Variant report

Variant	rs12174126
Chromosome Location	chr6:141474767-141474768
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:141474693..141476532-chr6:141479215..141481575,2	MCF-7	breast:

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs1414120	0.86[ASN][1000 genomes]
rs1452986	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1452993	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452995	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17070749	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1869273	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2167760	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2184531	0.86[ASN][1000 genomes]
rs57345729	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73776882	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73776884	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73778728	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73778734	0.91[ASN][1000 genomes]
rs73778750	0.86[ASN][1000 genomes]
rs7741795	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9321807	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9373299	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9373301	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9373303	0.91[ASN][1000 genomes]
rs9376580	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376582	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9376595	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9376596	0.91[ASN][1000 genomes]
rs9376598	0.91[ASN][1000 genomes]
rs9376604	0.87[ASN][1000 genomes]
rs9385936	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9385946	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9385947	0.89[ASN][1000 genomes]
rs9389877	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9389878	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9389880	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9389891	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9389898	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9389899	0.89[ASN][1000 genomes]
rs9389900	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9389902	0.91[ASN][1000 genomes]
rs9389903	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9399349	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9399351	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9399359	0.86[ASN][1000 genomes]
rs9399360	0.86[ASN][1000 genomes]
rs9403265	0.95[ASN][1000 genomes]
rs9403277	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9403283	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9403285	0.84[ASN][1000 genomes]
rs9403289	0.82[ASN][1000 genomes]
rs967794	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs967795	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs967796	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019459	chr6:141051249-141862727	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv538453	chr6:141051249-141862727	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv532070	chr6:141057326-141865359	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1025922	chr6:141090901-141865360	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv538454	chr6:141090901-141865360	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1028540	chr6:141121435-141740831	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv604780	chr6:141126080-141740918	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv1033387	chr6:141130072-141742682	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1030686	chr6:141130072-141749079	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1024981	chr6:141134064-141742682	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv916684	chr6:141149976-141682411	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv532071	chr6:141150099-141682503	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1035133	chr6:141156919-141650334	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv1029033	chr6:141156919-141740831	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv886720	chr6:141328865-141725335	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv886721	chr6:141328865-141739208	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
17	nsv1029550	chr6:141372610-142029669	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
18	nsv830822	chr6:141387803-141542998	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv886725	chr6:141428255-141718812	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv886726	chr6:141428255-141764919	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:141472600-141475200	Enhancers	Fetal Heart	heart
2	chr6:141473000-141475200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr6:141473200-141474800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr6:141473200-141475000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:141473200-141475200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:141473200-141475200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr6:141473200-141475200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr6:141473200-141475200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr6:141473200-141475200	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr6:141473400-141475000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:141473400-141475200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:141473400-141475200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:141473600-141474800	Weak transcription	Gastric	stomach
14	chr6:141473600-141475200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr6:141473600-141475600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr6:141473600-141475800	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr6:141473600-141476600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr6:141473600-141485200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:141473600-141485200	Weak transcription	Left Ventricle	heart
20	chr6:141474000-141475000	Enhancers	Aorta	Aorta
21	chr6:141474000-141475200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:141474200-141475000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr6:141474200-141475000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr6:141474200-141475000	Enhancers	HUVEC	blood vessel
25	chr6:141474200-141475200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr6:141474400-141475200	Enhancers	Primary T cells fromperipheralblood	blood
27	chr6:141474600-141475000	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr6:141474600-141475000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links