Variant report

Variant	rs71527450
Chromosome Location	chr7:3614019-3614020
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	chr7:3608810..3611760-chr7:3613102..3614702,2	MCF-7	breast:

Extended variants
information (count: 186 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10215198	0.83[ASN][1000 genomes]
rs10226719	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10245071	0.84[ASN][1000 genomes]
rs10257937	0.85[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs10485876	0.89[ASN][1000 genomes]
rs10951265	0.89[ASN][1000 genomes]
rs10951266	0.89[ASN][1000 genomes]
rs10951272	0.89[ASN][1000 genomes]
rs10951273	0.89[ASN][1000 genomes]
rs11763915	0.89[ASN][1000 genomes]
rs11766767	0.86[ASN][1000 genomes]
rs11768609	0.89[ASN][1000 genomes]
rs11769660	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11770829	0.89[ASN][1000 genomes]
rs11771990	0.89[ASN][1000 genomes]
rs12531560	0.89[ASN][1000 genomes]
rs12533563	0.89[ASN][1000 genomes]
rs12534865	0.89[ASN][1000 genomes]
rs12535467	0.89[ASN][1000 genomes]
rs12536371	0.89[ASN][1000 genomes]
rs12536753	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12537980	0.89[ASN][1000 genomes]
rs12538202	0.89[ASN][1000 genomes]
rs12539289	0.89[ASN][1000 genomes]
rs12539805	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12540148	0.89[ASN][1000 genomes]
rs12540209	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12701005	0.92[ASN][1000 genomes]
rs12701014	0.84[ASN][1000 genomes]
rs13239833	0.89[ASN][1000 genomes]
rs13240060	0.89[ASN][1000 genomes]
rs13240393	0.92[ASN][1000 genomes]
rs13242531	0.89[ASN][1000 genomes]
rs17320730	0.84[ASN][1000 genomes]
rs1922011	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1922016	0.89[ASN][1000 genomes]
rs2002669	0.84[ASN][1000 genomes]
rs2033441	0.89[ASN][1000 genomes]
rs2082360	0.89[ASN][1000 genomes]
rs2099302	0.89[ASN][1000 genomes]
rs2341579	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2341580	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2614950	0.92[ASN][1000 genomes]
rs2614951	0.92[ASN][1000 genomes]
rs2614955	0.81[ASN][1000 genomes]
rs2686851	0.83[ASN][1000 genomes]
rs2705609	0.83[ASN][1000 genomes]
rs2705614	0.83[ASN][1000 genomes]
rs2880085	0.89[ASN][1000 genomes]
rs34108699	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs34188874	0.89[ASN][1000 genomes]
rs34263851	0.89[ASN][1000 genomes]
rs34369020	0.89[ASN][1000 genomes]
rs34703718	0.92[ASN][1000 genomes]
rs34784806	0.89[ASN][1000 genomes]
rs35513976	0.89[ASN][1000 genomes]
rs35635220	0.89[ASN][1000 genomes]
rs36005986	0.89[ASN][1000 genomes]
rs4342491	0.89[ASN][1000 genomes]
rs4719998	0.89[ASN][1000 genomes]
rs4719999	0.89[ASN][1000 genomes]
rs4720001	0.86[ASN][1000 genomes]
rs4722903	0.86[ASN][1000 genomes]
rs4722976	0.89[ASN][1000 genomes]
rs4722993	0.89[ASN][1000 genomes]
rs4722994	0.84[ASN][1000 genomes]
rs4722995	0.89[ASN][1000 genomes]
rs4722997	0.89[ASN][1000 genomes]
rs4723001	0.81[ASN][1000 genomes]
rs62437895	0.89[ASN][1000 genomes]
rs62437901	0.89[ASN][1000 genomes]
rs6462216	0.89[ASN][1000 genomes]
rs67062941	0.89[ASN][1000 genomes]
rs6956079	0.89[ASN][1000 genomes]
rs6974350	0.89[ASN][1000 genomes]
rs6974872	0.84[ASN][1000 genomes]
rs956393	0.89[ASN][1000 genomes]
rs968775	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:108 , 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:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3600600-3616600	Weak transcription	Gastric	stomach
2	chr7:3610200-3615800	Weak transcription	Pancreas	Pancrea
3	chr7:3610400-3614400	Weak transcription	HepG2	liver
4	chr7:3612400-3617000	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:3613200-3625200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:3613800-3615800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:3614000-3614400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:3614000-3614400	Weak transcription	Stomach Mucosa	stomach

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