 genomes]
rs2389139	0.89[ASN][1000 genomes]
rs2892688	0.86[ASN][1000 genomes]
rs34536649	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4142020	0.86[ASN][1000 genomes]
rs4142021	0.86[ASN][1000 genomes]
rs4411370	0.89[ASN][1000 genomes]
rs4442657	0.87[ASN][1000 genomes]
rs4553470	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6492711	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs717769	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7317805	0.85[ASN][1000 genomes]
rs7318895	0.84[ASN][1000 genomes]
rs7323407	0.84[ASN][1000 genomes]
rs7325171	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7326382	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7327906	0.85[ASN][1000 genomes]
rs7329277	0.82[ASN][1000 genomes]
rs7330052	0.82[ASN][1000 genomes]
rs7330757	0.83[ASN][1000 genomes]
rs7334113	0.82[ASN][1000 genomes]
rs7334290	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7334716	0.82[ASN][1000 genomes]
rs7334829	0.82[ASN][1000 genomes]
rs7335126	0.82[ASN][1000 genomes]
rs7336995	0.84[ASN][1000 genomes]
rs7336997	0.84[ASN][1000 genomes]
rs7337026	0.82[ASN][1000 genomes]
rs7337275	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7338715	0.85[ASN][1000 genomes]
rs7338730	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7490774	0.82[ASN][1000 genomes]
rs7492025	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs767925	0.86[ASN][1000 genomes]
rs7997227	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7998655	0.85[EUR][1000 genomes]
rs8002991	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9284279	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9301971	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9301972	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9301973	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9301974	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9301975	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9556376	0.81[ASN][1000 genomes]
rs9556377	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9556378	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9556379	0.81[ASN][1000 genomes]
rs9556380	0.85[EUR][1000 genomes]
rs9556381	0.81[ASN][1000 genomes]
rs9556382	0.81[ASN][1000 genomes]
rs9556383	0.81[ASN][1000 genomes]
rs9556384	0.81[ASN][1000 genomes]
rs9556386	0.82[ASN][1000 genomes]
rs9556387	0.82[ASN][1000 genomes]
rs9556388	0.82[ASN][1000 genomes]
rs9556390	0.85[ASN][1000 genomes]
rs9556391	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9556392	0.85[ASN][1000 genomes]
rs9556397	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9556398	0.89[ASN][1000 genomes]
rs9561568	0.81[ASN][1000 genomes]
rs9561569	0.81[ASN][1000 genomes]
rs9561570	0.81[ASN][1000 genomes]
rs9561571	0.81[ASN][1000 genomes]
rs9561572	0.81[ASN][1000 genomes]
rs9561573	0.81[ASN][1000 genomes]
rs9561574	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9561575	0.81[ASN][1000 genomes]
rs9561576	0.81[ASN][1000 genomes]
rs9561577	0.81[ASN][1000 genomes]
rs9561578	0.82[ASN][1000 genomes]
rs9561579	0.81[ASN][1000 genomes]
rs9561580	0.82[ASN][1000 genomes]
rs9561581	0.82[ASN][1000 genomes]
rs9561582	0.82[ASN][1000 genomes]
rs9561583	0.82[ASN][1000 genomes]
rs9561584	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9561588	0.82[ASN][1000 genomes]
rs9561589	0.84[ASN][1000 genomes]
rs9561591	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9561592	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9561593	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9561595	0.85[ASN][1000 genomes]
rs9561596	0.85[ASN][1000 genomes]
rs9561597	0.85[ASN][1000 genomes]
rs9561599	0.86[ASN][1000 genomes]
rs9561600	0.86[ASN][1000 genomes]
rs9561601	0.86[ASN][1000 genomes]
rs9561602	0.86[ASN][1000 genomes]
rs9561603	0.83[ASN][1000 genomes]
rs9561604	0.84[ASN][1000 genomes]
rs9561605	0.84[ASN][1000 genomes]
rs9561606	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9561619	0.88[ASN][1000 genomes]
rs9561620	0.89[ASN][1000 genomes]
rs9561621	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9561622	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9561623	0.90[ASN][1000 genomes]
rs9561625	0.90[ASN][1000 genomes]
rs9561626	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9590029	0.86[ASN][1000 genomes]
rs9590030	0.86[ASN][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	esv34004	chr13:94906537-95392644	Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv562756	chr13:95178317-95238154	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv832685	chr13:95179676-95279966	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv832686	chr13:95206742-95400992	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95202400-95208800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr13:95202600-95221400	Weak transcription	Gastric	stomach
3	chr13:95202800-95208000	Weak transcription	Adipose Nuclei	Adipose
4	chr13:95202800-95208200	Weak transcription	Brain Germinal Matrix	brain
5	chr13:95202800-95210400	Weak transcription	Thymus	Thymus
6	chr13:95202800-95221400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr13:95202800-95222000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:95202800-95223600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr13:95203000-95221200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr13:95203000-95221400	Weak transcription	Fetal Intestine Small	intestine
11	chr13:95203000-95222400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr13:95203200-95220800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr13:95203200-95220800	Weak transcription	Fetal Intestine Large	intestine
14	chr13:95203200-95222200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr13:95203400-95222400	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr13:95203400-95222600	Weak transcription	A549	lung
17	chr13:95204800-95214000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr13:95205000-95208600	Weak transcription	Placenta	Placenta
19	chr13:95205200-95211200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:95206600-95207600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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