Variant report

Variant	rs17133566
Chromosome Location	chr7:3612421-3612422
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	chr7:3610768..3613073-chr7:3628327..3630622,2	MCF-7	breast:

Extended variants
information (count: 201 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10215541	0.94[ASN][1000 genomes]
rs10215554	0.83[CHB][hapmap];0.85[CHD][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs10215632	0.97[ASN][1000 genomes]
rs10216009	0.89[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs10227151	0.89[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs10236989	0.95[ASN][1000 genomes]
rs10238783	0.85[JPT][hapmap]
rs10241070	0.95[ASN][1000 genomes]
rs10243981	0.83[CHB][hapmap];0.90[JPT][hapmap];0.94[ASN][1000 genomes]
rs10263702	0.80[CHB][hapmap];0.85[JPT][hapmap];0.86[YRI][hapmap];0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10264275	0.94[ASN][1000 genomes]
rs10272876	0.89[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs10277776	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10951254	0.82[CHD][hapmap];0.82[JPT][hapmap]
rs11531493	0.94[ASN][1000 genomes]
rs11767639	0.82[CHD][hapmap];0.82[JPT][hapmap]
rs12055947	0.86[JPT][hapmap]
rs12111969	0.83[CHB][hapmap];0.88[JPT][hapmap];0.83[ASN][1000 genomes]
rs12670592	0.95[ASN][1000 genomes]
rs12672248	0.90[JPT][hapmap]
rs1522505	0.85[JPT][hapmap]
rs1608136	0.90[JPT][hapmap]
rs16870900	0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs17133300	0.81[GIH][hapmap]
rs17133409	0.80[TSI][hapmap]
rs17133420	0.90[JPT][hapmap]
rs17133426	0.90[JPT][hapmap]
rs17133432	0.90[JPT][hapmap]
rs17133501	0.85[JPT][hapmap]
rs17133520	0.90[JPT][hapmap]
rs17133523	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs17133533	0.87[ASN][1000 genomes]
rs17133535	0.90[ASN][1000 genomes]
rs17133554	0.94[ASN][1000 genomes]
rs17133555	0.89[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs17133591	0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs17751535	0.85[TSI][hapmap]
rs1882429	0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs1922015	0.80[ASN][1000 genomes]
rs1922017	0.90[JPT][hapmap]
rs1922019	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs1991758	0.80[ASN][1000 genomes]
rs2016197	0.82[ASN][1000 genomes]
rs2141819	0.86[JPT][hapmap]
rs2141821	0.85[JPT][hapmap]
rs2141825	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2177168	0.86[JPT][hapmap]
rs2178626	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2272526	0.89[JPT][hapmap]
rs2272527	0.90[JPT][hapmap]
rs2341578	0.81[CHD][hapmap]
rs2614966	0.86[JPT][hapmap]
rs2705606	0.82[CHD][hapmap];0.86[JPT][hapmap]
rs28412607	0.93[ASN][1000 genomes]
rs28451147	0.93[ASN][1000 genomes]
rs28832366	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs3817615	0.81[CHD][hapmap]
rs4291167	0.84[JPT][hapmap]
rs4496870	0.85[JPT][hapmap]
rs4722952	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs5022333	0.83[ASN][1000 genomes]
rs56329315	0.82[ASN][1000 genomes]
rs56669571	0.82[ASN][1000 genomes]
rs56995955	0.84[ASN][1000 genomes]
rs57125879	0.81[ASN][1000 genomes]
rs57462209	0.96[ASN][1000 genomes]
rs57473088	0.81[ASN][1000 genomes]
rs57480717	0.82[ASN][1000 genomes]
rs58498999	0.85[ASN][1000 genomes]
rs59465686	0.84[ASN][1000 genomes]
rs60372133	0.81[ASN][1000 genomes]
rs61425932	0.82[ASN][1000 genomes]
rs6462121	0.85[JPT][hapmap]
rs6947615	0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs6959706	0.81[JPT][hapmap]
rs6961261	0.81[ASN][1000 genomes]
rs6964347	0.83[CHD][hapmap]
rs6966652	0.90[ASN][1000 genomes]
rs6971989	0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs73673633	0.82[ASN][1000 genomes]
rs73673634	0.82[ASN][1000 genomes]
rs7779462	0.81[ASN][1000 genomes]
rs7782934	0.81[ASN][1000 genomes]
rs7787559	0.89[JPT][hapmap]
rs7791215	0.82[ASN][1000 genomes]
rs7794992	0.82[ASN][1000 genomes]
rs7795323	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs7800962	0.85[JPT][hapmap]
rs7802868	0.85[ASN][1000 genomes]
rs7805598	0.85[JPT][hapmap]
rs7807210	0.81[CHD][hapmap]
rs9638859	0.83[ASN][1000 genomes]
rs9654994	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9771445	0.90[JPT][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv2764026	chr7:3365002-3618361	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv916071	chr7:3423207-3697428	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1034716	chr7:3512406-3616155	Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv887334	chr7:3531275-3635105	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv1023888	chr7:3539750-3638242	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1034298	chr7:3539750-3646251	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1029264	chr7:3549193-3622532	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv830888	chr7:3577214-3776276	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv1840932	chr7:3585560-3618827	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv1792280	chr7:3592290-3668229	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv605907	chr7:3598581-3614784	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv1022135	chr7:3601840-3618349	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv1020806	chr7:3602348-3614788	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
18	esv2757205	chr7:3602348-3630349	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv2759501	chr7:3602348-3630349	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv1017012	chr7:3602397-3638242	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv538679	chr7:3602397-3638242	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv605908	chr7:3605340-3615334	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv605909	chr7:3605340-3638547	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv1028640	chr7:3606640-3617998	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv1025521	chr7:3606640-3618349	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
26	esv1838607	chr7:3606640-3618361	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
27	esv2752641	chr7:3609495-3631115	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
28	esv1835418	chr7:3609712-3618143	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
29	nsv517279	chr7:3609712-3618143	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
30	nsv818474	chr7:3609712-3618143	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
31	esv2752926	chr7:3609712-3631115	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
32	esv2754251	chr7:3609712-3631115	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
33	esv1841681	chr7:3609821-3614788	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
34	nsv605910	chr7:3609821-3618143	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
35	esv1835447	chr7:3609821-3618361	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
36	nsv1017452	chr7:3609821-3624792	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
37	nsv1016783	chr7:3609821-3624853	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
38	nsv1030806	chr7:3609821-3625238	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
39	nsv1022755	chr7:3609821-3626615	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
40	nsv1015396	chr7:3609821-3626689	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
41	nsv948390	chr7:3609821-3734421	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
42	esv1838067	chr7:3609843-3618361	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
43	esv1838414	chr7:3609843-3618361	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
44	nsv442026	chr7:3609843-3618361	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
45	esv1812450	chr7:3609982-3617808	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
46	esv1795945	chr7:3610182-3617608	Enhancers ZNF genes & repeats Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
47	esv1806284	chr7:3610182-3617608	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
48	esv1819441	chr7:3610182-3617608	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
49	esv1829974	chr7:3610182-3617608	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
50	esv1850048	chr7:3610182-3617608	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3600600-3616600	Weak transcription	Gastric	stomach
2	chr7:3608000-3612800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:3609200-3614000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:3610000-3612800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:3610200-3615800	Weak transcription	Pancreas	Pancrea
6	chr7:3610400-3614400	Weak transcription	HepG2	liver
7	chr7:3612200-3613400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr7:3612400-3613400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr7:3612400-3617000	Weak transcription	H9 Cell Line	embryonic stem cell

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